化学
电解
阳极
催化作用
导电体
膜
纳米颗粒
钙钛矿(结构)
化学工程
离子
无机化学
离子交换
电解水
电极
有机化学
电解质
复合材料
物理化学
生物化学
材料科学
工程类
作者
Tingting Zhai,Hao Wang,Sarah R. Beaudoin,Ran Zhang,Minkyoung Kwak,Shujin Hou,Zhengxiao Guo,Shannon W. Boettcher
摘要
Anion-exchange-membrane water electrolyzers (AEMWEs) are a possible low-capital-expense, efficient, and scalable hydrogen-production technology with inexpensive hardware, earth-abundant catalysts, and pure water. However, pure-water-fed AEMWEs remain at an early stage of development and suffer from inferior performance compared with proton-exchange-membrane water electrolyzers (PEMWEs). One challenge is to develop effective non-platinum-group-metal (non-PGM) anode catalysts and electrodes in pure-water-fed AEMWEs. We show how LaNiO3-based perovskite oxides can be tuned by cosubstitution on both A- and B-sites to simultaneously maintain high metallic electrical conductivity along with a degree of surface reconstruction to expose a stable Co-based active catalyst. The optimized perovskite, Sr0.1La0.9Co0.5Ni0.5O3, yielded pure-water AEMWEs operating at 1.97 V at 2.0 A cm-2 at 70 °C with a pure-water feed, thus illustrating the utility of the catalyst design principles.
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