Abstract
Singlet fission is a photophysical process in which an optically excited singlet exciton is converted into two triplet excitons. Singlet fission sensitized solar cells are expected to display a greatly enhanced power conversion efficiency compared to conventional single-junction cells, but the efficient design of such devices relies on the selection of materials capable of harvesting triplets generated in the fission chromophore. To this aim, the possibility of measuring triplet exciton dynamics with chemical selectivity paves the way for the rational design of complex heterojunctions, with optimized triplet conversion. Here we exploit the chemical sensitivity of X-ray absorption spectroscopy to track triplet exciton dynamics at the picosecond timescale in multilayer films of pentacene, the archetypal singlet fission material. We experimentally identify the signature of the triplet exciton in the Carbon K-edge absorption spectrum and measure its lifetime of about 300 ps. Our results are supported by state-of-the-art ab initio calculations.
Highlights
Singlet fission is a photophysical process in which an optically excited singlet exciton is converted into two triplet excitons
The molecular films have been deposited in situ in the ultra-high vacuum (UHV) experimental chamber to ensure the best molecular ordering and prevent contamination
We observe the pump-induced population of a short-lived state (
Summary
Singlet fission is a photophysical process in which an optically excited singlet exciton is converted into two triplet excitons. Singlet fission sensitized solar cells are expected to display a greatly enhanced power conversion efficiency compared to conventional singlejunction cells, but the efficient design of such devices relies on the selection of materials capable of harvesting triplets generated in the fission chromophore To this aim, the possibility of measuring triplet exciton dynamics with chemical selectivity paves the way for the rational design of complex heterojunctions, with optimized triplet conversion. Time resolved X-ray spectroscopies have been applied to the study of photoexcited states in molecules either in solution or in gas phase[18,19] Such techniques offer chemical selectivity since they probe excitations of localized core electrons to unoccupied valence states. To the best of our knowledge, this is the first extension of RI-CC2 to the calculation of core spectra (both excitation energies and intensities) of triplet excited states
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