WO3颗粒改性垂直排列TiO2纳米管阵列用于氢燃料生产

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Frontiers in Energy ›› 2018, Vol. 12 ›› Issue (2) : 249-258. DOI: 10.1007/s11708-018-0547-1

WO3颗粒改性垂直排列TiO2纳米管阵列用于氢燃料生产

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Decoration of vertically aligned TiO2 nanotube arrays with WO3 particles for hydrogen fuel production

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Abstract

WO3 decorated photoelectrodes of titanium nanotube arrays (W-oxide TNTAs) were synthesized via a two-step process, namely, electrochemical oxidation of titanium foil and electrodeposition of W-oxide for various interval times of 1, 2, 3, 5, and 20 min to improve the photoelectrochemical performance and the amount of hydrogen generated. The synthesized photoelectrodes were characterized by various characterization techniques. The presence of tungsten in the modified TNTAs was confirmed using energy dispersive X-ray spectroscopy (EDX). Field emission scanning electron microscopy (FESEM) and high resolution transmission electron microscope (HRTEM) proved the deposition of W-oxide as small particles staked up on the surface of the tubes at lower deposition time whereas longer times produced large and aggregate particles to mostly cover the surface of TiO2 nanotubes. Additionally, the incorporation of WO3 resulted in a shift of the absorption edge toward visible light as confirmed by UV-Vis diffuse reflectance spectroscopy and a decrease in the estimated band gap energy values hence, modified TNTAs facilitated a more efficient utilization of solar light for water splitting. From the photoelectrochemical measurement data, the optimal photoelectrode produced after 2 min of deposition time improved the photo conversion efficiency and the hydrogen generation by 30% compared to that of the pure TNTA.

Keywords

titanium dioxide nanotube arrays / potentiostaticanodization / electrodeposition method / tungsten oxide / photoelectrochemical water splitting

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. . Frontiers in Energy. 2018, 12(2): 249-258 https://doi.org/10.1007/s11708-018-0547-1

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Acknowledgments

This work was supported by the Science and Technology Development Fund (STDF) of Egypt (project number 3649).

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2018 Higher Education Press and Springer-Verlag GmbH Germany, part of Springer Nature
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