材料科学
电化学
电极
电解
氧化物
陶瓷
钙钛矿(结构)
电化学能量转换
化学工程
阳极
功率密度
储能
纳米技术
无机化学
电解质
化学
物理化学
复合材料
冶金
热力学
工程类
物理
功率(物理)
作者
Zuoqing Liu,Zhengjie Tang,Yufei Song,Guangming Yang,Wanru Qian,Meiting Yang,Yinlong Zhu,Ran Ran,Wei Wang,Wei Zhou,Zongping Shao
出处
期刊:Nano-micro Letters
[Springer Science+Business Media]
日期:2022-11-09
卷期号:14 (1): 217-217
被引量:159
标识
DOI:10.1007/s40820-022-00967-6
摘要
Reversible proton ceramic electrochemical cell (R-PCEC) is regarded as the most promising energy conversion device, which can realize efficient mutual conversion of electrical and chemical energy and to solve the problem of large-scale energy storage. However, the development of robust electrodes with high catalytic activity is the main bottleneck for the commercialization of R-PCECs. Here, a novel type of high-entropy perovskite oxide consisting of six equimolar metals in the A-site, Pr1/6La1/6Nd1/6Ba1/6Sr1/6Ca1/6CoO3-δ (PLNBSCC), is reported as a high-performance bifunctional air electrode for R-PCEC. By harnessing the unique functionalities of multiple elements, high-entropy perovskite oxide can be anticipated to accelerate reaction rates in both fuel cell and electrolysis modes. Especially, an R-PCEC utilizing the PLNBSCC air electrode achieves exceptional electrochemical performances, demonstrating a peak power density of 1.21 W cm-2 for the fuel cell, while simultaneously obtaining an astonishing current density of - 1.95 A cm-2 at an electrolysis voltage of 1.3 V and a temperature of 600 °C. The significantly enhanced electrochemical performance and durability of the PLNBSCC air electrode is attributed mainly to the high electrons/ions conductivity, fast hydration reactivity and high configurational entropy. This research explores to a new avenue to develop optimally active and stable air electrodes for R-PCECs.
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