Local Structure and Relaxation Dynamics in the Brush of Polymer-Grafted Silica Nanoparticles

被引:50
|
作者
Wei, Yuan [1 ]
Xu, Yifan [1 ]
Faraone, Antonio [2 ]
Hore, Michael J. A. [1 ]
机构
[1] Case Western Reserve Univ, Dept Macromol Sci & Engn, 10900 Euclid Ave, Cleveland, OH 44106 USA
[2] NIST, Ctr Neutron Res, Gaithersburg, MD 20899 USA
来源
ACS MACRO LETTERS | 2018年 / 7卷 / 06期
基金
美国国家科学基金会;
关键词
NANOCOMPOSITES; CONFORMATION; CHAIN; BEHAVIOR;
D O I
10.1021/acsmacrolett.8b00223
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
When grafted to spherical nanoparticles at high grafting densities, polymers adopt a variety of conformations. Because of strong confinement by neighboring chains, portions of the polymer near the nanoparticle core are highly stretched in the concentrated polymer brush region (CPB) of the polymer layer. Farther away from the core, where the polymer is less confined, the conformation becomes more ideal in the semidilute polymer brush (SDPB) region. Using a combination of small-angle neutron scattering (SANS) and neutron spin echo (NSE) spectroscopy, we directly characterized both the structure and dynamics of the CPB and SDPB on poly(methyl acrylate) (PMA) grafted SiO2 nanoparticles (NPs). Analysis of SANS measurements using a new core-chain-chain (CCC) model confirmed that the portion of the chain in the CPB region is highly stretched, and transitions to a more random conformation. Dynamics in the CPB region were found to be much slower than the SDPB region.
引用
收藏
页码:699 / 704
页数:11
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