Photoluminescence and relaxation processes in MEH-PPV

被引:38
作者
Cossiello, RF
Kowalski, E
Rodrigues, PC
Akcelrud, L
Bloise, AC
deAzevedo, ER
Bonagamba, TJ
Atvars, TDZ
机构
[1] Univ Estadual Campinas, Inst Quim, BR-13084971 Campinas, SP, Brazil
[2] Ctr Politecn, Inst Tecnol Desenvolvimiento LACTEC, BR-81531990 Curitiba, Parana, Brazil
[3] Univ Fed Parana, Ctr Politecn, Dept Quim, BR-81531990 Curitiba, Parana, Brazil
[4] Univ Sao Paulo, Inst Fis Sao Carlos, BR-13560970 Sao Carlos, SP, Brazil
关键词
D O I
10.1021/ma048340i
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A detailed description of the thermal relaxation processes in MEH-PPV is reported. Bulk methods such as DMTA were employed in conjunction with other techniques that probe molecular motions. such as fluorescence spectroscopy, thermal stimulated current. and C-13 NMR. From the two main transitions observed (glass transition process at 340 K and beta-relaxation between 200 and 220 K). it was demonstrated that the first is strongly correlated with the dissociation of a fluorescent emissive interchain complex and that the second relaxation involves movements of the lateral substituents of the polymer backbone and, more specifically, their CH2 groups. NMR dipolar chemical shift correlation experiments pointed an increasing gain in mobility through the side chain. the lateral carbons close to the aromatic ring being more rigid than those located more distant from be main polymer chain. A kinetic model involving the dissociation of interchains to re-form intrachain excitons was proposed to explain the profiles of the photolumineseence spectra at higher temperatures.
引用
收藏
页码:925 / 932
页数:8
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