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• W2963451768 abstract "Electronic polarization and charge transfer effects play a crucial role in thermodynamic, structural, and transport properties of room-temperature ionic liquids (RTILs). These nonadditive interactions constitute a useful tool for tuning physical chemical behavior of RTILs. Polarization and charge transfer generally decay as temperature increases, although their presence should be expected over an entire condensed state temperature range. For the first time, we use three popular pyridinium-based RTILs to investigate temperature dependence of electronic polarization in RTILs, based on a nonperiodic electronic density description for a cation–anion pair. Atom-centered density matrix propagation molecular dynamics, supplemented by a weak coupling to an external bath, is used to simulate the temperature impact on system properties. We show that, quite surprisingly, nonadditivity in the cation–anion interactions changes negligibly between 300 and 900 K, while the average dipole moment increases due to thermal fluctuations of geometries. Our results contribute to the fundamental understanding of electronic effects in the condensed phase of ionic systems and foster progress in physical chemistry and engineering." @default.
• W2963451768 created "2019-07-30" @default.
• W2963451768 creator A5049029786 @default.
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• W2963451768 date "2014-11-24" @default.
• W2963451768 modified "2023-09-26" @default.
• W2963451768 title "Polarization versus Temperature in Pyridinium Ionic Liquids" @default.
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• W2963451768 doi "https://doi.org/10.1021/jp5089788" @default.
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