Optimization of a direct carbon fuel cell for operation below 700°C

被引:33
|
作者
Xu, Xiaoyong [1 ]
Zhou, Wei [1 ]
Liang, Fengli [1 ]
Zhu, Zhonghua [1 ]
机构
[1] Univ Queensland, Sch Chem Engn, St Lucia, Qld 4072, Australia
基金
澳大利亚研究理事会;
关键词
Direct carbon fuel cell; Electrolyte-supported fuel cell; Solid carbon; Carbonates; SOLID OXIDE; ELECTROCHEMICAL OXIDATION; COMPLEXING PROCESS; DIRECT CONVERSION; ELECTROLYTE; PERFORMANCE; CATHODE; POWER; SLURRIES; ANODE;
D O I
10.1016/j.ijhydene.2013.02.066
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
Direct carbon fuel cells (DCFCs) are the most efficient technology to convert solid carbon energy to electricity and thus could have a major impact on reducing fuel consumption and CO2 emissions. The development of DCFCs to commercialisation stage is largely prohibited by their poor power densities due to the high resistive loss from anode. Here, we report a high-performance Sm0.2Ce0.8O1.9 electrolyte-supported hybrid DCFC with Ba0.5Sr0.5Co0.8Fe0.2O3-delta cathode and optimised anode configuration. The catalytic oxidation of carbon is improved, which results in an area specific resistance of only 0.41 Omega cm(2) at 650 degrees C at the anode. The hybrid DCFC achieves a peak power density of 113.1 mW cm(-2) at 650 degrees C operating on activated carbon. The stability of the fuel cell has also been improved due to the optimised current collection. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:5367 / 5374
页数:8
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