Effect of the Electrolyte on the Oxygen Reduction Reaction with a MOF Embedded Co‐Porphyrin

Abstract: Electrocatalysis in metal‐organic frameworks is an interplay between the diffusion of charges, the intrinsic catalytic rate, and the mass‐transport of reactants through the pores. Here a systematic study is carried out to investigate the role of the electrolyte nature and concentration on the oxygen reduction reaction (ORR) with the PCN‐224 (Co) MOF in aqueous electrolyte. It was found that the ORR activity is slightly influenced by the nature of the ions in solution, providing that the ionic strength is high enough to minimize the resistivity during the measurement. The ORR activity was found to be 1.3–1.5 times lower in lithium acetate compared to sodium acetate, while the ORR activity in cesium acetate was 1.3–1.6 times higher compared to the activity in sodium acetate. Moreover, there was no dependency found of the ORR catalysis on the size of the anion, buffer concentration, or oxygen concentration. These findings suggest that ORR catalysis in PCN‐224 (Co) is limited by the intrinsic ORR rate at the active site rather than charge transport through the porous structure or substrate transport in the pores. Therefore, optimization of ORR catalysis with this MOF might be achieved by the optimization of the electronics at the cobalt active site.

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

Erschienen in
Effect of the Electrolyte on the Oxygen Reduction Reaction with a MOF Embedded Co‐Porphyrin ; day:30 ; month:01 ; year:2025 ; extent:10
ChemSusChem ; (30.01.2025) (gesamt 10)

Urheber
Rademaker, Dana
Tanase, Stefania
Hetterscheid, Dennis G. H.

DOI
10.1002/cssc.202402295
URN
urn:nbn:de:101:1-2501311309394.715223819705
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
15.08.2025, 07:38 MESZ

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Beteiligte

  • Rademaker, Dana
  • Tanase, Stefania
  • Hetterscheid, Dennis G. H.

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