TY  - JOUR
AU  - Ivanović, Tijana
AU  - Popović, Daniela Ž.
AU  - Miladinović, Jelena
AU  - Miladinović, Zoran P.
AU  - Rajaković-Ognjanović, Vladana N.
AU  - Pastor, Ferenc
AU  - Mladenović, Anja
PY  - 2024-03
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/7259
AB  - This study present estimation of the thermodynamic parameters and the influence of ionic activity coefficient on the thermodynamic equilibrium constant of adsorption of phosphates on fly ash. The adsorption was conducted over a wide range of initial phosphate concentrations at different pH values pH = (3; 7; 10). The adsorption results were treated using the Langmuir, Freundlich and Sips adsorption isotherms, which provide information about the maximum adsorption capacity. The Langmuir and Sips isotherms were a satisfactory fit to the adsorption data, especially at pH = 3, with an acceptable regression coefficient over the entire concentration range, Langmuir (r2 = 0.9737) and Sips (r2 = 0.9969). The estimated maximum phosphate sorption capacity of fly ash was 6.21 ± 0.68 (mmol·g−1) according to Langmuir and 4.19 ± 0.16 (mmol·g−1) according to the Sips model, at pH = 3.0. However, there is no data in the published literature for estimating the thermodynamic parameters of the phosphate adsorption process using thermodynamic models for activity coefficients. Novel approach of this paper was determination of the thermodynamic equilibrium constant and Gibbs free energy, using the Pitzer ion-interaction model to predict the nature of adsorption. The Pitzer-ion interaction model was used for the mixed ionic systems, taking into consideration the effect of other present ions besides phosphates in the equilibrium solution resulting from fly ash desorption. The procedure for comprehensive estimation of the ion activity coefficient at maximum adsorption capacity and the dimensionless thermodynamic equilibrium constant using Langmuir's and Sips's constants was presented. The calculated value of the phosphate activity coefficient in the equilibrium solution was γH = 0.7003 ± 0.0027 and the converted molar activity coefficient was γH = 0.6903 ± 0.0027. The estimated values of Gibbs free energy were: ΔGL = −6.788 ± 0.521 kJ·mol−1 based on Langmuir equilibrium constant and ΔGa = −7.707 ± 0.527 kJ·mol−1 based on activity and thermodynamic equilibrium constant. According to Sips model, the adsorption process is even more spontaneous, with the Gibbs free energy calculated using the phosphate activity coefficient and the thermodynamic equilibrium constant, ΔGa = −9.707 ± 0.617 kJ·mol−1. Consideration of the ionic activity coefficient is particularly important for large, charged adsorbates at higher concentrations, as the absolute difference in free energy for adsorption is app. 12 %. The scientific contribution is reflected in obtaining the necessary and more accurate information for the improvement of adsorption processes and possibly for the upgrading of fly ash in overall wastewater treatment technology.
PB  - Elsevier B.V.
T2  - Journal of Molecular Liquids
T1  - Advanced thermodynamic approach to adsorption of charged adsorbates from aqueous electrolyte solutions
SP  - 124097
VL  - 397
DO  - 10.1016/j.molliq.2024.124097
ER  - 

@article{
author = "Ivanović, Tijana and Popović, Daniela Ž. and Miladinović, Jelena and Miladinović, Zoran P. and Rajaković-Ognjanović, Vladana N. and Pastor, Ferenc and Mladenović, Anja",
year = "2024-03",
abstract = "This study present estimation of the thermodynamic parameters and the influence of ionic activity coefficient on the thermodynamic equilibrium constant of adsorption of phosphates on fly ash. The adsorption was conducted over a wide range of initial phosphate concentrations at different pH values pH = (3; 7; 10). The adsorption results were treated using the Langmuir, Freundlich and Sips adsorption isotherms, which provide information about the maximum adsorption capacity. The Langmuir and Sips isotherms were a satisfactory fit to the adsorption data, especially at pH = 3, with an acceptable regression coefficient over the entire concentration range, Langmuir (r2 = 0.9737) and Sips (r2 = 0.9969). The estimated maximum phosphate sorption capacity of fly ash was 6.21 ± 0.68 (mmol·g−1) according to Langmuir and 4.19 ± 0.16 (mmol·g−1) according to the Sips model, at pH = 3.0. However, there is no data in the published literature for estimating the thermodynamic parameters of the phosphate adsorption process using thermodynamic models for activity coefficients. Novel approach of this paper was determination of the thermodynamic equilibrium constant and Gibbs free energy, using the Pitzer ion-interaction model to predict the nature of adsorption. The Pitzer-ion interaction model was used for the mixed ionic systems, taking into consideration the effect of other present ions besides phosphates in the equilibrium solution resulting from fly ash desorption. The procedure for comprehensive estimation of the ion activity coefficient at maximum adsorption capacity and the dimensionless thermodynamic equilibrium constant using Langmuir's and Sips's constants was presented. The calculated value of the phosphate activity coefficient in the equilibrium solution was γH = 0.7003 ± 0.0027 and the converted molar activity coefficient was γH = 0.6903 ± 0.0027. The estimated values of Gibbs free energy were: ΔGL = −6.788 ± 0.521 kJ·mol−1 based on Langmuir equilibrium constant and ΔGa = −7.707 ± 0.527 kJ·mol−1 based on activity and thermodynamic equilibrium constant. According to Sips model, the adsorption process is even more spontaneous, with the Gibbs free energy calculated using the phosphate activity coefficient and the thermodynamic equilibrium constant, ΔGa = −9.707 ± 0.617 kJ·mol−1. Consideration of the ionic activity coefficient is particularly important for large, charged adsorbates at higher concentrations, as the absolute difference in free energy for adsorption is app. 12 %. The scientific contribution is reflected in obtaining the necessary and more accurate information for the improvement of adsorption processes and possibly for the upgrading of fly ash in overall wastewater treatment technology.",
publisher = "Elsevier B.V.",
journal = "Journal of Molecular Liquids",
title = "Advanced thermodynamic approach to adsorption of charged adsorbates from aqueous electrolyte solutions",
pages = "124097",
volume = "397",
doi = "10.1016/j.molliq.2024.124097"
}

Ivanović, T., Popović, D. Ž., Miladinović, J., Miladinović, Z. P., Rajaković-Ognjanović, V. N., Pastor, F.,& Mladenović, A.. (2024-03). Advanced thermodynamic approach to adsorption of charged adsorbates from aqueous electrolyte solutions. in Journal of Molecular Liquids
Elsevier B.V.., 397, 124097.
https://doi.org/10.1016/j.molliq.2024.124097

Ivanović T, Popović DŽ, Miladinović J, Miladinović ZP, Rajaković-Ognjanović VN, Pastor F, Mladenović A. Advanced thermodynamic approach to adsorption of charged adsorbates from aqueous electrolyte solutions. in Journal of Molecular Liquids. 2024;397:124097.
doi:10.1016/j.molliq.2024.124097 .

Ivanović, Tijana, Popović, Daniela Ž., Miladinović, Jelena, Miladinović, Zoran P., Rajaković-Ognjanović, Vladana N., Pastor, Ferenc, Mladenović, Anja, "Advanced thermodynamic approach to adsorption of charged adsorbates from aqueous electrolyte solutions" in Journal of Molecular Liquids, 397 (2024-03):124097,
https://doi.org/10.1016/j.molliq.2024.124097 . .

TY  - JOUR
AU  - Kutyła, Dawid
AU  - Krstajić Pajić, Mila N.
AU  - Lačnjevac, Uroš Č.
AU  - Marzec, Mateusz M.
AU  - Elezović, Nevenka R.
AU  - Żabiński, Piotr
PY  - 2024-02
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6992
AB  - This study investigates the structure, electrochemical behavior and hydrogen evolution reaction (HER) performance of electrodeposited Ru–Co alloy coatings. The alloys were prepared from a 0.75 M Co2+ + 0.025 M Ru3+ solution at various potentials ranging from −0.5 to −1.2 V vs. SCE. Results reveal that the Ru and Co deposition processes are interdependent. The deposition of nobler Ru from the mixed metal solution reaches pure diffusion control already at −0.7 V compared to −1.0 V from a single Ru bath. On the other hand, Co deposition is significantly facilitated in the presence of Ru in the solution. Consequently, as the deposition potential changes from −0.6 to −1.0 V, Ru–Co solid solution coatings characterized by a distinct globular morphology are formed, with their Co content increasing from 22.1/7.4 to 70.2/86.1 wt% for the Cu/Ti2AlC MAX phase substrate applied. The alloy catalysts are found to show much better HER activity and stability in alkaline than in acidic solutions. The best Ru–Co@Ti2AlC sample, electrodeposited at −0.6 V, requires an overpotential of only −95 mV to deliver a current density of −100 mA cm−2 in 1 M KOH, thus outperforming most Ru–Co-based HER electrocatalysts reported to date.
PB  - Elsevier Ltd.
T2  - International Journal of Hydrogen Energy
T1  - Ru–Co alloy coatings electrodeposited on a MAX phase substrate as efficient catalysts for the hydrogen evolution reaction
EP  - 40
SP  - 28
VL  - 56
DO  - 10.1016/j.ijhydene.2023.11.296
ER  - 

@article{
author = "Kutyła, Dawid and Krstajić Pajić, Mila N. and Lačnjevac, Uroš Č. and Marzec, Mateusz M. and Elezović, Nevenka R. and Żabiński, Piotr",
year = "2024-02",
abstract = "This study investigates the structure, electrochemical behavior and hydrogen evolution reaction (HER) performance of electrodeposited Ru–Co alloy coatings. The alloys were prepared from a 0.75 M Co2+ + 0.025 M Ru3+ solution at various potentials ranging from −0.5 to −1.2 V vs. SCE. Results reveal that the Ru and Co deposition processes are interdependent. The deposition of nobler Ru from the mixed metal solution reaches pure diffusion control already at −0.7 V compared to −1.0 V from a single Ru bath. On the other hand, Co deposition is significantly facilitated in the presence of Ru in the solution. Consequently, as the deposition potential changes from −0.6 to −1.0 V, Ru–Co solid solution coatings characterized by a distinct globular morphology are formed, with their Co content increasing from 22.1/7.4 to 70.2/86.1 wt% for the Cu/Ti2AlC MAX phase substrate applied. The alloy catalysts are found to show much better HER activity and stability in alkaline than in acidic solutions. The best Ru–Co@Ti2AlC sample, electrodeposited at −0.6 V, requires an overpotential of only −95 mV to deliver a current density of −100 mA cm−2 in 1 M KOH, thus outperforming most Ru–Co-based HER electrocatalysts reported to date.",
publisher = "Elsevier Ltd.",
journal = "International Journal of Hydrogen Energy",
title = "Ru–Co alloy coatings electrodeposited on a MAX phase substrate as efficient catalysts for the hydrogen evolution reaction",
pages = "40-28",
volume = "56",
doi = "10.1016/j.ijhydene.2023.11.296"
}

Kutyła, D., Krstajić Pajić, M. N., Lačnjevac, U. Č., Marzec, M. M., Elezović, N. R.,& Żabiński, P.. (2024-02). Ru–Co alloy coatings electrodeposited on a MAX phase substrate as efficient catalysts for the hydrogen evolution reaction. in International Journal of Hydrogen Energy
Elsevier Ltd.., 56, 28-40.
https://doi.org/10.1016/j.ijhydene.2023.11.296

Kutyła D, Krstajić Pajić MN, Lačnjevac UČ, Marzec MM, Elezović NR, Żabiński P. Ru–Co alloy coatings electrodeposited on a MAX phase substrate as efficient catalysts for the hydrogen evolution reaction. in International Journal of Hydrogen Energy. 2024;56:28-40.
doi:10.1016/j.ijhydene.2023.11.296 .

Kutyła, Dawid, Krstajić Pajić, Mila N., Lačnjevac, Uroš Č., Marzec, Mateusz M., Elezović, Nevenka R., Żabiński, Piotr, "Ru–Co alloy coatings electrodeposited on a MAX phase substrate as efficient catalysts for the hydrogen evolution reaction" in International Journal of Hydrogen Energy, 56 (2024-02):28-40,
https://doi.org/10.1016/j.ijhydene.2023.11.296 . .

TY  - DATA
AU  - Ivanović, Tijana
AU  - Popović, Daniela Ž.
AU  - Miladinović, Jelena
AU  - Miladinović, Zoran P.
AU  - Rajaković-Ognjanović, Vladana N.
AU  - Pastor, Ferenc
AU  - Mladenović, Anja
PY  - 2024
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/7332
AB  - This study present estimation of the thermodynamic parameters and the influence of ionic activity coefficient on the thermodynamic equilibrium constant of adsorption of phosphates on fly ash. The adsorption was conducted over a wide range of initial phosphate concentrations at different pH values pH = (3; 7; 10). The adsorption results were treated using the Langmuir, Freundlich and Sips adsorption isotherms, which provide information about the maximum adsorption capacity. The Langmuir and Sips isotherms were a satisfactory fit to the adsorption data, especially at pH = 3, with an acceptable regression coefficient over the entire concentration range, Langmuir (r2 = 0.9737) and Sips (r2 = 0.9969). The estimated maximum phosphate sorption capacity of fly ash was 6.21 ± 0.68 (mmol·g−1) according to Langmuir and 4.19 ± 0.16 (mmol·g−1) according to the Sips model, at pH = 3.0. However, there is no data in the published literature for estimating the thermodynamic parameters of the phosphate adsorption process using thermodynamic models for activity coefficients. Novel approach of this paper was determination of the thermodynamic equilibrium constant and Gibbs free energy, using the Pitzer ion-interaction model to predict the nature of adsorption. The Pitzer-ion interaction model was used for the mixed ionic systems, taking into consideration the effect of other present ions besides phosphates in the equilibrium solution resulting from fly ash desorption. The procedure for comprehensive estimation of the ion activity coefficient at maximum adsorption capacity and the dimensionless thermodynamic equilibrium constant using Langmuir's and Sips's constants was presented. The calculated value of the phosphate activity coefficient in the equilibrium solution was γH = 0.7003 ± 0.0027 and the converted molar activity coefficient was γH = 0.6903 ± 0.0027. The estimated values of Gibbs free energy were: ΔGL = −6.788 ± 0.521 kJ·mol−1 based on Langmuir equilibrium constant and ΔGa = −7.707 ± 0.527 kJ·mol−1 based on activity and thermodynamic equilibrium constant. According to Sips model, the adsorption process is even more spontaneous, with the Gibbs free energy calculated using the phosphate activity coefficient and the thermodynamic equilibrium constant, ΔGa = −9.707 ± 0.617 kJ·mol−1. Consideration of the ionic activity coefficient is particularly important for large, charged adsorbates at higher concentrations, as the absolute difference in free energy for adsorption is app. 12 %. The scientific contribution is reflected in obtaining the necessary and more accurate information for the improvement of adsorption processes and possibly for the upgrading of fly ash in overall wastewater treatment technology.
PB  - Elsevier B.V.
T2  - Journal of Molecular Liquids
T1  - Supplementary material for the article: Ivanović, T.; Popović, D. Ž.; Miladinović, J.; Miladinović, Z. P.; Rajaković-Ognjanović, V. N.; Pastor, F. ; Mladenović, A. Advanced thermodynamic approach to adsorption of charged adsorbates from aqueous electrolyte solutions. Journal of Molecular Liquids 2024, 397, 124097. https://doi.org/10.1016/j.molliq.2024.124097
SP  - 124097
VL  - 397
UR  - https://hdl.handle.net/21.15107/rcub_technorep_7332
ER  - 

@misc{
author = "Ivanović, Tijana and Popović, Daniela Ž. and Miladinović, Jelena and Miladinović, Zoran P. and Rajaković-Ognjanović, Vladana N. and Pastor, Ferenc and Mladenović, Anja",
year = "2024",
abstract = "This study present estimation of the thermodynamic parameters and the influence of ionic activity coefficient on the thermodynamic equilibrium constant of adsorption of phosphates on fly ash. The adsorption was conducted over a wide range of initial phosphate concentrations at different pH values pH = (3; 7; 10). The adsorption results were treated using the Langmuir, Freundlich and Sips adsorption isotherms, which provide information about the maximum adsorption capacity. The Langmuir and Sips isotherms were a satisfactory fit to the adsorption data, especially at pH = 3, with an acceptable regression coefficient over the entire concentration range, Langmuir (r2 = 0.9737) and Sips (r2 = 0.9969). The estimated maximum phosphate sorption capacity of fly ash was 6.21 ± 0.68 (mmol·g−1) according to Langmuir and 4.19 ± 0.16 (mmol·g−1) according to the Sips model, at pH = 3.0. However, there is no data in the published literature for estimating the thermodynamic parameters of the phosphate adsorption process using thermodynamic models for activity coefficients. Novel approach of this paper was determination of the thermodynamic equilibrium constant and Gibbs free energy, using the Pitzer ion-interaction model to predict the nature of adsorption. The Pitzer-ion interaction model was used for the mixed ionic systems, taking into consideration the effect of other present ions besides phosphates in the equilibrium solution resulting from fly ash desorption. The procedure for comprehensive estimation of the ion activity coefficient at maximum adsorption capacity and the dimensionless thermodynamic equilibrium constant using Langmuir's and Sips's constants was presented. The calculated value of the phosphate activity coefficient in the equilibrium solution was γH = 0.7003 ± 0.0027 and the converted molar activity coefficient was γH = 0.6903 ± 0.0027. The estimated values of Gibbs free energy were: ΔGL = −6.788 ± 0.521 kJ·mol−1 based on Langmuir equilibrium constant and ΔGa = −7.707 ± 0.527 kJ·mol−1 based on activity and thermodynamic equilibrium constant. According to Sips model, the adsorption process is even more spontaneous, with the Gibbs free energy calculated using the phosphate activity coefficient and the thermodynamic equilibrium constant, ΔGa = −9.707 ± 0.617 kJ·mol−1. Consideration of the ionic activity coefficient is particularly important for large, charged adsorbates at higher concentrations, as the absolute difference in free energy for adsorption is app. 12 %. The scientific contribution is reflected in obtaining the necessary and more accurate information for the improvement of adsorption processes and possibly for the upgrading of fly ash in overall wastewater treatment technology.",
publisher = "Elsevier B.V.",
journal = "Journal of Molecular Liquids",
title = "Supplementary material for the article: Ivanović, T.; Popović, D. Ž.; Miladinović, J.; Miladinović, Z. P.; Rajaković-Ognjanović, V. N.; Pastor, F. ; Mladenović, A. Advanced thermodynamic approach to adsorption of charged adsorbates from aqueous electrolyte solutions. Journal of Molecular Liquids 2024, 397, 124097. https://doi.org/10.1016/j.molliq.2024.124097",
pages = "124097",
volume = "397",
url = "https://hdl.handle.net/21.15107/rcub_technorep_7332"
}

Ivanović, T., Popović, D. Ž., Miladinović, J., Miladinović, Z. P., Rajaković-Ognjanović, V. N., Pastor, F.,& Mladenović, A.. (2024). Supplementary material for the article: Ivanović, T.; Popović, D. Ž.; Miladinović, J.; Miladinović, Z. P.; Rajaković-Ognjanović, V. N.; Pastor, F. ; Mladenović, A. Advanced thermodynamic approach to adsorption of charged adsorbates from aqueous electrolyte solutions. Journal of Molecular Liquids 2024, 397, 124097. https://doi.org/10.1016/j.molliq.2024.124097. in Journal of Molecular Liquids
Elsevier B.V.., 397, 124097.
https://hdl.handle.net/21.15107/rcub_technorep_7332

Ivanović T, Popović DŽ, Miladinović J, Miladinović ZP, Rajaković-Ognjanović VN, Pastor F, Mladenović A. Supplementary material for the article: Ivanović, T.; Popović, D. Ž.; Miladinović, J.; Miladinović, Z. P.; Rajaković-Ognjanović, V. N.; Pastor, F. ; Mladenović, A. Advanced thermodynamic approach to adsorption of charged adsorbates from aqueous electrolyte solutions. Journal of Molecular Liquids 2024, 397, 124097. https://doi.org/10.1016/j.molliq.2024.124097. in Journal of Molecular Liquids. 2024;397:124097.
https://hdl.handle.net/21.15107/rcub_technorep_7332 .

Ivanović, Tijana, Popović, Daniela Ž., Miladinović, Jelena, Miladinović, Zoran P., Rajaković-Ognjanović, Vladana N., Pastor, Ferenc, Mladenović, Anja, "Supplementary material for the article: Ivanović, T.; Popović, D. Ž.; Miladinović, J.; Miladinović, Z. P.; Rajaković-Ognjanović, V. N.; Pastor, F. ; Mladenović, A. Advanced thermodynamic approach to adsorption of charged adsorbates from aqueous electrolyte solutions. Journal of Molecular Liquids 2024, 397, 124097. https://doi.org/10.1016/j.molliq.2024.124097" in Journal of Molecular Liquids, 397 (2024):124097,
https://hdl.handle.net/21.15107/rcub_technorep_7332 .

TY  - CONF
AU  - Milojković, Natalija D.
AU  - Simović, Bojana M.
AU  - Žunić, Milan M.
AU  - Radovanović, Lidija D.
AU  - Dapčević, Aleksandra H.
PY  - 2023
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/7403
AB  - Titan(IV)-oksid je jedan od najčešće korišćenih fotokatalizatora, dok za polipirol (PPy) postoje potvrde da je pogodan za ovu primenu. Cilj ovog rada bio je dobijanje kompozita TiO2/PPy sa boljom fotokatalitičkom aktivnosti u odnosu na TiO2. Kako bi se optimizovao sadržaj PPy u kompozitu, sintetisani su uzorci TiO2/x%PPy (x = 0, 0,5, 1, 1,5, 3, 5 mas.%), koji su okarakterisani TG/DTA, XRD, FTIR, FESEM i UV-Vis metodama, dok su njihova fotokatalitička svojstva ispitana kroz razgradnju tekstilne boje RO16. Nanokristalni TiO2 je dobijen u obliku anatasa veličine kristalita oko 2 nm, dok su izračunati parametri jedinične ćelije potvrdili da je kristalna struktura anatasa ostala nepromenjena nakon dodatka PPy. Gotovo svi uzorci (izuzev TiO2/3%PPy) su fotokatalitički aktivniji od TiO2, dok je TiO2/1%PPy pokazao najizraženiju fotokatalitičku aktivnost razgradivši 9 % boje nakon 75 min.
AB  - Titanium(IV) oxide is one of the most used photocatalysts while polypyrrole (PPy) is a promising material for photocatalytic application. The aim of this work was to obtain TiO2/PPy composites exhibiting higher photocatalytic activity than TiO2. In order to determine the optimal PPy content in a composite, TiO2/x%PPy (x = 0, 0.5, 1, 1.5, 3, 5 wt.%) samples were synthesized and characterized by TG/DTA, XRD, FTIR, FESEM and UV-Vis methods, while the photocatalytic behavior was examined towards the degradation of the textile dye RO16. Nanocrystalline TiO2 was obtained in anatase form with crystallite size around 26 nm and preserved anatase crystal structure despite the addition of PPy according to the calculated unit cell parameters. Almost all samples (except TiO2/3%PPy) showed better photocatalytic activity than TiO2 while the best photocatalytic activity was demonstrated by TiO2/1%PPy which degraded 98 % of the dye after 75 min.
PB  - Beograd : Srpsko hemijsko društvo = Serbian Chemical Society
C3  - Kratki izvodi radova ; Knjiga radova = Book of Abstracts ; Proceedings / 59. savetovanje Srpskog hemijskog društva, Novi Sad 1. i 2. jun 2023. godine = 59th meeting of the Serbian Chemical Society, Novi Sad, Serbia, June 1-2, 2023
T1  - Nanokompoziti TiO2/PPy za primenu u fotokatalizi
T1  - TiO2/PPy nanocomposites for photocatalytic application
SP  - 144
UR  - https://hdl.handle.net/21.15107/rcub_technorep_7403
ER  - 

@conference{
author = "Milojković, Natalija D. and Simović, Bojana M. and Žunić, Milan M. and Radovanović, Lidija D. and Dapčević, Aleksandra H.",
year = "2023",
abstract = "Titan(IV)-oksid je jedan od najčešće korišćenih fotokatalizatora, dok za polipirol (PPy) postoje potvrde da je pogodan za ovu primenu. Cilj ovog rada bio je dobijanje kompozita TiO2/PPy sa boljom fotokatalitičkom aktivnosti u odnosu na TiO2. Kako bi se optimizovao sadržaj PPy u kompozitu, sintetisani su uzorci TiO2/x%PPy (x = 0, 0,5, 1, 1,5, 3, 5 mas.%), koji su okarakterisani TG/DTA, XRD, FTIR, FESEM i UV-Vis metodama, dok su njihova fotokatalitička svojstva ispitana kroz razgradnju tekstilne boje RO16. Nanokristalni TiO2 je dobijen u obliku anatasa veličine kristalita oko 2 nm, dok su izračunati parametri jedinične ćelije potvrdili da je kristalna struktura anatasa ostala nepromenjena nakon dodatka PPy. Gotovo svi uzorci (izuzev TiO2/3%PPy) su fotokatalitički aktivniji od TiO2, dok je TiO2/1%PPy pokazao najizraženiju fotokatalitičku aktivnost razgradivši 9 % boje nakon 75 min., Titanium(IV) oxide is one of the most used photocatalysts while polypyrrole (PPy) is a promising material for photocatalytic application. The aim of this work was to obtain TiO2/PPy composites exhibiting higher photocatalytic activity than TiO2. In order to determine the optimal PPy content in a composite, TiO2/x%PPy (x = 0, 0.5, 1, 1.5, 3, 5 wt.%) samples were synthesized and characterized by TG/DTA, XRD, FTIR, FESEM and UV-Vis methods, while the photocatalytic behavior was examined towards the degradation of the textile dye RO16. Nanocrystalline TiO2 was obtained in anatase form with crystallite size around 26 nm and preserved anatase crystal structure despite the addition of PPy according to the calculated unit cell parameters. Almost all samples (except TiO2/3%PPy) showed better photocatalytic activity than TiO2 while the best photocatalytic activity was demonstrated by TiO2/1%PPy which degraded 98 % of the dye after 75 min.",
publisher = "Beograd : Srpsko hemijsko društvo = Serbian Chemical Society",
journal = "Kratki izvodi radova ; Knjiga radova = Book of Abstracts ; Proceedings / 59. savetovanje Srpskog hemijskog društva, Novi Sad 1. i 2. jun 2023. godine = 59th meeting of the Serbian Chemical Society, Novi Sad, Serbia, June 1-2, 2023",
title = "Nanokompoziti TiO2/PPy za primenu u fotokatalizi, TiO2/PPy nanocomposites for photocatalytic application",
pages = "144",
url = "https://hdl.handle.net/21.15107/rcub_technorep_7403"
}

Milojković, N. D., Simović, B. M., Žunić, M. M., Radovanović, L. D.,& Dapčević, A. H.. (2023). Nanokompoziti TiO2/PPy za primenu u fotokatalizi. in Kratki izvodi radova ; Knjiga radova = Book of Abstracts ; Proceedings / 59. savetovanje Srpskog hemijskog društva, Novi Sad 1. i 2. jun 2023. godine = 59th meeting of the Serbian Chemical Society, Novi Sad, Serbia, June 1-2, 2023
Beograd : Srpsko hemijsko društvo = Serbian Chemical Society., 144.
https://hdl.handle.net/21.15107/rcub_technorep_7403

Milojković ND, Simović BM, Žunić MM, Radovanović LD, Dapčević AH. Nanokompoziti TiO2/PPy za primenu u fotokatalizi. in Kratki izvodi radova ; Knjiga radova = Book of Abstracts ; Proceedings / 59. savetovanje Srpskog hemijskog društva, Novi Sad 1. i 2. jun 2023. godine = 59th meeting of the Serbian Chemical Society, Novi Sad, Serbia, June 1-2, 2023. 2023;:144.
https://hdl.handle.net/21.15107/rcub_technorep_7403 .

Milojković, Natalija D., Simović, Bojana M., Žunić, Milan M., Radovanović, Lidija D., Dapčević, Aleksandra H., "Nanokompoziti TiO2/PPy za primenu u fotokatalizi" in Kratki izvodi radova ; Knjiga radova = Book of Abstracts ; Proceedings / 59. savetovanje Srpskog hemijskog društva, Novi Sad 1. i 2. jun 2023. godine = 59th meeting of the Serbian Chemical Society, Novi Sad, Serbia, June 1-2, 2023 (2023):144,
https://hdl.handle.net/21.15107/rcub_technorep_7403 .

TY  - JOUR
AU  - Radovanović, Lidija
AU  - Radovanović, Željko
AU  - Simović, Bojana
AU  - Vasić, Milica V.
AU  - Balanč, Bojana
AU  - Dapčević, Aleksandra
AU  - Dramićanin, Miroslav D.
AU  - Rogan, Jelena
PY  - 2023
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5984
AB  - A biphasic [Mn(dipya)(H2O)4](tpht)/{[Zn(dipya)(tpht)]·H2O}n com­plex material, I (dipya = 2,2’-dipyridylamine, tpht2– = dianion of terephthalatic acid) was synthesized by ligand exchange reaction and characterized by XRPD and FTIR spectroscopy. A ZnO/ZnMn2O4 composite, II, has been prepared via thermal decomposition of I in an air atmosphere at 450 °C. XRPD, FTIR and FESEM analyses of II revealed the simultaneous presence of spherical nano­particles of wurtzite ZnO and elongated nanoparticles of spinel ZnMn2O4. The specific surface area of II was determined by the BET method, whereas the volume and average size of the mesopores were calculated in accordance with the BJH method. The measurements of the mean size, polydispersity index and zeta potential showed colloidal instability of II. Two band gap values of 2.4 and 3.3 eV were determined using UV–Vis diffuse reflectance spectroscopy, while the measurements of photoluminescence revealed that II is active in the blue region of the visible spectrum. Testing of composite II as a pigmentary material showed that it can be used for the colouring of a ceramic glaze.
AB  - Двофазни  [Mn(dipya)(H2O)4](tpht)/{[Zn(dipya)(tpht)]·H2O}n комплексни материјал, I,  (dipya  =  2,2’-дипиридиламин,  tpht2–  =  дианјон  1,4-бензендикарбоксилнекиселине) синтетисан је реакцијом измене лиганада и окарактерисан XRPD мeтoдоми FTIR спек-троскопијом. Композит ZnO/ZnMn2O4, II, добијен је термичком разградњом прекурcopa I у атмосфери ваздуха на  450  °C.  XRPD  мeтoдом,  FTIR  спектроскопијом и  FESEM  микроскопијом композита II утврђено је истовремено присуство сферних наночестица ZnO вирцитне структуре и издужених наночестица  ZnMn2O4 са структуром спинела. Специфична површина композита II одређена је BET методом, док су запремина и просечна величина мезопора израчунати у складу са  BJH  методом. Средња величина, индекс полидисперзије и цета потенцијал измерени су фотонском корелационом спектроскопијом и електрофоретским расејањем светлости и показали су нестабилност композита II. Вредности ширине забрањене зоне од  2,4  и  3,3  eV  одређене су  UV–Vis  дифузно-рефлексионом спектроскопијом, док су мерења фотолуминесценције показала да је композит II активан у плавој области видљивог дела спектра. Испитивање композита II као пигментног материјала показало је да се може користити за бојење керамичке глазуре.
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Structure and properties of ZnO/ZnMn2O4 composite obtained by thermal decomposition of terephthalate precursor
T1  - Структура и својства композита ZnO/ZnMn2O4 добијеног термичком разградњом терефталат-прекурсора
EP  - 325
IS  - 3
SP  - 313
VL  - 88
DO  - 10.2298/JSC221102090R
ER  - 

@article{
author = "Radovanović, Lidija and Radovanović, Željko and Simović, Bojana and Vasić, Milica V. and Balanč, Bojana and Dapčević, Aleksandra and Dramićanin, Miroslav D. and Rogan, Jelena",
year = "2023",
abstract = "A biphasic [Mn(dipya)(H2O)4](tpht)/{[Zn(dipya)(tpht)]·H2O}n com­plex material, I (dipya = 2,2’-dipyridylamine, tpht2– = dianion of terephthalatic acid) was synthesized by ligand exchange reaction and characterized by XRPD and FTIR spectroscopy. A ZnO/ZnMn2O4 composite, II, has been prepared via thermal decomposition of I in an air atmosphere at 450 °C. XRPD, FTIR and FESEM analyses of II revealed the simultaneous presence of spherical nano­particles of wurtzite ZnO and elongated nanoparticles of spinel ZnMn2O4. The specific surface area of II was determined by the BET method, whereas the volume and average size of the mesopores were calculated in accordance with the BJH method. The measurements of the mean size, polydispersity index and zeta potential showed colloidal instability of II. Two band gap values of 2.4 and 3.3 eV were determined using UV–Vis diffuse reflectance spectroscopy, while the measurements of photoluminescence revealed that II is active in the blue region of the visible spectrum. Testing of composite II as a pigmentary material showed that it can be used for the colouring of a ceramic glaze., Двофазни  [Mn(dipya)(H2O)4](tpht)/{[Zn(dipya)(tpht)]·H2O}n комплексни материјал, I,  (dipya  =  2,2’-дипиридиламин,  tpht2–  =  дианјон  1,4-бензендикарбоксилнекиселине) синтетисан је реакцијом измене лиганада и окарактерисан XRPD мeтoдоми FTIR спек-троскопијом. Композит ZnO/ZnMn2O4, II, добијен је термичком разградњом прекурcopa I у атмосфери ваздуха на  450  °C.  XRPD  мeтoдом,  FTIR  спектроскопијом и  FESEM  микроскопијом композита II утврђено је истовремено присуство сферних наночестица ZnO вирцитне структуре и издужених наночестица  ZnMn2O4 са структуром спинела. Специфична површина композита II одређена је BET методом, док су запремина и просечна величина мезопора израчунати у складу са  BJH  методом. Средња величина, индекс полидисперзије и цета потенцијал измерени су фотонском корелационом спектроскопијом и електрофоретским расејањем светлости и показали су нестабилност композита II. Вредности ширине забрањене зоне од  2,4  и  3,3  eV  одређене су  UV–Vis  дифузно-рефлексионом спектроскопијом, док су мерења фотолуминесценције показала да је композит II активан у плавој области видљивог дела спектра. Испитивање композита II као пигментног материјала показало је да се може користити за бојење керамичке глазуре.",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Structure and properties of ZnO/ZnMn2O4 composite obtained by thermal decomposition of terephthalate precursor, Структура и својства композита ZnO/ZnMn2O4 добијеног термичком разградњом терефталат-прекурсора",
pages = "325-313",
number = "3",
volume = "88",
doi = "10.2298/JSC221102090R"
}

Radovanović, L., Radovanović, Ž., Simović, B., Vasić, M. V., Balanč, B., Dapčević, A., Dramićanin, M. D.,& Rogan, J.. (2023). Structure and properties of ZnO/ZnMn2O4 composite obtained by thermal decomposition of terephthalate precursor. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 88(3), 313-325.
https://doi.org/10.2298/JSC221102090R

Radovanović L, Radovanović Ž, Simović B, Vasić MV, Balanč B, Dapčević A, Dramićanin MD, Rogan J. Structure and properties of ZnO/ZnMn2O4 composite obtained by thermal decomposition of terephthalate precursor. in Journal of the Serbian Chemical Society. 2023;88(3):313-325.
doi:10.2298/JSC221102090R .

Radovanović, Lidija, Radovanović, Željko, Simović, Bojana, Vasić, Milica V., Balanč, Bojana, Dapčević, Aleksandra, Dramićanin, Miroslav D., Rogan, Jelena, "Structure and properties of ZnO/ZnMn2O4 composite obtained by thermal decomposition of terephthalate precursor" in Journal of the Serbian Chemical Society, 88, no. 3 (2023):313-325,
https://doi.org/10.2298/JSC221102090R . .

TY  - JOUR
AU  - Simović, Bojana
AU  - Radovanović, Željko
AU  - Branković, Goran
AU  - Dapčević, Aleksandra
PY  - 2023
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6363
AB  - In this work, in order to improve the photocatalytic efficiency of ZnO, the optimal CeO2 content in ZnO powders was determined by varying the quantity of CeO2 from 0 to 10 mol%. The structural, microstructural, optical, textural, and photocatalytic properties of the hydrothermally obtained ZnO and CeO2/ZnO nanocomposites have been investigated by using the XRPD, FESEM, HRTEM/SAED, BET, and UV–Vis techniques. Detailed characterization revealed that CeO2, having spherical nanodots of about 5 nm with a large surface area, was distributed onto the ZnO surface, whose crystallites displayed a bimodal distribution, from nano-to micro-crystals. The morphology of ZnO is a combination of nanograins and microrods that further makes a 3-D tie-like morphology. The nanocomposite containing 5 mol% of CeO2 showed about 30% better photocatalytic efficiency in the degradation of Reactive Orange 16 dye compared to other samples under simulated solar radiation. In addition, the kinetics and mechanism of photocatalytic degradation were also proposed based on the photocatalytic activity and scavenger tests.
PB  - Elsevier Ltd.
T2  - Materials Science in Semiconductor Processing
T1  - Hydrothermally synthesized CeO2/ZnO nanocomposite photocatalysts for the enhanced degradation of Reactive Orange 16 dye
SP  - 107542
VL  - 162
DO  - 10.1016/j.mssp.2023.107542
ER  - 

@article{
author = "Simović, Bojana and Radovanović, Željko and Branković, Goran and Dapčević, Aleksandra",
year = "2023",
abstract = "In this work, in order to improve the photocatalytic efficiency of ZnO, the optimal CeO2 content in ZnO powders was determined by varying the quantity of CeO2 from 0 to 10 mol%. The structural, microstructural, optical, textural, and photocatalytic properties of the hydrothermally obtained ZnO and CeO2/ZnO nanocomposites have been investigated by using the XRPD, FESEM, HRTEM/SAED, BET, and UV–Vis techniques. Detailed characterization revealed that CeO2, having spherical nanodots of about 5 nm with a large surface area, was distributed onto the ZnO surface, whose crystallites displayed a bimodal distribution, from nano-to micro-crystals. The morphology of ZnO is a combination of nanograins and microrods that further makes a 3-D tie-like morphology. The nanocomposite containing 5 mol% of CeO2 showed about 30% better photocatalytic efficiency in the degradation of Reactive Orange 16 dye compared to other samples under simulated solar radiation. In addition, the kinetics and mechanism of photocatalytic degradation were also proposed based on the photocatalytic activity and scavenger tests.",
publisher = "Elsevier Ltd.",
journal = "Materials Science in Semiconductor Processing",
title = "Hydrothermally synthesized CeO2/ZnO nanocomposite photocatalysts for the enhanced degradation of Reactive Orange 16 dye",
pages = "107542",
volume = "162",
doi = "10.1016/j.mssp.2023.107542"
}

Simović, B., Radovanović, Ž., Branković, G.,& Dapčević, A.. (2023). Hydrothermally synthesized CeO2/ZnO nanocomposite photocatalysts for the enhanced degradation of Reactive Orange 16 dye. in Materials Science in Semiconductor Processing
Elsevier Ltd.., 162, 107542.
https://doi.org/10.1016/j.mssp.2023.107542

Simović B, Radovanović Ž, Branković G, Dapčević A. Hydrothermally synthesized CeO2/ZnO nanocomposite photocatalysts for the enhanced degradation of Reactive Orange 16 dye. in Materials Science in Semiconductor Processing. 2023;162:107542.
doi:10.1016/j.mssp.2023.107542 .

Simović, Bojana, Radovanović, Željko, Branković, Goran, Dapčević, Aleksandra, "Hydrothermally synthesized CeO2/ZnO nanocomposite photocatalysts for the enhanced degradation of Reactive Orange 16 dye" in Materials Science in Semiconductor Processing, 162 (2023):107542,
https://doi.org/10.1016/j.mssp.2023.107542 . .

TY  - JOUR
AU  - Krstajić Pajić, Mila N.
AU  - Dobrota, Ana S.
AU  - Mazare, Anca
AU  - Đurđić, Slađana
AU  - Hwang, Imgon
AU  - Skorodumova, Natalia V.
AU  - Manojlović, Dragan
AU  - Vasilić, Rastko
AU  - Pašti, Igor A.
AU  - Schmuki, Patrik
AU  - Lačnjevac, Uroš
PY  - 2023
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6576
AB  - Efficient cathodes for the hydrogen evolution reaction (HER) in acidic water electrolysis rely on the use of expensive platinum group metals (PGMs). However, to achieve economically viable operation, both the content of PGMs must be reduced and their intrinsically strong H adsorption mitigated. Herein, we show that the surface effects of hydrogenated TiO2 nanotube (TNT) arrays can make osmium, a so far less-explored PGM, a highly active HER electrocatalyst. These defect-rich TiO2 nanostructures provide an interactive scaffold for the galvanic deposition of Os particles with modulated adsorption properties. Through systematic investigations, we identify the synthesis conditions (OsCl3 concentration/temperature/reaction time) that yield a progressive improvement in Os deposition rate and mass loading, thereby decreasing the HER overpotential. At the same time, the Os particles deposited by this procedure remain mainly sub-nanometric and entirely cover the inner tube walls. An optimally balanced Os@TNT composite prepared at 3 mM/55 °C/30 min exhibits a record low overpotential (η) of 61 mV at a current density of 100 mA cm-2, a high mass activity of 20.8 A mgOs-1 at 80 mV, and a stable performance in an acidic medium. Density functional theory calculations indicate the existence of strong interactions between the hydrogenated TiO2 surface and small Os clusters, which may weaken the Os-H* binding strength and thus boost the intrinsic HER activity of Os centers. The results presented in this study offer new directions for the fabrication of cost-effective PGM-based catalysts and a better understanding of the synergistic electronic interactions at the PGM|TiO2 interface.
PB  - American Chemical Society
T1  - Activation of Osmium by the Surface Effects of Hydrogenated TiO2 Nanotube Arrays for Enhanced Hydrogen Evolution Reaction Performance
EP  - 31469
IS  - 26
SP  - 31459
VL  - 15
DO  - 10.1021/acsami.3c04498
ER  - 

@article{
author = "Krstajić Pajić, Mila N. and Dobrota, Ana S. and Mazare, Anca and Đurđić, Slađana and Hwang, Imgon and Skorodumova, Natalia V. and Manojlović, Dragan and Vasilić, Rastko and Pašti, Igor A. and Schmuki, Patrik and Lačnjevac, Uroš",
year = "2023",
abstract = "Efficient cathodes for the hydrogen evolution reaction (HER) in acidic water electrolysis rely on the use of expensive platinum group metals (PGMs). However, to achieve economically viable operation, both the content of PGMs must be reduced and their intrinsically strong H adsorption mitigated. Herein, we show that the surface effects of hydrogenated TiO2 nanotube (TNT) arrays can make osmium, a so far less-explored PGM, a highly active HER electrocatalyst. These defect-rich TiO2 nanostructures provide an interactive scaffold for the galvanic deposition of Os particles with modulated adsorption properties. Through systematic investigations, we identify the synthesis conditions (OsCl3 concentration/temperature/reaction time) that yield a progressive improvement in Os deposition rate and mass loading, thereby decreasing the HER overpotential. At the same time, the Os particles deposited by this procedure remain mainly sub-nanometric and entirely cover the inner tube walls. An optimally balanced Os@TNT composite prepared at 3 mM/55 °C/30 min exhibits a record low overpotential (η) of 61 mV at a current density of 100 mA cm-2, a high mass activity of 20.8 A mgOs-1 at 80 mV, and a stable performance in an acidic medium. Density functional theory calculations indicate the existence of strong interactions between the hydrogenated TiO2 surface and small Os clusters, which may weaken the Os-H* binding strength and thus boost the intrinsic HER activity of Os centers. The results presented in this study offer new directions for the fabrication of cost-effective PGM-based catalysts and a better understanding of the synergistic electronic interactions at the PGM|TiO2 interface.",
publisher = "American Chemical Society",
title = "Activation of Osmium by the Surface Effects of Hydrogenated TiO2 Nanotube Arrays for Enhanced Hydrogen Evolution Reaction Performance",
pages = "31469-31459",
number = "26",
volume = "15",
doi = "10.1021/acsami.3c04498"
}

Krstajić Pajić, M. N., Dobrota, A. S., Mazare, A., Đurđić, S., Hwang, I., Skorodumova, N. V., Manojlović, D., Vasilić, R., Pašti, I. A., Schmuki, P.,& Lačnjevac, U.. (2023). Activation of Osmium by the Surface Effects of Hydrogenated TiO2 Nanotube Arrays for Enhanced Hydrogen Evolution Reaction Performance. 
American Chemical Society., 15(26), 31459-31469.
https://doi.org/10.1021/acsami.3c04498

Krstajić Pajić MN, Dobrota AS, Mazare A, Đurđić S, Hwang I, Skorodumova NV, Manojlović D, Vasilić R, Pašti IA, Schmuki P, Lačnjevac U. Activation of Osmium by the Surface Effects of Hydrogenated TiO2 Nanotube Arrays for Enhanced Hydrogen Evolution Reaction Performance. 2023;15(26):31459-31469.
doi:10.1021/acsami.3c04498 .

Krstajić Pajić, Mila N., Dobrota, Ana S., Mazare, Anca, Đurđić, Slađana, Hwang, Imgon, Skorodumova, Natalia V., Manojlović, Dragan, Vasilić, Rastko, Pašti, Igor A., Schmuki, Patrik, Lačnjevac, Uroš, "Activation of Osmium by the Surface Effects of Hydrogenated TiO2 Nanotube Arrays for Enhanced Hydrogen Evolution Reaction Performance", 15, no. 26 (2023):31459-31469,
https://doi.org/10.1021/acsami.3c04498 . .

TY  - JOUR
AU  - Spasojević, Dragica
AU  - Prodanović, Olivera
AU  - Mutavdžić, Dragosav
AU  - Šekuljica, Nataša
AU  - Jovanović, Jelena
AU  - Maksimović, Vuk
AU  - Radotić, Ksenija
PY  - 2023
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6635
AB  - In recent years, versatile peroxidase (VP) has emerged as a promising enzyme for biotechnological applications, as it can oxidize lignin without the external mediators. To gain insights into the breakdown process of artificial lignin by VP, reaction between the two was studied. Degradation products were fractionated using ultrafiltration and analyzed by RP- high performance liquid chromatography with mass detection (HPLC-MS) chromatography. Four fractions were obtained based on their molecular sizes: >10, 3–10, 1–3, and <1 kDa. Interestingly, while VP did not significantly alter the yields of these fractions, the chromatograms revealed the presence of oligomers with different molecular weights (MWs) resulting from the enzymatic activity. The VP exhibits a dual role in its enzymatic activity: both degrading and synthesizing these oligomers. This was confirmed by principal component analysis (PCA). The positive correlations were found between certain oligomers (D1 and D2, D5 and D6, as well as between D7, D10, T2, and T4), suggesting their simultaneous degradation. On the other hand, a negative correlation was found between the monomer and some oligomers (D7, D10, T2, and T4), indicating the decomposition of these oligomers into monomers. These findings shed light on the intricate interplay between VP and artificial lignin, offering valuable insights for potential applications in lignin valorization.
PB  - John Wiley and Sons Inc
T2  - Biotechnology Journal
T1  - Two-way reaction of versatile peroxidase with artificial lignin enhances low-molecular weight fractions
DO  - 10.1002/biot.202300312
ER  - 

@article{
author = "Spasojević, Dragica and Prodanović, Olivera and Mutavdžić, Dragosav and Šekuljica, Nataša and Jovanović, Jelena and Maksimović, Vuk and Radotić, Ksenija",
year = "2023",
abstract = "In recent years, versatile peroxidase (VP) has emerged as a promising enzyme for biotechnological applications, as it can oxidize lignin without the external mediators. To gain insights into the breakdown process of artificial lignin by VP, reaction between the two was studied. Degradation products were fractionated using ultrafiltration and analyzed by RP- high performance liquid chromatography with mass detection (HPLC-MS) chromatography. Four fractions were obtained based on their molecular sizes: >10, 3–10, 1–3, and <1 kDa. Interestingly, while VP did not significantly alter the yields of these fractions, the chromatograms revealed the presence of oligomers with different molecular weights (MWs) resulting from the enzymatic activity. The VP exhibits a dual role in its enzymatic activity: both degrading and synthesizing these oligomers. This was confirmed by principal component analysis (PCA). The positive correlations were found between certain oligomers (D1 and D2, D5 and D6, as well as between D7, D10, T2, and T4), suggesting their simultaneous degradation. On the other hand, a negative correlation was found between the monomer and some oligomers (D7, D10, T2, and T4), indicating the decomposition of these oligomers into monomers. These findings shed light on the intricate interplay between VP and artificial lignin, offering valuable insights for potential applications in lignin valorization.",
publisher = "John Wiley and Sons Inc",
journal = "Biotechnology Journal",
title = "Two-way reaction of versatile peroxidase with artificial lignin enhances low-molecular weight fractions",
doi = "10.1002/biot.202300312"
}

Spasojević, D., Prodanović, O., Mutavdžić, D., Šekuljica, N., Jovanović, J., Maksimović, V.,& Radotić, K.. (2023). Two-way reaction of versatile peroxidase with artificial lignin enhances low-molecular weight fractions. in Biotechnology Journal
John Wiley and Sons Inc..
https://doi.org/10.1002/biot.202300312

Spasojević D, Prodanović O, Mutavdžić D, Šekuljica N, Jovanović J, Maksimović V, Radotić K. Two-way reaction of versatile peroxidase with artificial lignin enhances low-molecular weight fractions. in Biotechnology Journal. 2023;.
doi:10.1002/biot.202300312 .

Spasojević, Dragica, Prodanović, Olivera, Mutavdžić, Dragosav, Šekuljica, Nataša, Jovanović, Jelena, Maksimović, Vuk, Radotić, Ksenija, "Two-way reaction of versatile peroxidase with artificial lignin enhances low-molecular weight fractions" in Biotechnology Journal (2023),
https://doi.org/10.1002/biot.202300312 . .

TY  - JOUR
AU  - Vojisavljević, Katarina
AU  - Savić, Slavica
AU  - Počuča-Nešić, Milica
AU  - Hodžić, Aden
AU  - Kriechbaum, Manfred
AU  - Ribić, Vesna
AU  - Rečnik, Aleksander
AU  - Vukašinović, Jelena
AU  - Branković, Goran
AU  - Đokić, Veljko
PY  - 2023
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5919
AB  - Developing highly efficient semiconductor metal oxide (SMOX) sensors capable of accurate and fast responses to environmental humidity is still a challenging task. In addition to a not so pronounced sensitivity to relative humidity change, most of the SMOXs cannot meet the criteria of real-time humidity sensing due to their long response/recovery time. The way to tackle this problem is to control adsorption/desorption processes, i.e., water-vapor molecular dynamics, over the sensor’s active layer through the powder and pore morphology design. With this in mind, a KIT-5-mediated synthesis was used to achieve mesoporous tin (IV) oxide replica (SnO2-R) with controlled pore size and ordering through template inversion and compared with a sol-gel synthesized powder (SnO2-SG). Unlike SnO2-SG, SnO2-R possessed a high specific surface area and quite an open pore structure, similar to the KIT-5, as observed by TEM, BET and SWAXS analyses. According to TEM, SnO2-R consisted of fine-grained globular particles and some percent of exaggerated, grown twinned crystals. The distinctive morphology of the SnO2-R-based sensor, with its specific pore structure and an increased number of oxygen-related defects associated with the powder preparation process and detected at the sensor surface by XPS analysis, contributed to excellent humidity sensing performances at room temperature, comprised of a low hysteresis error (3.7%), sensitivity of 406.8 kΩ/RH% and swift response/recovery speed (4 s/6 s).
PB  - MDPI
T2  - Molecules
T1  - KIT-5-Assisted Synthesis of Mesoporous SnO2 for High-Performance Humidity Sensors with a Swift Response/Recovery Speed
IS  - 4
SP  - 1754
VL  - 28
DO  - 10.3390/molecules28041754
ER  - 

@article{
author = "Vojisavljević, Katarina and Savić, Slavica and Počuča-Nešić, Milica and Hodžić, Aden and Kriechbaum, Manfred and Ribić, Vesna and Rečnik, Aleksander and Vukašinović, Jelena and Branković, Goran and Đokić, Veljko",
year = "2023",
abstract = "Developing highly efficient semiconductor metal oxide (SMOX) sensors capable of accurate and fast responses to environmental humidity is still a challenging task. In addition to a not so pronounced sensitivity to relative humidity change, most of the SMOXs cannot meet the criteria of real-time humidity sensing due to their long response/recovery time. The way to tackle this problem is to control adsorption/desorption processes, i.e., water-vapor molecular dynamics, over the sensor’s active layer through the powder and pore morphology design. With this in mind, a KIT-5-mediated synthesis was used to achieve mesoporous tin (IV) oxide replica (SnO2-R) with controlled pore size and ordering through template inversion and compared with a sol-gel synthesized powder (SnO2-SG). Unlike SnO2-SG, SnO2-R possessed a high specific surface area and quite an open pore structure, similar to the KIT-5, as observed by TEM, BET and SWAXS analyses. According to TEM, SnO2-R consisted of fine-grained globular particles and some percent of exaggerated, grown twinned crystals. The distinctive morphology of the SnO2-R-based sensor, with its specific pore structure and an increased number of oxygen-related defects associated with the powder preparation process and detected at the sensor surface by XPS analysis, contributed to excellent humidity sensing performances at room temperature, comprised of a low hysteresis error (3.7%), sensitivity of 406.8 kΩ/RH% and swift response/recovery speed (4 s/6 s).",
publisher = "MDPI",
journal = "Molecules",
title = "KIT-5-Assisted Synthesis of Mesoporous SnO2 for High-Performance Humidity Sensors with a Swift Response/Recovery Speed",
number = "4",
pages = "1754",
volume = "28",
doi = "10.3390/molecules28041754"
}

Vojisavljević, K., Savić, S., Počuča-Nešić, M., Hodžić, A., Kriechbaum, M., Ribić, V., Rečnik, A., Vukašinović, J., Branković, G.,& Đokić, V.. (2023). KIT-5-Assisted Synthesis of Mesoporous SnO2 for High-Performance Humidity Sensors with a Swift Response/Recovery Speed. in Molecules
MDPI., 28(4), 1754.
https://doi.org/10.3390/molecules28041754

Vojisavljević K, Savić S, Počuča-Nešić M, Hodžić A, Kriechbaum M, Ribić V, Rečnik A, Vukašinović J, Branković G, Đokić V. KIT-5-Assisted Synthesis of Mesoporous SnO2 for High-Performance Humidity Sensors with a Swift Response/Recovery Speed. in Molecules. 2023;28(4):1754.
doi:10.3390/molecules28041754 .

Vojisavljević, Katarina, Savić, Slavica, Počuča-Nešić, Milica, Hodžić, Aden, Kriechbaum, Manfred, Ribić, Vesna, Rečnik, Aleksander, Vukašinović, Jelena, Branković, Goran, Đokić, Veljko, "KIT-5-Assisted Synthesis of Mesoporous SnO2 for High-Performance Humidity Sensors with a Swift Response/Recovery Speed" in Molecules, 28, no. 4 (2023):1754,
https://doi.org/10.3390/molecules28041754 . .

TY  - JOUR
AU  - Rakić, Jelena M.
AU  - Petrović, Rada D.
AU  - Radojević, Vesna J.
AU  - Baščarević, Zvezdana D.
PY  - 2023
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6458
AB  - Effects of Na2SO4, Na2CO3, and Na2SiO3 on setting time, compressive strength (up to 90 days), and hydration mechanism of binders with high volume (70 wt%, HVFA binders) of fly ash (FA) were investigated. Before chemical activation, FA was mechanically activated. Effects of the activators on hydration process were examined by isothermal calorimetry, X-ray diffraction and thermogravimetric analyses, and scanning electron microscopy. Pore solution analyses were also performed. It was found that, with addition of the chemical activators, Portland cement (PC) hydration was accelerated and the pozzolanic reaction started earlier, which resulted in shortening of setting time and increase in early compressive strength of the HVFA binders. Combination of mechanical activation of FA and the chemical activation by sodium silicate proved to be the best choice for synthesis of HVFA binder with good physicomechanical properties.
PB  - Elsevier Ltd.
T2  - Construction and Building Materials
T1  - Effects of selected inorganic chemical activators on properties and hydration mechanism of high volume fly ash (HVFA) binders
SP  - 131833
VL  - 391
DO  - 10.1016/j.conbuildmat.2023.131833
ER  - 

@article{
author = "Rakić, Jelena M. and Petrović, Rada D. and Radojević, Vesna J. and Baščarević, Zvezdana D.",
year = "2023",
abstract = "Effects of Na2SO4, Na2CO3, and Na2SiO3 on setting time, compressive strength (up to 90 days), and hydration mechanism of binders with high volume (70 wt%, HVFA binders) of fly ash (FA) were investigated. Before chemical activation, FA was mechanically activated. Effects of the activators on hydration process were examined by isothermal calorimetry, X-ray diffraction and thermogravimetric analyses, and scanning electron microscopy. Pore solution analyses were also performed. It was found that, with addition of the chemical activators, Portland cement (PC) hydration was accelerated and the pozzolanic reaction started earlier, which resulted in shortening of setting time and increase in early compressive strength of the HVFA binders. Combination of mechanical activation of FA and the chemical activation by sodium silicate proved to be the best choice for synthesis of HVFA binder with good physicomechanical properties.",
publisher = "Elsevier Ltd.",
journal = "Construction and Building Materials",
title = "Effects of selected inorganic chemical activators on properties and hydration mechanism of high volume fly ash (HVFA) binders",
pages = "131833",
volume = "391",
doi = "10.1016/j.conbuildmat.2023.131833"
}

Rakić, J. M., Petrović, R. D., Radojević, V. J.,& Baščarević, Z. D.. (2023). Effects of selected inorganic chemical activators on properties and hydration mechanism of high volume fly ash (HVFA) binders. in Construction and Building Materials
Elsevier Ltd.., 391, 131833.
https://doi.org/10.1016/j.conbuildmat.2023.131833

Rakić JM, Petrović RD, Radojević VJ, Baščarević ZD. Effects of selected inorganic chemical activators on properties and hydration mechanism of high volume fly ash (HVFA) binders. in Construction and Building Materials. 2023;391:131833.
doi:10.1016/j.conbuildmat.2023.131833 .

Rakić, Jelena M., Petrović, Rada D., Radojević, Vesna J., Baščarević, Zvezdana D., "Effects of selected inorganic chemical activators on properties and hydration mechanism of high volume fly ash (HVFA) binders" in Construction and Building Materials, 391 (2023):131833,
https://doi.org/10.1016/j.conbuildmat.2023.131833 . .

TY  - JOUR
AU  - Popović, Daniela Ž.
AU  - Ivanović, Tijana G.
AU  - Miladinović, Jelena
AU  - Miladinović, Zoran P.
AU  - Pastor, Ferenc T.
AU  - Zlatić, Aleksandra
PY  - 2023
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6994
AB  - The mean ionic activity coefficients of NaCl in a ternary system {yNaCl + (1 – y)Na2HPO4}(aq) were determined from measurements of the electromotive force (EMF) where the NaCl ionic strength fraction was y = (0.3012; 0.4015; 0.5011; 0.5988; 0.7706; 0.8997) in the range of total ionic strength of the solution Im = 0.0701–1.0161 mol kg–1 at temperature T = 298.15 K. A cell of the Na–ISE| (Formula presented.) |AgCl|Ag, type was employed for the EMF measurements. The experimental results from this work and the model of Pitzer’s were used to determine the mixing parameters. Good agreement was found between the experimental and calculated values of the mean ionic activity coefficients of NaCl with a standard deviation of fit 1.5 × 10–3. The values of the osmotic coefficients of the system {yNaCl + (1 – y)Na2HPO4}(aq) were estimated on the basis of the determined parameters and compared with literature data. The differences in the osmotic coefficients between the estimated and experimental values were negligible.
PB  - Pleiades Publishing
T2  - Russian Journal of Physical Chemistry A
T1  - Activity Coefficients of the System {yNaCl + (1 – y)Na2HPO4}(aq) at T = 298.15 K Determined by Electromotive Force Measurements
EP  - 2702
IS  - 12
SP  - 2693
VL  - 97
DO  - 10.1134/S0036024423120063
ER  - 

@article{
author = "Popović, Daniela Ž. and Ivanović, Tijana G. and Miladinović, Jelena and Miladinović, Zoran P. and Pastor, Ferenc T. and Zlatić, Aleksandra",
year = "2023",
abstract = "The mean ionic activity coefficients of NaCl in a ternary system {yNaCl + (1 – y)Na2HPO4}(aq) were determined from measurements of the electromotive force (EMF) where the NaCl ionic strength fraction was y = (0.3012; 0.4015; 0.5011; 0.5988; 0.7706; 0.8997) in the range of total ionic strength of the solution Im = 0.0701–1.0161 mol kg–1 at temperature T = 298.15 K. A cell of the Na–ISE| (Formula presented.) |AgCl|Ag, type was employed for the EMF measurements. The experimental results from this work and the model of Pitzer’s were used to determine the mixing parameters. Good agreement was found between the experimental and calculated values of the mean ionic activity coefficients of NaCl with a standard deviation of fit 1.5 × 10–3. The values of the osmotic coefficients of the system {yNaCl + (1 – y)Na2HPO4}(aq) were estimated on the basis of the determined parameters and compared with literature data. The differences in the osmotic coefficients between the estimated and experimental values were negligible.",
publisher = "Pleiades Publishing",
journal = "Russian Journal of Physical Chemistry A",
title = "Activity Coefficients of the System {yNaCl + (1 – y)Na2HPO4}(aq) at T = 298.15 K Determined by Electromotive Force Measurements",
pages = "2702-2693",
number = "12",
volume = "97",
doi = "10.1134/S0036024423120063"
}

Popović, D. Ž., Ivanović, T. G., Miladinović, J., Miladinović, Z. P., Pastor, F. T.,& Zlatić, A.. (2023). Activity Coefficients of the System {yNaCl + (1 – y)Na2HPO4}(aq) at T = 298.15 K Determined by Electromotive Force Measurements. in Russian Journal of Physical Chemistry A
Pleiades Publishing., 97(12), 2693-2702.
https://doi.org/10.1134/S0036024423120063

Popović DŽ, Ivanović TG, Miladinović J, Miladinović ZP, Pastor FT, Zlatić A. Activity Coefficients of the System {yNaCl + (1 – y)Na2HPO4}(aq) at T = 298.15 K Determined by Electromotive Force Measurements. in Russian Journal of Physical Chemistry A. 2023;97(12):2693-2702.
doi:10.1134/S0036024423120063 .

Popović, Daniela Ž., Ivanović, Tijana G., Miladinović, Jelena, Miladinović, Zoran P., Pastor, Ferenc T., Zlatić, Aleksandra, "Activity Coefficients of the System {yNaCl + (1 – y)Na2HPO4}(aq) at T = 298.15 K Determined by Electromotive Force Measurements" in Russian Journal of Physical Chemistry A, 97, no. 12 (2023):2693-2702,
https://doi.org/10.1134/S0036024423120063 . .

TY  - JOUR
AU  - Peleš Tadić, Adriana
AU  - Blagojević, Vladimir A.
AU  - Stojanović, Dušica
AU  - Ostojić, Sanja B.
AU  - Tasić, Nikola
AU  - Kosanović, Darko
AU  - Uskoković, Petar
AU  - Pavlović, Vladimir B.
PY  - 2023
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5264
AB  - Poly(vinylidenefluoride)–ZnO (PVDF–ZnO) nanocomposites with mechanically activated ZnO nanoparticle fillers were investigated using thermal and mechanical analysis and AFM and PFM. Differential scanning calorimetry (DSC) investigated the effect of ZnO nanoparticles on the crystallinity of the polymer, under controlled heating and cooling. Atomic force (AFM) microscopy was used to record the surfaces of the samples. Nanocomposite surface roughness shows the presence of the different phases inside of the matrix, where rough samples contain a higher proportion of the β phase. PFM was performed to investigate the piezoresponse of the composites. Nanoidentation showed that the mechanical activation of the filler (ZnO) increases the Young modulus with the activation time. Molecular simulations in periodic systems (PVDF–ZnO spherical nanocluster and nanocylinder composite) were used to investigate the influence of particle size and shape on the Young modulus of different phases of PVDF.
PB  - Elsevier Ltd
T2  - Materials Science and Engineering B: Solid-State Materials for Advanced Technology
T1  - Nanomechanical properties of PVDF–ZnO polymer nanocomposite
SP  - 116126
VL  - 287
DO  - 10.1016/j.mseb.2022.116126
ER  - 

@article{
author = "Peleš Tadić, Adriana and Blagojević, Vladimir A. and Stojanović, Dušica and Ostojić, Sanja B. and Tasić, Nikola and Kosanović, Darko and Uskoković, Petar and Pavlović, Vladimir B.",
year = "2023",
abstract = "Poly(vinylidenefluoride)–ZnO (PVDF–ZnO) nanocomposites with mechanically activated ZnO nanoparticle fillers were investigated using thermal and mechanical analysis and AFM and PFM. Differential scanning calorimetry (DSC) investigated the effect of ZnO nanoparticles on the crystallinity of the polymer, under controlled heating and cooling. Atomic force (AFM) microscopy was used to record the surfaces of the samples. Nanocomposite surface roughness shows the presence of the different phases inside of the matrix, where rough samples contain a higher proportion of the β phase. PFM was performed to investigate the piezoresponse of the composites. Nanoidentation showed that the mechanical activation of the filler (ZnO) increases the Young modulus with the activation time. Molecular simulations in periodic systems (PVDF–ZnO spherical nanocluster and nanocylinder composite) were used to investigate the influence of particle size and shape on the Young modulus of different phases of PVDF.",
publisher = "Elsevier Ltd",
journal = "Materials Science and Engineering B: Solid-State Materials for Advanced Technology",
title = "Nanomechanical properties of PVDF–ZnO polymer nanocomposite",
pages = "116126",
volume = "287",
doi = "10.1016/j.mseb.2022.116126"
}

Peleš Tadić, A., Blagojević, V. A., Stojanović, D., Ostojić, S. B., Tasić, N., Kosanović, D., Uskoković, P.,& Pavlović, V. B.. (2023). Nanomechanical properties of PVDF–ZnO polymer nanocomposite. in Materials Science and Engineering B: Solid-State Materials for Advanced Technology
Elsevier Ltd., 287, 116126.
https://doi.org/10.1016/j.mseb.2022.116126

Peleš Tadić A, Blagojević VA, Stojanović D, Ostojić SB, Tasić N, Kosanović D, Uskoković P, Pavlović VB. Nanomechanical properties of PVDF–ZnO polymer nanocomposite. in Materials Science and Engineering B: Solid-State Materials for Advanced Technology. 2023;287:116126.
doi:10.1016/j.mseb.2022.116126 .

Peleš Tadić, Adriana, Blagojević, Vladimir A., Stojanović, Dušica, Ostojić, Sanja B., Tasić, Nikola, Kosanović, Darko, Uskoković, Petar, Pavlović, Vladimir B., "Nanomechanical properties of PVDF–ZnO polymer nanocomposite" in Materials Science and Engineering B: Solid-State Materials for Advanced Technology, 287 (2023):116126,
https://doi.org/10.1016/j.mseb.2022.116126 . .

TY  - CONF
AU  - Rogan, Jelena
AU  - Radovanović, Lidija
AU  - Simović, Bojana
AU  - Radovanović, Željko
AU  - Mihajlovski, Katarina
AU  - Dapčević, Aleksandra
PY  - 2022
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/7404
AB  - Zinc oxide nanoparticles (ZnO-NPs) have been a subject of numerous researches owing to their multifunctional properties in many applications, such as solar cells, UV light-emitting devices, gas sensors and photocatalysts. ZnO-NPs can be synthesized through various methods and their features can be tailored by shape and size, resulting in new applications relevant to their structural properties. The synthesis of ZnO-NPs via controlled thermal decomposition of the single-source precursors represents a novel synthetic methodology. The basic goal of this study was to investigate the influence of precursors on crystallite size and morphology of the resulting ZnO-NPs. Four structurally characterized Zn complexes with different benzenepolycarboxylato ligands [1] were used as precursors for investigation of photocatalytic and antimicrobial effects of thermally obtained ZnO-NPs. The XRPD and FESEM analysis of ZnO-NPs, prepared by thermolysis of Zn precursors at 450 °C in the air atmosphere, revealed hexagonal wurtzite structure (space group P63mc, a ≈ 3.25 and c ≈ 5.21 Å) with an average crystallite size in the range of 39–47 nm and similar morphology. The best photocatalytic activity for degradation of Reactive orange 16 dye has been observed for ZnO-NPs where crystallites form the smallest agglomerates. All obtained ZnO-NPs showed excellent inhibitory effect against Gram-positive bacteria Staphylococcus aureus and Gram-negative bacteria Escherichia coli.
PB  - Zagreb : Croatian Association of Crystallographers
C3  - Book of Abstracts / The European Powder Diffraction Conference EPDIC 17, Šibenik, Croatia, 31 May – 03 June 2022
T1  - Photocatalytic and antimicrobial effects of zinc oxide nanoparticles prepared by thermal decomposition of zinc benzenepolycarboxylato complexes
SP  - 127
UR  - https://hdl.handle.net/21.15107/rcub_technorep_7404
ER  - 

@conference{
author = "Rogan, Jelena and Radovanović, Lidija and Simović, Bojana and Radovanović, Željko and Mihajlovski, Katarina and Dapčević, Aleksandra",
year = "2022",
abstract = "Zinc oxide nanoparticles (ZnO-NPs) have been a subject of numerous researches owing to their multifunctional properties in many applications, such as solar cells, UV light-emitting devices, gas sensors and photocatalysts. ZnO-NPs can be synthesized through various methods and their features can be tailored by shape and size, resulting in new applications relevant to their structural properties. The synthesis of ZnO-NPs via controlled thermal decomposition of the single-source precursors represents a novel synthetic methodology. The basic goal of this study was to investigate the influence of precursors on crystallite size and morphology of the resulting ZnO-NPs. Four structurally characterized Zn complexes with different benzenepolycarboxylato ligands [1] were used as precursors for investigation of photocatalytic and antimicrobial effects of thermally obtained ZnO-NPs. The XRPD and FESEM analysis of ZnO-NPs, prepared by thermolysis of Zn precursors at 450 °C in the air atmosphere, revealed hexagonal wurtzite structure (space group P63mc, a ≈ 3.25 and c ≈ 5.21 Å) with an average crystallite size in the range of 39–47 nm and similar morphology. The best photocatalytic activity for degradation of Reactive orange 16 dye has been observed for ZnO-NPs where crystallites form the smallest agglomerates. All obtained ZnO-NPs showed excellent inhibitory effect against Gram-positive bacteria Staphylococcus aureus and Gram-negative bacteria Escherichia coli.",
publisher = "Zagreb : Croatian Association of Crystallographers",
journal = "Book of Abstracts / The European Powder Diffraction Conference EPDIC 17, Šibenik, Croatia, 31 May – 03 June 2022",
title = "Photocatalytic and antimicrobial effects of zinc oxide nanoparticles prepared by thermal decomposition of zinc benzenepolycarboxylato complexes",
pages = "127",
url = "https://hdl.handle.net/21.15107/rcub_technorep_7404"
}

Rogan, J., Radovanović, L., Simović, B., Radovanović, Ž., Mihajlovski, K.,& Dapčević, A.. (2022). Photocatalytic and antimicrobial effects of zinc oxide nanoparticles prepared by thermal decomposition of zinc benzenepolycarboxylato complexes. in Book of Abstracts / The European Powder Diffraction Conference EPDIC 17, Šibenik, Croatia, 31 May – 03 June 2022
Zagreb : Croatian Association of Crystallographers., 127.
https://hdl.handle.net/21.15107/rcub_technorep_7404

Rogan J, Radovanović L, Simović B, Radovanović Ž, Mihajlovski K, Dapčević A. Photocatalytic and antimicrobial effects of zinc oxide nanoparticles prepared by thermal decomposition of zinc benzenepolycarboxylato complexes. in Book of Abstracts / The European Powder Diffraction Conference EPDIC 17, Šibenik, Croatia, 31 May – 03 June 2022. 2022;:127.
https://hdl.handle.net/21.15107/rcub_technorep_7404 .

Rogan, Jelena, Radovanović, Lidija, Simović, Bojana, Radovanović, Željko, Mihajlovski, Katarina, Dapčević, Aleksandra, "Photocatalytic and antimicrobial effects of zinc oxide nanoparticles prepared by thermal decomposition of zinc benzenepolycarboxylato complexes" in Book of Abstracts / The European Powder Diffraction Conference EPDIC 17, Šibenik, Croatia, 31 May – 03 June 2022 (2022):127,
https://hdl.handle.net/21.15107/rcub_technorep_7404 .

TY  - JOUR
AU  - Malesevic, Aleksandar
AU  - Radojkovic, Aleksandar
AU  - Zunic, Milan
AU  - Dapčević, Aleksandra
AU  - Perac, Sanja
AU  - Branković, Zorica
AU  - Brankovic, Goran
PY  - 2022
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4993
AB  - The properties of BaCe1-xInxO3-delta (x = 0.05, 0.10, 0.15, 0.20, 0.25, 0.30, 0.35, and 0.40) as proton conducting electrolyte are examined. The dense electrolyte is formed after sintering at 1300 degrees C for 5 h in air. The samples with In content > 25 mol% contain In2O3 as a secondary phase. The highest total conductivity is around 5x10(-3) S/cm for BaCe0.75In0.25O3-delta in the wet hydrogen atmosphere at 700 degrees C. After exposure to pure CO2 atmosphere at 700 degrees C for 5 h, the concentrations of at least 15 mol% In can completely suppress degradation of the electrolyte. The power density of Ni-BaCe0.75In0.25O3-delta/BaCe0.75In0.25O3-delta/LSCF-BaCe0.75In0.25O3-delta fuel cell tested in wet hydrogen atmosphere reaches 264 mW/cm(2) at 700 degrees C. This result is an indication of stability and functionality of this electrolyte and its versatility in respect to type of fuel and performing environment.
T2  - Journal of Advanced Ceramics
T1  - Evaluation of stability and functionality of BaCe1-xInxO3-delta electrolyte in a wider range of indium concentration
EP  - 453
IS  - 3
SP  - 443
VL  - 11
DO  - 10.1007/s40145-021-0547-1
ER  - 

@article{
author = "Malesevic, Aleksandar and Radojkovic, Aleksandar and Zunic, Milan and Dapčević, Aleksandra and Perac, Sanja and Branković, Zorica and Brankovic, Goran",
year = "2022",
abstract = "The properties of BaCe1-xInxO3-delta (x = 0.05, 0.10, 0.15, 0.20, 0.25, 0.30, 0.35, and 0.40) as proton conducting electrolyte are examined. The dense electrolyte is formed after sintering at 1300 degrees C for 5 h in air. The samples with In content > 25 mol% contain In2O3 as a secondary phase. The highest total conductivity is around 5x10(-3) S/cm for BaCe0.75In0.25O3-delta in the wet hydrogen atmosphere at 700 degrees C. After exposure to pure CO2 atmosphere at 700 degrees C for 5 h, the concentrations of at least 15 mol% In can completely suppress degradation of the electrolyte. The power density of Ni-BaCe0.75In0.25O3-delta/BaCe0.75In0.25O3-delta/LSCF-BaCe0.75In0.25O3-delta fuel cell tested in wet hydrogen atmosphere reaches 264 mW/cm(2) at 700 degrees C. This result is an indication of stability and functionality of this electrolyte and its versatility in respect to type of fuel and performing environment.",
journal = "Journal of Advanced Ceramics",
title = "Evaluation of stability and functionality of BaCe1-xInxO3-delta electrolyte in a wider range of indium concentration",
pages = "453-443",
number = "3",
volume = "11",
doi = "10.1007/s40145-021-0547-1"
}

Malesevic, A., Radojkovic, A., Zunic, M., Dapčević, A., Perac, S., Branković, Z.,& Brankovic, G.. (2022). Evaluation of stability and functionality of BaCe1-xInxO3-delta electrolyte in a wider range of indium concentration. in Journal of Advanced Ceramics, 11(3), 443-453.
https://doi.org/10.1007/s40145-021-0547-1

Malesevic A, Radojkovic A, Zunic M, Dapčević A, Perac S, Branković Z, Brankovic G. Evaluation of stability and functionality of BaCe1-xInxO3-delta electrolyte in a wider range of indium concentration. in Journal of Advanced Ceramics. 2022;11(3):443-453.
doi:10.1007/s40145-021-0547-1 .

Malesevic, Aleksandar, Radojkovic, Aleksandar, Zunic, Milan, Dapčević, Aleksandra, Perac, Sanja, Branković, Zorica, Brankovic, Goran, "Evaluation of stability and functionality of BaCe1-xInxO3-delta electrolyte in a wider range of indium concentration" in Journal of Advanced Ceramics, 11, no. 3 (2022):443-453,
https://doi.org/10.1007/s40145-021-0547-1 . .

TY  - JOUR
AU  - Tasic, Nikola
AU  - Cirković, Jovana
AU  - Ribic, Vesna
AU  - Zunic, Milan
AU  - Dapčević, Aleksandra
AU  - Brankovic, Goran
AU  - Branković, Zorica
PY  - 2022
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4999
AB  - We present the synthesis and photocatalytic properties of mixed-phase TiO2 nanoparticles decorated with silver nanodots obtained by environmental-friendly wet chemical method using low molecular weight chitosan as the silver reducing agent. Structural analysis of synthesized Ag nanoparticles revealed that they crystallized in a rare hexagonal modification. High-resolution transmission electron microscopy study shows that   lt 3-nm hexagonal-Ag nanoparticles are implanted on the surface of   lt 20-nm anatase grains. Compared to Ag-free TiO2 powders, implantation with Ag results in important increase in visible light absorption. The photocatalytic activity of the samples was measured by monitoring decolorization of concentrated textile dye solution (50 mg L-1 of Reactive Orange 16) under simulated solar irradiation of 280 W m(-2). The optimum photocatalytic properties are achieved with 5 wt% of silver. Based on the collected results, the operating mechanism of the degradation process is suggested, and the effects of the silver addition are explained.
T2  - Journal of the American Ceramic Society
T1  - Effects of the silver nanodots on the photocatalytic activity of mixed-phase TiO2
EP  - 347
IS  - 1
SP  - 336
VL  - 105
DO  - 10.1111/jace.18059
ER  - 

@article{
author = "Tasic, Nikola and Cirković, Jovana and Ribic, Vesna and Zunic, Milan and Dapčević, Aleksandra and Brankovic, Goran and Branković, Zorica",
year = "2022",
abstract = "We present the synthesis and photocatalytic properties of mixed-phase TiO2 nanoparticles decorated with silver nanodots obtained by environmental-friendly wet chemical method using low molecular weight chitosan as the silver reducing agent. Structural analysis of synthesized Ag nanoparticles revealed that they crystallized in a rare hexagonal modification. High-resolution transmission electron microscopy study shows that   lt 3-nm hexagonal-Ag nanoparticles are implanted on the surface of   lt 20-nm anatase grains. Compared to Ag-free TiO2 powders, implantation with Ag results in important increase in visible light absorption. The photocatalytic activity of the samples was measured by monitoring decolorization of concentrated textile dye solution (50 mg L-1 of Reactive Orange 16) under simulated solar irradiation of 280 W m(-2). The optimum photocatalytic properties are achieved with 5 wt% of silver. Based on the collected results, the operating mechanism of the degradation process is suggested, and the effects of the silver addition are explained.",
journal = "Journal of the American Ceramic Society",
title = "Effects of the silver nanodots on the photocatalytic activity of mixed-phase TiO2",
pages = "347-336",
number = "1",
volume = "105",
doi = "10.1111/jace.18059"
}

Tasic, N., Cirković, J., Ribic, V., Zunic, M., Dapčević, A., Brankovic, G.,& Branković, Z.. (2022). Effects of the silver nanodots on the photocatalytic activity of mixed-phase TiO2. in Journal of the American Ceramic Society, 105(1), 336-347.
https://doi.org/10.1111/jace.18059

Tasic N, Cirković J, Ribic V, Zunic M, Dapčević A, Brankovic G, Branković Z. Effects of the silver nanodots on the photocatalytic activity of mixed-phase TiO2. in Journal of the American Ceramic Society. 2022;105(1):336-347.
doi:10.1111/jace.18059 .

Tasic, Nikola, Cirković, Jovana, Ribic, Vesna, Zunic, Milan, Dapčević, Aleksandra, Brankovic, Goran, Branković, Zorica, "Effects of the silver nanodots on the photocatalytic activity of mixed-phase TiO2" in Journal of the American Ceramic Society, 105, no. 1 (2022):336-347,
https://doi.org/10.1111/jace.18059 . .

TY  - JOUR
AU  - Zemljak, Olivera
AU  - Golić Luković, Danijela
AU  - Počuča-Nešić, Milica
AU  - Dapčević, Aleksandra
AU  - Šenjug, Pavla
AU  - Pajić, Damir
AU  - Radošević, Tina
AU  - Branković, Goran
AU  - Branković, Zorica
PY  - 2022
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5204
AB  - Yttrium manganite, YMnO3, was doped with different concentrations of titanium (x = 0, 0.04, 0.08, 0.10, 0.15, 0.20) in order to improve the microstructural and multiferroic properties. The powders were prepared using sol-gel polymerization complex method from citrate precursors. Depending on the titanium concentration, the hexagonal structure and/or the rhombohedral superstructure are present in the sintered samples. The YMn1–xTixO3+δ (x = 0.10, 0.15, 0.20) ceramic samples showed significantly reduced density of microcracks, and of inter- and intragranular pores, and relative densities greater than 90%. The structural parameters for YMn1–xTixO3+δ (x = 0, 0.10, 0.15) were correlated with the results of magnetic and ferroelectric measurements. The most of titanium-doped samples showed a reduction of the leakage current density in comparison with undoped YMnO3, and their ferroelectric responses were slightly improved. The modifications in structural arrangement resulted in partial suppression of ideal antiferromagnetic ordering visible through decrease of the Néel temperature and Weiss parameter, as well as the appearance of weak ferromagnetism and increase of magnetization (especially, in samples x = 0.08, 0.10, 0.15). These changes in physical quantities most likely originated from incorporation of the uncompensated magnetic moments and possible spin canting induced by enhanced symmetry break of the superexchange bridges.
PB  - Springer
T2  - Journal of Sol-Gel Science and Technology
T1  - Titanium doped yttrium manganite: improvement of microstructural properties and peculiarities of multiferroic properties
EP  - 819
IS  - 3
SP  - 807
VL  - 103
DO  - 10.1007/s10971-022-05872-3
ER  - 

@article{
author = "Zemljak, Olivera and Golić Luković, Danijela and Počuča-Nešić, Milica and Dapčević, Aleksandra and Šenjug, Pavla and Pajić, Damir and Radošević, Tina and Branković, Goran and Branković, Zorica",
year = "2022",
abstract = "Yttrium manganite, YMnO3, was doped with different concentrations of titanium (x = 0, 0.04, 0.08, 0.10, 0.15, 0.20) in order to improve the microstructural and multiferroic properties. The powders were prepared using sol-gel polymerization complex method from citrate precursors. Depending on the titanium concentration, the hexagonal structure and/or the rhombohedral superstructure are present in the sintered samples. The YMn1–xTixO3+δ (x = 0.10, 0.15, 0.20) ceramic samples showed significantly reduced density of microcracks, and of inter- and intragranular pores, and relative densities greater than 90%. The structural parameters for YMn1–xTixO3+δ (x = 0, 0.10, 0.15) were correlated with the results of magnetic and ferroelectric measurements. The most of titanium-doped samples showed a reduction of the leakage current density in comparison with undoped YMnO3, and their ferroelectric responses were slightly improved. The modifications in structural arrangement resulted in partial suppression of ideal antiferromagnetic ordering visible through decrease of the Néel temperature and Weiss parameter, as well as the appearance of weak ferromagnetism and increase of magnetization (especially, in samples x = 0.08, 0.10, 0.15). These changes in physical quantities most likely originated from incorporation of the uncompensated magnetic moments and possible spin canting induced by enhanced symmetry break of the superexchange bridges.",
publisher = "Springer",
journal = "Journal of Sol-Gel Science and Technology",
title = "Titanium doped yttrium manganite: improvement of microstructural properties and peculiarities of multiferroic properties",
pages = "819-807",
number = "3",
volume = "103",
doi = "10.1007/s10971-022-05872-3"
}

Zemljak, O., Golić Luković, D., Počuča-Nešić, M., Dapčević, A., Šenjug, P., Pajić, D., Radošević, T., Branković, G.,& Branković, Z.. (2022). Titanium doped yttrium manganite: improvement of microstructural properties and peculiarities of multiferroic properties. in Journal of Sol-Gel Science and Technology
Springer., 103(3), 807-819.
https://doi.org/10.1007/s10971-022-05872-3

Zemljak O, Golić Luković D, Počuča-Nešić M, Dapčević A, Šenjug P, Pajić D, Radošević T, Branković G, Branković Z. Titanium doped yttrium manganite: improvement of microstructural properties and peculiarities of multiferroic properties. in Journal of Sol-Gel Science and Technology. 2022;103(3):807-819.
doi:10.1007/s10971-022-05872-3 .

Zemljak, Olivera, Golić Luković, Danijela, Počuča-Nešić, Milica, Dapčević, Aleksandra, Šenjug, Pavla, Pajić, Damir, Radošević, Tina, Branković, Goran, Branković, Zorica, "Titanium doped yttrium manganite: improvement of microstructural properties and peculiarities of multiferroic properties" in Journal of Sol-Gel Science and Technology, 103, no. 3 (2022):807-819,
https://doi.org/10.1007/s10971-022-05872-3 . .

TY  - CONF
AU  - Milojković, Natalija
AU  - Orlić, Marina
AU  - Dikić, Jelena
AU  - Zunic, Milan
AU  - Simović, Bojana
AU  - Dapčević, Aleksandra
PY  - 2022
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6478
AB  - Regarding enormous expansion of bacterial contamination as well as their increase resistivity to commonly used disinfectants, there is a great demand for antibacterial material, which will not be based on organic compounds. Among various inorganic substances, environmentally friendly, low-cost and chemically stable ZnO and TiO2 demonstrate considerable antibacterial activity.This work primarily focuses on idea of developing novel disinfectant based on both, ZnO and TiO2, which would integrate all the worthy properties of both oxides. For that matter, titanium(IV) butoxide was dissolved in a solution of zinc acetate following with the ammonia addition until pH value was 8.5. Half of the initial solution was hydrothermally treated, dried and calcined at 500 (H-ZnTi-500) and 800°C (H-ZnTi-800). Two other samples (ZnTi-500 and ZnTi-800) were obtained from the other half of the initial solution which was directly dried and calcined under the same conditions. The samples were characterized by XRD including Rietveld refinement, FESEMand TG/DTA. Antibacterial activity was examined towards Gram-positive S. aureus and Gram-negative E. coli .The results showed that only ZnTi-800 consisted of pure Zn2TiO4 (Fd-3m) while Zn TiO was the major phase in three other samples. In the case of samples calcined at 500 °C, traces of ZnO were found. H-ZnTi-800 contained three phases: Zn2TiO4, ZnO and Zn2Ti3O8 (P4332). Cubic Zn2TiO4 contains two cation sites: tetrahedrally coordinated Zn at 0,0,0 and octahedral site at 5/8,5/8,5/8 shared between Zn and Ti. The calculated a-parameters of all obtained Zn2TiO4 as well as Zn–O and Zn/Ti–O bond distances were independent of synthesis. At 500 °C nanocrystalline Zn2TiO4 were obtained with the crystallite sizes 26 and 71 nm for H-ZnTi-500 and ZnTi-500, respectively, while microcrystalline phases were obtained at 800 °C with the crystallite sizes larger than 110 nm. The soft agglomerates consisted of smaller particles were obtained at 500 °C comparing to samples at 800 °C having more compact agglomerates.The best antibacterial activity with high reduction in the number of bacteria cells (87.6 % of E. coli and 63.4 % of S. aureus) was exhibited by the ZnTi-500. It means that the purity of samples, crystallite size and softness of agglomerates, influence antibacterial activity and that optimal level of all factors should be reached since ZnTi-500 was almost pure with sufficiently small crystallites and soft agglomerates.
PB  - European Powder Diffraction Conference (17 ; 2022 ; Šibenik)
C3  - European Powder Diffraction Conference -ЕPDIC17, Šibenik, Croatia, Book of Abstracts
T1  - A novel disinfectant based on zinc orthotitanate
SP  - 206
UR  - https://hdl.handle.net/21.15107/rcub_rimsi_1969
ER  - 

@conference{
author = "Milojković, Natalija and Orlić, Marina and Dikić, Jelena and Zunic, Milan and Simović, Bojana and Dapčević, Aleksandra",
year = "2022",
abstract = "Regarding enormous expansion of bacterial contamination as well as their increase resistivity to commonly used disinfectants, there is a great demand for antibacterial material, which will not be based on organic compounds. Among various inorganic substances, environmentally friendly, low-cost and chemically stable ZnO and TiO2 demonstrate considerable antibacterial activity.This work primarily focuses on idea of developing novel disinfectant based on both, ZnO and TiO2, which would integrate all the worthy properties of both oxides. For that matter, titanium(IV) butoxide was dissolved in a solution of zinc acetate following with the ammonia addition until pH value was 8.5. Half of the initial solution was hydrothermally treated, dried and calcined at 500 (H-ZnTi-500) and 800°C (H-ZnTi-800). Two other samples (ZnTi-500 and ZnTi-800) were obtained from the other half of the initial solution which was directly dried and calcined under the same conditions. The samples were characterized by XRD including Rietveld refinement, FESEMand TG/DTA. Antibacterial activity was examined towards Gram-positive S. aureus and Gram-negative E. coli .The results showed that only ZnTi-800 consisted of pure Zn2TiO4 (Fd-3m) while Zn TiO was the major phase in three other samples. In the case of samples calcined at 500 °C, traces of ZnO were found. H-ZnTi-800 contained three phases: Zn2TiO4, ZnO and Zn2Ti3O8 (P4332). Cubic Zn2TiO4 contains two cation sites: tetrahedrally coordinated Zn at 0,0,0 and octahedral site at 5/8,5/8,5/8 shared between Zn and Ti. The calculated a-parameters of all obtained Zn2TiO4 as well as Zn–O and Zn/Ti–O bond distances were independent of synthesis. At 500 °C nanocrystalline Zn2TiO4 were obtained with the crystallite sizes 26 and 71 nm for H-ZnTi-500 and ZnTi-500, respectively, while microcrystalline phases were obtained at 800 °C with the crystallite sizes larger than 110 nm. The soft agglomerates consisted of smaller particles were obtained at 500 °C comparing to samples at 800 °C having more compact agglomerates.The best antibacterial activity with high reduction in the number of bacteria cells (87.6 % of E. coli and 63.4 % of S. aureus) was exhibited by the ZnTi-500. It means that the purity of samples, crystallite size and softness of agglomerates, influence antibacterial activity and that optimal level of all factors should be reached since ZnTi-500 was almost pure with sufficiently small crystallites and soft agglomerates.",
publisher = "European Powder Diffraction Conference (17 ; 2022 ; Šibenik)",
journal = "European Powder Diffraction Conference -ЕPDIC17, Šibenik, Croatia, Book of Abstracts",
title = "A novel disinfectant based on zinc orthotitanate",
pages = "206",
url = "https://hdl.handle.net/21.15107/rcub_rimsi_1969"
}

Milojković, N., Orlić, M., Dikić, J., Zunic, M., Simović, B.,& Dapčević, A.. (2022). A novel disinfectant based on zinc orthotitanate. in European Powder Diffraction Conference -ЕPDIC17, Šibenik, Croatia, Book of Abstracts
European Powder Diffraction Conference (17 ; 2022 ; Šibenik)., 206.
https://hdl.handle.net/21.15107/rcub_rimsi_1969

Milojković N, Orlić M, Dikić J, Zunic M, Simović B, Dapčević A. A novel disinfectant based on zinc orthotitanate. in European Powder Diffraction Conference -ЕPDIC17, Šibenik, Croatia, Book of Abstracts. 2022;:206.
https://hdl.handle.net/21.15107/rcub_rimsi_1969 .

Milojković, Natalija, Orlić, Marina, Dikić, Jelena, Zunic, Milan, Simović, Bojana, Dapčević, Aleksandra, "A novel disinfectant based on zinc orthotitanate" in European Powder Diffraction Conference -ЕPDIC17, Šibenik, Croatia, Book of Abstracts (2022):206,
https://hdl.handle.net/21.15107/rcub_rimsi_1969 .

TY  - JOUR
AU  - Petričević, Aleksandar
AU  - Jović, Vladimir D.
AU  - Krstajić Pajić, Mila N.
AU  - Zabinski, Piotr
AU  - Elezović, Nevenka R.
PY  - 2022
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5353
AB  - Catalytic activity towards the oxygen reduction reaction (ORR) in 0.5 M H2SO4 was investigated at sub-monolayers and ultra-thin layers (corresponding to 10, 30 and 100 monolayers, (MLs)) of Pt electrochemically deposited on (Nb-Ti)2AlC substrate. Electrochemical deposition of Pt layers on (Nb-Ti)2AlC substrate was achieved from the solution containing 3 mM K2PtCl4 + 0.5 M NaCl (pH 4) under the conditions of convective diffusion (RPM = 400) using linear sweep voltammetry (LSV) at a sweep rate of 2 mV s-1, by determining limiting potential for deposition of each Pt sample from the QPt vs. E curves. The Pt samples were characterized X-ray photoelectron spectroscopy (XPS). XPS analysis showed that practically the whole surface of (Nb-Ti)2AlC substrate is covered with homogeneous layer of Pt, while Pt ion reduction was complete to metallic form – Pt(0) valence state. Then oxygen reduction was studied at rotating disc electrode by cyclic voltammetry and linear sweep voltammetry. Two different Tafel slopes were observed, one close to 60 mV dec-1 in low current densities region and second one ~ 120 mV dec-1 in high current densities region. This novel catalyst exhibited higher activity in comparison to carbon supported one, in terms of mass activity – kinetic current density normalized to Pt loading.
AB  - Ispitivana je reakcija redukcije kiseonika na tankim slojevima platine u 0.5 mol dm-3 H2SO4. Tanki
slojevi platine – čija količina naelektrisanja odgovara 10, 30 i 100 teorijskih monoslojeva Pt su
istaloženi na nosaču od (Nb-Ti)2AlC. Za elektrohemijsko taloženje je korišćen rastvor 3 mM
K2PtCl4 + 0.5 M NaCl pH = 4, u uslovima konvektivne difuzije (RPM = 400) primenom metode
linearne skenirajuće voltametrije (LSV) pri brzini promene potencijala od 2 mV s-1
. Elektrohemijski
dobijeni platinski katalizatori na pomenutom nosaču su okarakterisani metodom fotoelektronske
spektroskopija X-zraka (XPS), kao i elektrohemijskim tehnikama.
Za određivanje realne elektrohemijski aktivne površine elektrode je primenjena ciklična
voltametrija, integracijom ispod anodnog dela voltamograma u oblasti adsorpcije vodonika na
potpotencijalima. Za ispitivanje kinetike reakcije redukcije kiseonika je korišćena metoda linearne
skenirajuće voltametrije na rotirajućoj disk elektrodi. Dobijene su dve vrednosti Tafelovog nagiba,
jedna približno 60 mV dek-1
u oblasti malih prenapetosti, a druga ~ 120 mV dek-1
, u oblasti većih
gustina struje. Katalitička aktivnost katalizatora je poređena sa vrednostima iz literature dobijenim
na platini na ugljeničim nosačima na 0.85 V prema reverzibilnoj vodoničnoj elektrodi, izražena kao
kinetička gustina struje po realnoj površini electrode, ili specifična aktivnost – izražena kao
kinetička gustina struje po masi platine. Pokazano je da katalizator sa 10 monoslojeva platine
poseduje veoma dobru katalitičku aktivnost, posebno izraženu po masi istaložene platine.
PB  - Engineers Society for Corrosion
T2  - Zaštita materijala
T1  - Oxygen reduction reaction on electrochemically deposited sub-monolayers and ultra-thin layers of Pt on (Nb-Ti)2AlC substrate
T1  - Reakcija redukcije kiseonika na elektrohemijski istaloženim tankim slojevima platine na (Nb-Ti)2alc nosaču
EP  - 164
IS  - 2
SP  - 153
VL  - 63
DO  - 10.5937/zasmat2202153P
ER  - 

@article{
author = "Petričević, Aleksandar and Jović, Vladimir D. and Krstajić Pajić, Mila N. and Zabinski, Piotr and Elezović, Nevenka R.",
year = "2022",
abstract = "Catalytic activity towards the oxygen reduction reaction (ORR) in 0.5 M H2SO4 was investigated at sub-monolayers and ultra-thin layers (corresponding to 10, 30 and 100 monolayers, (MLs)) of Pt electrochemically deposited on (Nb-Ti)2AlC substrate. Electrochemical deposition of Pt layers on (Nb-Ti)2AlC substrate was achieved from the solution containing 3 mM K2PtCl4 + 0.5 M NaCl (pH 4) under the conditions of convective diffusion (RPM = 400) using linear sweep voltammetry (LSV) at a sweep rate of 2 mV s-1, by determining limiting potential for deposition of each Pt sample from the QPt vs. E curves. The Pt samples were characterized X-ray photoelectron spectroscopy (XPS). XPS analysis showed that practically the whole surface of (Nb-Ti)2AlC substrate is covered with homogeneous layer of Pt, while Pt ion reduction was complete to metallic form – Pt(0) valence state. Then oxygen reduction was studied at rotating disc electrode by cyclic voltammetry and linear sweep voltammetry. Two different Tafel slopes were observed, one close to 60 mV dec-1 in low current densities region and second one ~ 120 mV dec-1 in high current densities region. This novel catalyst exhibited higher activity in comparison to carbon supported one, in terms of mass activity – kinetic current density normalized to Pt loading., Ispitivana je reakcija redukcije kiseonika na tankim slojevima platine u 0.5 mol dm-3 H2SO4. Tanki
slojevi platine – čija količina naelektrisanja odgovara 10, 30 i 100 teorijskih monoslojeva Pt su
istaloženi na nosaču od (Nb-Ti)2AlC. Za elektrohemijsko taloženje je korišćen rastvor 3 mM
K2PtCl4 + 0.5 M NaCl pH = 4, u uslovima konvektivne difuzije (RPM = 400) primenom metode
linearne skenirajuće voltametrije (LSV) pri brzini promene potencijala od 2 mV s-1
. Elektrohemijski
dobijeni platinski katalizatori na pomenutom nosaču su okarakterisani metodom fotoelektronske
spektroskopija X-zraka (XPS), kao i elektrohemijskim tehnikama.
Za određivanje realne elektrohemijski aktivne površine elektrode je primenjena ciklična
voltametrija, integracijom ispod anodnog dela voltamograma u oblasti adsorpcije vodonika na
potpotencijalima. Za ispitivanje kinetike reakcije redukcije kiseonika je korišćena metoda linearne
skenirajuće voltametrije na rotirajućoj disk elektrodi. Dobijene su dve vrednosti Tafelovog nagiba,
jedna približno 60 mV dek-1
u oblasti malih prenapetosti, a druga ~ 120 mV dek-1
, u oblasti većih
gustina struje. Katalitička aktivnost katalizatora je poređena sa vrednostima iz literature dobijenim
na platini na ugljeničim nosačima na 0.85 V prema reverzibilnoj vodoničnoj elektrodi, izražena kao
kinetička gustina struje po realnoj površini electrode, ili specifična aktivnost – izražena kao
kinetička gustina struje po masi platine. Pokazano je da katalizator sa 10 monoslojeva platine
poseduje veoma dobru katalitičku aktivnost, posebno izraženu po masi istaložene platine.",
publisher = "Engineers Society for Corrosion",
journal = "Zaštita materijala",
title = "Oxygen reduction reaction on electrochemically deposited sub-monolayers and ultra-thin layers of Pt on (Nb-Ti)2AlC substrate, Reakcija redukcije kiseonika na elektrohemijski istaloženim tankim slojevima platine na (Nb-Ti)2alc nosaču",
pages = "164-153",
number = "2",
volume = "63",
doi = "10.5937/zasmat2202153P"
}

Petričević, A., Jović, V. D., Krstajić Pajić, M. N., Zabinski, P.,& Elezović, N. R.. (2022). Oxygen reduction reaction on electrochemically deposited sub-monolayers and ultra-thin layers of Pt on (Nb-Ti)2AlC substrate. in Zaštita materijala
Engineers Society for Corrosion., 63(2), 153-164.
https://doi.org/10.5937/zasmat2202153P

Petričević A, Jović VD, Krstajić Pajić MN, Zabinski P, Elezović NR. Oxygen reduction reaction on electrochemically deposited sub-monolayers and ultra-thin layers of Pt on (Nb-Ti)2AlC substrate. in Zaštita materijala. 2022;63(2):153-164.
doi:10.5937/zasmat2202153P .

Petričević, Aleksandar, Jović, Vladimir D., Krstajić Pajić, Mila N., Zabinski, Piotr, Elezović, Nevenka R., "Oxygen reduction reaction on electrochemically deposited sub-monolayers and ultra-thin layers of Pt on (Nb-Ti)2AlC substrate" in Zaštita materijala, 63, no. 2 (2022):153-164,
https://doi.org/10.5937/zasmat2202153P . .

TY  - JOUR
AU  - Pantić, Nevena
AU  - Spasojević, Milica
AU  - Stojanović, Željko
AU  - Veljović, Đorđe
AU  - Krstić, Jugoslav
AU  - Balaž, Ana Marija
AU  - Prodanović, Radivoje
AU  - Prodanović, Olivera
PY  - 2022
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5096
AB  - Novel macroporous copolymers of glycidyl methacrylate and ethylene glycol dimethacrylate with mean pore size diameters ranging from 150 to 310 nm were synthesized by dispersion polymerization and modified with ethylenediamine. The glutaraldehyde and periodate method were employed to immobilize horseradish peroxidase (HRP) onto these carriers. The activity of the immobilized enzyme was greatly affected by the pore size of the carrier. The highest specific activities of 9.65 and 8.94 U/g of dry weight were obtained for HRP immobilized by the periodate-route onto poly(GMA‐co‐EGDMA) carriers with pore size diameters of 234 and 297 nm, respectively. Stability studies showed an improved operational stability of immobilized peroxidase at 65 °C and in an organic solvent. HRP immobilized on a copolymer with a pore size of 234 nm, showing the highest specific activity and good stability, had higher activities at almost all pH values than the native enzyme and the increased Km value for pyrogallol oxidation. Immobilized HRP retained 80% of its original activity after five consecutive cycles of the pyrogallol oxidation and 98% of its initial activity in a storage stability study. Enzyme immobilized onto the macroporous copolymer with the pore size diameter of 234 nm showed a substantial degree of phenol removal achieved by immobilized peroxidase.
PB  - Springer
T2  - Journal of Polymers and the Environment
T1  - Immobilization of Horseradish Peroxidase on Macroporous Glycidyl-Based Copolymers with Different Surface Characteristics for the Removal of Phenol
DO  - 10.1007/s10924-021-02364-3
ER  - 

@article{
author = "Pantić, Nevena and Spasojević, Milica and Stojanović, Željko and Veljović, Đorđe and Krstić, Jugoslav and Balaž, Ana Marija and Prodanović, Radivoje and Prodanović, Olivera",
year = "2022",
abstract = "Novel macroporous copolymers of glycidyl methacrylate and ethylene glycol dimethacrylate with mean pore size diameters ranging from 150 to 310 nm were synthesized by dispersion polymerization and modified with ethylenediamine. The glutaraldehyde and periodate method were employed to immobilize horseradish peroxidase (HRP) onto these carriers. The activity of the immobilized enzyme was greatly affected by the pore size of the carrier. The highest specific activities of 9.65 and 8.94 U/g of dry weight were obtained for HRP immobilized by the periodate-route onto poly(GMA‐co‐EGDMA) carriers with pore size diameters of 234 and 297 nm, respectively. Stability studies showed an improved operational stability of immobilized peroxidase at 65 °C and in an organic solvent. HRP immobilized on a copolymer with a pore size of 234 nm, showing the highest specific activity and good stability, had higher activities at almost all pH values than the native enzyme and the increased Km value for pyrogallol oxidation. Immobilized HRP retained 80% of its original activity after five consecutive cycles of the pyrogallol oxidation and 98% of its initial activity in a storage stability study. Enzyme immobilized onto the macroporous copolymer with the pore size diameter of 234 nm showed a substantial degree of phenol removal achieved by immobilized peroxidase.",
publisher = "Springer",
journal = "Journal of Polymers and the Environment",
title = "Immobilization of Horseradish Peroxidase on Macroporous Glycidyl-Based Copolymers with Different Surface Characteristics for the Removal of Phenol",
doi = "10.1007/s10924-021-02364-3"
}

Pantić, N., Spasojević, M., Stojanović, Ž., Veljović, Đ., Krstić, J., Balaž, A. M., Prodanović, R.,& Prodanović, O.. (2022). Immobilization of Horseradish Peroxidase on Macroporous Glycidyl-Based Copolymers with Different Surface Characteristics for the Removal of Phenol. in Journal of Polymers and the Environment
Springer..
https://doi.org/10.1007/s10924-021-02364-3

Pantić N, Spasojević M, Stojanović Ž, Veljović Đ, Krstić J, Balaž AM, Prodanović R, Prodanović O. Immobilization of Horseradish Peroxidase on Macroporous Glycidyl-Based Copolymers with Different Surface Characteristics for the Removal of Phenol. in Journal of Polymers and the Environment. 2022;.
doi:10.1007/s10924-021-02364-3 .

Pantić, Nevena, Spasojević, Milica, Stojanović, Željko, Veljović, Đorđe, Krstić, Jugoslav, Balaž, Ana Marija, Prodanović, Radivoje, Prodanović, Olivera, "Immobilization of Horseradish Peroxidase on Macroporous Glycidyl-Based Copolymers with Different Surface Characteristics for the Removal of Phenol" in Journal of Polymers and the Environment (2022),
https://doi.org/10.1007/s10924-021-02364-3 . .

TY  - JOUR
AU  - Ivanović, Tijana G.
AU  - Popović, Daniela Ž.
AU  - Miladinović, Jelena
AU  - Miladinović, Zoran P.
AU  - Pastor, Ference
AU  - Nikolić, Anastasija
PY  - 2022
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5079
AB  - The mean activity coefficients of KCl in the ternary system {y KCl + (1 – y) K2HPO4}(aq) were experimentally determined at T = (298.15 ± 0.01) K by the electromotive force measurement (EMF method) using the cell of the type, K–ISE∣KCl(mKCl), K2HPO4(mK)∣Ag∣AgCl (ISE = ion-selective electrode), in the range of total ionic strength of the solution Im = (0.10 to 1.00) mol·kg−1 at different ionic strength fractions of KCl being y = (0.1011; 0.1997; 0.3016; 0.4027; 0.5006; 0.6018; 0.7018; 0.8051; 0.8988; 1). In addition, the osmotic coefficients of the system have been measured at the same temperature by the isopiestic vapor pressure method over the range of ionic strengths from (0.96698 to 2.21602) mol⋅kg−1 using KCl(aq) as the reference solution, at ionic strength fractions of KCl being y = (0.2063; 0.3849; 0.6099; 0.8011; 1). Values of the mean ionic activity coefficients of KCl and osmotic coefficients in the system {yKCl+(1–y)K2HPO4}(aq) were treated by an extended form of Pitzer's ion-interaction model, Scatchard's neutral-electrolyte model and Clegg–Pitzer–Brimblecombe's equations based on the mole-fraction-composition scale. All three models gave similar quality representations of both sets of experimental results. There are two sets of previously published isopiestic data that were taken into consideration during treatment. The model parameters were fitted and optimized to all available thermodynamic data from EMF and isopiestic measurements to obtain an accurate and self-consistent description of properties and to form a set of parameters that can be used in a wide range of ionic strength of the system. The standard deviation of the fit for the ionic strength range from Im = (0.0897 to 10.4350) mol·kg−1 with two optimized mixing parameters of Pitzer's model without higher–order electrostatic terms was for the mean ionic activity coefficients of KCl and osmotic coefficients, s.d. (γ±) = 3.5⋅10–3 and s.d. (ϕ) = 4.7⋅10–3 respectively, with two optimized mixing parameters of the Scatchard model standard deviations were s.d. (γ±) = 4.9⋅10–3 and s.d. (ϕ) = 5.0⋅10–3 and with Clegg–Pitzer–Brimblecombe's model higher–order electrostatic terms not included, standard deviations were s.d. (γ±) = 4.2⋅10–3 and s.d. (ϕ) = 4.8⋅10–3.
PB  - Elsevier B.V.
T2  - Journal of Molecular Liquids
T1  - Isopiestic determination of osmotic coefficients in the ionic strength range Im = (0.9670–2.2160) mol⋅kg−1 and activity coefficients determined by electromotive force measurements in the range Im = (0.0897–1.0054) mol⋅kg−1 of the {yKCl + (1 – y) K2HPO4}(aq) system at T = 298.15 K
SP  - 118767
VL  - 353
DO  - 10.1016/j.molliq.2022.118767
ER  - 

@article{
author = "Ivanović, Tijana G. and Popović, Daniela Ž. and Miladinović, Jelena and Miladinović, Zoran P. and Pastor, Ference and Nikolić, Anastasija",
year = "2022",
abstract = "The mean activity coefficients of KCl in the ternary system {y KCl + (1 – y) K2HPO4}(aq) were experimentally determined at T = (298.15 ± 0.01) K by the electromotive force measurement (EMF method) using the cell of the type, K–ISE∣KCl(mKCl), K2HPO4(mK)∣Ag∣AgCl (ISE = ion-selective electrode), in the range of total ionic strength of the solution Im = (0.10 to 1.00) mol·kg−1 at different ionic strength fractions of KCl being y = (0.1011; 0.1997; 0.3016; 0.4027; 0.5006; 0.6018; 0.7018; 0.8051; 0.8988; 1). In addition, the osmotic coefficients of the system have been measured at the same temperature by the isopiestic vapor pressure method over the range of ionic strengths from (0.96698 to 2.21602) mol⋅kg−1 using KCl(aq) as the reference solution, at ionic strength fractions of KCl being y = (0.2063; 0.3849; 0.6099; 0.8011; 1). Values of the mean ionic activity coefficients of KCl and osmotic coefficients in the system {yKCl+(1–y)K2HPO4}(aq) were treated by an extended form of Pitzer's ion-interaction model, Scatchard's neutral-electrolyte model and Clegg–Pitzer–Brimblecombe's equations based on the mole-fraction-composition scale. All three models gave similar quality representations of both sets of experimental results. There are two sets of previously published isopiestic data that were taken into consideration during treatment. The model parameters were fitted and optimized to all available thermodynamic data from EMF and isopiestic measurements to obtain an accurate and self-consistent description of properties and to form a set of parameters that can be used in a wide range of ionic strength of the system. The standard deviation of the fit for the ionic strength range from Im = (0.0897 to 10.4350) mol·kg−1 with two optimized mixing parameters of Pitzer's model without higher–order electrostatic terms was for the mean ionic activity coefficients of KCl and osmotic coefficients, s.d. (γ±) = 3.5⋅10–3 and s.d. (ϕ) = 4.7⋅10–3 respectively, with two optimized mixing parameters of the Scatchard model standard deviations were s.d. (γ±) = 4.9⋅10–3 and s.d. (ϕ) = 5.0⋅10–3 and with Clegg–Pitzer–Brimblecombe's model higher–order electrostatic terms not included, standard deviations were s.d. (γ±) = 4.2⋅10–3 and s.d. (ϕ) = 4.8⋅10–3.",
publisher = "Elsevier B.V.",
journal = "Journal of Molecular Liquids",
title = "Isopiestic determination of osmotic coefficients in the ionic strength range Im = (0.9670–2.2160) mol⋅kg−1 and activity coefficients determined by electromotive force measurements in the range Im = (0.0897–1.0054) mol⋅kg−1 of the {yKCl + (1 – y) K2HPO4}(aq) system at T = 298.15 K",
pages = "118767",
volume = "353",
doi = "10.1016/j.molliq.2022.118767"
}

Ivanović, T. G., Popović, D. Ž., Miladinović, J., Miladinović, Z. P., Pastor, F.,& Nikolić, A.. (2022). Isopiestic determination of osmotic coefficients in the ionic strength range Im = (0.9670–2.2160) mol⋅kg−1 and activity coefficients determined by electromotive force measurements in the range Im = (0.0897–1.0054) mol⋅kg−1 of the {yKCl + (1 – y) K2HPO4}(aq) system at T = 298.15 K. in Journal of Molecular Liquids
Elsevier B.V.., 353, 118767.
https://doi.org/10.1016/j.molliq.2022.118767

Ivanović TG, Popović DŽ, Miladinović J, Miladinović ZP, Pastor F, Nikolić A. Isopiestic determination of osmotic coefficients in the ionic strength range Im = (0.9670–2.2160) mol⋅kg−1 and activity coefficients determined by electromotive force measurements in the range Im = (0.0897–1.0054) mol⋅kg−1 of the {yKCl + (1 – y) K2HPO4}(aq) system at T = 298.15 K. in Journal of Molecular Liquids. 2022;353:118767.
doi:10.1016/j.molliq.2022.118767 .

Ivanović, Tijana G., Popović, Daniela Ž., Miladinović, Jelena, Miladinović, Zoran P., Pastor, Ference, Nikolić, Anastasija, "Isopiestic determination of osmotic coefficients in the ionic strength range Im = (0.9670–2.2160) mol⋅kg−1 and activity coefficients determined by electromotive force measurements in the range Im = (0.0897–1.0054) mol⋅kg−1 of the {yKCl + (1 – y) K2HPO4}(aq) system at T = 298.15 K" in Journal of Molecular Liquids, 353 (2022):118767,
https://doi.org/10.1016/j.molliq.2022.118767 . .

TY  - JOUR
AU  - Ivanović, Tijana
AU  - Popović, Daniela Ž.
AU  - Miladinović, Jelena
AU  - Miladinović, Zoran P.
AU  - Pastor, Ferenc
PY  - 2022
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5863
AB  - Zero-current cell potential measurements were used to determine the solution activity coefficient in a ternary system {yKCl + (1 - y) KH2PO4}(aq) at temperature T = 298.15 K. The cell of the type K-ISE|KCl(mKCl), KH2PO4(mKH2PO4)|Ag|AgCl was used in the total ionic strength range, Im = 0.0886-1.0046 mol kg-1. In order to generate a set of parameters that can be applied in a wide range of mixed solution ionic strengths, the Pitzer, Scatchard, and Clegg-Pitzer-Brimblecombe models were used to fit all available experimental data, including cell potential and isopiestic measurements from the literature. The experimental and calculated values of thermodynamic properties for the studied system are in excellent agreement. Potential interactions and solution structure were discussed by means of the excess free energy of mixing via potential pairs, triplets, or quads for the investigated solution using the Scatchard model mixing parameters.
PB  - American Chemical Society
T2  - Journal of Chemical and Engineering Data
T1  - Activity Coefficients of the System { yKCl + (1 - y)KH2PO4}(aq) at T = 298.15 K Determined by Cell Potential Measurements
DO  - 10.1021/acs.jced.2c00704
ER  - 

@article{
author = "Ivanović, Tijana and Popović, Daniela Ž. and Miladinović, Jelena and Miladinović, Zoran P. and Pastor, Ferenc",
year = "2022",
abstract = "Zero-current cell potential measurements were used to determine the solution activity coefficient in a ternary system {yKCl + (1 - y) KH2PO4}(aq) at temperature T = 298.15 K. The cell of the type K-ISE|KCl(mKCl), KH2PO4(mKH2PO4)|Ag|AgCl was used in the total ionic strength range, Im = 0.0886-1.0046 mol kg-1. In order to generate a set of parameters that can be applied in a wide range of mixed solution ionic strengths, the Pitzer, Scatchard, and Clegg-Pitzer-Brimblecombe models were used to fit all available experimental data, including cell potential and isopiestic measurements from the literature. The experimental and calculated values of thermodynamic properties for the studied system are in excellent agreement. Potential interactions and solution structure were discussed by means of the excess free energy of mixing via potential pairs, triplets, or quads for the investigated solution using the Scatchard model mixing parameters.",
publisher = "American Chemical Society",
journal = "Journal of Chemical and Engineering Data",
title = "Activity Coefficients of the System { yKCl + (1 - y)KH2PO4}(aq) at T = 298.15 K Determined by Cell Potential Measurements",
doi = "10.1021/acs.jced.2c00704"
}

Ivanović, T., Popović, D. Ž., Miladinović, J., Miladinović, Z. P.,& Pastor, F.. (2022). Activity Coefficients of the System { yKCl + (1 - y)KH2PO4}(aq) at T = 298.15 K Determined by Cell Potential Measurements. in Journal of Chemical and Engineering Data
American Chemical Society..
https://doi.org/10.1021/acs.jced.2c00704

Ivanović T, Popović DŽ, Miladinović J, Miladinović ZP, Pastor F. Activity Coefficients of the System { yKCl + (1 - y)KH2PO4}(aq) at T = 298.15 K Determined by Cell Potential Measurements. in Journal of Chemical and Engineering Data. 2022;.
doi:10.1021/acs.jced.2c00704 .

Ivanović, Tijana, Popović, Daniela Ž., Miladinović, Jelena, Miladinović, Zoran P., Pastor, Ferenc, "Activity Coefficients of the System { yKCl + (1 - y)KH2PO4}(aq) at T = 298.15 K Determined by Cell Potential Measurements" in Journal of Chemical and Engineering Data (2022),
https://doi.org/10.1021/acs.jced.2c00704 . .

TY  - JOUR
AU  - Rizzotto, Francesco
AU  - Vasiljević, Zorka Ž.
AU  - Stanojević, Gordana
AU  - Dojčinović, Milena P.
AU  - Janković-Častvan, Ivona
AU  - Vujančević, Jelena D.
AU  - Tadić, Nenad B.
AU  - Branković, Goran O.
AU  - Magniez, Aurélie
AU  - Vidić, Jasmina
AU  - Nikolić, Maria Vesna
PY  - 2022
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/5147
AB  - An emerging technology of active packaging enables prolongation of food shelf life by limiting the oxygen transfer and the reactivity of free radicals, which both destruct food freshness. In this work, Fe2TiO5 nanoparticles were synthesized using a modified sol–gel method and evaluated as an enforcement of alginate food packaging film. Pure phase Fe2TiO5 nanoparticles had an average particle size of 44 nm and rhombohedral morphology. Fe2TiO5 nanoparticles induce no cell damage of human Caco-2 epithelial cells and show no inhibitory effect towards growth of a panel of bacterial strains, suggesting good biocompatibility. Films obtained by incorporation of Fe2TiO5 nanoparticles into alginate using the solvent casting method show no migration of iron or titanium ions from films to food simulants again suggesting their safety as a packaging material. Fe2TiO5 nanoparticles also showed strong antioxidant efficiency as determined using the DPPḢ assay, and confirmed further in a preservation test on fresh fruit.
PB  - Elsevier Ltd
T2  - Food Chemistry
T1  - Antioxidant and cell-friendly Fe2TiO5 nanoparticles for food packaging application
SP  - 133198
VL  - 390
DO  - 10.1016/j.foodchem.2022.133198
ER  - 

@article{
author = "Rizzotto, Francesco and Vasiljević, Zorka Ž. and Stanojević, Gordana and Dojčinović, Milena P. and Janković-Častvan, Ivona and Vujančević, Jelena D. and Tadić, Nenad B. and Branković, Goran O. and Magniez, Aurélie and Vidić, Jasmina and Nikolić, Maria Vesna",
year = "2022",
abstract = "An emerging technology of active packaging enables prolongation of food shelf life by limiting the oxygen transfer and the reactivity of free radicals, which both destruct food freshness. In this work, Fe2TiO5 nanoparticles were synthesized using a modified sol–gel method and evaluated as an enforcement of alginate food packaging film. Pure phase Fe2TiO5 nanoparticles had an average particle size of 44 nm and rhombohedral morphology. Fe2TiO5 nanoparticles induce no cell damage of human Caco-2 epithelial cells and show no inhibitory effect towards growth of a panel of bacterial strains, suggesting good biocompatibility. Films obtained by incorporation of Fe2TiO5 nanoparticles into alginate using the solvent casting method show no migration of iron or titanium ions from films to food simulants again suggesting their safety as a packaging material. Fe2TiO5 nanoparticles also showed strong antioxidant efficiency as determined using the DPPḢ assay, and confirmed further in a preservation test on fresh fruit.",
publisher = "Elsevier Ltd",
journal = "Food Chemistry",
title = "Antioxidant and cell-friendly Fe2TiO5 nanoparticles for food packaging application",
pages = "133198",
volume = "390",
doi = "10.1016/j.foodchem.2022.133198"
}

Rizzotto, F., Vasiljević, Z. Ž., Stanojević, G., Dojčinović, M. P., Janković-Častvan, I., Vujančević, J. D., Tadić, N. B., Branković, G. O., Magniez, A., Vidić, J.,& Nikolić, M. V.. (2022). Antioxidant and cell-friendly Fe2TiO5 nanoparticles for food packaging application. in Food Chemistry
Elsevier Ltd., 390, 133198.
https://doi.org/10.1016/j.foodchem.2022.133198

Rizzotto F, Vasiljević ZŽ, Stanojević G, Dojčinović MP, Janković-Častvan I, Vujančević JD, Tadić NB, Branković GO, Magniez A, Vidić J, Nikolić MV. Antioxidant and cell-friendly Fe2TiO5 nanoparticles for food packaging application. in Food Chemistry. 2022;390:133198.
doi:10.1016/j.foodchem.2022.133198 .

Rizzotto, Francesco, Vasiljević, Zorka Ž., Stanojević, Gordana, Dojčinović, Milena P., Janković-Častvan, Ivona, Vujančević, Jelena D., Tadić, Nenad B., Branković, Goran O., Magniez, Aurélie, Vidić, Jasmina, Nikolić, Maria Vesna, "Antioxidant and cell-friendly Fe2TiO5 nanoparticles for food packaging application" in Food Chemistry, 390 (2022):133198,
https://doi.org/10.1016/j.foodchem.2022.133198 . .

TY  - JOUR
AU  - Dapčević, Aleksandra
AU  - Radojkovic, A.
AU  - Zunic, M.
AU  - Pocuca-Nesic, M.
AU  - Milosevic, O.
AU  - Brankovic, G.
PY  - 2021
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4939
AB  - In this study, the possibility to stabilize O-2 ion conductors in Bi2O3-V2O5 system was investigated. Six pseudo-binary Bi2O3-V2O5 mixtures [3.50   lt x(V2O5)   lt 8.50 mol%] were thermally treated at 1000 degrees C for 1 h. The samples were characterized by XRD, HRTEM/SAED, DTA and EIS techniques. The high-temperature reaction between alpha Bi2O3 and V2O5 resulted in formation of microcrystalline single-phase specimens containing the phase based on delta-Bi2O3 if V2O5 content was >= 4.63 mol%. The obtained phases exhibited main diffraction peaks corresponding to the simple cubic delta-Bi2O3 (space group Fm-3m) but Rietveld refinement showed a threefold repeat on a simple cubic sublattice indicating that the true unit cell is 3x3x3 supercell. Within proposed supercell, the octahedrally coordinated V5+ ions fully occupy 4a Wyckoff position and partially occupy 32f. The Bi3+ ions are placed at the rest of 32f and at 24e and 48h with full occupation. In total, 22 % of anionic sites are vacant. The ionic conductivity of phase with the lowest dopant content, i.e. Bi103V5O167, amounts 0.283 S cm(-1) at 800 degrees C with the activation energy of 0.64(5) eV, which is comparable to the undoped delta-Bi2O3 known as the fastest ion conductor.
T2  - Science of Sintering
T1  - Fast Oxide-Ion Conductors in Bi2O3-V2O5 System: Bi108-xVxO162+x(x=4-9) with 3 x 3 x 3 Superstructure
EP  - 66
IS  - 1
SP  - 55
VL  - 53
DO  - 10.2298/SOS2101055D
ER  - 

@article{
author = "Dapčević, Aleksandra and Radojkovic, A. and Zunic, M. and Pocuca-Nesic, M. and Milosevic, O. and Brankovic, G.",
year = "2021",
abstract = "In this study, the possibility to stabilize O-2 ion conductors in Bi2O3-V2O5 system was investigated. Six pseudo-binary Bi2O3-V2O5 mixtures [3.50   lt x(V2O5)   lt 8.50 mol%] were thermally treated at 1000 degrees C for 1 h. The samples were characterized by XRD, HRTEM/SAED, DTA and EIS techniques. The high-temperature reaction between alpha Bi2O3 and V2O5 resulted in formation of microcrystalline single-phase specimens containing the phase based on delta-Bi2O3 if V2O5 content was >= 4.63 mol%. The obtained phases exhibited main diffraction peaks corresponding to the simple cubic delta-Bi2O3 (space group Fm-3m) but Rietveld refinement showed a threefold repeat on a simple cubic sublattice indicating that the true unit cell is 3x3x3 supercell. Within proposed supercell, the octahedrally coordinated V5+ ions fully occupy 4a Wyckoff position and partially occupy 32f. The Bi3+ ions are placed at the rest of 32f and at 24e and 48h with full occupation. In total, 22 % of anionic sites are vacant. The ionic conductivity of phase with the lowest dopant content, i.e. Bi103V5O167, amounts 0.283 S cm(-1) at 800 degrees C with the activation energy of 0.64(5) eV, which is comparable to the undoped delta-Bi2O3 known as the fastest ion conductor.",
journal = "Science of Sintering",
title = "Fast Oxide-Ion Conductors in Bi2O3-V2O5 System: Bi108-xVxO162+x(x=4-9) with 3 x 3 x 3 Superstructure",
pages = "66-55",
number = "1",
volume = "53",
doi = "10.2298/SOS2101055D"
}

Dapčević, A., Radojkovic, A., Zunic, M., Pocuca-Nesic, M., Milosevic, O.,& Brankovic, G.. (2021). Fast Oxide-Ion Conductors in Bi2O3-V2O5 System: Bi108-xVxO162+x(x=4-9) with 3 x 3 x 3 Superstructure. in Science of Sintering, 53(1), 55-66.
https://doi.org/10.2298/SOS2101055D

Dapčević A, Radojkovic A, Zunic M, Pocuca-Nesic M, Milosevic O, Brankovic G. Fast Oxide-Ion Conductors in Bi2O3-V2O5 System: Bi108-xVxO162+x(x=4-9) with 3 x 3 x 3 Superstructure. in Science of Sintering. 2021;53(1):55-66.
doi:10.2298/SOS2101055D .

Dapčević, Aleksandra, Radojkovic, A., Zunic, M., Pocuca-Nesic, M., Milosevic, O., Brankovic, G., "Fast Oxide-Ion Conductors in Bi2O3-V2O5 System: Bi108-xVxO162+x(x=4-9) with 3 x 3 x 3 Superstructure" in Science of Sintering, 53, no. 1 (2021):55-66,
https://doi.org/10.2298/SOS2101055D . .

TY  - JOUR
AU  - Elezović, Nevenka R.
AU  - Zabinski, P.
AU  - Lačnjevac, Uroš
AU  - Krstajić-Pajić, Mila
AU  - Jović, V. D.
PY  - 2021
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/10
AB  - Two types of iridium oxide films formed at the Ti-2 AlC substrate were investigated: (1) anodically electrodeposited iridium oxide film from the solution based on IrCl(3)xH(2)O; (2) iridium oxide film prepared by cycling thin layer of electrodeposited Ir in the 0.5 M H2SO4 from - 0.25 to 1.20 V. It was shown that during anodic electrodeposition of iridium oxide film (1) coulombic efficiency decreases with increasing anodic potential, being only 3% atE = 0.7 V vs. SCE and 26% atE = 0.62 V vs. SCE. A pair of peaks corresponding to the transition Ir(III)-oxide/Ir(IV)-oxide was present on the CVs recorded in 0.5 M H2SO4. While cycling pure Ir thin layer in the solution of 0.5 M H2SO4 from - 0.25 to 1.20 V (2) up to 100 cycles, typical CV response was characterized with the prepeak and a pair of peaks corresponding to the Ir(III)/Ir(IV)-oxide transition. With the increase of cycles number to 150, additional peak at potential of 1.0 V appeared. This peak was formed on the account of pair of peaks corresponding to the Ir(III)/Ir(IV)-oxide transition. The oxygen evolution reaction (OER) was investigated at both iridium oxide films. It was shown that the Tafel slope for the OER was similar to 40 mV dec(-1)for the first polarization curve, confirming that the rds was a reaction S-OH - gt  S-O-ads + H++ e(-). As the number of recorded polarization curves increased, the activity of both types of iridium oxide films decreased, due to dissolution of iridium oxide films at the potentials of the OER. It is shown that anodically electrodeposited iridium oxide film is more active for the OER than that obtained by cycling electrodeposited iridium layer. However, both iridium oxide films exhibited insufficient stability.
PB  - Springer, New York
T2  - Journal of Solid State Electrochemistry
T1  - Electrochemical deposition and characterization of iridium oxide films on Ti2AlC support for oxygen evolution reaction
EP  - 363
IS  - 1
SP  - 351
VL  - 25
DO  - 10.1007/s10008-020-04816-7
ER  - 

@article{
author = "Elezović, Nevenka R. and Zabinski, P. and Lačnjevac, Uroš and Krstajić-Pajić, Mila and Jović, V. D.",
year = "2021",
abstract = "Two types of iridium oxide films formed at the Ti-2 AlC substrate were investigated: (1) anodically electrodeposited iridium oxide film from the solution based on IrCl(3)xH(2)O; (2) iridium oxide film prepared by cycling thin layer of electrodeposited Ir in the 0.5 M H2SO4 from - 0.25 to 1.20 V. It was shown that during anodic electrodeposition of iridium oxide film (1) coulombic efficiency decreases with increasing anodic potential, being only 3% atE = 0.7 V vs. SCE and 26% atE = 0.62 V vs. SCE. A pair of peaks corresponding to the transition Ir(III)-oxide/Ir(IV)-oxide was present on the CVs recorded in 0.5 M H2SO4. While cycling pure Ir thin layer in the solution of 0.5 M H2SO4 from - 0.25 to 1.20 V (2) up to 100 cycles, typical CV response was characterized with the prepeak and a pair of peaks corresponding to the Ir(III)/Ir(IV)-oxide transition. With the increase of cycles number to 150, additional peak at potential of 1.0 V appeared. This peak was formed on the account of pair of peaks corresponding to the Ir(III)/Ir(IV)-oxide transition. The oxygen evolution reaction (OER) was investigated at both iridium oxide films. It was shown that the Tafel slope for the OER was similar to 40 mV dec(-1)for the first polarization curve, confirming that the rds was a reaction S-OH - gt  S-O-ads + H++ e(-). As the number of recorded polarization curves increased, the activity of both types of iridium oxide films decreased, due to dissolution of iridium oxide films at the potentials of the OER. It is shown that anodically electrodeposited iridium oxide film is more active for the OER than that obtained by cycling electrodeposited iridium layer. However, both iridium oxide films exhibited insufficient stability.",
publisher = "Springer, New York",
journal = "Journal of Solid State Electrochemistry",
title = "Electrochemical deposition and characterization of iridium oxide films on Ti2AlC support for oxygen evolution reaction",
pages = "363-351",
number = "1",
volume = "25",
doi = "10.1007/s10008-020-04816-7"
}

Elezović, N. R., Zabinski, P., Lačnjevac, U., Krstajić-Pajić, M.,& Jović, V. D.. (2021). Electrochemical deposition and characterization of iridium oxide films on Ti2AlC support for oxygen evolution reaction. in Journal of Solid State Electrochemistry
Springer, New York., 25(1), 351-363.
https://doi.org/10.1007/s10008-020-04816-7

Elezović NR, Zabinski P, Lačnjevac U, Krstajić-Pajić M, Jović VD. Electrochemical deposition and characterization of iridium oxide films on Ti2AlC support for oxygen evolution reaction. in Journal of Solid State Electrochemistry. 2021;25(1):351-363.
doi:10.1007/s10008-020-04816-7 .

Elezović, Nevenka R., Zabinski, P., Lačnjevac, Uroš, Krstajić-Pajić, Mila, Jović, V. D., "Electrochemical deposition and characterization of iridium oxide films on Ti2AlC support for oxygen evolution reaction" in Journal of Solid State Electrochemistry, 25, no. 1 (2021):351-363,
https://doi.org/10.1007/s10008-020-04816-7 . .

TY  - JOUR
AU  - Vasiljević, Zorka Ž.
AU  - Dojčinović, Milena P.
AU  - Vujančević, Jelena D.
AU  - Spreitzer, Matjaz
AU  - Kovač, Janez
AU  - Bartolić, Dragana
AU  - Marković, Smilja
AU  - Janković-Častvan, Ivona
AU  - Tadić, Nenad B.
AU  - Nikolić, Maria Vesna
PY  - 2021
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4845
AB  - Nanostructured Fe2TiO5 (pseudobrookite), a mixed metal oxide material holds significant promise for utilization in energy and environmental applications. However, its full application is still hindered due to the difficulty to synthesize monophasic Fe2TiO5 with high crystallinity and a large specific surface area. Herein, Fe2TiO5 nanofibers were synthesized via a versatile and low-cost electrospinning method, followed by a calcination process at different temperatures. We found a significant effect of the calcination process and its duration on the crystalline phase in the form of either pseudobrookite or pseudobrookite-hematite-rutile and the morphology of calcined nanofibers. The crystallite size increased whereas the specific surface area decreased with an increase in calcination temperature. At higher temperatures, the growth of Fe2TiO5 nanoparticles and simultaneous coalescence of small particles was noted. The highest specific surface area was obtained for the sample calcined at 500 degrees C for 6 h (S-BET = 64.4 m(2) g(-1)). This work opens new opportunities in the synthesis of Fe2TiO5 nanostructures using the electrospinning method and a subsequent optimized calcination process for energy-related applications.
PB  - Royal Society of Chemistry
T2  - RSC Advances
T1  - Exploring the impact of calcination parameters on the crystal structure, morphology, and optical properties of electrospun Fe2TiO5 nanofibers
EP  - 32368
IS  - 51
SP  - 32358
VL  - 11
DO  - 10.1039/d1ra05748k
ER  - 

@article{
author = "Vasiljević, Zorka Ž. and Dojčinović, Milena P. and Vujančević, Jelena D. and Spreitzer, Matjaz and Kovač, Janez and Bartolić, Dragana and Marković, Smilja and Janković-Častvan, Ivona and Tadić, Nenad B. and Nikolić, Maria Vesna",
year = "2021",
abstract = "Nanostructured Fe2TiO5 (pseudobrookite), a mixed metal oxide material holds significant promise for utilization in energy and environmental applications. However, its full application is still hindered due to the difficulty to synthesize monophasic Fe2TiO5 with high crystallinity and a large specific surface area. Herein, Fe2TiO5 nanofibers were synthesized via a versatile and low-cost electrospinning method, followed by a calcination process at different temperatures. We found a significant effect of the calcination process and its duration on the crystalline phase in the form of either pseudobrookite or pseudobrookite-hematite-rutile and the morphology of calcined nanofibers. The crystallite size increased whereas the specific surface area decreased with an increase in calcination temperature. At higher temperatures, the growth of Fe2TiO5 nanoparticles and simultaneous coalescence of small particles was noted. The highest specific surface area was obtained for the sample calcined at 500 degrees C for 6 h (S-BET = 64.4 m(2) g(-1)). This work opens new opportunities in the synthesis of Fe2TiO5 nanostructures using the electrospinning method and a subsequent optimized calcination process for energy-related applications.",
publisher = "Royal Society of Chemistry",
journal = "RSC Advances",
title = "Exploring the impact of calcination parameters on the crystal structure, morphology, and optical properties of electrospun Fe2TiO5 nanofibers",
pages = "32368-32358",
number = "51",
volume = "11",
doi = "10.1039/d1ra05748k"
}

Vasiljević, Z. Ž., Dojčinović, M. P., Vujančević, J. D., Spreitzer, M., Kovač, J., Bartolić, D., Marković, S., Janković-Častvan, I., Tadić, N. B.,& Nikolić, M. V.. (2021). Exploring the impact of calcination parameters on the crystal structure, morphology, and optical properties of electrospun Fe2TiO5 nanofibers. in RSC Advances
Royal Society of Chemistry., 11(51), 32358-32368.
https://doi.org/10.1039/d1ra05748k

Vasiljević ZŽ, Dojčinović MP, Vujančević JD, Spreitzer M, Kovač J, Bartolić D, Marković S, Janković-Častvan I, Tadić NB, Nikolić MV. Exploring the impact of calcination parameters on the crystal structure, morphology, and optical properties of electrospun Fe2TiO5 nanofibers. in RSC Advances. 2021;11(51):32358-32368.
doi:10.1039/d1ra05748k .

Vasiljević, Zorka Ž., Dojčinović, Milena P., Vujančević, Jelena D., Spreitzer, Matjaz, Kovač, Janez, Bartolić, Dragana, Marković, Smilja, Janković-Častvan, Ivona, Tadić, Nenad B., Nikolić, Maria Vesna, "Exploring the impact of calcination parameters on the crystal structure, morphology, and optical properties of electrospun Fe2TiO5 nanofibers" in RSC Advances, 11, no. 51 (2021):32358-32368,
https://doi.org/10.1039/d1ra05748k . .