Understanding Cation Effects on the Hydrogen Evolution Reaction

被引:104
作者
Bender, Jay T. [1 ]
Petersen, Amanda S. [2 ]
ostergaard, Frederik C. [2 ]
Wood, Mikayla A. [1 ]
Heffernan, Sean M. J. [1 ]
Milliron, Delia J. [1 ]
Rossmeisl, Jan [2 ]
Resasco, Joaquin [1 ]
机构
[1] Univ Texas Austin, McKetta Dept Chem Engn, Austin, TX 78712 USA
[2] Univ Copenhagen, Dept Chem, DK-2100 Copenhagen, Denmark
基金
新加坡国家研究基金会; 美国国家科学基金会;
关键词
APPARENT PH-DEPENDENCE; ALKALI-METAL CATIONS; ELECTROCHEMICAL REDUCTION; REACTION-KINETICS; OXIDATION; ELECTROCATALYSTS; ELECTROLYTES; ELECTRODES; ADSORPTION; INTERFACES;
D O I
10.1021/acsenergylett.2c02500
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
The hydrogen evolution reaction (HER) is known to be influenced by the identity of alkali metal cations in the electrolyte. But a clear understanding of this behavior has not been developed. Here, we present the results of experimental and theoretical studies that describe how alkali metal cations influence the HER in acidic and basic electrolytes. Alkali metal cations are shown to have no systematic effect on HER rates in acid. In alkaline media, rates decrease with increasing cation size over Ir, Pd, and Pt (Li+ > Na+ > K+ > Cs+) and increase with cation size over Cu, Ag, and Au (Li+ < Na+ < K+ < Cs+). We argue that interfacial cations lower the activation barrier for water dissociation, an elementary step unique to the HER in alkaline media. HER rates are limited by this step on Cu, Ag, and Au but are not over Ir, Pd, and Pt, explaining the inverted activity trend. Based on ab initio molecular dynamics simulations, we suggest that trends with cation size are attributable to the greater willingness of large, weakly solvated cations to approach the electrode surface.
引用
收藏
页码:657 / 665
页数:9
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