Published January 1, 2017
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Temperature-dependence of oxygen reduction activity on Pt/C and PtCr/C electrocatalysts synthesized from microwave-heated diethylene glycol method
Creators
- 1. Univ Poitiers, IC2MP, UMR 7285, CNRS,Equipe SAMCat, 4 Rue Michel Brunet,B27,TSA 51106, F-86073 Poitiers 09, France
- 2. Univ Joseph Fourier, Lab Electrochim & Physicochim Mat & Interfaces LE, UMR 5279, CNRS,Grenoble INP,Univ Savoie, BP 75, F-38402 St Martin Dheres, France
- 3. Istanbul Tech Univ, Fac Sci & Letters, Dept Chem, TR-34469 Istanbul, Turkey
Description
This work reports first the synthesis of carbon supported Pt and Pt-Cr electrode materials from microwave-heated diethylene glycol (DEG) without additional protective agents. The prepared electro-catalysts have superior electrochemical activity and stability than those previously reported in acidic medium. Transmission electron microscopy (TEM) characterizations of these materials reveal uniformly dispersed particles with a mean size of ca. 1.20 nm. The morphological changes of these two materials were investigated by identical location-transmission electron microscopy (IL-TEM) after classical durability test. The electrocatalytic activity towards the oxygen reduction reaction (ORR) was investigated using rotating disk electrode (RDE) and rotating ring disk electrode (RRDE) techniques in 0.1 mol L-1 HClO4. The kinetic parametdrs were assessed through the Koutecky-Levich equation at 20, 30 and 40 degrees C. Electrochemical measurements demonstrate that significantly higher catalytic activity was observed on the Pt-Cr/C electrocatalyst than on Pt/C. The RRDE analysis shows that the ORR mainly involves a four-electron reduction mechanism to water with the formation of a very low H2O2 amount as reaction intermediate. (C) 2016 Elsevier B.V. All rights reserved.
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