Ultrafast real-time vibronic coupling dynamics of a breather soliton in trans-polyacetylene with a few-optical-cycle-pulse laser

被引:3
作者
Kobayashi, Takayoshi [1 ,2 ,3 ,4 ,5 ]
Teramoto, Takahiro [1 ,2 ,3 ]
Kobryanskii, Valerii M. [6 ]
Taneichi, Takashi [1 ,2 ,3 ]
机构
[1] Univ Electrocommun, Dept Appl Phys & Chem, Tokyo 1828585, Japan
[2] Univ Electrocommun, Inst Laser Sci, Tokyo 1828585, Japan
[3] Japan Sci & Technol Agcy, ICORP, Kawaguchi, Saitama 3320012, Japan
[4] Natl Chiao Tung Univ, Dept Electrophys, Hsinchu 30010, Taiwan
[5] Osaka Univ, Inst Laser Engn, Osaka 5650871, Japan
[6] Russian Acad Sci, Inst Chem Phys, Moscow 117977, Russia
关键词
Ultrafast spectroscopy; Coherent vibration; Nuclear wave packets; Polymers; SUBSTITUTED POLYACETYLENES; PARAMETRIC AMPLIFICATION; PHOTOINDUCED ABSORPTION; CONJUGATED POLYMERS; EXCITATIONS; GENERATION; STATES;
D O I
10.1016/j.synthmet.2009.05.021
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The dynamics preceding the spatial separation of a charged soliton pair after photoexcitation in trans-polyacetylene was successfully investigated by using ultrafast spectroscopy with a 6.2 fs pulse laser. It was directly verified that after photoexcitation, the electron-hole pair relaxes with a breather mode (i.e. multi-quanta vibronic states), as theory predicts, with an electron-hole pair lifetime of 33-50 fs. By applying spectrogram analysis to the time trace of the absorbance change, the ultrafast amplitude and frequency modulations of C-C and C=C stretching modes, induced by breathers and lasting no longer than 100 fs, can be observed Simultaneously for the first time. The frequency shifts of both modes were in good agreement with a simulation based on the Su-Schrieffer-Heeger model. It was found that the intensities of transition dipoles changed due to breathers, whereas transition energies were dominantly modulated by C=C stretching modes as recent theoretical work predicted. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:1751 / 1756
页数:6
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