Journal
JOURNAL OF MATERIALS CHEMISTRY
Volume 19, Issue 10, Pages 1483-1489Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b813368a
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Funding
- Ministry of Science and Technology (MOST), Korea
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A new, well-defined diblock copolymer (P3HT-b-C-60) based on regioregular poly(3-hexylthiophene) (P3HT) and fullerene was synthesized. First, regioregular P3HT was synthesized through Grignard metathesis polymerization, and then methyl methacrylate (MMA) and 2-hydroxyethyl methacrylate (HEMA) were copolymerized by using an end-functionalized P3HT as a macroinitiator for the atom transfer radical polymerization to yield a diblock copolymer (P3HT-b-P(MMA-r-HEMA)). A fullerene derivative functionalized with carboxylic acid, [6,6]-phenyl-C-61-butyric acid (PCBA), was then chemically linked to the HEMA unit in the second block (P(MMA-r-HEMA)) to produce a diblock copolymer with the second block containing fullerenes. Annealing thin films of the copolymer revealed nanometer-scale phase separation, a more suitable morphology for enabling excitons generated in the P3HT domain to more efficiently reach the donor-acceptor interface, relative to simple blends of P3HT and C-60. As a result, photoluminescence of the P3HT-b-C-60 diblock copolymer in the films showed a complete quenching of photoluminescence of P3HT, which is indicative of charge transfer between P3HT and fullerene.
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