Resolving ultrafast exciton migration in organic solids at the nanoscale
arXiv:1706.08460 · doi:10.1038/nmat4975
Abstract
The effectiveness of molecular-based light harvesting relies on transport of optical excitations, excitons, to charg-transfer sites. Measuring exciton migration has, however, been challenging because of the mismatch between nanoscale migration lengths and the diffraction limit. In organic semiconductors, common bulk methods employ a series of films terminated at quenching substrates, altering the spatioenergetic landscape for migration. Here we instead define quenching boundaries all-optically with sub-diffraction resolution, thus characterizing spatiotemporal exciton migration on its native nanometer and picosecond scales without disturbing morphology. By transforming stimulated emission depletion microscopy into a time-resolved ultrafast approach, we measure a 16-nm migration length in CN-PPV conjugated polymer films. Combining these experiments with Monte Carlo exciton hopping simulations shows that migration in CN-PPV films is essentially diffusive because intrinsic chromophore energetic disorder is comparable to inhomogeneous broadening among chromophores. This framework also illustrates general trends across materials. Our new approach's sub-diffraction resolution will enable previously unattainable correlations of local material structure to the nature of exciton migration, applicable not only to photovoltaic or display-destined organic semiconductors but also to explaining the quintessential exciton migration exhibited in photosynthesis.
References in corpus (1)
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