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          Institute: MPI für Polymerforschung     Collection: MPI Polymerforschung     Display Documents



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ID: 28440.0, MPI für Polymerforschung / MPI Polymerforschung
Exciton and polaron dynamics in a step-ladder polymeric semiconductor: the influence of interchain order
Authors:Silva, C.; Russell, D. M.; Dhoot, A. S.; Herz, L. M.; Daniel, C.; Greenham, N. C.; Arias, A. C.; Setayesh, S.; Müllen, Klaus; Friend, R. H.
Language:English
Date of Publication (YYYY-MM-DD):2002-10-28
Title of Journal:Journal of Physics-Condensed Matter
Journal Abbrev.:J. Phys.-Condes. Matter
Volume:14
Issue / Number:42
Start Page:9803
End Page:9824
Review Status:No review
Audience:Not Specified
Abstract / Description:We present combined results of femtosecond transient photoluminescence (PL), femtosecond transient absorption and quasi-steady-state photoinduced absorption spectroscopy on the organic semiconductor poly-6, 6', 12, 12'-tetraalkyl-2, 8- indenofluorene (PIF). By control of interchain order via the choice of the side-chain substituents, we have investigated its effect on exciton and polaron dynamics in this model, electronic material. We show that interfaces between ordered and disordered domains play a significant role in the photophysics. At high photoexcitation fluence, a high yield (similar to10%) of polarons is only observed in the ordered semiconductor. This process arises from two-step photoexcitation, first to the lowest exciton, and then to a high-energy state of opposite symmetry. In contrast, triplet exciton population is generated via sequential excitation with smaller yield (<1%) in both ordered and disordered materials. In the low fluence regime, triplet excitons are found to arise from evolution of polarons generated with low efficiency (also <1%) by diffusion-limited processes. The triplet generation yield is strongly dependent on order, with the disordered material displaying a higher yield. Polaron decay is found to be thermally activated, with a higher activation energy and lower room-temperature recombination rate in the ordered material. Furthermore, we do not find that emissive keto defects play a defining role in the PL properties of our PIF samples. Instead, absorption features of aggregate-like species, which we believe to lead to sub-gap emission, are evident in the photocurrent action spectrum of the more ordered PIF derivative.
Comment of the Author/Creator:Date: 2002, OCT 28
External Publication Status:published
Document Type:Article
Affiliations:MPI für Polymerforschung
External Affiliations:Univ Cambridge, Cavendish Lab, Madingley Rd, Cambridge CB3 0HE, England
Identifiers:ISI:000179480700003 [ID No:1]
ISSN:0953-8984 [ID No:2]
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