Insight into the Carbon Monoxide Reduction Reaction on Cu(111) from <i>Operando</i> Electrochemical X‐ray Photoelectron Spectroscopy

B Bernadette Davies (Department of Physics, Alba Nova Research Center) F Fernando Garcia‐Martinez (Photon Science Deutsches Elektronen‐Synchrotron DESY Notkestr. 85 22607 Hamburg Germany) C Christopher M. Goodwin D David Degerman (Department of Physics, Alba Nova Research Center) M Markus Soldemo P Patrick Lömker V Vladimir Grigorev (Department of Physics, Alba Nova Research Center) S Sara Boscolo Bibi (Department of Physics Stockholm University AlbaNova University Center Stockholm SE‐106 91 Sweden) H Harri Ali‐Löytty (Faculty of Engineering and Natural Sciences Tampere University P.O. Box 692 Tampere FI‐33014 Finland) R Robin Y. Engel (Department of Physics Stockholm University AlbaNova University Center Stockholm SE‐106 91 Sweden) J Joakim Halldin Stenlid (Department of Physics, Alba Nova Research Center) G Gabriel L. S. Rodrigues T Tony Hansson (Department of Physics Stockholm University AlbaNova University Center Stockholm SE‐106 91 Sweden) C Christoph Schlueter X Xiaodong Zou (Department of Chemistry) A Anders Nilsson (Department of Physics, Alba Nova Research Center) S Sergey Koroidov (Department of Physics, Alba Nova Research Center)

Abstract

Abstract In this work, we introduce a modified dip‐and‐pull electrochemical X‐ray photoelectron spectroscopy (ECXPS) approach that offers new mechanistic insight into the alkaline carbon monoxide reduction reaction (CORR) over a Cu(111) single crystal surface. We tackle two major unresolved questions in the CORR mechanism that persist in the literature. Firstly, we address the mechanism for methane formation on Cu(111) and show that the mechanism likely proceeds via atomic carbon, which subsequently couples, leading to the accumulation of amorphous carbon on the surface. Secondly, we provide insight into whether the mechanism for acetate formation occurs entirely on the surface or partially within the solution phase, showing that acetate is present on the surface, indicating a surface‐based reaction. These insights into surface‐based mechanisms provide a handle for designing future catalysts that can efficiently target the binding of specific intermediates. Furthermore, we expect that our modified approach to dip‐and‐pull ECXPS – in which we have changed the electrode geometry, the method of introducing the reactant gas and used hard x‐rays – will significantly expand the technique's applicability, enabling studies of the CO (2) RR and beyond.

Article Details

Volume / Issue Vol. 64, Issue 33
Published August 11, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (17)

B

Bernadette Davies

Department of Physics, Alba Nova Research Center

F

Fernando Garcia‐Martinez

Photon Science Deutsches Elektronen‐Synchrotron DESY Notkestr. 85 22607 Hamburg Germany

C

Christopher M. Goodwin

D

David Degerman

Department of Physics, Alba Nova Research Center

M

Markus Soldemo

P

Patrick Lömker

V

Vladimir Grigorev

Department of Physics, Alba Nova Research Center

S

Sara Boscolo Bibi

Department of Physics Stockholm University AlbaNova University Center Stockholm SE‐106 91 Sweden

H

Harri Ali‐Löytty

Faculty of Engineering and Natural Sciences Tampere University P.O. Box 692 Tampere FI‐33014 Finland

R

Robin Y. Engel

Department of Physics Stockholm University AlbaNova University Center Stockholm SE‐106 91 Sweden

J

Joakim Halldin Stenlid

Department of Physics, Alba Nova Research Center

G

Gabriel L. S. Rodrigues

T

Tony Hansson

Department of Physics Stockholm University AlbaNova University Center Stockholm SE‐106 91 Sweden

C

Christoph Schlueter

X

Xiaodong Zou

Department of Chemistry

A

Anders Nilsson

Department of Physics, Alba Nova Research Center

S

Sergey Koroidov

Department of Physics, Alba Nova Research Center