Direct carbon dioxide-methane solid oxide fuel cells integrated for high-efficiency power generation with La0.75Sr0.25Cr0.5Fe0.4Ni0.1O3-δ-based dry reforming catalyst

被引:7
作者
Rao, Mumin [1 ]
Li, Mingfei [1 ]
Chen, Zhengpeng [1 ]
Xiong, Kai [2 ]
Huang, Hui [2 ]
Yang, Weiguo [3 ]
Ling, Yihan [4 ]
Chen, Chuangting [1 ]
Zhang, Zongming [3 ]
Lin, Bin [5 ]
机构
[1] Guangdong Energy Grp Sci & Technol Res Inst Co Ltd, Guangzhou 510000, Peoples R China
[2] Guangdong Energy Grp Co Ltd, Guangzhou 510000, Peoples R China
[3] Guangdong Huizhou Lng Power Co Ltd, Huizhou 516000, Peoples R China
[4] China Univ Min & Technol, Sch Mat Sci & Phys, Xuzhou 221116, Peoples R China
[5] Univ Elect Sci & Technol China, Sch Mech & Elect Engn, Chengdu 611731, Peoples R China
基金
中国国家自然科学基金;
关键词
Solid oxide fuel cells; Cermet anode; Carbon deposition; Dry reforming catalyst; Thermodynamic calculation; IN-SITU; ELECTROCHEMICAL PERFORMANCE; RAMAN-SPECTROSCOPY; DEPOSITION; STABILITY; IMPEDANCE; ANODE; OXIDATION; ELECTRODE; CATHODES;
D O I
10.1016/j.seppur.2022.122831
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Solid oxide fuel cell (SOFC) can directly convert carbon-based fuels to power with low environmental impact and high energy efficiency, while there is still one of the key challenges that carbon deposition over Ni-based cermet anodes causes serious performance degradation. Herein, a Ni-doped perovskite, La0.75Sr0.25Cr0.5Fe0.4Ni0.1O3-delta (LSCFN), is prepared to design exsolution systems and evaluated as the dry reforming catalyst for direct carbon dioxide-methane SOFCs. It is demonstrated that the reducing atmosphere in anode effectively induce the NiFe alloy nanoparticles exsolution from LSCFN, and provide abundant active sites for dry reforming. Anode sup-ported single cells with LSCFN-Ce0.9Gd0.1O2-delta (LSCFN-GDC) composite reforming catalyst show excellent elec-trochemical performance in both H-2 and CH4-CO2, and the peak power densities of 686.05 and 684.83 mW.cm(-2) are obtained at 800 degrees C, respectively. The dry reforming of 50 %CH(4-)50 %CO2 integrated with LSCFN-GDC reforming catalyst is sustained for 100 h stable performance at 700 degrees C without any degradation, which are further confined by the experimental verification and thermodynamic calculation. These results demonstrate that additional dry reforming catalyst is an effective strategy to effectively manipulate CH4-CO2 reforming and electrochemical performance for energy purposes.
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页数:10
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