In situ X-ray absorption spectroscopy of germanium evaporated thin film electrodes

被引:45
作者
Baggetto, Loic [1 ]
Hensen, Emiel J. M. [1 ]
Notten, Peter H. L. [1 ]
机构
[1] Eindhoven Univ Technol, Dept Chem Engn & Chem, NL-5600 MB Eindhoven, Netherlands
关键词
Evaporated germanium; Lithium-ion thin film electrodes; In situ electrochemical experiments; X-ray near-edge spectroscopy (XANES); Extended X-ray absorption fine structure (EXAFS); LITHIUM; ANODE; GE; NANOPARTICLES; SN;
D O I
10.1016/j.electacta.2010.06.087
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The understanding of germanium Li-ion insertion/extraction reaction mechanism is drawing more and more attention in the field of Li-ion batteries. When a germanium thin film electrode is inserted with Li ions, the material remains amorphous until it crystallizes into Li15Ge4 as evidenced by X-ray diffraction. The local coordination environment of the Ge atoms of the intermediate amorphous phases was investigated by in situ X-ray absorption spectroscopy. Li-ion insertion and extraction were electrochemically controlled by continuous and intermittent galvanostatic methods. The evolution of the coordination number and interatomic distance of Ge-Ge and Ge-Li shells was determined as a function of Li composition. From a short range ordering perspective, it was observed that the first Ge-Ge interatomic distance increases and the Ge-Ge coordination number decreases with increasing Li content. The opposite is observed for the first Li-Ge interaction. Moreover, it was found that electrochemical lithiation is reversible at the atomic scale. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7074 / 7079
页数:6
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