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:4
标识
DOI:10.1002/anie.202513592
摘要
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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