Visualizing the chemistry and structure dynamics in lithium-ion batteries by in-situ neutron diffraction

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作者
Xun-Li Wang
Ke An
Lu Cai
Zhili Feng
Stephen E. Nagler
Claus Daniel
Kevin J. Rhodes
Alexandru D. Stoica
Harley D. Skorpenske
Chengdu Liang
Wei Zhang
Joon Kim
Yue Qi
Stephen J. Harris
机构
[1] Oak Ridge National Laboratory,Chemical and Engineering Materials Division
[2] City University of Hong Kong Tat Chee Avenue,Department of Physics and Materials Science
[3] Oak Ridge National Laboratory,Materials Science and Technology Division
[4] Oak Ridge National Laboratory,Quantum Condensed Matter Division
[5] University of Tennessee,Department of Materials Science and Engineering
[6] Center for Nanophase Materials Sciences,undefined
[7] Oak Ridge National Laboratory,undefined
[8] Dow Kokam LLC,undefined
[9] General Motors R&D Center,undefined
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摘要
We report an in-situ neutron diffraction study of a large format pouch battery cell. The succession of Li-Graphite intercalation phases was fully captured under an 1C charge-discharge condition (i.e., charge to full capacity in 1 hour). However, the lithiation and dilithiation pathways are distinctively different and, unlike in slowing charging experiments with which the Li-Graphite phase diagram was established, no LiC24 phase was found during charge at 1C rate. Approximately 75 mol. % of the graphite converts to LiC6 at full charge and a lattice dilation as large as 4% was observed during a charge-discharge cycle. Our work demonstrates the potential of in-situ, time and spatially resolved neutron diffraction study of the dynamic chemical and structural changes in “real-world” batteries under realistic cycling conditions, which should provide microscopic insights on degradation and the important role of diffusion kinetics in energy storage materials.
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