Affiliation:
1. School of Environment and Energy South China University of Technology Guangzhou 510006 China
2. Beijing Huairou Laboratory Beijing 101400 China
3. Research Institute of Renewable Energy and Advanced Materials Zijin Mining Group Co. Ltd. Xiamen Fujian 361101 China
4. South China Advanced Institute for Soft Matter Science and Technology School of Emergent Soft Matter, Guangdong Provincial Key Laboratory of Functional and Intelligent Hybrid Materials and Devices South China University of Technology Guangzhou 510640 China
Abstract
AbstractReversible protonic ceramic electrochemical cells (R‐PCECs) have received increasing focus for their good capability of converting and storing energy. However, the widely used cobalt‐based air electrodes are less thermomechanically compatible with the electrolyte and lack stability, which largely limits the development of R‐PCECs. Herein, a cobalt‐free perovskite with a nominal composition of PrBa0.8Ca0.2Fe1.8Ce0.2O6δ (PBCFC) is reported, which is in–situ engineered to a (Ba, Ce) deficient‐PBCFC phase, a BaCeO3, and a CeO2 phase under typical operating conditions, delivering a low area–specific resistance of 0.10 Ωcm2 at 700 oC. The generated BaCeO3 and CeO2 particles increase the conduction/transfer of protons and oxygen ions, thus providing extra active sites for the oxygen reactions. When utilized as an air electrode on a single cell, it achieves encouraging performance at 700 °C: a peak power density of 1.78 Wcm−2 and a current density of 5.00 Acm−2 at 1.3 V in the dual mode of the fuel cell (FC) and electrolysis (EL) mode with reasonable Faradaic efficiencies. In addition, the cells exhibit favorable operational durability of 65 h (FC mode), 95 h (EL mode), and promising cycling stability of 200 h.
Funder
National Natural Science Foundation of China
Fundamental Research Funds for the Central Universities
Subject
Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials
Cited by
9 articles.
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