4.6 Article

Exploiting Additives for Directing the Adsorption and Organization of Colloid Particles at Fluid Interfaces

Journal

LANGMUIR
Volume 37, Issue 31, Pages 9302-9335

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.langmuir.1c01029

Keywords

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Funding

  1. European Union [888076]
  2. Luxembourg National Research Fund (CORE COReLIGHT grant) [C18/MS/12701231]
  3. Marie Curie Actions (MSCA) [888076] Funding Source: Marie Curie Actions (MSCA)

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The self-assembly of colloids at fluid interfaces, driven by additives, is a well-studied research field. The critical analysis of mechanisms, interactions, and experimental protocols provides insights into controlling the organization of particles at interfaces. Structures formed by colloid self-organization at fluid interfaces have potential applications and unique properties, making this research area exciting and valuable for scientists from various fields.
The self-assembly of colloids at fluid interfaces is a well-studied research field both for gaining fundamental insights and for material fabrication. The fluid interface allows the confinement of particles in two dimensions and may act as a template for guiding their organization into soft and reconfigurable structures. Additives (e.g., surfactants, salts, and polymers) in the colloidal suspension are routinely used as a practical and effective tool to drive particle adsorption and tune their interfacial organization. However, some phenomena lying at the heart of the accumulation and self-assembly of particles at fluid interfaces remain poorly understood. This Feature Article aims to critically analyze the mechanisms involved in the adsorption and self-organization of micro- and nanoparticles at various fluid interfaces. In particular, we address the role of additives in both promoting the adsorption of particles from the bulk suspension to the fluid interface and in mediating the interactions between interfacial particles. We emphasize how different types of additives play a crucial role in controlling the interactions between suspended particles and the fluid interface as well as the interactions between adsorbed particles, thus dictating the final self-assembled structure. We also critically summarize the main experimental protocols developed for the complete adsorption of particles initially suspended in the bulk. Furthermore, we highlight some special properties (e.g., reconfigurability upon external stimulation and dissipative self-assembly) and the application potential of structures formed by colloid self-organization at fluid interfaces mediated/promoted by additives. We believe our contribution serves both as a practical roadmap to scientists coming from other fields and as a valuable information resource for all researchers interested in this exciting research field.

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