Performance and durability of a layered proton conducting solid oxide fuel cell fueled by the dry reforming of methane

被引:12
作者
Guo, Youmin [1 ]
Wan, Tingting [1 ]
Zhu, Ankang [1 ]
Shi, Tingting [1 ]
Zhang, Guilin [1 ]
Wang, Chunchang [1 ]
Yu, Hao [2 ]
Shao, Zongping [3 ,4 ]
机构
[1] Anhui Univ, Sch Phys & Mat Sci, 111 Jiulong Rd, Hefei 230601, Anhui, Peoples R China
[2] Shandong Univ Sci & Technol, Coll Chem & Environm Engn, Qingdao 266590, Peoples R China
[3] Nanjing Tech Univ, Coll Energy, Jiangsu Natl Synerget Innovat Ctr Adv Mat, State Key Lab Mat Oriented Chem Engn, Nanjing 210009, Jiangsu, Peoples R China
[4] Curtin Univ, Dept Chem Engn, Perth, WA 6845, Australia
来源
RSC ADVANCES | 2017年 / 7卷 / 70期
基金
中国国家自然科学基金;
关键词
SUPPORTED NICKEL-CATALYSTS; OF-THE-ART; CARBON-DIOXIDE; SYNTHESIS GAS; RAMAN-SPECTROSCOPY; SOFCS; DEPOSITION; PRECURSOR; NI/LA2O3; HYDROGEN;
D O I
10.1039/c7ra07710f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Catalyst layers derived from La2NiO4, LaNiO3 and Ni/La2O3 precursors were applied to a conventional Ni-based anode in a proton conducting solid oxide fuel cell (H+-SOFC) for the dry reforming of methane with CO2. The phase structures, microstructures and catalytic activities of catalysts from the different precursors were systematically investigated. The cell performance and durability of a H+-SOFC with a catalyst layer (layered H+-SOFC) were examined. The layered H+-SOFC had higher cell performances than the conventional H+-SOFC. However, catalyst deactivation and degradation of the cell performance were observed as carbon deposition occurred on the catalyst layer due to CO disproportionation in exhaust gas at a high partial pressure of CO. The structure of carbon deposited on the catalysts was also investigated.
引用
收藏
页码:44319 / 44325
页数:7
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