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      Towards efficient photoinduced charge separation in carbon nanodots and TiO2 composites in the visible region

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          Abstract

          The visible photoinduced electrons and holes in CDs-V/TiO 2 composites could be effectively separated, indicating that a well performing CD-based photovoltaic system could be realized.

          Abstract

          In this work, photoinduced charge separation behaviors in non-long-chain-molecule-functionalized carbon nanodots (CDs) with visible intrinsic absorption (CDs-V) and TiO 2 composites were investigated. Efficient photoinduced electron injection from CDs-V to TiO 2 with a rate of 8.8 × 10 8 s −1 and efficiency of 91% was achieved in the CDs-V/TiO 2 composites. The CDs-V/TiO 2 composites exhibited excellent photocatalytic activity under visible light irradiation, superior to pure TiO 2 and the CDs with the main absorption band in the ultraviolet region and TiO 2 composites, which indicated that visible photoinduced electrons and holes in such CDs-V/TiO 2 composites could be effectively separated. The incident photon-to-current conversion efficiency (IPCE) results for the CD-sensitized TiO 2 solar cells also agreed with efficient photoinduced charge separation between CDs-V and the TiO 2 electrode in the visible range. These results demonstrate that non-long-chain-molecule-functionlized CDs with a visible intrinsic absorption band could be appropriate candidates for photosensitizers and offer a new possibility for the development of a well performing CD-based photovoltaic system.

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          Most cited references27

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          Fluorescence lifetime measurements and biological imaging.

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            A biocompatible fluorescent ink based on water-soluble luminescent carbon nanodots.

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              Upconversion and downconversion fluorescent graphene quantum dots: ultrasonic preparation and photocatalysis.

              A facile ultrasonic route for the fabrication of graphene quantum dots (GQDs) with upconverted emission is presented. The as-prepared GQDs exhibit an excitation-independent downconversion and upconversion photoluminescent (PL) behavior, and the complex photocatalysts (rutile TiO(2)/GQD and anatase TiO(2)/GQD systems) were designed to harness the visible spectrum of sunlight. It is interesting that the photocatalytic rate of the rutile TiO(2)/GQD complex system is ca. 9 times larger than that of the anatase TiO(2)/GQD complex under visible light (λ > 420 nm) irradiation in the degradation of methylene blue.
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                Author and article information

                Journal
                PPCPFQ
                Physical Chemistry Chemical Physics
                Phys. Chem. Chem. Phys.
                Royal Society of Chemistry (RSC)
                1463-9076
                1463-9084
                2015
                2015
                : 17
                : 12
                : 7966-7971
                Article
                10.1039/C5CP00444F
                90ae82e6-cdf9-4ddf-b769-0adfc41d8988
                © 2015
                History

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