skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Direct formation of new, phase-stable, and photoactive anatase-type Ti{sub 1-2X}Nb{sub X}Sc{sub X}O{sub 2} solid solution nanoparticles by hydrothermal method

Journal Article · · Materials Research Bulletin
 [1];  [1]
  1. Department of Applied Chemistry, Faculty of Engineering, Aichi Institute of Technology, Yakusa, Toyota 470-0392 (Japan)

A new anatase phase of photoactive Ti{sub 1-2X}Nb{sub X}Sc{sub X}O{sub 2} (X = 0-0.2) solid solutions was directly formed as nanoparticles from precursor solutions of TiOSO{sub 4}, NbCl{sub 5}, and Sc(NO{sub 3}){sub 3} under mild hydrothermal conditions at 180 deg. C for 5 h using the hydrolysis of urea. With the increase of the content of niobium and scandium from X = 0 to 0.2, the lattice parameters a{sub 0} and c{sub 0}, the crystallite size, and the optical band gap of anatase gradually increased. Their photocatalytic activity and adsorptivity were evaluated separately by the measurement of the concentration of methylene blue (MB) remained in the solution in the dark or under UV-light irradiation. The anatase-type Ti{sub 1-2X}Nb{sub X}Sc{sub X}O{sub 2} (X = 0.05) showed approximately two times and three times as high photocatalytic activity as those of the hydrothermal anatase-type pure TiO{sub 2} and commercially available reference pure TiO{sub 2} (ST-01), respectively. The anatase phase of Ti{sub 1-2X}Nb{sub X}Sc{sub X}O{sub 2} (X = 0-0.2) existed stably up to 900 deg. C during heat treatment in air. New rutile-type Ti{sub 1-2X}Nb{sub X}Sc{sub X}O{sub 2} solid solutions are formed through the phase transformation. The starting temperature of anatase-to-rutile phase transformation for Ti{sub 1-2X}Nb{sub X}Sc{sub X}O{sub 2} (X = 0-0.2) solid solutions was delayed but its completing temperature was accelerated.

OSTI ID:
21144083
Journal Information:
Materials Research Bulletin, Vol. 43, Issue 8-9; Other Information: DOI: 10.1016/j.materresbull.2007.08.027; PII: S0025-5408(07)00385-6; Copyright (c) 2007 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0025-5408
Country of Publication:
United States
Language:
English