无定形固体
催化作用
材料科学
电解水
氧气
析氧
化学工程
膜
离子交换
钴
电解
纳米结构
离子
纳米技术
化学
无机化学
降级(电信)
质子交换膜燃料电池
无定形碳
格子(音乐)
膜反应器
电催化剂
纳米颗粒
晶体结构
作者
Jingxuan Zhao,Kunjie Wang,Xiangyang Li,Xiangyang Li,Xinmei Li,Xinmei Li,Xingyu Cui,Xu Zhao
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-09-23
卷期号:64 (47): e202513592-e202513592
被引量:19
标识
DOI:10.1002/anie.202513592
摘要
Abstract Controlling the long‐range disorder of dynamically reconstructed nanostructures represents a challenging but important approach for achieving practical catalysts with high performance. Here, we report a facile fluoride‐mediated‐stabilization strategy to finely localize the long‐range disorder of reconstructed amorphous Co‐based oxyhydroxide (CoOOH) nanosheets under oxygen evolution reaction (OER) conditions with compatible lattice‐oxygen activation and regeneration for robust anion exchange membrane water electrolysis (AEMWE). The stabilized lattice Co by fluoride‐induced bond reinforcing in pre‐catalysts enabled localized long‐range disorder of reconstructed amorphous oxyhydroxides. The localized long‐range disorder can promote Co─O covalency for activating lattice oxygen and also induce tensile strain as an oxygen pump for regenerating lattice oxygen. The corresponding AEMWE yielded a cutting‐edge current of 3.4 A cm −2 at 2.0 V and remarkable stability with imperceptible degradation of 0.09 mV h −1 in 1200 h. This work opens up a feasible avenue for developing targeted catalysts under operating conditions by finely tuning the long‐range disorder during reconstruction.
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