材料科学
纳米晶
阴极
离子
化学物理
锂(药物)
扩散
微晶
热传导
纳米技术
扫描透射电子显微镜
透射电子显微镜
粒子(生态学)
分析化学(期刊)
化学
物理化学
热力学
复合材料
医学
海洋学
物理
有机化学
色谱法
内分泌学
地质学
冶金
作者
Yuki Nomura,Kazuo Yamamoto,Tsukasa Hirayama,Emiko Igaki,Koh Saitoh
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2020-05-27
卷期号:5 (6): 2098-2105
被引量:59
标识
DOI:10.1021/acsenergylett.0c00942
摘要
The rate capability of bulk-type solid-state Li-ion batteries is limited by the solid-state diffusion of Li ions in the cathodes that typically form micrometer-sized polycrystalline particles composed of aggregated nanocrystals. This necessitates nanoscale and dynamic observations of Li ions to establish a detailed understanding of Li conduction in the complicated particle structure. This study demonstrates Li-ion dynamics in particle cathodes under low- and high-rate charge–discharge reaction conditions using operando scanning transmission electron microscopy coupled with electron energy-loss spectroscopy. Direct observation results reveal the slow diffusion through nanocrystal grain boundaries as the primary factor limiting Li conduction in particle cathodes. Therefore, rate-capability enhancement of Li-ion batteries requires either optimization of the interfacial structure along with nanocrystal orientation or the use of large single crystals without boundaries.
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