电解质
化学
电极
溶解
薄膜
电化学
锂(药物)
透射电子显微镜
外延
电子衍射
曲面重建
脉冲激光沉积
分析化学(期刊)
图层(电子)
化学工程
衍射
纳米技术
材料科学
物理化学
曲面(拓扑)
光学
医学
几何学
物理
工程类
内分泌学
色谱法
有机化学
数学
作者
Masaaki Hirayama,Hedekazu Ido,KyungSu Kim,Woosuk Cho,Kazuhisa Tamura,J. Mizuki,Ryoji Kanno
摘要
Gaining a thorough understanding of the reactions on the electrode surfaces of lithium batteries is critical for designing new electrode materials suitable for high-power, long-life operation. A technique for directly observing surface structural changes has been developed that employs an epitaxial LiMn2O4 thin-film model electrode and surface X-ray diffraction (SXRD). Epitaxial LiMn2O4 thin films with restricted lattice planes (111) and (110) are grown on SrTiO3 substrates by pulsed laser deposition. In situ SXRD studies have revealed dynamic structural changes that reduce the atomic symmetry at the electrode surface during the initial electrochemical reaction. The surface structural changes commence with the formation of an electric double layer, which is followed by surface reconstruction when a voltage is applied in the first charge process. Transmission electron microscopy images after 10 cycles confirm the formation of a solid electrolyte interface (SEI) layer on both the (111) and (110) surfaces and Mn dissolution from the (110) surface. The (111) surface is more stable than the (110) surface. The electrode stability of LiMn2O4 depends on the reaction rate of SEI formation and the stability of the reconstructed surface structure.
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