Journal
NANO ENERGY
Volume 9, Issue -, Pages 383-391Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.nanoen.2014.06.032
Keywords
Li-ion batteries; Li4Ti5O12-TiO2; Dual phase; Nanowire arrays
Categories
Funding
- Natural Sciences and Engineering Research Council of Canada (NSERC) [CRDPJ418270]
- University of Waterloo
- Waterloo Institute for Nanotechnology
- Energy Efficiency and Renewable Energy, Vehicle Technologies Office of the U.S. Department of Energy [DE-AC02-05CH11231]
- Batteries for Advanced Transportation Technologies (BATT) Program [7056410]
- Chemical Imaging Initiative at Pacific Northwest National Laboratory (PNNL)
- U.S. Department of Energy (DOE) [DE-AC05-76RLO1830]
- DOE's Office of Biological and Environmental Research and located at PNNL
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Lithium titanate (Li4Ti5O12) is well known as a zero strain material inherently, which provides excellent long cycle stability as a negative electrode for lithium ion batteries. However, the low specific capacity (175 mA h g(-1)) limits it to power batteries although the low electrical conductivity is another intrinsic issue need to be solved. In this work, we developed a facile hydrothermal and ionexchange route to synthesize the self-supported dual-phase Li4Ti5O12-TiO2 nanowire arrays to further improve its capacity as well as rate capability. The ratio of Li4Ti5O12 to TiO2 in the dual phase Li4Ti5O12-TiO2 nanowire is around 2:1. The introduction of TiO2 into Li4Ti5O12 increases the specific capacity. More importantly, by interface design, it creates a dual-phase nanostructure with high grain boundary density that facilitates both electron and Li ion transport. Compared with phase-pure nanowire Li4Ti5O12 and TiO2 nanaowire arrays, the dual-phase nanowire electrode yielded superior rate capability (135.5 at 5 C, 129.4 at 10 C, 120.2 at 20 C and 115.5 mA h g(-1) at 30 C). In-situ transmission electron microscope clearly shows the near zero deformation of the dual phase structure, which explains its excellent cycle stability. (C) 2014 Elsevier Ltd. All rights reserved.
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