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Reversible Aggregation and Dispersion of Particles at a Liquid–Liquid Interface Using Space Charge Injection
Author(s) -
Jia Yankai,
Huang Renjing,
Lan Yang,
Ren Yukun,
Jiang Hongyuan,
Lee Daeyeon
Publication year - 2019
Publication title -
advanced materials interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.671
H-Index - 65
ISSN - 2196-7350
DOI - 10.1002/admi.201801920
Subject(s) - chemical physics , materials science , surface charge , dispersion (optics) , colloid , particle (ecology) , charge (physics) , space charge , monolayer , suspension (topology) , electrophoresis , nanotechnology , electron , chemistry , optics , physics , chromatography , oceanography , mathematics , quantum mechanics , homotopy , pure mathematics , geology
Colloids at water–oil interfaces can form ordered monolayers when surface charge–induced repulsion overcomes capillary attraction. Such particle monolayers play an important role in the stabilization of emulsions and also can serve as an exquisite model system to study fundamental physical phenomena. However, it is challenging to dynamically control the relative magnitudes of repulsion and attraction between the particles, especially with reversibility, to induce reversible aggregation and dispersion because forces that are relevant tend to be much greater than those induced by thermal fluctuation. Here, the authors show that reversible assembly, that is reversible aggregation and dispersion, can be induced by space charge injection from corona discharge. The authors find that space charge injection modulates the strength of charge‐induced repulsion. By injecting charges, it is possible to either induce aggregation of repulsion‐dominated colloids or dispersion of aggregated particles. Interfacial electrophoretic experiments show that the alteration of the repulsion is caused by the variation of the particle surface charge that results from charge injection. The authors also demonstrate that even particles that initially form aggregated clusters due to low surface charge can be induced to organize into a hexagonally ordered structure. This method can be a powerful tool for studying phenomena involving interface‐trapped particles.