Study on proton-conducting solid oxide fuel cells with a conventional nickel cermet anode operating on dimethyl ether

被引:11
|
作者
Liu, Yu [1 ]
Guo, Youmin [1 ]
Wang, Wei [1 ]
Su, Chao [1 ]
Ran, Ran [1 ]
Wang, Huanting [2 ]
Shao, Zongping [1 ,2 ]
机构
[1] Nanjing Univ Technol, State Key Lab Mat Oriented Chem Engn, Nanjing 210009, Peoples R China
[2] Monash Univ, Dept Chem Engn, Clayton, Vic 3800, Australia
基金
澳大利亚研究理事会; 美国国家科学基金会;
关键词
Dimethyl ether; Proton conductor; Solid oxide fuel cells; Coke formation; Steam reforming; HIGH-PERFORMANCE; HYDROGEN-PRODUCTION; TEMPERATURE; CATHODE; ELECTROLYTES; GENERATION; CATALYST; AMMONIA;
D O I
10.1016/j.jpowsour.2011.07.051
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
This study investigates dimethyl ether (DME) as a potential fuel for proton-conducting SOFCs with a conventional nickel cermet anode and a BaZr0.4Ce0.4Y0.2O3-delta (BZCY4) electrolyte. A catalytic test demonstrates that the sintered Ni + BZCY4 anode has an acceptable catalytic activity for the decomposition and steam reforming of DME with CO, CH4 and CO2 as the only gaseous carbon-containing products. An O-2-TPO analysis demonstrates the presence of a large amount of coke formation over the anode catalyst when operating on pure DME, which is effectively suppressed by introducing steam into the fuel gas. The selectivity towards CH4 is also obviously reduced. Peak power densities of 252, 280 and 374 mW cm(-2) are achieved for the cells operating on pure DME, a DME + H2O gas mixture (1:3) and hydrogen at 700 degrees C, respectively. After the test, the cell operating on pure DME is seriously cracked whereas the cell operating on DME + H2O maintains its original integrity. A lower power output is obtained for the cell operating on DME + H2O than on H-2 at low temperature, which is mainly due to the increased electrode polarization resistance. The selection of a better proton-conducting phase in the anode is critical to further increase the cell power output. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:9246 / 9253
页数:8
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