Li-ion battery material under high pressure: amorphization and enhanced conductivity of Li4Ti5O12

Author:

Huang Yanwei12,He Yu31,Sheng Howard14,Lu Xia5,Dong Haini13,Samanta Sudeshna1,Dong Hongliang1,Li Xifeng6,Kim Duck Young1,Mao Ho-kwang17,Liu Yuzi8,Li Heping3,Li Hong9,Wang Lin1

Affiliation:

1. Center for High Pressure Science and Technology Advanced Research, Shanghai 201203, China

2. College of Materials and Environmental Engineering, Hangzhou Dianzi University, Hangzhou 310018, China

3. Key Laboratory of High-temperature and High-pressure Study of the Earth's Interior, Institute of Geochemistry, Chinese Academy of Sciences, Guiyang 550081, China

4. Department of Physics and Astronomy, George Mason University, Fairfax VA 22030, USA

5. State Key Laboratory of Organic-Inorganic Composites, Beijing Advanced Innovation Center for Soft Matter Science and Engineering, College of Energy, Beijing University of Chemical Engineering, Beijing 100029, China

6. School of Mechatronic Engineering and Automation, Shanghai University, Shanghai 200072, China

7. Geophysical Laboratory, Carnegie Institution, Washington, DC 20015, USA

8. Center for Nanoscale Materials, Argonne National Laboratory, Argonne, IL 60439, USA

9. Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China

Abstract

Abstract Lithium titanium oxide (Li4Ti5O12, LTO), a ‘zero-strain’ anode material for lithium-ion batteries, exhibits excellent cycling performance. However, its poor conductivity highly limits its applications. Here, the structural stability and conductivity of LTO were studied using in situ high-pressure measurements and first-principles calculations. LTO underwent a pressure-induced amorphization (PIA) at 26.9 GPa. The impedance spectroscopy revealed that the conductivity of LTO improved significantly after amorphization and that the conductivity of decompressed amorphous LTO increased by an order of magnitude compared with its starting phase. Furthermore, our calculations demonstrated that the different compressibility of the LiO6 and TiO6 octahedra in the structure was crucial for the PIA. The amorphous phase promotes Li+ diffusion and enhances its ionic conductivity by providing defects for ion migration. Our results not only provide an insight into the pressure depended structural properties of a spinel-like material, but also facilitate exploration of the interplay between PIA and conductivity.

Funder

National Natural Science Foundation of China

National Science Associated Funding

Science Challenging Program

China Postdoctoral Science Foundation

State Key Laboratory of Organic-Inorganic Composites

Fundamental Research Funds for the Central Universities

Publisher

Oxford University Press (OUP)

Subject

Multidisciplinary

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