WCU program of Chemical Convergence for Energy and Environment (C2E2), School of Chemical and Biological Engineering, College of Engineering, Seoul National University, 599 Gwanak-ro, Gwanak-gu, Seoul 151-742, Korea.
ACS Appl Mater Interfaces. 2012 Sep 26;4(9):4603-9. doi: 10.1021/am300979s. Epub 2012 Sep 7.
Highly conductive silica/polyaniline (PANi) core/shell nanoparticles (NPs) were synthesized in various diameters (from 18 to 130 nm) using self-stabilized dispersion polymerization. The polymerization was carried out in an aqueous/organic liquid system at -30 °C. In this system, the organic phase plays a key role in directing para-direction oriented polymerization of the PANi on the surface of silica NPs. Because of its para-direction polymerized structure, the synthesized silica/PANi core/shell NPs exhibited enhanced electrical conductivity (25.6 S cm(-1)) compared with NPs (1.4 S cm(-1)) prepared by homogeneous polymerization. The conductivities and BET surface areas were 25.6 S cm(-1)/170 m(2) g(-1) (18 nm in diameter), 22.5 S cm(-1)/111 m(2) g(-1) (35 nm in diameter), 18.3 S cm(-1)/78 m(2) g(-1) (63 nm in diameter), and 16.4 S cm(-1)/53 m(2) g(-1) (130 nm in diameter). In this series, increased para-coupling along the polymer backbone was elucidated using several characterization techniques, including Fourier transform infrared (FTIR), X-ray diffraction (XRD), and nuclear magnetic resonance (NMR) spectroscopy. As-prepared silica/PANi core/shell NPs exhibited capacitance as high as 305 F g(-1).
采用自稳定分散聚合的方法合成了不同粒径(18-130nm)的高导电二氧化硅/聚苯胺(PANI)核/壳纳米粒子(NPs)。聚合反应在-30°C的水/有机液体体系中进行。在该体系中,有机相在指导PANI沿二氧化硅 NPs 表面进行对位聚合方面起着关键作用。由于其对位聚合结构,与通过均相聚合制备的 NPs(1.4Scm(-1))相比,合成的二氧化硅/PANI 核/壳 NPs 表现出增强的电导率(25.6Scm(-1))。电导率和 BET 比表面积分别为 25.6Scm(-1)/170m(2)g(-1)(直径 18nm)、22.5Scm(-1)/111m(2)g(-1)(直径 35nm)、18.3Scm(-1)/78m(2)g(-1)(直径 63nm)和 16.4Scm(-1)/53m(2)g(-1)(直径 130nm)。在该系列中,使用傅里叶变换红外(FTIR)、X 射线衍射(XRD)和核磁共振(NMR)光谱等几种表征技术阐明了沿聚合物主链增加的对位偶联。所制备的二氧化硅/PANI 核/壳 NPs 表现出高达 305Fg(-1)的电容。