材料科学
透射电子显微镜
循环伏安法
锂(药物)
图层(电子)
锂钴氧化物
锂电池
锂离子电池
电池(电)
化学工程
电解质
扫描电子显微镜
电化学
电极
分析化学(期刊)
化学
离子
纳米技术
离子键合
物理化学
复合材料
内分泌学
功率(物理)
医学
物理
有机化学
工程类
色谱法
量子力学
作者
Ki–Hyun Kim,Yasutoshi Iriyama,Kazuo Yamamoto,Shota Kumazaki,Toru Asaka,Kinuka Tanabe,Craig A. J. Fisher,Tsukasa Hirayama,Ramaswamy Murugan,Zempachi Ogumi
标识
DOI:10.1016/j.jpowsour.2010.07.073
摘要
The interfacial layer formed between a lithium-ion conducting solid electrolyte, Li7La3Zr2O12 (LLZ), and LiCoO2 during thin film deposition was characterized using a combination of microscopy and electrochemical measurement techniques. Cyclic voltammetry confirmed that lithium extraction occurs across the interface on the first cycle, although the nonsymmetrical redox peaks indicate poor electrochemical performance. Using analytical transmission electron microscopy, the reaction layer (∼50 nm) was analyzed. Energy dispersive X-ray spectroscopy revealed that the concentrations of some of the elements (Co, La, and Zr) varied gradually across the layer. Nano-beam electron diffraction of this layer revealed that the layer contained neither LiCoO2 nor LLZ, but some spots corresponded to the crystal structure of La2CoO4. It was also demonstrated that reaction phases due to mutual diffusion are easily formed between LLZ and LiCoO2 at the interface. The reaction layer formed during high temperature processing is likely one of the major reasons for the poor lithium insertion/extraction at LLZ/LiCoO2 interfaces.
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