Abstract

Many self-assembly approaches of colloidal monolayers have flourished but with some shortages, such as complexity, time-consumption, parameter sensitivity, and high-cost. This paper presents a facile, rapid, well-controlled, and low-cost method to prepare monolayers by directly adding silica particle suspensions containing water and ethanol to different liquids. A detailed analysis of the self-assembly process was conducted. The particles dove into water firstly, then moved up under the effect of the buoyancy and the tension gradient. The tension gradient induced the Marangoni convection and the relative motion between the water and the particles. At last, the particles were adsorbed at the air-water interface to minimize the free energy. The quality of the monolayers depended on the addition of sodium dodecyl sulfonate or ethanol in the water subphase. An interfacial polymerization of ethyl 2-cyanoacrylate was used to determine the contact angles of the particles at different subphase surfaces. The value of the detachment energy was positively associated with the contact angle and the surface tension. When the detachment energy decreased to a certain value, some particles detached from the surface, leading to the formation of a quasi-double layer. We also observed that the content of ethanol in suspensions influenced the arrangement of particles.

Highlights

  • Two-dimensional ordered arrangements of colloidal particles, commonly referred to as crystalline colloidal monolayers, have a wide range of applications in surface-enhanced Raman scattering (SERS) [1], patterned surface fabrication [2], photonic crystals [3], wetting property modification [4] and so on

  • To clarify the formation mechanism of the monolayer, the motion of particles was recorded by Particle image velocimetry (PIV) from a side view

  • The suspension drop dove into the water after it was added above the air-water interface

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Summary

Introduction

Two-dimensional ordered arrangements of colloidal particles, commonly referred to as crystalline colloidal monolayers, have a wide range of applications in surface-enhanced Raman scattering (SERS) [1], patterned surface fabrication [2], photonic crystals [3], wetting property modification [4] and so on. As for the second case, particles with some extent hydrophobicity float at the air-liquid interface, which provides the required particle mobility for defect-free packing These processes generally consist of floating particles at the interfaces, crystallizing the particle films with a mobile barrier (Langmuir–Blodgett technique) [9] or a surfactant [10], and transferring the films onto substrates. The position of the needle tip was controlled carefully to enable the spreading of the particles along the meniscus formed between the tip and the water surface Another method was adding water to a level where a meniscus was formed around the periphery of a glass slide in a Petri dish, followed by dropping colloidal suspensions on the glass slide. Once the suspensions contacted water, the particles spread at the water surface [14] In these methods, the precise control was needed to form the meniscus. We found that the arrangement of particles was affected by the content of ethanol in the suspension

Materials
Monolayer Preparation
Characterization
Self-Assembly Process of the Colloidal Monolayer at the Air-Water Interface
Conclusions
References φ

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