Published May 2009 | Version v1
Journal article

A convenient sol-gel route for the synthesis of salicylate-titania nanocomposites having visible absorption and blue luminescence

  • 1. Department of Materials Science, Indian Association for the Cultivation of Science, Jadavpur, Kolkata 700032 (India)
  • 2. Haldia Government College, Purba Medinipur 721657, West Bengal (India)

Description

Syntheses of titania-based nanomaterials by simple sol-gel route using a mixture of CTAB and salicylate as well as salicylate ions as templates have been reported. The materials are characterized by the powder X-ray diffraction (XRD), thermal analysis, transmission electron microscopy (TEM), scanning electron microscopy (SEM) and spectroscopic (FT IR, UV-VIS) analyses. A disordered mesoscale orientation of nanoparticles (ca. 2-4 nm) composed of TiO2-salicylate surface complex has been obtained when 1:1 mixing ratio of CTAB and salicylate at the CTAB concentration of 0.001 M was employed as a template. All these nanocomposites exhibit a considerable red shift at the onsets of their absorption band compared to pure (organic-free) nanocrystalline TiO2 and show blue luminescence at room temperature. This assembly of nanoparticles is highly interesting in the context of visible light sensitization and nanodevice fabrication. - Graphical abstract: A new titania-salicylate nanostructure material has been synthesized, which exhibit a considerable red shift towards the visible region vis-a-vis nanocrystalline (organic-free) TiO2 and blue luminescence at room temperature.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jssc.2009.02.004

Additional details

Identifiers

DOI
10.1016/j.jssc.2009.02.004;
PII
S0022-4596(09)00048-6;

Publishing Information

Journal Title
Journal of Solid State Chemistry
Journal Volume
182
Journal Issue
5
Journal Page Range
p. 1200-1205
ISSN
0022-4596
CODEN
JSSCBI

Optional Information

Copyright
Copyright (c) 2009 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.