电解
电催化剂
材料科学
海水
对偶(语法数字)
无机化学
类金属
膜
离子交换
离子
化学工程
电极
电化学
冶金
金属
化学
物理化学
有机化学
海洋学
电解质
艺术
生物化学
文学类
工程类
地质学
作者
Wen‐Li Yu,Zengfeng Qiu,Jinsong Wang,Zexing Wu,Bin Dong,Yong‐Ming Chai,Lei Wang
标识
DOI:10.1002/adfm.202423537
摘要
Abstract Constructing synergistic dual sites has been well‐recognized as an updated avenue in constructing binary‐component Pt/support compounds such materials undergo undesirable interfacial barriers and complicated synthesis. Here an integration of ultrafine Pt nanocrystals on oxygen‐deficient CoMoO 4 nanosheets is reported that achieved superior alkaline hydrogen evolution reaction (HER) activity (110 mV @ 1000 mA cm −2 ) with a reversed hydrogen deliver effect between bifunctional active sites. With perceptions from comprehensive experimental and theoretical results, the HER process occurs in three steps: pronounced water dissociation capability on CoMoO 4 , facile hydrogen transfer to Pt nanoparticles, and optimized hydrogen desorption on the Pt catalytic site. Thanks to the dual site effect, the Pt/CoMoO 4 catalyst boosts HER activity in alkaline large‐density seawater electrolysis and anion exchange membrane electrolyzer (AEM). This work not only provides a valid intensification strategy aimed at support‐type electrocatalysts but also takes insights into dual‐site mechanisms for high‐performance HER.
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