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      Incorporating graphene quantum dots to enhance the photoactivity of CdSe-sensitized TiO 2nanorods for solar hydrogen production

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          Abstract

          By introducing GQDs to promote vectorial charge transfer, photocorrosion of CdSe-sensitized TiO 2toward solar hydrogen production can be resolved.

          Abstract

          This work demonstrated that the incorporation of graphene quantum dots (GQDs) can greatly improve the photoelectrochemical (PEC) efficiency of CdSe-sensitized TiO 2nanorods (TiO 2/CdSe), a TiO 2-based visible light-responsive photoelectrode paradigm, for solar hydrogen production. For TiO 2/CdSe, the accumulated holes at CdSe may induce photocorrosive oxidation to decompose CdSe, deteriorating the long-term stability of the photoelectrode and degrading the PEC performance. With the introduction of GQDs, the delocalized holes can further transfer from CdSe to the GQDs, which eases the hole accumulation at the CdSe sites, thus retarding photocorrosion. Compared to the binary TiO 2/CdSe photoanode, the ternary TiO 2/CdSe/GQD photoanode displays higher photocurrent and better photostability toward PEC hydrogen production. This superiority can be attributed to vectorial charge transfer and enhanced reaction kinetics provided by the introduction of GQDs. The findings from this work highlight the importance of the introduction of GQDs as a potential solution to the photocorrosion issue of chalcogenide-sensitized semiconductor photoelectrodes.

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          Electrochemical Photolysis of Water at a Semiconductor Electrode

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            Preparation of Graphitic Oxide

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              Large-scale pattern growth of graphene films for stretchable transparent electrodes.

              Problems associated with large-scale pattern growth of graphene constitute one of the main obstacles to using this material in device applications. Recently, macroscopic-scale graphene films were prepared by two-dimensional assembly of graphene sheets chemically derived from graphite crystals and graphene oxides. However, the sheet resistance of these films was found to be much larger than theoretically expected values. Here we report the direct synthesis of large-scale graphene films using chemical vapour deposition on thin nickel layers, and present two different methods of patterning the films and transferring them to arbitrary substrates. The transferred graphene films show very low sheet resistance of approximately 280 Omega per square, with approximately 80 per cent optical transparency. At low temperatures, the monolayers transferred to silicon dioxide substrates show electron mobility greater than 3,700 cm(2) V(-1) s(-1) and exhibit the half-integer quantum Hall effect, implying that the quality of graphene grown by chemical vapour deposition is as high as mechanically cleaved graphene. Employing the outstanding mechanical properties of graphene, we also demonstrate the macroscopic use of these highly conducting and transparent electrodes in flexible, stretchable, foldable electronics.
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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                July 21 2020
                2020
                : 8
                : 28
                : 13971-13979
                Affiliations
                [1 ]Department of Materials Science and Engineering
                [2 ]National Chiao Tung University
                [3 ]Hsinchu 30010
                [4 ]Taiwan
                [5 ]Institute of Innovative Research
                [6 ]Tokyo Institute of Technology
                [7 ]Yokohama 226-8503
                [8 ]Japan
                [9 ]Center for Emergent Functional Matter Science
                Article
                10.1039/D0TA02359K
                32032976-5ff9-4b97-94d0-4c93afc3580b
                © 2020

                http://rsc.li/journals-terms-of-use

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