Surface Charge Effects for the Hydrogen Evolution Reaction on Pt(111) Using a Modified Grand-Canonical Potential Kinetics Method
Shaoyu Kong, Min Ouyang, Yi An, Wei Cao, Xiaobo Chen

TL;DR
This paper introduces a modified method to study how surface charges on catalysts affect electrochemical reactions like hydrogen evolution.
Contribution
A modified grand-canonical potential kinetics method is proposed to track surface charge effects on reaction energetics.
Findings
Surface charges on Pt(111) significantly alter hydrogen adsorption energy under standard conditions.
The modified method accurately predicts Tafel barriers consistent with experimental results.
Surface charge changes during reactions stabilize or destabilize different energy components.
Abstract
Surface charges of catalysts have important influences on the thermodynamics and kinetics of electrochemical reactions. Herein, we develop a modified version of the grand-canonical potential kinetics (GCP-K) method based on density functional theory (DFT) calculations to explore the effect of surface charges on reaction thermodynamics and kinetics. Using the hydrogen evolution reaction (HER) on the Pt(111) surface as an example, we show how to track the change of surface charge in a reaction and how to analyze its influence on the kinetics. Grand-canonical calculations demonstrate that the optimum hydrogen adsorption energy on Pt under the standard hydrogen electrode condition (SHE) is around −0.2 eV, rather than 0 eV established under the canonical ensemble, due to the high density of surface negative charges. By separating the surface charges that can freely exchange with the external…
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Taxonomy
TopicsAdvanced Chemical Physics Studies · Electrocatalysts for Energy Conversion · nanoparticles nucleation surface interactions
