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Encapsulating a Co(II) Molecular Photocatalyst in Metal–Organic Framework for Visible-Light-Driven H2 Production: Boosting Catalytic Efficiency via Spatial Charge Separation
The photodriven H2 generation from water splitting, providing a high-performance energy source, has been recognized to be a promising pathway for solar energy conversion. However, the efficient charge separation for photocatalysts remains a critical issue. In this work, we have rationally encapsulat...
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Published in: | ACS catalysis 2016-08, Vol.6 (8), p.5359-5365 |
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container_title | ACS catalysis |
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creator | Li, Zhe Xiao, Juan-Ding Jiang, Hai-Long |
description | The photodriven H2 generation from water splitting, providing a high-performance energy source, has been recognized to be a promising pathway for solar energy conversion. However, the efficient charge separation for photocatalysts remains a critical issue. In this work, we have rationally encapsulated a Co(II) molecular photcatalyst, [CoII(TPA)Cl][Cl] (TPA = tris(2-pyridylmethyl)amine), inside the cages of a metal–organic framework (MOF) photosensitizer, MIL-125-NH2, for visible-light-driven H2 production. This noble-metal-free composite photocatalyst facilitates the photoinduced charge transfer from MIL-125-NH2 to the Co(II) complex and greatly improves the spatial charge separation, thus significantly boosting the photocatalytic efficiency of H2 production. In addition, MIL-125-NH2 behaves as a host matrix to achieve hetrogenization of the Co(II) complex, and thus, the composite can be well-recycled. |
doi_str_mv | 10.1021/acscatal.6b01293 |
format | article |
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However, the efficient charge separation for photocatalysts remains a critical issue. In this work, we have rationally encapsulated a Co(II) molecular photcatalyst, [CoII(TPA)Cl][Cl] (TPA = tris(2-pyridylmethyl)amine), inside the cages of a metal–organic framework (MOF) photosensitizer, MIL-125-NH2, for visible-light-driven H2 production. This noble-metal-free composite photocatalyst facilitates the photoinduced charge transfer from MIL-125-NH2 to the Co(II) complex and greatly improves the spatial charge separation, thus significantly boosting the photocatalytic efficiency of H2 production. 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However, the efficient charge separation for photocatalysts remains a critical issue. In this work, we have rationally encapsulated a Co(II) molecular photcatalyst, [CoII(TPA)Cl][Cl] (TPA = tris(2-pyridylmethyl)amine), inside the cages of a metal–organic framework (MOF) photosensitizer, MIL-125-NH2, for visible-light-driven H2 production. This noble-metal-free composite photocatalyst facilitates the photoinduced charge transfer from MIL-125-NH2 to the Co(II) complex and greatly improves the spatial charge separation, thus significantly boosting the photocatalytic efficiency of H2 production. In addition, MIL-125-NH2 behaves as a host matrix to achieve hetrogenization of the Co(II) complex, and thus, the composite can be well-recycled.</abstract><pub>American Chemical Society</pub><doi>10.1021/acscatal.6b01293</doi><tpages>7</tpages></addata></record> |
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title | Encapsulating a Co(II) Molecular Photocatalyst in Metal–Organic Framework for Visible-Light-Driven H2 Production: Boosting Catalytic Efficiency via Spatial Charge Separation |
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