Stoppa Alexander, Hunger Johannes, Buchner Richard, Hefter Glenn, Thoman Andreas, Helm Hanspeter
Institut für Physikalische und Theoretische Chemie, Universität Regensburg, D-93040 Regensburg, Germany.
J Phys Chem B. 2008 Apr 24;112(16):4854-8. doi: 10.1021/jp800852z. Epub 2008 Mar 28.
Precise dielectric spectra have been determined at 25 degrees C over the exceptionally broad frequency range of 0.1 <or= nu/GHz <or= 3000 for the imidazolium-based room-temperature ionic liquids (RTILs) [bmim][BF4], [bmim][PF6], [bmim][DCA], and [hmim][BF4]. The spectra are dominated by a low-frequency process at approximately 1 GHz with a broad relaxation time distribution of the Cole-Davidson or Cole-Cole type, which is thought to correspond to the rotational diffusion of the dipolar cations. In addition, these RTILs possess two Debye relaxations at approximately 5 GHz and approximately 0.6 THz and a damped harmonic oscillation at approximately 2.5 THz. The two higher-frequency modes are almost certainly due to cation librations, but the origin of the approximately 5 GHz mode remains obscure.
在25摄氏度下,针对基于咪唑鎓的室温离子液体(RTILs)[bmim][BF4]、[bmim][PF6]、[bmim][DCA]和[hmim][BF4],在0.1≤ν/GHz≤3000这一异常宽广的频率范围内测定了精确的介电谱。这些谱图主要由一个约1 GHz的低频过程主导,其具有科尔 - 戴维森或科尔 - 科尔类型的宽弛豫时间分布,这被认为对应于偶极阳离子的旋转扩散。此外,这些RTILs在约5 GHz和约0.6 THz处具有两个德拜弛豫,以及在约2.5 THz处具有一个阻尼谐波振荡。这两个高频模式几乎肯定是由于阳离子的振动,但约5 GHz模式的起源仍不清楚。