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RISS 인기검색어
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- 저자 : Cirpan, Ali (검색결과 2 건)
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Lee, Jea Uk,Cirpan, Ali,Emrick, Todd,Russell, Thomas P.,Jo, Won Ho Royal Society of Chemistry 2009 Journal of materials chemistry Vol.19 No.10
<P>A new, well-defined diblock copolymer (P3HT-<I>b</I>-C<SUB>60</SUB>) 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-<I>b</I>-P(MMA-<I>r</I>-HEMA)). A fullerene derivative functionalized with carboxylic acid, [6,6]-phenyl-C<SUB>61</SUB>-butyric acid (PCBA), was then chemically linked to the HEMA unit in the second block (P(MMA-<I>r</I>-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<SUB>60</SUB>. As a result, photoluminescence of the P3HT-<I>b</I>-C<SUB>60</SUB> diblock copolymer in the films showed a complete quenching of photoluminescence of P3HT, which is indicative of charge transfer between P3HT and fullerene.</P> <P>Graphic Abstract</P><P>A new, well-defined diblock copolymer (P3HT-<I>b</I>-C<SUB>60</SUB>) based on regioregular P3HT and fullerene showed phase separation on a nanometer scale, which allows the excitons generated in the P3HT domain to reach the donor–acceptor interface more efficiently. <IMG SRC='http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=b813368a'> </P>
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Emission tuning study of RGB blends. Interaction of two EL polymers and a red dye
Jeferson Ferreira de Deus,Ali Cirpan,Frank Karasz,Leni Akcelrud 한국물리학회 2010 Current Applied Physics Vol.10 No.2
A study of light emission in photo- and electroluminescence in blends composed of a blue and a green emitting polymers with a red dye was performed. To gain information about the tunability of the RGB mixture, the blends varied in composition. The polymers were poly(2,7-9,90-dihexylfluorenediyl) (blue),poly(9,9-di-hexylfluorenediyl divinylene-alt-1,4-phenylenevinylene) (green) and the dye was 4-(dicyanomethylene)-2-methyl-6-(dimethylaminostyryl)-4H-pyrane (red). It was verified that in photoluminescence Forster type energy transfer plays the main role in the emission. In solution a large concentration of the acceptors is needed to attain the transfer radii, whereas in the solid state, the transfer is very sensitive to small variations in the acceptor content, with large changes in emission spectra. The band gaps of the components allowed a cascade energy transfer mechanism. In electroluminescence, apart from the energy transfer mechanism, an important role is played by the trapping of charge carriers, resulting in significant differences between the PL and EL spectra.
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