Operando Tracking the Interactions between CoOx and CeO2 during Oxygen Evolution Reaction
Source abstract
Abstract
Abstract CeO2 greatly enhances the electrocatalytic oxygen evolution reaction (OER) activity of CoOx, though the enhancement mechanism beyond this synergy is yet to be understood. Here, operando hard X‐ray absorption spectroscopy (hXAS) is applied to monitor the Co K edge and Ce L3 edge in CoOx/CeO2 to shed light on the evolution of the Co and Ce oxidation states during OER. In addition, ex situ soft XAS (sXAS) characterizations provide information on the irreversible surface‐specific transformations of the Co L3 edge as well as of the O K edge. Combining the operando and ex situ spectroscopic characterizations with comprehensive electrochemical analyses, it is confirmed that CeO2 is not the active center for the OER. However, coupling CeO2 with CoOx introduces significant modifications in the Co and O species at the CoOx surface and alters the flat band potential (Efb), leading to more favorable Co oxidation state transformations during OER and possibly modifying the preferential reaction pathway. This work establishes the connections between electronic structures, Co oxidation state and the OER reaction mechanism for CoOx/CeO2 composites electrodes.
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Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Catalytic Processes in Materials Science · Electrochemical Analysis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Electrochemistry Laboratory Paul Scherrer Institut Villigen PSI CH‐5232 Switzerland
Photon Science Division Paul Scherrer Institute Villigen PSI CH‐5232 Switzerland
Laboratory for High Performance Ceramics Empa – Swiss Federal Laboratories for Materials Science and Technology Dübendorf CH‐8600 Switzerland
Institute for Physical Molecular Sciences ETH Zürich Zürich CH‐8093 Switzerland
Funding
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
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