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Pr2Ni0.8Co0.2O4+δ impregnated La0.6Sr0.4CoO3-δ oxygen electrode for efficient CO2 electroreduction in solid oxide electrolysis cells.
Liu, Binbin; Li, Zeming; Xiao, Guoping; Du, Xian-Long; Yao, Huichao; Dai, Ruoyun; Wang, Xiulin; Wang, Jian-Qiang; Li, Tao.
  • Liu B; Engineering Research Center of Large-Scale Reactor Engineering and Technology, Ministry of Education, State Key Laboratory of Chemical Engineering, East China University of Science and Technology Shanghai 200237 China.
  • Li Z; Key Laboratory of Interfacial Physics and Technology, Shanghai Institute of Applied Physics, Chinese Academy of Sciences Shanghai 201800 China duxianlong@sinap.ac.cn.
  • Xiao G; University of Chinese Academy of Sciences Beijing 100049 China.
  • Du XL; Key Laboratory of Interfacial Physics and Technology, Shanghai Institute of Applied Physics, Chinese Academy of Sciences Shanghai 201800 China duxianlong@sinap.ac.cn.
  • Yao H; University of Chinese Academy of Sciences Beijing 100049 China.
  • Dai R; Key Laboratory of Interfacial Physics and Technology, Shanghai Institute of Applied Physics, Chinese Academy of Sciences Shanghai 201800 China duxianlong@sinap.ac.cn.
  • Wang X; University of Chinese Academy of Sciences Beijing 100049 China.
  • Wang JQ; CNOOC Gas and Power Group Co., Ltd Beijing 100020 China.
  • Li T; CNOOC Gas and Power Group Co., Ltd Beijing 100020 China.
RSC Adv ; 14(19): 13251-13257, 2024 Apr 22.
Article en En | MEDLINE | ID: mdl-38655465
ABSTRACT
The solid oxide electrolysis cell (SOEC) is an advanced electrochemical device with a promising future in reducing CO2 emissions. Currently, the insufficient oxygen evolution reaction activity in conventional anode materials severely restricts the development of electrolytic CO2. Herein, the PNCO-LSC composite oxygen electrode was exploited by impregnating Pr2Ni0.8Co0.2O4+δ (PNCO) on the surface of La0.6Sr0.4CoO3-δ (LSC) oxygen electrode. The results of electrochemical tests and various physicochemical characterizations indicate that the infiltration of PNCO can lead to a significant improvement in the performance of the cell for CO2 electroreduction by increasing the surface oxygen exchange. The current density of the PNCO-LSC oxygen electrode infiltrated twice at 800 °C and 1.5 V reaches 0.917 A cm-2, which is about 40% higher than that of the bare LSC oxygen electrode. In addition, the single cell did not show significant degradation in a long-term stability test at a current density of 0.4 A cm-2 for 100 h of electrolysis. Therefore, the PNCO-LSC composite oxygen electrode material is effective in enhancing electrolytic CO2 performance.