Femtosecond study of self-trapped vibrational excitons in crystalline acetanilide

被引:89
作者
Edler, J
Hamm, P
Scott, AC
机构
[1] Max Born Inst Nichtlineare Opt & Kurzzeitspekt, D-12489 Berlin, Germany
[2] Univ Arizona, Dept Math, Tucson, AZ 85721 USA
[3] Tech Univ Denmark, Dept Informat & Math Modelling, DK-2800 Lyngby, Denmark
关键词
D O I
10.1103/PhysRevLett.88.067403
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Femtosecond IR spectroscopy of delocalized NH excitations of crystalline acetanilide confirms that self-trapping in hydrogen-bonded peptide units exists and does stabilize the excitation. Two phonons with frequencies of 48 and 76 cm(-1) are identified as the major degrees of freedom that mediate self-trapping. After selective excitation of the free exciton, self-trapping occurs within a few 100 fs. Excitation of the self-trapped states disappears from the spectral window of this investigation on a 1 ps time scale, followed by a slow ground state recovery of the hot ground state within 18 ps.
引用
收藏
页码:67403/1 / 67403/4
页数:4
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