化学
单重态裂变
准分子
裂变
单重态
光化学
光致发光
吸收(声学)
激发态
化学物理
荧光
三重态
原子物理学
光学
分子
中子
有机化学
物理
量子力学
作者
Miroslav Dvořák,Shyamal K. K. Prasad,Cameron B. Dover,Chelsea R. Forest,Akasha Kaleem,Rowan W. MacQueen,Anthony J. Petty,Roslyn Forecast,Jonathon E. Beves,John E. Anthony,Murad J. Y. Tayebjee,Asaph Widmer‐Cooper,Pall Thordarson,Timothy W. Schmidt
摘要
The excited-state dynamics of 6,13-bis(triisopropylsilylethynyl)pentacene is investigated to determine the role of excimer and aggregate formation in singlet fission in high-concentration solutions. Photoluminescence spectra were measured by excitation with the evanescent wave in total internal reflection, in order to avoid reabsorption effects. The spectra over nearly two magnitudes of concentration were nearly identical, with no evidence for excimer emission. Time-correlated single-photon counting measurements confirm that the fluorescence lifetime shortens with concentration. The observed rate constant grows at high concentrations, and this effect is modeled in terms of the hard-sphere radial distribution function. NMR measurements confirm that aggregation takes place with a binding constant of between 0.14 and 0.43 M-1. Transient absorption measurements are consistent with a diffusive encounter mechanism for singlet fission, with hints of more rapid singlet fission in aggregates at the highest concentration measured. These data show that excimers do not play the role of an emissive intermediate in exothermic singlet fission in solution and that, while aggregation occurs at higher concentrations, the mechanism of singlet fission remains dominated by diffusive encounters.
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