期刊
JOURNAL OF MATERIALS CHEMISTRY A
卷 8, 期 36, 页码 18745-18754出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d0ta06442d
关键词
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资金
- National Key RAMP
- D Program of China [2017YFB0702800]
- National Natural Science Foundation of China [21733009]
- Strategic Priority Research Program of the Chinese Academy of Sciences [XDB17020200]
Herein, we report the design and fabrication of QH-COF@TiO(2)and TiO2@QH-COF (QH-COF: tetrahydroquinoline-linked COFs) core-shell structured heterojunctions for photocatalytic oxidation of alcohols. For the first time, the spatial location of two semiconductors either in the core or on the shell is precisely designed, and their corresponding photocatalytic performance has been well investigated. For photocatalytic benzyl alcohol oxidation, the activity of QH-COF@TiO(2)is almost three times higher than that of TiO2@QH-COF (reaction rate: 1.19vs.0.44 mmol g(-1)h(-1)), although they exhibit similar capability for light harvesting and charge separation. The higher photocatalytic activity of QH-COF@TiO(2)is due to its easier donation of electrons to O-2. A similar tendency was also observed for the visible-light photocatalytic aerobic cross-dehydrogenative coupling reaction. Our spatial location engineering of semiconductor heterojunctions provides an efficient strategy that facilitates the modulation of charge separation and mass diffusion to enhance the photocatalytic activity of semiconductors.
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