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The biocompatibility and adaptability of hydrogels make them ideal candidates for use as artificial tendons and muscles in clinical applications, where both muscle-like strength and low hysteresis are essential. However, achieving a balance between a high strength and low hysteresis in hydrogels remains a significant challenge. Herein, we demonstrated a self-assembly process of heterogeneous hydrogels to meet the dilemma. And the hydrogels are composed of both hydrophilic and hydrophobic polymers. The hydrophilic network absorbs water, causing phase separation into a water-rich phase and a water-poor phase, while hydrophobic polymers and entanglement of the network arrest phase separation. Our results demonstrated that these hydrogels achieve remarkable mechanical properties, with a strength of 848.8 kPa, a low energy loss of 19.6 kJ/m 3 , and minimal hysteresis (0.046) during loading-unloading cycles. The reinforcing mechanisms underlying these properties are attributed to crystallization, molecular entanglement, and chain rearrangement induced by stretching. Furthermore, the combination of hydrophilic and hydrophobic networks is exceedingly rare in reported hydrogels.

Dew harvesting, minimally influenced by climate and geographical locations, is an ideal method for addressing water shortage problems. Superhydrophilic surfaces, characterized by their highest affinity for water, are particularly attractive for this purpose as they can attract more water molecules via condensation. However, a significant challenge arises from the high surface capillary force that impedes water from sliding down and being effectively collected. The resulting water film on the superhydrophilic surface tends to stay around the edge of the water collection surface, leading to evaporation loss and reduced collection efficacy. To overcome this problem, triangular patterns with low surface adhesion to water were introduced at the edge of superhydrophilic surfaces. This modification, achieved through a wet chemical method and masked oxygen plasma treatment, has significantly improved the efficiency of water collection. Results indicate that the hybrid surface reduced the time for the first water droplet to slide down by half and increased water collection efficiency by 78% compared to uniform superhydrophilic surfaces and by 536% compared to uniform superhydrophobic surfaces under a relative humidity of 55% with a temperature difference of 15 °C. The underlying principles were elucidated through computational simulations, and the mechanisms driving the enhancement in collection efficiency were explained.

Enhancing the hydrophilicity and UV protective property of poly(ethylene terephthalate) (PET) fabric are two significant ways to upgrade its quality and enlarge the applicable area. Biobased finishes are greatly welcomed for the fabrication of sustainable textiles; however, their application on PET fabric is still challenging compared with the case of natural fabric. This study presents a strategy that immobilizes epigallocatechin gallate (EGCG) onto PET fabric using citric acid (CA) for durably hydrophilic and UV-proof properties with negligible color change. A controllable surface-activating method integrating alkaline and deep eutectic solvent (DES) is customized for the PET fabric to promote the reactions among PET, CA, and EGCG. The hydrophilic, antistatic, and UV protective properties of functionalized PET fabric were explored. Results show that the hydrophilicity of the PET fabric after direct EGCG treatment increases but drops sharply after first-round washing due to weak interactions. The combined alkaline/DES pretreatment increases the number of hydrophilic groups and the roughness of PET fibers. After EGCG modification, the moisture regain (MR) of PET fabric increases from 0.41 to 0.64%. The contact angle and electrostatic charge half-life ( T 1/2 ) decreases from >120 to 23°, and from >60 to 0.13 s, respectively. The MR and T 1/2 are well retained after a 10-cycle washing. In addition, the UV protective factor of the PET fabric increases from 18 to 36. A very slight yellowing phenomenon occurs on the PET fabric after the treatment. In all, this research attempts to integrate a biobased finishing agent and an eco-friendly cross-linker on synthetic fiber for durable functions, which is transferrable to the sustainable fabrication of other polymeric materials such as fibers or films.

Radiative cooling fabrics have gained significant attention for their ability to enhance comfort without consuming extra energy. Nevertheless, sweat accumulation on the skin and diminishing cooling efficiency usually exist in the reported polymer cooling membranes. Herein, we report a universal method to obtain a calcium (Ca)-salt-enhanced fiber membrane with high infrared emission and hydrophilicity for efficient passive cooling and flame retardancy. The modification by Ca salts (including CaSiO 3 , CaSO 3 , and CaHPO 4 ) with strong infrared emission results in an improvement in hygrothermal management ability, especially for moisture absorption and perspiration regulation in hot and humid environments. As an example, the CaSiO 3 @PMMA fiber membrane exhibits exceptional reflectivity in the solar spectrum (∼94.5%), high emittance in the atmospheric window (∼96.7%), and superhydrophilicity with a contact angle of 31°. Under direct sunlight, the CaSiO 3 @PMMA membrane exhibits an obvious temperature drop of 11.7 °C and moisture management achieves an additional cooling of 8.9 °C, as further confirmed by the ability to reduce the rate of ice melting. Additionally, the composite membrane provides notable flame retardancy and UV resistance. This work paves a new path in developing new materials with perspiration management and flame retardancy for zero energy consumption cooling in hot and humid environments.

It is imperative to induce hydrophilicity in intrinsically hydrophobic carbon nanotubes (CNTs) without losing their superior properties for applications that specifically deal with aqueous media. A method for transforming a CNTs sheet from hydrophobic to hydrophilic by treatment with N -methyl-2-pyrrolidone (NMP) is explored. The NMP-treated CNT sheets are assessed based on complementing characterization, and it is concluded that the binding of NMP to a CNTs surface is through noncovalent interaction without the incorporation of defects in CNTs. The induced hydrophilicity in the CNTs sheet is stable for water exposure over a longer duration while it displays a semireversible nature upon heat treatment. The mechanical and electrical properties of the NMP-treated CNTs sheet revealed enhancement in the tensile strength from 221 to 421 MPa while maintaining a good electrical conductivity of ∼1.22 × 10 4 S/m because of the improved interfacial properties. The hydrophilic CNTs exhibited excellent adsorption capacity for methylene blue dye. The NMP-treated CNTs sheets demonstrated their suitability in flexible hybrid supercapacitor (FHSC) devices with improved electrochemical performance with enhancement in the capacitance from 5.4 to 7.6 F/g and a decrease in the equivalent series resistance from 53 to 34 Ω compared to pristine CNTs-based devices. These solid-state FHSC devices displayed excellent cyclic charge-discharge performance along with robust behavior over thousands of bending cycles without significant performance degradation. The excellent dye removal capability and superior electrochemical performance of the NMP-treated CNTs sheet is a consequence of their improved interface with aqueous media, which is governed by the hydrophilic nature of the CNTs sheet.

Increased particulate matter (PM) concentrations in our ambient air are the cause of various life-threatening diseases and consequently need to be reduced to nonhazardous levels. The natural PM removal capabilities of leaves inspired the development of a low-cost coating technology that exploits natural weather phenomena for its PM catching and removal processes. The herein presented coating is based on microparticle-filled silicone with optimized chemical and physical surface properties. Its surface roughness was tuned using differently sized spray-dried particles, and its surface contact angle was adjusted through silicone tensides, polar ether groups incorporated in the silicon backbone, and the used amount of spray-dried particles. In such a way, optimized silicone coatings showed in laboratory experiments improved catching abilities (>300% relative to glass surfaces), a full retention of adsorbed PM during wind events, and the formation of large PM aggregates. Upon (simulated) rain events, these coatings were regenerated, and the content of harmful PM of various sizes dispersed in water was reduced between ∼73 and 100%. Furthermore, an outdoor test over 100 days showed the functioning of the coating under real-world conditions. These regenerative coatings are readily applicable on diverse surfaces and do not require any further technical infrastructure. Thus, they present an extension of the toolbox for PM reduction technologies.

Developing effective synthetic strategies as well as broadening functionalities for zwitterionic materials that comprise moieties with equimolar cationic and anionic groups still remains a huge challenge. Herein, we develop two zwitterionic vinylene-linked covalent organic frameworks (Zi-VCOF-1 and Zi-VCOF-2) that are a type of novel hydrophilic material. Zi-VCOF-1 and Zi-VCOF-2 are obtained directly through the convenient Knoevenagel condensation of new sulfonic-pyridinium zwitterionic monomers with aromatic aldehyde derivatives. This is the first report on zwitterionic COFs being constructed by the bottom-up functionalization approach from predesigned zwitterionic monomers. Both Zi-VCOFs exhibit a high photocatalytic hydrogen evolution rate (HER) because of their appropriate optical property and outstanding hydrophilicity. Specifically, Zi-VCOF-1 and Zi-VCOF-2 show photocatalytic HER of 13,547 and 5057 μmol h -1 g -1 , respectively. Interestingly, the photocatalytic HER of Zi-VCOF-1 is about 2.68 times of that of Zi-VCOF-2, although they differ by only one methyl group in sulfonic-pyridinium zwitterionic pairs. The photocatalytic HER of Zi-VCOF-1 is not only the highest in the vinylene-linked COFs but also outstanding among the most reported COFs. This is the first application of zwitterionic COFs for photocatalytic hydrogen evolution, which would open a new frontier in zwitterionic COFs and be helpful for the design of other photocatalytic materials.

β-Alkoxyalcohols generated from epoxide ring-opening reactions are significant due to their enormous value as pharmaceutical intermediates and fine chemicals. Using a phenyl-substituted double-decker-type silsesquioxane as the precursor, a hybrid porous material (PCS-DDSQ) was synthesized through a Scholl coupling reaction with an AlCl 3 catalyst. Then, novel excellent Brønsted acid-derived silsesquioxane solid catalysts (PCS-DDSQ-SO 3 H- x ) were successfully obtained through an electrophilic aromatic substitution reaction of chlorosulfonic acid on phenyl rings of PCS-DDSQ, fully characterized by Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, energy-dispersive X-ray spectroscopy, powder X-ray diffraction, temperature-programmed desorption, water contact angle, Brunauer-Emmett-Teller model, thermogravimetric analysis, and solid-state 13 C and 29 Si nuclear magnetic resonance techniques. The catalytic behavior of the PCS-DDSQ-SO 3 H- x with different SO 3 H loadings for the methanolysis of styrene oxide was compared and evaluated. The presence of SO 3 H groups endows them with excellent catalytic abilities, achieving the highest values from PCS-DDSQ-SO 3 H-1 (the acid site of its catalyst is 1.84 mmol/g) as 99% conversion and 100% selectivity for the methanolysis of styrene oxide in 30 min, which shows superior catalytic properties of low dosage and high efficiency. Furthermore, the PCS-DDSQ-SO 3 H-1 catalyst can maintain high activity and selectivity after three cycles. This study provides a feasible method for the preparation of Brønsted solid acid catalysts with different acid loadings by introducing the sulfonic group into PCS-DDSQ.

In the last few decades, numerous studies have focused on designing suitable hydrophilic materials to inhibit surface-induced fog or frost under extreme conditions. As fogging and condensation frosting on a film involves molecular interaction with water prior to forming discrete droplets on the surface, it is essential to control the extent of a film to strongly bind with water molecules for antifogging coatings. While the water contact angle measurement is commonly used to probe the hydrophilicity of a film, it oftentimes fails to predict the antifogging and antifrosting performance as this value only reflects the wettability of a given surface to water droplet. In this work, a polysaccharide-based film composed of chitosan (CHI) and carboxymethyl cellulose (CMC) is used as the model system and oligo(ethylene glycol) (OEG) moieties are additionally introduced to study the effect of OEG moieties on antifogging and condensation frosting. We show that the film containing OEG-grafted CHI exhibits excellent frost-resistant capability due to the OEG moieties in the film that serve as active sites for water molecules to strongly interact in a nonfreezable state.

The crystalline porous organic framework offers a highly ordered and stable structure under hydrated conditions at high temperatures. Here, we demonstrated a method for preparing high-performance membrane buildup using "heterogeneous networks" and "polymer phase-separated nanochannels". A well-interconnected "nanochannel" with a "crystalline organic framework" forms a highly stable hybrid membrane above 80 °C under 100% hydration under acidic and basic conditions. The prepared structure provides a self-standing membrane that easily overcomes the problem faced by conventional high ion-exchange capacity (IEC)-based membranes such as swelling, gelling, fragility, and dissolving at elevated temperatures. Apart from structural stability, it also shows better chemical stability with enhanced proton conduction at elevated temperatures. This proton conduction with better structural stability in the high IEC sample confirms from thermal analysis, whereas it also offers relatively low in-plane membrane swelling as compared to the conventional membranes. These hybrid membranes were further combined with the FAA-3 membrane to manufacture a reverse electrodialysis system for generating a power output. We also evaluated the maximum power density ( P max ) of the stack theoretically and experimentally. The determined net power density ( P net ) is reported to be 0.45 W m -2 at a flow rate of 40 mL min -1 . These results confirm that the developed membrane can withstand robustly under realistic ambient conditions maintaining stable cell performance.

Herein, we successfully synthesized high-quality Hf-ZnO thin films with various Hf contents (0, 3, 6, 9, 12, and 15 at. %), which showed both superhydrophilic (6% Hf-ZnO) and ultrahydrophobic (15% Hf-ZnO) wetting behavior. Different characterization methods were opted to recognize the structural (XRD, SEM, AFM) and defect properties (XPS) of the pristine and doped materials, to understand the mechanisms underlying the tuning of wetting behavior (contact angle). Hafnium doping plays a noteworthy role in tuning the morphology of the ZnO nanostructures, roughness of the material surface, generation of defects, Lewis acid-base interactions, and wettability properties. We achieved a superhydrophilic surface with 6% Hf-ZnO owing to a smooth surface, less basicity, and maximum concentration of oxygen vacancies, and also an ultrahydrophobic surface with 15% Hf-ZnO because of the rough surface, high basicity, and minimum concentration of oxygen vacancies. The as prepared Hf-ZnO samples showed stable performance (stability, wearability, weatherability, and antifouling) under real-life conditions marking them multifunctional and biosafe material to be effectively used in solar and building's window. A wetting mechanism was established to relate the wetting behavior of the samples to oxygen vacancies (active sites for water dissociation: resulted due to charge mismatch of host cation (Zn 2+ ) by the doped cation (Hf 4+ )), roughness (smooth surface (Wenzel) with minimum R (0.588) portraying hydrophilic property and rough caltropic surface (Cassie-Baxter) with maximum rms (0.588) portraying hydrophilic property and rough caltropic surface (Cassie-Baxter) with maximum R rms (2.522) portraying hydrophobic property), basicity (H 2 O: Lewis Base; ZnO: Lewis acid; HfO 2 : Lewis base) and morphology (tube-like structure (0-6% Hf-ZnO) and caltrop-like structure (12-15% Hf-ZnO)).

The development and application of natural antibacterial materials have always been the focus of biomedical research. Borneol as a natural antibacterial compound has received extensive attention. However, the hydrophobicity caused by its unique structure limits its application range to a certain extent. In this study, we combine zwitterionic 2-methacryloyloxyethyl phosphorylcholine (MPC) with a complex bicyclic monoterpene structure borneol compound and prepare an excellent antifouling and antibacterial surface via the Schiff-base bond. The prepared coating has excellent hydrophilicity verified by the contact angle (CA), and its polymer layer is confirmed by X-ray photoelectron spectroscopy (XPS). The zwitterion MPC and borneol moieties in the copolymer play a coordinating role, relying on super hydration and the special stereochemical structure to prevent protein adsorption and inhibit bacterial adhesion, respectively, which are demonstrated by bovine serum albumin (BSA) adsorption and antibacterial activity test. Moreover, the water-soluble borneol derivative as the antibacterial surfaces we designed here was biocompatible toward MRC-5 (lung fibroblasts), as showed by in vitro cytotoxicity assays. Such results indicate the potential application of the as-prepared hydrophilic surfaces in the biomedical materials.

Development of a robust self-cleaning oil-repellent surface in a cost-efficient and green manner is highly desirable, yet still difficult to realize. Herein, we develop a poly(vinyl alcohol) (denoted as PVA) composite hydrogel on which the oily contaminations can be removed efficiently by water merely. Owing to its high affinity to water and resistance to oils, the water-wetted hydrogel establishes a slippery oil-repellent state in air, displays underwater superoleophobicity with ultralow adhesion to all probe oils, and blocks oil from permeating when immersed into an oil surrounding. Oily contaminations on the PVA hydrogel surface are removed just by titling or water immersion, with no oil residue left behind. This enhanced oil repellency was retained after hand-bending, water-jetting, and even 1000 cycles of sand abrasion, demonstrating mechanical robustness. Application of the PVA hydrogel-coated copper mesh is demonstrated to separate oil/water and oil/oil mixtures, with separation efficiency being greater than 98%.

This work provides a simple method to prepare a hydrophilic/oleophobic coating using polyester filter cloth as the substrate, a mixture of three hydrophilic polymers (poly(aspartic acid), poly(acrylic acid), and poly(vinyl alcohol)); SiO 2 with an average particle size of 30 nm is used to improve the surface roughness of the filter cloth. Then, a long fluorocarbon chain of 1 H ,1 H ,2 H ,2 H -perfluorooctyltriethoxysilane is grafted onto the surface by a vacuum silanization coupling reaction to obtain hydrophilic/oleophobic properties. The water and hexadecane contact angles of the treated filter cloth are 3 and 99.8°, respectively. A separation efficiency of 98% was achieved in hexadecane/water separation. The durability test shows that the separation efficiency of toward hexadecane-water mixture remains more than 98% after 20 cycles. The obtained material also presents a strong underwater antipollution property when using hexane, rapeseed oil, mineral oil, and pump oil as model pollutants. For oils with higher viscosity, the separation efficiency remains above 97%. However, the separation efficiency is ∼80% when treating emulsions.

Hydrogels, as a representative of soft and biocompatible materials, have been widely used in biosensors, biomedical devices, soft robotics, and the marine industry. However, the ir-recoverability of hydrogels after dehydration, which causes the loss of original mechanical, optical, and wetting properties, has severely restricted their practical applications. At present, this critical challenge of maintaining hydrogels' accurate character has attracted less attention. To address this, here we report a hydrogel based on synergistic effects to achieve both well-regulated rehydration and deswelling properties. The hydrogel after dehydration can quickly restore its original state both on the macro- and microscale. In addition, the hydrogel has excellent mechanical stability after several dehydration-rehydration cycles. All of these properties offer a possibility of water condition endurance and increase the service life. The robust property is attributed to the hydrophilic-hydrophobic and ionic interactions induced by the synergy of hydrophilic/oleophilic heteronetworks. Moreover, zwitterionic segments as hydrophilic network play a vital role in fabricating anti-biofouling hydrogels. The durable and reusable hydrogel may have promising applications for biomedical materials, flexible devices, and the marine industry.

Although graphitic carbon nitride (g-C 3 N 4 ) has been identified as a promising photocatalyst, pristine g-C 3 N 4 has a limited light absorption, insolubility, small specific surface area, and rapid electron-hole pair recombination. In this study, hydroxyl-grafted oxygen-linked tri-s-triazine-based polymer (HGONTP) is achieved through the polycondensation of hydrothermally pretreated dicyandiamide (DCDA). The content of C-O-C linkers and terminal OH groups in HGONTP can be regulated by the cyclization and hydrolysis degrees of DCDA through the replacement of the pendant NH 2 groups with OH groups. The HGONTP photocatalyst exhibits an outstanding light absorption from UV to near-IR, possessing a narrow band gap of 2.18 eV, a hydrophilic surface, a large specific surface area of 96.1 m 2 g -1 , and reduced charge recombination. As a result, HGONTP exhibits a hydrogen evolution rate 27.7-fold higher than that for pristine g-C 3 N 4 (6.54 vs 0.236 mmol g -1 h -1 ). The apparent quantum yield reaches 12.6% at 420 nm and 4.1% at 500 nm. In addition, the photocatalytic conversion efficiency of CO 2 to CO reaches as high as 3.3 μmol g -1 h -1 without cocatalysts and sacrificial agents. The selectivity of CO 2 to CO achieves 88.4%. The proposed strategy paves a new avenue to design high-performance polymeric photocatalysts used in water.

Sponges based on short electrospun fibers have received significant attention due to their ultrahigh porosity, lightweight, and multifunctional characteristics. In particular, polyimide (PI) sponges have been researched due to their exceptional mechanical properties and thermal stability. Nevertheless, a number of sponges, including PI, are usually hydrophobic and synthesized in toxic, nonwater solvents (e.g., 1,4-dioxane). Conversely, hydrophilic sponges disintegrate upon contact with water. Here, we suggest a new strategy to fabricate PI sponges in water by introducing a suitable surfactant, sodium dodecylbenzenesulfonate (SDBS) (sPI sponges). With less than 1 wt % of SDBS with respect to PI short fibers, they can be homogeneously dispersed in water and mixed well with poly(amic acid) (PAA) solution. The synthesized sponge, depending on the concentration of SDBS, showed hydrophilic properties and substantial water uptake above 5000%. The hydrophilic properties of the sponges, which are not common, and the preparation from aqueous solution introduce new research opportunities. Such hydrophilic sponges are particularly special because they do not swell in contact with water, which makes them dimensionally stable. The methods presented here can serve as a milestone for the future development of various kinds of hydrophilic sponges applied for various applications, ranging from tissue engineering to oil/water separation.

Water is the basis of life in the world. Unfortunately, resources are shrinking at an alarming rate. The lack of access to water is still the biggest problem in the modern world. The key to solving it is to find new unconventional ways to obtain water from alternative sources. Fog collectors are becoming an increasingly important way of water harvesting as there are places in the world where fog is the only source of water. Our aim is to apply electrospun fiber technology, due to its high surface area, to increase fog collection efficiency. Therefore, composites consisting of hydrophobic and hydrophilic fibers were successfully fabricated using a two-nozzle electrospinning setup. This design enables the realization of optimal meshes for harvesting water from fog. In our studies we focused on combining hydrophobic polystyrene (PS) and hydrophilic polyamide 6 (PA6), surface properties in the produced meshes, without any chemical modifications, on the basis of new hierarchical composites for collecting water. This combination of hydrophobic and hydrophilic materials causes water to condense on the hydrophobic microfibers and to run down on the hydrophilic nanofibers. By adjusting the fraction of PA6 nanofibers, we were able to tune the mechanical properties of PS meshes and importantly increase the efficiency in collecting water. We combined a few characterization methods together with novel image processing protocols for the analysis of fiber fractions in the constructed meshes. The obtained results show a new single-step method to produce meshes with enhanced mechanical properties and water collecting abilities that can be applied in existing fog water collectors. This is a new promising design for fog collectors with nano- and macrofibers which are able to efficiently harvest water, showing great application in comparison to commercially available standard meshes.

The microdroplets in fog flow have been considered as an important resource for supplying fresh drinking water. Most of the reported works of fog collection focus on the water-collecting ability rather than the environmental reliability of selected materials. In this work, a beetle-inspired hierarchical fog-collecting interface based on the antibacterial needle-array (ABN) and hydrophilic/hydrophobic cooperative structure is displayed. The hydrophilic ABN is coated with zwitterionic carboxybetaine (CB) brushes that endow the fog collector with a long-term cleaning in harsh environment. Due to its strong affinity to water molecules, the tilted needles with a CB coating can facilitate the capture of fog and the rapid delivery of condensed water driven by gravity. After being transported to the connected hydrophobic sheet, the collected droplets can be rapidly detached and stored in the container, achieving a high fog-harvesting rate. Furthermore, CB-patterned channels are integrated on the hydrophobic sheet for the pathway-controlled water delivery. The CB coating is able to efficiently resist bacterial adhesion and contamination during fog harvesting, protecting the device from microbiological corrosion. The current design provides a promising method to incorporate antibacterial ability into fog collectors, which offer great opportunity to develop water harvesters for real-world applications.

Although there are plenty of merits for lithium-sulfur (Li-S) batteries, their undesired shuttle effect and insulated nature are hindering the practical applications. Here, a conductive metal-organic framework (MOF)-modified separator has been designed and fabricated through a facile filtration method to address the issues. Specifically, its intrinsic microporous structure, hydrophilic polar property, and conductive feature could make it easy to contact with and trap polysulfides and boost the kinetics of electrochemical reactions. Both the physical and chemical properties of the as-prepared separator are beneficial to alleviating the shuttle effect and enhancing the rate capability. Accordingly, the electrochemical performance of the battery with a MOF-modified separator was significantly improved.

Rooftop solar thermal collectors have the potential to meet residential heating demands if deployed efficiently at low solar irradiance (i.e., 1 sun). The efficiency of solar thermal collectors depends on their ability to absorb incoming solar energy and minimize thermal losses. Most techniques utilize a vacuum gap between the solar absorber and the surroundings to eliminate conduction and convection losses, in combination with surface coatings to minimize reradiation losses. Here, we present an alternative approach that operates at atmospheric pressure with simple, black, absorbing surfaces. Silica based aerogels coated on black surfaces have the potential to act as simple and inexpensive solar thermal collectors because of their high transmission to solar radiation and low transmission to thermal radiation. To demonstrate their heat-trapping properties, we fabricated tetramethyl orthosilicate-based silica aerogels. A hydrophilic aerogel with a thickness of 1 cm exhibited a solar-averaged transmission of 76% and thermally averaged transmission of ≈1% (at 100 °C). To minimize unwanted solar absorption by O-H groups, we functionalized the aerogel to be hydrophobic, resulting in a solar-averaged transmission of 88%. To provide a deeper understanding of the link between aerogel properties and overall efficiency, we developed a coupled radiative-conductive heat transfer model and used it to predict solar thermal performance. Instantaneous solar thermal efficiencies approaching 55% at 1 sun and 80 °C were predicted. This study sheds light on the applicability of silica aerogels on black coatings for solar thermal collectors and offers design priorities for next-generation solar thermal aerogels.

Liquid jet impingement on porous materials is particularly important in many applications of heat transfer, filtration, or in incontinence products. Generally, it is desired that the liquid not penetrate the substrate at or near the point of jet impact, but rather be distributed over a wider area before reaching the back side. A facile wettability-patterning technique is presented, whereby a water jet impinging orthogonally on a wettability-patterned nonwoven substrate is distributed on the top surface and through the porous matrix, and ultimately dispensed from prespecified points underneath the sample. A systematic approach is adopted to identify the optimum design that allows for a uniform distribution of the liquid on horizontally mounted substrates of ∼50 cm 2 area, with minimal or no spilling over the sample edges at jet flow rates exceeding 1 L/min. The effect of the location of jet impingement on liquid distribution is also studied, and the design is observed to perform well even under offset jet impact conditions.

Carbon Nanomaterials are excellent electrode materials due to their extraordinary conductivity, prolific structures, and morphologies. Herein, a novel nanocarbon-based material (Au@NCNC) was synthesized by embedding gold nanoparticles (AuNPs) inside the pores of three-dimensional hierarchical nitrogen-doped carbon nanocages (NCNC) through an in situ chemical deposition method. The resultant Au@NCNC was employed as an electrochemical catalyst for the oxygen reduction reaction (ORR) and as an electrode material for supercapacitors. The conductivity and hydrophilicity of Au@NCNC were much more improved than those of pristine NCNC. Meanwhile, the bubble adhesive force on the Au@NCNC film was much lower underwater than that of NCNC, which provided easy accessibility to the active sites of reactants, such as hydrated O 2 . Therefore, the deposition of AuNPs inside pores of NCNC facilitated the transfer of electrons and diffusion of ions, promoting the electrocatalytic performance of Au@NCNC. As a result, Au@NCNC exhibited high performance toward ORR, which manifested in high numbers of electron transfer (3.7-3.9), high kinetic current density, enhanced electrocatalytic stability, and remarkable methanol durability. Moreover, Au@NCNC displayed high specific capacitance, good rate capability, and cycling stability with ∼97% of its initial capacitance retained at the high current density of 10 A g -1 after 5000 cycles. This could be attributed to the synergetic effect of ultrafine gold nanoparticles, the hierarchical porous structure, and the hydrophilic surface of NCNC as well. This work offers an excellent alternative for Pt-based catalysts in fuel cells, ORR, and supercapacitive electrode materials by enhancing the conductivity and surface hydrophilicity of electrocatalysts.

The growing need to develop surfaces able to effectively resist biological fouling has resulted in the widespread investigation of nanomaterials with potential antifouling properties. However, the preparation of effective antifouling coatings is limited by the availability of reactive surface functional groups and our ability to carefully control and organize chemistries at a materials' interface. Here, we present two methods of preparing hydrophilic low-fouling surface coatings through reaction of silica-nanoparticle suspensions and predeposited silica-nanoparticle films with zwitterionic sulfobetaine (SB). Silica-nanoparticle suspensions were functionalized with SB across three pH conditions and deposited as thin films via a simple spin-coating process to generate hydrophilic antifouling coatings. In addition, coatings of predeposited silica nanoparticles were surface functionalized via exposure to zwitterionic solutions. Quartz crystal microgravimetry with dissipation monitoring was employed as a high throughput technique for monitoring and optimizing reaction to the silica-nanoparticle surfaces. Functionalization of nanoparticle films was rapid and could be achieved over a wide pH range and at low zwitterion concentrations. All functionalized particle surfaces presented a high degree of wettability and resulted in large reductions in adsorption of bovine serum albumin protein. Particle coatings also showed a reduction in adhesion of fungal spores (Epicoccum nigrum) and bacteria (Escherichia coli) by up to 87 and 96%, respectively. These results indicate the potential for functionalized nanosilicas to be further developed as versatile fouling-resistant coatings for widespread coating applications.

Strong, reversible underwater adhesion using gecko-inspired surfaces is achievable through the use of a hydrophobic structural material and does not require surface modification or suction cup effects for this adhesion to be effective. Increased surface energy can aid in dry adhesion in an air environment but strongly degrades wet adhesion via reduction of interfacial energy underwater. A direct comparison of structurally identical but chemically different mushroom shaped fibers shows that strong, reversible adhesion, even in a fully wetted, stable state, is feasible underwater if the structural material of the fibers is hydrophobic and the mating surface is not strongly hydrophilic. The exact adhesion strength will be a function of the underwater interfacial energy between surfaces and the specific failure modes of individual fibers. This underwater adhesion has been calculated to be potentially greater than the dry adhesion for specific combinations of hydrophobic surfaces.

A robust and simple method is provided to fabricate Janus polymer/carbon nanotube (CNT) hybrid membranes for oil/water separation. Starting from CNT membranes formed by dispensing, hydrophobic poly(styrene) (PS) and hydrophilic poly(N,N-dimethylaminoethyl methacrylate) (PDMAEMA) were grated from different sides of the photoactive CNT membranes via self-initiated photografting and photopolymerization (SIPGP) to achieve Janus polymer/CNTs hybrid membranes. The obtained membranes have excellent oil/water selectivity in the removal of oil from water. Moreover, they can effectively separate both surfactant-stabilized oil-in-water and water-in-oil emulsions because of the anisotropic wettability of the membranes.