Structuring in Thin Films during Meniscus-Guided Deposition

TL;DR

This paper presents a theoretical study of phase separation in thin films during meniscus-guided deposition, highlighting how different mass transport mechanisms influence coarsening dynamics under various evaporation conditions.

Contribution

It introduces a comprehensive model accounting for hydrodynamic, diffusive, and evaporative transport, revealing new coarsening regimes and mechanisms in thin film phase separation.

Findings

Hydrodynamic coarsening dominates in slow evaporation regimes.

Rapid evaporation suppresses hydrodynamic and diffusive coarsening.

A novel hydrodynamic coarsening regime involves droplet motion and coalescence.

Abstract

We study theoretically the evaporation-driven phase separation of a binary fluid mixture in a thin film deposited on a moving substrate, as occurs in meniscus-guided deposition for solution-processed materials. Our focus is on rapid substrate motion during, where phase separation takes place far removed from the coating device under conditions where the mixture is essentially stationary with respect to the substrate. We account for the hydrodynamic transport of the mixture within the lubrication approximation. In the early stages of demixing, diffusive and evaporative mass transport predominates, consistent with earlier studies on evaporation-driven spinodal decomposition. By contrast, in the late-stage coarsening of the demixing process, the interplay of solvent evaporation, diffusive, and hydrodynamic mass transport results in a number of distinct coarsening mechanisms. The effective coarsening rate is dictated by the (momentarily) dominant mass transport mechanism and therefore depends on the material properties, evaporation rate and time: slow solvent evaporation results in initially diffusive coarsening that for sufficiently strong hydrodynamic transport transitions to hydrodynamic coarsening, whereas rapid solvent evaporation can preempt and suppress either or both hydrodynamic and diffusive coarsening. We identify a novel hydrodynamic coarsening regime for off-critical mixtures, arising from the interaction of the interfaces between solute-rich and solute-poor regions in the film with the solution-gas interface. This interaction induces directional motion of solute-rich droplets along gradients in the film thickness, from regions where the film is relatively thick to where it is thinner. The solute-rich domains subsequently accumulate and coalesce in the thinner regions, enhancing domain growth.