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Published on: December 20, 2016
Do Ionic Liquids Slow Down in Stages?
Bichitra Borah1, Gobin Raj Acharya2, Diana Grajeda2
1Department of Chemistry, The University of Iowa, Iowa City, Iowa 52242, United States.
Ionic liquids (ILs) with the trihexyltetradecylphosphonium cation show distinct stages when cooling from liquid to glass. The charge network slows first, followed by the apolar domain, suggesting separate structural-dynamic changes.
Area of Science:
- Materials Science
- Physical Chemistry
- Chemical Physics
Background:
- Recent studies highlight liquid-liquid (L-L) phase transitions in ionic liquids (ILs) with the trihexyltetradecylphosphonium cation (P666,14+).
- This cation is known as the "universal liquifier" due to its unique properties.
- Understanding the transition from liquid to glass state in these ILs is crucial for their application.
Purpose of the Study:
- To investigate the structural-dynamic pathway of ionic liquids containing the P666,14+ cation from a liquid to a glassy state.
- To elucidate the distinct stages and molecular dynamics involved in this transition.
- To explore the potential relationship between these stages and observed L-L and glass transitions.
Main Methods:
- Experimental characterization of ionic liquid behavior.
- Computational modeling and simulations.
- Analysis of structural and dynamic changes upon cooling.
Main Results:
- Evidence suggests a two-stage process during cooling from liquid to glass.
- The first stage involves the slowdown of the charge network while the apolar subcomponent remains mobile.
- The second stage involves the subsequent slowdown of the apolar domain.
Conclusions:
- The pathway from liquid to glass in P666,14+-based ILs involves separate structural-dynamic changes.
- These distinct stages may be linked to liquid-liquid and glass transitions, but further research is needed.
- The findings provide insight into the complex behavior of "universal liquifier" ionic liquids.
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