Extremely stable photoinduced charge separation in a colloidal system composed of semiconducting niobate and clay nanosheets.
Extremely stable photoinduced charge separation in a colloidal system composed of semiconducting niobate and clay nanosheets.
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DOI:
10.1002/anie.200604483
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发表时间:
2007-05
影响因子:
--
通讯作者:
N. Miyamoto;Yoshimi Yamada;S. Koizumi;T. Nakato
中科院分区:
文献类型:
--
作者:
N. Miyamoto;Yoshimi Yamada;S. Koizumi;T. Nakato
Colloidal semiconductor particles have been investigated because of their applications in photoenergy conversion and photocatalysis.[1] Electrons and holes generated upon bandgap photoexcitation of the semiconductor particles are separated by subsequent interfacial electron transfer to acceptor and donor molecules. The stabilization of the charge-separated state is key for controlling the photochemical reactions induced by photoexcitation of the semiconductor particles.The spatial separation of the acceptor and donor species can be used effectively to stabilize the charge-separated state by suppressing back electron transfer. Heterogeneous media, such as micelles and vesicles, have been utilized for such purposes;[2] for example, the photoinduced charge separation between semiconducting particles and acceptor or sensitizer molecules has been achieved by using vesicles,[3] microemulsions,[4] and SiO2 particles [5] as the heterogeneous media. However, in these colloidal systems the photogenerated charge-separated states are still short-lived (with lifetimes of only a few minutes). The incorporation of acceptor and donor components into nanostructured solids, such as layered [6, 7] and porous materials,[8] stabilizes effectively the chargeseparated state (with lifetimes of up to several hours). Nevertheless, solid systems have a drawback regarding the difficulty of being penetrated by both light and molecules. Another disadvantage is that the charge-separated products which store the photoenergy cannot undergo further reactions easily.