Single-atom catalysts for CO2 electroreduction with significant activity and selectivity improvements

A single-atom catalyst (SAC) has an electronic structure that is very different from its bulk counterparts, and has shown an unexpectedly high specific activity with a significant reduction in noble metal usage for CO oxidation, fuel cell and hydrogen evolution applications, although physical origins of such performance enhancements are still poorly understood. Herein, by means of density functional theory (DFT) calculations, we for the first time investigate the great potential of single atom catalysts for CO2 electroreduction applications. In particular, we study a single transition metal atom anchored on defective graphene with single or double vacancies, denoted M@sv-Gr or M@dv-Gr, where M = Ag, Au, Co, Cu, Fe, Ir, Ni, Os, Pd, Pt, Rh or Ru, as a CO2 reduction catalyst. Many SACs are indeed shown to be highly selective for the CO2 reduction reaction over a competitive H-2 evolution reaction due to favorable adsorption of carboxyl (*COOH) or formate (*OCHO) over hydrogen (*H) on the catalysts. On the basis of free energy profiles, we identified several promising candidate materials for different products; Ni@dv-Gr (limiting potential U-L = -0.41 V) and Pt@dv-Gr (-0.27 V) for CH3OH production, and Os@dvGr (-0.52 V) and Ru@dv-Gr (-0.52 V) for CH4 production. In particular, the Pt@dv-Gr catalyst shows remarkable reduction in the limiting potential for CH3OH production compared to any existing catalysts, synthesized or predicted. To understand the origin of the activity enhancement of SACs, we find that the lack of an atomic ensemble for adsorbate binding and the unique electronic structure of the single atom catalysts as well as orbital interaction play an important role, contributing to binding energies of SACs that deviate considerably from the conventional scaling relation of bulk transition metals.
Publisher
ROYAL SOC CHEMISTRY
Issue Date
2017-08
Language
English
Keywords

ELECTROCHEMICAL REDUCTION; CARBON-DIOXIDE; METAL-SURFACES; H-2 EVOLUTION; OXIDATION; GRAPHENE; AU; ELECTROCATALYSTS; HYDROCARBONS; PERFORMANCE

Citation

CHEMICAL SCIENCE, v.8, no.2, pp.1090 - 1096

ISSN
2041-6520
DOI
10.1039/c6sc03911a
URI
http://hdl.handle.net/10203/220963
Appears in Collection
NT-Journal Papers(저널논문)EEW-Journal Papers(저널논문)
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