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Photocathode functionalized with a molecular cobalt catalyst for selective carbon dioxide reduction in water

Artificial photosynthesis is a vibrant field of research aiming at converting abundant, low energy molecules such as water, nitrogen or carbon dioxide into fuels or useful chemicals by means of solar energy input. Photo-electrochemical reduction of carbon dioxide is an appealing strategy, aiming at...

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Detalles Bibliográficos
Autores principales: Pati, Palas Baran, Wang, Ruwen, Boutin, Etienne, Diring, Stéphane, Jobic, Stéphane, Barreau, Nicolas, Odobel, Fabrice, Robert, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7358214/
https://www.ncbi.nlm.nih.gov/pubmed/32661340
http://dx.doi.org/10.1038/s41467-020-17125-4
Descripción
Sumario:Artificial photosynthesis is a vibrant field of research aiming at converting abundant, low energy molecules such as water, nitrogen or carbon dioxide into fuels or useful chemicals by means of solar energy input. Photo-electrochemical reduction of carbon dioxide is an appealing strategy, aiming at reducing the greenhouse gas into valuable products such as carbon monoxide at low or without bias voltage. Yet, in such configuration, there is no catalytic system able to produce carbon monoxide selectively in aqueous media with high activity, and using earth-abundant molecular catalyst. Upon associating a p-type Cu(In,Ga)Se(2) semi-conductor with cobalt quaterpyridine complex, we herein report a photocathode complying with the aforementioned requirements. Pure carbon dioxide dissolved in aqueous solution (pH 6.8) is converted to carbon monoxide under visible light illumination with partial current density above 3 mA cm(−2) and 97% selectivity, showing good stability over time.