阴极
材料科学
阳极
氧化物
质子
氢
钙钛矿(结构)
陶瓷
化学工程
氧气
扩散
无机化学
电极
化学
复合材料
物理化学
冶金
有机化学
热力学
工程类
物理
量子力学
作者
Xiaoyu Wang,Wenhuai Li,Chuan Zhou,Meigui Xu,Zhiwei Hu,Chih‐Wen Pao,Wei Zhou,Zongping Shao
标识
DOI:10.1021/acsami.2c19343
摘要
Protonic ceramic fuel cells (PCFCs), as an efficient energy storage and conversion device, have great potential to solve the serious problems of energy shortage and environmental pollution. Improving the proton conductivity of the promising cathode materials is an effective solution to promote the widespread application of PCFCs at low temperatures (450-650 °C). Herein, considering the high oxygen reduction reaction (ORR) activity of BaCoO3-based perovskite oxide and beneficial proton uptake capacity of Zn-doping, we construct BaCo0.4Fe0.4Zn0.1Y0.1O3-δ (BCFZnY) as the PCFCs cathode, and compare it with the classic triple-conducting cathode BaCo0.4Fe0.4Zr0.1Y0.1O3-δ (BCFZrY). Different from the general strategy of increasing the initial oxygen vacancy concentration of cathode materials, this work unveils that enhancing the hydration of perovskite oxide with low oxygen vacancy concentration is a more effective strategy to accelerate the proton diffusion in the electrode. Therefore, the BCFZnY cathode achieved excellent proton conductivities of 8.05 × 10-3 and 6.38 × 10-3 S cm-1 as obtained by hydrogen permeation measurements and peak power densities of 982 and 320 mW cm-2 in a BaZr0.1Ce0.7Y0.1Yb0.1O3-δ-based anode-supported fuel cell at 600 and 450 °C, respectively.
科研通智能强力驱动
Strongly Powered by AbleSci AI