Scaling Relations on Basal Plane Vacancies of Transition Metal Dichalcogenides for CO2 Reduction
Author(s) -
Yongfei Ji,
Jens K. Nørskov,
Karen Chan
Publication year - 2019
Publication title -
the journal of physical chemistry c
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.401
H-Index - 289
eISSN - 1932-7455
pISSN - 1932-7447
DOI - 10.1021/acs.jpcc.8b11628
Subject(s) - transition metal , density functional theory , scaling , vacancy defect , basal plane , catalysis , materials science , hydrogen , metal , chemistry , electrocatalyst , transition state , kinetic energy , chemical physics , crystallography , computational chemistry , physics , metallurgy , electrochemistry , quantum mechanics , geometry , mathematics , organic chemistry , electrode , biochemistry
Transition metal dichalcogenides (TMDs) have shown promising electrocatalytic performance for CO2 reduction (CO2R) recently. However, the development of efficient and selective catalysts remains a major challenge. Although recent studies have suggested the importance of activation energies as activity descriptors for CO2R beyond CO, the scaling of intermediate binding energies presents the first step in computational catalyst screening. Here, we investigate the basal vacancy on 2H and 1T/1T′ phase group V, VI, and X TMDs for CO2 reduction. We find that the change of oxophicility and carbophilicity on each group of TMDs follows different trends, which leads to different scaling relations amongst key intermediates. Our thermochemical analysis also suggests group V and VI TMDs to be either selective for hydrogen evolution reaction or prone to OH poisoning. However, the initial analysis suggests group X TMDs to be possible candidates for active and selective CO2 reduction without suffering from OH poisoning, ...
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