Simple jQuery Dropdowns
Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/23388
Title: Spectroscopic study of photophysical change in collapsed coils of conjugated polymers: Effects of solvent and temperature
Authors: Rakchart Traiphol
Patrapon Sanguansat
Toemsak Srikhirin
Teerakiat Kerdcharoen
Tanakorn Osotchan
Naresuan University
Mahidol University
Keywords: Materials Science
Issue Date: 7-Feb-2006
Citation: Macromolecules. Vol.39, No.3 (2006), 1165-1172
Abstract: A relationship between conformation and photophysics of poly[2-methoxy-5-(2′-ethylhexoxy)-p-phenylenevinylene] (MEH-PPV) in dilute solution was investigated by utilizing UV/vis absorption, excitation, and emission spectroscopy. By tuning polymer-solvent interactions, a control of conjugation length which relates to state of chain collapse is achieved. Position of absorption and emission spectra can be systematically moved within 60 nm by using a series of alcohols and aromatic solvents as well as mixed solvents. In addition to a decrease of conjugation length, the collapsed chain exhibit optical characteristics different from that of the extended counterpart. While a single type of emitter is present in the extended chain, separate emission from multiple emitters with various conjugation lengths is detected from the collapsed coils. Fluorescence decay measurements support the presence of multiple emitters. Studies of UV/vis absorption and photoluminescence upon increasing temperature detect a blue shift of transition energies and a decrease of absorption and emission efficiency. In addition, rate of the shift is found to decrease with increasing magnitude of chain collapse. © 2006 American Chemical Society.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=32544431948&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/23388
ISSN: 00249297
Appears in Collections:Scopus 2006-2010

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.