Defect by design: Harnessing the "petal effect" for advanced hydrophobic surface applications.

HYPOTHESIS: In the interfacial wetting boundary, the superhydrophobic surface is often damaged, and the anisotropic wettability of its surface has attracted many researchers' attention. The "petal effect" surface has typical anisotropic wettability. We predict that under the dual conditions of structural defects and high impact velocity, the "petal effect" becomes more adhesive on the surface. EXPERIMENTS: This study refers to the droplet state on rose petals, structural defects were constructed on the superhydrophobic surface. This paper studies the influence of macro-structural defects on the wettability change from natural to bionic "lotus effect" to "petal effect" in both static and dynamic angles. FINDINGS: Macro defects significantly change the static contact angle of the superhydrophobic surface. The higher the impact velocity of the droplet, the higher the energy dissipation of the "petal effect" surface (DSHS), which improves the adhesion of the surface to the droplet and prolongs the contact time. It is found that the defect structure and high impact velocity will directly affect the deposition and desorption of droplets on the superhydrophobic surface, and they are both essential. This wetting dynamic law is very likely to be helpful in the quantitative design of defect structure scale for dynamic desorption of droplets on superhydrophobic surfaces.

Ultrafast and Eco-Friendly Fabrication Process for Robust, Repairable Superhydrophobic Metallic Surfaces with Tunable Water Adhesion.

Superhydrophobic metallic surfaces with a water contact angle greater than 150° have attracted considerable attention in both fundamental research and industrial applications due to their special properties such as antibiofouling, drag reduction, self-cleaning, anti-icing, anticorrosion, and oil-water separation. Until now, the development of superhydrophobic practical applications is mainly limited by the process complexity, long fabrication time, coating with toxic materials, and easily damaged surface structure. To reduce the fabrication time, and simplify the process for industrial applications, an eco-friendly postprocess has been developed in this research. The superhydrophobic surfaces on the laser-textured titanium, aluminum, copper, stainless steel, and nickel substrates were fabricated extremely rapidly by a simple surface modification of only a 10 min heat treatment with nontoxic silicone oil. Hydrophobic organic group absorption has been accelerated on the silicone oil heat-treated surface and has created a low-energy surface. In addition, we demonstrated the potential of using the laser areal fluence parameter, which could be an alternative to single-laser process parameters such as scanning speed, power, and step size, to fine-tune the water adhesion behavior. Therefore, a surface that integrates different water adhesion behaviors can be easily fabricated for more complex practical applications such as controlled microdroplet transportation, microfluidic systems, and certain biomedical processes. Moreover, the robustness of superhydrophobic surfaces was confirmed by abrasion tests, knife-scratch tests, chemical durability tests, and aging tests, and their repairability was evaluated for product applications in practice.

Vapor Lubrication for Reducing Water and Ice Adhesion on Poly(dimethylsiloxane) Brushes.

Fast removal of small water drops from surfaces is a challenging issue in heat transfer, water collection, or anti-icing. Poly(dimethylsiloxane) (PDMS) brushes show good prospects to reach this goal because of their low adhesion to liquids. To further reduce adhesion of water drops, here, the surface to the vapor of organic solvents such as toluene or n-hexane is exposed. In the presence of such vapors, water drops slide at lower tilt angle and move faster. This is mainly caused by the physisorption of vapor and swelling of the PDMS brushes, which serves as a lubricating layer. Enhanced by the toluene vapor lubrication, the limit departure volume of water drop on PDMS brushes decreases by one order of magnitude compared to that in air. As a result, the water harvesting efficiency in toluene vapor increases by 65%. Benefits of vapor lubrication are further demonstrated for de-icing: driven by gravity, frozen water drops slide down the vertical PDMS brush surface in the presence of vapor.

Micellar formation by soft template electropolymerization in organic solvents.

HYPOTHESIS: The formation of porous nanostructures on surfaces and the control of their size and shape is fundamental for various applications. The creation of nanotubes is particularly difficult to implement without the aid of hard and rigid templates. Recently, methods that form nanotubular structures in a straightforward manner and without direct templating, e.g. soft templating, have been highly sought after. Here we propose the use of "soft templating" via self-assembly of conducting monomers during electropolymerization in organic solvents as a mean to form porous, nanotubular features. EXPERIMENTS: Naphtho[2,3-b]thieno[3,4-e][1,4]dioxine (NaphDOT) is employed as monomer for electropolymerizations conducted in dichloromethane and chloroform containing varying amounts of water. SEM analyses of the resulting surfaces confirms the strong capacity of NaphDOT to form vertically aligned nanotubes. Polymerization solutions analyzed by DLS and TEM reveal the presence of micelles prior to electropolymerization, and the size of the micelles correlates with the inner diameter of the nanotubes formed. FINDINGS: We show that micelles in polymerization solutions are stabilized by both monomers and electrolytes. We propose a mechanism where reverse micelles are forming a soft-template responsible for the formation of porous nanostructures during electropolymerization in organic, non-polar solvents. In this mechanism, the monomer and electrolyte assume the role of surfactant in the reverse micelle system.

Spraying Preparation of Eco-Friendly Superhydrophobic Coatings with Ultralow Water Adhesion for Effective Anticorrosion and Antipollution.

Sustainability, eco-efficiency, and green chemistry guide the development of new materials in various fields. Herein, we designed and fabricated bio-based superhydrophobic coatings by means of a facile spraying synthesized method. The as-prepared superhydrophobic coatings exhibited high water repellency with higher water contact angle being up to 156.9 ± 2.7° and a lower sliding angle of only 4.3 ± 0.6°. Also, the water adhesion on the superhydrophobic coatings was as low as 11 µN, which was far less than that (346 µN) of the normal polyurethane surfaces. The superhydrophobic properties still retained high stability under the conditions of soaking in acid solution (pH = 1) and alkaline solution (pH = 13). Meanwhile, the as-prepared bio-based superhydrophobic coatings were verified for effective corrosion and pollution protection ability. The electrochemical measurements showed excellent corrosion resistance with a higher corrosion voltage of -204.7 mV and lower corrosion current of 1.494 × 10-5 A/cm2. The corrosion protection efficiency reached a value of 95.2%, and meantime, the superhydrophobic coatings displayed higher antipollution performance without any stains when they were removed from the polluted liquids. On this basis, the underlying physical-chemical mechanisms clearly revealed that the surface micro-nanostructures could capture the continuous and stable air layer to segregate the corrosion and pollution media.

Dynamic Wetting Properties of Mesh Substrates with Tunable Water Adhesion.

In nature, wetting phenomena are present nearly everywhere and are a source of inspiration for liquid transportation. A good understanding of the underlying dynamic phenomena that governs wettability is therefore extremely important for researchers involved in bio-inspired surfaces. Herein, we study the adhesive behavior with water of mesh substrates modified with structured copolymers in order to tune the surfaces from parahydrophobic states (high water adhesion) to superhydrophobic states (low water adhesion). Using the ejection test method (ETM), a new technique that consists of the ejection of water droplets deposited onto a substrate with the aid of a catapult system, we experimentally demonstrate that the elasticity of the mesh substrate can be exploited for efficient vertical actuation of droplets.

Synthesis of low surface-energy polyepichlorohydrin triazoles thin film.

In this investigation, a new polymer with low surface energy was synthesized by grafting a triazole group onto polyepichlorohydrin (PECH) rubber that contained no halogens. The chlorine on PECH was first replaced by an azide group, and this attached azide was then converted to a triazole group with alkyl chains using the azide-alkyne Huisgen cycloaddition reaction. Analyses confirmed the structure of final product, PECH-triazole polymer. The grafting reactions increased the surface roughness. The static contact angles of water or CH2I2 droplets on the PECH-azole film were 101.7° and 71.3°, respectively. The advancing and receding contact angles for water on PECH-azide were 119.8° and 13.7°, respectively. The PECH-triazole polymer has omniphobic properties with rose petal characteristics. The PECH-triazole has low dispersive surface energy (21 mN/m) and negligible non-dispersive surface energy, giving a wetting envelope that is similar to the one of PTFE polymer. X-ray photoelectron spectroscopy and transmission infrared spectroscopy suggested that the interactions of the N atoms on the triazole ring and the O atoms on the PECH backbone constrained the orientation of CH2 groups and reduced the surface energy of the thin film.

Maskless Hydrophilic Patterning of the Superhydrophobic Aluminum Surface by an Atmospheric Pressure Microplasma Jet for Water Adhesion Controlling.

Superhydrophobic surfaces with hydrophilic patterns have great application potential in various fields, such as microfluidic systems and water harvesting. However, many reported preparation methods involve complicated devices and/or masks, making fabrication of these patterned surfaces time-consuming and inefficient. Here, we propose a highly efficient, simple, and maskless microplasma jet (MPJ) treatment method to prepare hydrophilic patterns such as dots, lines, and curves on superhydrophobic aluminum substrates. Contact angles, sliding angles, adhesive forces, and droplet impact behavior of the created patterns are investigated and analyzed. The prepared "dot" patterns exhibit great water adhesion, whereas the "line" patterns show anisotropic adhesion. Additionally, the MPJ treatment does not obviously change the surface structures, which makes it possible to achieve repeatable patterning on one substrate. The adhesion behavior of these patterns could be adjusted using MPJs with different diameters. MPJs with larger diameters are efficient for the creation of patterns with high water adhesion, which can be potentially used for open-channel lab-on-chip systems (e.g., continuous water transportation), whereas MPJs with smaller diameters are preferable in preparing patterns with low water adhesion for diverse applications in biomedical fields (e.g., lossless liquid droplet mixing and cell screening).

Structural and wetting properties of nature's finest silks (order Embioptera).

Insects from the order Embioptera (webspinners) spin silk fibres which are less than 200 nm in diameter. In this work, we characterized and compared the diameters of single silk fibres from nine species-Antipaluria urichi, Pararhagadochir trinitatis, Saussurembia calypso, Diradius vandykei, Aposthonia ceylonica, Haploembia solieri, H. tarsalis, Oligotoma nigra and O. saundersii. Silk from seven of these species have not been previously quantified. Our studies cover five of the 10 named taxonomic families and represent about one third of the known taxonomic family-level diversity in the order Embioptera. Naturally spun silk varied in diameter from 43.6 ± 1.7 nm for D. vandykei to 122.4 ± 3.2 nm for An. urichi. Mean fibre diameter did not correlate with adult female body length. Fibre diameter is more similar in closely related species than in more distantly related species. Field observations indicated that silk appears shiny and smooth when exposed to rainwater. We therefore measured contact angles to learn more about interactions between silk and water. Higher contact angles were measured for silks with wider fibre diameter and higher quantity of hydrophobic amino acids. High static contact angles (ranging up to 122° ± 3° for An. urichi) indicated that silken sheets spun by four arboreal, webspinner species were hydrophobic. A second contact angle measurement made on a previously wetted patch of silk resulted in a lower contact angle (average difference was greater than 27°) for all four species. Our studies suggest that silk fibres which had been previously exposed to water exhibited irreversible changes in hydrophobicity and water adhesion properties. Our results are in alignment with the 'super-pinning' site hypothesis by Yarger and co-workers to describe the hydrophobic, yet water adhesive, properties exhibited by webspinner silk fibres. The physical and chemical insights gained here may inform the synthesis and development of smaller diameter silk fibres with unique water adhesion properties.

Collective Molecular Mechanisms in the CH3NH3PbI3 Dissolution by Liquid Water.

The origin of the dissolution of methylammonium lead trihalide (MAPI) crystals in liquid water is clarified by finite-temperature molecular dynamics by developing a MYP-based force field (MYP1) for water-MAPI systems. A thermally activated process is found with an energy barrier of 0.36 eV consisting of a layer-by-layer degradation with generation of inorganic PbI2 films and solvation of MA and I ions. We rationalize the effect of water on MAPI by identifying a transition from a reversible absorption and diffusion in the presence of vapor to the irreversible destruction of the crystal lattice in liquid due to a cooperative action of water molecules. A strong water-MAPI interaction is found with a binding energy of 0.41 eV/H2O and wetting energy of 0.23 N/m. The water vapor absorption is energetically favored (0.29 eV/H2O), and the infiltrated molecules can migrate within the crystal with a diffusion coefficient D = 1.7 × 10-8 cm2/s and activation energy of 0.28 eV.

Physical and chemical quality, biodiversity, and thermodynamic prediction of adhesion of bacterial isolates from a water purification system: a case study

ABSTRACT The objective of this study was to evaluate the quality of water purification system and identify the bacteria this system, predict bacterial adherence according to the hydrophobicity of these microorganisms and of the polypropylene distribution loop for purified water. The assessment of drinking water that supplies the purification system allowed good-quality physical, chemical, and microbiological specifications. The physicochemical specifications of the distributed purified water were approved, but the heterotrophic bacteria count was higher than allowed (>2 log CFU mL-1).The sanitation of the storage tank with chlorine decreased the number of bacteria adhered to the surface (4.34 cycles log). By sequencing of the 16SrDNA genes, six species of bacteria were identified. The contact angle was determined and polypropylene surface and all bacteria were considered to be hydrophilic, and adhesion was thermodynamically unfavorable. This case study showed the importance of monitoring the water quality in the purified water systems and the importance of sanitization with chemical agents. The count of heterotrophic bacteria on the polypropylene surface was consistent with the predicted thermodynamics results because the number of adhered cells reached approximate values of 5 log CFU cm-2.

Graphical analysis of mammalian cell adhesion in vitro.

Short-term (<2h) cell adhesion kinetics of 3 different mammalian cell types: MDCK (epithelioid), MC3T3-E1 (osteoblastic), and MDA-MB-231 (cancerous) on 7 different substratum surface chemistries spanning the experimentally-observable range of water wettability (surface energy) are graphically analyzed to qualitatively elucidate commonalities and differences among cell/surface/suspending media combinations. We find that short-term mammalian cell attachment/adhesion in vitro correlates with substratum surface energy as measured by water adhesion tension, τ≡γlvcosθ, where γlv is water liquid-vapor interfacial energy (72.8 mJ/m2) and cosθ is the cosine of the advancing contact angle subtended by a water droplet on the substratum surface. No definitive functional relationships among cell-adhesion kinetic parameters and τ were observed as in previous work, but previously-observed general trends were reproduced, especially including a sharp transition in the magnitude of kinetic parameters from relatively low-to-high near τ=0mJ/m2, although the exact adhesion tension at which this transition occurs is difficult to accurately estimate from the current data set. We note, however, that the transition is within the hydrophobic range based on the τ=30mJ/m2 surface-energetic dividing line that has been proposed to differentiate "hydrophobic" surfaces from "hydrophilic". Thus, a rather sharp hydrophobic/hydrophilic contrast is observed for cell adhesion for disparate cell/surface combinations.

Sticky or Slippery Wetting: Network Formation Conditions Can Provide a One-Way Street for Water Flow on Platinum-cured Silicone.

In the course of studies on Sylgard 184 (S-PDMS), we discovered strong effects on receding contact angles (CAs), θrec, while cure conditions have little effect on advancing CAs. Network formation at high temperatures resulted in high θadv of 115-120° and high θrec ≥ 80°. After network formation at low temperatures (≤25 °C), θadv was still high but θrec was 30-50°. Uncertainty about compositional effects on wetting behavior resulted in similar experiments with a model D(V)D(H) silicone elastomer (Pt-PDMS) composed of a vinyl-terminated poly(dimethylsiloxane) (PDMS) base and a polymeric hydromethylsilane cross-linker. Again, network formation at high temperature (∼100 °C) resulted in high CAs, while low-temperature curing retained high advancing CAs but gave low receding CAs (θrec 30-50°). These changes in receding CAs translate to strong effects on water adhesion, wp, which is the actual work required to separate a liquid (water) from a surface: wp ∝ (1 + θrec). When the values θrec 84° for high-temperature and θrec 50° for low-temperature network formation are used, wp is ∼1.5 times higher for curing at low temperature. The origin of low receding contact angles was investigated by attenuated total reflectance IR spectroscopy. Absorptions for Si-OH hydrogen-bonded to water (3350 cm(-1)) were stronger for low- versus high-temperature curing. This result is attributed to faster hydrosilylation during curing at higher temperatures that consumes Si-H before autoxidation to Si-OH. Sharp bands at 3750 and 3690 cm(-1) due to isolated -Si-OH are more prominent for Pt-PDMS than those for S-PDMS, which may be due to an effect of functionalized nanofiller. To explore the impact of wp on water droplet flow, gradient coatings of S-PDMS and Pt-PDMS elastomers were prepared by coating a slide, maintaining opposite ends at high and low temperatures and thus forming a thermal gradient. When the slide was tilted, a droplet moved easily on the high-temperature end (slippery surface) but became pinned at the low-temperature end (sticky surface) and did not move when the slide was rotated 180°. The surface was therefore a "one-way street" for water droplet flow. Theory provides fundamental understanding for slippery/sticky behavior for gradient S-PDMS and Pt-PDMS coatings. A model for network formation is based on hydrosilylation at high temperature and condensation curing of Si-OH from autoxidation of Si-H at low temperatures. In summary, network formation conditions strongly affect receding contact angles and water adhesion for Sylgard 184 and the filler-free mimic Pt-PDMS. These findings suggest careful control of curing conditions is important to silicones used in microfluidic devices or as biomedical materials. Network-forming conditions also impact bulk mechanical properties for Sylgard 184, but the range that can be obtained has not been critically examined for specific applications.

Superhydrophobic surfaces fabricated by femtosecond laser with tunable water adhesion: from lotus leaf to rose petal.

Superhydrophobic surfaces with tunable water adhesion have attracted much interest in fundamental research and practical applications. In this paper, we used a simple method to fabricate superhydrophobic surfaces with tunable water adhesion. Periodic microstructures with different topographies were fabricated on copper surface via femtosecond (fs) laser irradiation. The topography of these microstructures can be controlled by simply changing the scanning speed of the laser beam. After surface chemical modification, these as-prepared surfaces showed superhydrophobicity combined with different adhesion to water. Surfaces with deep microstructures showed self-cleaning properties with extremely low water adhesion, and the water adhesion increased when the surface microstructures became flat. The changes in surface water adhesion are attributed to the transition from Cassie state to Wenzel state. We also demonstrated that these superhydrophobic surfaces with different adhesion can be used for transferring small water droplets without any loss. We demonstrate that our approach provides a novel but simple way to tune the surface adhesion of superhydrophobic metallic surfaces for good potential applications in related areas.

Switchable water-adhesive, superhydrophobic palladium-layered silicon nanowires potentiate the angiogenic efficacy of human stem cell spheroids.

A switchable water-adhesive, super-hydrophobic nanowire surface is developed for the formation of functional stem cell spheroids. The sizes of hADSC spheroids are readily controllable on the surface. Our surface increases cell-cell and cell-matrix interaction, which improves viability and paracrine secretion of the spheroids. Accordingly, the hADSC spheroids produced on the surface exhibit significantly enhanced angiogenic efficacy.

Superhydrophobic ZnO networks with high water adhesion.

ZnO structures were deposited using a simple chemical bath deposition technique onto interdigitated electrodes fabricated by a conventional photolithography method on SiO2/Si substrates. The X-ray diffraction studies show that the ZnO samples have a hexagonal wurtzite crystalline structure. The scanning electron microscopy observations prove that the substrates are uniformly covered by ZnO networks formed by monodisperse rods. The ZnO rod average diameter and length were tuned by controlling reactants' concentration and reaction time. Optical spectroscopy measurements demonstrate that all the samples display bandgap values and emission bands typical for ZnO. The electrical measurements reveal percolating networks which are highly sensitive when the samples are exposed to ammonia vapors, a variation in their resistance with the exposure time being evidenced. Other important characteristics are that the ZnO rod networks exhibit superhydrophobicity, with water contact angles exceeding 150° and a high water droplet adhesion. Reproducible, easily scalable, and low-cost chemical bath deposition and photolithography techniques could provide a facile approach to fabricate such ZnO networks and devices based on them for a wide range of applications where multifunctionality, i.e., sensing and superhydrophobicity, properties are required. PACS: 81.07.-b; 81.05.Dz; 68.08.Bc.

Bioinspired superhydrophobic carbonaceous hairy microstructures with strong water adhesion and high gas retaining capability.

Various hydrophobic hairy carbonaceous fibers are obtained by a low-temperature CVD process on catalyst-patterned surface patches which are selectively coated with silica to make the surface superhydrophobic and yet allow strong water adhesion for the "Salvinia effect". The versatility of the functional hairy fiber surfaces is demonstrated with a liquid barrier grid for cell microarray, a gas retaining capability under water/liquid for a membrane-free microfluidic chemical process, and functionalized papillae for cell immobilization with green algae.

Gas-driven ultrafast reversible switching of super-hydrophobic adhesion on palladium-coated silicon nanowires.

A gas-driven ultrafast adhesion switching of water droplets on palladium-coated Si nanowire arrays is demonstrated. By regulating the gas-ambient between the atmosphere and H2 , the super-hydrophobic adhesion is repeatedly switched between water-repellent and water-adhesive. The capability of modulating the super-hydrophobic adhesion on a super-hydrophobic surface with a non-contact mode could be applicable to novel functional lab-on-a-chip platforms.