Decoupling of the Liquid Response of a Superhydrophobic Quartz Crystal Microbalance

• Published in: Langmuir Vol. 23; no. 19; pp. 9823 - 9830
• Main Authors: Roach, P, McHale, G, Evans, C. R, Shirtcliffe, N. J, Newton, M. I
• Format: Journal Article
• Language: English
• Published: Washington, DC American Chemical Society 11-09-2007
• Subjects: Chemistry; Colloidal state and disperse state; Exact sciences and technology; General and physical chemistry; Surface physical chemistry; Water; Viscosity; Slippage; Shear; Force; Hydrophobicity; Immersion; Density; Solid; Particle; Energy dissipation; Topography; Oscillation; Rheometer; Diameter; Crystals; Glycerol; Contact angle; Quartz; Conversion; Plate; Chemistry; Storage; Frequency; Models; Resonance; High frequency; Newtonian liquid; Interface; Quartz microbalance
• ISSN: 0743-7463; 1520-5827
• DOI: 10.1021/la701089a

Recent reports using particle image velocimetry and cone-and-plate rheometers have suggested that a simple Newtonian liquid flowing across a superhydrophobic surface demonstrates a finite slip length. Slippage on a superhydrophobic surface indicates that the combination of topography and hydrophobicity may have consequences for the coupling at the solid−liquid interface observed using the high-frequency shear-mode oscillation of a quartz crystal microbalance (QCM). In this work, we report on the response of a 5 MHz QCM possessing a superhydrophobic surface to immersion in water−glycerol mixtures. QCM surfaces were prepared with a layer of SU-8 photoresist and lithographically patterned to produce square arrays of 5 μm diameter circular cross-section posts spaced 10 μm center-to-center and with heights of 5, 10, 15, and 18 μm. Non-patterned layers were also created for comparison, and both non-hydrophobized and chemically hydrophobized surfaces were investigated. Contact angle measurements confirmed that the hydrophobized post surfaces were superhydrophobic. QCM measurements in water before and after applying pressure to force a Cassie−Baxter (non-penetrating) to Wenzel (penetrating) conversion of state showed a larger frequency decrease and higher dissipation in the Wenzel state. QCM resonance spectra were fitted to a Butterworth−van Dyke model for the full range of water−glycerol mixtures from pure water to (nominally) pure glycerol, thus providing data on both energy storage and dissipation. The data obtained for the post surfaces show a variety of types of behavior, indicating the importance of the surface chemistry in determining the response of the quartz crystal resonance, particularly on topographically structured surfaces; data for hydrophobized post surfaces imply a decoupling of the surface oscillation from the mixtures. In the case of the 15 μm tall hydrophobized post surfaces, crystal resonance spectra become narrower as the viscosity−density product increases, which is contrary to the usual behavior. In the most extreme case of the 18 μm tall hydrophobized post surfaces, both the frequency decrease and bandwidth increase of the resonance spectra are significantly lower than that predicted by the Kanazawa and Gordon model, thus implying a decoupling of the oscillating surface from the liquid, which can be interpreted as interfacial slip.