Constructing High-Loading Single-Atom/Cluster Catalysts via an Electrochemical Potential Window Strategy

被引:174
|
作者
Liu, Jin-Cheng [1 ]
Xiao, Hai [1 ]
Li, Jun [1 ,2 ]
机构
[1] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
[2] Southern Univ Sci & Technol, Dept Chem, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
WATER-GAS SHIFT; TOTAL-ENERGY CALCULATIONS; FOCK WAVE-FUNCTIONS; ATOM CATALYSTS; AB-INITIO; CO OXIDATION; PLATINUM CLUSTERS; SUPPORTED SINGLE; OXYGEN REDUCTION; RATIONAL DESIGN;
D O I
10.1021/jacs.9b06808
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Single-atom catalysts (SACs) and single-cluster catalysts (SCCs) are the new frontier of heterogeneous catalysis, which exhibit high activity, selectivity, stability, and atomic efficiency as well as precise tunability. However, the lack of efficient methods for producing high-loading and high-purity SACs and SCCs hinders their industrial applications. In this work, we propose a general and efficient strategy for the production of high-loading and high-purity SACs and SCCs anchored on suitable substrates. Our strategy relies on the existence of an electrochemical potential window (EcPW) we predict within which any aggregate forms of the target metal on the substrate are leached away by electrochemical oxidation, while the strongly bound single atoms or single clusters remain at the substrate. We demonstrate the applicability of this strategy with modeling the production of Pt, Pd, and Ni SACs anchored on N-doped graphene and Fe2O3 as well as Pt-3 and Ni-3 SCCs anchored on graphdiyne.
引用
收藏
页码:3375 / 3383
页数:9
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