Effect of Surface‐Adsorbed and Intercalated (Oxy) anions on the Oxygen Evolution Reaction

Abstract: As the kinetically demanding oxygen evolution reaction (OER) is crucial for the decarbonization of our society, a wide range of (pre) catalysts with various non‐active‐site elements (e.g., Mo, S, Se, N, P, C, Si…) have been investigated. Thermodynamics dictate that these elements oxidize during industrial operation. The formed oxyanions are water soluble and thus predominantly leach in a reconstruction process. Nevertheless, recently, it was unveiled that these thermodynamically stable (oxy) anions can adsorb on the surface or intercalate in the interlayer space of the active catalyst. There, they tune the electronic properties of the active sites and can interact with the reaction intermediates, changing the OER kinetics and potentially breaking the persisting OER *OH/*OOH scaling relations. Thus, the addition of (oxy) anions to the electrolyte opens a new design dimension for OER catalysis and the herein discussed observations deepen the understanding of the role of anions in the OER.

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch

Erschienen in
Effect of Surface‐Adsorbed and Intercalated (Oxy) anions on the Oxygen Evolution Reaction ; day:04 ; month:08 ; year:2022 ; extent:1
Angewandte Chemie ; (04.08.2022) (gesamt 1)

Urheber
Hausmann, J. Niklas
Menezes, Prashanth W.

DOI
10.1002/ange.202207279
URN
urn:nbn:de:101:1-2022080515091310021187
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
15.08.2025, 07:30 MESZ

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