| Literature DB >> 36194638 |
Jana M Becker1, Anna Lielpetere1, Julian Szczesny1, João R C Junqueira1, Patricia Rodríguez-Maciá2, James A Birrell2, Felipe Conzuelo3, Wolfgang Schuhmann1.
Abstract
The development of electrodes for efficient CO2 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 (ChCODH II) using a cobaltocene-based low-potential redox polymer for the selective reduction of CO2 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 CO2 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 CO2 into CO without any parasitic co-reactions at the applied potentials.Entities:
Keywords: CO2 reduction; carbon monoxide dehydrogenase; enzymes; gas diffusion electrodes; redox polymers
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Year: 2022 PMID: 36194638 PMCID: PMC9585511 DOI: 10.1021/acsami.2c09547
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 10.383