Self-Assembly of Star-Polymer-Attached Nanospheres for Polymer Nanocomposites

被引:13
|
作者
Cheng, Lisheng [1 ]
Cao, Dapeng [1 ]
机构
[1] Beijing Univ Chem Technol, Key Lab Nanomat, Div Mol & Mat Simulat, Beijing 100029, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2010年 / 114卷 / 13期
基金
中国国家自然科学基金;
关键词
MOLECULAR-DYNAMICS SIMULATION; HOLLOW NANOSPHERES; GOLD NANOPARTICLES; COMPOSITE-MATERIAL; CLICK CHEMISTRY; ELECTROCHEMICAL SYNTHESIS; POLYELECTROLYTE BRUSHES; BIOMIMETIC SYNTHESIS; SILICA NANOSPHERES; OPTICAL-PROPERTIES;
D O I
10.1021/jp908421q
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Self-assembly is a versatile approach for the preparation of polymer nanocomposites with prescribed morphologies in the high-technology applications. Here, we use a Brownian dynamics (BD) method to explore the self-assembly of star-polymer-attached nanospheres and propose that a star polymer attached to the nanosphere brings anisotropy and induces the formation of polymer nanocomposites with different morphologies. These morphologies include hollow sphere, porous structure, lamella, perforated lamella with star polymer through nanosphere, and cylinder-like nanosphere, core shell micelle, gyroid-like network, and star-polymer-formed cylindrical structure, depending on temperature, concentration, and nanosphere size. To give a framework of these mesostructures, a temperature versus concentration phase diagram is presented for each case of nanospheres. In order to better understand the self-assembly of star-polymer-attached nanospheres, we also explore the mechanism of the formation of these morphologies by examining the packing details of star polymers. It is expected that this work would provide useful information for engineering novel polymer nanocomposite materials by means of the mesophase self-assembly.
引用
收藏
页码:5732 / 5740
页数:9
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