Lithium storage in nanostructured TiO2 made by hydrothermal growth

被引:407
作者
Kavan, L
Kalbác, M
Zukalová, M
Exnar, I
Lorenzen, V
Nesper, R
Graetzel, M
机构
[1] Acad Sci Czech Republ, J Heyrovsky Inst Phys Chem, CZ-18223 Prague 8, Czech Republic
[2] SusTech GmbH & Co KG, EPFL, PSE B, D-64287 Darmstadt, Germany
[3] ETHZ, Lab Inorgan Chem, CH-8093 Zurich, Switzerland
[4] Ecole Polytech Fed Lausanne, Lab Photon & Interfaces, CH-1015 Lausanne, Switzerland
关键词
D O I
10.1021/cm035046g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Nanostructured titania materials were prepared from TiCl4 via autoclaving in 10 M NaOH at 250 degreesC and subsequent treatment in aqueous and/or acidic media. XRD and Raman spectroscopy evidenced the presence of anatase as the main phase, but most materials contained also some XRD-silent component. Cyclic voltammograms of lithium insertion demonstrate two pairs of reversible pseudocapacitive peaks (S-peaks) in addition to the ordinary peaks of diffusion-controlled Li insertion into the anatase lattice. The occurrence of S-peaks is associated with the nanosheet- and/or nanotubular morphology of the materials. This structure developed at hydrothermal conditions via exfoliation of the layered Na+/H+ titanate precursors. The S-peaks were suggested to be the signatures of quantum-size confinement in titania nanosheets. The nanosheet-containing materials are reducible by n-butyllithium to cubic LiTiO2 (at conditions when the ordinary nanocrystalline anatase gives only the orthorhombic Li0.5TiO2). Consequently, the electrochemical Li-storage capacity is larger compared to that of crystalline anatase. The prepared materials also show better insertion kinetics; hence, they are promising for applications in Li-ion batteries. Depending on the applied voltage, they can be charged/discharged either as ordinary Li-insertion hosts or as supercapacitors.
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页码:477 / 485
页数:9
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