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离子液体增强质子转移并促进中性析氧反应

陈明星 刘念 杜子翯 齐静 曹睿

电化学(中英文)2025,Vol.31Issue(7):27-36,10.
电化学(中英文)2025,Vol.31Issue(7):27-36,10.DOI:10.61558/2993-074X.3549

离子液体增强质子转移并促进中性析氧反应

Ionic Liquid Enhanced Proton Transfer for Neutral Oxygen Evolution Reaction

陈明星 1刘念 1杜子翯 1齐静 1曹睿2

作者信息

  • 1. 河南师范大学材料科学与工程学院,河南省先进电化学储能材料设计与循环利用工程技术研究中心,河南 新乡 453007
  • 2. 陕西师范大学化学化工学院,应用表面与胶体化学教育部重点实验室,陕西 西安 710119
  • 折叠

摘要

Abstract

The development of highly active catalyst in pH-neutral media for oxygen evolution reaction(OER)is critical in the field of renewable energy storage and conversion.Nevertheless,the slow kinetics of proton-coupled electron transfer(PCET)hinders the overall OER efficiency.Herein,we report an ionic liquid(IL)modified CoSn(OH)6 nanocubes(denoted as CoS-n(OH)6-IL),which could be prepared through a facile strategy.The modified IL would not change the structural character-istics of CoSn(OH)6,but could effectively regulate the local proton activity near the active sites.The CoSn(OH)6-IL exhibited higher intrinsic OER performances than the pristine CoSn(OH)6 in neutral media.For example,the current density of CoS-n(OH)6-IL at 1.8 V versus reversible hydrogen electrode(RHE)was about 4 times higher than that of CoSn(OH)6.According to the pH-dependent kinetic investigations,operando electrochemical impedance spectroscopic,chemical probe tests,and deuterium kinetic isotope effects,the interfacial layer of IL could be utilized as a proton transfer mediator to promote the proton transfer,which enhances the surface coverage of OER intermediates and reduces the activation barrier.Consequent-ly,the sluggish OER kinetics would be efficiently accelerated.This study provides a facile and effective strategy to facilitate the PCET processes and is beneficial to guide the rational design of OER electrocatalysts.

关键词

电催化/析氧反应/离子液体/质子转移/CoSn(OH)6立方体

Key words

Electrocatalysis/Oxygen evolution reaction/Ionic liquid/Proton transfer/CoSn(OH)6 nanocube

引用本文复制引用

陈明星,刘念,杜子翯,齐静,曹睿..离子液体增强质子转移并促进中性析氧反应[J].电化学(中英文),2025,31(7):27-36,10.

基金项目

This work was supported by the National Natural Science Foundation of China(22209040,22202063). (22209040,22202063)

电化学(中英文)

OA北大核心

1006-3471

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