SearcharxivSearch

arXiv subjects

Jesse M. Steenhoff

Publications and source records attributed to Jesse M. Steenhoff.

2 recordsLinked to original sources

Substrate-Directed Wetting Layers in Bicontinuous Particle-Stabilised Emulsions

Bicontinuous interfacially jammed emulsion gels (bijels) facilitate efficient mass transport across multiple length scales due to their interwoven structure of particle-stabilised liquid channels. This unique morphology imparts considerable potential for applications in separation and catalysis, particularly when fabricated \textit{via} solvent-transfer-induced phase separation (STrIPS). STrIPS enables the continuous, large-scale production of nanostructured bijel films on solid substrates, yet the influence of the substrate properties on the formation dynamics and final morphology remains insufficiently understood. In this study, this relationship is elucidated by preparing STrIPS bijel films on silane-functionalised glass substrates with selectively controlled wettability and analysing the resulting structure with confocal microscopy. The results showed the presence of notable wetting layers at the bijel-substrate interface, whose thicknesses could be tuned through the nanoparticle weight fraction. In line with numerical simulations, increasing the substrate hydrophobicity drove a transition from a laminar, water-rich surface layer to a patch-like, progressively oil-rich structure. These findings provide crucial insight into the structure-directing role of substrates in supported bijel films, which aids their application as functional materials.

cond-mat.soft

Phase-Field Models for Particle-Stabilised Emulsions

Particle-stabilised emulsions are a cornerstone of soft matter science due to their broad application and fundamental relevance. Computer simulations provide key insights into the formation and behaviour of these emulsions, yet current methods are limited by the spatiotemporal scales accessible for study. The principal issue is that particles are resolved individually. In this work, an alternative strategy is introduced based on phase-field theory, for which we establish the framework. By evolving continuous fields, large-scale dynamics can be simulated in a computationally efficient manner. Our approach is then applied to model the complex formation of a bicontinuous interfacially jammed emulsion gel (bijel) via solvent-transfer induced phase separation (STrIPS). By resolving the coupled dynamics of liquid phase separation and nanoparticle adsorption, the model allows for the characterisation of the influence of nanoparticles on the morphology. Higher concentrations of nanoparticles are found to reduce the average domain size of STrIPS bijels, in line with previous experimental evidence. The presented phase-field model thus represents a promising approach for the morphological investigation of complex particle-stabilised emulsions.

cond-mat.soft