Evaluation of the corrosion of Sb-doped SnO2 supports for electrolysis systems

被引:15
作者
Gurrola, M. P. [1 ]
Gutierrez, J. [1 ]
Rivas, S. [2 ]
Guerra-Balcazar, M. [2 ]
Ledesma-Garda, J. [2 ]
Arriaga, L. G. [1 ]
机构
[1] Ctr Invest & Desarrollo Tecnol Electroquim, Queretaro 76703, Mexico
[2] Univ Autonoma Queretaro, Fac Ingn, Div Invest & Posgrado, Queretaro 76010, Mexico
关键词
ATO support; Corrosion resistance; High surface area; Solid polymer electrolyser; THIN-FILMS; ELECTROCATALYTIC ACTIVITY; PLATINUM NANOPARTICLES; CERAMIC ELECTRODES; CARBON NANOTUBES; OXYGEN EVOLUTION; TITANIUM-OXIDES; TEMPERATURE; EBONEX(R); TIN;
D O I
10.1016/j.ijhydene.2014.02.156
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The corrosion behaviour and electrochemical stability of two different electrocatalyst supports based on Sb-doped SnO2 (ATO) were evaluated in an acidic medium over a wide potential range (0-1.8 V vs. NHE). The results were compared with those from a commercial Vulcan carbon XC-72 (254 m(2) g(-1)) support. ATO (85 m(2) g(-1)) and modified-ATO (216 m(2) g(-1)) were synthesized by the sol-gel method and were then characterized by XRD, BET and TEM. The modification of the ATO consisted of adding dodecylamine as a surfactant to generate a surface area similar to that of Vulcan carbon. The electrochemical characterization conditions were chosen to match the operating conditions of a proton exchange membrane fuel cell (PEMFC) and a solid polymer electrolyser (SPE), where the oxygen-evolution reaction takes place at a potential near 1.6 V with respect to normal hydrogen electrode (NHE). The results show good chemical stability when the ATO and the modified-ATO are subjected to these conditions, whereas Vulcan carbon corrodes easily. This indicates that Sb-doped SnO2 is a good candidate for electrocatalyst supports for energy-conversion systems such as electrolysers and unified regenerative fuel cells. Copyright (C) 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:16763 / 16770
页数:8
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