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Bioelectrocatalytic CO 2 Reduction by Redox Polymer-Wired Carbon Monoxide Dehydrogenase Gas Diffusion Electrodes.

Jana M BeckerAnna LielpetereJulian SzczesnyJoão R C JunqueiraPatricia Rodríguez-MaciáJames A BirrellFelipe ConzueloWolfgang Schuhmann
Published in: ACS applied materials & interfaces (2022)
The development of electrodes for efficient CO 2 reduction while forming valuable compounds is critical. The use of enzymes as catalysts provides the advantage of high catalytic activity in combination with highly selective transformations. We describe the electrical wiring of a carbon monoxide dehydrogenase II from Carboxydothermus hydrogenoformans ( Ch CODH II) using a cobaltocene-based low-potential redox polymer for the selective reduction of CO 2 to CO over gas diffusion electrodes. High catalytic current densities of up to -5.5 mA cm -2 are achieved, exceeding the performance of previously reported bioelectrodes for CO 2 reduction based on either carbon monoxide dehydrogenases or formate dehydrogenases. The proposed bioelectrode reveals considerable stability with a half-life of more than 20 h of continuous operation. Product quantification using gas chromatography confirmed the selective transformation of CO 2 into CO without any parasitic co-reactions at the applied potentials.
Keyphrases
  • gas chromatography
  • room temperature
  • mass spectrometry
  • reduced graphene oxide
  • tandem mass spectrometry
  • gold nanoparticles
  • carbon dioxide
  • solid phase extraction
  • ionic liquid
  • liquid chromatography
  • transition metal