Radović, M.

Link to this page

Authority KeyName Variants
f76a71f8-2440-49ba-83b0-8091028ec585
  • Radović, M. (2)
  • Radović, Miladin (1)
Projects

Author's Bibliography

Ru layers electrodeposited onto highly stable Ti2AlC substrates as cathodes for hydrogen evolution in sulfuric acid solutions

Jović, Borka M.; Jović, Vladimir D.; Lačnjevac, Uroš; Stevanović, Sanja; Kovač, Janez; Radović, Miladin; Krstajić, Nedeljko V.

(Elsevier, 2016)

TY  - JOUR
AU  - Jović, Borka M.
AU  - Jović, Vladimir D.
AU  - Lačnjevac, Uroš
AU  - Stevanović, Sanja
AU  - Kovač, Janez
AU  - Radović, Miladin
AU  - Krstajić, Nedeljko V.
PY  - 2016
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4297
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6365
AB  - In this work, the hydrogen evolution reaction (HER) was studied on Ru coated Ti2AlC electrodes in 1.0 mol dm(-3) H2SO4 at 25 degrees C. Ti2AlC was found to be a highly stable substrate in sulfuric acid solutions due to the formation of a passivating oxide layer on the surface, which was confirmed by the X-ray photoelectron spectroscopy (XPS) analysis of as-prepared and anodically treated Ti2AlC samples. Ru films were electrodeposited onto Ti2AlC substrates by cycling the potential of Ti2AlC in the solution containing 0.01 mol dm(-3) RuCl3 + 0.1 mol dm(-3) H2SO4 between -0.5 V and 0.4 V vs. a saturated calomel electrode (SCE) at the sweep rate of 20 mV s(-1). Four Ru/Ti2AlC samples were prepared, obtained at 5, 10, 15 and 20 cycles of Ru electrodeposition. Characterization of samples was performed by scanning electron microscopy (SEM) and cyclic voltammetry (CV), while the thickness of the electrodeposited Ru layers was determined by atomic force microscopy (AFM). It was found that the most compact sample with the thickness of about 0.42 mu m was obtained after 5 cycles. Electrochemical impedance spectroscopy (EIS) and steady-state polarization measurements showed that all Ru/Ti2AlC electrodes were exceptionally active for the HER. A Tafel slope of about -60 mV dec(-1) was observed on all polarization curves in the range of high cathodic current densities. Based on formal kinetics analysis, an appropriate mechanism for the HER on Ru/Ti2AlC was suggested.
PB  - Elsevier
T2  - Journal of Electroanalytical Chemistry
T1  - Ru layers electrodeposited onto highly stable Ti2AlC substrates as cathodes for hydrogen evolution in sulfuric acid solutions
EP  - 86
SP  - 78
VL  - 766
DO  - 10.1016/j.jelechem.2016.01.038
ER  - 
@article{
author = "Jović, Borka M. and Jović, Vladimir D. and Lačnjevac, Uroš and Stevanović, Sanja and Kovač, Janez and Radović, Miladin and Krstajić, Nedeljko V.",
year = "2016",
abstract = "In this work, the hydrogen evolution reaction (HER) was studied on Ru coated Ti2AlC electrodes in 1.0 mol dm(-3) H2SO4 at 25 degrees C. Ti2AlC was found to be a highly stable substrate in sulfuric acid solutions due to the formation of a passivating oxide layer on the surface, which was confirmed by the X-ray photoelectron spectroscopy (XPS) analysis of as-prepared and anodically treated Ti2AlC samples. Ru films were electrodeposited onto Ti2AlC substrates by cycling the potential of Ti2AlC in the solution containing 0.01 mol dm(-3) RuCl3 + 0.1 mol dm(-3) H2SO4 between -0.5 V and 0.4 V vs. a saturated calomel electrode (SCE) at the sweep rate of 20 mV s(-1). Four Ru/Ti2AlC samples were prepared, obtained at 5, 10, 15 and 20 cycles of Ru electrodeposition. Characterization of samples was performed by scanning electron microscopy (SEM) and cyclic voltammetry (CV), while the thickness of the electrodeposited Ru layers was determined by atomic force microscopy (AFM). It was found that the most compact sample with the thickness of about 0.42 mu m was obtained after 5 cycles. Electrochemical impedance spectroscopy (EIS) and steady-state polarization measurements showed that all Ru/Ti2AlC electrodes were exceptionally active for the HER. A Tafel slope of about -60 mV dec(-1) was observed on all polarization curves in the range of high cathodic current densities. Based on formal kinetics analysis, an appropriate mechanism for the HER on Ru/Ti2AlC was suggested.",
publisher = "Elsevier",
journal = "Journal of Electroanalytical Chemistry",
title = "Ru layers electrodeposited onto highly stable Ti2AlC substrates as cathodes for hydrogen evolution in sulfuric acid solutions",
pages = "86-78",
volume = "766",
doi = "10.1016/j.jelechem.2016.01.038"
}
Jović, B. M., Jović, V. D., Lačnjevac, U., Stevanović, S., Kovač, J., Radović, M.,& Krstajić, N. V.. (2016). Ru layers electrodeposited onto highly stable Ti2AlC substrates as cathodes for hydrogen evolution in sulfuric acid solutions. in Journal of Electroanalytical Chemistry
Elsevier., 766, 78-86.
https://doi.org/10.1016/j.jelechem.2016.01.038
Jović BM, Jović VD, Lačnjevac U, Stevanović S, Kovač J, Radović M, Krstajić NV. Ru layers electrodeposited onto highly stable Ti2AlC substrates as cathodes for hydrogen evolution in sulfuric acid solutions. in Journal of Electroanalytical Chemistry. 2016;766:78-86.
doi:10.1016/j.jelechem.2016.01.038 .
Jović, Borka M., Jović, Vladimir D., Lačnjevac, Uroš, Stevanović, Sanja, Kovač, Janez, Radović, Miladin, Krstajić, Nedeljko V., "Ru layers electrodeposited onto highly stable Ti2AlC substrates as cathodes for hydrogen evolution in sulfuric acid solutions" in Journal of Electroanalytical Chemistry, 766 (2016):78-86,
https://doi.org/10.1016/j.jelechem.2016.01.038 . .
18
14
19

A new electrolyte based on Tm3+-doped delta-Bi2O3-type phase with enhanced conductivity

Dapčević, Aleksandra; Poleti, Dejan; Rogan, Jelena; Radojković, Aleksandar; Radović, M.; Branković, Goran

(Elsevier Science Bv, Amsterdam, 2015)

TY  - JOUR
AU  - Dapčević, Aleksandra
AU  - Poleti, Dejan
AU  - Rogan, Jelena
AU  - Radojković, Aleksandar
AU  - Radović, M.
AU  - Branković, Goran
PY  - 2015
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3135
AB  - The possibility to stabilize the delta-Bi2O3-type polymorph with high ionic conductivity by doping with Tm2O3 was investigated in this study. Five microaystalline samples were synthesized at 750 degrees C from alpha-Bi2O3 and Tm2O3 mixtures with compositions (Bi1-xTmx)(2)O-3, where x = 0.04, 0.08, 0.11, 0.14 and 0.20. The XRD, SEM, HRTEM and SAED results showed that the targeted delta-Bi2O3-type single-phase (space group Fm (3) over barm) was formed for 0.11  lt = x  lt = 0.20. The unit cell parameter of delta-Bi2O3-type phase decreases with increase in Tm content. According to DTA, no phase transitions were observed in the sample with x = 020, indicating that the obtained delta-Bi2O3-type phase is structurally stable from room temperature to 985 degrees C. Based on EIS, (Bi0.80Tm0.20)(2)O-3 exhibits high conductivity (0.117 S cm(-1) at 550 degrees C) with activation energies: 0.38(4) eV above 550 degrees C and 127(2) eV below 550 degrees C, due to the change in charge carrier mobility. The effect of thermal aging was investigated and discussed.
PB  - Elsevier Science Bv, Amsterdam
T2  - Solid State Ionics
T1  - A new electrolyte based on Tm3+-doped delta-Bi2O3-type phase with enhanced conductivity
EP  - 23
SP  - 18
VL  - 280
DO  - 10.1016/j.ssi.2015.08.004
ER  - 
@article{
author = "Dapčević, Aleksandra and Poleti, Dejan and Rogan, Jelena and Radojković, Aleksandar and Radović, M. and Branković, Goran",
year = "2015",
abstract = "The possibility to stabilize the delta-Bi2O3-type polymorph with high ionic conductivity by doping with Tm2O3 was investigated in this study. Five microaystalline samples were synthesized at 750 degrees C from alpha-Bi2O3 and Tm2O3 mixtures with compositions (Bi1-xTmx)(2)O-3, where x = 0.04, 0.08, 0.11, 0.14 and 0.20. The XRD, SEM, HRTEM and SAED results showed that the targeted delta-Bi2O3-type single-phase (space group Fm (3) over barm) was formed for 0.11  lt = x  lt = 0.20. The unit cell parameter of delta-Bi2O3-type phase decreases with increase in Tm content. According to DTA, no phase transitions were observed in the sample with x = 020, indicating that the obtained delta-Bi2O3-type phase is structurally stable from room temperature to 985 degrees C. Based on EIS, (Bi0.80Tm0.20)(2)O-3 exhibits high conductivity (0.117 S cm(-1) at 550 degrees C) with activation energies: 0.38(4) eV above 550 degrees C and 127(2) eV below 550 degrees C, due to the change in charge carrier mobility. The effect of thermal aging was investigated and discussed.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Solid State Ionics",
title = "A new electrolyte based on Tm3+-doped delta-Bi2O3-type phase with enhanced conductivity",
pages = "23-18",
volume = "280",
doi = "10.1016/j.ssi.2015.08.004"
}
Dapčević, A., Poleti, D., Rogan, J., Radojković, A., Radović, M.,& Branković, G.. (2015). A new electrolyte based on Tm3+-doped delta-Bi2O3-type phase with enhanced conductivity. in Solid State Ionics
Elsevier Science Bv, Amsterdam., 280, 18-23.
https://doi.org/10.1016/j.ssi.2015.08.004
Dapčević A, Poleti D, Rogan J, Radojković A, Radović M, Branković G. A new electrolyte based on Tm3+-doped delta-Bi2O3-type phase with enhanced conductivity. in Solid State Ionics. 2015;280:18-23.
doi:10.1016/j.ssi.2015.08.004 .
Dapčević, Aleksandra, Poleti, Dejan, Rogan, Jelena, Radojković, Aleksandar, Radović, M., Branković, Goran, "A new electrolyte based on Tm3+-doped delta-Bi2O3-type phase with enhanced conductivity" in Solid State Ionics, 280 (2015):18-23,
https://doi.org/10.1016/j.ssi.2015.08.004 . .
36
18
38

Influence of Fe3+ on Photo catalytic Efficiency of Nanopowder-TiO2 and CeO2 - Comparative Study

Kuburović, Nataša; Golubović, Aleksandar; Radović, M.; Dohcević-Mitrović, Zorana; Orlović, Aleksandar

(ICT Press, Prague, 2010)

TY  - CONF
AU  - Kuburović, Nataša
AU  - Golubović, Aleksandar
AU  - Radović, M.
AU  - Dohcević-Mitrović, Zorana
AU  - Orlović, Aleksandar
PY  - 2010
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/1740
PB  - ICT Press, Prague
C3  - Proceedings of the 6th European Meeting on Solar Chemistry & Photocatalysis: Environmental Applicati
T1  - Influence of Fe3+ on Photo catalytic Efficiency of Nanopowder-TiO2 and CeO2 - Comparative Study
EP  - 135
SP  - 135
UR  - https://hdl.handle.net/21.15107/rcub_technorep_1740
ER  - 
@conference{
author = "Kuburović, Nataša and Golubović, Aleksandar and Radović, M. and Dohcević-Mitrović, Zorana and Orlović, Aleksandar",
year = "2010",
publisher = "ICT Press, Prague",
journal = "Proceedings of the 6th European Meeting on Solar Chemistry & Photocatalysis: Environmental Applicati",
title = "Influence of Fe3+ on Photo catalytic Efficiency of Nanopowder-TiO2 and CeO2 - Comparative Study",
pages = "135-135",
url = "https://hdl.handle.net/21.15107/rcub_technorep_1740"
}
Kuburović, N., Golubović, A., Radović, M., Dohcević-Mitrović, Z.,& Orlović, A.. (2010). Influence of Fe3+ on Photo catalytic Efficiency of Nanopowder-TiO2 and CeO2 - Comparative Study. in Proceedings of the 6th European Meeting on Solar Chemistry & Photocatalysis: Environmental Applicati
ICT Press, Prague., 135-135.
https://hdl.handle.net/21.15107/rcub_technorep_1740
Kuburović N, Golubović A, Radović M, Dohcević-Mitrović Z, Orlović A. Influence of Fe3+ on Photo catalytic Efficiency of Nanopowder-TiO2 and CeO2 - Comparative Study. in Proceedings of the 6th European Meeting on Solar Chemistry & Photocatalysis: Environmental Applicati. 2010;:135-135.
https://hdl.handle.net/21.15107/rcub_technorep_1740 .
Kuburović, Nataša, Golubović, Aleksandar, Radović, M., Dohcević-Mitrović, Zorana, Orlović, Aleksandar, "Influence of Fe3+ on Photo catalytic Efficiency of Nanopowder-TiO2 and CeO2 - Comparative Study" in Proceedings of the 6th European Meeting on Solar Chemistry & Photocatalysis: Environmental Applicati (2010):135-135,
https://hdl.handle.net/21.15107/rcub_technorep_1740 .
1