Nataša M. Petrović

Dr. Nataša M. Petrović

Department of Electrochemistry, Institute of Chemistry, Technology and Metallurgy, University of Belgrade
orcid

Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 March 2020 in Transactions of Nonferrous Metals Society of China
Verified
Journal Article
Closed access
VCVesna S. Cvetković
Vesna S. Cvetković
Nataša M. PetrovićNataša M. Petrović
Nataša M. Petrović
NJNiko Jovićević
Niko Jovićević
JSJasmina S. Stevanović
Jasmina S. Stevanović
JJJovan N. Jovićević
Jovan N. Jovićević

1 April 2018 in Electrochimica Acta
Verified
Journal Article
Closed access
Vesna S. CvetkovicVesna S. Cvetkovic
Vesna S. Cvetkovic
Nataša M. PetrovićNataša M. Petrović
Nataša M. Petrović
Nebojša NikolićNebojša Nikolić
Nebojša Nikolić
GBGoran Branković
Goran Branković
TBTanja Barudzija
Tanja Barudzija
Jovan N. JovićevićJovan N. Jovićević
Jovan N. Jovićević

28 April 2020 in Metals
Verified
Journal Article
Open access
PDF file
Vesna S. CvetkovicVesna S. Cvetkovic
Vesna S. Cvetkovic
Dominic FeldhausDominic Feldhaus
Dominic Feldhaus
Nataša M. PetrovićNataša M. Petrović
Nataša M. Petrović
TBTanja Barudzija
Tanja Barudzija
Bernd FriedrichBernd Friedrich
Bernd Friedrich
Jovan N. JovićevićJovan N. Jovićević
Jovan N. Jovićević
Neodymium was electrochemically deposited from NdF3–LiF–Nd2O3 molten salt electrolyte onto the Mo electrode at temperatures close to 1273 K. Cyclic voltammetry and chronoamperometry measurements were the applied electrochemical methods. Metallic neodymium is obtained by potentiostatic deposition. The optical microscopy and XRD were used to analyze the electrolyte, the working electrode surface, and the deposit on the electrode. It was established that Nd(III) ions were reduced to Nd metals in two steps: Nd(III) + e− → Nd(II) at potential ≈−0.55 V vs. W and Nd(II) + 2e− → Nd(0) at ≈−0.83 V vs. W. Both of these processes are reversible and under mass transfer control. Upon deposition under the regime of relatively small deposition overpotential of −0.10 V to −0.20 V, and after the electrolyte was cooled off, Nd metal was observed at the surface of the Mo electrode. CO and CF4 were gases registered as being evolved at the anode. CO and CF4 evolution were observed in quantities below 600 ppm and 10 ppm, respectively.

1 July 2020 in International Journal of Electrochemical Science
Verified
Journal Article
Open access
Vesna S. CvetkovicVesna S. Cvetkovic
Vesna S. Cvetkovic
Nataša M. PetrovićNataša M. Petrović
Nataša M. Petrović
DFDominic Feldhaus
Dominic Feldhaus
TBTanja Barudzija
Tanja Barudzija
JSJasmina S. Stevanović
Jasmina S. Stevanović
JJJovan N. Jovićević
Jovan N. Jovićević

1 June 2019 in Journal of Electroanalytical Chemistry
Verified
Journal Article
Closed access
Vesna S. CvetkovicVesna S. Cvetkovic
Vesna S. Cvetkovic
Nataša M. PetrovićNataša M. Petrović
Nataša M. Petrović
Nebojša NikolićNebojša Nikolić
Nebojša Nikolić
ZBZvezdana Baščarević
Zvezdana Baščarević
TBTanja Barudzija
Tanja Barudzija
JJJovan N. Jovićević
Jovan N. Jovićević

15 March 2017 in Metals
Verified
Journal Article
Open access
PDF file
Vesna S. CvetkovicVesna S. Cvetkovic
Vesna S. Cvetkovic
NJNiko Jovićević
Niko Jovićević
JSJasmina S. Stevanović
Jasmina S. Stevanović
MPMiomir G. Pavlović
Miomir G. Pavlović
Nataša M. PetrovićNataša M. Petrović
Nataša M. Petrović
Jovan N. JovićevićJovan N. Jovićević
Jovan N. Jovićević
Magnesium underpotential deposition on gold electrodes from magnesium nitrate –ammonium nitrate melts has been investigated. Linear sweep voltammetry and potential step were used as electrochemical techniques. Scanning electron microscopy (SEM), energy dispersive spectrometry (EDS) and X-ray diffraction (XRD) were used for characterization of obtained electrode surfaces. It was observed that reduction processes of nitrate, nitrite and traces of water (when present), in the Mg underpotential range studied, proceeded simultaneously with magnesium underpotential deposition. There was no clear evidence of Mg/Au alloy formation induced by Mg UPD from the melt made from eutectic mixture [Mg(NO3)2·6H2O + NH4NO3·XH2O]. However, EDS and XRD analysis showed magnesium present in the gold substrate and four different Mg/Au alloys being formed as a result of magnesium underpotential deposition and interdiffusion between Mg deposit and Au substrate from the melt made of a nonaqueous [Mg(NO3)2 + NH4NO3] eutectic mixture at 460 K.