Rajić, Vladimir

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  • Rajić, Vladimir (3)

Author's Bibliography

Synergy of Nd:YAG Picosecond Pulsed Laser Irradiation and Electrochemical Anodization in the Formation of TiO2 Nanostructures for the Photocatalytic Degradation of Pesticide Carbofuran

Tošić, Miloš; Rajić, Vladimir; Pjević, Dejan; Stojadinović, Stevan; Krstulović, Nikša; Dimitrijević-Branković, Suzana; Momčilović, Miloš

(2024)

TY  - JOUR
AU  - Tošić, Miloš
AU  - Rajić, Vladimir
AU  - Pjević, Dejan
AU  - Stojadinović, Stevan
AU  - Krstulović, Nikša
AU  - Dimitrijević-Branković, Suzana
AU  - Momčilović, Miloš
PY  - 2024
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/7412
AB  - This study proposes a simple and controlled method for producing TiO2 with phase junction, oxygen vacancies, and Ti3+ by combining picosecond pulsed laser irradiation and electrochemical anodization. Ti mesh was pretreated by irradiating with a picosecond pulsed laser technique using an Nd:YAG laser (1064 nm) at two fluencies, 15 J/cm2 and 30 J/cm2 . The samples were then subjected to electrochemical anodization to form TiO2 nanotube arrays on the previously laser-treated surface. This study will investigate the possibility of forming TiO2 nanotube arrays on a pre-laser-treated Ti substrate and determine their physicochemical and photocatalytic properties. The samples were characterized by FESEM, XRD, Raman, XPS, and UV-Vis DRS. UV-Vis spectroscopy was used to observe the progress of photocatalytic degradation for all samples, and degradation products were determined using GC-MS. With the synergistic effects of phase junction, oxygen vacancies, and Ti3+, the laser-treated TiO2 with 30 J/cm2 showed a higher photocatalytic degradation rate (85.1%) of the pesticide carbofuran compared to non-laser-treated TiO2 (54.8%), remaining stable during successive degradation cycles, which has promising practical applications.
T2  - Photonics
T1  - Synergy of Nd:YAG Picosecond Pulsed Laser Irradiation and Electrochemical Anodization in the Formation of TiO2 Nanostructures for the Photocatalytic Degradation of Pesticide Carbofuran
IS  - 3
SP  - 284
VL  - 11
DO  - 10.3390/photonics11030284
ER  - 
@article{
author = "Tošić, Miloš and Rajić, Vladimir and Pjević, Dejan and Stojadinović, Stevan and Krstulović, Nikša and Dimitrijević-Branković, Suzana and Momčilović, Miloš",
year = "2024",
abstract = "This study proposes a simple and controlled method for producing TiO2 with phase junction, oxygen vacancies, and Ti3+ by combining picosecond pulsed laser irradiation and electrochemical anodization. Ti mesh was pretreated by irradiating with a picosecond pulsed laser technique using an Nd:YAG laser (1064 nm) at two fluencies, 15 J/cm2 and 30 J/cm2 . The samples were then subjected to electrochemical anodization to form TiO2 nanotube arrays on the previously laser-treated surface. This study will investigate the possibility of forming TiO2 nanotube arrays on a pre-laser-treated Ti substrate and determine their physicochemical and photocatalytic properties. The samples were characterized by FESEM, XRD, Raman, XPS, and UV-Vis DRS. UV-Vis spectroscopy was used to observe the progress of photocatalytic degradation for all samples, and degradation products were determined using GC-MS. With the synergistic effects of phase junction, oxygen vacancies, and Ti3+, the laser-treated TiO2 with 30 J/cm2 showed a higher photocatalytic degradation rate (85.1%) of the pesticide carbofuran compared to non-laser-treated TiO2 (54.8%), remaining stable during successive degradation cycles, which has promising practical applications.",
journal = "Photonics",
title = "Synergy of Nd:YAG Picosecond Pulsed Laser Irradiation and Electrochemical Anodization in the Formation of TiO2 Nanostructures for the Photocatalytic Degradation of Pesticide Carbofuran",
number = "3",
pages = "284",
volume = "11",
doi = "10.3390/photonics11030284"
}
Tošić, M., Rajić, V., Pjević, D., Stojadinović, S., Krstulović, N., Dimitrijević-Branković, S.,& Momčilović, M.. (2024). Synergy of Nd:YAG Picosecond Pulsed Laser Irradiation and Electrochemical Anodization in the Formation of TiO2 Nanostructures for the Photocatalytic Degradation of Pesticide Carbofuran. in Photonics, 11(3), 284.
https://doi.org/10.3390/photonics11030284
Tošić M, Rajić V, Pjević D, Stojadinović S, Krstulović N, Dimitrijević-Branković S, Momčilović M. Synergy of Nd:YAG Picosecond Pulsed Laser Irradiation and Electrochemical Anodization in the Formation of TiO2 Nanostructures for the Photocatalytic Degradation of Pesticide Carbofuran. in Photonics. 2024;11(3):284.
doi:10.3390/photonics11030284 .
Tošić, Miloš, Rajić, Vladimir, Pjević, Dejan, Stojadinović, Stevan, Krstulović, Nikša, Dimitrijević-Branković, Suzana, Momčilović, Miloš, "Synergy of Nd:YAG Picosecond Pulsed Laser Irradiation and Electrochemical Anodization in the Formation of TiO2 Nanostructures for the Photocatalytic Degradation of Pesticide Carbofuran" in Photonics, 11, no. 3 (2024):284,
https://doi.org/10.3390/photonics11030284 . .

IDENTIFICATION OF Fe-BEARING PHASES IN THE AS-CAST MICROSTRUCTURE OF AA6026 ALLOY AND THEIR EVOLUTION DURING HOMOGENIZATION TREATMENT

Radetić, Tamara; Popović, Miljana; Novaković, Mirjana; Rajić, Vladimir; Romhanji, Endre

(Technical Faculty in Bor, 2023)

TY  - JOUR
AU  - Radetić, Tamara
AU  - Popović, Miljana
AU  - Novaković, Mirjana
AU  - Rajić, Vladimir
AU  - Romhanji, Endre
PY  - 2023
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/7159
AB  - The Fe-bearing intermetallic phases present in the as-cast AA6026 alloy and their evolution during homogenization treatments at 480-550°C were investigated using optical microscopy, SEM, and TEM techniques in combination with EDS analysis. In addition to the α-Al(Fe,Mn)Si phase with dendritic morphology, two types of plate-like Fe-bearing microconstituents were revealed in the microstructure of the as-cast alloy. The EDS microanalysis and electron diffraction showed that one set of platelets represented thin sections of α-Al(Fe,Mn)Si microconstituent. The other set of plate-like microconstituents was identified as a tetragonal, silicon-rich δ-Al4(Fe,Mn)Si2 phase. The formation of the δ-Al4(Fe,Mn)Si2 phase was attributed to the chemical composition of the alloy. During homogenization, the metastable δ-Al4(Fe,Mn)Si2 transformed into the α-Al(Fe,Mn)Si phase and fragmented. The dendritic α-Al(Fe,Mn)Si microconstituents underwent fragmentation. However, while the α-Al(Fe,Mn)Si microconstituents preserved a b.c.c. crystal lattice throughout the process, the product of the transformation of the δ-Al4(Fe,Mn)Si2 phase exhibited primitive cubic lattice.
AB  - Ispitivanje prisustva faza koje sadrže Fe u mikrostrukturi livene legure AA6026, kao i njihova evolucija tokom postupaka
homogenizacije na temperaturama od 480-550 °C, sprovedena su korišćenjem optičke mikroskopije, skenirajuće
elektronske mikroskopije (SEM) i transmisione elektronske mikroskopije (TEM) u kombinaciji sa analizom EDS-a. Osim
faze α-Al(Fe,Mn)Si sa dendritskom morfologijom, identifikovane su dve vrste pločastih mikrokonstituenata koji sadrže Fe
u mikrostrukturi livene legure. EDS mikroanaliza i elektronska difrakcija pokazali su da jedan skup ploča predstavlja samo
tanke sekcije mikrokonstituente α-Al(Fe,Mn)Si. Drugi skup pločastih mikrokonstituenata identifikovan je kao četvrtasta,
silicijumom bogata faza δ-Al4
(Fe,Mn)Si2
. Formiranje faze δ-Al4
(Fe,Mn)Si2
 povezano je sa hemijskim sastavom legure.
Tokom homogenizacije, metastabilna faza δ-Al4
(Fe,Mn)Si2
 transformisala se u fazu α-Al(Fe,Mn)Si i fragmentirala.
Dendritski mikrokonstituenti α-Al(Fe,Mn)Si takođe su fragmentirali. Međutim, dok su mikrokonstituenti α-Al(Fe,Mn)Si
sačuvali kubnu kristalnu rešetku tipa b.c.c. tokom procesa, proizvod transformacije faze δ-Al4(Fe,Mn)Si2
 pokazao je prostu
kubnu rešetku.
PB  - Technical Faculty in Bor
T2  - Journal of Mining and Metallurgy, Section B: Metallurgy
T1  - IDENTIFICATION OF Fe-BEARING PHASES IN THE AS-CAST MICROSTRUCTURE OF AA6026 ALLOY AND THEIR EVOLUTION DURING HOMOGENIZATION TREATMENT
T1  - PREPOZNAVANJE FAZA KOJE SADRŽE Fe U MIKROSTRUKTURI LIVENE LEGURE AA6026 I NJIHOVA EVOLUCIJA TOKOM POSTUPKA HOMOGENIZACIJE
EP  - 338
IS  - 2
SP  - 327
VL  - 59
DO  - 10.2298/JMMB230611028R
ER  - 
@article{
author = "Radetić, Tamara and Popović, Miljana and Novaković, Mirjana and Rajić, Vladimir and Romhanji, Endre",
year = "2023",
abstract = "The Fe-bearing intermetallic phases present in the as-cast AA6026 alloy and their evolution during homogenization treatments at 480-550°C were investigated using optical microscopy, SEM, and TEM techniques in combination with EDS analysis. In addition to the α-Al(Fe,Mn)Si phase with dendritic morphology, two types of plate-like Fe-bearing microconstituents were revealed in the microstructure of the as-cast alloy. The EDS microanalysis and electron diffraction showed that one set of platelets represented thin sections of α-Al(Fe,Mn)Si microconstituent. The other set of plate-like microconstituents was identified as a tetragonal, silicon-rich δ-Al4(Fe,Mn)Si2 phase. The formation of the δ-Al4(Fe,Mn)Si2 phase was attributed to the chemical composition of the alloy. During homogenization, the metastable δ-Al4(Fe,Mn)Si2 transformed into the α-Al(Fe,Mn)Si phase and fragmented. The dendritic α-Al(Fe,Mn)Si microconstituents underwent fragmentation. However, while the α-Al(Fe,Mn)Si microconstituents preserved a b.c.c. crystal lattice throughout the process, the product of the transformation of the δ-Al4(Fe,Mn)Si2 phase exhibited primitive cubic lattice., Ispitivanje prisustva faza koje sadrže Fe u mikrostrukturi livene legure AA6026, kao i njihova evolucija tokom postupaka
homogenizacije na temperaturama od 480-550 °C, sprovedena su korišćenjem optičke mikroskopije, skenirajuće
elektronske mikroskopije (SEM) i transmisione elektronske mikroskopije (TEM) u kombinaciji sa analizom EDS-a. Osim
faze α-Al(Fe,Mn)Si sa dendritskom morfologijom, identifikovane su dve vrste pločastih mikrokonstituenata koji sadrže Fe
u mikrostrukturi livene legure. EDS mikroanaliza i elektronska difrakcija pokazali su da jedan skup ploča predstavlja samo
tanke sekcije mikrokonstituente α-Al(Fe,Mn)Si. Drugi skup pločastih mikrokonstituenata identifikovan je kao četvrtasta,
silicijumom bogata faza δ-Al4
(Fe,Mn)Si2
. Formiranje faze δ-Al4
(Fe,Mn)Si2
 povezano je sa hemijskim sastavom legure.
Tokom homogenizacije, metastabilna faza δ-Al4
(Fe,Mn)Si2
 transformisala se u fazu α-Al(Fe,Mn)Si i fragmentirala.
Dendritski mikrokonstituenti α-Al(Fe,Mn)Si takođe su fragmentirali. Međutim, dok su mikrokonstituenti α-Al(Fe,Mn)Si
sačuvali kubnu kristalnu rešetku tipa b.c.c. tokom procesa, proizvod transformacije faze δ-Al4(Fe,Mn)Si2
 pokazao je prostu
kubnu rešetku.",
publisher = "Technical Faculty in Bor",
journal = "Journal of Mining and Metallurgy, Section B: Metallurgy",
title = "IDENTIFICATION OF Fe-BEARING PHASES IN THE AS-CAST MICROSTRUCTURE OF AA6026 ALLOY AND THEIR EVOLUTION DURING HOMOGENIZATION TREATMENT, PREPOZNAVANJE FAZA KOJE SADRŽE Fe U MIKROSTRUKTURI LIVENE LEGURE AA6026 I NJIHOVA EVOLUCIJA TOKOM POSTUPKA HOMOGENIZACIJE",
pages = "338-327",
number = "2",
volume = "59",
doi = "10.2298/JMMB230611028R"
}
Radetić, T., Popović, M., Novaković, M., Rajić, V.,& Romhanji, E.. (2023). IDENTIFICATION OF Fe-BEARING PHASES IN THE AS-CAST MICROSTRUCTURE OF AA6026 ALLOY AND THEIR EVOLUTION DURING HOMOGENIZATION TREATMENT. in Journal of Mining and Metallurgy, Section B: Metallurgy
Technical Faculty in Bor., 59(2), 327-338.
https://doi.org/10.2298/JMMB230611028R
Radetić T, Popović M, Novaković M, Rajić V, Romhanji E. IDENTIFICATION OF Fe-BEARING PHASES IN THE AS-CAST MICROSTRUCTURE OF AA6026 ALLOY AND THEIR EVOLUTION DURING HOMOGENIZATION TREATMENT. in Journal of Mining and Metallurgy, Section B: Metallurgy. 2023;59(2):327-338.
doi:10.2298/JMMB230611028R .
Radetić, Tamara, Popović, Miljana, Novaković, Mirjana, Rajić, Vladimir, Romhanji, Endre, "IDENTIFICATION OF Fe-BEARING PHASES IN THE AS-CAST MICROSTRUCTURE OF AA6026 ALLOY AND THEIR EVOLUTION DURING HOMOGENIZATION TREATMENT" in Journal of Mining and Metallurgy, Section B: Metallurgy, 59, no. 2 (2023):327-338,
https://doi.org/10.2298/JMMB230611028R . .

Bifunctional catalytic activity of Zn1-xFexO toward the OER/ORR: seeking an optimal stoichiometry

Rajić, Vladimir; Stojković-Simatović, Ivana; Veselinović, Ljiljana; Belošević-Čavor, Jelena; Novaković, Mirjana; Popović, Maja; Škapin, Srečo Davor; Mojović, Miloš; Stojadinović, Stevan; Rac, Vladislav; Janković-Častvan, Ivona; Marković, Smilja

(Royal Soc Chemistry, Cambridge, 2020)

TY  - JOUR
AU  - Rajić, Vladimir
AU  - Stojković-Simatović, Ivana
AU  - Veselinović, Ljiljana
AU  - Belošević-Čavor, Jelena
AU  - Novaković, Mirjana
AU  - Popović, Maja
AU  - Škapin, Srečo Davor
AU  - Mojović, Miloš
AU  - Stojadinović, Stevan
AU  - Rac, Vladislav
AU  - Janković-Častvan, Ivona
AU  - Marković, Smilja
PY  - 2020
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/4368
AB  - Eco-friendly and rapid microwave processing of a precipitate was used to produce Fe-doped zinc oxide (Zn1-xFexO,x= 0, 0.05, 0.1, 0.15 and 0.20; ZnO:Fe) nanoparticles, which were tested as catalysts toward the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) in a moderately alkaline solution. The phase composition, crystal structure, morphology, textural properties, surface chemistry, optical properties and band structure were examined to comprehend the influence of Zn(2+)partial substitution with Fe(3+)on the catalytic activity of ZnO:Fe. Linear sweep voltammetry showed an improved catalytic activity of ZnO:5Fe toward the ORR, compared to pure ZnO, while with increased amounts of the Fe-dopant the activity decreased. The improvement was suggested by a more positive onset potential (0.394 Vvs.RHE), current density (0.231 mA cm(-2)at 0.150 Vvs.RHE), and faster kinetics (Tafel slope,b= 248 mV dec(-1)), and it may be due to the synergistic effect of (1) a sufficient amount of surface oxygen vacancies, and (2) a certain amount of plate-like particles composed of crystallites with well developed (0001) and (0001x304;) facets. Quite the contrary, the OER study showed that the introduction of Fe(3+)ions into the ZnO crystal structure resulted in enhanced catalytic activity of all ZnO:Fe samples, compared to pure ZnO, probably due to the modified binding energy and an optimized band structure. With the maximal current density of 1.066 mA cm(-2)at 2.216 Vvs.RHE, an onset potential of 1.856 Vvs.RHE, and the smallest potential difference between the OER and ORR (Delta E= 1.58 V), ZnO:10Fe may be considered a promising bifunctional catalyst toward the OER/ORR in moderately alkaline solution. This study demonstrates that the electrocatalytic activity of ZnO:Fe strongly depends on the defect chemistry and consequently the band structure. Along with providing fundamental insight into the electrocatalytic activity of ZnO:Fe, the study also indicates an optimal stoichiometry for enhanced bifunctional activity toward the OER/ORR, compared to pure ZnO.
PB  - Royal Soc Chemistry, Cambridge
T2  - Physical Chemistry Chemical Physics
T1  - Bifunctional catalytic activity of Zn1-xFexO toward the OER/ORR: seeking an optimal stoichiometry
EP  - 22095
IS  - 38
SP  - 22078
VL  - 22
DO  - 10.1039/d0cp03377d
ER  - 
@article{
author = "Rajić, Vladimir and Stojković-Simatović, Ivana and Veselinović, Ljiljana and Belošević-Čavor, Jelena and Novaković, Mirjana and Popović, Maja and Škapin, Srečo Davor and Mojović, Miloš and Stojadinović, Stevan and Rac, Vladislav and Janković-Častvan, Ivona and Marković, Smilja",
year = "2020",
abstract = "Eco-friendly and rapid microwave processing of a precipitate was used to produce Fe-doped zinc oxide (Zn1-xFexO,x= 0, 0.05, 0.1, 0.15 and 0.20; ZnO:Fe) nanoparticles, which were tested as catalysts toward the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) in a moderately alkaline solution. The phase composition, crystal structure, morphology, textural properties, surface chemistry, optical properties and band structure were examined to comprehend the influence of Zn(2+)partial substitution with Fe(3+)on the catalytic activity of ZnO:Fe. Linear sweep voltammetry showed an improved catalytic activity of ZnO:5Fe toward the ORR, compared to pure ZnO, while with increased amounts of the Fe-dopant the activity decreased. The improvement was suggested by a more positive onset potential (0.394 Vvs.RHE), current density (0.231 mA cm(-2)at 0.150 Vvs.RHE), and faster kinetics (Tafel slope,b= 248 mV dec(-1)), and it may be due to the synergistic effect of (1) a sufficient amount of surface oxygen vacancies, and (2) a certain amount of plate-like particles composed of crystallites with well developed (0001) and (0001x304;) facets. Quite the contrary, the OER study showed that the introduction of Fe(3+)ions into the ZnO crystal structure resulted in enhanced catalytic activity of all ZnO:Fe samples, compared to pure ZnO, probably due to the modified binding energy and an optimized band structure. With the maximal current density of 1.066 mA cm(-2)at 2.216 Vvs.RHE, an onset potential of 1.856 Vvs.RHE, and the smallest potential difference between the OER and ORR (Delta E= 1.58 V), ZnO:10Fe may be considered a promising bifunctional catalyst toward the OER/ORR in moderately alkaline solution. This study demonstrates that the electrocatalytic activity of ZnO:Fe strongly depends on the defect chemistry and consequently the band structure. Along with providing fundamental insight into the electrocatalytic activity of ZnO:Fe, the study also indicates an optimal stoichiometry for enhanced bifunctional activity toward the OER/ORR, compared to pure ZnO.",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "Physical Chemistry Chemical Physics",
title = "Bifunctional catalytic activity of Zn1-xFexO toward the OER/ORR: seeking an optimal stoichiometry",
pages = "22095-22078",
number = "38",
volume = "22",
doi = "10.1039/d0cp03377d"
}
Rajić, V., Stojković-Simatović, I., Veselinović, L., Belošević-Čavor, J., Novaković, M., Popović, M., Škapin, S. D., Mojović, M., Stojadinović, S., Rac, V., Janković-Častvan, I.,& Marković, S.. (2020). Bifunctional catalytic activity of Zn1-xFexO toward the OER/ORR: seeking an optimal stoichiometry. in Physical Chemistry Chemical Physics
Royal Soc Chemistry, Cambridge., 22(38), 22078-22095.
https://doi.org/10.1039/d0cp03377d
Rajić V, Stojković-Simatović I, Veselinović L, Belošević-Čavor J, Novaković M, Popović M, Škapin SD, Mojović M, Stojadinović S, Rac V, Janković-Častvan I, Marković S. Bifunctional catalytic activity of Zn1-xFexO toward the OER/ORR: seeking an optimal stoichiometry. in Physical Chemistry Chemical Physics. 2020;22(38):22078-22095.
doi:10.1039/d0cp03377d .
Rajić, Vladimir, Stojković-Simatović, Ivana, Veselinović, Ljiljana, Belošević-Čavor, Jelena, Novaković, Mirjana, Popović, Maja, Škapin, Srečo Davor, Mojović, Miloš, Stojadinović, Stevan, Rac, Vladislav, Janković-Častvan, Ivona, Marković, Smilja, "Bifunctional catalytic activity of Zn1-xFexO toward the OER/ORR: seeking an optimal stoichiometry" in Physical Chemistry Chemical Physics, 22, no. 38 (2020):22078-22095,
https://doi.org/10.1039/d0cp03377d . .
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