Transient birefringence of liquids induced by terahertz electric-field torque on permanent molecular dipoles

被引:67
作者
Sajadi, Mohsen [1 ]
Wolf, Martin [1 ]
Kampfrath, Tobias [1 ]
机构
[1] Fritz Haber Inst Max Planck Soc, Dept Phys Chem, D-14195 Berlin, Germany
基金
欧洲研究理事会;
关键词
DIELECTRIC-RELAXATION; SECONDARY RELAXATIONS; DIMETHYL-SULFOXIDE; GLASS-TRANSITION; VISCOUS-LIQUIDS; DYNAMICS; SPECTROSCOPY;
D O I
10.1038/ncomms14963
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Collective low-frequency molecular motions have large impact on chemical reactions and structural relaxation in liquids. So far, these modes have mostly been accessed indirectly by off-resonant optical pulses. Here, we provide evidence that intense terahertz (THz) pulses can resonantly excite reorientational-librational modes of aprotic and strongly polar liquids through coupling to the permanent molecular dipole moments. We observe a significantly enhanced response because the transient optical birefringence is up to an order of magnitude higher than obtained with optical excitation. Frequency-dependent measurements and a simple analytical model indicate that the enhancement arises from resonantly driven librations and their coupling to reorientational motion, assisted by the pump field and/or a cage translational mode. Our results open up the path to applications such as efficient molecular alignment, enhanced transient Kerr signals and systematic resonant nonlinear THz spectroscopy of the coupling between intermolecular modes in liquids.
引用
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页数:8
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