TY  - JOUR
AU  - Elezović, Nevenka R.
AU  - Zabinski, Piotr
AU  - Krstajic-Pajic, M. N.
AU  - Tokarski, Tomasz
AU  - Jović, Borka M
AU  - Jović, Vladimir D
PY  - 2018
UR  - http://rimsi.imsi.bg.ac.rs/handle/123456789/1131
AB  - The AgPd alloys were electrodeposited onto Au and glassy carbon disc electrodes from the solution containing 0 001 mol dm(-3) PdCl2 + 0.04 mol dm(-3) AgCl + 0.1 mol dm(-3) HCl + 12 mol dm(-3) LiCl under the non-stationary diffusion (quiescent electrolyte) and convective diffusion (omega = 1000 rpm) to the different amounts of charge and at different current densities. Electro-deposited alloy layers were characterized by the anodic linear sweep voltam-metry (ALSV), scanning electron microscopy, energy dispersive X-ray spectro-scopy (EDS) and X-ray photoelectron spectroscopy (XPS). The compositions of the AgPd alloys determined by the EDS were almost identical to the theoretically predicted ones, while the compositions obtained by XPS and ALSV analysis were similar to each other, but different from those obtained by EDS. Deviation from the theoretically predicted values (determined by the ratio j(L)(Pd)/j(Ag)) was more pronounced at lower current densities and lower charges of AgPd alloys electrodeposition, due to the lower current efficiencies for alloys electrodeposition. The ALSV analysis indicated the presence of Ag and Pd, expressed by two ALSV peaks, and in some cases the presence of the additional peak, which was found to correspond to the dissolution of large AgPd crystals, formed at thicker electrodeposits (higher electrodeposition charge), indicating, for the first time, that besides the phase structure, the morphology of alloy electrodeposit could also influence the shape of the ALSV response. In addition to Ag and Pd, the XPS analysis confirmed the presence of AgCl at the surface of samples electrodeposited to low thicknesses (amounts of charge).
PB  - Srpsko hemijsko društvo, Beograd
T2  - Journal of the Serbian Chemical Society
T1  - Electrochemical deposition and characterization of AgPd alloy layers
EP  - 609
IS  - 5
SP  - 593
VL  - 83
DO  - 10.2298/JSC171103011E
ER  - 

@article{
author = "Elezović, Nevenka R. and Zabinski, Piotr and Krstajic-Pajic, M. N. and Tokarski, Tomasz and Jović, Borka M and Jović, Vladimir D",
year = "2018",
abstract = "The AgPd alloys were electrodeposited onto Au and glassy carbon disc electrodes from the solution containing 0 001 mol dm(-3) PdCl2 + 0.04 mol dm(-3) AgCl + 0.1 mol dm(-3) HCl + 12 mol dm(-3) LiCl under the non-stationary diffusion (quiescent electrolyte) and convective diffusion (omega = 1000 rpm) to the different amounts of charge and at different current densities. Electro-deposited alloy layers were characterized by the anodic linear sweep voltam-metry (ALSV), scanning electron microscopy, energy dispersive X-ray spectro-scopy (EDS) and X-ray photoelectron spectroscopy (XPS). The compositions of the AgPd alloys determined by the EDS were almost identical to the theoretically predicted ones, while the compositions obtained by XPS and ALSV analysis were similar to each other, but different from those obtained by EDS. Deviation from the theoretically predicted values (determined by the ratio j(L)(Pd)/j(Ag)) was more pronounced at lower current densities and lower charges of AgPd alloys electrodeposition, due to the lower current efficiencies for alloys electrodeposition. The ALSV analysis indicated the presence of Ag and Pd, expressed by two ALSV peaks, and in some cases the presence of the additional peak, which was found to correspond to the dissolution of large AgPd crystals, formed at thicker electrodeposits (higher electrodeposition charge), indicating, for the first time, that besides the phase structure, the morphology of alloy electrodeposit could also influence the shape of the ALSV response. In addition to Ag and Pd, the XPS analysis confirmed the presence of AgCl at the surface of samples electrodeposited to low thicknesses (amounts of charge).",
publisher = "Srpsko hemijsko društvo, Beograd",
journal = "Journal of the Serbian Chemical Society",
title = "Electrochemical deposition and characterization of AgPd alloy layers",
pages = "609-593",
number = "5",
volume = "83",
doi = "10.2298/JSC171103011E"
}

Elezović, N. R., Zabinski, P., Krstajic-Pajic, M. N., Tokarski, T., Jović, B. M.,& Jović, V. D.. (2018). Electrochemical deposition and characterization of AgPd alloy layers. in Journal of the Serbian Chemical Society
Srpsko hemijsko društvo, Beograd., 83(5), 593-609.
https://doi.org/10.2298/JSC171103011E

Elezović NR, Zabinski P, Krstajic-Pajic MN, Tokarski T, Jović BM, Jović VD. Electrochemical deposition and characterization of AgPd alloy layers. in Journal of the Serbian Chemical Society. 2018;83(5):593-609.
doi:10.2298/JSC171103011E .

Elezović, Nevenka R., Zabinski, Piotr, Krstajic-Pajic, M. N., Tokarski, Tomasz, Jović, Borka M, Jović, Vladimir D, "Electrochemical deposition and characterization of AgPd alloy layers" in Journal of the Serbian Chemical Society, 83, no. 5 (2018):593-609,
https://doi.org/10.2298/JSC171103011E . .

TY  - JOUR
AU  - Krstajic, Mila N
AU  - Obradović, Maja D
AU  - Babić, Biljana M.
AU  - Radmilović, Velimir R
AU  - Lačnjevac, Uroš
AU  - Krstajić, Nedeljko V
AU  - Gojković, Snežana Lj
PY  - 2013
UR  - http://rimsi.imsi.bg.ac.rs/handle/123456789/640
AB  - Ru-doped SnO2 powder, (RuxSn1-x)O-2, with a Sn:Ru atomic ratio of 9:1 was synthesized and used as a support for Pt nanoparticles (30 mass % loading). The (RuxSn1-x)O-2 support and the Pt/(RuxSn1-x)O-2 catalyst were characterized by X-ray diffraction measurements, energy dispersive X-ray spectroscopy and transmission electron microscopy (TEM). The (RuxSn1-x)O-2 was found to be a two-phase material consisting of probably a solid solution of RuO2 in SnO2 and pure RuO2. The average Pt particle size determined by TEM was 5.3 nm. Cyclic voltammetry of Pt/(RuxSn1-x)O-2 indicated good conductivity of the support and displayed the usual features of Pt. The results of the electrochemical oxidation of COad, and methanol on Pt/(RuxSn1-x)O-2 were compared with those on commercial Pt/C and PtRu/C catalysts. Oxidation of COads on Pt/(RuxSn1-x)O-2 starts at lower positive potentials than on PtRu/C and Pt/C. Potentiodynamic polarization curves and chronoamperometric curves of methanol oxidation indicated higher initial activity of the Pt/(RuxSn1-x)O-2 catalyst compared to PtRu/C, but also a greater loss in current density over time. A potentiodynamic stability test of the catalysts revealed that deactivation of Pt/(RuxSn1-x)O-2 and Pt/C was primarily caused by poisoning of the Pt surface by residues of methanol oxidation, which mostly occurred during the first potential cycle. In the case of PtRu/C, the poisoning of the surface was minor and deactivation was caused by surface area loss of the PtRu.
PB  - Srpsko hemijsko društvo, Beograd
T2  - Journal of the Serbian Chemical Society
T1  - Electrochemical oxidation of methanol on Pt/(RuxSn1-x)O-2 nanocatalyst
EP  - 1716
IS  - 11
SP  - 1703
VL  - 78
DO  - 10.2298/JSC130718091K
ER  - 

@article{
author = "Krstajic, Mila N and Obradović, Maja D and Babić, Biljana M. and Radmilović, Velimir R and Lačnjevac, Uroš and Krstajić, Nedeljko V and Gojković, Snežana Lj",
year = "2013",
abstract = "Ru-doped SnO2 powder, (RuxSn1-x)O-2, with a Sn:Ru atomic ratio of 9:1 was synthesized and used as a support for Pt nanoparticles (30 mass % loading). The (RuxSn1-x)O-2 support and the Pt/(RuxSn1-x)O-2 catalyst were characterized by X-ray diffraction measurements, energy dispersive X-ray spectroscopy and transmission electron microscopy (TEM). The (RuxSn1-x)O-2 was found to be a two-phase material consisting of probably a solid solution of RuO2 in SnO2 and pure RuO2. The average Pt particle size determined by TEM was 5.3 nm. Cyclic voltammetry of Pt/(RuxSn1-x)O-2 indicated good conductivity of the support and displayed the usual features of Pt. The results of the electrochemical oxidation of COad, and methanol on Pt/(RuxSn1-x)O-2 were compared with those on commercial Pt/C and PtRu/C catalysts. Oxidation of COads on Pt/(RuxSn1-x)O-2 starts at lower positive potentials than on PtRu/C and Pt/C. Potentiodynamic polarization curves and chronoamperometric curves of methanol oxidation indicated higher initial activity of the Pt/(RuxSn1-x)O-2 catalyst compared to PtRu/C, but also a greater loss in current density over time. A potentiodynamic stability test of the catalysts revealed that deactivation of Pt/(RuxSn1-x)O-2 and Pt/C was primarily caused by poisoning of the Pt surface by residues of methanol oxidation, which mostly occurred during the first potential cycle. In the case of PtRu/C, the poisoning of the surface was minor and deactivation was caused by surface area loss of the PtRu.",
publisher = "Srpsko hemijsko društvo, Beograd",
journal = "Journal of the Serbian Chemical Society",
title = "Electrochemical oxidation of methanol on Pt/(RuxSn1-x)O-2 nanocatalyst",
pages = "1716-1703",
number = "11",
volume = "78",
doi = "10.2298/JSC130718091K"
}

Krstajic, M. N., Obradović, M. D., Babić, B. M., Radmilović, V. R., Lačnjevac, U., Krstajić, N. V.,& Gojković, S. L.. (2013). Electrochemical oxidation of methanol on Pt/(RuxSn1-x)O-2 nanocatalyst. in Journal of the Serbian Chemical Society
Srpsko hemijsko društvo, Beograd., 78(11), 1703-1716.
https://doi.org/10.2298/JSC130718091K

Krstajic MN, Obradović MD, Babić BM, Radmilović VR, Lačnjevac U, Krstajić NV, Gojković SL. Electrochemical oxidation of methanol on Pt/(RuxSn1-x)O-2 nanocatalyst. in Journal of the Serbian Chemical Society. 2013;78(11):1703-1716.
doi:10.2298/JSC130718091K .

Krstajic, Mila N, Obradović, Maja D, Babić, Biljana M., Radmilović, Velimir R, Lačnjevac, Uroš, Krstajić, Nedeljko V, Gojković, Snežana Lj, "Electrochemical oxidation of methanol on Pt/(RuxSn1-x)O-2 nanocatalyst" in Journal of the Serbian Chemical Society, 78, no. 11 (2013):1703-1716,
https://doi.org/10.2298/JSC130718091K . .