Cargando…

A Precious‐Metal‐Free Hybrid Electrolyzer for Alcohol Oxidation Coupled to CO(2)‐to‐Syngas Conversion

Electrolyzers combining CO(2) reduction (CO(2)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‐tetra...

Descripción completa

Detalles Bibliográficos
Autores principales: Bajada, Mark A., Roy, Souvik, Warnan, Julien, Abdiaziz, Kaltum, Wagner, Andreas, Roessler, Maxie M., Reisner, Erwin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496929/
https://www.ncbi.nlm.nih.gov/pubmed/32250531
http://dx.doi.org/10.1002/anie.202002680
Descripción
Sumario:Electrolyzers combining CO(2) reduction (CO(2)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–CO(2)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:H(2) 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 CO(2)R to less energy demanding, and value‐added, oxidative chemistry.