Abstract
Natural photosynthesis, which achieves efficient solar energy conversion through the combined actions of many types of molecules ingeniously arranged in a nanospace, highlights the importance of a technique for site-selective coupling of different materials to realize artificial high-efficiency devices1. In view of increasingly serious energy and environmental problems, semiconductor-based artificial photosynthetic systems consisting of isolated photochemical system 1 (PS1), PS2 and the electron-transfer system have recently been developed2,3. However, the direct coupling of the components is crucial for retarding back reactions to increase the reaction efficiency. Here, we report a simple technique for forming an anisotropic CdS–Au–TiO2 nanojunction, in which PS1(CdS), PS2(TiO2) and the electron-transfer system (Au) are spatially fixed. This three-component system exhibits a high photocatalytic activity, far exceeding those of the single- and two-component systems, as a result of vectorial electron transfer driven by the two-step excitation of TiO2 and CdS.
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Acknowledgements
H.T. thanks T. Kawahara for discussions throughout this work. This work was partially supported by a Grant-in-Aid for Scientific Research (C) No. 16550169 from the Ministry of Education, Science, Sport, and Culture, Japan.
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H.T.: project planning, data analysis. T.M. and T.K.: experimental work (electronic absorption spectra, TEM and photocatalytic reactions). T.A. and K.T.: experimental work (HRTEM and EELS).
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Tada, H., Mitsui, T., Kiyonaga, T. et al. All-solid-state Z-scheme in CdS–Au–TiO2 three-component nanojunction system. Nature Mater 5, 782–786 (2006). https://doi.org/10.1038/nmat1734
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DOI: https://doi.org/10.1038/nmat1734
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