Lithium Ion Solvation in Room-Temperature Ionic Liquids Involving Bis(trifluoromethanesulfonyl) Imide Anion Studied by Raman Spectroscopy and DFT Calculations

2007 ◽  
Vol 111 (45) ◽  
pp. 13028-13032 ◽  
Author(s):  
Yasuhiro Umebayashi ◽  
Takushi Mitsugi ◽  
Shuhei Fukuda ◽  
Takao Fujimori ◽  
Kenta Fujii ◽  
...  



2007 ◽  
Vol 174 (2) ◽  
pp. 1021-1026 ◽  
Author(s):  
Hiroe Nakagawa ◽  
Yukiko Fujino ◽  
Suguru Kozono ◽  
Yoshihiro Katayama ◽  
Toshiyuki Nukuda ◽  
...  


2013 ◽  
Vol 42 (1) ◽  
pp. 63-65 ◽  
Author(s):  
Rong Lu ◽  
Wei Wang ◽  
Shuwei Yuan ◽  
Anchi Yu


2015 ◽  
pp. 317-332
Author(s):  
Kenta Fujii ◽  
Shiro Seki ◽  
Hiroyuki Doi ◽  
Yasuhiro Umebayashi


2012 ◽  
Vol 14 (39) ◽  
pp. 13676 ◽  
Author(s):  
Akira Kobayashi ◽  
Koji Osawa ◽  
Masahide Terazima ◽  
Yoshifumi Kimura


2020 ◽  
Vol 861 ◽  
pp. 264-269
Author(s):  
Masahiro Ikeda ◽  
Masaru Aniya

The clarification of the degree of ionic dissociation occurring in liquid-electrolyte systems such as those used in current lithium-ion batteries is important from both, fundamental and application points of views. In the present study, based on the bond strength–coordination number fluctuation (BSCNF) model proposed by the authors, we consider the relation between the ionic diffusion and dissociation in room-temperature ionic liquids. Specifically, we show firstly, that the molar conductivity Λ is well correlated with the degree of molecular cooperativity NB defined by the BSCNF model. This correlation enables to connect the cooperativity with the degree of ionic dissociation in ionic liquids. Through the comparison between the ionic diffusion coefficients and the molar conductivity, we discuss on a possible relation between these quantities.



2011 ◽  
Vol 2011 ◽  
pp. 1-5 ◽  
Author(s):  
Naohiro Hatano ◽  
Takahiro Takekiyo ◽  
Hiroshi Abe ◽  
Yukihiro Yoshimura

We have investigated the nonspherical anion effect on the trans-trans (TT) and gauche-trans (GT) equilibrium in pure 1-butyl-3-methylimidazolium ([bmim]+)-based room temperature ionic liquids (RTILs) by the Raman spectroscopy. The intensity ratio of the [bmim]+ cation in [bmim]+-based RTILs having nonspherical anions changes with nature of the anions. However, the enthalpy change of the [bmim]+ cation is approximately −1.0 kJ/mol for all [bmim]+-based RTILs used in this study and is independent of the anionic species. The present results indicate that the conformational stability of the [bmim]+ cation in [bmim]+-based RTILs including nonspherical anions is driven by the entropic contribution associated with the orientation and configuration of the [bmim]+ cation with respect to the counteranion.



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