Synthesis and evaluation of ATO as a support for Pt-IrO2 in a unitized regenerative fuel cell

被引:48
作者
Cruz, J. C. [1 ]
Rivas, S. [2 ]
Beltran, D. [1 ]
Meas, Y. [1 ]
Ornelas, R. [3 ]
Osorio-Monreal, G. [1 ]
Ortiz-Frade, L. [1 ]
Ledesma-Garcia, J. [4 ]
Arriaga, L. G. [1 ]
机构
[1] Ctr Invest & Desarrollo Tecnol Electroquim SC, Pedro Escobedo 76703, Queretaro, Mexico
[2] Ctr Invest Energia, Temixco 62580, Morelos, Mexico
[3] Tozzi Renewable Energy SpA, I-1048010 Mezzano, RA, Italy
[4] Univ Autonoma Queretaro, Div Invest & Posgrado, Fac Ingn, Queretaro 76010, Mexico
关键词
Water electrolysis; ATO support; Unitized regenerative fuel cell; Oxygen evolution; Oxygen reduction; OXYGEN EVOLUTION REACTION; CATALYST SUPPORT; PEM ELECTROLYSIS; TUNGSTEN CARBIDE; PLATINUM; ELECTRODES; ELECTROCATALYSTS; HYDROGEN; BEHAVIOR; PERFORMANCE;
D O I
10.1016/j.ijhydene.2012.06.095
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
An IrO2 catalyst was prepared using a colloidal method followed by a thermal treatment. The catalyst was later mixed with Pt-Black and supported on the Sb-doped SnO2 (ATO), synthesized through the same colloidal method. ATO was investigated as a possible catalyst support in an electrode of a regenerative fuel cell (URFC), where Pt-IrO2 was used as the catalyst for the oxygen evolution and reduction reactions. The morphology and composition of the ATO support was investigated through transmission electron microscopy, X-ray diffraction (including Rietveld Refinement), BET analysis, and X-ray fluorescence. An ATO support was obtained with a highly homogeneous distribution and crystal sizes, measuring approximately 4-6 nm. The Pt-IrO2/ATO material was deposited on a Nafion 115 membrane with 0.5 mg cm(-2) of catalyst loading. Pt/Vulcan XC-72 (30 wt. %, E-TEK) was used as the catalyst in the H-2 compartment with a Pt loading of 0.4 mg cm(-2). The electrochemical activity of the Pt IrO2/ATO for oxygen evolution/reduction in the URFC system was investigated by AC-impedance spectroscopy, linear voltammetry, and chronoamperometry techniques. The maximum mass current activity was 1118 A g(-1) at 1.8 V in proton-exchange membrane water electrolyser mode (PEMWE) and 565 A g(-1) at 0.3 V in proton-exchange membrane fuel cell mode (PEMFC), both at 80 degrees C. The value of the round-trip energy efficiency was approximately 48% at 50 A g(-1). Copyright (C) 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:13522 / 13528
页数:7
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