Abstract
Li4Ti5O12, Li2TiO3, and dual-phase Li4Ti5O12/Li2TiO3 composite were prepared by sol-gel method with average particle size of 1, 0.3, and 0.4 respectively. Though Li2TiO3 is electrochemically inactive, the rate capability of Li4Ti5O12/Li2TiO3 is comparable to that of Li4Ti5O12 at different current rates. Li4Ti5O12/Li2TiO3 also shows a good rate performance of 90 mA h g-1 at a high rate of 10 C in the voltage range 1-3 V, attributable to increased interfaces in the composite. While Li4Ti5O12 delivers a capacity retention of 88.6% at 0.2 C over 50 cycles, Li4Ti5O12/Li2TiO3 exhibits no capacity fading at 0.2 C (40 cycles) and a capacity retention of 98.45% at 0.5 C (50 cycles). This highly stable cycling performance is attributed to the contribution of Li2TiO3 in preventing the undesirable reaction of Li4Ti5O12 with the electrolyte during cycling. Cyclic voltammetric curves of Li4Ti5O12/Li2TiO3 in the 0-3 V range exhibit two anodic peaks at 1.51 and 0.7-0.0 V, indicating two modes of lithium intercalation into the lattice sites of active material. Owing to enhanced intercalation/deintercalation kinetics in 0-3 V, the composite electrode delivers a superior rate performance of 203 mAh/g at 2.85 C and 140 mAh/g at 5.7 C with good reversible capacity retention over 100 cycles.
Original language | British English |
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Pages (from-to) | 9553-9561 |
Number of pages | 9 |
Journal | Journal of Physical Chemistry C |
Volume | 120 |
Issue number | 18 |
DOIs | |
State | Published - 12 May 2016 |