Third-order optical nonlinearities of α,ω-dithienylpolyenes and oligo(thienylvinylene)
α,ω-Dithienylpolyenes and oligo(thienylvinylene) are interesting third-order nonlinear optical materials for a variety of device applications. To better understand the third-order nonlinear response of these materials, the third-order susceptibilities ( χ (3)) and nonlinear absorption behaviors of t...
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Published in: | Optics communications Vol. 215; no. 1; pp. 185 - 190 |
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Main Authors: | , , |
Format: | Journal Article |
Language: | English |
Published: |
Amsterdam
Elsevier B.V
01-01-2003
Elsevier Science |
Subjects: | |
Online Access: | Get full text |
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Summary: | α,ω-Dithienylpolyenes and oligo(thienylvinylene) are interesting third-order nonlinear optical materials for a variety of device applications. To better understand the third-order nonlinear response of these materials, the third-order susceptibilities (
χ
(3)) and nonlinear absorption behaviors of two α,ω-dithienylpolyenes with different conjugation length and two oligo(thienylvinylene) with different substituents on the thiophene rings have been studied using degenerate four wave mixing (DFWM) and nonlinear transmission techniques at 532 nm. The
χ
(3) values of 1×10
−3 mol/l solutions are all of the order of 10
−13 esu. The
χ
(3) values increase with the increase of the linear absorption coefficient. In addition, these compounds exhibit reverse saturable absorption for nanosecond laser pulses. The strength of reverse saturable absorption varies when the conjugation length and substituents change. Moreover, the nonlinear absorption characteristics of these compounds in the picosecond regime differ from those in the nanosecond regime. The different nonlinear absorption behavior is due to the relative contributions from excited singlet–singlet and triplet–triplet absorption. The strong reverse saturable absorption characteristics of two of the compounds suggest that they could be potential candidates for optical limiting applications in the nanosecond regime. |
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ISSN: | 0030-4018 1873-0310 |
DOI: | 10.1016/S0030-4018(02)02187-9 |