Abstract
Low-gap conjugated polymers have enabled an impressive increase in the efficiencies of organic solar cells, primarily due to their red absorption that allows harvesting of that part of the solar spectrum. Here we report that the true optical gap of one prototypical material, PTB7, is in fact at significantly higher energy than has previously been reported, indicating that the red absorption ...
Abstract
Low-gap conjugated polymers have enabled an impressive increase in the efficiencies of organic solar cells, primarily due to their red absorption that allows harvesting of that part of the solar spectrum. Here we report that the true optical gap of one prototypical material, PTB7, is in fact at significantly higher energy than has previously been reported, indicating that the red absorption utilized in these materials in solar cells is entirely due to chain aggregation. Using single-molecule spectroscopy we find that PL from isolated nanoscale aggregates consists of multiple independently emitting chromophores. At the single-molecule level, however, straight single chains with a high degree of emission polarization are observed. The PL is found to be similar to 0.4 eV higher in energy, with a longer lifetime than the red aggregates, and is attributed to single chromophores. Our findings indicate that the impressive light-harvesting abilities of PTB7 in the red spectral region arise solely from chain aggregation.
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