Double perovskite decorated with in situ exsolved Fe nanoparticles as active catalyst for CO2 electrolysis

被引:0
|
作者
Tan, Yuan [1 ]
Tang, Jiangcheng [2 ]
Yang, Caichen [2 ]
Tian, Yunfeng [3 ]
Wang, Ziling [4 ]
Pu, Jian [2 ]
Chi, Bo [2 ]
机构
[1] Jianghan Univ, Sch Optoelect Mat & Technol, Key Lab Optoelect Chem Mat & Devices, Wuhan 430056, Peoples R China
[2] Huazhong Univ Sci & Technol, Sch Mat Sci & Engn, Wuhan 430074, Peoples R China
[3] China Univ Min & Technol, Sch Mat Sci & Phys, Jiangsu Key Lab Coal Based Greenhouse Gas Control, Xuzhou 221116, Peoples R China
[4] Nanjing Univ Sci & Technol, Sch New Energy, Jiangyin 214443, Peoples R China
基金
中国国家自然科学基金;
关键词
CO; 2; electrolysis; Solid oxide electrolysis cells; Cathode catalyst; Exsolution of Fe nanoparticles; Double perovskite; OXYGEN-ELECTRODE; FUEL ELECTRODE; OXIDE; CATHODE; STEAM; PERFORMANCE; CELL; EXSOLUTION; ANODE; CU;
D O I
10.1016/j.ceramint.2023.10.064
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The double perovskite (Pr0.5Ba0.5)1.8Fe1.8Mn0.2O5-delta decorated with in situ exsolved Fe nanoparticles (Fe@PBFM) was used as the cathode in a solid oxide electrolysis cell (SOEC) to convert CO2 to CO and exhibited high efficiency and stability. This catalyst is synthesized from the simple perovskite (Pr0.5Ba0.5)0.9Fe0.9Mn0.1O3-delta (PBFM) by annealing it under an H2-N2 atmosphere at 850 degrees C for 15 h. The cell fabricated with the Fe@PBFM cathode shows a higher current density of 1.6 A/cm2 at 850 degrees C and 1.8 V than the cell with the unreduced PBFM. The increased current density can be attributed to the in situ exsolved Fe nanoparticles and generation of the Fe@PBFM double perovskite. Furthermore, the cell containing this active catalyst exhibits stable CO2 electrolysis performance for 100 h at a stable voltage of 1.3 V, suggesting that Fe@PBFM is an attractive candidate as SOEC cathode for CO2 electrolysis.
引用
收藏
页码:40797 / 40803
页数:7
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