You are in the accessibility menu

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/65924
Title: 
Study of Hybrid Silica-Polyethyleneglycol Xerogels by Eu3+ Luminescence Spectroscopy
Author(s): 
Institution: 
Universidade Estadual Paulista (UNESP)
ISSN: 
0928-0707
Abstract: 
Good optical quality Eu3+-doped silica-polyethyleneglycol hybrids were prepared by the sol-gel process. Thermomechanical analysis showed an increase of the glass transition temperature, due to the stiffness of the polymeric network, as the amount of Eu3+ increased. Europium luminescent properties were used to study structural evolution during the sol-gel transition. For lower doping concentrations dried gels present statistical distributions of Eu3+, typical of an amorphous environment, while for higher concentrations a crystalline-like environment of Eu3+ was observed. A broad emission band was observed in the visible part of the electromagnetic spectrum and assigned to the intrinsic emission from the hybrid polymeric network.
Issue Date: 
1-Dec-1999
Citation: 
Journal of Sol-Gel Science and Technology, v. 13, n. 1-3, p. 427-432, 1999.
Time Duration: 
427-432
Keywords: 
  • Eu3+ spectroscopy
  • Hybrid gels
  • Optical probes
  • Polymer electrolytes
  • Sol-gel
  • Crystal structure
  • Doping (additives)
  • Glass transition
  • Ionic conduction
  • Luminescence
  • Polyelectrolytes
  • Polyethylene glycols
  • Sol-gels
  • Spectroscopic analysis
  • Thermal expansion
  • Thermomechanical treatment
  • Composition effects
  • Emission spectroscopy
  • Europium
  • Luminescence of solids
  • Stiffness
  • Optical quality
  • Spectrofluorimeters
  • Statistical distributions
  • Xerogels
  • Silica
  • Silica gel
Source: 
http://dx.doi.org/10.1023/A:1008673211834
URI: 
Access Rights: 
Acesso restrito
Type: 
outro
Source:
http://repositorio.unesp.br/handle/11449/65924
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

There are no files associated with this item.
 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.