Using Molecular Structure to Tune Intrachain and Interchain Charge Transport in Indacenodithiophene-Based Copolymers

In this work, we compare two structurally near-amorphous rigid-rod polymerspoly­(indaceno­dithiophene-co-benzo­thiadiazole), p­(IDT-BT), and poly­(indaceno­dithiophene-co-benzo­pyrollodione), p­(IDT-BPD)with orders of magnitude different mobilities to understand the effect charge carrier intrachain delocalization has on electronic transport. Quantum chemical calculations show that p­(IDT-BPD) has a barrier to torsion that is significantly lower than that of p­(IDT-BT) and is thus more likely to have reduced conjugation lengths. We utilize absorption and photoluminescence spectroscopy to characterize energetic disorder and show that p­(IDT-BPD) has higher energetic disorder. Charge modulation spectroscopy (CMS) and model calculations are used to show that charge carriers are substantially delocalized in p­(IDT-BT) and occupy near-uniform energetic environments. We find that mobility activated hopping barriers are similar in these two materials. Electronic structure calculations show that both intrachain and interchain couplings of monomer units are poor enough in p­(IDT-BPD) that charge carriers collapse to single IDT units and transport via a through-space tunneling mechanism. This work highlights the remarkable charge transport properties of p­(IDT-BT) by showing that high mobilities are achievable on device-relevant length scales with only 1D carrier delocalization.