The electro-chemical properties and intercalation mechanism of low strain Li2TiO3 as a high-performance anode material for lithium-ion batteries

YT Xie and QY Wang and FP Gu and KS Dai and M Shui and J Shu, JOURNAL OF ALLOYS AND COMPOUNDS, 893, 162348 (2022).

DOI: 10.1016/j.jallcom.2021.162348

In this article, the sol-gel synthesized beta-Li2TiO3, referred to as sg-beta-Li2TiO3, exhibits superior electro-chemical performance, compared with the theoretical specific capacities of frequently investigated Titanium based oxides, for example, LiTiO2 (143 mAh g(-1)), Li4Ti5O12 (175 mAh g(-1)) and Li2Ti3O7 (198 mAh g(-1)). It delivers a considerable specific capacity of more than 200 mAh g(-1) within 100 cycles and close to 200 mAh g(-1) after 200 cycles and preserves coulombic efficiency above 97% for all the cycles. After more than 500 cycles, the reversible specific capacity of sg-beta-Li2TiO3 is more than 170 mAh g(-1) and a less than 2% capacity degeneration is observed for the followed several hundreds of cycles. DFT calculations and MD simulations show 8 f void mediated diffusion comprise the two dimensional diffusion layer on a-b plane and the neighboring diffusion layers are interconnected by two 8 f voids via a Li2 atom. Low energy barriers and high Li+ activities are observed. Three intermediate phases, corresponding to intercalation level x = 0.5, 0.75 and 0.875 in beta-Li2+xTiO3, are identified for the intercalation process with the maximal intercalation level 0.875. Both ex-situ XRD and theoretical calculations reveal low volume change or strain less than 5% in the intercalation process. Also, an insulator-metal transition upon lithiation is observed by the electronic structure analysis. (C) 2021 Elsevier B.V. All rights reserved.

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