Perovskite Catalysts for Pure-Water-Fed Anion-Exchange-Membrane Electrolyzer Anodes: Co-design of Electrically Conductive Nanoparticle Cores and Active Surfaces
Tingting Zhai, Hao Wang, Sarah R. Beaudoin, Ran Zhang, Minkyoung Kwak, Shujin Hou, Zhengxiao Guo, Shannon W. Boettcher
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引用次数: 0
Abstract
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.
阴离子交换膜水电解槽(AEMWEs)是一种可能的低资本成本、高效、可扩展的制氢技术,具有廉价的硬件、丰富的催化剂和纯净水。然而,纯水AEMWEs仍处于早期发展阶段,与质子交换膜水电解槽(PEMWEs)相比,其性能较差。其中一个挑战是在纯水AEMWEs中开发有效的非铂族金属(non-PGM)阳极催化剂和电极。我们展示了基于lanio3的钙钛矿氧化物如何通过在A位和b位上的共取代来调节,同时保持高金属导电性以及一定程度的表面重建,从而暴露出稳定的co基活性催化剂。优化后的钙钛矿Sr0.1La0.9Co0.5Ni0.5O3在70°C、2.0 A cm-2、1.97 V条件下产生了纯水AEMWEs,从而说明了催化剂设计原则的实用性。
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