Hydrothermal Sm-doped tungsten oxide vertically plate-like array photoelectrode and its enhanced photoelectrocatalytic efficiency for degradation of organic dyes |
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Authors: | Qiong Liu Yang Liu Chang Li Jie Li Haizhou He Yaomin Li Wenzhang Li |
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Affiliation: | 1.School of Chemistry and Chemical Engineering,Central South University,Changsha,China;2.Key Laboratory of Metallogenic Prediction of Nonferrous Metals and Geological Environment Monitoring (Central South University),Ministry of Education,Changsha,China;3.Key Laboratory of Hunan Province for Metallurgy and Material Processing of Rare Metals,Changsha,China;4.Department of Chemistry,University College London,London,UK |
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Abstract: | Samarium doped tungsten oxide film was synthesized by a hydrothermal method with sodium tungstate as W precursor and samarium oxide as dopant. After annealing at 450 °C for 0.5 h, the morphology and structural characterization of as-prepared films were determined with scanning electron microscopy, X-ray diffraction and high-resolution transmission electron microscope. For the pure and Sm-doped WO3 films serving as the photoanodes, photoelectrocatalytic properties were demonstrated by degrading methyl orange and methylene blue solution, showing that Sm-doped WO3 film has faster degrading rate than pure WO3 film. Photoelectrochemical properties were investigated using linear sweep voltammetry, electrochemical impedance spectroscopy, Mott–Schottky and incident photon to current conversion efficiency. Sm-doped WO3 achieves a high photocurrent of 1.50 mA cm?2 at 1.4 V versus. Ag/AgCl, which is 1.8 times as high as that of pure WO3 film (0.83 mA cm?2). Moreover, photogenerated hole injection efficiency was improved by retarding the recombination at the interface of electrode/electrolyte. The results indicate the Sm2O3 formed by excess doping led to a better photoelectrocatalytic and photoelectrochemical activities of Sm-doped WO3 film, suggesting that the doping of Sm is a favorable strategy to improve the performance of WO3 film photoanode. |
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