A soluble, asymmetrically substituted polydiacetylene, poly(BPOD), has been reported to form stable monolayers at the air-water interface by the Langmuir-Blodgett (LB) technique [2]. Preformed polydiacetylene has been deposited onto hydrophobic substrates as multilayers to form second order nonlinear optical thin films. Second harmonic generation was found to increase with the number of layers. From previous atomic force microscopy (AFM) studies backbone orientation along the dipping direction with an interchain spacing of about 5 A° was indicated [2].The film morphology and preferential molecular orientation of these LB films are further investigated by transmission electron microscopy (TEM). A specifically tailored sample preparation method for the ultrathin LB films was used. Multilayer films were deposited on hydrophobic collodion covered glass substrates for this purpose. Electron diffraction was employed to study the crystalline organization of mono and multilayers of LB films as well as cast films.
Nonlinear optical (NLO) ultrathin films of a preforrned asymmetric polydiacetylene have been fabricated by Z-type Langmuir-Blodgett film deposition from the air-water interface. Induced in-plane orientation of the polydiacetylene backbone on the substrates has been confirmed by UV/Vis, FT-IR dichroism, and degenerate four wave mixing (DFWM) studies. All the measurements indicate that the backbone is prefe rentially oriented along the dipping direction. Second harmonic generation study suggests that the LB multilayers form an asymmetric structure (Z-type) due to the accumulation of 2-dimensional ordered monolayer and the dominant induced second order polarization is in the plane of the film. The film morphology and molecular orientation have been investigated by atomic force microscopy (AFM).
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