Orientational dynamics of the ionic organic liquid 1-ethyl-3-methylimidazolium nitrate

被引:147
作者
Cang, H [1 ]
Li, J [1 ]
Fayer, MD [1 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
关键词
D O I
10.1063/1.1628668
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Optical heterodyne-detected optical Kerr effect (OHD-OKE) experiments are used to study the orientational dynamics of the ionic organic liquid 1-ethyl-3-methylimidazolium nitrate (EMIM+NO3-) over time scales from similar to1 ps to similar to2 ns, and the temperatures range from 410 to 295 K. The temperatures cover the normal liquid state and the weakly supercooled state. The orientational dynamics exhibit characteristics typical of normal organic glass-forming liquids. The longest time scale portion of the data decays as a single exponential and obeys the Debye-Stokes Einstein relation. The decay of the OHD-OKE signal begins (similar to1 ps) with a temperature independent power law, t(-z), z=1.02+/-0.05, the "intermediate power law.'' The power law decay is followed by a crossover region, modeled as a second power law, the von Schweidler power law. The longest time scale decay is the exponential a relaxation. The intermediate power law decay has been observed in van der Waals supercooled liquids previously. These are the first such observations on an ionic organic liquid. The observation of the dynamical signatures observed in other liquids demonstrates that the orientational dynamics of ionic organic liquids are fundamentally the same as van der Waals liquids and supports the universality of the intermediate power law decay in the dynamics of complex liquids. Within the mode-coupling theory (MCT) framework, the MCT critical temperature T-C is estimated to be T(C)congruent to255 K. (C) 2003 American Institute of Physics.
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页码:13017 / 13023
页数:7
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