Electroreduction of CO2 on Au(310)@Cu High‐index Facets

Author:

Liang Liang1,Feng Quanchen1ORCID,Wang Xingli1ORCID,Hübner Jessica1,Gernert Ulrich2,Heggen Marc3,Wu Longfei1,Hellmann Tim4,Hofmann Jan P.4ORCID,Strasser Peter1ORCID

Affiliation:

1. Department of Chemistry Chemical Engineering Division Technical University Berlin Straße des 17. Juni 124 10623 Berlin Germany

2. Institutes of Physical Science and Information Technology Center for Electron Microscopy (ZELMI) Technical University Berlin Straße des 17. Juni 124 10623 Berlin Germany

3. Ernst Ruska-Centre for Microscopy and Spectroscopy with Electrons Forschungszentrum Jülich GmbH 52425 Jülich Germany

4. Surface Science Laboratory Department of Materials and Earth Sciences Technical University of Darmstadt Otto-Berndt-Straße 3 64287 Darmstadt Germany

Abstract

AbstractThe chemical selectivity and faradaic efficiency of high‐index Cu facets for the CO2 reduction reaction (CO2RR) is investigated. More specifically, shape‐controlled nanoparticles enclosed by Cu {hk0} facets are fabricated using Cu multilayer deposition at three distinct layer thicknesses on the surface facets of Au truncated ditetragonal nanoprisms (Au DTPs). Au DTPs are shapes enclosed by 12 high‐index {310} facets. Facet angle analysis confirms DTP geometry. Elemental mapping analysis shows Cu surface layers are uniformly distributed on the Au {310} facets of the DTPs. The 7 nm Au@Cu DTPs high‐index {hk0} facets exhibit a CH4 : CO product ratio of almost 10 : 1 compared to a 1 : 1 ratio for the reference 7 nm Au@Cu nanoparticles (NPs). Operando Fourier transform infrared spectroscopy spectra disclose reactive adsorbed *CO as the main intermediate, whereas CO stripping experiments reveal the high‐index facets enhance the *CO formation followed by rapid desorption or hydrogenation.

Funder

Horizon 2020 Framework Programme

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

General Chemistry,Catalysis

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