Hunger Johannes, Stoppa Alexander, Schrödle Simon, Hefter Glenn, Buchner Richard
Institut für Physikalische und Theoretische Chemie, Universität Regensburg, 93040 Regensburg, Germany.
Chemphyschem. 2009 Mar 9;10(4):723-33. doi: 10.1002/cphc.200800483.
Dielectric spectra were measured for eight, mostly imidazolium-based, room temperature ionic liquids (RTILs) over a wide range of frequencies (0.2 < or = nu/GHz < or = 89) and temperatures (5 < or = theta/degrees C < or = 65). Detailed analysis of the spectra shows that the dominant low frequency process centred at ca. 0.06 to 10 GHz (depending on the salt and the temperature) is better described using a symmetrically broadened Cole-Cole model rather than the asymmetric Cole-Davidson models used previously. Evaluation of the temperature dependence of the static permittivities, effective dipole moments, volumes of rotation, activation energies, and relaxation times derived from the dielectric data indicates that the low frequency process cannot be solely due to rotational diffusion of the dipolar imidazolium cations, as has been thought, but must also include other contributions, probably from cooperative motions. Analysis of the Debye process observed at higher frequencies for these RTILs is not undertaken because it overlaps with even faster processes that lie outside the range of the present instrumentation.
在很宽的频率范围(0.2≤ν/GHz≤89)和温度范围(5≤θ/℃≤65)内,测量了8种主要基于咪唑鎓的室温离子液体(RTILs)的介电谱。对光谱的详细分析表明,以约0.06至10 GHz为中心的主要低频过程(取决于盐和温度),使用对称展宽的Cole-Cole模型比之前使用的不对称Cole-Davidson模型能更好地描述。对由介电数据得出的静态介电常数、有效偶极矩、旋转体积、活化能和弛豫时间的温度依赖性进行评估表明,低频过程不能像之前所认为的那样仅仅归因于偶极咪唑鎓阳离子的旋转扩散,还必须包括其他贡献,可能来自协同运动。由于在这些RTILs中在较高频率观察到的德拜过程与超出当前仪器范围的更快过程重叠,因此未对其进行分析。