电解质
电化学
锂(药物)
电极
材料科学
电池(电)
快离子导体
锂钴氧化物
透射电子显微镜
分析化学(期刊)
化学工程
扩散
锂电池
锂离子电池
离子
化学
纳米技术
离子键合
物理化学
色谱法
内分泌学
工程类
医学
功率(物理)
量子力学
热力学
物理
有机化学
作者
Atsushi Sakuda,Akitoshi Hayashi,Masahiro Tatsumisago
摘要
In all-solid-state lithium secondary batteries, both the electrode and electrolyte materials are solid. The electrode and solid electrolyte interface's structure and morphology affect a battery's electrochemical performance. Observation of the interface between LiCoO2 positive electrode and highly lithium-ion-conducting Li2S−P2S5 solid electrolyte was conducted using transmission electron microscopy. An interfacial layer was formed at the interface between LiCoO2 electrode and Li2S−P2S5 solid electrolyte after the battery's initial charge. Furthermore, mutual diffusions of Co, P, and S at the interface between LiCoO2 and Li2S−P2S5 were observed. The mutual diffusion and the formation of the interfacial layer were suppressed using LiCoO2 particles coated with Li2SiO3 thin film. Results showed that all-solid-state cells using Li2SiO3-coated LiCoO2 had better electrochemical performance than those using noncoated LiCoO2. The all-solid-state cells functioned at −30 °C. Moreover, the all-solid-state cell using Li2SiO3-coated LiCoO2 was charged and discharged under a high current density of 40 mA cm−2 at 100 °C.
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