期刊
CERAMICS INTERNATIONAL
卷 40, 期 4, 页码 6115-6125出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.ceramint.2013.11.063
关键词
Powders: chemical preparation; X-ray methods; Electrical properties; Batteries; V2O5
资金
- National 863 Program [2013A A050901]
- National Natural Science Foundation of China [51104092]
- K.C. Wong Magna Fund in Ningbo University
- Scientific Research Foundation of Graduate School of Ningbo University [G13032]
- Open Foundation of State Key Laboratory of Materials Processing and Die & Mould Technology [2012-P01]
- Open Foundation of State Key Laboratory of Electronic Thin Films and Integrated Devices [KFJJ201209]
In this paper, V2O5 sheets and bulks are prepared by a low temperature sol gel method with and without tartaric acid as chelating agent, respectively. Owing to short diffusion pathways for lithium ions, V2O5 sheets display the reversible lithium storage capacities of 243.2, 167.5, 124.3 mAh g(-1) at 0.2C, 1C and 2C in 1.5-4.1 V, respectively. Electroanalytical results reveal that the chemical diffusion coefficient (3.4 x 10(-12) CM2 s(-1)) in Li-deficient LixV(2)O(5) sheets (x=0.681) is almost one order of magnitude higher than that (3.7 x 10(-13) cm(2) s(-1))) in Li-rich phase (x=2.824). As a result, V2O5 sheets show an outstanding capacity retention of 92.7% after 22 cycles due to 0.912 Li per formula storage in Li-deficient LixV2O5 at 2C. In-situ structural analysis shows that the electrochemical reactions of V2O5 sheets with Li are associated with the formation of alpha-Li,V2O5, alpha-LixV(2)O(5),.delta-Li,V2O5 and gamma-LixV(2)O(5) in 1.5 +/- 4.1 V. In the reverse delithiation process, y-Li,V2O5 can transforms back into.delta-Li(x)V205, epsilon-LixV2O5 and alpha-LixV2O5, but cannot return to the pristine V2O5. Upon an over-lithiation process to 0.0 V, the crystal structure of LixV(2)O(5) (x> 3) sheets will collapse and cannot be rebuilt in 0.0-4.1 V. (C) 2013 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
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