In nature, durable self-cleaning surfaces such as the Lotus leaf rely on the multiscale architecture and cohesive regenerative properties of organic tissue. Real-world impact of synthetic replicas has been limited by the poor mechanical and chemical stability of the ultrafine hierarchical textures required for attaining a highly dewetting superhydrophobic state. Here, we present the low-cost synthesis of large-scale ultradurable superhydrophobic coatings by rapid template-free micronano texturing of interpenetrated polymer networks (IPNs). A highly transparent texture of soft yielding marshmallow-like pillars with an ultralow surface energy is obtained by sequential spraying of a novel polyurethane-acrylic colloidal suspension and a superhydrophobic nanoparticle solution. The resulting coatings demonstrate outstanding antiabrasion resistance, maintaining superhydrophobic water contact angles and a pristine lotus effect with sliding angles of below 10° for up to 120 continuous abrasion cycles. Furthermore, they also have excellent chemical- and photostability, preserving the initial performance upon more than 50 h exposure to intense UVC light (254 nm, 3.3 mW cm(-2)), 24 h of oil contamination, and highly acidic conditions (1 M HCl). This sprayable polyurethane-acrylic colloidal suspension and surface texture provide a rapid and low-cost approach for the substrate-independent fabrication of ultradurable transparent self-cleaning surfaces with superior abrasion, chemical, and UV-resistance.
Engineering surface textures that are highly transparent and repel water, oil, and other low surface energy fluids can transform our interaction with wet environments. Despite extensive progress, current top-down methods are based on directional line-of-sight fabrication mechanisms that are limited by scale and cannot be applied to highly uneven, curved, and enclosed surfaces, while bottom-up techniques often suffer from poor optical transparency. Here, we present an approach that enables the rapid, omnidirectional synthesis of flexible and up to 99.97% transparent superhydrophobic and -oleophobic textures on many variable surface types. These features are obtained by the spontaneous formation of a multi re-entrant morphology during the controlled self-assembly of nanoparticle aerosols. We also develop a mathematical model to explain and control the self-assembly dynamics, providing important insights for the rational engineering of functional materials. We envision that our findings represent a significant advance in imparting superoleophobicity and superamphiphobicity to a so-far inapplicable family of materials and geometries for multifunctional applications.
One of the innate fundamentals of living systems is their ability to respond toward distinct stimuli by various selforganization behaviors. Despite extensive progress, the engineering of spontaneous motion in man-made inorganic materials still lacks the directionality and scale observed in nature. We report the directional self-organization of soft materials into three-dimensional geometries by the rapid propagation of a folding stimulus along a predetermined path. We engineer a unique Janus bilayer architecture with superior chemical and mechanical properties that enables the efficient transformation of surface energy into directional kinetic and elastic energies. This Janus bilayer can respond to pinpoint water stimuli by a rapid, several-centimeters-long self-assembly that is reminiscent of the Mimosa pudica's leaflet folding. The Janus bilayers also shuttle water at flow rates up to two orders of magnitude higher than traditional wicking-based devices, reaching velocities of 8 cm/s and flow rates of 4.7 ml/s. This self-organization regime enables the ease of fabricating curved, bent, and split flexible channels with lengths greater than 10 cm, demonstrating immense potential for microfluidics, biosensors, and water purification applications.
This review is dedicated to bridging the fields of wetting and catalysis by introducing the fundamentals of various in-air/underwater wetting states and reviewing the cutting-edge design methodologies of corresponding (photo)electrocatalytic systems.
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