材料科学
电解质
X射线光电子能谱
碳酸乙烯酯
分解
合金
电极
无定形固体
电池(电)
离子
化学工程
锂(药物)
无机化学
分析化学(期刊)
物理化学
结晶学
化学
冶金
热力学
功率(物理)
内分泌学
有机化学
工程类
色谱法
医学
物理
作者
Giulio Ferraresi,Claire Villevieille,Izabela Czekaj,M. Horisberger,Petr Novák,Mario El Kazzi
标识
DOI:10.1021/acsami.7b19481
摘要
SnO2 is an attractive negative electrode for Li-ion battery owing to its high specific charge compared to commercial graphite. However, the various intermediate conversion and alloy reactions taking place during lithiation/delithiation, as well as the electrolyte stability, have not been fully elucidated, and many ambiguities remain. An amorphous SnO2 thin film was investigated for use as a model electrode by a combination of postmortem X-ray photoelectron spectroscopy supported by density functional theory calculations and scanning electron microscopy to shed light on these different processes. The early stages of lithiation reveal the presence of multiple overlapping reactions leading to the formation of Li2SnO3 and Sn0 phases between 2 and 0.8 V vs Li+/Li. Between 0.45 V and 5 mV vs Li+/Li Li8SnO6, Li2O and Li xSn phases are formed. Electrolyte reduction occurs simultaneously in two steps, at 1.4 and 1 V vs Li+/Li, corresponding to the decomposition of the LiPF6 salt and ethylene carbonate/dimethyl carbonate solvents, respectively. Most of the reactions during delithiation are reversible up to 1.5 V vs Li+/Li, with the reappearance of Sn0 accompanied by the decomposition of Li2O. Above 1.5 V vs Li+/Li, Sn0 is partially reoxidized to SnO x. This process tends to limit the conversion reactions in favor of the alloy reaction, as also confirmed by the long-term cycling samples.
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