Toward Realistic Models of the Electrocatalytic Oxygen Evolution Reaction.


Journal

Chemical reviews
ISSN: 1520-6890
Titre abrégé: Chem Rev
Pays: United States
ID NLM: 2985134R

Informations de publication

Date de publication:
22 Jul 2024
Historique:
medline: 22 7 2024
pubmed: 22 7 2024
entrez: 22 7 2024
Statut: aheadofprint

Résumé

The electrocatalytic oxygen evolution reaction (OER) supplies the protons and electrons needed to transform renewable electricity into chemicals and fuels. However, the OER is kinetically sluggish; it operates at significant rates only when the applied potential far exceeds the reversible voltage. The origin of this overpotential is hidden in a complex mechanism involving multiple electron transfers and chemical bond making/breaking steps. Our desire to improve catalytic performance has then made mechanistic studies of the OER an area of major scientific inquiry, though the complexity of the reaction has made understanding difficult. While historically, mechanistic studies have relied solely on experiment and phenomenological models, over the past twenty years

Identifiants

pubmed: 39038270
doi: 10.1021/acs.chemrev.4c00171
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Travis E Jones (TE)

Theoretical Division, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, United States.
Department of Inorganic Chemistry, Fritz-Haber-Institute of the Max-Planck-Society, Berlin 14195, Germany.

Detre Teschner (D)

Department of Inorganic Chemistry, Fritz-Haber-Institute of the Max-Planck-Society, Berlin 14195, Germany.
Department of Heterogeneous Reactions, Max-Planck-Institute for Chemical Energy Conversion, Mülheim an der Ruhr 45470, Germany.

Simone Piccinin (S)

Consiglio Nazionale delle Ricerche, Istituto Officina dei Materiali, Trieste 34136, Italy.

Classifications MeSH