Design and development of dithienopyrrolobenzothiadiazole (DTPBT)-based rigid conjugated polymers with improved hole mobilities

Autor: Sanjio S. Zade, Hiren K. Machhi, Saurabh S. Soni, Arun L. Patel, Viraj J. Bhanvadia
Rok vydání: 2020
Předmět:
Zdroj: Polymer. 211:123089
ISSN: 0032-3861
DOI: 10.1016/j.polymer.2020.123089
Popis: Donor-acceptor integrated ladder-type dithienopyrrolobenzothiadiazole (DTPBT)-based conjugated building blocks have been used to develop rigid conjugated polymers by copolymerizing them with synthesized ladder-type indoloquinoxaline, π-extended isoindigo and π-extended 2,1,3-benzothiadiazole-based conjugated building blocks. Structural aspects of synthesized building blocks are studied by single-crystal X-ray diffraction, which revealed the co-planar structure of indoloquinoxaline-scaffold while twisted but intramolecularly hydrogen-bonded structures of π-extended isoindigo- and 2,1,3-benzothiadiazole-scaffolds with number of intermolecular non-bonding interactions. The synthesized DTPBT-based conjugated polymers P-1, P-2 and P-3 are studied for photophysical and electrochemical properties and are found to have moderate to good visible light absorptivity with HOMO energy levels below −5.0 eV. The X-ray diffraction studies indicate strong π−π stacking interactions induced face-on arrangement of polymer chains respective to the substrate. Polymers show π−π stacks promoted high space-charge limited current (SCLC) hole mobilities ranging between 5.6 × 10−4 –1.3 × 10−3 cm2V−1s−1. The obtained SCLC hole mobility data in tandem with the studied structural aspects of monomers and morphological aspects of polymers, suggest that the combination of ladder-type DTPBT-scaffolds (capable of intermolecular π−π interactions) with non-ladder-type planar and structurally rigid π-extended conjugated scaffolds (capable of intermolecular π−π and other non-bonding interactions) is beneficial for getting good hole mobilities.
Databáze: OpenAIRE