Structuring in Thin Films during Meniscus-Guided Deposition
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 rem...
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Main Authors | , , , |
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Format | Journal Article |
Language | English |
Published |
28.06.2024
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Subjects | |
Online Access | Get full text |
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Summary: | 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. |
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DOI: | 10.48550/arxiv.2406.19779 |