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Integration of bio-inspired lanthanide-transition metal cluster and P-doped carbon nitride for efficient photocatalytic overall water splitting

Photosynthesis in nature uses the Mn(4)CaO(5) cluster as the oxygen-evolving center to catalyze the water oxidation efficiently in photosystem II. Herein, we demonstrate bio-inspired heterometallic LnCo(3) (Ln = Nd, Eu and Ce) clusters, which can be viewed as synthetic analogs of the CaMn(4)O(5) clu...

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Detalles Bibliográficos
Autores principales: Chen, Rong, Zhuang, Gui-Lin, Wang, Zhi-Ye, Gao, Yi-Jing, Li, Zhe, Wang, Cheng, Zhou, Yang, Du, Ming-Hao, Zeng, Suyuan, Long, La-Sheng, Kong, Xiang-Jian, Zheng, Lan-Sun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433082/
https://www.ncbi.nlm.nih.gov/pubmed/34691725
http://dx.doi.org/10.1093/nsr/nwaa234
Descripción
Sumario:Photosynthesis in nature uses the Mn(4)CaO(5) cluster as the oxygen-evolving center to catalyze the water oxidation efficiently in photosystem II. Herein, we demonstrate bio-inspired heterometallic LnCo(3) (Ln = Nd, Eu and Ce) clusters, which can be viewed as synthetic analogs of the CaMn(4)O(5) cluster. Anchoring LnCo(3) on phosphorus-doped graphitic carbon nitrides (PCN) shows efficient overall water splitting without any sacrificial reagents. The NdCo(3)/PCN-c photocatalyst exhibits excellent water splitting activity and a quantum efficiency of 2.0% at 350 nm. Ultrafast transient absorption spectroscopy revealed the transfer of a photoexcited electron and hole into the PCN and LnCo(3) for hydrogen and oxygen evolution reactions, respectively. A density functional theory (DFT) calculation showed the cooperative water activation on lanthanide and O−O bond formation on transition metal for water oxidation. This work not only prepares a synthetic model of a bio-inspired oxygen-evolving center but also provides an effective strategy to realize light-driven overall water splitting.