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 in | Electrochimica acta Vol. 54; no. 4; pp. 1312 - 1318 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Kidlington
Elsevier Ltd
30.01.2009
Elsevier |
Subjects | |
Online Access | Get full text |
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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. |
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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 |