4.7 Article

Performance optimization of Ca and Y co-doped CeO2-based electrolyte for intermediate-temperature solid oxide fuel cells

期刊

JOURNAL OF ALLOYS AND COMPOUNDS
卷 913, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2022.165317

关键词

Solid oxide fuel cells; Electrolyte; Scavenging factor; Oxygen vacancy formation energy

资金

  1. Natural Science Foundation of China [61775011]
  2. Collaborative Education Project of Industry University Cooperation of the Ministry of Education [20215921028, 20215921027]
  3. Natural Science Foundation of Liaoning [LJKZ0296, LJKZ0295]
  4. Innovation and en-trepreneurship training program for college students of University of Science and Technology Liaoning [S202110146014]

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The study prepared Ca and Y co-doped Ce0.8Y0.2-xCaxO2-delta electrolytes and evaluated their performance in intermediate-temperature solid oxide fuel cells. The co-doped electrolyte exhibited high conductivity and reduced blocking factor, indicating superior performance.
The CeO2-based electrolytes of solid oxide fuel cells (SOFCs) with high ionic conductivity have attracted considerable attention. In this study, Ca and Y co-doped Ce0.8Y0.2-xCaxO2-delta (x = 0, 0.05, 0.1, and 0.15, abbreviated as YDC, YCDC05, YCDC10, and YCDC15) electrolytes were prepared, and their properties were investigated for intermediate-temperature solid oxide fuel cells (IT-SOFCs). All samples formed a cubic fluorite structure at a low sintering temperature (600 degrees C). At 800 degrees C, the YCDC05 electrolyte exhibited the highest conductivity (0.10 S cm(-1)), which was approximately 54% higher than that of the YDC electrolyte. The YCDC05 had the highest grain boundary scavenging factor and the smallest blocking factor. The blocking factor of YCDC05 was reduced by 49%, compared with that of YDC at 400 degrees C. The density functional theory calculation results showed that the oxygen vacancy formation energy of the Y and Ca co-doped (YCDC) electrolyte was lower than that of YDC. Therefore, Ce0.8Y0.15Ca0.05O2-delta may be a potential electrolyte material for IT-SOFCs. (C) 2022 Elsevier B.V. All rights reserved.

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