Generating Long-Lived Triplet Excited States in Narrow Bandgap Conjugated Polymers
José Manuel Marín‐Beloqui, Daniel G. Congrave, Daniel T. W. Toolan, Stephanie Montanaro, Junjun Guo, Iain A. Wright, Tracey M. Clarke, Hugo Bronstein, Stoichko D. Dimitrov
Abstract
High Resolution Image Download MS PowerPoint Slide Narrow bandgap conjugated polymers are a heavily studied class of organic semiconductors, but their excited states usually have a very short lifetime, limiting their scope for applications. One approach to overcome the short lifetime is to populate long-lived triplet states for which relaxation to the ground state is forbidden. However, the triplet lifetime of narrow bandgap polymer films is typically limited to a few microseconds. Here, we investigated the effect of film morphology on triplet dynamics in red-emitting conjugated polymers based on the classic benzodithiophene monomer unit with the solubilizing alkyl side chains C 16 and C 2 C 6 and then used Pd porphyrin sensitization as a further strategy to change the triplet dynamics. Using transient absorption spectroscopy, we demonstrated a 0.45 ms triplet lifetime for the more crystalline nonsensitized polymer C 2 C 6, 2–3 orders of magnitude longer than typically reported, while the amorphous C 16 had only a 5 μs lifetime. The increase is partly due to delaying bimolecular electron–hole recombination in the more crystalline C 2 C 6, where a higher energy barrier for charge recombination is expected. A triplet lifetime of 0.4 ms was also achieved by covalently incorporating 5% of Pd porphyrin into the C 16 polymer, which introduced extra energy transfer steps between the polymer and porphyrin that delayed triplet dynamics and increased the polymer triplet yield by 7.9 times. This work demonstrates two synthetic approaches to generate the longest-lived triplet excited states in narrow bandgap conjugated polymers, which is of necessity in a wide range of fields that range from organic electronics to sensors and bioapplications.