A simple method of electrochemical lithium intercalation within graphite from a propylene carbonate-based solution

Electrochemical lithium intercalation within graphite from 1moldm−3 solution of LiClO4 in propylene carbonate (PC) was investigated at 25 and −15°C. Lithium ions were intercalated into and de-intercalated from graphite reversibly at −15°C despite the use of pure PC as the solvent. However, ceaseless...

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Published inElectrochemistry communications Vol. 31; pp. 24 - 27
Main Authors Jeong, Soon-Ki, Song, Hee-Youb, Kim, Seong In, Abe, Takeshi, Jeon, Woo Sung, Yin, Ri-Zhu, Kim, Yang Soo
Format Journal Article
LanguageEnglish
Published Lausanne Elsevier B.V 01.06.2013
Amsterdam Elsevier
New York, NY
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Summary:Electrochemical lithium intercalation within graphite from 1moldm−3 solution of LiClO4 in propylene carbonate (PC) was investigated at 25 and −15°C. Lithium ions were intercalated into and de-intercalated from graphite reversibly at −15°C despite the use of pure PC as the solvent. However, ceaseless solvent decomposition and intense exfoliation of graphene layers occurred at 25°C. The results of the Raman spectroscopic analysis indicated that the interaction between PC molecules and lithium ions became weaker at −15°C by chemical exchange effects, which suggested that the thermodynamic stability of the solvated lithium ions was an important factor that determined the formation of a solid electrolyte interface (SEI) in PC-based solutions. Charge–discharge analysis revealed that the nature of the SEI formed at −15°C in 1moldm−3 of LiClO4 in PC was significantly different from that formed at 25°C in 1moldm−3 of LiClO4 in PC containing vinylene carbonate, 3.27molkg−1 of LiClO4 in PC, and 1moldm−3 of LiClO4 in ethylene carbonate. •Lithium ion was intercalated into graphite in a PC-based solution at −15°C.•An effective SEI was formed on graphite by lowering of the reaction temperature.•The SEI formed at −15°C was stable and effective for protecting graphite at 25°C.
ISSN:1388-2481
1873-1902
DOI:10.1016/j.elecom.2013.02.019