Lithium storage in amorphous TiO2 nanoparticles
Wouter J.H. Borghols (Jülich Centre for Neutron Science at FRM II)
D. Lützenkirchen-Hecht (Bergische Universität Wuppertal )
Ullrich Haake (Bergische Universität Wuppertal )
U Lafont (TU Delft - Novel Aerospace Materials)
E. M. Kelder (TU Delft - RST/Storage of Electrochemical Energy)
Ernst R.H. van Eck (Radboud Universiteit Nijmegen)
A. P.M. Kentgens (Radboud Universiteit Nijmegen)
F. M. Mulder (TU Delft - ChemE/Materials for Energy Conversion and Storage)
M Wagemaker (TU Delft - RST/Storage of Electrochemical Energy)
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Abstract
Amorphous titanium oxide nanoparticles were prepared from titanium isopropoxide. In situ measurements reveal an extraordinary high capacity of 810 mAh/g on the first discharge. Upon cycling at a charge/discharge rate of 33.5 mA/g, this capacity gradually decreases to 200 mAh/g after 50 cycles. The origin of this fading was investigated using X-ray absorption spectroscopy and solid-state nuclear magnetic resonance. These measurements reveal that a large fraction of the total amount of the consumed Li atoms is due to the reaction of H2 O/OH species adsorbed at the surface to Li2 O, explaining the irreversible capacity loss. The reversible capacity of the bulk, leading to the Li0.5 TiO2 composition, does not explain the relatively large reversible capacity, implying that part of Li2 O at the TiO2 surface may be reversible. The high reversible capacity, also at large (dis)charge rates up to 3.35 A/g (10C), makes this amorphous titanium oxide material suitable as a low cost electrode material in a high power battery.
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