Mechanisms for hydrogen evolution on transition metal phosphide catalysts and a comparison to Pt(111). Issue 44 (5th November 2019)

• Record Type: Journal Article
• Authors: Li, Chenyang; Gao, Hao; Wan, Wan; Mueller, Tim
• Is Part Of: Physical chemistry chemical physics. Volume 21:Issue 44(2019)
• Page Start: 24489
• Page End: 24498
• Publication Date: 2019-11-05
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c9cp05094a
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : Cluster expansions and Monte Carlo simulations provide insights into the mechanisms for the hydrogen evolution reaction and the effects of potential and surface coverage on Pt(111) and model transition metal phosphide surfaces. Abstract : Earth-abundant transition metal phosphides have been demonstrated to be promising alternative catalysts to replace Pt for hydrogen evolution reaction (HER). However, the mechanism for the hydrogen evolution reaction on transition metal phosphides remains unclear. Here, we explore the catalytically active sites and the reaction mechanisms on a variety of model transition metal phosphide surfaces by building cluster expansion models and running Monte Carlo simulations. We demonstrate that the effect of hydrogen coverage, interaction between hydrogen atoms and desorption kinetics all dictate the HER mechanisms and the active sites, and we propose mechanisms that are in good agreement with experimental studies. The present method provides a general and effective way to probe the active sites and study the mechanisms of catalytic reactions, which can facilitate the rational design of highly active electrocatalysts.