Ravindranath Renu, Ajikumar Parayil Kumaran, Advincula Rigoberto C, Knoll Wolfgang, Valiyaveettil Suresh
Department of Chemistry, National University of Singapore, Singapore 117543.
Langmuir. 2006 Oct 10;22(21):9002-8. doi: 10.1021/la060539w.
Over the past two decades, considerable efforts have been devoted to the development of conjugated polymeric materials for electronic applications due to the tunability of their properties through variation of their chemical structure. The LB technique is one of the most effective and precise methods for controlling the organization and thereby the properties of polymer films at the nanoscale for device fabrication. A detailed study was performed on the Langmuir-Schaefer (LS) monolayer and Langmuir-Blodgett-Kuhn (LBK) multilayer formation of newly designed conjugated poly(p-phenylene)s (C(n)PPPOH), incorporated with alkoxy groups with different chain lengths (C(6)H(13)O-, C(12)H(25)O-, and C(18)H(37)O-) and hydroxyl groups on the polymer backbone. The monolayer formed at the air-water interface was characterized using surface pressure-area isotherms, including hysteresis measurements. The films were then transferred to different hydrophilic solid substrates and analyzed using surface plasmon resonance spectroscopy, UV-vis spectroscopy, fluorescence spectroscopy, and AFM measurements. The results showed that the polymer with a short alkoxy chain (C(6)PPPOH) forms uniform monolayers at the air-water interface and can be transferred as multilayer films compared to C(12)PPPOH and C(18)PPPOH. The observed film thicknesses measured by SPR and AFM studies were similar to the theoretical value obtained in the case of C(6)PPPOH, whereas this was not the case with the other two polymers. The present study shows that the polymer C(n)PPPOH with short alkoxy chain can be transferred onto different solid substrates for device fabrication with molecular level control.
在过去二十年中,由于共轭聚合物材料可通过改变化学结构来调节其性能,人们投入了大量精力来开发用于电子应用的共轭聚合物材料。LB技术是在纳米尺度上控制聚合物薄膜的组织从而控制其性能以用于器件制造的最有效、最精确的方法之一。对新设计的带有不同链长的烷氧基(C₆H₁₃O-、C₁₂H₂₅O-和C₁₈H₃₇O-)以及聚合物主链上的羟基的共轭聚对苯撑(C(n)PPPOH)的朗缪尔-谢弗(LS)单层和朗缪尔-布洛杰特-库恩(LBK)多层膜的形成进行了详细研究。利用表面压力-面积等温线对在空气-水界面形成的单层进行了表征,包括滞后测量。然后将薄膜转移到不同的亲水性固体基板上,并使用表面等离子体共振光谱、紫外-可见光谱、荧光光谱和原子力显微镜测量进行分析。结果表明,与C₁₂PPPOH和C₁₈PPPOH相比,具有短烷氧基链的聚合物(C₆PPPOH)在空气-水界面形成均匀的单层,并且可以作为多层膜转移。通过SPR和AFM研究测量的观察到的膜厚度与C₆PPPOH情况下获得 的理论值相似,而其他两种聚合物则并非如此。本研究表明,具有短烷氧基链的聚合物C(n)PPPOH可以转移到不同的固体基板上,以进行分子水平控制的器件制造。