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Journal of Sol-Gel Science and Technology

, Volume 79, Issue 2, pp 270–278 | Cite as

Lithium insertion properties of mesoporous nanocrystalline TiO2 and TiO2–V2O5 microspheres prepared by non-hydrolytic sol–gel

  • A. M. Escamilla-Pérez
  • N. Louvain
  • M. Kaschowitz
  • S. Freunberger
  • O. Fontaine
  • B. Boury
  • N. Brun
  • P. H. Mutin
Original Paper: Nano- and macroporous materials (aerogels, xerogels, cryogels, etc.)

Abstract

Mesoporous nanocrystalline TiO2 and TiO2–V2O5 microspheres were prepared by non-hydrolytic sol–gel from TiCl4, VOCl3, and iPr2O at 110 °C without any solvent or additives. The samples were characterized by elemental analysis, X-ray diffraction, Raman spectroscopy, scanning electron microscopy, nitrogen physisorption, and impedance measurements. At low vanadium loadings, only TiO2 anatase was detected, and V2O5 scherbinaite was also detected at high vanadium loadings. The texture of the samples depended on the V loading, but all the samples appeared built of primary nanoparticles (≈10–20 nm in size) that aggregate to form mesoporous micron-sized spheres. The lithium insertion properties of these materials were evaluated by galvanostatic measurements taken using coin-type cells, in view of their application as electrode for rechargeable Li-ion batteries. The mesoporous TiO2 microspheres showed good performances, with a specific reversible capacity of 145 and 128 mAh g−1 at C/2 and C, respectively (C = 335.6 mA g−1), good coulombic efficiency, and a moderate capacity fade (6 %) from the 2nd to the 20th cycle at C/20. Although the addition of V effectively increased the electronic conductivity of the powders, the specific reversible capacity and cycling performances of the TiO2–V2O5 samples were only minimally improved for a 5 at% V loading and were lower at higher V loading.

Graphical Abstract

Keywords

Non-hydrolytic sol–gel Mesoporous xerogel Titania Vanadia Lithium battery 

Notes

Acknowledgments

This work was supported by the “Centre National de la Recherche Scientifique” and the University of Montpellier, and through a PhD grant of the “Consejo Nacional de Ciencia y Tecnología” in Mexico.

Supplementary material

10971_2016_4037_MOESM1_ESM.docx (229 kb)
Supplementary material 1 (DOCX 229 kb)

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Copyright information

© Springer Science+Business Media New York 2016

Authors and Affiliations

  • A. M. Escamilla-Pérez
    • 1
  • N. Louvain
    • 1
    • 2
  • M. Kaschowitz
    • 3
  • S. Freunberger
    • 3
  • O. Fontaine
    • 1
    • 2
  • B. Boury
    • 1
  • N. Brun
    • 1
  • P. H. Mutin
    • 1
  1. 1.Institut Charles Gerhardt Montpellier, UMR 5253Université Montpellier 2Montpellier Cedex 5France
  2. 2.Réseau sur le Stockage Electrochimique de l’Energie (RS2E)AmiensFrance
  3. 3.Institute for Chemistry and Technology of MaterialsGraz University of TechnologyGrazAustria

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