Multifunctional Superamphiphobic Coating Based on Fluorinated TiO2 toward Effective Anti-Corrosion.

The application of superamphiphobic coatings improves the surface's ability to repel fluids, thereby greatly enhancing its various functions, including anti-fouling, anti-corrosion, anti-icing, anti-bacterial, and self-cleaning properties. This maximizes the material's potential for industrial applications. This work utilized the agglomeration phenomenon exhibited by nano-spherical titanium dioxide (TiO2) particles to fabricate 1H,1H,2H,2H-perfluorodecyltriethoxysilane (PFDTES) modified TiO2 (TiO2@fluoroPOS) fillers with low surface energy. This was achieved through the in-situ formation of protective armor on the surface of the agglomerates using the sol-gel method and fluorination modification. Polyvinylidene fluoride-tetrafluoropropylene (PVDF-HFP) and TiO2@fluoroPOS fillers were combined using a spraying technique to prepare P/TiO2@fluoroPOS coatings with superamphiphobicity. Relying on the abundance of papillae, micropores, and other tiny spaces on the surface, the coating can capture a stable air film and reject a variety of liquids. When the coatings were immersed in solutions of 2 mol/L HCl, NaCl, and NaOH for a duration of 12 h, they retained their exceptional superamphiphobic properties. Owing to the combined influence of the armor structure and the organic binder, the coating exhibited good liquid repellency during water jetting and sandpaper abrasion tests. Furthermore, the coating has shown exceptional efficacy in terms of its ability to be anti-icing, anti-waxing, and self-cleaning.

Super-amphiphobic arabic gum-based coatings on textile for on-demand oily and dye wastewater treatment.

Different membrane materials have broadly been constructed for oil-containing water separation, but most of preparation routes involve corrosive or toxic chemicals and especially many materials have only single superwetting property. Herein, a novel and eco-friendly cellulose-based textile membrane is developed by incorporating the composite coating consisting of arabic gum (AG), attapulgite (APT), and iron (Fe) onto cellulose textiles. The functionalized textile is superoleophobic underwater and superhydrophobic underoil. As a result, the textile prewetted with water or oil can be employed to separate light oil layer/water and heavy oil layer/water mixtures, respectively, and the separation efficiency to the two types of mixtures is larger than 98.3 %. Results also reveal that the decorated textile possesses superior stability and recyclability in purifying oily wastewater. More importantly, such coated textile is capable of filtrating water-soluble contaminants (dyes) from polluted water. Due to the versatility and environmental compatibility of product as well as the accessibility as agricultural and forestry product as raw materials, the advanced textiles may offer effective solutions to oily wastewater purification and water-soluble contaminant removal.

Preparation of Hybrid Nanopigments with Excellent Environmental Stability, Antibacterial and Antioxidant Properties Based on Monascus Red and Sepiolite by One-Step Grinding Process.

This study is focused on the preparation, characterization, and multifunctional properties of intelligent hybrid nanopigments. The hybrid nanopigments with excellent environmental stability and antibacterial and antioxidant properties were fabricated based on natural Monascus red, surfactant, and sepiolite via a facile one-step grinding process. The density functional theory calculations demonstrated that the surfactants loaded on sepiolite were in favor of enhancing the electrostatic, coordination, and hydrogen bonding interactions between Monascus red and sepiolite. Thus, the obtained hybrid nanopigments exhibited excellent antibacterial and antioxidant properties, with an inhibition effect on Gram-positive bacteria that was superior to that of Gram-negative bacteria. In addition, the scavenging activity on DPPH and hydroxyl free radicals as well as the reducing power of hybrid nanopigments were higher than those of hybrid nanopigments prepared without the addition of the surfactant. Inspired by nature, gas-sensitive reversible alochroic superamphiphobic coatings with excellent thermal and chemical stability were successfully designed by combining hybrid nanopigments and fluorinated polysiloxane. Therefore, intelligent multifunctional hybrid nanopigments have great application foreground in related fields.

Performance of a superamphiphobic self-cleaning passive subambient daytime radiative cooling coating on grain and oil storage structures.

The thermal performance of a novel exterior coating material for commonly used grain and food-grain oil structures was investigated. Grain structures included a concrete squat silo and a concrete warehouse while the edible oil structure was a concrete sided tank. The exterior coating provided excellent moisture runoff and solar reflectance properties and is best described as a superamphiphobic self-cleaning passive subambient daytime radiative cooling (SSC-PSDRC) coating. The coating exhibited a remarkable subambient daytime cooling effect in various structures in different climatic regions. Compared with the roof surface temperatures of a cool white-coated concrete grain silo and a gray carbon iron-based edible oil storage tank, those of the PSDRC coated top surfaces could be reduced by 37 °C and 33 °C, respectively. The roof surface temperature of a warehouse painted with a cool-white coating-with a solar reflectance of 0.9 and an emissivity of 0.85-and that of a warehouse with the roof installed with aluminised polymer waterproof membranes were 19 °C and 18 °C higher than that of the PSDRC warehouse, respectively. Consequently, the interior temperature of the wheat pile in the PSDRC grain silo was 10 °C lower than that in the control squat silo. With the inner loop flow temperature control system operating, the interior air temperatures of the PSDRC west-facing separate space were 6 °C and 3 °C higher than those of the cool-white coated and control west-facing separate spaces, respectively. Even after the application of PSDRC coating for only a few days, the interior air temperature of the PSDRC oil storage tank was reduced by 38 °C, and the interior temperature of the oil storage tank was reduced by 4 °C. Furthermore, in practical applications, the coating showed impressive superamphiphobic self-cleaning capabilities and super aging resistance. The wide applications of the coating would have far-reaching, global implications for maintaining grain and edible oil products, particularly in the sub-tropical climates.

Facile Preparation of Robust Superamphiphobic Coatings on Complex Substrates via Nonsolvent-Induced Phase Separation.

Superamphiphobic surfaces have great potential in many fields but often suffer from complicated, expensive, and time-consuming preparation methods, difficulty in applying them on complex substrates, and low stability. Herein, we show a facile fabrication of robust superamphiphobic coatings on complex substrates. A stock suspension was prepared by nonsolvent-induced phase separation of a silicone-modified polyurethane (Si-PU) adhesive containing fluorinated silica (FD-silica) nanoparticles. Then, superamphiphobic surfaces could be easily fabricated via dip coating in the suspension. The influences of phase separation and Si-PU/FD-silica ratio on the wettability and morphology of the coatings were studied. The coatings feature a microscale dense and nanoscale rough texture due to phase separation and rapid solvent evaporation, which enhances the stability by forming strong linkages among the nanoparticles while achieving high superamphiphobicity by trapping air stably in the nanopores. Consequently, the coatings show excellent static/dynamic superamphiphobicity, superior impalement resistance, and good mechanical, chemical, thermal, and UV aging stability. Additionally, the coatings have good anti-icing performance as demonstrated by the greatly extended water freezing time and weakened ice adhesion force in both simulated and real conditions.

Enhancing the lifespan and durability of superamphiphobic surfaces for potential industrial applications: A review.

A superamphiphobic surface is a special wettability surface that repels liquids with lower surface tension than water. Superamphiphobic surface has a variety of applications, such as: self-cleaning, anticorrosion, electrical conductivity, flame retardant, flexible sensors, super-fast bubble bursting, droplet control. With the improvement of the theory of wettability, the superamphiphobic surface has developed rapidly recently. However, due to the problems of poor durability and short service life, the field of superamphiphobic has not been well promoted and applied in real life. These questions are also concerned by many researchers, and many related studies have been published in recent years. However, these studies lack logic and organization, and fail to obtain systematic induction and summary, which is not conducive to the follow-up research of subsequent researchers. Therefore, the main purpose of this review is to summarize and review the development, basic principles, preparation methods, durability characterization methods and applications of superamphiphobic surfaces, and the efforts made by researchers in recent years to enhance the durability of superamphiphobic surfaces. The main directions of durability enhancement are: structures, surface chemistry conditioning, adhesive, and versatile coating.

A Short Overview of Recent Developments in the Application of Polymeric Materials for the Conservation of Stone Cultural Heritage Elements.

Stones are ones of the most ancient natural materials exploited by humans, with different uses, from tools to buildings, that have endured over time in better conditions than other objects belonging to cultural heritage. Given the importance of those silent witnesses of our past, as well as our duty to preserve all parts of cultural heritage for future generations, much effort was put into the development of materials for their consolidation, protection, self-cleaning, or restoration. Protection of ancient stone monuments and objects has gained the interest of researchers in the last decades in the field of conservation of cultural heritage. In this respect, the present paper aims to be a critical discussion regarding potential polymeric materials, which can be used in restorative and conservative approaches for stone materials of cultural heritage importance, against physical degradation phenomena. Recent advances in this area are presented, as well as the current bottle-necks and future development perspectives.

Controlling supraparticle shape and structure by tuning colloidal interactions.

HYPOTHESIS: Assembly of colloids in drying colloidal suspensions on superhydrophobic surface is influenced by the colloidal interactions, which determine the shape and interior structure of the assembled supraparticle. The introduction of salt (electrolyte) into the assembly system is expected to influence the colloid interactions and packing during the evaporation process. Hence, both the outer shape and internal structure of supraparticles should be controlled by varying salt concentrations. EXPERIMENTS: Suspensions of electrostatically stabilized polystyrene particles with specified salt concentrations were chosen as model systems to conduct the evaporation on a superhydrophobic surface. A systematic study was performed by regulating the concentration and valency of salt. The morphology and interior of supraparticles were carefully characterized with electron scanning microscopy, while the colloidal interaction was established using colloidal probe atomic force microscopy. FINDINGS: Supraparticles displayed a spherical-to-nonspherical shape change due to the addition of salts. The extent of crystallization depended on salt concentration. These changes in shape and structure were correlated with salt-dependent single colloid interaction forces, which were not previously investigated in detail in radially symmetric evaporation geometry. Our findings are crucial for understanding assembly behavior during the drying process and offer guidance for preparing complex supraparticles to meet specific applications requirement.

Femtosecond Laser Regulated Ultrafast Growth of Mushroom-Like Architecture for Oil Repellency and Manipulation.

Natural organisms can create various microstructures via a spontaneous growth mode. In contrast, artificial protruding microstructures are constructed by subtractive methods that waste materials and time or by additive methods that require additional materials. Here, we report a facile and straightforward strategy for a laser-induced self-growing mushroom-like microstructure on a flat surface. By simply controlling the localized femtosecond laser heating and ablation on the poly(ethylene terephthalate) tape/heat-shrinkable polystyrene bilayer surface, it is discovered that a mushroom-like architecture can spontaneously and rapidly grow out from the original surface within 0.36 s. The dimension of the re-entrant micropillar array (cap diameter, pillar spacing, and height) can be accurately controlled through the intentional control of laser scanning. Followed by a fluorination and spray coating, the obtained surface can realize the repellency and manipulation of oil droplets. This work provides new opportunities in the fields of microfabrication, microfluidics, microreactor engineering, and wearable antifouling electronics.

Ultrafast Bubble Bursting by Superamphiphobic Coatings.

Controlling bubble motion or passively bursting bubbles using solid interfaces is advantageous in numerous industrial applications including flotation, catalysis, electrochemical processes, and microfluidics. Current research has explored the formation, dissolution, pinning, and rupturing of bubbles on different surfaces. However, the ability to tune and control the rate of bubble bursting is not yet achieved. Scaling down surface-induced bubble bursting to just a few milliseconds is important for any application. In this work, the hierarchical structure of superamphiphobic surfaces is tuned in order to rapidly rupture contacting bubbles. Surfaces prepared using liquid flame spray show ultrafast bubble bursting (down to 2 ms) and superior durability. The coatings demonstrate excellent mechanical and chemical stability even in the presence of surface-active species. Air from the ruptured bubble is absorbed into the aerophilic Cassie-state. Long-term applicability is demonstrated by preventing the accumulation of air in the plastron via a connection of the plastron to the environment. The times recorded for bubble rupture and complete reorganization of air are reduced by approximately a factor of 3 compared to previously reported values. The concept is utilized to passively control surfactant-rich foam in froth flotation. Material collection efficiency increased by more than 60 times compared to controls.

Improvement mechanism of NO photocatalytic degradation performance of self-cleaning synergistic photocatalytic coating under high humidity.

Photocatalytic coating has been widely studied as a promising material to remove air pollutants. However, the effectiveness and long-term effect of photocatalysis in high relative humidity environment is still the main challenge in this field. In this study, a fluorinated WO3-TiO2 nanorods/SiO2 epoxy photocatalytic superamphiphobic coating (FTSE coating) was prepared using a simple spraying method. The micromorphology and chemical composition of FTSE coating was characterized by SEM, EDS, FT-IR, XPS and TGA techniques. The advanced contact angle and hysteresis angle test show that the FTSE coating had excellent superamphiphobicity. The mechanical abrasions, corrosion resistance and UV aging tests show that the FTSE coating exhibited reasonable durability. Besides, the NO degradation efficiency of hydrophilic and superamphiphobic coatings with contact angles of 20.19°, 87.74°, 162.93° and 164.47° was tested in different humidity environment. The results showed that the superamphiphobic coating exhibited more superior photocatalytic degradation efficiency (84.02%) than the hydrophilic coating (51.38%) at a high relative humidity (RH=98%). Finally, FTSE coating exhibited prominent photocatalytic stability and the synergistic effect of photocatalysis and self-cleaning. After 30 d outdoor weathering test, the NO degradation efficiency decreased by 13.07% and recovered to the original level after flushing. The improvement mechanism of NO degradation performance was proposed based on the characteristics of superamphiphobic surface.

In Situ, One-Pot Method to Prepare Robust Superamphiphobic Cotton Fabrics for High Buoyancy and Good Antifouling.

Multifunctional superamphiphobic cotton fabrics are in high demand. However, preparation of such fabrics is often difficult or complicated. Herein, a novel superamphiphobic fabric is constructed by a simple one-pot method with an in situ growth process. Under suitable alkaline conditions, dopamine (DA) can be oxidized to benzoquinone. Meanwhile, 3-aminopropyltriethoxysilane (APTES), 1H,1H,2H,2H-perfluorodecyltriethoxysilane (FAS-17) molecules undergo the hydrolysis reaction and bond together. Besides, benzoquinone can react with APTES by Schiff base and hollow nanoclusters can be finally obtained because of the steric hindrance effect of benzene ring and long alkyl chain. Such nanoclusters are formed on the surface of fabric, which endows the fabric with extreme liquid repellence. The effects of pH value and DA concentration on the surface morphology and lyophobic properties of the fabric are systematically studied. The water and pump oil contact angles of the superamphiphobic fabric obtained under the optimal reaction conditions can reach 160 and 151°, respectively. The lyophobicity of the fabric is maintained even after undergoing various harsh tests, showing significant durability and stability. In addition, the superamphiphobic fabric exhibits good antifouling and strong buoyancy ability. The superamphiphobic fabric can load 35 and 27.4 times its own weight in water and oil, respectively, which shows great potential in the field of functional textiles such as swimming suits, protective clothing, and life jackets in the future.

Long-term corrosion protection for magnesium alloy by two-layer self-healing superamphiphobic coatings based on shape memory polymers and attapulgite.

Magnesium (Mg) alloy has wide potential applications due to its unique properties, but is apt to corrosion. Recently, superhydrophobic coatings are receiving great interest for corrosion protection of metals but suffer from short lifespan. Here, we report a strategy for long-term corrosion protection of Mg alloy by designing two-layer self-healing superamphiphobic coatings based on shape memory polymers (SMP) and attapulgite. The superamphiphobic coatings are composed of a bottom SMP coating containing a corrosion inhibitor (1, 2, 3-benzotriazole, BTA) and ceresine wax microparticles and a top superamphiphobic attapulgite coating. The two-layer self-healing coatings have excellent superamphiphobicity and initial anti-corrosion performance. The Mg alloy with the coatings can withstand immersion in 3.5 wt% NaCl solution for 80 days and neutral salt spray with 5 wt% NaCl for 54 days. Furthermore, the coatings show excellent self-healing capability towards various physical damages, such as 10 scratching/self-healing cycles at the same position, hexagonal star scratching and grid scratching. Moreover, the physically damaged coatings exhibit self-healing behavior of the microstructure and superhydrophobicity, driven by the shape memory effect of the bottom SMP layer. Thus, the self-healed coatings can still withstand 60 days of 3.5 wt% NaCl solution immersion and 30 days of 5 wt% NaCl salt spray. This study paves the way for applying super anti-wetting coatings for long-term corrosion protection of metals.

Polymeric Microparticles Generated via Confinement-Free Fluid Instability.

In-fiber fluid instability can be harnessed to realize scalable microparticles fabrication with tunable sizes and multifunctional characteristics making it competitive in comparison to conventional microparticles fabrication methods. However, since in-fiber fluid instability has to be induced via thermal annealing and the resulting microparticles can only be collected after dissolving the fiber cladding, obtaining contamination-free particles for high-temperature incompatible materials remains great challenge. Herein, confinement-free fluid instability is demonstrated to fabricate polymeric microparticles in a facile manner induced by the ultralow surface energy of the superamphiphobic surface. The polymer solution columns break up into uniform droplets then form spherical particles spontaneously in seconds at ambient temperature. This method can be applied to a variety of polymers spanning an exceptionally wide range of sizes: from 1 mm down to 1 µm. With the aid of microfluidic spinning instrument, a large quantity of microparticles can be obtained, making this method promising for scaling up production. Notably, through simple modification of the feed solution configuration, composite/structured micromaterials can also be produced, including quantum-dots-labeled fluorescent particles, magnetic particles, core-shell particles, microcapsules, and necklace-like microfibers. This method, with general applicability and facile control, is envisioned to have great prospects in the field of polymer microprocessing.

Randomly heterogeneous oleophobic/pH-responsive polymer coatings with reversible wettability transition for multifunctional fabrics and controllable oil-water separation.

Stimuli-responsive surfaces with wettability change between superhydrophilic and superhydrophobic are susceptible to oil contamination which often ruins the surface. Herein, a coating with pH-switchable wettability transition between superamphiphobic and superhydrophilic-superoleophobic is achieved by rationally designing oleophobic/pH-responsive polymer heterogeneous chemistry. Fabrics modified with this coating show repellency to both water and oils, while upon exposure to acidic water (pH = 1) the fabrics change to be superhydrophilic-superoleophobic within a short response time of <5 s. More importantly, the superamphiphobicity of the fabric can be restored under mild alkaline condition (pH = 10), and the transition is reversible for many cycles. The effective in situ or ex situ wettability change under acidic/alkaline water treatment makes the coated fabric capable of separating oil-water mixture or even some mixtures of immiscible organic solvents. In addition, the coated fabric is also demonstrated to be promising as a new class of functional fabrics that provide protection against water and many oils in one condition, and can change to be hygroscopic, anti-static, oil-repellent and anti-oil-fouling in the other condition for improved wear comfort and self-cleaning.

Photocatalytic Superamphiphobic Coatings and the Effect of Surface Microstructures on Superamphiphobicity.

In recent years, superamphiphobic coatings have been widely used in industrial transportation and environmental treatments because of their unique liquid repellency. In this study, WO3-TiO2 nanorods/SiO2 were used as the constructor of surface microstructures, and 1H,1H,2H,2H-perfluorodecyltriethoxysilane was used as the provider of low surface energy, and a photocatalytic superamphiphobic coating (FTS coating) was prepared. The microstructure and chemical composition of the coating was characterized by scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS), Fourier-transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), and thermogravimetric analysis (TGA). The coating exhibited excellent photocatalytic activity toward degradation methyl red and nitric oxide (NO), and the degradation efficiency to NO reached 47.8%. Also, the advanced contact angle and the hysteresis angle of water, glycol, glycerol, and olive oil was used to evaluate the superamphiphobicity. After 7 days of ultraviolet (UV) aging, five cycles of airbrush flushing and 48 h of immersion in acid, salt, and alkali solutions, the FTS coating still exhibits excellent amphiphobicity, which lays a foundation for its large-scale applications in the concrete exterior wall. The surface microstructure and the formation of air pockets are a prerequisite for superamphiphobicity, which promotes the liquid on the coating surface into the Cassie-Baxter state. Furthermore, the formation of air pockets is closely related to the gas adsorption capacity and the specific surface area (SBET) of the surface microstructure on the coating surface. The coatings with different SBET constructed and the advanced contact angle were measured. The influence of air pockets on the superamphiphobicity of coatings was studied in combination with the optical microscope. The understanding that SBET further influences superamphiphobicity by affecting the surface air pockets is proposed.

Fluorinated Carbon Nanotube Superamphiphobic Coating for High-Efficiency and Long-Lasting Underwater Antibiofouling Surfaces.

Biofilm formation on the surface of materials has brought great troubles to various industries. Designing surfaces with long-lasting antibiofouling properties can help restrain primary bacterial and protein attachment and subsequent biofilm formation for a long time, which is also of great significance for industrial applications. In this work, we successfully prepared fluorinated carbon nanotubes through a one-step fluorination method using fluorosilane and fabricated a superamphiphobic coating using a simple spray method. This coating with ultralow surface free energy and stable micro/nano structures achieved highly efficient and long-term underwater antibiofouling properties. Tea, milk, BSA, and bacterial solution can bounce highly on this surface without wetting the surface in air. The long-term existence of the underwater air-bubble layer on the surface of the superamphiphobic coating was observed. Thus, this surface can effectively resist BSA and bacterial attachment (E. coli), and the efficiency, respectively, reaches 97.5 and 98.2%. Even if it is fully soaked in BSA and BS solution for 120 h, the whole surface is still able to repel water, BSA, and BS solution very well. In addition, the coating possessed excellent wear resistance, the CAs of BSA and BS solution just decreased slightly (higher than 158°), and the sliding angles increased slightly (lower than 4°) after 50 tape abrasion cycles. Therefore, this superamphiphobic coating may have promising applications for marine devices, biomedical materials, protective clothing, and chemical shielding.

Effect of Silica Size and Content on Superamphiphobic Properties of Silica-Fluoropolymer Core-Shell Coatings.

We present a facile approach to fabricate superamphiphobic surfaces by spray coating silica-fluoropolymer core-shell particles without substrate pretreatment with an additional binder resin. A series of SiO2@poly(1H,1H,2H,2H-heptadecafluorodecyl methacrylate) (SiO2@PFMA) core-shell particles with core particles of different sizes were prepared via thiol-lactam initiated radical polymerization (TLIRP). The surface of each SiO2 particle with an average particle size of 12, 80, 150, and 350 nm was modified with (3-mercaptopropyl) trimethoxysilane and used as a seed for TLIRP. The SiO2@PFMA particles with various SiO2 sizes and contents were coated on aluminum substrates by a spray gun and then thermally treated to form a stable, rough composite layer. During the spray coating, the core-shell particles were aggregated by rapid evaporation of the solvent and then irregularly adhered to the substrate resulting in hierarchical structures. In the case of SiO2@PFMAs with low SiO2 contents, the roughness created mainly by the polymer shell disappeared during heat treatment. However, the substrates coated with SiO2@PFMAs with high SiO2 contents maintained the roughness even after heat treatment. The core-shell particles prepared with 12 nm SiO2 formed a stable superamphiphobic surface. The water/hexadecane contact and sliding angles on an aluminum plate coated with SiO2@PFMA, prepared using 12 nm silica at 46 wt% silica content (12 nm-SiO2(46)@PFMA), were 178.5°/159.2° and 1°/7°, respectively. The cross-cut tape test showed that adhesion between the 12nm-SiO2(46)@PFMA and the aluminum substrate was classified as 5B. A glass surface spray-coated with the core-shell composite particles exhibited transparent superhydrophobicity and translucent superamphiphobicity by controlling the concentration of the coating solution.

Novel Strategy To Prepare Hierarchically Porous Ceramic Microspheres via a Self-Assembly Method on Tunable Superamphiphobic Surfaces.

Porous ceramic microspheres have been widely used in many fields such as drug delivery, chemical catalysis, environmental protection, noise reduction by absorption, and separation and purification. However, the methodology to prepare porous ceramic microspheres based on traditional colloidal processing routes faces the problems of precise control of the diameter, degree of sphericity, uniformity of the microstructure (size, porosity, shape, etc.), and so forth. Herein, we propose a new methodology to prepare hierarchically porous ceramic microspheres with a mechanism based on the superwettability strategy without the requirement of any special equipment or complicated procedures. In such an approach, a ceramic emulsion with an extremely low viscosity was prepared by an emulsion-assisted self-assembly method, which would be repelled on the superamphiphobic surface to form a submillimeter-sized Al2O3 microsphere. Compared with the traditional colloidal processing approaches to prepare ceramic microspheres, the homogeneity and precision of the ceramic microspheres prepared via our approach are much finer, while our approach is quite simple, highly efficient, and cost-saving. Moreover, the diameter of the microspheres and the microstructure of the pores (size, density, porosity, etc.) in the ceramic microspheres could be flexibly manipulated. Our methodology has solved the key problems in the preparation of ceramic microspheres which have not been solved in the past decades and provided the solution for engineering through the delicate scientific design. We anticipate that this example of the combination of superwettability science with traditional structural ceramics could provide an important application direction of advanced techniques for fabricating ceramics.

A self-healing superamphiphobic coating for efficient corrosion protection of magnesium alloy.

Magnesium alloys have many excellent properties, but the poor corrosion resistance seriously hinders their widespread applications. Here, we report a self-healing superamphiphobic coating for efficient corrosion protection of magnesium alloy by the combination of a compact self-healing epoxy resin (SHEP) coating and a porous superamphiphobic coating. The coating shows (i) excellent superamphiphobicity with high contact angle, low sliding angle and robust impact/bounce behavior, (ii) excellent anti-corrosion performance as demonstrated by the potentiodynamic polarization curves and electrochemical impedance spectroscopy, and (iii) excellent self-healing performance as proved by the scanning electron microscopy and electrochemical impedance spectroscopy. This is owing to synergistic effect of the bi-layer structure. Furthermore, the healed coating retained excellent anti-corrosion performance according to the immersion test and neutral salt spray test. This is because the SHEP layer can effectively drive repair of microstructure of the superamphiphobic layer, and then recover of superamphiphobicity. Therefore, the contact area and contact time of corrosive solutions with the pristine and healed coatings are limited, which efficiently prevents diffusion of corrosive substances such as water, chloride ions and oxygen. The self-healing superamphiphobic coating may find applications in protection of various metal alloys.