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      Efficient visible light-induced photoelectrocatalytic hydrogen production using CdS sensitized TiO 2 nanorods on TiO 2 nanotube arrays

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          Abstract

          CdS/TNRs/TNTs were synthesized by combining a hydrothermal method with a sequential-chemical bath deposition method and displayed enhanced visible light-induced photoelectrocatalytic hydrogen production activity compared with TNTs, TNRs/TNTs and CdS/TNTs.

          Abstract

          A novel CdS/TiO 2 nanorods/TiO 2 nanotube array (CdS/TNRs/TNT) photocatalyst was prepared. The self-organized highly oriented TiO 2 nanotube arrays (TNTs) were first synthesized by anodizing Ti sheets. The “flower-like” rutile TiO 2 nanorods (TNRs) were then grafted on the TNTs by a hydrothermal method. Subsequently, the CdS quantum dots (CdS QDs) were deposited on the surface of the resulting TNRs/TNTs using a sequential-chemical bath deposition (S-CBD) method. UV-vis diffuse reflectance spectra indicated that the CdS/TNRs/TNTs sample showed significantly enhanced absorption in the range from 350 to 700 nm. The photoelectrocatalytic hydrogen production activities of all samples were evaluated by using Na 2S and Na 2SO 3 as sacrificial reagents in water under a 300 W Xe lamp with a UV-light filter ( λ > 420 nm). The results showed that CdS/TNRs/TNTs prepared by hydrothermal reactions for 4 h and S-CBD 15 cycles showed a hydrogen production rate approximately 14 times that of the TNTs. When compared to CdS/TNTs, CdS/TNRs/TNTs showed a 2.3 fold increase in hydrogen production, which can be attributed to the enlarged effective deposition area for CdS QDs by depositing “flower-like” rutile TiO 2 nanorods on the TNTs. In addition, CdS/TNRs/TNTs exhibited excellent hydrogen production stability using Na 2S and Na 2SO 3 as sacrificial reagents.

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          Most cited references37

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          Electrochemical Photolysis of Water at a Semiconductor Electrode

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            Alternative energy technologies.

            Fossil fuels currently supply most of the world's energy needs, and however unacceptable their long-term consequences, the supplies are likely to remain adequate for the next few generations. Scientists and policy makers must make use of this period of grace to assess alternative sources of energy and determine what is scientifically possible, environmentally acceptable and technologically promising.
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              Photoelectrochemical cells.

              M Grätzel (2001)
              Until now, photovoltaics--the conversion of sunlight to electrical power--has been dominated by solid-state junction devices, often made of silicon. But this dominance is now being challenged by the emergence of a new generation of photovoltaic cells, based, for example, on nanocrystalline materials and conducting polymer films. These offer the prospect of cheap fabrication together with other attractive features, such as flexibility. The phenomenal recent progress in fabricating and characterizing nanocrystalline materials has opened up whole new vistas of opportunity. Contrary to expectation, some of the new devices have strikingly high conversion efficiencies, which compete with those of conventional devices. Here I look into the historical background, and present status and development prospects for this new generation of photoelectrochemical cells.
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                Author and article information

                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                2015
                2015
                : 3
                : 44
                : 22218-22226
                Affiliations
                [1 ]State Key Laboratory of Physical Chemistry of Solid Surfaces
                [2 ]Department of Chemistry
                [3 ]College of Chemistry and Chemical Engineering
                [4 ]Xiamen University
                [5 ]Xiamen
                Article
                10.1039/C5TA04107D
                fd5f5f10-61c8-4a18-a8ee-77c0b3b2036e
                © 2015
                History

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