Energy transfer in PPV-based conjugated polymers: a defocused widefield fluorescence microscopy study

被引:13
作者
Hooley, E. N. [1 ,2 ]
Tilley, A. J. [1 ,2 ]
White, J. M. [1 ,2 ]
Ghiggino, K. P. [1 ,2 ]
Bell, T. D. M. [3 ]
机构
[1] Univ Melbourne, Sch Chem, Parkville, Vic 3010, Australia
[2] Univ Melbourne, Inst Bio21, Parkville, Vic 3010, Australia
[3] Monash Univ, Sch Chem, Clayton, Vic 3800, Australia
基金
澳大利亚研究理事会;
关键词
TEMPORAL HETEROGENEITY; SINGLE; CONFORMATION; SPECTROSCOPY; PHOTOPHYSICS; CHAINS; DIFFUSION; MOLECULES; EMISSION; DYNAMICS;
D O I
10.1039/c4cp00276h
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Both pendant and main chain conjugated MEH-PPV based polymers have been studied at the level of single chains using confocal and widefield fluorescence microscopy techniques. In particular, defocused widefield fluorescence is applied to reveal the extent of energy transfer in these polymers by identifying whether they act as single emitters. For main chain conjugated MEH-PPV, molecular weight and the surrounding matrix play a primary role in determining energy transport processes and whether single emitter behaviour is observed. Surprisingly in polymers with a saturated backbone but containing the same pendant MEH-PPV oligomer on each repeating unit, intra-chain energy transfer to a single emitter is also apparent. The results imply there is chromophore heterogeneity that can facilitate energy funneling to the emitting site. Both main chain conjugated and pendant MEH-PPV polymers exhibit changes in orientation of the emission dipole during a fluorescence trajectory of many seconds, whereas a model MEH-PPV oligomer does not. The results suggest that, in the polymers, the nature of the emitting chromophores can change during the time trajectory.
引用
收藏
页码:7108 / 7114
页数:7
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