Synthesis of silica-polypyrrole core-shell nanocomposite using in situ γ-aminopropyltriethoxysilane (APTES)-modified nanosilica

被引:17
作者
Jafarzadeh, Mohammad [1 ]
Ab Rahman, Ismail [2 ]
Sipaut, Coswald Stephen [3 ]
机构
[1] Univ Sains Malaysia, Sch Chem Sci, George Town 11800, Malaysia
[2] Univ Sains Malaysia, Sch Dent Sci, Kubang Kerian 16150, Kelantan, Malaysia
[3] Univ Malaysia Sabah, Sch Engn & Informat Technol, Kota Kinabalau 88999, Sabah, Malaysia
关键词
Modified silica; Polypyrrole; Core-shell; Nanocomposite; SILANE COUPLING AGENT; COLLOIDAL DISPERSIONS; NANOPARTICLES; SURFACE; MICROSPHERES; COMPOSITES; ADSORPTION; C-13; NMR;
D O I
10.1016/j.synthmet.2012.01.001
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A well dispersed core-shell, silica-polypyrrole nanocomposites, with particle size of similar to 70 nm were synthesized using a new approach. The polypyrrole conducting layer was deposited directly on the in situ-modified silica via an oxidative polymerization without the utilizing a steric stabilizer. The composites were characterized by TEM, C-13 and Si-29 NMR, thermogravimetric analysis (TGA), photoluminescence (PL) and UV-vis. The in situ gamma-aminopropyltriethoxysilane (APTES)-modified silica has shown a higher deposited polypyrrole which led to effective polymerization and higher conductivity compared to the unmodified silica (2.26 x S cm(-1) vs. 3.94 x 10(-5) S cm(-1)). This might be due to the presence of an aminopropyl group on the silica surface that improved compatibility and effective interactions. The existence of a core-shell system has been proven by TEM, through energy spectroscopic imaging (ESI) and PL analysis. The particle sizes and conductivity of the nanocomposites were found to be dependent on the mode of preparation, deposition time and the type of oxidants (FeCl3.6H(2)O and (NH4)(2)S2O4 (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:466 / 476
页数:11
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