Mixed Nanosphere Assemblies at a Liquid–Liquid Interface

• Published in: Small (Weinheim an der Bergstrasse, Germany) Vol. 20; no. 15
• Main Authors: Fink, Zachary, Wu, Xuefei, Kim, Paul Y., McGlasson, Alex, Abdelsamie, Maged, Emrick, Todd, Sutter‐Fella, Carolin M., Ashby, Paul D., Helms, Brett A., Russell, Thomas P.
• Format: Journal Article
• Language: English
• Published: United States Wiley 22-11-2023
• Subjects: INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; liquid interface; nanoparticle adsorption; phase separation; plasmon resonance; UV–vis reflection spectroscopy
• ISSN: 1613-6810; 1613-6829

Abstract
The in‐plane packing of gold (Au), polystyrene (PS), and silica (SiO
2
) spherical nanoparticle (NP) mixtures at a water–oil interface is investigated in situ by UV–vis reflection spectroscopy. All NPs are functionalized with carboxylic acid such that they strongly interact with amine‐functionalized ligands dissolved in an immiscible oil phase at the fluid interface. This interaction markedly increases the binding energy of these nanoparticle surfactants (NPSs). The separation distance between the Au NPSs and Au surface coverage are measured by the maximum plasmonic wavelength (λ
max
) and integrated intensities as the assemblies saturate for different concentrations of non‐plasmonic (PS/SiO
2
) NPs. As the PS/SiO
2
content increases, the time to reach intimate Au NP contact also increases, resulting from their hindered mobility. λ
max
changes within the first few minutes of adsorption due to weak attractive inter‐NP forces. Additionally, a sharper peak in the reflection spectrum at NP saturation reveals tighter Au NP packing for assemblies with intermediate non‐plasmonic NP content. Grazing incidence small angle X‐ray scattering (GISAXS) and scanning electron microscopy (SEM) measurements confirm a decrease in Au NP domain size for mixtures with larger non‐plasmonic NP content. The results demonstrate a simple means to probe interfacial phase separation behavior using in situ spectroscopy as interfacial structures densify into jammed, phase‐separated NP films.