Self-assembled FeRu bimetallic nanocatalysts for efficient and durable mutual CO-CO2 conversion in a reversible solid oxide electrochemical cell

被引:8
|
作者
Wang, Jing [1 ]
Zhang, Dong [2 ]
Liu, Tong [1 ]
Xu, Anqi [1 ]
Luo, Yao [2 ]
Hu, Xuelei [1 ]
Wang, Yao [2 ]
机构
[1] Wuhan Inst Technol, Sch Chem Engn & Pharm, Hubei Key Lab Novel Reactor & Green Chem Technol, Key Lab Green Chem Proc,Minist Educ, Wuhan 430205, Peoples R China
[2] Wuhan Univ, Sch Power & Mech Engn, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
Ruddlesden-Popper oxide; CO-CO2; conversion; cycling test; perovskite oxide; reversible solid oxide cells; distribution of relaxation times; electrochemical impedance spectra; fuel electrode; IN-SITU EXSOLUTION; ALLOY NANOPARTICLES; CARBON DEPOSITION; CO2; ELECTROLYSIS; OXYGEN REDUCTION; FUEL-CELLS; LAYERED PEROVSKITE; ANODE MATERIAL; CATHODE; PERFORMANCE;
D O I
10.1007/s40843-024-2922-8
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Herein, we report a phase-transformed fuel electrode to carry out the reversible CO-CO2 conversion in a reversible solid oxide electrochemical cell (RSOC), which is composed of self-assembled FeRu bimetallic nanoparticles and Ruddlesden-Popper Pr0.8Sr1.2Fe1-x-yRuxMoyO4 (FeRu@PSFRM). Electrochemical impedance spectra and their corresponding distribution of relaxation time demonstrate that the sub-electrode reaction process in the frequency ranging 10(0)-10(2) Hz, including the gas adsorption, dissociation, and ionization reactions on the electrode surface, predominantly dominates the entire electrode reaction process. The single cell with the FeRu@PSFRM fuel electrode generates a maximum output power density of 170 W cm(-2) at 800 degrees C in the solid oxide fuel cell (SOFC) mode, while yields a current density of -0.256 A cm(-2) at 1.3 V in the solid oxide electrolysis cell (SOEC) mode. In addition, the reliable reversible CO-CO2 mutual conversion has experienced "activation-stabilization-degradation" three obvious stages in the first 42-h SOFC-SOEC cycling testing. Fortunately, the degraded fuel electrode can be regenerated by oxidizing it in the oxidizing gas and then retreating in the reductive atmosphere. Our findings reveal that the FeRu@PSFRM material generated by the in-situ exsolution technique is a promising fuel electrode candidate for efficient and durable mutual CO-CO2 conversion in a RSOC.
引用
收藏
页码:1471 / 1480
页数:10
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