多金属氧酸盐
过电位
析氧
材料科学
阳极
电化学
化学工程
催化作用
溴化物
石墨烯
分解水
阴极
超分子化学
纳米技术
电流密度
电催化剂
电解水
无机化学
电解
电极
化学
物理化学
有机化学
分子
光催化
工程类
物理
量子力学
电解质
作者
Rong‐Zhi Sun,Xiang Ma,Kai Chen,Jian Yang,Yixin Liu,Xin‐Xiong Li,Pingwei Cai,Zhenhai Wen,Shou‐Tian Zheng
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-08-11
卷期号:64 (40): e202513915-e202513915
被引量:13
标识
DOI:10.1002/anie.202513915
摘要
Abstract Superstructures assembled from nanoscale polyoxometalates (POMs) attract considerable interest due to their well‐defined architectures and outstanding physicochemical properties. However, the targeted synthesis of self‐assembled POM‐based superstructures with high‐efficiency electrocatalytic performance remains a significant challenge. Herein, we report the rational design and construction of three POM‐based superstructures with ultrathin graphene‐like morphologies and well‐organized frameworks via a simple self‐assembled method, in which transition metals (TMs) bridge POMs into graphene‐like planes, while cetyltrimethylammonium bromide (CTAB) serves as an intercalation agent, endowing the structures with high surface area and enhanced electronic conductivity. Among the resulting materials (denote as POM‐CTAB‐TM, TM═Co, Ni, or Cu), POM‐CTAB‐Co exhibits the highest catalytic activity toward oxygen evolution reaction (OER), achieving a low overpotential of 292 mV at a current density of 10 mA cm −2 . In situ electrochemical spectroscopy and theoretical calculations underscore that the Co atoms within the POM serve as active sites and facilitate the rate‐determining step of *OOH formation. Moreover, an anion exchange membrane water electrolyzer employing POM‐CTAB‐Co as the anode and Pt/C as the cathode demonstrates exceptional performance, delivering a current density of 2 A cm −2 at a cell voltage of 2.247 V, along with remarkable durability exceeding 2000 h at an industrial‐grade current density of 500 mA cm −2 . This study develops a simple and efficient method for synthesizing supramolecular POM‐based nanosheets as OER electrocatalysts.
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