Influence of amide-containing side chains on the mechanical properties of diketopyrrolopyrrole-based polymers

• Published in: Polymer chemistry Vol. 9; no. 46; pp. 5531 - 5542
• Main Authors: Ocheje, Michael U., Selivanova, Mariia, Zhang, Song, Van Nguyen, Thi Hai, Charron, Brynn P., Chuang, Ching-Heng, Cheng, Yu-Hsuan, Billet, Blandine, Noori, Suendues, Chiu, Yu-Cheng, Gu, Xiaodan, Rondeau-Gagné, Simon
• Format: Journal Article
• Language: English
• Published: Cambridge Royal Society of Chemistry 14.12.2018
• Subjects: Atomic beam spectroscopy; Atomic force microscopy; Conjugation; Crystal structure; Crystallinity; Disruption; Elongation; Fracture mechanics; Hydrogen bonding; Mechanical properties; Modulus of elasticity; Morphology; Polymer chemistry; Polymers; Regeneration; Stretchability; X ray spectra; X-ray diffraction
• DOI: 10.1039/C8PY01207E
• ISSN: 1759-9954

An efficient strategy to modulate the mechanical properties of conjugated polymers has been developed through the incorporation of amide-containing alkyl chains in diketopyrrolopyrrole-based conjugated polymers. The side-chain engineering performed with hydrogen bonding moieties (up to 20 mol% of amide-containing side-chains) was found to reduce the crystallinity of the conjugated polymers in the solid state. Interestingly, this reduction in crystallinity drastically influenced the mechanical properties of the new DPP-polymers, by promoting their stretching ability, reducing the elastic modulus of the polymers, and facilitating the molecular alignment after stretch. The resulting polymers with 10% hydrogen bonding side chains showed a maximum stretchability of 75% elongation, without the appearance of nanoscale cracks, and a detailed investigation of the mechanical properties was performed by a combination of morphological characterization tools, including grazing-incidence X-ray diffraction, polarized UV-Vis spectroscopy and optical/atomic force microscopy to support our finding. Additionally, incorporation of amide-containing side-chains also enabled the regeneration of the conjugated polymer morphology after damage. Our results demonstrate that the introduction of amide-containing alkyl chains is an effective strategy to enhance the mechanical properties of π-conjugated polymers without disrupting the π-conjugation, and to enable new properties such as morphological healing.