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      Combinatorial aerosol assisted chemical vapour deposition of a photocatalytic mixed SnO2/TiO2 thin film

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          Abstract

          A mixed phase TiO 2 and SnO 2 film was deposited by combinatorial aerosol assisted CVD and composition was related to photocatalysis, hydrophobicity and microstructure not inherent to TiO 2 or SnO 2.

          Abstract

          Combinatorial Aerosol Assisted Chemical Vapour Deposition (cAACVD) was used to grow a thin film that graduated across its width from tin dioxide to titanium dioxide. This is a relatively new technique that can be used to create a variety of mixed phase and composition thin films on a single substrate. Here cAACVD was used to deposit a mixed phase TiO 2 and SnO 2 film and composition was related to UV photocatalysis, hydrophobicity and microstructure not inherent to anatase TiO 2 or cassiterite SnO 2. Characterisation was achieved using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX) and UV-Vis spectroscopy. Functional testing to elucidate the differences in functional properties across the film was undertaken by the photo-induced degradation of a resazurin ‘intelligent’ ink, a photo-induced wettability study and two-point resistivity measurements. Functional properties showed enhanced photocatalysis in comparison to Pilkington Activ™ with similar formal quantum yield (molecules destroyed per absorbed photon) and formal quantum efficiency (molecules destroyed per incident photon) values.

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          Most cited references24

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          Chemical vapour deposition of coatings

          S K Choy (2003)
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            Electrons in nanostructured TiO2 solar cells: transport, recombination and photovoltaic properties

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              Visible Light-Induced Water Oxidation on Mesoscopic α-Fe2O3Films Made by Ultrasonic Spray Pyrolysis

              Alpha-Fe(2)O(3) films having a mesoscopic leaflet type structure were produced for the first time by ultrasonic spray pyrolysis (USP) to explore their potential as oxygen-evolving photoanodes. The target of these studies is to use translucent hematite films deposited on conducting fluorine doped tin oxide (FTO) glass as top electrodes in a tandem cell that accomplishes the cleavage of water into hydrogen and oxygen by sunlight. The properties of layers made by USP were compared to those deposited by conventional spray pyrolysis (SP). Although both types of films show similar XRD and UV-visible and Raman spectra, they differ greatly in their morphology. The mesoscopic alpha-Fe(2)O(3) layers produced by USP consist mainly of 100 nm-sized platelets with a thickness of 5-10 nm. These nanosheets are oriented mainly perpendicularly to the FTO support, their flat surface exposing (001) facets. The mesoscopic leaflet structure has the advantage that it allows for efficient harvesting of visible light, while offering at the same time the very short distance required for the photogenerated holes to reach the electrolyte interface before recombining with conduction band electrons. This allows for water oxidation by the valence band holes even though their diffusion length is only a few nanometers. Distances are longer in the particles produced by SP favoring recombination of photoinduced charge carriers. Open-circuit photovoltage measurements indicate a lower surface state density for the nanoplatelets as compared to the round particles. These factors explain the much higher photoactivity of the USP compared to the SP deposited alpha-Fe(2)O(3) layers. Addition of hydrogen peroxide to the alkaline electrolyte further improves the photocurrent-voltage characteristics of films generated by USP indicating the hole transfer from the valence band of the semiconductor oxide to the adsorbed water to be the rate-limiting kinetic step in the oxygen generation reaction.
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                Author and article information

                Journal
                JMCAET
                J. Mater. Chem. A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                2014
                2014
                : 2
                : 14
                : 5108-5116
                Affiliations
                [1 ]Materials Chemistry Research Centre
                [2 ]Department of Chemistry
                [3 ]University College London
                [4 ]London, UK
                [5 ]Bio Nano Consulting Ltd
                [6 ], UK
                [7 ]Chemistry Department
                [8 ]King Abdulaziz University
                [9 ]Saudi Arabia
                Article
                10.1039/C4TA00545G
                ffb7e4be-b546-40bd-ad91-7d89ef50a917
                © 2014
                History

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