4.7 Article

A two-step synthesis of NaTaO3 microspheres for photocatalytic water splitting

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 39, Issue 25, Pages 13481-13485

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2014.03.023

Keywords

NaTaO3; Microspheres; Photocatalytic water splitting; Rough surface

Funding

  1. Excellent Youth Foundation of Xinjiang Uygur Autonomous Region [2013711004]
  2. National Nature Science Foundation of China [21001113, 21173261]
  3. One Hundred Talents Project Foundation Program of Chinese Academy of Sciences, International Science & Technology Cooperation Program of Xinjiang Uygur Autonomous Region [20126017]
  4. CAS Western Action Plan [KGZD-EW-502]
  5. Cross-Cooperation Program for Creative Research Teams of Chinese Academy of Sciences
  6. Western Light Program of Chinese Academy of Sciences [YB201303]

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NaTaO3 photocatalyst has been successfully synthesized by a two-step synthesis approach, namely, molten salt in combination with hydrothermal processing at a relatively low temperature. The key concept of the approach is using molten salt to convert Ta2O5 to a soluble Ta-precursor, and the aqueous solution of the obtained Ta-precursor is then transferred as a starting source of Ta to synthesize NaTaO3 by a hydrothermal process. The obtained sample was characterized by powder X-ray diffraction (XRD), inductively coupled plasma emission spectrometry (ICP), field emission scanning electron microscopy (FESEM) and ultraviolet visible (UV-vis) spectroscopy. A spherical morphology for NaTaO3 has been observed by FESEM. Comparative study on hydrogen production from water splitting under UV-light irradiation evinces that the obtained sample exhibits more than 4 times higher photoactivity than its counterpart prepared by a solid state method. In addition, loading of NiO co-catalyst onto the surface of NaTaO3 improves its efficiency for water splitting. Copyright (C) 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

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