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Utilize este identificador para citar ou criar um link para este item: http://acervodigital.unesp.br/handle/11449/40603
Título: 
CeO2 nanoparticles synthesized by a microwave-assisted hydrothermal method: evolution from nanospheres to nanorods
Autor(es): 
Instituição: 
  • Universidade de São Paulo (USP)
  • Universidade Federal de Alfenas (UNIFAL)
  • Universidade Estadual Paulista (UNESP)
  • Empresa Brasileira de Pesquisa Agropecuária (EMBRAPA)
ISSN: 
1466-8033
Financiador: 
  • Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
  • Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
Resumo: 
Ceria (CeO2) plays a vital role in emerging technologies for environmental and energy-related applications. The catalytic efficiency of ceria nanoparticles depends on its morphology. In this study, CeO2 nanoparticles were synthesized by a microwave-assisted hydrothermal method under different synthesis temperatures. The samples were characterized by X-ray diffraction, transmission electron microscopy, Raman scattering spectroscopy, electron paramagnetic resonance spectroscopy and by the Brunauer-Emmett-Teller method. The X-ray diffraction and Raman scattering results indicated that all the synthesized samples had a pure cubic CeO2 structure. Rietveld analysis and Raman scattering also revealed the presence of structural defects due to an associated reduction in the valence of the Ce4+ ions to Ce3+ ions caused by an increasing molar fraction of oxygen vacancies. The morphology of the samples was controlled by varying the synthesis temperature. The TEM images show that samples synthesized at 80 degrees C consisted of spherical particles of about 5 nm, while those synthesized at 120 degrees C presented a mix of spherical and rod-like nanoparticles and the sample synthesized at 160 degrees C consisted of nanorods with 10 nm average diameter and 70 nm length. The microwave-assisted method proved to be highly efficient for the synthesis of CeO2 nanoparticles with different morphologies.
Data de publicação: 
1-Jan-2012
Citação: 
Crystengcomm. Cambridge: Royal Soc Chemistry, v. 14, n. 3, p. 1150-1154, 2012.
Duração: 
1150-1154
Publicador: 
Royal Soc Chemistry
Fonte: 
http://dx.doi.org/10.1039/c1ce06188g
Endereço permanente: 
Direitos de acesso: 
Acesso restrito
Tipo: 
outro
Fonte completa:
http://repositorio.unesp.br/handle/11449/40603
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