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A Precious-Metal-Free Hybrid Electrolyzer for Alcohol Oxidation Coupled to CO2 -to-Syngas Conversion.
Bajada, Mark A; Roy, Souvik; Warnan, Julien; Abdiaziz, Kaltum; Wagner, Andreas; Roessler, Maxie M; Reisner, Erwin.
Afiliación
  • Bajada MA; Department of Chemistry, University of Cambridge, Cambridge, CB2 1EW, UK.
  • Roy S; Department of Chemistry, University of Cambridge, Cambridge, CB2 1EW, UK.
  • Warnan J; Department of Chemistry, University of Cambridge, Cambridge, CB2 1EW, UK.
  • Abdiaziz K; Department of Chemistry, Imperial College London, Molecular Sciences Research Hub, White City Campus, London, W12 0BZ, UK.
  • Wagner A; School of Biological and Chemical Sciences and Materials Research Institute, Queen Mary University of London, London, E1 4NS, UK.
  • Roessler MM; Department of Chemistry, University of Cambridge, Cambridge, CB2 1EW, UK.
  • Reisner E; Department of Chemistry, Imperial College London, Molecular Sciences Research Hub, White City Campus, London, W12 0BZ, UK.
Angew Chem Int Ed Engl ; 59(36): 15633-15641, 2020 Sep 01.
Article en En | MEDLINE | ID: mdl-32250531
Electrolyzers combining CO2 reduction (CO2 R) with organic substrate oxidation can produce fuel and chemical feedstocks with a relatively low energy requirement when compared to systems that source electrons from water oxidation. Here, we report an anodic hybrid assembly based on a (2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO) electrocatalyst modified with a silatrane-anchor (STEMPO), which is covalently immobilized on a mesoporous indium tin oxide (mesoITO) scaffold for efficient alcohol oxidation (AlcOx). This molecular anode was subsequently combined with a cathode consisting of a polymeric cobalt phthalocyanine on carbon nanotubes to construct a hybrid, precious-metal-free coupled AlcOx-CO2 R electrolyzer. After three-hour electrolysis, glycerol is selectively oxidized to glyceraldehyde with a turnover number (TON) of ≈1000 and Faradaic efficiency (FE) of 83 %. The cathode generated a stoichiometric amount of syngas with a CO:H2 ratio of 1.25±0.25 and an overall cobalt-based TON of 894 with a FE of 82 %. This prototype device inspires the design and implementation of nonconventional strategies for coupling CO2 R to less energy demanding, and value-added, oxidative chemistry.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2020 Tipo del documento: Article Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2020 Tipo del documento: Article Pais de publicación: Alemania