材料科学
耐久性
分解水
阳极
电解水
电解
钛
接口(物质)
氧化物
腐蚀
降级(电信)
氢
化学工程
催化作用
电极
复合材料
计算机科学
光催化
冶金
润湿
电信
生物化学
化学
有机化学
物理化学
工程类
电解质
坐滴法
作者
Chang Liu,Meital Shviro,Aldo Saul Gago,Sarah Zaccarine,Guido Bender,Pawel Gazdzicki,Tobias Morawietz,Indro Biswas,M. Rasiński,Andreas Everwand,Roland Schierholz,Jason Pfeilsticker,Martin Müller,Pietro Papa Lopes,Rüdiger‐A. Eichel,Bryan S. Pivovar,Svitlana Pylypenko,K. Andreas Friedrich,Werner Lehnert,Marcelo Carmo
标识
DOI:10.1002/aenm.202002926
摘要
Abstract Water electrolysis is the key to a decarbonized energy system, as it enables the conversion and storage of renewably generated intermittent electricity in the form of hydrogen. However, reliability challenges arising from titanium‐based porous transport layers (PTLs) have hitherto restricted the deployment of next‐generation water‐splitting devices. Here, it is shown for the first time how PTLs can be adapted so that their interface remains well protected and resistant to corrosion across ≈4000 h under real electrolysis conditions. It is also demonstrated that the malfunctioning of unprotected PTLs is a result triggered by additional fatal degradation mechanisms over the anodic catalyst layer beyond the impacts expected from iridium oxide stability. Now, superior durability and efficiency in water electrolyzers can be achieved over extended periods of operation with less‐expensive PTLs with proper protection, which can be explained by the detailed reconstruction of the interface between the different elements, materials, layers, and components presented in this work.
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