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Direct Evidence of Subsurface Oxygen Formation in Oxide-Derived Cu by X-ray Photoelectron Spectroscopy
Stockholm University, Faculty of Science, Department of Physics.ORCID iD: 0000-0002-6379-9759
Stockholm University, Faculty of Science, Department of Physics.ORCID iD: 0000-0003-0483-0602
Stockholm University, Faculty of Science, Department of Physics.ORCID iD: 0000-0001-6085-2916
Stockholm University, Faculty of Science, Department of Physics. Deutsches Elektronen-Synchrotron (DESY), Germany.ORCID iD: 0000-0002-5297-710x
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Number of Authors: 72022 (English)In: Angewandte Chemie International Edition, ISSN 1433-7851, E-ISSN 1521-3773, Vol. 61, no 3, article id e202111021Article in journal (Refereed) Published
Abstract [en]

Subsurface oxygen has been proposed to be crucial in oxide-derived copper (OD-Cu) electrocatalysts for enhancing the binding of CO intermediates during CO2 reduction reaction (CO2RR). However, the presence of such oxygen species under reductive conditions still remains debated. In this work, the existence of subsurface oxygen is validated by grazing incident hard X-ray photoelectron spectroscopy, where OD-Cu was prepared by reduction of Cu oxide with H2 without exposing to air. The results suggest two types of subsurface oxygen embedded between the fully reduced metallic surface and the Cu2O buried beneath: (i) oxygen staying at lattice defects and/or vacancies in the surface-most region and (ii) interstitial oxygen intercalated in metal structure. This study adds convincing support to the presence of subsurface oxygen in OD-Cu, which previously has been suggested to play an important role to mitigate the σ-repulsion of Cu for CO intermediates in CO2RR. 

Place, publisher, year, edition, pages
2022. Vol. 61, no 3, article id e202111021
Keywords [en]
CO2 reduction, grazing incident XPS, oxide-derived Cu, subsurface oxygen, surface-sensitive measurement
National Category
Chemical Sciences
Identifiers
URN: urn:nbn:se:su:diva-204015DOI: 10.1002/anie.202111021ISI: 000773454800008PubMedID: 34758161Scopus ID: 2-s2.0-85120917441OAI: oai:DiVA.org:su-204015DiVA, id: diva2:1652635
Available from: 2022-04-19 Created: 2022-04-19 Last updated: 2022-04-19Bibliographically approved

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Wang, Hsin-YiSoldemo, MarkusDegerman, DavidLömker, PatrickNilsson, AndersAmann, Peter

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