Non-close-packed plasmonic Bravais lattices through a fluid interface-assisted colloidal assembly and transfer process

IF 2.2 4区 化学 Q3 CHEMISTRY, PHYSICAL
Déborah Feller, Marius Otten, Michael S. Dimitriyev, Matthias Karg
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Abstract

The assembly of colloids at fluid interfaces followed by their transfer to solid substrates represents a robust bottom-up strategy for creating colloidal monolayers over large, macroscopic areas. In this study, we showcase how subtle adjustments in the transfer process, such as varying the contact angle of the substrate and controlling deposition speed and direction, enable the realization of all five two-dimensional Bravais lattices. Leveraging plasmonic core–shell microgels as the building blocks, we successfully engineered non-close-packed plasmonic lattices exhibiting hexagonal, square, rectangular, centered rectangular, and oblique symmetries. Beyond characterizing the monolayer structures and their long-range order, we employed extinction spectroscopy alongside finite difference time domain simulations to comprehensively investigate and interpret the plasmonic response of these monolayers. Additionally, we probed the influence of the refractive index environment on the plasmonic properties by two methods: first, by plasma treatment to remove the microgel shells, and second, by overcoating the resulting gold nanoparticle lattices with a homogeneous refractive index polymer film.

Graphical Abstract

Abstract Image

通过流体界面辅助胶体组装和转移过程实现非紧密堆积的等离子体布拉维晶格
在流体界面上组装胶体,然后将其转移到固体基底上,是在大面积宏观区域上形成胶体单层的一种强有力的自下而上的策略。在这项研究中,我们展示了转移过程中的微妙调整,如改变基底的接触角以及控制沉积速度和方向,是如何实现所有五种二维布拉维晶格的。利用等离子核壳微凝胶作为构建模块,我们成功地设计出了非紧密堆积的等离子晶格,呈现出六边形、正方形、长方形、居中长方形和斜对称性。除了表征单层结构及其长程有序性,我们还利用消光光谱和有限差分时域模拟来全面研究和解释这些单层的等离子响应。此外,我们还通过两种方法探究了折射率环境对等离子特性的影响:第一种是通过等离子处理去除微凝胶壳,第二种是用均匀的折射率聚合物薄膜覆盖由此产生的金纳米粒子晶格。
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来源期刊
Colloid and Polymer Science
Colloid and Polymer Science 化学-高分子科学
CiteScore
4.60
自引率
4.20%
发文量
111
审稿时长
2.2 months
期刊介绍: Colloid and Polymer Science - a leading international journal of longstanding tradition - is devoted to colloid and polymer science and its interdisciplinary interactions. As such, it responds to a demand which has lost none of its actuality as revealed in the trends of contemporary materials science.
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