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Wetting phenomena have been widely observed in our daily lives, such as dew on lotus leaf, and applied in technical applications, e.g., ink-jet printing. In contrast to constant liquid–solid and solid–gas interfacial tensions in Young's law, we here focus on the wetting phenomena by considering varying fluid–solid interfacial tensions. We analyze the energy landscape, the map of Young's contact angle, the number and corresponding contact angle of local energy minima, and the contact angle hysteresis for a liquid droplet on a solid substrate in a gas phase. In addition, a gas bubble on a solid substrate in a liquid phase has been scrutinized from the aspect of surface energy minimization. The wetting effect has been regarded, where the liquid and gas species penetrate into the solid phase on the microscopic scale [F. Wang and B. Nestler, Phys. Rev. Lett. 132, 126202 (2024)]. We assume the liquid–solid and the solid–gas interfacial tensions to be a function dependent on the volume fraction of the liquid and the gas species and investigate the impact of the size ratio of the droplet to the solid surface that is overlooked in existing theories on the wetting phenomena. Our finding sheds light on the microscopic origin of the contact angle hysteresis and the droplet size effect on the wetting phenomena. [ABSTRACT FROM AUTHOR]

We demonstrate the change of the sign from negative to positive of the self-powered photovoltaic photocurrent in core–shell n-InGaN/p-GaN nanowire heterojunctions within the visible to UV wavelength range. Such dual-polarity photodetectors are of broad interest to provide extended functionalities for optoelectronic devices, starting with dual-wavelength photodetectors. The physics of the photocurrent sign reversal is understood by a well-balanced selective absorption and photocarrier generation, photocarrier transfer, and thermal excitation paths in the core–shell n-InGaN/p-GaN nanowire functional absorber with different bandgap energies and opposite inner- and surface energy band bendings. The basic dual-wavelength photodetector operation parameters are given. [ABSTRACT FROM AUTHOR]

The design of heterogeneous catalysts generally involves optimizing the reactivity descriptor of adsorption energy, which is inevitably governed by the structure of surface-active sites. A prerequisite for understanding the structure–properties relationship is the precise identification of real surface-active site structures, rather than relying on conceived structures derived from bulk alloy properties. However, it remains a formidable challenge due to the dynamic nature of nanoalloys during catalytic reactions and the lack of accurate and efficient interatomic potentials for simulations. Herein, a generalizable deep-learning potential for the Ag–Pd–F system is developed based on a dataset encompassing the bulk, surface, nanocluster, amorphous, and point defected configurations with diverse compositions to achieve a comprehensive description of interatomic interactions, facilitating precise prediction of adsorption energy, surface energy, formation energy, and diffusion energy barrier and is utilized to investigate the structural evolutions of AgPd nanoalloys during fluorination. The structural evolutions involve the inward diffusion of F, the outward diffusion of Ag in Ag@Pd nanoalloys, the formation of surface AgFx species in mixed and Janus AgPd nanoalloys, and the shape deformation from cuboctahedron to sphere in Ag and Pd@Ag nanoalloys. Moreover, the effects of atomic diffusion and dislocation formation and migration on the reconstructing pathway of nanoalloys are highlighted. It is demonstrated that the stress relaxation upon F adsorption serves as the intrinsic driving factor governing the surface reconstruction of AgPd nanoalloys. [ABSTRACT FROM AUTHOR]

The preparation of rigid polyurethane foam with uniform pore size is extremely challenging. In this work, double-effect baking powder was used as foaming agent, and rigid polyurethane foam with regular morphology was successfully prepared through semi-prepolymerization. The rigid polyurethane foam apertures with regular morphology were controlled by the secondary release of C[O.sub.2] when the content of baking powder is 0.30 part. Combined with theoretical calculation and experimental test, it is found that the particle size distribution, wall thickness, and hole shape are uniform, regular, thin, polygonal, and few broken holes. The compression strength, contact angle, and surface energy of the rigid polyurethane foam are 33.36 kPa, 109.6[degrees], and 21.8 mJ/[m.sup.2] after adding 0.20 part of double-effect baking powder, respectively. By adjusting the amount of double-acting baking powder, the porosity, mechanical properties and foam rate of the polyurethane foams could be significantly improved. Due to the molecular solvation effect, rigid polyurethane foams will deform in the water and oil due phase, but it can remain stable for a long time at room temperature without solvent. It provides a new method for the preparation of rigid polyurethane foam, which is expected to be widely used in transportation and other fields. Highlights * Baking powder was firstly used as a foaming modifier for rigid polyurethane. * Baking powder releases C[O.sub.2] twice to ensure uniform structure of polyurethane cell. * Rigid polyurethane foam has long-term stability and regular, uniform cell holes. * The porosity and mechanical properties of foams could be significantly improved. * Foaming mechanism of rigid polyurethane using baking powder was firstly revealed. KEYWORDS blowing agent, foam, mechanical properties, microstructure, polyurethane, 1 | INTRODUCTION With the rapid development of the transportation and logistics industry, there is an increasing demand for high-performance materials, particularly in enhancing fuel efficiency, safety, and passenger comfort. [...]

Polymers are known to wet nanopores with high surface energy through an atomically thin precursor film followed by slower capillary filling. We present here light interference spectroscopy using a mesoporous membrane-based chip that allows us to observe the dynamics of these phenomena in situ down to the sub-nanometer scale at milli- to microsecond temporal resolution. The device consists of a mesoporous silicon film (average pore size 6 nm) with an integrated photonic crystal, which permits to simultaneously measure the phase shift of thin film interference and the resonance of the photonic crystal upon imbibition. For a styrene dimer, we find a flat fluid front without a precursor film, while the pentamer forms an expanding molecular thin film moving in front of the menisci of the capillary filling. These different behaviors are attributed to a significantly faster pore-surface diffusion compared to the imbibition dynamics for the pentamer and vice versa for the dimer. In addition, both oligomers exhibit anomalously slow imbibition dynamics, which could be explained by apparent viscosities of six and eleven times the bulk value, respectively. However, a more consistent description of the dynamics is achieved by a constriction model that emphasizes the increasing importance of local undulations in the pore radius with the molecular size and includes a sub-nanometer hydrodynamic dead, immobile zone at the pore wall but otherwise uses bulk fluid parameters. Overall, our study illustrates that interferometric, opto-fluidic experiments with mesoporous media allow for a remarkably detailed exploration of the nano-rheology of polymeric liquids. [ABSTRACT FROM AUTHOR]

We present a robust strategy to numerically sample the Coulomb potential in reciprocal space for periodic Born–von Karman cells of general shape. Our approach tackles two common issues of plane-wave based implementations of Coulomb integrals under periodic boundary conditions: the treatment of the singularity at the Brillouin-zone center and discretization errors, which can cause severe convergence problems in anisotropic cells, necessary for the calculation of low-dimensional systems. We apply our strategy to the Hartree–Fock and coupled cluster (CC) theories and discuss the consequences of different sampling strategies on different theories. We show that sampling the Coulomb potential via the widely used probe-charge Ewald method is unsuitable for CC calculations in anisotropic cells. To demonstrate the applicability of our developed approach, we study two representative, low-dimensional use cases: the infinite carbon chain, for which we report the first periodic CCSD(T) potential energy surface, and a surface slab of lithium hydride, for which we demonstrate the impact of different sampling strategies for calculating surface energies. We find that our Coulomb sampling strategy serves as a vital solution, addressing the critical need for improved accuracy in plane-wave based CC calculations for low-dimensional systems. [ABSTRACT FROM AUTHOR]

Many modern anti-icing and anti-fouling coatings rely on soft, low surface energy elastomeric materials such as polydimethylsiloxane for their functionality. While the low surface energy is desirable for reducing adhesion, very little work considers the larger contribution to adhesive failure caused by the viscoelastic nature of elastomers. Here we examine several different siloxane elastomers using a JKR adhesion test, which was operated over a range of different speeds and temperatures. Additionally, we characterize the dynamic mechanical modulus over a large range of frequencies for each material. We note that surface energies of the materials are all similar, but variation in adhesion strength is clear in the data. The variation at low speeds is related to elastomer architecture but the speed dependence itself is independent of architecture. Qualitative correlations are noted between the JKR adhesion measurements and the dynamic moduli. Finally, an attempt is made to directly compare moduli and adhesion through the recent Persson–Brener model. Approximations of the model are shown to be inaccurate. The full model is found to be accurate at low speeds, although it fails to precisely capture higher speed behaviour. [ABSTRACT FROM AUTHOR]

The formation process of Pd-based bimetallic nanoparticles synthesized by co-sputtering is investigated by performing in situ morphological observation using resistive spectroscopy. The segregation of the metal with lower surface energy on the nanoparticle surface is observed, and it is found that the formation process of the alloy nanoparticles tends to be similar to that of the nanoparticles composed of the core metal even when the atomic fraction of the shell metal is higher than that of the core metal. The co-sputtering process is simulated by the molecular dynamics analysis, and the observed formation process is theoretically confirmed. [ABSTRACT FROM AUTHOR]

In this study, Fe 80 Ce 20 films were deposited on Si(100) and glass substrates using sputtering in a high-vacuum environment and subsequently heat-treated in a vacuum annealing furnace. The films, with thicknesses ranging from 10 nm to 50 nm, were annealed at temperatures of 100 °C, 200 °C, and 300 °C. The objective was to investigate the effects of film thickness and annealing temperature on the structural, surface energy, and magnetic properties of the material. X-ray diffraction (XRD) analysis confirmed the crystalline nature of both Si(100)/Fe 80 Ce 20 and Glass/Fe 80 Ce 20 films. Atomic force microscopy (AFM) revealed a smooth film surface that became rougher after annealing. Contact angle measurements indicated hydrophilic properties, with the highest surface energy observed in the as-deposited films due to a higher density of defects and grain boundaries. The hysteresis loop demonstrated exceptional soft magnetic properties and a high saturation magnetization (Ms) of approximately 2000 emu/cm³. Annealing at 100 °C altered the magnetic domain structure from a striped labyrinthine configuration to an aligned pattern. At higher annealing temperatures, the films exhibited grain growth, increased surface roughness, and new grain formation. Following annealing, the grains in the Fe 80 Ce 20 films became larger, surface roughness increased, and the water contact angle increased, rendering the films more hydrophobic. The as-deposited films displayed the highest surface energy due to the high density of defects and grain boundaries. Increased surface roughness led to more grain boundary defects and irregularities, which served as pinning points for magnetic domain walls, thus increasing coercivity (Hc). Rough surfaces induced local stress fields, increased magnetic anisotropy, and decreased saturation magnetization. Thermal perturbations from higher annealing temperatures further disrupted the alignment of the magnetic moments, leading to a reduction in saturation magnetization. [ABSTRACT FROM AUTHOR]

The petal effect is a well-known natural phenomenon in surface science and has served as inspiration for the creation of several materials with superhydrophobic qualities and high adhesion. As surface roughness has a crucial role in these properties, being able to modulate it could help us design materials at will. Capillary penetration frustrates diffusion and promotes large contact angles as well as high adhesion. Polystyrene surfaces were created using the spin-coating technique. By varying the polymer concentration, the surface roughness was modified. To determine the roughness parameters, atomic force microscopy was used. We recorded advancing and receding contact angles using water and glycerol as test liquids to study contact angle hysteresis, the work of adhesion and the apparent surface energy, which was determined with the Chibowski and Perea–Carpio method. For the purpose of elucidating the wetting states, captive bubble experiments were conducted. Using an easy method, we create polystyrene surfaces with both superhydrophobicity and strong adhesion, where the roughness area factor regulates wetting transitions from Cassie–Baxter to Wenzel. The receding contact angle suggests capillary penetration, which we demonstrate by captive bubble experiments. In addition, a link was found between the surface roughness and apparent surface energy. [ABSTRACT FROM AUTHOR]

Unstable Zn metal anodes with dendrites/side reactions are becoming the main obstacle to the practical application of zinc‐based aqueous batteries. Epitaxial growth has been considered to be an effective strategy for solving these issues, especially for inducing the (002) plane growth. Nonetheless, the (002)‐textured Zn is difficult to achieve highly stable Zn anode under high capacity resulting from its large lattice distortion. Herein, the Cu single atom anchored polymeric carbon nitride (Cu@PCN) is synthesized by a facile thermal polymerization method. Serving as multifunctional protective layer on Zn surface, the Cu@PCN can provide massive nucleation sites at a nano‐level and uniformize the electron distribution through coordination engineering. Optimizing the coordination structures of single Cu and N atoms within the carbon matrix enables a redistribution for electric field and regulates ion flux. More importantly, this coordination strategy with single atoms is first reported to customize oriented and continuous phase epitaxy along highly dendrite‐resistant Zn(101) plane by reducing (101) surface energy. This pattern of oriented dense deposition leads to stable and reversible Zn plating/stripping is achieved, which delivers an extended cycling life of 550 h at 10 A cm−2, 20 mAh cm−2. The practical full cell also displays stable performance for 1200 cycles. [ABSTRACT FROM AUTHOR]

Durable superhydrophobic fabrics with electromagnetic wave absorption were highly valuable in practical applications. In this work, durable superhydrophobic cotton fabrics with electromagnetic wave absorption were successfully prepared by modifying the cotton fabrics with polydopamine (PDA) and then depositing MoS2/RGO (MR) composites and polydimethylsiloxane (PDMS). The surface morphology, crystal structure, and thermal degradation properties of the obtained products were evaluated. The PDA modification enhanced the affinity and adsorption saturation between the fabrics and the MR composites. Here, the MR composites provided the fabrics with wave-absorbing components and rough micro/nanostructure, and the PDMS offered lower surface energy for the treated fabrics. Ultimately, the water contact angle (WCA) of the obtained cotton fabrics could reach 157.2 ± 0.4 ° and the minimum reflection loss (RLmin) was −45.3 dB at 11.1 GHz, which showed excellent superhydrophobicity and microwave absorption properties. In addition, the obtained cotton fabrics displayed excellent robustness against rubbing, bending, and laundrying and satisfactory chemical stability. This research showed promising prospects for the development of wearable materials with durable electromagnetic wave absorption. [ABSTRACT FROM AUTHOR]

Highlights This work investigates the effects of laser processing parameters on basalt fiber‐reinforced composites for the optimization of surface processing without fiber damage. Various conditions of laser power, speed, and stand‐off distance were applied using a CO₂ laser. Consequently, a well‐processed morphology with full matrix removal and clear fiber exposure was achieved under optimized conditions of 32 W power, 200 mm/s speed, and 5 mm SOD. Those parameters resulted in a surface roughness Sa of 6.11 μm. Using the optimum parameters obtained from the experiments, the surface energy density was computed as 0.89 J/mm2, while ensuring adequate material removal without damage to the fiber. Lower power input of 20 W resulted in incomplete removal of the matrix; on the other extreme, unreasonably high powers resulted in fiber degradation. The experiments determined that optimum laser parameters indeed play a critical role in the processing of basalt fiber composites surfaces. Ideal laser settings: 32 W, 200 mm/s, 5 mm SOD. Full‐matrix removal and fiber exposition realized without any damage. The achieved surface roughness Sa is 6.11 μm for optimized laser parameters. Excessive laser power leads to a fiber damage. [ABSTRACT FROM AUTHOR]

Highlights Boron nitride (BN) has excellent thermal conductivity (TC), however, it exhibits high surface energy, strong chemical inertness, poor interface compatibility with polymer matrices, and difficulty in even dispersion within‐polymer matrix, preventive effective construction of TC pathways. Four kinds of modified boron nitride/polyurethane composites (BTPUC) were prepared by different silane‐functionalized BN with polyurethane (TPU). Among them, 3‐trimethoxysilylpropylmethacrylate (TMSPMA)‐functionalized BN demonstrated better interface compatibility with TPU, significantly improving the mechanical properties and TC of the composites compared to the other three functionalized BN addition. The BN@TMSPMA/PU exhibited good TC and mechanical properties, with a TC of 0.865 W/mK, a tensile stress and a tensile strain of 9.65 ± 1.40 MPa and 759.88 ± 67.93%, respectively. It also showed good electrical insulation properties and mechanical durability. Therefore, the as‐prepared BN@TMSPMA/PU have broad prospects as flexible thermal‐management materials. The composites are constructed by TMSPMA‐modified BN and polyurethane by NIPS. The composites show good mechanical properties and cyclic failure resistance. The composites exhibit good thermal conductivity and electrical insulation. [ABSTRACT FROM AUTHOR]

We report a micro-fractionation device for high performance liquid chromatography-mass spectrometry to archive chromatographic separations on an array of optimized surface energy traps (SETs). The method has the potential to significantly alter nanoflow LC-MS workflow, decoupling separation and analysis. The wetting characteristics of the SETs cause the HPLC eluent stream to spontaneously split into droplet microfractions. The droplet mirofractions are then dried down to enable facile storage and transport of the archived separation. Discontinuously dewetting array parameters were explored to maximize array volume and resolution using a combination of SET design, shape, size, and spacing. Mass spectrometry analysis is performed utilizing a liquid micro-junction surface sampling probe to extract dried analytes from the surface of the SETs followed by electrospray ionisation. A reverse phase separation of pharmaceutical compounds is "recorded" using the micro-fractionation device followed by "reading" the chromatographic trace with a mass spectrometer 24 hours after the separation was performed/archived, demonstrating a true decoupling of LC, and MS. Additionally, we demonstrate the ability to collect microfractions with sub-one-second integration time, approaching the scan time of a mass spectrometer or UV-Vis detector. With further improvements to the device, sub-1-second micro-fractionation may enable seamless reconstruction of archived chromatograms indistinguishable from online LC-MS data, while also providing the benefits of easy storage and transport of archived separations. [ABSTRACT FROM AUTHOR]

Non-Newtonian viscous fluids such as yogurt, honey, etc., due to their extremely high viscosity and complex fluidity, remain on food containers after use, where adhesion and staining occurs, which is a great inconvenience and causes a lot of wasted resources. Hydrophobic coatings can be an excellent candidate for eliminating liquid waste. Inexpensive wollastonite nanoparticles were used to build rough micro- and nano-structures, and chitosan was used to emulsify rice bran wax to prepare green and low surface energy emulsions. The above two were mechanically mixed to obtain the hydrophobic emulsion, and coated on the paper surface and heat-treated to prepare the hydrophobic paper. Contact angles up to 157.3°. The coating exhibits good self-cleaning properties for a wide range of non-Newtonian viscous food liquids and shows excellent resistance to repeated machine bending and multiple abrasion damages, while maintaining its hydrophobicity. After 40 cycles of friction, the contact angle is 148.1°, which is still close to 150° and has good hydrophobicity. In addition, the coating has great potential for application to the interior surfaces of various food packages to reduce or even eliminate liquid food residues. [ABSTRACT FROM AUTHOR]

Conventional approaches to creating high‐resolution electric circuits face challenges such as the requirement for skilled personnel and expensive equipment. In response, we propose an innovative strategy that leverages a photochemically modified porous polymer skeleton for in‐situ circuit fabrication. By developing maskless surface energy manipulation that guides PEDOT:PSS‐based conductive ink deposition, electric circuits with high precision, density, stability and adaptability are effortlessly engineered within or atop the porous skeleton, enabling transitions between 2D and 3D circuit configurations. This process simplifies prototyping while significantly reducing costs and maintaining efficiency, promising advancements across various technological sectors. [ABSTRACT FROM AUTHOR]

Hydroxyapatite (HA) bioceramics are widely used materials for orthopaedic applications, offering enhanced cellular adhesion and differentiation. However, the lack of antibacterial features makes the HA biomaterials prone to bacterial infections in in-vivo conditions. The osteomyelitis-like conditions are often treated with prolonged doses of antibiotics and may require surgical removal. Such problems can be tackled by inducing the antibacterial characteristics in the biomaterials which prevent such infections. Various research studies have been conducted to improve the mechanical and antibacterial characteristics of biomaterials like HA through doping. The present study focuses on the synthesis, characterization, and antibacterial study of Zn and Fe doped HA (ZFHAp) for application in the treatment of osteomyelitis. Response Surface Methodology (RSM) based Central Composite Design (CCD) approach was used to optimize the process parameters using the Design Expert software. The analyses indicated the presence of Calcium Iron Hydrogen Phosphate (CIHP) and Parascholzite (PS) as major phases. The optimized experimental conditions were estimated as 0.09 M Zn and 0.04 M Fe at 65 °C, corresponding to 71.29 % and 28.71 % of the CIHP and PS phases, respectively. The synthesized nanopowder showed mixed morphology comprising spherical and rod-shaped particles due to biphasic composition. The ZFHAp sample showed a broad-spectrum antibacterial activity, with IC 50 values of 4.02 mg/ml and 4.79 mg/ml against E. coli and S. aureus , respectively. The optimized sample showed excellent biocompatibility with the osteoblast-like cells (MG-63) with improved biomineralization properties. The antibacterial and osteoinductive characteristics of the synthesized biphasic Fe and Zn doped HA suggest its potential application against osteomyelitis-related conditions. • Biphasic composite was prepared with Fe containing CIHP and Zn containing PS phases. • RSM-CCD optimization process suggested conditions as 0.09 M Zn and 0.04 M Fe at 65 °C. • Excellent alkaline phosphatase activity with increased cell proliferation. • Broad spectrum antibacterial activities with IC 50 values less than 5 mg/ml. • Decreased surface energy of ZHHAp than HA indicating increased surface hydrophobicity. [ABSTRACT FROM AUTHOR]

This study establishes a finite element model based on the Iwan model to accurately characterize the force–displacement relationship and energy dissipation in bolted joints under small-amplitude tangential displacement. The force–displacement behavior of the Iwan model is transformed into a stress–strain relationship using a hybrid hardened intrinsic model. A subroutine developed with UMAT and UHARD is used to simulate the elastic–plastic behavior of the Iwan model during surface contact in the finite element model. Three-dimensional modeling and joint simulation are conducted using ABAQUS software. Experimental data verify the model's validity, and the effects of multiple factors on the bolted bonding surface are analyzed. The influence of friction coefficient, cyclic displacement amplitude, and preload on the force–displacement relationship of the bolted bonding surface is explored. Polynomial interpolation of the loading and unloading curves is applied to investigate the energy dissipation phenomenon. Results show that the finite element method can effectively reflect the hysteresis and energy dissipation behavior of the bonding surface. Increased friction coefficient and preload improve residual stiffness and energy dissipation capacity, while larger cyclic displacement amplitudes increase energy dissipation but have a minimal effect on residual stiffness. [ABSTRACT FROM AUTHOR]

In order to achieve flame retardant, hydrophobic, and toughened epoxy resins, phosphorus/fluorine‐containing block copolymer (FBCP) was synthesized by reversible addition‐fragmentation chain transfer polymerization, and then the as‐synthesized PMADOPO‐b‐PHFBA block copolymer was used as additive to modify the epoxy resin, accompanying with a random copolymer (FRCP) serving as control group. It showed that due to the regular arrangement of molecular chains, FBPC formed a fibrous‐like structure at the fracture interface of epoxy/PMADOPO‐b‐PHFBA (EP/FBCP) samples, effectively enhancing the toughness of epoxy composite materials. The fracture energy of EP90/FBCP‐10 was higher than that of EP90/FRCP‐10 and was about twice than that of pure EP. The addition of 3 wt% FBCP could enhance the limited oxygen index (LOI) of EP97/FBCP‐3 to 33.2% and reached a V‐1 UL‐94 rating. As the addition of FBCP increased, the LOI gradually increased. When the addition of FBCP was 10%, the LOI and UL‐94 of EP90/FBCP‐10 was 38.2% and V‐0 grade, respectively. Meanwhile, the presence of fluorine element effectively reduced the surface energy of the composite EP material. Compared with pure EP, the water contact angle of EP90/FBCP‐10 was about 101° with an increasing of 20.8%. Furthermore, the flame‐retardant mechanism of EP/FBCP epoxy composites was discussed. [ABSTRACT FROM AUTHOR]

In this paper, we report a simple yet efficient method for rapid and high-performance SERS substrate fabrication by a combination of cold plasma and laser treatment. Our analysis reveals that cold plasma pre-treatment significantly reduced surface roughness, transforming 200 nm spikes into an almost perfectly uniform surface, while enhancing the substrate's surface energy by lowering the water contact angle from 59° to 0°, all achieved within just 30 s of 0.9-mW plasma treatment, while 15-min green-laser treatment facilitated more uniform deposition of AuNPs across the entire treated area, effectively creating the SERS substrates. The combined treatments result in enhancement of the Raman intensity (11 times) and consistency over the whole area of the SERS substrates, and their reusability (up to 10 times). The fabricated SERS substrates exhibit a significant enhancement factor of approximately 3 × 10⁸ with R6G, allowing detection down to a concentration of 10−12 M. We demonstrate the application of these SERS substrates by detecting amoxicillin—an antibiotic used worldwide to treat a diversity of bacterial infections—in a dynamic expanded linear range of seven orders (from 10−3 to 10−9 M) with high reliability (R2 = 0.98), and a detection limit of 9 × 10−10 M. Our approach to high-performance SERS substrate fabrication holds potential for further expansion to other metallic NPs like Ag, or magnetic NPs (Fe3O4). [ABSTRACT FROM AUTHOR]

Since breast cancer is one of the most common forms of cancer in women, silicone mammary implants have been extensively employed in numerous breast reconstruction procedures. However, despite the crucial role they play, their interaction with the host's immune system and microbiome is poorly understood. Considering this, the present work investigates the immunomodulatory and bacterial mitigation potential of six textured surfaces, based on linear step-like features with various regular and irregular multiscaled arrangements, in comparison to a flat PDMS surface. We hypothesise that the chosen surface geometries are capable of modulating the cellular response through mechanical interdigitation within the multiscaled surface morphology, independent of the surface chemical properties. Each type of sample was characterised from a physico-chemical and biological points of view and by comparison to the flat PDMS surface. The overall results proved that the presence of linear multiscaled step-like features on the PDMS surface influenced both the surface's characteristics (e.g., surface energy, wettability, and roughness parameters), as well as the cellular response. Thus, the biological evaluation revealed that, to different degrees, biomaterial-induced macrophage activation can be mitigated by the newly designed microtextured surfaces. Moreover, the reduction in bacteria adherence up to 90%, suggested that the topographical altered surfaces are capable of suppressing bacterial colonisation, therefore demonstrating that in a surgical environment at risk of bacterial contamination, they can be better tolerated. [ABSTRACT FROM AUTHOR]

Wood–plastic composites (WPCs) combine the properties of plastics and lignocellulosic fillers. A particular limitation in their use is usually a hydrophobic, poorly wettable surface. The surface properties of materials can be modified using ion implantation. The research involved using composites based on polyethylene (PE) filled with sawdust or bark (40%, 50%, and 60%). Their surfaces were modified by argon ion implantation in three fluencies (1 × 1015, 1 × 1016, and 1 × 1017 cm−2) at an accelerating voltage of 60 kV. Changes in the wettability, surface energy, and surface colour of the WPCs were analysed. It was shown that argon ion implantation affects the distinct colour change in the WPC surface. The nature of the colour changes depends on the filler used. Implantation also affects the colour balance between the individual variants. Implantation of the WPC surface with argon ions resulted in a decrease in the wetting angle. In most of the variants tested, the most significant effect on the wetting angle changes was the ion fluence of 1 × 1017 cm−2. Implantation of the WPC surface also increased the surface free energy of the composites. The highest surface free energy values were also recorded for the argon ion fluence of 1 × 1017 cm−2. [ABSTRACT FROM AUTHOR]

This study focuses on formulating a low-surface-energy, water-resistant, and anti-condensation coating utilizing a fluorocarbon and acrylic resins composite (FAC), enhanced by six functional additives: antistatic agents, water-repellent agents, nanofillers, anti-mold and anti-algae agent, leveling agents, and wetting and dispersing agents. An orthogonal experimental design was implemented to systematically investigate the effects of varying concentrations of these additives on the surface tension of the coating. The results show that the optimized combination of fluorocarbon and acrylic resins composite (OFAC)with functional additives significantly reduces the surface tension, thereby improving both water resistance and anti-condensation properties. This research advances the development of more efficient surface treatment technologies, particularly for applications requiring enhanced water resistance and anti-condensation performance. [ABSTRACT FROM AUTHOR]

Facilitating (002)‐textured zinc growth is crucial for achieving dendrite‐free zinc deposition in zinc‐ion batteries. Electrolyte engineering holds promise in directing zinc electrodeposition toward this desired orientation. However, despite the (002) plane's lower surface energy compared to other facets, it remains unclear why this plane does not dominate zinc crystal faces during electrodeposition under normal conditions. This knowledge gap underscores the need to better understand zinc electrodeposition behaviors and the influence of electrolyte compositions on its crystallographic texture. This study explores different tetraazamacrocycle derivatives as electrolyte additives. It reveals that achieving (002)‐textured zinc deposition is not solely dictated by thermodynamic equilibrium but also significantly influenced by interface dynamics. In typical ZnSO4 electrolytes, imbalanced kinetics among reduction, ion diffusion, and adatom diffusion processes lead to electroconvection and disorderly zinc accumulation, hindering proper zinc growth. In contrast, introducing specific tetraazamacrocycle derivative in the electrolyte regulates reduction rate, enhances limiting current density, and expedites adatom diffusion, mitigating hydrodynamic instability and dendrite growth. This regulation restores the thermodynamically favorable flat (002)‐textured zinc deposition, extending the zinc anode's lifespan to 1800 h at 5 mA cm−2 and 5 mAh cm−2, enabling the fabrication of a high‐performance zinc ion hybrid capacitor prototype capable of stable operation for 40 000 cycles. [ABSTRACT FROM AUTHOR]

Poly(lactic acid) (PLA)/poly (3‐hydroxybutyrate‐co‐3‐hydroxyvalerate) (PHBV) blends are typically phase‐separated, and there is limited research on using graphene oxide (GO) as their matrix filler. PLA/PHBV/GO composites using 1, 3, or 5 wt% GO were prepared by melt mixing, after which their morphology and thermal properties were determined. All the components were hydrophilic (Contact angles less than 90°), and the wetting coefficient value of 3.52 suggested that GO would be dispersed in PLA during surface energy evaluations (SEES). Scanning electron microscopy (SEM) showed that PLA/PHBV blends are immiscible and phase‐separated; however, adding GO brought partial miscibility. Differential scanning calorimetry (DSC) showed that GO plasticized the polymers at lower contents (1 wt%) and inhibited their crystallization at higher contents (3 and 5 wt%). Fourier‐transform infrared spectroscopy (FTIR) measurements showed that a chemical interaction exists between GO and the polymers, and X‐ray diffraction (XRD) results confirmed that GO inhibited crystallization in the polymers at high contents. Adding GO to the polymers generally improved the thermal stability of PLA, verifying the affinity thereof during thermogravimetric (TGA) analyses. Merging of the thermal degradation steps implied that GO induced partial miscibility on polymers. Concurrently, the polymers thermally masked the GO to prolong its lifespan. Composites with 1 wt% GO were the optimal and ideal materials. Highlights: Melt mixed PLA/PHBV blends and their composites with GO as a filler.GO brought partial miscibility to the blends and favored the PLA phase.1 wt% GO contents provide optimal thermal and morphological properties.3 and 5 wt% GO contents form chemical bonds with the polymers.Initial GO loadings increase the crystallinity of the polymers. [ABSTRACT FROM AUTHOR]

This study developed a freshness indicator based on poly(vinyl alcohol) (PVA) and a biohybrid (BH) of Laponite® and anthocyanins adhered to linear low‐density polyethylene (LLDPE) using cold atmospheric plasma (CAP). LLDPE was treated with CAP for 0 to 300 s, which resulted in an increased surface energy, characterized by an important increase in its polar component up to 120 s of treatment, due to the formation of polar groups on the surface of LLDPE. No changes in mechanical properties and water vapor permeability of LLDPE were observed. LLDPE–PVA–BH films were more homogeneous if BH was added before the acidification of the film‐forming solution due to more negative zeta potential and lower particle size of BH in basic medium. Indicators made with BH were able to maintain color after 8 weeks of exposure to light, while those made with anthocyanin extract had fully degraded after 3 weeks. The freshness indicator's color changed from purple to blue and finally to green when exposed to ammonia hydroxide (30% NH3) and from purple to blue when exposed to a simulant liquid of spoiled meat (0.03% NH3). Similar color variance was observed when the indicator was applied to monitor shrimp freshness, changing from purple to blue when the shrimp pH reached pH 7.6. Thus, bilayer films of LLDPE–PVA and natural BH produced using CAP have potential food packaging applications. © 2024 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

Lubricant‐infused organo‐gels with low surface energy solvents represent an environment‐friendly lubricating material, while the poor mechanical performance incapacitates them to harsh and intricate service conditions. To address this challenge, a simple yet highly effective strategy to prepare strong, smart, and slippery organo‐gels by glassifying the polymer network is reported. As a proof of concept, appropriate amounts of rigid solvophobic poly(phenyl methacrylate) (PPMA) units are integrated into a solvophilic poly(cyclohexyl acrylate) (PCHA) network infiltrated with lubricant. Upon forming bicontinuous phase‐separated structures, the rigid solvent‐free PPMA segments stay in glassy states, serving as a load‐bearing phase to toughen the materials effectively. Meanwhile, the soft PCHA phase maintains lubricity and extensibility by holding a substantial amount of lubricant. Owing to the synergistic effect, the gels manifest glass‐like mechanical performance with high rigidity (46.6 MPa), strength (7.7 MPa), and toughness (23.7 kJ m−2). Moreover, the materials exhibit high thermo‐sensitivity with the elastic modulus reversibly decreasing from 46.6 MPa at 20 °C to 0.23 MPa at 50 °C, endowing the gels with shape‐memory properties. Furthermore, the organo‐gels display satisfactory anti‐adhesiveness to various foreign matters. Taken together, the work represents a facile and universal strategy to reinforce organo‐gels, thereby adapting them to various applications. [ABSTRACT FROM AUTHOR]

The further applications of silicon carbide (SiC) are limited due to the ease of being contaminated and tendency for icing at low temperature caused by its intrinsically hydrophilicity. In recent years, superhydrophobic surface has been widely employed due to the potential value in anti-fouling and passive anti-icing. In this work, a novel laser ablation-silicone oil heat treatment (LASH) composite process is proposed to fabricate superhydrophobic SiC surface. Many microscale "fence" structures and nanoscale "broccoli" fragmental structures are successfully obtained, which can be adjusted by using different laser processing parameters. Besides, the X-ray photoelectron spectroscopy analysis demonstrates that the effective deposition of low surface energy chemical functional groups is the key to realize the superhydrophobic properties of SiC surface. The coupling effect between the micro/nano structures and low surface energy is confirmed to be important for the stability of Cassie-Baxter state at low temperature. In addition, the freezing process of water droplets on the LASH surface at low temperature and the mechanism of the rapid transition from Wenzel state to Cassie-Baxter state are analyzed. The experimental results indicate that the LASH surface possesses a longer static icing time and keeps good hydrophobicity at −5 °C. The icing temperature of the LASH surface decreases to −17.6 °C while the temperature of the untreated surface is −3.7 °C. Moreover, the LASH surface possesses a lower ice adhesion strength which means it is easier for the ice droplets to break away from the surface. After 20 cycles of icing-deicing experiments, the WCA of the LASH surface is still higher than 150° and its ice adhesion strength slightly increases to 240 kPa. Finally, the mechanical robustness of the LASH surface is studied through the abrasive belt and tape stripping tests, and the anti-fouling property is also evaluated. The change of ice adhesion strength on the LASH surface under cyclic icing experiment is analyzed. The experimental results show that the LASH surface has great mechanical durability and anti-fouling property, which is expected to further expand the application prospects of SiC in different fields. [Display omitted] • LASH composite process is developed to fabricate superhydrophobic silicon carbide surface. • Micro/nano structures and surface chemistry play important roles for superhydrophobicity. • Wettability of the surface can be controlled by adjusting the laser processing parameters. • LASH surface can achieve free transition from Wenzel state to Cassie-Baxter state. • LASH surface possesses excellent mechanical durability and anti-icing properties. [ABSTRACT FROM AUTHOR]

Cesium lead iodide (CsPbI3) exhibits great potential in developing photovoltaic cells due to suitable optical bandgap and thermal stability. However, the photoactive γ‐phase normally exists at high‐temperatures ≈180 °C, and it is challenging to obtain γ‐phase CsPbI3 at room temperature. Here, it discovers that γ‐phase CsPbI3 is achievable by reducing the underlayer surface roughness to a certain level. This method is universal as demonstrated on the surface of poly(3,4‐ethylenedioxythiophene) poly(styrene sulfonate) (PEDOT:PSS), poly[bis(4‐phenyl)(2,4,6‐trimethylphenyl)amine] (PTAA), polystyrene (PS), and silicon substrates. Moreover, it is found that lower surface roughness resulted in smaller crystallite size in the CsPbI3 film, which is an important reason for achieving γ‐phase because the decrease in crystallite size will increase grain surface energy to suppress tilting of PbI6 octahedra and lattice distortion. This study offers a universal approach to obtain γ‐phase CsPbI3 for the development of high‐performance all‐inorganic perovskite solar cells and other optoelectronic devices. [ABSTRACT FROM AUTHOR]

In wide-bandgap semiconductor power device packaging, die bonding refers to attaching the die to substrate. Thereby, the process temperature of Ag sintering for the die bonding should be low to prevent damage to fragile dies. Herein, an organic-free strategy using Ag nanostructures derived from the thermal decomposition of metal–organic decomposition (MOD) was proposed to achieve low-temperature bonding. Significant effects on bonding performance were determined by the thermal decomposition temperature, which in turn determined the organic content and sintering degree of Ag nanostructures. At a low thermal decomposition temperature of 160 °C, incomplete decomposition resulted in high organic content in the Ag nanostructures, causing large pores inside the Ag joints owing to the generation of gaseous products. Owing to the Ag particles with naked surfaces and wide size distribution, the Ag nanostructure obtained at 180 °C showed an excellent bonding performance, resulting in a high shear strength of 31.1 MPa at a low bonding temperature of 160 °C. As the thermal decomposition temperature was 200 °C, sintering among Ag particles increased the particle size, resulting in a reduction of surface energy and driving force for sintering. We think that uncovering this underlying mechanism responsible for the bonding performance will promote the application of Ag MOD in the die bonding of WBG power devices. [ABSTRACT FROM AUTHOR]

Controlling the polymorphism of metal nanocrystals is a promising strategy for enhancing properties and discovering new phenomena. However, previous studies on Rh nanocrystals have focused on their thermodynamically stable face‐centered‐cubic (fcc) phase. Herein, a facile synthesis of Rh‐based nanocrystals featuring the metastable hexagonal close‐packed (hcp) phase is reported by using Ru seeds in their native hcp phase to template the deposition of Rh atoms. The success of such phase‐controlled synthesis relies on the templating effect promoted by the small lattice mismatch between Ru and Rh and the slow dropwise titration of the precursor at an elevated temperature, ensuring the layer‐by‐layer growth mode and thus the formation of a conformal hcp‐Rh shell. Faster injection rate of Rh(III) precursor leads to the formation of a rough Rh shell in the conventional fcc phase due to accelerated reaction kinetics. Considering both thermodynamic and kinetic aspects of this system, the hcp‐Rh phase is favored when the low surface energy from smooth overlayers balances the high bulk energy of the metastable phase, achieved through tight control of reaction rates and deposition patterns. These Ruhcp@Rhhcp core–shell nanocrystals demonstrate thermal stability up to 400 °C, while exhibiting higher catalytic activity toward ethanol oxidation reaction compared to Ruhcp@Rhfcc counterparts. [ABSTRACT FROM AUTHOR]

Super‐hydrophobic surface has excellent waterproof, self‐cleaning and delayed icing properties, and is widely used in various fields, but its lack of durability restricts its large‐scale use. In this paper, carbon fiber composite material with excellent mechanical properties is selected as the substrate, PTFE nanoparticles with excellent hydrophobicity are used as the surface energy substance, and metal screen is selected as the template, combined with hot pressing molding process, a super‐hydrophobic surface with multi‐level micro‐nano structure is successfully constructed. The test shows that the water contact angle of the surface is 169°, and the rolling angle is about 2°. The contact angle of the surface is also over 150° for other liquids, and it bounces off the external water droplets for three times, so it can easily take away pollutants and keep the surface dry and clean under the action of water flow. In the same icing environment, compared with the original surface, it can prolong the freezing time of droplets by 5 times. After repeated rubbing, the surface still has superhydrophobic properties until the whole surface is completely destroyed. The preparation method used in this study is simple, and the prepared superhydrophobic surface has excellent performance, which is expected to promote the application of superhydrophobic surface in practical working conditions. Highlights: The preparation method is fast, efficient, low‐energy and environment‐friendly, and the used materials are simple and economical, and can be reused.The prepared surface has excellent hydrophobic performance for different media.The prepared superhydrophobic surface has low adhesion and droplet rebound performance.The prepared superhydrophobic surface has excellent delayed icing performance.The prepared superhydrophobic surface has excellent wear resistance. [ABSTRACT FROM AUTHOR]

Despite the impressing advances on sizing agents for CF/PEEK composites, the aromatic backbone of the polymer precursors utilized in the vast majority of reports compromises the dispersity and ductility of the slurry, subsequently resulting in inferior overall performance of the composites. Meanwhile, most resins employed for sizing agents in existing reports are based on petroleum resources. Herein, a bio‐based waterborne sizing agent utilizing semi‐aromatic poly ether ketones (PIEK‐C) derived from isosorbide and phenolphthalein has been disclosed, featured by its salutary dispersity, exceptional thermal stability, higher glass transition temperatures, and broader applicability. Due to the structural similarity between the sizing and resin matrix, the protocol endowed CF/PEEK composites with ameliorated overall performance, addressing issues related to inadequate adhesion of CF with PEEK resin, as well as environmental pollution commonly associated with existing commercial epoxy and solvent‐based sizing agents. The Tg and T5% of PIEK‐C‐5050 were 205.08 and 427.16°C, respectively. The particle size range of the PIEK‐C sizing agents spanned from 66.32 to 84.63 nm. The flexural strength and interlaminar shear strength of the composites experienced a respective 993.92 MPa (30.73%) and 83.32 MPa (36.97%) increase compared to untreated CF/PEEK composites following sizing treatment with PIEK‐C‐5050, underscoring expedient intermolecular interactions based on comparable solubility and π‐π stacking effects between the PEEK and PIEK‐C components. This study introduced an efficient and eco‐friendly approach to enhance the interfacial properties of CF/PEEK composites. Highlights: PIEK‐C resin is employed for the first time to prepare carbon fiber sizing agents.The PIEK‐C sizing agent significantly fortified the surface energy and wettability of carbon fibers.The CF/PEEK composites after treatment with PIEK‐C sizing agent showed excellent heat resistance.The ILSS and bending strength of the composites were significantly increased by 36.97% and 30.73%, respectively. [ABSTRACT FROM AUTHOR]

The cysteine and alkanethiol adsorption on Au(111) surfaces is investigated using density functional theory (DFT) and classic molecular dynamics (MD). Understanding the S–Au interaction across different scales poses major challenges. DFT provides atomic‐level precision but it hardly provides insight on nanosecond scale dynamics of this interface. Alternatively, MD, although it enables modeling larger systems for longer periods, its accuracy heavily relies on the parameterization of the force fields (FF). To address this, an MD potential is fitted using DFT calculations, bridging the gap in accuracy and efficiency. At the DFT level, it is found that PBE with DFT‐D3 reproduces complex approaches at a fraction of the computational cost. Separating PBE and DFT‐D3 contributions reveals consistent PBE energy across molecules (chemisorption), while dispersion varies (physisorption). Thus, the interaction energy of cysteine and two short‐chain alkanethiols is calculated to parameterize both Morse and Lennard–Jones (LJ) potentials. The parameterization improves the potential energy in the preferred adsorption sites: the threefold hcp and fcc with respect to the previous proposals in the literature. Furthermore, the transferability is here demonstrated. At last, these results show that LJ potentials outperform more complex Morse potentials. The procedure is general, and the codes and supporting inputs are publicly available, allowing swift generation of potential energy surfaces (PES) at the DFT level, and fitted LJ or Morse potentials to any molecular interface. [ABSTRACT FROM AUTHOR]

To improve anti-icing traits of outdoor coatings, a synergy between photothermal and hydrophobic anti-icings was utilized to fabricate copolymer/Ti3C2Tx MXene composite coatings with good transparency and adhesion. MXene contributes to photothermal trait from local surface plasmon resonance effect. Copolymer enables hydrophobicity from perfluoroalkyls-induced low surface energy and high surface roughness. An increase in MXene dose results in an increased surface roughness. With 140.0 ± 2.2° of water contact angle and 70% of light transmittance, the optimal film bears 2 wt% of MXene. High MXene dose results in large temperature-increase of film under sunlight. After 15 min of sunlight exposure, the temperature of optimal film surface in icing simulation increases from − 18 ℃ to 7.2 ℃. After 48 h of acid immersion, the temperature-increase of optimal film surface based on 300 s of sunlight irradiation reaches 28.7 ± 1.2 ℃. After 48 h of ultraviolet irradiation, the temperature-increase of optimal film surface is 30.7 ± 0.8 ℃. This surface has a water contact angle of 132.7 ± 1.1° after 48 h of acid immersion. This study gives impetus to a preparation of various composite coatings for outdoor anti-icing/deicing. [ABSTRACT FROM AUTHOR]

Robust, accurate, and direct measurements of evaporation and related energy fluxes on the Laurentian Great Lakes are necessary to understand the large historical range in water levels, regional climatology, lake hydrodynamics, and lake-effect snowfall, all of which inform water management. Despite the societal and scientific importance of this information, few long-term, full-year, in situ measurements exist due to logistical, financial, and safety-related challenges. We present 15 years (2008–2022) of eddy covariance data from Stannard Rock, a historic lighthouse on Lake Superior located 38 km southeast of Manitou Island and 72 km north of Marquette, Michigan. We provide information about the site and instrumentation, as well as data availability and processing. Analysis of this unique long-term dataset, available through the AmeriFlux network (US-GL1), will improve our ability to understand the drivers and patterns of large-lake surface energy fluxes and will advance predictions of evaporative regimes over Lake Superior. [ABSTRACT FROM AUTHOR]

The linear diblock copolymer polystyrene-b-poly(4-vinylpyridine) (PS-P4VP) is an important copolymer recently used in many applications such as optoelectronics, sensors, catalysis, membranes, energy conversion, energy storage devices, photolithography, and biomedical applications. (1) Background: The surface thermodynamic properties of PS-P4VP copolymers are of great importance in many chemical and industrial processes. (2) Methods: The inverse gas chromatography (IGC) at infinite dilution was used for the experimental determination of the retention volumes of organic solvents adsorbed on copolymer surfaces as a function of temperature. This led to the variations in the free energy of interaction necessary to the evaluation of the London dispersive and polar acid–base surface energies, the polar enthalpy and entropy, the Lewis acid–base constants, and the transition temperatures of the PS-P4VP copolymer. (3) Results: The application of the thermal Hamieh model led to an accurate determination of the London dispersive surface energy of the copolymer that showed non-linear variations versus the temperature, highlighting the presence of two transition temperatures. It was observed that the Lewis acid–base parameters of the copolymer strongly depend on the temperature, and the Lewis base constant of the solid surface was shown to be higher than its acid constant. (4) Conclusions: An important effect of the temperature on the surface thermodynamic properties of PS-P4VP was proven and new surface correlations were determined. [ABSTRACT FROM AUTHOR]

Aqueous zinc-ion batteries (AZIBs) have become a promising and cost-effective alternative to lithium-ion batteries due to their low cost, high energy, and high safety. However, dendrite growth, hydrogen evolution reactions (HERs), and corrosion significantly restrict the performance and scalability of AZIBs. We propose the introduction of a BaTiO3 (BTO) piezoelectric polarized coating as an interface modification strategy for ZIBs. The low surface energy of the BTO (110) crystal plane ensures its thermodynamic preference during crystal growth in experimental processes and exhibits very low reactivity toward oxidation and corrosion. Calculations of interlayer coupling mechanisms reveal a stable junction between BTO (110) and Zn (002), ensuring system stability. Furthermore, the BTO (110) coating also effectively inhibits HERs. Diffusion kinetics studies of Zn ions demonstrate that BTO effectively suppresses the dendrite growth of Zn due to its piezoelectric effect, ensuring uniform zinc deposition. Our work proposes the introduction of a piezoelectric material coating into AZIBs for interface modification, which provides an important theoretical perspective for the mechanism of inhibiting dendrite growth and side reactions in AZIBs. [ABSTRACT FROM AUTHOR]

The abnormal grain growth of high-purity cobalt during high-temperature annealing was analyzed in this work. The microstructure and orientation evolutions were characterized using the in situ electron backscatter diffraction technique. It was found that the HCP ↔ FCC phase transformation follows the orientation relationships of {0001}HCP//{111}FCC, < 11–20 > HCP// < 1–10 > FCC during both the heating and cooling process. At around 500 °C, the {100} oriented FCC grains exhibited abnormal growth, with the size exceeding 300 μm. The origin of this phenomenon was analyzed from the perspectives of grain orientation distribution and surface energy. The growth of {111} oriented grains is inhibited by the {111} texture, leading to the abnormal growth of {100} oriented grains, which have the second lowest surface energy. Additionally, the transformation microstructure of the abnormally large grains after cooling is analyzed. This work provides insights into the microstructure stability of high-purity cobalt sputtering targets during their service. [ABSTRACT FROM AUTHOR]

Programmed droplet transport which is typically directed by surface energy gradients or external fields, is crucial in domains ranging from chemical reaction modulation to self‐powered intelligent sensing. However, droplet motion control remains constrained by path reconfiguration, requirements on chemical surface modification, and platform complexity. Here, a more universal plug‐and‐play droplet manipulation paradigm based on liquid‐solid contact electrification and triboelectricwetting on common dielectric surfaces is reported. By regulating the electrical double layer via asymmetric ion dynamics, the triboelectric charge polarity of droplets can be adjusted, enabling in situ manipulation without path reconfiguration dictated by the conventional droplet motion output. Droplets achieved an ultrahigh velocity of 450 mm s−1 on general surfaces, significantly exceeding the speeds observed in droplets subjected to constant electrostatic fields with chemical modifications. This flexible and modular functionally decoupled manipulation strategy offers an environmentally friendly, cost‐effective, and versatile paradigm, facilitating applications in chemical analysis and smart sensing. [ABSTRACT FROM AUTHOR]

Evaporative fraction (EF) is a useful measure for quantifying land surface energy partitioning processes and determining evaporative regimes; however, its influencing factors remain highly uncertain. Here, global data sets were compiled to disentangle the effects of environmental variables on EF variations along climate and land surface gradients. We found that (a) at annual timescales, ecosystem‐level EF could be expressed as a power law function of aridity index. The relationships of mean annual soil water content (SWC) and leaf area index (LAI) with mean annual EF resembled the traditional evaporative regime theory; (b) at daily timescales, the boosted regression tree method quantitatively revealed that the impacts of environmental variables (including meteorological variables) on EF showed equal importance, especially at humid sites, primarily due to the different response direction and magnitude of latent heat (LE) and sensible heat (H) fluxes to environmental changes. Particularly, the contrasting responses of LE (positive) and H (negative) to SWC, LAI, and relative humidity enhanced the positive effects of those influencing variables on EF; whereas, the correlations between EF and energy‐related factors (i.e., net radiation‐Rn and air temperature‐Ta) deteriorated as both LE and H showed positive response patterns to those variables; (c) meteorological factors were also found to have nonlinear effects on daily EF, further modified by climatic conditions. Rn near 150 W/m2 and Ta near 15°C appeared to be important energy‐partitioning thresholds at drier and humid sites, respectively. Moreover, changing interactions among environmental variables with climates were demonstrated to be important for better explaining EF variations. Plain Language Summary: Evaporative fraction (EF; defined as latent heat flux‐LE divided by the sum of LE and sensible heat flux‐H) can vary under different climatic and land surface conditions, but its influencing factors remain poorly understood. To this end, we explored the effects of environmental variables on annual and daily EF variations at different sites around the globe. We found that mean annual EF decreased with increasing aridity index and increased with mean annual soil water content and leaf area index. By comparison, the boosted regression tree method quantitatively showed that environmental variables exerted equally important roles in regulating daily EF, especially at humid sites. The complex interplays of daily EF with environmental variables were mainly due to the different responses of LE and H to surrounding environments and the strong nonlinear and interactive effects of environmental variables. These results are important for understanding the driving mechanisms of EF and land surface energy partitioning processes along climate and land surface gradients. Key Points: Environmental variables exerted equally important roles in regulating daily evaporative fraction, especially at humid sitesSynchronous responses of latent and sensible heat to surroundings determined how environmental variables affected evaporative fractionEnvironmental factors had strong nonlinear and interactive effects on daily evaporative fraction, which was further modified by climates [ABSTRACT FROM AUTHOR]

Transformations of solid samples under solvent‐free or minimal solvent conditions set the future trend and define a modern strategy for the production of new materials. Of the various technologies tested in recent years, the mechanochemical approach seems to be the most promising for economic and ecological reasons. The aim of this review article is to present the current state of art in solid state research on binary systems, which have found numerous applications in the pharmaceutical and materials science industries. This article is divided into three sections. In the first part, we describe the new equipment improvements, which include the innovative application of thermo‐mechanochemistry, sono‐mechanochemistry, photo‐mechanochemistry, electro‐mechanochemistry, as well as resonant acoustic mixing (RAM), and transformation under high‐speed sample spinning (“SpeedMixing”). A brief description of techniques dedicated to ex‐situ and in‐situ studies of progress and the mechanism of solid matter transformation (PXRD, FTIR, Raman and NMR spectroscopy) is presented. In the second section, we discuss the problem of cocrystal polymorphism highlighting the issue related with correlation between mechanochemical parameters (time, temperature, energy, molar ratio, solvent used as a liquid assistant, surface energy, crystal size, crystal shape) and preference for the formation of requested polymorph. The last part is devoted to the description of the processes of coformer exchange in binary systems forced by mechanical and/or thermal stimuli. The influence of the thermodynamic factor on the selection of the best‐suited partner for the formation of a two‐component stable structure is presented. [ABSTRACT FROM AUTHOR]

Metal oxide thin‐film transistors (TFTs) offer remarkable opportunities for applications in emerging transparent and flexible microelectronics. Unfortunately, their performance is hindered by limitations associated with parasitic effects, such as parasitic electrode overlap capacitances and high contact resistance, which can severely limit their dynamic behavior. Here, an innovative method is reported to fabricate coplanar self‐aligned‐gate (SAG) indium‐gallium‐zinc‐oxide (IGZO) transistors with engineered source/drain contacts. The manufacturing process starts with the deposition and patterning of a gate electrode/dielectric stack and its functionalization with an organic self‐assembled monolayer (SAM) as the surface energy modifier. A second gold (Au) electrode is subsequently deposited over the gate electrode stack. The overlapping region between the two electrodes is removed via self‐delamination under mild sonication, forming perfectly aligned coplanar Au‐Gate‐Au electrodes. Device fabrication is completed with the spin coating of the IGZO precursor, followed by rapid photonic curing. Replacing the gold source/drain contact with bimetallic electrodes such as Au/In and Au/ITO enables a reduction in contact resistance and improves the transistor performance remarkably without increasing manufacturing complexity. The method is highly scalable, robust, and applicable to other semiconductor materials. [ABSTRACT FROM AUTHOR]

Sweat wearable biosensors facilitate continuous monitoring of individuals' in‐depth body physiological state with real‐time and molecular‐level insight. However, limited detection accuracy and sensitivity resulted from insufficient amount of sweat sampling and impurities interferences still hinder their practical applications. Here, a miniature wearable skin‐interfaced intelligent graphene nano‐electronic (SIGN) patch employing a novel Janus membrane integrated surface wettability switchable microfluidic module with autonomous sweat sampling and purification capabilities is presented for in situ analysis of sweat biomarkers. Due to the asymmetric surface energy distribution characteristics of the microfluidic surfaces, rapid, directional transport of sufficient amount of sweat to the Janus membrane is achieved. The Janus membrane purifies the sweat sample and transport the sample to the sensing surface autonomously, thus eliminating impurities interferences and enhancing the sensing performance. An ultra‐flexible bio‐receptor functionalized graphene transistor for accurately monitoring sweat biomarkers such as lactate, with outstanding signal reproducibility and good long‐term (over 1 month) stability, and a signal processing unit are employed incorporating with the microfluidic module. In practical wearing tests, the SIGN patch enables the continuous measuring of sweat lactate levels for volunteers during exercises and intelligently providing a preliminary diagnostic assessment on their exercise intensity successfully, suggesting its potential commercialization prospects. [ABSTRACT FROM AUTHOR]

The surfaces of solids (gold, silver, and polymers) have been modified with adsorption layers of various compounds. Optimal modification conditions have been determined using the methods of contact angle measuring and quartz crystal microbalance. The degree of surface coverage with the adsorption layer has been calculated and the data obtained have been compared with the results of the direct measurements of adsorption. The surface energy of the modifying layers has been determined and the potential application fields of the modified solids as functional materials have been demonstrated. [ABSTRACT FROM AUTHOR]

The numerical analysis focuses on investigating head-on collisions between two miscible drops composed of distinct fluids, specifically ethanol and water. The simulations are performed using a coupled level set and volume of fluid approach with different Weber numbers to study the effect of drop inertia. The code is validated against experimental and numerical results from earlier investigations. Additionally, a comparative study involving both water drops and ethanol–water drops is conducted to explore the impact of varying surface tension ratios on collision outcomes. Results show that when miscible drops collide, the merged liquid drop exhibits asymmetric behavior, such as an asymmetric combined drop shape in cases of permanent coalescence or an asymmetric end droplet breakup in cases of reflexive separation. The collision outcome undergoes significant variation as the Weber number changes. At lower Weber numbers, permanent coalescence is observed, while at medium Weber numbers, reflexive separation occurs without the formation of a secondary drop. For medium to large Weber numbers, reflexive separation with the generation of one secondary drop becomes prominent, and in the case of very large Weber numbers, multiple satellite drops form. The maximum vertical elongation of the merged drop and corresponding surface energy increase as the surface tension ratio rises, irrespective of the Weber number. However, for a fixed surface tension ratio, the maximum vertical elongation and associated surface energy vary with an increase in the Weber number. The findings also shed light on the enhanced internal mixing arising from the mismatched surface tension of the colliding drops as the Weber number increases. Furthermore, the study explores the effect of drop inertia on various aspects, including asymmetric collision behavior, energy budget, and mixing index. [ABSTRACT FROM AUTHOR]

In this study, the dynamic behaviors of non-Newtonian fluid droplets with shear-thinning properties eccentrically impacting hydrophobic particle surfaces are investigated through a combination of numerical simulations and experiments. The simulation integrates the dynamic contact angle and a non-Newtonian fluid power-law model within the volume of fluid model framework. The effects of apparent viscosity (η), impact velocity (v0), and dimensionless eccentricity parameter (B) on the dynamic behaviors of non-Newtonian droplets are analyzed. Furthermore, the study offers insight into the progression of pressure distribution, kinetic energy, and liquid viscosity across droplets during the entire impact process. An energy balance analysis, which includes kinetic energy, surface energy, potential energy, and viscous dissipation, is employed to elucidate the fundamental physical mechanisms that govern the dynamics of eccentric impacts of non-Newtonian droplets. Finally, a model (Recr D* = −95.7 + 11 450.6e−B/0.18) is proposed to predict the adhesion or detachment of shear-thinning droplets eccentrically impacting hydrophobic particle surfaces. [ABSTRACT FROM AUTHOR]

The surface thermodynamic properties of polymers and copolymers modified by supramolecular structures are used in several industrial processes, such as selective adsorption, paints, coatings, colloids, and adhesion applications. Background: Inverse gas chromatography at infinite dilution was proved to be the best technique to determine the surface properties of solid surfaces by studying the adsorption of some model polar and non-polar organic molecules adsorbed on solid surfaces at different temperatures. Methods: The retention volume of adsorbed solvents is a valuable parameter that was used to obtain the London dispersive and polar free energies and the London dispersive surface energy of styrene–divinylbenzene copolymer modified by supramolecular structure of melamine using both the Hamieh thermal model and our new methodology consisting of the separation of the two polar molecules and the dispersive free energy of their interaction. This led to the determination of the polar acid and base surface energy, and the Lewis acid–base constants of the various solid materials. Results: Following our new methodology, all surface energetic properties of styrene–divinylbenzene copolymer modified by melamine at different percentages were determined as a function of temperature. Conclusions: It was observed that the styrene–divinylbenzene copolymer exhibited the highest London dispersive surface energy, which decreased when the melamine percentage increased. All materials presented higher Lewis basicity and this Lewis basicity increased with the percentage of melamine. [ABSTRACT FROM AUTHOR]