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Solvent-Mediated Forces between Ellipsoidal Nanoparticles Adsorbed at Liquid–Vapor Interfaces
[Image: see text] Classical capillary theory predicts that a non-neutrally wetting ellipsoidal particle adsorbed at a liquid–vapor interface will deform the interface. The deformation gives rise to anisotropic capillary forces of a quadrupolar nature that induce strong directionality in the particle...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735740/ https://www.ncbi.nlm.nih.gov/pubmed/33236631 http://dx.doi.org/10.1021/acs.langmuir.0c02243 |
Sumario: | [Image: see text] Classical capillary theory predicts that a non-neutrally wetting ellipsoidal particle adsorbed at a liquid–vapor interface will deform the interface. The deformation gives rise to anisotropic capillary forces of a quadrupolar nature that induce strong directionality in the particle interactions. Here, we investigate the interactions between nanoparticles with characteristic lengths of 1–5 nm. We show that the near-field interactions are dominated by solvent-mediated forces, which arise from the fluid packing between the nanoparticles and direct nanoparticle–nanoparticle interactions. The solvent-mediated forces are two orders of magnitude larger than the estimated capillary force. We find that interacting ellipsoidal nanoparticles adsorbed at the liquid–vapor interface have a larger repulsion in the depletion region than the nanoparticles submerged in a dense bulk phase and argue that this is because of a negative line tension associated with the three-phase line. |
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