Electrochemical hydrogen evolution on Pt-based catalysts from a theoretical perspective

被引:6
|
作者
Zhang, Ke-Xiang [1 ]
Liu, Zhi-Pan [1 ,2 ,3 ]
机构
[1] Fudan Univ, Collaborat Innovat Ctr Chem Energy Mat, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat,Key L, Shanghai 200433, Peoples R China
[2] Shanghai Qi Zhi Inst, Shanghai 200030, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Organ Chem, Key Lab Synthet & Selfassembly Chem Organ Funct Mo, Shanghai 200032, Peoples R China
来源
JOURNAL OF CHEMICAL PHYSICS | 2023年 / 158卷 / 14期
基金
美国国家科学基金会;
关键词
DENSITY-FUNCTIONAL THEORY; SINGLE-CRYSTAL SURFACES; ACTIVE EDGE SITES; PLATINUM NANOPARTICLES; ELECTROLYTIC HYDROGEN; MOLECULAR-STRUCTURE; WATER ELECTROLYSIS; REACTION-KINETICS; EXCHANGE CURRENT; GRAPHENE;
D O I
10.1063/5.0142540
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hydrogen evolution reaction (HER) by splitting water is a key technology toward a clean energy society, where Pt-based catalysts were long known to have the highest activity under acidic electrochemical conditions but suffer from high cost and poor stability. Here, we overview the current status of Pt-catalyzed HER from a theoretical perspective, focusing on the methodology development of electrochemistry simulation, catalytic mechanism, and catalyst stability. Recent developments in theoretical methods for studying electrochemistry are introduced, elaborating on how they describe solid-liquid interface reactions under electrochemical potentials. The HER mechanism, the reaction kinetics, and the reaction sites on Pt are then summarized, which provides an atomic-level picture of Pt catalyst surface dynamics under reaction conditions. Finally, state-of-the-art experimental solutions to improve catalyst stability are also introduced, which illustrates the significance of fundamental understandings in the new catalyst design.
引用
收藏
页数:11
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