access icon free Well-defined structures and nanoscale morphology for all-conjugated BCPs

A series of conjugated donor–acceptor (D–A) block copolymers (BCPs) were synthesised using a one-pot Stille coupling polycondensation reaction. This involved reaction between a series of mono-bromo-functionalised Poly3-hexylthiophene (P3HT) polymers (P3HT-Br, Mn : 17, 21 and 43 kg/mol) and [N, N′-bis(2-decyl-tetradecyl)-1,7-dibromo-3,4,9,10-perylene diimide (PBI) and [2,5-bis(trimethylstannyl)-thiophene] (T) monomers. Purification using preparative gel permeation chromatography (GPC) removed any excess P3HT and resulted in BCPs with low polydispersity index values. The P3HT-b-PBIT BCPs were characterised using 1H-NMR and Fourier-transform infrared spectroscopy. When compared to a P3HT/PBIT polymer blend, the D–A BCP films exhibited a remarkably fine structure with a nanoscale morphology. These results indicated that these D–A BCPs have the potential for use as nanostructured active layers in polymer solar cells.

Inspec keywords: Fourier transform infrared spectra; ultraviolet spectra; condensation; thermal stability; visible spectra; conducting polymers; polymer blends; polymerisation

Other keywords: nanoscale morphology; polycondensation reaction; polydispersity index; [N, N’-bis(2-decyl-tetradecyl)-1,7-dibromo-3,4,9,10-perylene diimide; mono-bromo-functionalised P3HT polymers; 1H-NMR; Fourier-transform infrared spectroscopy; P3HT-PBIT polymer blend

Subjects: Visible and ultraviolet spectra of other nonmetals; Photoluminescence in organic materials; Solid surface structure; Electrochemistry and electrophoresis; Polymer reactions and polymerization; Photoconduction and photovoltaic effects; photodielectric effects; Structure of polymers, elastomers, and plastics; Infrared and Raman spectra in disordered solids (inc. glasses and polymers); Preparation of organic materials, polymers and plastics

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http://iet.metastore.ingenta.com/content/journals/10.1049/mnl.2019.0002
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