Publication: Effects of conformational change and segmental aggregation on photoemission of illuminophores in conjugated polymer MEH-PPV: Blue shift versus red shift
Issued Date
2008-02-01
Resource Type
ISSN
03796779
Other identifier(s)
2-s2.0-40849095854
Rights
Mahidol University
Rights Holder(s)
SCOPUS
Bibliographic Citation
Synthetic Metals. Vol.158, No.3-4 (2008), 135-142
Suggested Citation
Rakchart Traiphol, Nipaphat Charoenthai Effects of conformational change and segmental aggregation on photoemission of illuminophores in conjugated polymer MEH-PPV: Blue shift versus red shift. Synthetic Metals. Vol.158, No.3-4 (2008), 135-142. doi:10.1016/j.synthmet.2007.12.014 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/19219
Research Projects
Organizational Units
Authors
Journal Issue
Thesis
Title
Effects of conformational change and segmental aggregation on photoemission of illuminophores in conjugated polymer MEH-PPV: Blue shift versus red shift
Author(s)
Other Contributor(s)
Abstract
In this contribution, we report experimental results to demonstrate the effects of chain collapse and segmental aggregation of conjugated polymer, poly[2-methoxy, 5-(2′-ethylhexyloxy)-1,4-phenylenevinylene](MEH-PPV), on its photophysics. We have found that the photoemission spectrum of isolated chains in toluene constitutes of high- and low-energy peaks at ∼385 nm and ∼558 nm. This is attributed to simultaneous emissions of short and long illuminophores within the same conjugated chain. When the system is perturbed by addition of a poor solvent, the chains minimize polymer-solvent interactions by undergoing segmental aggregation and/or chain collapse causing drastic change of the optical properties. We demonstrate that the aggregation is responsible for red-shift peaks in absorption and emission spectra detected at ∼550 nm and ∼580 nm, respectively. The chain collapse, on the other hand, causes a blue shift of the spectra. Furthermore, the measurements of emission spectra by using excitation wavelength of 350 nm detect novel high-energy peaks with λmaxat ∼414 nm. The results obtained from temperature-dependent experiments suggest that the detection of high-energy peaks arises from the collapse of individual chains. © 2008 Elsevier B.V. All rights reserved.