4.7 Article

A stable chromite anode for SOFC with Ce/Ni exsolution for simultaneous electricity generation and CH4 reforming

Journal

SEPARATION AND PURIFICATION TECHNOLOGY
Volume 315, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.seppur.2023.123739

Keywords

Solid oxide fuel cell; Perovskite anode; Ce; Ni-doping; Hydrogen energy

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This study explores the in-situ decoration of CeO2 and Ni nanoparticles on the surface of a chromite anode in order to enhance the performance and stability of solid oxide fuel cells (SOFCs). The exsolution of CeO2 and Ni0 nanoparticles significantly improves the performance of the Ce-LCN anode under propane and H2 fuel conditions. Injecting 20% H2 in volume into CH4 has been found to effectively enhance the coking resistance of the anode, resulting in a CH4 conversion rate of approximately 85% and close to unity selectivity for CO. This study provides a viable solution for the simultaneous production of electricity and syngas from CH4 using complex perovskite SOFCs.
Solid oxide fuel cells (SOFCs) operating at a high temperature can be used to generate electricity and produce syngas from hydrocarbon fuels. In this work, the in-situ decoration of CeO2 and Ni nanoparticles on the surface of chromite anode has been explored; i.e., the exsolution of CeO2 from La0.75Ce0.05Ca0.2Cr0.9Ni0.1O3 (Ce-LCN) can be achieved in the oxygenation in air to boost the exsolution of Ni0 under the fuel condition. The SOFC with a Ce-LCN anode showed higher performance and better stability under propane and H2 fuel than the one La0.8Ca0.2Cr0.9Ni0.1O3 (LCN) anode because of the formation of CeO2 and Ni0 nanoparticles. Setting in the dis-tribution of H2 in the existing natural gas pipeline, hydrogen-injection in CH4 (20% H2 in volume in CH4) was found for the first time to efficiently improve the coking resistance of the anode because the H2 was able to boost the transfer of oxygen from the anode to the direct internal reforming. The conversion of CH4 was found to be around 85% and the selectivity for CO was close to unity. This study provides a viable solution to the design of complex perovskite SOFC to produce electricity and syngas simultaneously from CH4.

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