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Non-wetting droplets on hot superhydrophilic surfaces

Author

Listed:
  • Solomon Adera

    (Device Research Laboratory, Massachusetts Institute of Technology)

  • Rishi Raj

    (Device Research Laboratory, Massachusetts Institute of Technology
    Present address: Department of Mechanical Engineering, Indian Institute of Technology, Patna 800013, India)

  • Ryan Enright

    (Thermal Management Research Group, Bell Labs Ireland, Alcatel-Lucent, Ireland Ltd., Blanchardstown Business & Technology Park
    Work initiated while affiliated with Device Research Laboratory, Massachusetts Institute of Technology and Stokes Institute, University of Limerick, Limerick, Ireland)

  • Evelyn N. Wang

    (Device Research Laboratory, Massachusetts Institute of Technology)

Abstract

Controlling wettability by varying surface chemistry and roughness or by applying external stimuli is of interest for a wide range of applications including microfluidics, drag reduction, self-cleaning, water harvesting, anti-corrosion, anti-fogging, anti-icing and thermal management. It has been well known that droplets on textured hydrophilic, that is superhydrophilic, surfaces form thin films with near-zero contact angles. Here we report an unexpected behaviour where non-wetting droplets are formed by slightly heating superhydrophilic microstructured surfaces beyond the saturation temperature (>5 °C). Although such behaviour is generally not expected on superhydrophilic surfaces, an evaporation-induced pressure in the structured region prevents wetting. In particular, the increased thermal conductivity and decreased vapour permeability of the structured region allows this behaviour to be observed at such low temperatures. This phenomenon is distinct from the widely researched Leidenfrost and offers an expanded parametric space for fabricating surfaces with desired temperature-dependent wettability.

Suggested Citation

  • Solomon Adera & Rishi Raj & Ryan Enright & Evelyn N. Wang, 2013. "Non-wetting droplets on hot superhydrophilic surfaces," Nature Communications, Nature, vol. 4(1), pages 1-7, December.
  • Handle: RePEc:nat:natcom:v:4:y:2013:i:1:d:10.1038_ncomms3518
    DOI: 10.1038/ncomms3518
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