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Branimir N. Grgur
Researcher at University of Belgrade
Publications - 139
Citations - 6633
Branimir N. Grgur is an academic researcher from University of Belgrade. The author has contributed to research in topics: Polyaniline & Corrosion. The author has an hindex of 34, co-authored 130 publications receiving 6078 citations. Previous affiliations of Branimir N. Grgur include Ben-Gurion University of the Negev & Lawrence Berkeley National Laboratory.
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Temperature-dependent oxygen electrochemistry on platinum low-index single crystal surfaces in acid solutions
TL;DR: Using the rotating ring disk technique (RRDPt(hkl)E), the ORR was studied in sulfuric acid solution over the temperature range 298 −333 K at the same temperature, the exc...
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Temperature-dependent hydrogen electrochemistry on platinum low-index single-crystal surfaces in acid solutions
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Methanol electrooxidation on supported Pt and PtRu catalysts in acid and alkaline solutions
Amalija V. Tripković,K.D Popović,Branimir N. Grgur,Berislav Blizanac,Philip N. Ross,Nenad M. Markovic +5 more
TL;DR: In this article, it was found that the activity of Pt and Pt-Ru catalysts for methanol oxidation is a strong function of pH of solution and temperature, which is attributed to the pH competitive adsorption of oxygenated species with anions from supporting electrolytes.
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Oxygen reduction reaction on Pt(111): effects of bromide
TL;DR: In this paper, the same authors showed that strongly adsorbed Br − can simultaneously suppress both the adsorption of O 2 molecule and the formation of pairs of platinum sites needed for the breaking of the O-O bond.
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Effect of temperature on surface processes at the Pt(111)-liquid interface: Hydrogen adsorption, oxide formation and CO oxidation
Nenad M. Markovic,Thomas J. Schmidt,Branimir N. Grgur,Hubert A. Gasteiger,Rolf Jürgen Behm,Philip N. Ross +5 more
TL;DR: In this article, it was shown that the heat of adsorption of hydrogen on Pt(111) at the electrochemical interface is essentially independent of either the pH of the electrolyte or the nature of the supporting anion.