Dynamic Structural Changes at LiMn2O4/Electrolyte Interface during Lithium Battery Reaction

被引:333
作者
Hirayama, Masaaki [1 ]
Ido, Hedekazu [1 ]
Kim, KyungSu [1 ]
Cho, Woosuk [1 ]
Tamura, Kazuhisa [2 ]
Mizuki, Jun'ichiro [2 ]
Kanno, Ryoji [1 ]
机构
[1] Tokyo Inst Technol, Dept Elect Chem, Interdisciplinary Grad Sch Sci & Engn, Midori Ku, Yokohama, Kanagawa 2268502, Japan
[2] Japan Atom Energy Agcy, Synchrotron Radiat Res Ctr, Kansai Res Estab, Sayo, Hyogo 6795148, Japan
基金
日本学术振兴会;
关键词
X-RAY REFLECTOMETRY; ELEVATED-TEMPERATURE PERFORMANCE; PULSED-LASER DEPOSITION; ION BATTERIES; ELECTRODE/ELECTROLYTE INTERFACE; ATOMISTIC SIMULATION; CATHODE MATERIALS; SURFACE-STRUCTURE; LIMN2O4; CATHODE; SPINEL;
D O I
10.1021/ja105389t
中图分类号
O6 [化学];
学科分类号
0703 ;
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.
引用
收藏
页码:15268 / 15276
页数:9
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