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Structural transformation of LiVOPO4 to Li3V2(PO4)3 with enhanced capacity.
Kuo, H T; Bagkar, N C; Liu, R S; Shen, C H; Shy, D S; Xing, X K; Lee, J-F; Chen, J M.
Afiliação
  • Kuo HT; Department of Chemistry, National Taiwan University, Taipei 106, Taiwan.
J Phys Chem B ; 112(36): 11250-7, 2008 Sep 11.
Article em En | MEDLINE | ID: mdl-18636763
In the present investigation, we report the transformation of alpha-LiVOPO 4 to alpha-Li 3V 2(PO 4) 3, leading to an enhancement of capacity. The alpha-LiVOPO 4 sample was synthesized by a sol-gel method, followed by sintering at 550-650 degrees C in a flow of 5% H 2/Ar. The structural transformation of a triclinic alpha-LiVOPO 4 structure to a monoclinic alpha-Li 3V 2(PO 4) 3 structure was observed at higher sintering temperatures (700-800 degrees C in a flow of 5% H 2/Ar). The alpha-Li 3V 2(PO 4) 3 phase was characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, thermal gravimetric analysis, and X-ray absorption near edge spectrum (XANES) techniques. The valence shift of vanadium ions from +4 to +3 states was observed using in situ XANES experiments at V K-edge. The structural transformation is ascertained by the shape changes in pre-edge and near edge area of X-ray absorption spectrum. It was observed that the capacity was enhanced from 140 mAh/g to 164 mAh/g via structural transformation process of LiVOPO 4 to Li 3V 2(PO 4) 3.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2008 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2008 Tipo de documento: Article