4.4 Article

Birefringence dynamics of poly{1-[4-(3-carboxy-4-hydroxyphenylazo)benzenesulfonamido]-1,2-ethanediyl, sodium salt} cast films

Journal

THIN SOLID FILMS
Volume 519, Issue 22, Pages 8191-8196

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.tsf.2011.06.102

Keywords

Photoisomerization; Polyelectrolytes; Relaxation; Thin films

Funding

  1. Fundacao para a Ciencia e Tecnologia (FCT/MCTES) [SFRH/BPD/35471/2007]
  2. CAPES-Brazil/Grices-Portugal
  3. DAAD-Germany/Grices-Portugal
  4. ECCL [COST actionCM0601]
  5. Fundação para a Ciência e a Tecnologia [SFRH/BPD/35471/2007] Funding Source: FCT

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Photoinduced birefringence creation/decay dynamics in poly{1-14-(3-carboxy-4-hydroxyphenylazo) benzenesulfonamido]-1,2-ethanediyl, sodium salt)cast films, has been characterized in the 5 to 100 mW writing laser power range at the wavelength of 514 nm. The maximum birefringence magnitude increased with laser beam power, being the largest value of 0.03, measured at 632.8 nm. Birefringence creation kinetics followed a biexponential behavior, where a slow process and a fast process could be clearly distinguished. The fast process accounted for more than 60% of birefringence. The time constants for both fast and slow processes decreased with increasing power of writing beam. Birefringence relaxation after removal of writing laser beam revealed to be independent of beam power and, was found to be ruled by two processes, described by a biexponential curve plus a constant term accounting for residual birefringence. A high residual birefringence signal of 85 +/- 3% was attained, with the fast process contributing to 67% of decay from maximum value. The large values obtained for time constants for both birefringence creation and relaxation processes are believed to arise from stabilization of azo-group either by the formation of an ionic network, or by local short range interactions that are coming through as a result polyelectrolyte coiling due to its high degree of ionization. (C) 2011 Elsevier B.V. All rights reserved.

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