Published February 2007 | Version v1
Journal article

Synthesis and characterization of Ti1-2x Nb x Ni x O2-x/2 solid solutions

  • 1. Departamento de Quimica Inorganica y Organica, Universitat Jaume I, 12071, Castellon (Spain)
  • 2. Laboratoire de Chimie de la Matiere Condensee, CNRS-UMR 7574, 75231, Paris (France)

Description

Doped-rutile has been traditionally used in ceramic pigments for its intense optical properties. In this paper, we compare the classical ceramic synthesis of Ti1-2x Nb x Ni x O2-x/2 system with the sol-gel methodology, which allows a reduction of the anatase-rutile transformation temperature. The composition was optimised in order to obtain a unique rutile phase with the minimum amount of pollutant Ni(II) and enhanced chromatic coordinates. Incorporation of the doping ions in the rutile structure was corroborated by XRD and Rietveld refinements. The species responsible for the colour mechanism were studied by different techniques. UV-VIS spectroscopy showed the characteristic features of Ni2+ ions, whose existence was corroborated by EPR and magnetic measurements. From these results, (Ni,Nb)doped-TiO2 powder samples can be now shaped as thin films, monoliths, etc. by using sol-gel methodology without modifying their properties. This study introduces new possibilities of coloured TiO2-based solid solutions in new combined advanced applications (colouring agent and photocatalyst, etc.). - Graphical abstract: The synthesis and characterization of the Ti1-2x Nb x Ni x O2-x/2 system prepared by traditional solid-state and sol-gel methodologies is reported. The incorporation of the doping ions in the rutile structure by Rietveld refinements and the magnetic response are discussed. The similarity found by both procedures introduces new possibilities of coloured TiO2-based solid solutions

Additional details

Identifiers

DOI
10.1016/j.jssc.2006.11.026;
PII
S0022-4596(06)00605-0;

Publishing Information

Journal Title
Journal of Solid State Chemistry
Journal Volume
180
Journal Issue
2
Journal Page Range
p. 679-687
ISSN
0022-4596
CODEN
JSSCBI

Optional Information

Copyright
Copyright (c) 2006 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.