Single chain versus single aggregate spectroscopy of conjugated polymers. Where is the border?
(2010) In Physical chemistry chemical physics : PCCP 12. p.11770-11777- Abstract
- Single chains of conjugated polymers e.g. MEH-PPV (poly(2-methoxy-5-(2'-ethylhexyloxy)-1,4-phenylenevinylene) have become interesting objects for single molecule spectroscopy (SMS) studies. However, most of the experiments so far were performed without full awareness of the isolation status of the polymer chains in host matrices. We used steady-state and time-resolved fluorescence methods and 2D polarization single molecule imaging technique to unravel the isolation/aggregation status of MEH-PPV in spin-coated films prepared at different conditions. It turned out that a sample showing isolated bright spots in fluorescence images could be obtained in a very broad concentration range of MEH-PPV when toluene was used as a solvent and PMMA as... (More)
- Single chains of conjugated polymers e.g. MEH-PPV (poly(2-methoxy-5-(2'-ethylhexyloxy)-1,4-phenylenevinylene) have become interesting objects for single molecule spectroscopy (SMS) studies. However, most of the experiments so far were performed without full awareness of the isolation status of the polymer chains in host matrices. We used steady-state and time-resolved fluorescence methods and 2D polarization single molecule imaging technique to unravel the isolation/aggregation status of MEH-PPV in spin-coated films prepared at different conditions. It turned out that a sample showing isolated bright spots in fluorescence images could be obtained in a very broad concentration range of MEH-PPV when toluene was used as a solvent and PMMA as a matrix. If the MEH-PPV concentration was not sufficiently low, a substantial fraction of the fluorescence spots should be assigned to individual nano-aggregates rather than truly isolated chains of the polymer. Contrary to single aggregates, truly isolated MEH-PPV chains showed blue-shifted emission spectra, mono-exponential fluorescence decay dynamics with relatively long lifetimes (0.4-1.2 ns), and high polarization anisotropy. We argue that insufficient control of the concentration in the published SMS studies of MEH-PPV resulted in incorrect assigning of some spectroscopic properties of single aggregates to isolated MEH-PPV chains. We believe this to be the main origin of discrepancies among the published data in this field. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/1665442
- author
- Lin, Hongzhen LU ; Hania, Ralph LU ; Bloem, Robert ; Mirzov, Oleg LU ; Thomsson, Daniel LU and Scheblykin, Ivan LU
- organization
- publishing date
- 2010
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Physical chemistry chemical physics : PCCP
- volume
- 12
- pages
- 11770 - 11777
- publisher
- Royal Society of Chemistry
- external identifiers
-
- wos:000281726800067
- pmid:20694242
- scopus:77956505293
- ISSN
- 1463-9084
- DOI
- 10.1039/c001120g
- language
- English
- LU publication?
- yes
- additional info
- The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Chemical Physics (S) (011001060)
- id
- d21ec41f-1be2-4015-9db1-8ceb71f282f2 (old id 1665442)
- date added to LUP
- 2016-04-01 13:30:26
- date last changed
- 2024-04-24 09:21:59
@article{d21ec41f-1be2-4015-9db1-8ceb71f282f2, abstract = {{Single chains of conjugated polymers e.g. MEH-PPV (poly(2-methoxy-5-(2'-ethylhexyloxy)-1,4-phenylenevinylene) have become interesting objects for single molecule spectroscopy (SMS) studies. However, most of the experiments so far were performed without full awareness of the isolation status of the polymer chains in host matrices. We used steady-state and time-resolved fluorescence methods and 2D polarization single molecule imaging technique to unravel the isolation/aggregation status of MEH-PPV in spin-coated films prepared at different conditions. It turned out that a sample showing isolated bright spots in fluorescence images could be obtained in a very broad concentration range of MEH-PPV when toluene was used as a solvent and PMMA as a matrix. If the MEH-PPV concentration was not sufficiently low, a substantial fraction of the fluorescence spots should be assigned to individual nano-aggregates rather than truly isolated chains of the polymer. Contrary to single aggregates, truly isolated MEH-PPV chains showed blue-shifted emission spectra, mono-exponential fluorescence decay dynamics with relatively long lifetimes (0.4-1.2 ns), and high polarization anisotropy. We argue that insufficient control of the concentration in the published SMS studies of MEH-PPV resulted in incorrect assigning of some spectroscopic properties of single aggregates to isolated MEH-PPV chains. We believe this to be the main origin of discrepancies among the published data in this field.}}, author = {{Lin, Hongzhen and Hania, Ralph and Bloem, Robert and Mirzov, Oleg and Thomsson, Daniel and Scheblykin, Ivan}}, issn = {{1463-9084}}, language = {{eng}}, pages = {{11770--11777}}, publisher = {{Royal Society of Chemistry}}, series = {{Physical chemistry chemical physics : PCCP}}, title = {{Single chain versus single aggregate spectroscopy of conjugated polymers. Where is the border?}}, url = {{http://dx.doi.org/10.1039/c001120g}}, doi = {{10.1039/c001120g}}, volume = {{12}}, year = {{2010}}, }