Coherent vibrational dynamics of intermolecular hydrogen bonds in acetic acid dimers studied by ultrafast mid-infrared spectroscopy

被引:28
|
作者
Heyne, K [1 ]
Huse, N [1 ]
Nibbering, ETJ [1 ]
Elsaesser, T [1 ]
机构
[1] Max Born Inst Nickhlineare Opt & Kurzzeitspekt, D-12489 Berlin, Germany
关键词
D O I
10.1088/0953-8984/15/1/316
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
Ultrafast vibrational motions and the underlying microscopic couplings in hydrogen-bonded cyclic dimers. of acetic acid are studied by pump-probe and photon echo experiments in the mid-infrared. Upon feratosecond excitation of the O-H stretching mode, we demonstrate coherent nuclear motions along the in-plane dimer stretching mode which persist for picoseconds. The anharmonic coupling of the O-H stretching and the low-frequency mode is isolated in the nonlinear vibrational response, whereas other couplings are suppressed. Three-pulse photon echo experiments demonstrate a dephasing of O-H stretching excitations on a femtosecond timescale and quantum beats due to the anharmonically coupled dimer stretching mode.
引用
收藏
页码:S129 / S136
页数:8
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