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电子供体-受体相互作用增强金属有机聚合物对氧还原的电催化活性

Electron-Donors-Acceptors Interaction Enhancing Electrocatalytic Activity of Metal-Organic Polymers for Oxygen Reduction.

作者信息

Huang Bingyu, Tang Xiannong, Hong Yaoshuai, Li Longbin, Hu Ting, Yuan Kai, Chen Yiwang

机构信息

Institute of Polymers and Energy Chemistry (IPEC), College of Chemistry and Chemical Engineering, Nanchang University, 999 Xuefu Avenue, Nanchang, 330031, China.

School of Physics and Materials Science, Nanchang University, 999 Xuefu Avenue, Nanchang, 330031, China.

出版信息

Angew Chem Int Ed Engl. 2023 Aug 14;62(33):e202306667. doi: 10.1002/anie.202306667. Epub 2023 Jul 11.

Abstract

Catalysts with metal-N sites have long been considered as effective electrocatalysts for oxygen reduction reaction (ORR), yet the accurate structure-property correlations of these active sites remain debatable. Report here is a proof-of-concept method to construct 1,4,8,11-tetraaza[14]annulene (TAA)-based polymer nanocomposites with well-managed electronic microenvironment via electron-donors/acceptors interaction of altering electron-withdrawing β-site substituents. DFT calculation proves the optimal -Cl substituted catalyst (CoTAA-Cl@GR) tailored the key OH* intermediate interaction with Co-N sites under the d-orbital regulation, hence reaching the top of ORR performance with excellent turnover frequency (0.49 e s site ). The combination of in situ scanning electrochemical microscopy and variable-frequency square wave voltammetry techniques contribute the great ORR kinetics of CoTAA-Cl@GR to the relatively high accessible site density (7.71×10  site g ) and fast electron outbound propagation mechanism. This work provides theoretical guidance for rational design of high-performance catalysts for ORR and beyond.

摘要

长期以来,含金属 - N 位点的催化剂一直被视为氧还原反应(ORR)的有效电催化剂,然而这些活性位点准确的结构 - 性能关系仍存在争议。本文报道了一种概念验证方法,通过改变吸电子β位取代基的供体/受体相互作用,构建具有良好调控电子微环境的基于 1,4,8,11 - 四氮杂[14]环烯(TAA)的聚合物纳米复合材料。密度泛函理论(DFT)计算证明,优化的 - Cl 取代催化剂(CoTAA - Cl@GR)在 d 轨道调控下调整了关键 OH*中间体与 Co - N 位点的相互作用,从而以优异的周转频率(0.49 e s 位点)达到 ORR 性能的顶峰。原位扫描电化学显微镜和变频方波伏安法技术的结合将 CoTAA - Cl@GR 出色的 ORR 动力学归因于相对较高的可及位点密度(7.71×10 位点 g)和快速的电子外输传播机制。这项工作为合理设计用于 ORR 及其他领域的高性能催化剂提供了理论指导。

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