Photoinduced Neutral-to-Ionic Phase Transition in Tetrathiafulvalene-p-chloranil Studied by Time-Resolved Vibrational Spectroscopy

被引:20
|
作者
Matsubara, Yoshitaka [1 ]
Okimoto, Yoichi [1 ]
Yoshida, Tatsushi [1 ]
Ishikawa, Tadahiko [1 ]
Koshihara, Shin-ya [1 ,2 ]
Onda, Ken [3 ]
机构
[1] Tokyo Inst Technol, Dept Chem & Mat Sci, Meguro Ku, Tokyo 1528551, Japan
[2] Japan Sci & Technol Agcy JST, CREST, Kawaguchi, Saitama 3320012, Japan
[3] Tokyo Inst Technol, Dept Environm Chem & Engn, Yokohama, Kanagawa 2268502, Japan
关键词
photoinduced phase transition; femtosecond pump-probe spectroscopy; infrared vibrational spectroscopy; neutral-ionic phase transition; organic charge transfer complex; CHARGE-TRANSFER COMPLEXES; TTF-CA; TRANSFER CRYSTAL; SPECTROMETER; DYNAMICS; ORDER; RAMAN; BAND;
D O I
10.1143/JPSJ.80.124711
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
We studied the photoinduced neutral-to-ionic phase transition in tetrathiafulvalene-p-chloranil (TTF-CA) using time-resolved infrared (IR) vibrational spectroscopy with a broadband femtosecond IR laser pulse and a linear IR detector array. After photoexcitation, the strength of the TTF a(g)upsilon(3) band increased, indicating that dimerization is activated within similar to 1 ps. In contrast, the strength of the CAb(1u)upsilon(10) band, whose frequency is proportional to the degree of charge transfer (rho), decreased, and a broad weak band appeared in the lower-frequency region. This implies that large fluctuations in charge transfer continued until about 20 ps after the photoexcitation. These results indicate a large difference between the electronic structures of the ionic phases generated by thermalexcitation and photoexcitation, although a dimerized structure was observed in both cases.
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页数:5
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