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SnO 2 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 SnO 2 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 Li 2 SnO 3 and Sn 0 phases between 2 and 0.8 V vs Li + /Li. Between 0.45 V and 5 mV vs Li + /Li Li 8 SnO 6, Li 2 O and Li x Sn 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 LiPF 6 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 Sn 0 accompanied by the decomposition of Li 2 O. Above 1.5 V vs Li + /Li, Sn 0 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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Ferraresi et al. (2018) studied this question.
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