Scholay

学术搜索 · AI 审稿 · LaTeX 协作

Synergistic O-Containing Triazine and Imidazole Linker in Covalent Organic Frameworks for Electrochemical Hydrogen Evolution

作者:Qiushuang Li, Lantian Li, Bing Zhao, Yuqian He, Xiuwen Wang, Wei Kan, Li Sun, Liyan Wang · 发表于:ACS Applied Polymer Materials · 年份:2025 · DOI:10.1021/acsapm.4c03046 · 被引用次数:10 · 研究领域:Electrocatalysts for Energy Conversion、Electrochemical Analysis and Applications、Advanced Photocatalysis Techniques

Electrochemical hydrogen evolution systems with water based on covalent organic frameworks (COFs) provide a promising platform for replacing metal catalysts to drive sustainable development. Until now, rational design of the structure of COFs poses a significant challenge because of the largely overlooked individual or synergistic effects of building blocks and linkers in COFs on their electrocatalytic abilities. Herein, a building block-dependent linker integration pattern is illuminated, and the combination of an O-containing triazine building block with phenanthro[9,10- d ]imidazole linker successfully yields a COF material, namely, TFPT–PI-COF, which exhibits a distinctive porous structure and high thermal stability. The composite TFPT-PI-COF@NF as the catalyst demonstrates a promising overpotential value of 120 mV for hydrogen evolution reaction (HER) and delivers a current density of 10 mA cm –2 in alkaline media. The collaborative contributions of O-containing triazine and phenanthro[9,10- d ]imidazole are experimentally verified, and the computation analysis of the Gibbs free energy further confirms the presence of the abundant and accessible active sites in the porous TFPT-PI-COF for HER. This integrated strategy furnishes a vast foreground for designing and developing other COF-based electrocatalysts.