Composite manganate oxygen electrode enhanced with iron oxide nanocatalyst for high temperature steam electrolysis in a proton-conducting solid oxide electrolyzer

被引:32
|
作者
Li, Huaxin [1 ]
Chen, Xiaoli [1 ]
Chen, Shigang [1 ]
Wu, Yucheng [1 ]
Xie, Kui [1 ,2 ]
机构
[1] Hefei Univ Technol, Sch Mat Sci & Engn, Hefei 230009, Anhui, Peoples R China
[2] Chinese Acad Sci, Fujian Inst Res Struct Matter, Key Lab Design & Assembly Funct Nanostruct, Fuzhou 350002, Fujian, Peoples R China
关键词
Iron oxide; Manganate; Proton conductor; Steam electrolysis; RAY PHOTOELECTRON-SPECTROSCOPY; HYDROGEN-PRODUCTION; FUEL-CELLS; COPPER NANOCATALYST; CATHODE; CARBON; PERFORMANCE; ANODES; POLARIZATION; IMPREGNATION;
D O I
10.1016/j.ijhydene.2015.04.067
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
Composite electrode based on La0.8Sr0.2MnO3-delta (LSM) can be utilized in a proton-conducting solid oxide electrolyzer for steam electrolysis; however, the insufficient electro-catalytic activity of LSM still restricts the electrode performance and Faraday current efficiency. In this work, catalytic-active iron oxide nanoparticles are loaded on the surface of LSM composite oxygen electrode to improve electro-catalytic performance as well as extend the three-phase boundaries. SEM and EDS results together confirm the loading of Fe2O3 nanoparticles with the size of approximately 20-40 nm on the surface of LSM composite oxygen electrode. The effects on electrode performance due to different contents of Fe2O3 are loaded into LSM composite electrodes are systemically studied using symmetric cells. The electrical property of LSM is investigated and correlated to the electrochemical performance of the composite oxygen electrode in electrolysis cells. The maximum Faraday current efficiency is approximately 65% with the Fe2O3-loaded LSM composite electrode for steam electrolysis in a proton-conducting solid oxide electrolyzer at 800 degrees C. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:7920 / 7931
页数:12
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