Mesoporous Tin Phosphate as Anode Material for Lithium-Ion Cells

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Mesoporous SnP2O7 was synthesized via a surfactant templating method where an anionic surfactant, sodium dodecyl sulfate was used. X-ray diffraction (XRD) analysis indicates presence of mesostructure when the precursors were calcined at 200, 300 and 400 °C. Cyclic voltammetry tests carried out within 0-2.0 V (vs. Li/Li+) indicated that irreversible reduction of tin phosphate to form lithium phosphate phases and metallic tin occurred around 1.10 V and 0.69 V whereas the reversible alloying and de-alloying reaction involving lithium with tin occurred at 0.19 V and 0.52 V, respectively. Galvanostatic charge-discharge cycling tests carried out within 0-1.2V (vs. Li/Li+) showed that the mesoporous tin phosphate calcined at 400 °C exhibited a reversible discharge capacity of 738 mAh/g in the second cycle and upon reaching the tenth cycle, it retained a discharge capacity of 461 mAh/g. The relatively high capacity obtained for this anode was attributed to the mesoporous framework which provided larger surface area for reaction with lithium and minimized effect of volume changes experienced by the anode during repeated charging and discharging cycling.

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175-181

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July 2012

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© 2012 Trans Tech Publications Ltd. All Rights Reserved

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[1] M. Winter and J.O. Besenhard, Electrochemical Lithiation of Tin and Tin-based Intermetallics and Composites, Electrochemica Acta, vol. 45, 1999, pp.31-50.

DOI: 10.1016/s0013-4686(99)00191-7

Google Scholar

[2] I.A. Courtney and J.R. Dahn. J. Electrochemical Society 144, (1997) p.2045-(2052).

Google Scholar

[3] I.A. Courtney and J.R. Dahn. J. Electrochemical Society 144, (1997) pp.2943-2948.

Google Scholar

[4] J. Yang, M. Winter and J. O Besenhard. Solid State Ionics 90, (1996) pp.281-287.

Google Scholar

[5] O. Mao, R.L. Turner, I.A. Courtney, B.D. Frederickson, M.I. Buckett, L.J. Krause and J.R. Dahn, Electrochemical and Solid State Letters 2, (1999) pp.3-5.

Google Scholar

[6] J.H. Ahn, G.X. Wang, J. Yao, H.K. Liu and S.X. Dou. J. Power Sources 119-121, (2003) pp.45-49.

Google Scholar

[7] F.L. Chen, Z. Shi and M. L Liu. Chemical Communications, (2000) p.2095-(2096).

Google Scholar

[8] A. Yu and R. Frech. J. Power Sources 104, (2002) pp.97-100.

Google Scholar

[9] E. Kim, D. Son, T.G. Kim, J. Cho, B. Park, K.S. Ryu and S.H. Chang. Angewandte Chemie Int. Ed. 43, (2004) pp.5587-5590.

Google Scholar

[10] C. Velásquez, F. Rojas, V.H. Lara and A. Campero. Physical Chemistry Chemical Physics 6, (2004) pp.4714-4721.

Google Scholar

[11] M. Behm and J.T.S. Irvine. Electrochimica Acta 47, (2002) pp.1727-1738.

Google Scholar

[12] J. Rouquerol, D. Avnir, C.W. Fairbridge, D.H. Everett, J.H. Haynes, N. Pernicone, J.D.F. Ramsay, K.S.W. Sing and K.K. Unger. Pure and Applied Chemistry 66, (1994) pp.1739-1758.

DOI: 10.1351/pac199466081739

Google Scholar

[13] J.Z. Li, H. Li, Z.X. Wang, X.J. Huang and L.Q. Chen. J. Power Sources 81-82, (1999) pp.346-351.

Google Scholar

[14] Y.W. Xiao, J.Y. Lee, A.S. Yu and Z.L. Liu. J. Electrochemical Society 146, (1999) pp.3623-3629.

Google Scholar

[15] I.A. Courtney, W.R. McKinnon & J.R. Dahn. J. Electrochemical Society 146, (1999) pp.59-68.

Google Scholar

[16] M. Wachtler, J.O. Besenhard and M. Winter. J. Power Sources 94, (2001) pp.189-193.

Google Scholar