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Multiexciton Dynamics Depending on Intramolecular Orientations in Pentacene Dimers: Recombination and Dissociation of Correlated Triplet Pairs

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Details

Original languageEnglish
Pages (from-to)3354-3360
Number of pages7
JournalJournal of Physical Chemistry Letters
Volume9
Issue number12
DOIs
Publication statusPublished - 21 Jun 2018
Publication typeA1 Journal article-refereed

Abstract

Pentacene dimers bridged by a phenylene at ortho and meta positions [denoted as o-(Pc)2 and m-(Pc)2] were synthesized to examine intramolecular orientation-dependent multiexciton dynamics, especially focusing on singlet fission (SF) and recombination from correlated triplet pairs [(TT)]. Absorption and electrochemical measurements indicated strong intramolecular couplings of o-(Pc)2 relative to m-(Pc)2. Femtosecond and nanosecond TA measurements successfully demonstrated efficient SF in both dimers. In contrast, the dissociation process from the (TT) to the individual triplets [(2 × T)] was clearly observed in m-(Pc)2, which is in sharp contrast to a major recombination process in o-(Pc)2. Time-resolved electron spin resonance (TR-ESR) measurements demonstrated that the recombination and dissociation proceed from the quintet state of 5(TT) in m-(Pc)2. The rate constant of the SF was 2 orders of magnitude greater in o-(Pc)2 than that in m-(Pc)2 and was rationalized by enhanced electronic coupling between adjacent HOMOs of the Pc units.

Publication forum classification

Field of science, Statistics Finland