材料科学
纳米颗粒
电解质
钙钛矿(结构)
阳极
氧化物
无机化学
乙二醇
化学工程
电化学
纳米技术
电极
化学
物理化学
冶金
工程类
作者
Yun Fan,Xiuan Xi,Jun Li,Qi Wang,Ming Ming Li,Li Juan Wang,Dmitry Medvedev,Jing Luo,Xian Zhu Fu
标识
DOI:10.1016/j.electacta.2021.139096
摘要
Proton-conducting solid oxide fuel cells have the potential ability to simultaneously convert ethane to electrical energy and value-added ethylene with high selectivity and the absence of CO2 emissions. However, their development is impeded by a lack of efficient and stable anode materials. Herein, in-situ exsolved FeNi nanoparticles on (La0.6Sr0.4)0.95Fe0.8Ni0.1Mo0.1O3-δ (LSFNM) perovskite oxide are realised by controlling A-site deficiency and Mo-doping. The introduction of high-valence molybdenum ions in (La0.6Sr0.4)0.95Fe0.8Ni0.2O3-δ (LSFN) not only stabilises its cubic perovskite structure under a reducing atmosphere, but also facilities the exsolution of FeNi nanoparticles from the parent perovskite matrix. The power density of the BaZr0.1Ce0.7Y0.2O3−δ (BZCY) electrolyte-supported single cells with a LSFNM/BZCY/LSCF-SDC configuration reaches 172mW•cm−2 at 750°C in C2H6; meanwhile, the ethylene yield also reaches approximately 40.5%. The presented results extend the functionality and applicability of proton conducting fuel cells for carrying out efficient hydrocarbon-related electrochemical conversion for producing power and co-production of value-added chemicals.
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