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Crystalline Structure and Ferroelectric Response of Poly(vinylidene fluoride)/Organically Modified Silicate Thin Films Prepared by Heat Controlled Spin Coating

机译:热控制旋涂法制备的聚偏二氟乙烯/有机改性硅酸盐薄膜的晶体结构和铁电响应

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摘要

Ultra-thin films of poly(vinylidene fluoride) (PVDF) and its organically modified silicate (OMS) nanocomposites were prepared by heat-controlled spin coating and characterized using FTIR-GIRAS, AFM, DC-EFM, and P-E measurements. Incorporation of OMS, Lucentite STN into the PVDF matrix favored the preferential formation of beta-phase in nanoscale thin films, irrespective of preparation temperature. The PVDF-OMS nanocomposite films have a little higher degree of orientation of molecular chains along the ITO substrate surface than that of the neat PVDF film. This gave the PVDF-OMS nanocomposite higher remanent polarization and better contrast in a DC-EFM phase image. Unlike the thick PVDF-OMS nanocomposites films showing only alpha-crystalline phase after quenching and slow cooling from the melt, the nanoscale thin PVDF-Oms films showed a mixture of beta- and gamma-crystalline phases without any trace of alpha-crystalline phase.
机译:通过热控制旋涂法制备了聚偏二氟乙烯(PVDF)及其有机改性的硅酸盐(OMS)纳米复合材料的超薄膜,并使用FTIR-GIRAS,AFM,DC-EFM和P-E测量进行了表征。将OMS,Lucentite STN掺入PVDF基质中,无论制备温度如何,都有利于在纳米级薄膜中优先形成β相。与纯PVDF膜相比,PVDF-OMS纳米复合膜的分子链沿着ITO基板表面的取向度略高。这使PVDF-OMS纳米复合材料在DC-EFM相位图像中具有更高的剩余极化率和更好的对比度。不同于厚的PVDF-OMS纳米复合材料薄膜在淬火和从熔体中缓慢冷却后仅显示α晶相,纳米级PVDF-Oms薄膜却显示出β和γ晶相的混合物,而没有任何痕量的α晶相。

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