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Photodriven water oxidation initiated by a surface bound chromophore-donor-catalyst assembly

In photosynthesis, solar energy is used to produce solar fuels in the form of new chemical bonds. A critical step to mimic photosystem II (PS II), a key protein in nature's photosynthesis, for artificial photosynthesis is designing devices for efficient light-driven water oxidation. Here, we de...

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Detalles Bibliográficos
Autores principales: Wang, Degao, Xu, Zihao, Sheridan, Matthew V., Concepcion, Javier J., Li, Fei, Lian, Tianquan, Meyer, Thomas J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580115/
https://www.ncbi.nlm.nih.gov/pubmed/34880995
http://dx.doi.org/10.1039/d1sc03896f
Descripción
Sumario:In photosynthesis, solar energy is used to produce solar fuels in the form of new chemical bonds. A critical step to mimic photosystem II (PS II), a key protein in nature's photosynthesis, for artificial photosynthesis is designing devices for efficient light-driven water oxidation. Here, we describe a single molecular assembly electrode that duplicates the key components of PSII. It consists of a polypyridyl light absorber, chemically linked to an intermediate electron donor, with a molecular-based water oxidation catalyst on a SnO(2)/TiO(2) core/shell electrode. The synthetic device mimics PSII in achieving sustained, light-driven water oxidation catalysis. It highlights the value of the tyrosine–histidine pair in PSII in achieving efficient water oxidation catalysis in artificial photosynthetic devices.