4.7 Article

Operando tracking of oxidation-state changes by coupling electrochemistry with time-resolved X-ray absorption spectroscopy demonstrated for water oxidation by a cobalt-based catalyst film

Journal

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
Volume 413, Issue 21, Pages 5395-5408

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-021-03515-0

Keywords

Electrocatalysts; Time-resolved X-ray absorption spectroscopy; Transition metal oxides; Water oxidation

Funding

  1. Projekt DEAL
  2. German Federal Ministry of Education and Research (Bundesministerium fur Bildung und Forschung, BMBF) [05K16KE2, 05K19KE1]
  3. Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under Germany's Excellence Strategy [EXC 2008 -390540038 -UniSysCat]
  4. Alexander-von-Humboldt (AvH) Foundation
  5. Chinese Scholarship Council (CSC)

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Transition metal oxides show promise as electrocatalysts for water oxidation, with a proposed strategy of using single-energy X-ray absorption spectroscopy to monitor metal oxidation-state changes during operation. This approach allows for the investigation of redox kinetics and differentiation of catalytic current from redox current.
Transition metal oxides are promising electrocatalysts for water oxidation, i.e., the oxygen evolution reaction (OER), which is critical in electrochemical production of non-fossil fuels. The involvement of oxidation state changes of the metal in OER electrocatalysis is increasingly recognized in the literature. Tracing these oxidation states under operation conditions could provide relevant information for performance optimization and development of durable catalysts, but further methodical developments are needed. Here, we propose a strategy to use single-energy X-ray absorption spectroscopy for monitoring metal oxidation-state changes during OER operation with millisecond time resolution. The procedure to obtain time-resolved oxidation state values, using two calibration curves, is explained in detail. We demonstrate the significance of this approach as well as possible sources of data misinterpretation. We conclude that the combination of X-ray absorption spectroscopy with electrochemical techniques allows us to investigate the kinetics of redox transitions and to distinguish the catalytic current from the redox current. Tracking of the oxidation state changes of Co ions in electrodeposited oxide films during cyclic voltammetry in neutral pH electrolyte serves as a proof of principle.

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