4.8 Article

A Pyrene-Triazacyclononane Anchor Affords High Operational Stability for CO2RR by a CNT-Supported Histidine-Tagged CODH

期刊

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202117212

关键词

Azamacrocycles; CO2 Reduction; Carbon Monoxide Dehydrogenase; Carbon Nanotubes; Pyrene

资金

  1. Agence Nationale de la Recherche through the LabEx ARCANE program [ANR-11-LABX-0003-01]
  2. Graduate School on Chemistry, Biology and Health of Univ Grenoble Alpes CBH-EUR-GS [ANR-17-EURE-0003]
  3. CNRS
  4. plateforme de Chimie NanoBio ICMG FR 2607 (PCN-ICMG)
  5. Plateau Synthese Organique (PSO-DCM)

向作者/读者索取更多资源

An AcPyTACN compound was synthesized for immobilizing recombinant CODH on carbon-nanotube electrodes, resulting in high current density and stability for electroenzymatic CO2 reduction.
An original 1-acetato-4-(1-pyrenyl)-1,4,7-triazacyclononane (AcPyTACN) was synthesized for the immobilization of a His-tagged recombinant CODH from Rhodospirillum rubrum (RrCODH) on carbon-nanotube electrodes. The strong binding of the enzyme at the Ni-AcPyTACN complex affords a high current density of 4.9 mA cm(-2) towards electroenzymatic CO2 reduction and a high stability of more than 6x10(6) TON when integrated on a gas-diffusion bioelectrode.

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