Surface layer formation on Sn anode: ATR FTIR spectroscopic characterization

Surface layer formed on Sn thin film electrode in 1 M LiPF 6/EC:DMC electrolyte was characterized using ex situ FTIR spectroscopy with the attenuated total reflection technique. IR spectral analyses showed that the immersion of Sn film in the electrolyte resulted in a chemical interfacial reaction l...

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Published inElectrochimica acta Vol. 54; no. 4; pp. 1312 - 1318
Main Authors Song, Seung-Wan, Baek, Seung-Won
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier Ltd 30.01.2009
Elsevier
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Summary:Surface layer formed on Sn thin film electrode in 1 M LiPF 6/EC:DMC electrolyte was characterized using ex situ FTIR spectroscopy with the attenuated total reflection technique. IR spectral analyses showed that the immersion of Sn film in the electrolyte resulted in a chemical interfacial reaction leading to the passivation of Sn surface with primarily PF-containing inorganic surface species and small amount of organics. When constant current cycling was conducted with lithium cells with Sn film electrode at 0.1–1.0 V vs. Li/Li +, the interfacial reaction between Sn and electrolyte appeared significantly intensified that the features of PF-containing species became enhanced and new IR features of organic species (e.g. alkyl carbonate/carboxylate metal salts and ester functionalities) were observed. The surface layer continued to form with cycling, partly due to non-effective surface passivation as well as particle pulverization accompanied by enlargement of active surface area. Comparative IR spectral analyses indicated that the interfacial reaction between Sn and PF 6 − anion played a leading role in forming the surface layer, which is different from lithiated graphite that had mainly organic surface species. The data contribute to a better understanding of the interfacial processes occurring on Sn-based anode materials in lithium-ion batteries.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0013-4686
1873-3859
DOI:10.1016/j.electacta.2008.09.021