电解
海水
阴极
镍
化学工程
催化作用
电解水
电极
材料科学
膜
化学
无机化学
冶金
地质学
电解质
物理化学
工程类
海洋学
生物化学
作者
Marvin Frisch,Trung Ngo Thanh,Aleks Arinchtein,Linus Hager,Johannes Schmidt,Sven Brückner,Jochen Kerres,Peter Strasser
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-04-26
卷期号:8 (5): 2387-2394
被引量:81
标识
DOI:10.1021/acsenergylett.3c00492
摘要
In arid coastal zones, direct seawater electrolysis appears particularly intriguing for green hydrogen production. State-of-the-art direct seawater electrolyzers, however, show unsatisfactory performance and rely on large amounts of platinum-group metals (PGMs) in the electrodes or hidden as transport layer coatings. Herein, we report an asymmetric-feed electrolyzer design, in which all cell components consist of PGM-free materials. Cobalt- and nickel-based phosphides/chalcogenides not only serve as active and robust electrocatalysts but also are put forth as porous transport layer (PTL) surface coatings enhancing selective seawater splitting performance. In a systematic design study at the single-cell level, we report the integration of our catalysts and PTLs into a membrane–electrode assembly (MEA) using a customized, terphenyl-based anion-exchange membrane (AEM). The presented entirely PGM-free electrolyzer achieves industrially relevant current densities of up to 1.0 A cm–2 below 2.0 Vcell in standardized alkaline seawater and dry cathode operation.
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