Tailoring of Active Sites from Single to Dual Atom Sites for Highly Efficient Electrocatalysis

电催化剂 活动站点 材料科学 应变工程 纳米技术 电子转移 化学物理 Atom(片上系统) 催化作用 化学 光化学 计算机科学 物理化学 电化学 光电子学 有机化学 电极 嵌入式系统
作者
Hongwei Zhang,Xindie Jin,Jong‐Min Lee,Xin Wang
出处
期刊:ACS Nano [American Chemical Society]
卷期号:16 (11): 17572-17592 被引量:97
标识
DOI:10.1021/acsnano.2c06827
摘要

Single atom catalysts (SACs) have been attracting extensive attention in electrocatalysis because of their unusual structure and extreme atom utilization, but the low metal loading and unified single site induced scaling relations may limit their activity and practical application. Tailoring of active sites at the atomic level is a sensible approach to break the existing limits in SACs. In this review, SACs were first discussed regarding carbon or non-carbon supports. Then, five tailoring strategies were elaborated toward improving the electrocatalytic activity of SACs, namely strain engineering, spin-state tuning engineering, axial functionalization engineering, ligand engineering, and porosity engineering, so as to optimize the electronic state of active sites, tune d orbitals of transition metals, adjust adsorption strength of intermediates, enhance electron transfer, and elevate mass transport efficiency. Afterward, from the angle of inducing electron redistribution and optimizing the adsorption nature of active centers, the synergistic effect from adjacent atoms and recent advances in tailoring strategies on active sites with binuclear configuration which include simple, homonuclear, and heteronuclear dual atom catalysts (DACs) were summarized. Finally, a summary and some perspectives for achieving efficient and sustainable electrocatalysis were presented based on tailoring strategies, design of active sites, and in situ characterization.
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