Correlative full field X-ray Compton scattering imaging and X-ray computed tomography for in situ observation of Li ion batteries

Correlative full field X-ray Compton scattering imaging and X-ray computed tomography for in situ observation of Li ion batteries
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DOI:
10.1016/j.mtener.2022.101224
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发表时间:
2022-12
影响因子:
9.3
通讯作者:
Chu Lun Alex Leung;M. Wilson;T. Connolley;S. Collins;O. Magdysyuk;Matthieu Boone;Kosuke Suzuki;M. Veale;E. Liotti;F. Van Assche;A. Lui;Chun Huang
Chu Lun Alex Leung;M. Wilson;T. Connolley;S. Collins;O. Magdysyuk;Matthieu Boone;Kosuke Suzuki;M. Veale;E. Liotti;F. Van Assche;A. Lui;Chun Huang
中科院分区:
材料科学3区
文献类型:
--
作者:
Chu Lun Alex Leung;M. Wilson;T. Connolley;S. Collins;O. Magdysyuk;Matthieu Boone;Kosuke Suzuki;M. Veale;E. Liotti;F. Van Assche;A. Lui;Chun Huang

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Increasing electrode thickness is gaining more attention as a potential route to increase energy density for Li ion batteries although the realizable capacity and rate capability are usually limited by Li+ion diffusion during (dis)charge, especially at increased (dis)charge rates. It remains challenging to visualize and quantify the low atomic number Li+chemical stoichiometry distribution inside the electrode within commercially standard battery geometry, e.g. coin cells with stainless steel casings. Here, we map the distribution of Li+chemical stoichiometry in the electrode microstructure inside a working coin cell battery to show the amount of electrode materials contributing to energy storage performance using innovativein situcorrelative full-field X-ray Compton scattering imaging (XCS-I) and X-ray computed tomography (XCT). We design and fabricate an ultra-thick (∼1 mm) cathode of LiNi0.8Mn0.1Co0.1O2with a microstructure containing vertically oriented pore arrays using a directional ice templating method. This novel technique paves a new way to map low atomic number elements in 3D structures and study how the microstructure improves Li+ion diffusivity and energy storage performance.