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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/111747
Title: 
Insight into the Effects of Fe Addition on the Local Structure and Electronic Properties of SrTiO3
Author(s): 
Institution: 
  • Universidade de São Paulo (USP)
  • Univ Jaume 1
  • Universidade Estadual Paulista (UNESP)
  • Universidade Federal de São Paulo (UNIFESP)
  • Universidade Federal de Pelotas (UFPEL)
ISSN: 
1932-7447
Sponsorship: 
  • Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
  • Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
  • Generalitat Valenciana
  • Ministerio de Ciencia e Innovacion
  • Programa de Cooperacion Cientifica con Iberoamerica (Brazil)
  • Ministerio de Educacion
Sponsorship Process Number: 
  • CNPq: 70/2008
  • CNPq: 150753/2013-6
  • FAPESP: 13/09573-3
  • Generalitat ValencianaPrometeo/2009/053
  • Ministerio de Ciencia e InnovacionCTQ2009-14541-C02
  • Ministerio de EducacionPHB2009-0065-PC
Abstract: 
This paper reports an experimental and theoretical investigation of the effects of adding Fe to the perovskite strontium titanate SrTiO3. The effects include changes in the short-order range structure as well as in the electronic and electrical properties. X-ray diffraction analysis reveals that the SrTi1-xFexO3 network shrinks with increasing Fe content, while X-ray absorption spectroscopy measurements of the Ti and Fe K-edge revealed the presence of some under-coordinated TiO5 units created because of the partial replacement of Fe3+ ions in the Ti4+. site. UV-visible absorption spectra indicated a reduction in optical gap with increasing Fe content. The electronic structure and spin densities of STFO with x = 0, 0.0625, 0.125, 0.5, and 1 are calculated by the OFT method at the B3LYP computational level, showing a Jahn-Teller distortion of O atoms surrounding the Fe as well as the formation of under-coordinated TiO5 units. From the electrical viewpoint, the results show that STFO is a mixed (ionic and electronic) conductor and that the electronic contribution becomes dominant with increasing Fe content.
Issue Date: 
6-Mar-2014
Citation: 
Journal Of Physical Chemistry C. Washington: Amer Chemical Soc, v. 118, n. 9, p. 4930-4940, 2014.
Time Duration: 
4930-4940
Publisher: 
Amer Chemical Soc
Source: 
http://dx.doi.org/10.1021/jp408839q
URI: 
Access Rights: 
Acesso restrito
Type: 
outro
Source:
http://repositorio.unesp.br/handle/11449/111747
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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