Influence of the chromophore ionization potential on speed and magnitude of photorefractive effects in poly(N-vinylcarbazole) based polymer composites

Citation
D. Van Steenwinckel et al., Influence of the chromophore ionization potential on speed and magnitude of photorefractive effects in poly(N-vinylcarbazole) based polymer composites, J CHEM PHYS, 112(24), 2000, pp. 11030-11037
Citations number
31
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF CHEMICAL PHYSICS
ISSN journal
00219606 → ACNP
Volume
112
Issue
24
Year of publication
2000
Pages
11030 - 11037
Database
ISI
SICI code
0021-9606(20000622)112:24<11030:IOTCIP>2.0.ZU;2-6
Abstract
We report on the synthesis of three highly polar chromophores and their use as dopants in poly(N-vinylcarbazole) based photorefractive polymer composi tes sensitized with (2,4,7-trinitro-9-fluorenylidene)malononitrile. Small a lterations in the amino donor group substituents were used to tune the dye' s ionization potential (IP) by 0.2 eV. At 780 nm, 5 degrees C above the gla ss transition temperature (T-g), and with an applied field of 59 V/mu m, we observed complete internal diffraction and a gain coefficient of 167 cm(-1 ). In this temperature range, diffraction efficiency, gain coefficient, and photorefractive phase shift were found to correlate with the chromophore I P. At 20 degrees C below Tg, the contribution from birefringence to the ind ex modulation is insignificant, and the speed of the photorefractive effect correlates well with the chromophore IP. Analysis of the results suggests that the space-charge field is influenced by the chromophore IP. (C) 2000 A merican Institute of Physics. [S0021-9606(00)70224-8].