Zhai Tingting, Wang Hao, Beaudoin Sarah R, Zhang Ran, Kwak Minkyoung, Hou Shujin, Guo Zhengxiao, Boettcher Shannon W
Department of Mechanical Engineering, The University of Hong Kong,Hong Kong (SAR), Pokfulam 999077, China.
Oregon Center for Electrochemistry, Department of Chemistry and Biochemistry, University of Oregon, Eugene, Oregon 97403, United States.
J Am Chem Soc. 2025 May 7;147(18):15448-15458. doi: 10.1021/jacs.5c01621. Epub 2025 Apr 24.
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 LaNiO-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, SrLaCoNiO, yielded pure-water AEMWEs operating at 1.97 V at 2.0 A cm at 70 °C with a pure-water feed, thus illustrating the utility of the catalyst design principles.