杂原子
催化作用
材料科学
电化学
双金属片
制氢
氧化还原
电催化剂
无机化学
化学工程
电极
化学
有机化学
工程类
物理化学
戒指(化学)
作者
Penghui Xu,Zhenyu Bao,Yujian Zhao,Lingxia Zheng,Zhuoqing Lv,Xiaowei Shi,Hong‐En Wang,Xiaosheng Fang,Huajun Zheng
标识
DOI:10.1002/aenm.202303557
摘要
Abstract Electrocatalytic biomass valorization coupled with hydrogen production provides an efficient and economical way to achieve a zero‐carbon economy. Ni‐based electrocatalysts are promising candidates due to their intrinsic redox capabilities, but the rational design of active Ni site coordination is still a huge challenge. Herein, the combined strategies of surface reconstruction and heteroatom doping are adopted to modify Ni 3 S 2 pre‐catalysts and the obtained bimetallic catalyst exhibits superior electrocatalytic performance toward 5‐hydroxymethylfurfural (HMF) oxidation to 2,5‐furanedicarboxylic acid (FDCA). Specifically, the oxysulfide‐coordinated amorphous NiOOH (NiOOH‐SO x ) active phase is in situ constructed following the anionic regulation mechanism, which endows numerous defects and unsaturated sites for anodic HMF oxidation. Cu heteroatom doping further modulates the electronic structure of active sites with abundant Lewis acidic sites, offering advanced capability for HMF adsorption. Several operando characterization techniques (in situ Raman, infrared, and electrochemical impedance spectroscopies) are performed to disclose the reaction pathway and structure‐activity‐potential relationship. Theoretical results further demonstrate that Cu doping and oxyanionic regulation effectively modulate the local coordination environment of Ni sites and correspondingly tailor the intermediate adsorption behavior and then promote the reaction kinetics. Moreover, a two‐electrode system is assembled to pair HMF oxidation with cathode hydrogen production, demonstrating better energy conversion efficiency.
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