Directed Nanoparticle Assembly through Polymer Crystallization

被引:33
作者
Mei, Shan [1 ]
Staub, Mark [1 ]
Li, Christopher Y. [1 ]
机构
[1] Drexel Univ, Dept Mat Sci & Engn, Philadelphia, PA 19104 USA
基金
美国国家科学基金会;
关键词
nanoparticle assemblies; nanoparticles; polymer crystallization; polymer single crystals; self-assembly; SINGLE-CRYSTALS; GOLD NANOPARTICLES; POLY(ETHYLENE OXIDES); AUTONOMOUS MOVEMENT; OXIDIZED SILICON; ULTRATHIN FILMS; SHISH-KEBABS; IN-SITU; NANOCRYSTALS; FIELD;
D O I
10.1002/chem.201903022
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanoparticles can be assembled into complex structures and architectures by using a variety of methods. In this review, we discuss recent progress of using polymer crystallization (particularly polymer single crystals, PSCs) to direct nanoparticle assembly. PSCs have been extensively studied since 1957. Mainly appearing as quasi-two-dimensional (2D) lamellae, PSCs are typically used as model systems to determine polymer crystalline structures, or as markers to investigate the crystallization process. Recent research has demonstrated that they can also be used as nanoscale functional materials. Herein, we show that nanoparticles can be directed to assemble into complex shapes by using in situ or ex situ polymer crystal growth. End-functionalized polymers can crystallize into 2D nanosheet PSCs, which are used to conjugate with complementary nanoparticles, leading to a nanosandwich structure. These nanosandwiches can find interesting applications for catalysis, surface-enhanced Raman spectroscopy, and nanomotors. Dissolution of the nanosandwich leads to the formation of Janus nanoparticles, providing a unique method for asymmetric nanoparticle synthesis.
引用
收藏
页码:349 / 361
页数:13
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