Surface-Initiated Polymerization as an Enabling Tool for Multifunctional (Nano-)Engineered Hybrid Materials

被引:329
作者
Hui, Chin Ming [1 ]
Pietrasik, Joanna [1 ]
Schmitt, Michael [2 ]
Mahoney, Clare [2 ]
Choi, Jihoon [2 ]
Bockstaller, Michael R. [2 ]
Matyjaszewski, Krzysztof [1 ]
机构
[1] Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Dept Mat Sci & Engn, Pittsburgh, PA 15213 USA
基金
美国国家科学基金会;
关键词
nanocomposite; particle brush; ATRP; nanostructure; controlled radical polymerization; TRANSFER RADICAL POLYMERIZATION; ACTIVATION-DEACTIVATION EQUILIBRIUM; MOLECULAR-WEIGHT; POLYELECTROLYTE BRUSHES; METHYL-METHACRYLATE; ELECTRON-TRANSFER; FUNCTIONAL MATERIALS; COMPUTER-SIMULATION; COPOLYMER BRUSHES; COATED PARTICLES;
D O I
10.1021/cm4023634
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
Surface-initiated atom transfer radical polymerization (SI-ATRP) has become an indispensable tool for engineering the structure and properties of polymer/inorganic and polymer/organic interfaces. This article describes the progress and challenges that are associated with the application of SI-ATRP to precisely control the molecular characteristics of polymer chains tethered to nanoparticle surfaces and explores the properties and potential applications of the resulting particle brush materials. Even for the conceptually most "simple" particle brush systems that is, spherical particles uniformly grafted with amorphous nonpolar polymers the complex superposition of interactions as well as time- and length-scales related to particle core and tethered chains provides a rich and largely unexplored parameter space for the design of novel functional materials. The application of the particle brush approach to the development of materials for applications ranging from photonic inks and paints to advanced high "k" dielectrics for energy storage and advanced nanocomposite materials with improved optical, mechanical, or transport characteristics is discussed.
引用
收藏
页码:745 / 762
页数:18
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