结晶度
材料科学
共价键
循环伏安法
亚胺
化学工程
纳米技术
催化作用
电化学
化学
电极
有机化学
复合材料
工程类
物理化学
作者
Yuxin Ren,Shuang Li,Meidi Wang,Xue‐Qian Wu,Ya‐Pan Wu,Bojing Sun,Jun Zhao,Fangyuan Kang,Qichun Zhang,Dong‐Sheng Li
出处
期刊:Advanced Science
[Wiley]
日期:2025-03-19
卷期号:12 (18): e2501442-e2501442
被引量:6
标识
DOI:10.1002/advs.202501442
摘要
Abstract Developing diverse methods to approach highly crystalline covalent organic frameworks (COFs) for improvement of their electrocatalytic hydrogen evolution reaction (HER) activity is important but very challenging. Herein, for the first time, an electrochemically‐driven reconstruction strategy is demonstrated to convert semi‐polymerized low‐crystalline COFs into highly crystalline, structurally ordered COFs with enhanced HER activity. In situ and ex situ characterizations reveal that cyclic voltammetry (CV) cycles can promote crystallinity, thereby leading to improved conductivity, increased active site density, and superior stability. As a result, the highly crystalline COF achieves low overpotentials of 103.6 and 219.4 mV at 10 and 50 mA cm −2 , respectively, with excellent stability (1200 h at 50 mA cm −2 ). More importantly, this strategy is generalizable and effective for various imine‐linked COFs with different bonding types, significantly improving their crystallinity and HER activity. This work not only establishes a novel method for constructing highly crystalline COFs but also demonstrates the versatility of electrochemically driven structural modulation in enhancing the catalytic performance of COFs.
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