电极
材料科学
陶瓷
路易斯酸
电解
兴奋剂
氧化物
极化(电化学)
氧气
电流密度
无机化学
析氧
耐久性
化学工程
催化作用
分析化学(期刊)
化学
复合材料
电化学
物理化学
冶金
光电子学
电解质
工程类
有机化学
物理
量子力学
作者
Yangsen Xu,Kang Xu,Feng Zhu,Fan He,Hua Zhang,Chong Fang,Ying Liu,Yucun Zhou,YongMan Choi,Yu Chen
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-09-13
卷期号:8 (10): 4145-4155
被引量:16
标识
DOI:10.1021/acsenergylett.3c01722
摘要
Improving the reaction kinetics and durability of air electrodes on protonic ceramic cells is effective for their commercialization but challenging. Here, we report our electrode design via a low-Lewis-acid-strength cation (Cs+) doping strategy on a double perovskite oxide with a detailed formula of PrBa0.9Cs0.1Co2O5+δ (PBCsC). At 600 °C, the PBCsC electrode demonstrates a low area-specific resistance (ASR) value of 0.3 Ω cm2 within 100 h without significant degradation due likely to the electron pair shift by the polarization distribution of ionic Lewis acid strength at A and B sites. At 650 °C, a full cell with the PBCsC electrode displays an encouraging peak power density of 1.66 W cm–2 in the fuel cell (FC) mode, a high current density of −2.85 A cm–2 (at 1.3 V) in the electrolysis (EC) mode, good operational stability in dual modes of FC and EC, and promising cycling durability of 20 cycles in ∼80 h.
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