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Local Chain Alignment via Nematic Ordering Reduces Chain Entanglement in Conjugated Polymers

Caggiano, N.J. (author)
Pennsylvania State University
Su, Tang (author)
Pennsylvania State University
Weisen, Albree R (author)
Pennsylvania State University
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Aplan, M.P. (author)
Pennsylvania State University
Xie, Renxuan (author)
Pennsylvania State University
Segad, Mo (author)
Pennsylvania State University
Müller, Christian, 1980 (author)
Chalmers tekniska högskola,Chalmers University of Technology
Colby, R.H. (author)
Pennsylvania State University
Gomez, Enrique D. (author)
Pennsylvania State University
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 (creator_code:org_t)
2018-12-14
2018
English.
In: Macromolecules. - : American Chemical Society (ACS). - 1520-5835 .- 0024-9297. ; 51:24, s. 10271-10284
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Chain entanglements govern the dynamics of polymers and will therefore affect the processability and kinetics of ordering; it follows that through these parameters chain dynamics can also affect charge transport in conjugated polymers. The effect of nematic coupling on chain entanglements is probed by linear viscoelastic measurements on poly[N-9′-heptadecanyl-2,7-carbazole-alt-5,5-(4′,7′-di-2-thienyl-2′,1′,3′-benzothiadiazole)] (PCDTBT) and poly((9,9-dioctylfluorene-2,7-diyl)-alt-(4,7-di(thiophene-2-yl)-2,1,3-benzothiadiazole)-5′,5″-diyl) (PFTBT) with varying molecular weights. We first verify the existence of nematic phases in both PFTBT and PCDTBT and identify nematic-isotropic transition temperatures, TIN, between 260 and 300 °C through a combination of differential scanning calorimetry, polarized optical microscopy, temperature-dependent X-ray scattering, and rheology. In addition, both PCDTBT and PFTBT show a glass transition temperature (Tg) and TIN, whereas only PFTBT has a melting temperature Tm of 260 °C. Comparing the molecular weight dependence of TIN with theoretical predictions of nematic phases in conjugated polymers yields the nematic coupling constant, α = (550 ± 80 K)/T + (2.1 ± 0.1), and the long-chain limit TIN as 350 ± 10 °C for PFTBT. The entanglement molecular weight (Me) in the isotropic phase is extracted to be 11 ± 1 kg/mol for PFTBT and 22 ± 2 kg/mol for PCDTBT by modeling the linear viscoelastic response. Entanglements are significantly reduced through the isotropic-to-nematic transition, leading to a 10-fold increase in Me for PFTBT and a 15-fold increase for PCDTBT in the nematic phase.

Subject headings

NATURVETENSKAP  -- Kemi -- Polymerkemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Polymer Chemistry (hsv//eng)
NATURVETENSKAP  -- Kemi -- Fysikalisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Physical Chemistry (hsv//eng)
NATURVETENSKAP  -- Fysik -- Den kondenserade materiens fysik (hsv//swe)
NATURAL SCIENCES  -- Physical Sciences -- Condensed Matter Physics (hsv//eng)

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