Micro-scale 2D quasi-nanosheets formed by 0D nanocrystals: from single to multicomponent building blocks

被引:10
|
作者
Chang, Yu [1 ]
Xu, Meng [1 ]
Huang, Liu [1 ]
Pan, Rongrong [1 ]
Liu, Jiajia [1 ]
Liu, Jia [1 ]
Rong, Hongpan [1 ]
Chen, Wenxing [1 ]
Zhang, Jiatao [1 ]
机构
[1] Beijing Inst Technol, Expt Ctr Adv Mat, Beijing Key Lab Construct Tailorable Adv Funct Ma, Sch Mat Sci & Engn, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
nanocrystals; self-assembly; plasmonic superstructures; 2D nanosheets; CORE-SHELL NANOCRYSTALS; AQUEOUS CATION-EXCHANGE; NANOPARTICLES; TRANSITION; NANORODS; DESIGN; CRYSTALLIZATION; SUPERSTRUCTURES; FABRICATION; ASSEMBLIES;
D O I
10.1007/s40843-020-1295-3
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Self-assembly of colloidal nanocrystals (NCs) into large-scale superlattices with complex and controllable structures has attracted extensive attention due to their collective properties and promising device applications. Plasmonic NCs are very popular for long-range ordered superstructures by virtue of their collective nanogaps for electromagnetic field enhancement, in particular bulk-scale single-layer assembly. Large-area two-dimensional (2D) quasinanosheets (QNSs) composed of mono-component Au NCs or multi-component Au@ZnS core-shell hetero-nanocrystals (HNCs) were successfully prepared, via careful solvent evaporation-induced interfacial self-assembly. The entire self-assembly process was carried out on the liquid-air surface and mediated simply by tuning the operating temperatures and concentrations of the NCs. Specifically, monolayer and double-layer 2D QNSs in tens of micrometers scale with different stacking models were fabricated by precisely controlling the solvent evaporation rate and colloidal concentration.
引用
收藏
页码:1265 / 1271
页数:7
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