Effect of ether group on the electrochemical stability of zwitterionic imidazolium compounds

The cathodic stability of the zwitterionic imidazolium compounds was significantly enhanced by the introduction of an ether group at 1 or 2-position on the imidazolium ring. The cycle performance tests showed that the initial cell capacity was maintained almost unchanged up to 100 cycles at 0.5 and...

Full description

Saved in:
Bibliographic Details
Published inElectrochemistry communications Vol. 10; no. 11; pp. 1761 - 1764
Main Authors Kim, H., Nguyen, D.Q., Bae, H.W., Lee, J.S., Cho, B.W., Kim, H.S., Cheong, M., Lee, H.
Format Journal Article
LanguageEnglish
Published Lausanne Elsevier B.V 01.11.2008
Amsterdam Elsevier
New York, NY
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The cathodic stability of the zwitterionic imidazolium compounds was significantly enhanced by the introduction of an ether group at 1 or 2-position on the imidazolium ring. The cycle performance tests showed that the initial cell capacity was maintained almost unchanged up to 100 cycles at 0.5 and 1 C when 2.5 wt.% of 2-butoxymethyl-1-methylimidazolium-3-propylsulfonate or 2-butoxymethyl-1-butylimidazolium-3-propylsulfonate was added to the model electrolyte (1 M LiPF 6 in ethylene carbonate, dimethyl carbonate and ethylmethyl carbonate (1/1/1 v/v/v)). Structures of zwitterionic compounds and their interactions with lithium ions were theoretically investigated.
ISSN:1388-2481
1873-1902
DOI:10.1016/j.elecom.2008.09.006