Paper
1 December 1997 Ultrafast femtosecond relaxation processes in luminescent and nonluminescent conducting polymers
Jiandong D. Huang, Sergey V. Frolov, Z. Valy Vardeny, W. Chen, Thomas J. Barton, R. Sugimoto, Masanori Ozaki, Katsumi Yoshino
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Abstract
We have employed the time-resolved photomodulation (PM) technique to study the photoexcitation dynamics of a luminescent (Si-PT) and nonluminescent (s-(CH)x) conducting polymers in the low signal limit. In each polymer, we identify two exponential decay processes in the PM decay, with characteristic time constants T1 and T2, where T1 is of order 1 ps and T2 depends on the specific polymer; T2 in Si-PT is about 50 ps, whereas T2 in s-(CH)x is about 5 ps. The difference in T2 is tentatively attributed to radiative and non-radiative recombination kinetics, respectively. We also found that the PM decay does not show any obvious temperature and intensity dependences, whereas the polarization memory decay is longer at low temperatures.
© (1997) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Jiandong D. Huang, Sergey V. Frolov, Z. Valy Vardeny, W. Chen, Thomas J. Barton, R. Sugimoto, Masanori Ozaki, and Katsumi Yoshino "Ultrafast femtosecond relaxation processes in luminescent and nonluminescent conducting polymers", Proc. SPIE 3145, Optical Probes of Conjugated Polymers, (1 December 1997); https://doi.org/10.1117/12.284153
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KEYWORDS
Picosecond phenomena

Polymers

Absorption

Modulation

Polarization

Phase modulation

Ultrafast phenomena

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