Lović, J. D.

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  • Lović, J. D. (2)
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Synthesis and characterization of AgPd alloy coatings as beneficial catalysts for low temperature fuel cells application

Elezović, Nevenka R.; Lović, J. D.; Jović, Borka M; Zabinski, P.; Wloch, Grzegorz; Jović, Vladimir D

(Pergamon-Elsevier Science Ltd, Oxford, 2019)

TY  - JOUR
AU  - Elezović, Nevenka R.
AU  - Lović, J. D.
AU  - Jović, Borka M
AU  - Zabinski, P.
AU  - Wloch, Grzegorz
AU  - Jović, Vladimir D
PY  - 2019
UR  - http://rimsi.imsi.bg.ac.rs/handle/123456789/1207
AB  - The Ag, Pd and AgPd alloys of different morphologies and compositions were electrodeposited onto Au and glassy carbon (GC) disc electrodes from the solution containing 0.001 M PdCl2 + 0.04 M AgCl + 0.1 M HCl + 12 M LiCl under the conditions of non-stationary (RPM = 0, samples AgPd1 and AgPd2) and convective diffusion (RPM = 1000, sample AgPd3). Electrodeposited alloy layers were characterized by the scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), and X-ray photoelectron spectroscopy (XPS). Oxygen reduction reaction (ORR) was investigated on all coatings in 0.1 M NaOH solution saturated with oxygen. The j-E curves for the ORR were recorded by two procedures: (1) samples were cycled with 5 mV s(-1) from open circuit potential (OCP) to -0.8 V for Ag and AgPd alloys (or -0.6 V for pure Pd) and back; (2) samples were cycled with 5 mV s(-1) from open circuit potential to 0.45 V (formation of Ag2O, in the case of Pd formation of PdO and PdO2), from 0.45 V to -0.60 V and back to the OCP. Significant catalytic activity for the Ag and AgPd alloys was detected after cycling electrodes in the potential region of Ag2O formation and reduction. Increase of the catalytic activity for AgPd alloys was, for the first time in the literature, ascribed to the presence of a certain amount of Ag2O which could not be completely reduced during the reverse sweep from 0.45 V to -0.6 V. Catalytic activity of AgPd alloys was found to be closely related to the amount of non-reduced Ag2O (most probably in the form of Ag-hydroxide). In the absence of such treatment, the catalytic activity for the ORR on electrodeposited Ag and AgPd alloy coatings was not detected.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Electrochimica Acta
T1  - Synthesis and characterization of AgPd alloy coatings as beneficial catalysts for low temperature fuel cells application
EP  - 368
SP  - 360
VL  - 307
DO  - 10.1016/j.electacta.2019.03.177
ER  - 
@article{
author = "Elezović, Nevenka R. and Lović, J. D. and Jović, Borka M and Zabinski, P. and Wloch, Grzegorz and Jović, Vladimir D",
year = "2019",
abstract = "The Ag, Pd and AgPd alloys of different morphologies and compositions were electrodeposited onto Au and glassy carbon (GC) disc electrodes from the solution containing 0.001 M PdCl2 + 0.04 M AgCl + 0.1 M HCl + 12 M LiCl under the conditions of non-stationary (RPM = 0, samples AgPd1 and AgPd2) and convective diffusion (RPM = 1000, sample AgPd3). Electrodeposited alloy layers were characterized by the scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), and X-ray photoelectron spectroscopy (XPS). Oxygen reduction reaction (ORR) was investigated on all coatings in 0.1 M NaOH solution saturated with oxygen. The j-E curves for the ORR were recorded by two procedures: (1) samples were cycled with 5 mV s(-1) from open circuit potential (OCP) to -0.8 V for Ag and AgPd alloys (or -0.6 V for pure Pd) and back; (2) samples were cycled with 5 mV s(-1) from open circuit potential to 0.45 V (formation of Ag2O, in the case of Pd formation of PdO and PdO2), from 0.45 V to -0.60 V and back to the OCP. Significant catalytic activity for the Ag and AgPd alloys was detected after cycling electrodes in the potential region of Ag2O formation and reduction. Increase of the catalytic activity for AgPd alloys was, for the first time in the literature, ascribed to the presence of a certain amount of Ag2O which could not be completely reduced during the reverse sweep from 0.45 V to -0.6 V. Catalytic activity of AgPd alloys was found to be closely related to the amount of non-reduced Ag2O (most probably in the form of Ag-hydroxide). In the absence of such treatment, the catalytic activity for the ORR on electrodeposited Ag and AgPd alloy coatings was not detected.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Electrochimica Acta",
title = "Synthesis and characterization of AgPd alloy coatings as beneficial catalysts for low temperature fuel cells application",
pages = "368-360",
volume = "307",
doi = "10.1016/j.electacta.2019.03.177"
}
Elezović, N. R., Lović, J. D., Jović, B. M., Zabinski, P., Wloch, G.,& Jović, V. D.. (2019). Synthesis and characterization of AgPd alloy coatings as beneficial catalysts for low temperature fuel cells application. in Electrochimica Acta
Pergamon-Elsevier Science Ltd, Oxford., 307, 360-368.
https://doi.org/10.1016/j.electacta.2019.03.177
Elezović NR, Lović JD, Jović BM, Zabinski P, Wloch G, Jović VD. Synthesis and characterization of AgPd alloy coatings as beneficial catalysts for low temperature fuel cells application. in Electrochimica Acta. 2019;307:360-368.
doi:10.1016/j.electacta.2019.03.177 .
Elezović, Nevenka R., Lović, J. D., Jović, Borka M, Zabinski, P., Wloch, Grzegorz, Jović, Vladimir D, "Synthesis and characterization of AgPd alloy coatings as beneficial catalysts for low temperature fuel cells application" in Electrochimica Acta, 307 (2019):360-368,
https://doi.org/10.1016/j.electacta.2019.03.177 . .
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Electrodeposited AgPd alloy coatings as efficient catalysts for the ethanol oxidation reaction

Lović, J. D.; Elezović, Nevenka R.; Jović, Borka M; Zabinski, P.; Gajić-Krstajić, Ljiljana M; Jović, Vladimir D

(Pergamon-Elsevier Science Ltd, Oxford, 2018)

TY  - JOUR
AU  - Lović, J. D.
AU  - Elezović, Nevenka R.
AU  - Jović, Borka M
AU  - Zabinski, P.
AU  - Gajić-Krstajić, Ljiljana M
AU  - Jović, Vladimir D
PY  - 2018
UR  - http://rimsi.imsi.bg.ac.rs/handle/123456789/1153
AB  - The Pd and three AgPd alloy layers (AgPd1, AgPd2 and AgPd3) were electrodeposited onto Au disc electrodes from the solution containing high concentration of chloride ions (>12 M). All coatings were investigated by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), anodic linear sweep voltammetry (ALSV), while their surface composition was investigated by X-ray photoelectron spectroscopy (XPS). The AgPd1 and AgPd2 samples were electrodeposited at different constant current densities (-0.178 mA cm(-2) and -0.415 mA cm(-2) respectively) to the charge of -0.2 C cm(-2) (thickness similar to 0.18 mu m) at a stationary disc electrode, while the sample AgPd3 was electrodeposited to the charge of -3.0 C cm(-2) (thickness similar to 2.8 mu m) at a constant current density of -7.0 mA cm(-2) under the conditions of convective diffusion. Samples AgPd1 and AgPd2 had similar morphologies of low roughness, while the morphology of AgPd3 was characterized by large crystals and higher roughness. The most active and the most poisoning tolerant coatings for ethanol oxidation reaction (EOR) are the AgPd3 and AgPd1 alloy samples, containing 72.6 at.% Ag - 27.4 at.% Pd and 84.7 at.% Ag - 15.2 at.% Pd respectively (XPS analysis). In this study, we demonstrated for the first time that the activity for the EOR at AgPd alloys was closely related to the amount of non-reduced Ag2O (most probably as Ag - hydroxide). Accordingly, all AgPd alloy samples had to be cycled in the potential region of Ag2O formation and reduction before the investigation of the EOR, in order to provide their catalytic activity towards the EOR.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - International Journal of Hydrogen Energy
T1  - Electrodeposited AgPd alloy coatings as efficient catalysts for the ethanol oxidation reaction
EP  - 18508
IS  - 39
SP  - 18498
VL  - 43
DO  - 10.1016/j.ijhydene.2018.08.056
ER  - 
@article{
author = "Lović, J. D. and Elezović, Nevenka R. and Jović, Borka M and Zabinski, P. and Gajić-Krstajić, Ljiljana M and Jović, Vladimir D",
year = "2018",
abstract = "The Pd and three AgPd alloy layers (AgPd1, AgPd2 and AgPd3) were electrodeposited onto Au disc electrodes from the solution containing high concentration of chloride ions (>12 M). All coatings were investigated by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), anodic linear sweep voltammetry (ALSV), while their surface composition was investigated by X-ray photoelectron spectroscopy (XPS). The AgPd1 and AgPd2 samples were electrodeposited at different constant current densities (-0.178 mA cm(-2) and -0.415 mA cm(-2) respectively) to the charge of -0.2 C cm(-2) (thickness similar to 0.18 mu m) at a stationary disc electrode, while the sample AgPd3 was electrodeposited to the charge of -3.0 C cm(-2) (thickness similar to 2.8 mu m) at a constant current density of -7.0 mA cm(-2) under the conditions of convective diffusion. Samples AgPd1 and AgPd2 had similar morphologies of low roughness, while the morphology of AgPd3 was characterized by large crystals and higher roughness. The most active and the most poisoning tolerant coatings for ethanol oxidation reaction (EOR) are the AgPd3 and AgPd1 alloy samples, containing 72.6 at.% Ag - 27.4 at.% Pd and 84.7 at.% Ag - 15.2 at.% Pd respectively (XPS analysis). In this study, we demonstrated for the first time that the activity for the EOR at AgPd alloys was closely related to the amount of non-reduced Ag2O (most probably as Ag - hydroxide). Accordingly, all AgPd alloy samples had to be cycled in the potential region of Ag2O formation and reduction before the investigation of the EOR, in order to provide their catalytic activity towards the EOR.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "International Journal of Hydrogen Energy",
title = "Electrodeposited AgPd alloy coatings as efficient catalysts for the ethanol oxidation reaction",
pages = "18508-18498",
number = "39",
volume = "43",
doi = "10.1016/j.ijhydene.2018.08.056"
}
Lović, J. D., Elezović, N. R., Jović, B. M., Zabinski, P., Gajić-Krstajić, L. M.,& Jović, V. D.. (2018). Electrodeposited AgPd alloy coatings as efficient catalysts for the ethanol oxidation reaction. in International Journal of Hydrogen Energy
Pergamon-Elsevier Science Ltd, Oxford., 43(39), 18498-18508.
https://doi.org/10.1016/j.ijhydene.2018.08.056
Lović JD, Elezović NR, Jović BM, Zabinski P, Gajić-Krstajić LM, Jović VD. Electrodeposited AgPd alloy coatings as efficient catalysts for the ethanol oxidation reaction. in International Journal of Hydrogen Energy. 2018;43(39):18498-18508.
doi:10.1016/j.ijhydene.2018.08.056 .
Lović, J. D., Elezović, Nevenka R., Jović, Borka M, Zabinski, P., Gajić-Krstajić, Ljiljana M, Jović, Vladimir D, "Electrodeposited AgPd alloy coatings as efficient catalysts for the ethanol oxidation reaction" in International Journal of Hydrogen Energy, 43, no. 39 (2018):18498-18508,
https://doi.org/10.1016/j.ijhydene.2018.08.056 . .
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