1988
DOI: 10.1016/0379-6779(88)90110-5
|View full text |Cite
|
Sign up to set email alerts
|

Thermochromic and solvatochromic effects in poly(3-hexylthiophene)

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

13
189
1

Year Published

1997
1997
2015
2015

Publication Types

Select...
6
2
1

Relationship

0
9

Authors

Journals

citations
Cited by 482 publications
(203 citation statements)
references
References 19 publications
13
189
1
Order By: Relevance
“…For conducting polymers, changes in the relative orientation of aromatic rings and/or overall backbone confi guration with temperature, are commonly observed [1][2][3][4]. Such structural changes lead to reduced π-π intermolecular interactions and/or create defects that can have a profound effect on conductivity and π-band localization in the highest occupied molecular orbitals.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…For conducting polymers, changes in the relative orientation of aromatic rings and/or overall backbone confi guration with temperature, are commonly observed [1][2][3][4]. Such structural changes lead to reduced π-π intermolecular interactions and/or create defects that can have a profound effect on conductivity and π-band localization in the highest occupied molecular orbitals.…”
Section: Introductionmentioning
confidence: 99%
“…Head-to-tail regioregular (98.5%) poly(3-hexylthiophene-2,5-diyl) (RR-P3HT) was one of the fi rst aromatic polymers found to exhibit a temperature dependent change in optical absorption and metallicity due to changes in backbone geometry (i.e., thermochromism [1,2,6]). Unfortunately, models of thermochromism have never deeply considered the role of defects other than those introduced by structural distortions.…”
Section: Introductionmentioning
confidence: 99%
“…5, a). The shift of the π-π* transition absorption peaks to higher energy indicates an increasing density of conformational defects, equivalent to non-planarity, and causes loss in conjugation (Hotta et al, 1987;Inganäs et al, 1988). The observed red-shift of the absorption maximum in chlorobenzene deposited layers indicates a better crystallinity of P3HT.…”
Section: Inks and Solventsmentioning
confidence: 80%
“…2), as expected for poly(3-alkylthiophenes). 16 The absorption spectrum of the P3TOT film shows no vibronic structure and a less pronounced bathochromic shift.…”
mentioning
confidence: 97%