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H(2)O(2) Production at Low Overpotentials for Electroenzymatic Halogenation Reactions

Various enzymes utilize hydrogen peroxide as an oxidant. Such “peroxizymes” are potentially very attractive catalysts for a broad range of oxidation reactions. Most peroxizymes, however, are inactivated by an excess of H(2)O(2). The electrochemical reduction of oxygen can be used as an in situ gener...

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Detalles Bibliográficos
Autores principales: Bormann, Sebastian, van Schie, Morten M. C. H., De Almeida, Tiago Pedroso, Zhang, Wuyuan, Stöckl, Markus, Ulber, Roland, Hollmann, Frank, Holtmann, Dirk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899481/
https://www.ncbi.nlm.nih.gov/pubmed/31557410
http://dx.doi.org/10.1002/cssc.201902326
Descripción
Sumario:Various enzymes utilize hydrogen peroxide as an oxidant. Such “peroxizymes” are potentially very attractive catalysts for a broad range of oxidation reactions. Most peroxizymes, however, are inactivated by an excess of H(2)O(2). The electrochemical reduction of oxygen can be used as an in situ generation method for hydrogen peroxide to drive the peroxizymes at high operational stabilities. Using conventional electrode materials, however, also necessitates significant overpotentials, thereby reducing the energy efficiency of these systems. This study concerns a method to coat a gas‐diffusion electrode with oxidized carbon nanotubes (oCNTs), thereby greatly reducing the overpotential needed to perform an electroenzymatic halogenation reaction. In comparison to the unmodified electrode, with the oCNTs‐modified electrode the overpotential can be reduced by approximately 100 mV at comparable product formation rates.