The Sabatier Principle in Electrocatalysis: Basics, Limitations, and Extensions

被引:273
|
作者
Ooka, Hideshi [1 ]
Huang, Jun [2 ]
Exner, Kai S. [3 ,4 ]
机构
[1] RIKEN, Ctr Sustainable Resource Sci CSRS, Wako, Saitama, Japan
[2] Ulm Univ, Inst Theoret Chem, Ulm, Germany
[3] Univ Duisburg Essen, Fac Chem Theoret Inorgan Chem, Essen, Germany
[4] Cluster Excellence RESOLV, Bochum, Germany
基金
中国国家自然科学基金; 日本学术振兴会;
关键词
electrocatalysis; Sabatier principle; thermodynamics; kinetics; theory; OXYGEN EVOLUTION REACTION; ELECTROCHEMICAL HYDROGEN OXIDATION; SURFACE POURBAIX DIAGRAMS; COUPLED ELECTRON-TRANSFER; EVANS-POLANYI RELATION; FREE-ENERGY DIAGRAM; CHLORINE EVOLUTION; PROTON-TRANSFER; SCALING RELATIONS; CARBON-DIOXIDE;
D O I
10.3389/fenrg.2021.654460
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
The Sabatier principle, which states that the binding energy between the catalyst and the reactant should be neither too strong nor too weak, has been widely used as the key criterion in designing and screening electrocatalytic materials necessary to promote the sustainability of our society. The widespread success of density functional theory (DFT) has made binding energy calculations a routine practice, turning the Sabatier principle from an empirical principle into a quantitative predictive tool. Given its importance in electrocatalysis, we have attempted to introduce the reader to the fundamental concepts of the Sabatier principle with a highlight on the limitations and challenges in its current thermodynamic context. The Sabatier principle is situated at the heart of catalyst development, and moving beyond its current thermodynamic framework is expected to promote the identification of next-generation electrocatalysts.
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页数:20
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