单层
超晶格
纳米颗粒
自组装
纳米尺度
纳米技术
化学
光催化
聚乙二醇
分子
拉曼光谱
化学工程
材料科学
光电子学
有机化学
光学
催化作用
物理
工程类
作者
Yu Zhao,Xiaoyuan Wang,Xiaoning Luo,Liping Song,Fengmei Su,Youju Huang
标识
DOI:10.1002/cjoc.202200559
摘要
Comprehensive Summary Plasmonic superlattices of nanoparticles (NPs) possess unique “surface lattice resonances” properties that facilitates their wide applications in plasmonic sensing, photocatalysis, and nanoscale light manipulation. However, it is still challenging to manufacture superlattices with precisely controllable NPs distance and break the size limitation of NPs. Herein, we provided an effective strategy to construct NPs superlattices via shape‐persistent polyhedral oligosilsesquioxane (POSS) molecular nanoparticles govern interfacial assembly. As a nanoscale molecule with diameter of 1.5 nm, the POSS‐SH molecule provides sufficient rigid steric hindrance and hydrophobic effect for tailoring the uniformity and controllable distance between NPs in superlattices. Interestingly, synergistically with hydrophilic ligands of polyethylene glycol (PEG‐SH) with optimized ratio, the rigid POSS ligands can effectively regulate the distance between NPs in a fixed range of 2.3—2.8 nm, which is independent of ligands molecular weight and particle size. Furthermore, the effective approach can be universal to anisotropic NPs for manufacturing monolayer films with high NPs density. We believe this nanoscale molecule tailored interfacial self‐assembly strategy can effectively break the size of NPs and assembly obstacles for superlattice monolayer film. Additionally, the definite distance between NPs in superlattices can minimize optical energy attenuation and facilitates the applications such as surface‐enhanced Raman spectroscopy and photocatalysis.
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