Issue 40, 2013

Carbon nanocage supported synthesis of V2O5 nanorods and V2O5/TiO2 nanocomposites for Li-ion batteries

Abstract

We present the facile synthesis of crystalline V2O5 nanorods and V2O5/TiO2 nanocomposites structures by a carbon nanocage (CNC)-assisted growth process, using vanadium triisopropoxide oxide and titanium isopropoxide precursors in air at 500 °C. The diameters of the resultant V2O5 nanorods ranged between ∼10 and 70 nm, while the crystalline V2O5/TiO2 nanocomposite structures adopted a unique morphology, due to both crystallisation and templating processes, with V2O5 adopting small-diameter nanowire and nanorod morphologies surrounded by sub-30 nm TiO2 nanoparticles. The V2O5 nanorods and V2O5/TiO2 nanocomposites were characterised by electron microscopy and X-ray diffraction techniques and subsequently reviewed as positive Li-ion electrodes. The phase-pure V2O5 nanorod structures exhibited appreciable Li+ storage properties over the potential range of 2.0–4.0 V vs. Li/Li+, displaying capacities of up to 288 mA h g−1 with appreciable cyclic behaviour at test rates of up to ∼1 C. The crystalline V2O5/TiO2 nanocomposite structures displayed similar Li+ storage properties, however, increasing molar fractions of TiO2 led to a decline in the overall capacity versus the single-phase V2O5 counterparts. Interestingly, the Li+ insertion behaviour of the V2O5/TiO2 nanocomposite displayed character more-typical of amorphous V2O5, which was ascribed to a structural buffering effect of the inactive TiO2 phase.

Graphical abstract: Carbon nanocage supported synthesis of V2O5 nanorods and V2O5/TiO2 nanocomposites for Li-ion batteries

Supplementary files

Article information

Article type
Paper
Submitted
08 Jul 2013
Accepted
27 Aug 2013
First published
28 Aug 2013

J. Mater. Chem. A, 2013,1, 12568-12578

Carbon nanocage supported synthesis of V2O5 nanorods and V2O5/TiO2 nanocomposites for Li-ion batteries

M. J. Armstrong, D. M. Burke, T. Gabriel, C. O'Regan, C. O'Dwyer, N. Petkov and J. D. Holmes, J. Mater. Chem. A, 2013, 1, 12568 DOI: 10.1039/C3TA12652H

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