电解
氯
阳极
催化作用
材料科学
析氧
电解质
海水
电解水
制氢
氯化物
纳米技术
分解水
化学工程
氢
腐蚀
可持续能源
环境科学
氢经济
生化工程
反应性(心理学)
工艺工程
作者
Y Zhang,Xinling Tian,Aiqing Cao,Zudong Shen,Ende Yu,Linlin Zhou,Dan Kang,Gang Ma,Yun Hu,Y Li,Yun Kuang,Xiaoming Sun,Daojin Zhou
摘要
ABSTRACT The global transition toward low‐carbon energy systems drives the urgent need for scalable green hydrogen production. Although water electrolysis is technologically mature, its reliance on freshwater limits large‐scale deployment. Direct seawater electrolysis therefore emerges as an attractive alternative, yet its practical implementation is hindered by chloride‐induced corrosion and the competing chlorine oxidation reaction at the anode. Overcoming these challenges requires moving beyond a sole focus on intrinsic catalytic activity toward a holistic design paradigm that integrates interface and microenvironment engineering. Recent multidimensional strategies, including physical protective layers, dynamic catalyst surface reconstruction, interlayer anion engineering, and electrolyte engineering, enable the construction of selectively permeable anode interfaces that suppress deleterious chloride interactions while sustaining efficient oxygen evolution. Beyond passive protection, an emerging research direction shifts from chlorine resistance to chlorine utilization, in which chloride species are deliberately incorporated as functional elements to synergistically enhance catalytic activity and facilitate stable operation. Looking forward, transformative progress is expected from interface designs that exploit cooperative mechanisms across multiple length scales, guided by theoretical insights and data‐driven methodologies. A mechanistic understanding of interfacial evolution under industrially relevant conditions will be essential for translating direct seawater electrolysis into a stable, efficient, and economically viable hydrogen production technology.
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