Revisiting the Critical Condition for the Cassie-Wenzel Transition on Micropillar-Structured Surfaces.

Biological and engineering applications of superhydrophobic surfaces are limited by the stability of the wetting state determined by the transition from the Cassie-Baxter state to the Wenzel state (C-W transition). In this paper, we performed water droplet squeeze tests to investigate the critical conditions for the C-W transition for solid surfaces with periodic micropillar arrays. The experimental results indicate that the critical transition pressures for the samples with varying micropillar dimensions are all significantly higher than the theoretical predictions. Through independent measurements, we attributed the disparity to the incorrect assessment of the contact angle on the sidewall surfaces of the micropillars. We also showed that the theoretical models are still applicable when the correct contact angle of the sidewall surfaces is adopted. Our work directly validates and improves the theoretical models regarding the C-W transition and suggests a potential route of tuning superhydrophobicity using finer scale surface features.

Line tension effects on the wetting of nanostructures: an energy method.

The superhydrophobicity and self-cleaning property of micro/nano-structured solid surfaces require a stable Cassie-Baxter (CB) wetting state at the liquid-solid interface. We present an energy method to investigate how the three-phase line tension affects the CB wetting state on nanostructured materials. For some nanostructures, the line tension may engender a distinct energy barrier, which restricts the position of the three-phase contact line and affects the stability of the CB wetting state. We ascertain the upper and lower limits of the critical pressure at the CB-Wenzel transition. Our results suggest that superhydrophobicity on nanostructures can be modulated by tailoring the line tension and harnessing the curvature effect. This study also provides new insights into the sinking phenomena observed in the nanoparticle-floating experiment.

Synergistic adhesion mechanisms of spider capture silk.

It is well known that capture silk, the main sticky component of the orb web of a spider, plays an important role in the spider's ability to capture prey via adhesion. However, the detailed mechanism with which the spider achieves its unparalleled high-adhesion performance remains elusive. In this work, we combine experiments and theoretical analysis to investigate the adhesion mechanisms of spider silk. In addition to the widely recognized adhesion effect of the sticky glue, we reveal a synergistic enhancement mechanism due to the elasticity of silk fibres. A balance between silk stiffness, strength and glue stickiness is crucial to endow the silk with superior adhesion, as well as outstanding energy absorption capacity and structural robustness. The revealed mechanisms deepen our understanding of the working principles of spider silk and suggest guidelines for biomimetic designs of spider-inspired adhesion and capture devices.

Frogs use a viscoelastic tongue and non-Newtonian saliva to catch prey.

Frogs can capture insects, mice and even birds using only their tongue, with a speed and versatility unmatched in the world of synthetic materials. How can the frog tongue be so sticky? In this combined experimental and theoretical study, we perform a series of high-speed films, material tests on the tongue, and rheological tests of the frog saliva. We show that the tongue's unique stickiness results from a combination of a soft, viscoelastic tongue coupled with non-Newtonian saliva. The tongue acts like a car's shock absorber during insect capture, absorbing energy and so preventing separation from the insect. The shear-thinning saliva spreads over the insect during impact, grips it firmly during tongue retraction, and slides off during swallowing. This combination of properties gives the tongue 50 times greater work of adhesion than known synthetic polymer materials such as the sticky-hand toy. These principles may inspire the design of reversible adhesives for high-speed application.

Stability of Cassie-Baxter wetting states on microstructured surfaces.

A stable Cassie-Baxter (CB) wetting state is indispensable for the superhydrophobicity of solid surfaces. In this paper, we analyze the equilibrium and stability of CB wetting states. Using an energy approach, the stability criteria of CB wetting states are established for solid surfaces with either two- or three-dimensional symmetric microstructures. A generic method is presented to calculate the critical pressure at which the CB state on a microstructured solid surface collapses. The method holds for microstructures with arbitrary generatrix, and explicit solutions are derived for a few representative microstructures with a straight or circular generatrix. In addition, some possible strategies are proposed to design surface structures with stable CB wetting states from the viewpoints of geometry and chemistry.

Efficient Self-Propelling of Small-Scale Condensed Microdrops by Closely Packed ZnO Nanoneedles.

Realizing the efficient self-propelling of small-scale condensed microdrops is very challenging but extremely important to design and develop advanced condensation heat transfer nanomaterials and devices, for example, for power generation and thermal management. Here, we present the efficient self-propelling of small-scale condensed microdrops on the surface of closely packed ZnO nanoneedles, as-synthesized by facile, rapid, and inexpensive wet chemical crystal growth followed by hydrophobic modification. Compared with flat surfaces, the nanostructured surfaces with the same low-surface-energy chemistry possess far higher time-averaged density of condensed droplets at the microscale, among which those with diameters below 10 µm occupy more than 80% of the total drop number of residual condensates. Theoretical analyses clearly reveal that this remarkable property should be ascribed to the extremely low solid-liquid adhesion of the surface nanostructure, where excess surface energy released from the coalescence of smaller condensed microdrops can be sufficient to ensure the self-propelled jumping of merged microdrops.