PICOSECOND PHOTOINDUCED ABSORPTION AND POLARIZATION MEMORY IN POLYTHIOPHENE DERIVATIVES

被引:30
作者
MCBRANCH, D [1 ]
HAYS, A [1 ]
SINCLAIR, M [1 ]
MOSES, D [1 ]
HEEGER, AJ [1 ]
机构
[1] UNIV CALIF SANTA BARBARA,DEPT PHYS,SANTA BARBARA,CA 93106
来源
PHYSICAL REVIEW B | 1990年 / 42卷 / 05期
关键词
D O I
10.1103/PhysRevB.42.3011
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Although the fast dynamics of photoexcitations has been thoroughly explored in the conjugated polymer trans-polyacetylene, the experimental picture is much less complete for polymers in which the ground state is nondegenerate. We report time-resolved photoinduced-absorption data from films of one family of such polymers: the soluble polythiophene derivatives, poly(3-hexylthiophene-2,5- yl) and poly(3-octylthiophene-2,5-yl). Fast (<10-12 s) bleaching of the interband transition is observed at 2.06 eV, accompanied by photoinduced absorption in the band gap at 1.17 eV. The results indicate a shift of a fraction of the oscillator strength, consistent with rapid structural relaxation to form polarons with associated band-gap states. By varying the polarization of the optical probe relative to that of the pump, photoinduced dichroism is observed. The magnitude of the initial dichroism implies that in spin-cast films the polymers are (locally) chain extended and chain aligned. The time decay of the polarization memory is consistent with rapid trapping of the initially mobile charged excitations. © 1990 The American Physical Society.
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收藏
页码:3011 / 3016
页数:6
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