Structural Transformation of LiVOPO4 to Li3V2(PO4)3 with Enhanced Capacity
Author(s) -
Hung-Chi Kuo,
Nitin Bagkar,
RuShi Liu,
C. H. Shen,
D.S. Shy,
X. K. Xing,
J.-F. Lee,
J. M. Chen
Publication year - 2008
Publication title -
the journal of physical chemistry b
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.864
H-Index - 392
eISSN - 1520-6106
pISSN - 1520-5207
DOI - 10.1021/jp803210w
Subject(s) - xanes , analytical chemistry (journal) , monoclinic crystal system , crystallography , materials science , triclinic crystal system , transmission electron microscopy , vanadium , extended x ray absorption fine structure , k edge , absorption spectroscopy , chemistry , spectroscopy , crystal structure , nanotechnology , physics , chromatography , quantum mechanics , metallurgy
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.
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