Large electro‐optic activity and enhanced temporal stability of methacrylate‐based crosslinking hyperbranched nonlinear optical polymer |
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Authors: | Yuichi Mori Kosei Nakaya Xianqing Piao Kazuhiro Yamamoto Akira Otomo Shiyoshi Yokoyama |
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Affiliation: | 1. Institute for Materials Chemistry and Engineering, Kyushu University, 6‐1 Kasuga, Fukuoka 815‐8580, Japan;2. National Institute for Information and Communications Technology, 588‐2 Iwaoka, Nishi‐ku, Kobe 651‐2492, Japan |
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Abstract: | A methacrylate‐based crosslinking hyperbranced polymers have been synthesized through initiator‐fragment incorporation radical polymerization and used for the temperature stable electro‐optic (EO) polymer application. This polymer consists of methyl methacrylate, 2‐metacryloxyethyl isocyanate, and ethylene glycol dimethacrylate (EGDMA) monomers. The use of EGDMA as a bifunctional unit resulted in the solvent‐soluble crosslinking hyperbranched chain, so that the EO polymer enhanced glass transition temperatures. A phenyl vinylene thiophene vinylene bridge nonlinear optical chromophore was attached to the polymer backbone as the side‐chain by a post‐functionalization reaction. The loading concentration of the chromophore was varied between 30 and 50 wt % by simply changing the mixing ratio of the precursor polymer to the chromophore. The synthesized EO polymers produced optical quality films with a light propagation loss of 0.61 dB/cm in a slab waveguide at 1.31 μm. The electrically poled film had an EO coefficient (r33) of 139 pm/V at 1.31 μm. The EO crosslinking hyperbranced polymer had a high‐glass transition temperature of 170 °C, and exhibited excellent temporal stability of the EO activity at 85 °C for 500 h. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 |
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Keywords: | crosslinking electro‐optic polymer high‐glass transition temperature hyperbranched NLO post‐functionalization temporal stability |
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