4.7 Article

Transport and trapping of nanosheets via hydrodynamic forces and curvature-induced capillary quadrupolar interactions

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 531, Issue -, Pages 352-359

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2018.07.068

Keywords

Nanosheet; Capillary interactions; Quadrupolar; Hydrodynamic; Trapping; Microfluidics

Funding

  1. Allen Institute for Brain Science, Seattle, WA
  2. National Institutes of Health [1-U01-MH106027-01, R01 EY023173]
  3. National Science Foundation [EHR 0965945, CISE 1110947]

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Hypothesis: The manipulation of nanosheets on a fluid-fluid interface remains a significant challenge. At this interface, hydrodynamic forces can be used for long-range transport (>1 x capillary length) but are difficult to utilize for accurate and repeatable positioning. While capillary multipole interactions have been used for particle trapping, how these interactions manifest on large but thin objects, i.e., nanosheets, remains an open question. Hence, we posit hydrodynamic forces in conjunction with capillary multipole interactions can be used for nanosheet transport and trapping. Experiments: We designed and characterized a fluidic device for transporting and trapping nanosheets on the water-air interface. Analytical models were compared against optical measurements of the nanosheet behavior to investigate capillary multipole interactions. Energy-based modeling and dimensional analysis were used to study trapping stability. Findings: Hydrodynamic forces and capillary interactions successfully transported and trapped nanosheets at a designated trapping location with a repeatability of 10% of the nanosheet's length and 12% of its width (length = 1500 mu m, width = 1000 mu m) and an accuracy of 20% of their length and width. Additionally, this is the first report that surface tension forces acting upon nanoscale-thick objects manifest as capillary quadrupolar interactions and can be used for precision manipulation of nanosheets. (C) 2018 Elsevier Inc. All rights reserved.

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