Quaternization-Assisted Assembly of Polymer-Tethered Gold Nanoparticles into Superlattices with a Tunable Structure

被引:2
|
作者
Yu, Xin [1 ,2 ]
Li, Jinlan [1 ,2 ]
Yan, Nan [1 ,3 ]
Jiang, Wei [2 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
[2] Univ Sci & Technol China, Hefei 230026, Peoples R China
[3] Changchun Normal Univ, Coll Chem, Changchun 130032, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2023年 / 127卷 / 21期
基金
中国国家自然科学基金;
关键词
GRAFTED NANOPARTICLES; VESICLES; NANOSPHERES; COPOLYMER;
D O I
10.1021/acs.jpcc.3c01826
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
Programmable organization of functional inorganic nanoparticles(NPs) into well-defined hierarchical superstructures has raised considerableconcern due to the enhanced magnetic, electronic, and optical propertiesarising from the strong plasmonic coupling effect. However, the spontaneousself-assembly of inorganic NPs into uniform superlattices with thedesired or tunable shape remains a formidable challenge. Herein, wereport the quaternization-assisted hierarchical assembly of gold nanoparticles(AuNPs) tethered with polystyrene (PS) and quaternized poly-(2-vinylpyridine)(P2VP) ligands into controllable superstructures in emulsion droplets.The quaternization interaction between bromoalkyl molecular additives(e.g., C (n) H2n+1Br) and P2VP ligands results in the increase ofthe hydrophilicity degree of quaternized P2VP ligands and triggersthe interfacial instability of emulsion droplets, achieving the continuoustransformation of generated superstructures from solid assembliesto hollow colloidosomes and then to the multilayer sheet-like superlattices.Furthermore, the degree of quaternization can be readily tuned bythe added content of additives and the length of the alkyl chain,providing a unique and promising approach to prepare contrivable superstructuresand functional materials.
引用
收藏
页码:10253 / 10260
页数:8
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