Ultrasonic spraying quercetin chitosan nonwovens with antibacterial and deodorizing properties for sanitary napkin.

With economic and social development, there is a growing focus on menstrual hygiene, and traditional sanitary napkins are no longer sufficient to meet women's needs. In this study, quercetin (QC) was efficiently and uniformly ultrasonic sprayed on thermally bonded chitosan nonwovens (CS) to prepare a multifunctional surface layer of sanitary napkins (QCX@CS). CS sprayed with 3 layers of QC (QC3@CS) exhibits excellent mechanical properties and high antibacterial rates against Escherichia coli (99.51 %) and Staphylococcus aureus (99.87 %), respectively. Besides, QC3@CS demonstrates strong free radical scavenging abilities, which have great potential to reduce the effects of reactive oxygen species on immune and metabolic functions during menstruation. QC3@CS demonstrates strong deodorizing abilities, with rates of 87.22 % for acetic acid and 90.88 % for ammonia, which could effectively eliminate the unpleasant odor associated with menstruation. Moreover, QC3@CS ensures excellent water absorption, anti-return properties, and cytocompatibility. This study may provide valuable insights into developing functional sanitary napkin materials based on natural extracts.

High-Performance Flexible Hybrid Silica Membranes with an Ultrasonic Atomization-Assisted Spray-Coated Active Layer on Polymer for Isopropanol Dehydration.

Organic-inorganic hybrid silica materials, incorporating an organic group bridging two silicon atoms, have demonstrated great potential in creating membranes with excellent permselectivity. Yet, the large-scale production of polymer-supported flexible hybrid silica membranes has remained a significant challenge. In this study, we present an easy and scalable approach for fabricating these membranes. By employing a sol-gel ultrasonic spray process with a single-pass method, we deposited a thin and uniform hybrid active layer onto a porous polymer substrate. We first optimized the deposition conditions, including substrate temperature, the binary solvent ratio of the silica sol, and various ultrasonic spray parameters. The resulting flexible hybrid silica membranes exhibited exceptional dehydration performance for isopropanol (IPA)/water solutions (IPA: 90 wt%) in the pervaporation process, achieving a water flux of 0.6 kg/(m2 h) and a separation factor of around 1300. This work demonstrates that the single-pass ultrasonic spray method is an effective strategy for the large-scale production of polymer-supported flexible hybrid silica membranes.

Efficient Pervaporation for Ethanol Dehydration: Ultrasonic Spraying Preparation of Polyvinyl Alcohol (PVA)/Ti3C2Tx Nanosheet Mixed Matrix Membranes.

Polyvinyl alcohol (PVA) pervaporation (PV) membranes have been extensively studied in the field of ethanol dehydration. The incorporation of two-dimensional (2D) nanomaterials into the PVA matrix can greatly improve the hydrophilicity of the PVA polymer matrix, thereby enhancing its PV performance. In this work, self-made MXene (Ti3C2Tx-based) nanosheets were dispersed in the PVA polymer matrix, and the composite membranes were fabricated by homemade ultrasonic spraying equipment with poly(tetrafluoroethylene) (PTFE) electrospun nanofibrous membrane as support. Due to the gentle coating of ultrasonic spraying and following continuous steps of drying and thermal crosslinking, a thin (~1.5 µm), homogenous and defect-free PVA-based separation layer was fabricated on the PTFE support. The prepared rolls of the PVA composite membranes were investigated systematically. The PV performance of the membrane was significantly improved by increasing the solubility and diffusion rate of the membranes to the water molecules through the hydrophilic channels constructed by the MXene nanosheets in the membrane matrix. The water flux and separation factor of the PVA/MXene mixed matrix membrane (MMM) were dramatically increased to 1.21 kg·m-2·h-1 and 1126.8, respectively. With high mechanical strength and structural stability, the prepared PGM-0 membrane suffered 300 h of the PV test without any performance degradation. Considering the promising results, it is likely that the membrane would improve the efficiency of the PV process and reduce energy consumption in the ethanol dehydration.

Fabrication of folded MXene/MoS2 composite microspheres with optimal composition and their microwave absorbing properties.

In this work, ultrasonic spray technology is utilized for build up MXene and MoS2 nanosheets to three-dimensional MXene/MoS2 fold microspheres by one-step method. By skillfully assembling two kinds of functional two-dimensional materials, the microspheres have abundant heterogeneous interfaces and huge specific surface area. The optimum feed ratio of MXene and MoS2 is determined by comparing the absorbing properties, and the mass ratio is 5:1. With 30% filler, the material shows the best absorption performance. At 10.4 GHz, the minimal reflection loss (RLmin) reach -51.21 dB, and the thickness is merely 2.5 mm. At the thickness in 1.6 mm, the efficacious absorption bandwidth (RL < -10 dB) reaches 4.4 GHz. The outstanding microwave absorbing properties with MXene/MoS2 folded microspheres is resulted in the multiple interfaces in the heterostructure and above the average conductivity of MXene. The results show that MXene/MoS2 folded microsphere is a prospective electromagnetic absorbing material. The construction of MXene/MoS2 folded microsphere provides an effective method to devise new high-performance microwave absorbing materials.

Effect of Li+ Doping on Photoelectric Properties of Double Perovskite Cs2SnI6: First Principles Calculation and Experimental Investigation.

Double perovskite Cs2SnI6 and its doping products (with SnI2, SnF2 or organic lithium salts added) have been utilized as p-type hole transport materials for perovskite and dye-sensitized solar cells in many pieces of research, where the mechanism for producing p-type Cs2SnI6 is rarely reported. In this paper, the mechanism of forming p-type Li+ doped Cs2SnI6 was revealed by first-principles simulation. The simulation results show that Li+ entered the Cs2SnI6 lattice by interstitial doping to form strong interaction between Li+ and I-, resulting in the splitting of the α spin-orbital of I-p at the top of the valence band, with the intermediate energy levels created and the absorption edge redshifted. The experimental results confirmed that Li+ doping neither changed the crystal phase of Cs2SnI6, nor introduced impurities. The Hall effect test results of Li+ doped Cs2SnI6 thin film samples showed that Li+ doping transformed Cs2SnI6 into a p-type semiconductor, and substantially promoted its carrier mobility (356.6 cm2/Vs), making it an ideal hole transport material.

Manipulate Micrometer Surface and Nanometer Bulk Phase Separation Structures in the Active Layer of Organic Solar Cells via Synergy of Ultrasonic and High-Pressure Gas Spraying.

For organic solar cells, the vertical and lateral micro-/nanometer-scale structure in the active layer largely determines the device performance. In this work, the surface and bulk domain size of the photoactive layer are successfully manipulated with a facile two-step spraying method, that is, an ultrathin active layer by high-pressure spraying is deliberately stacked on top of the thick active layer by ultrasonic spraying. Thus, the morphology is effectively optimized with the comprehensive study of optical and electrical characteristics, such as photon absorption, exciton dissociation efficiency, and bimolecular recombination. Moreover, the novel method can be used not only in the fullerene system but also in the nonfullerene system, demonstrating the remarkable universality through this synergy method. This work provides an easy and reliable strategy to improve photovoltaic device performance in the industrial large-area spray-coating process.

Bactericidal and Hemocompatible Coating via the Mixed-Charged Copolymer.

Cationic antibacterial coating based on quaternary ammonium compounds, with an efficient and broad spectrum bactericidal property, has been widely used in various fields. However, the high density of positive charges tends to induce weak hemocompatibility, which hinders the application of the cationic antibacterial coating in blood-contacting devices and implants. It has been reported that a negatively charged surface can reduce blood coagulation, showing improved hemocompatibility. Here, we describe a strategy to combine the cationic and anionic groups by using mixed-charged copolymers. The copolymers of poly (quaternized vinyl pyridine- co- n-butyl methacrylate- co-methacrylate acid) [P(QVP- co- nBMA- co-MAA)] were synthesized through free radical copolymerization. The cationic group of QVP, the anionic group of MAA, and the hydrophobic group of nBMA were designed to provide bactericidal capability, hemocompatibility, and coating stability, respectively. Our findings show that the hydrophilicity of the copolymer coating increased, and its zeta potential decreased from positive charge to negative charge with the increase of the anionic/cationic ratio. Meanwhile, the bactericidal property of the copolymer coating was kept around a similar level compared with the pure quaternary ammonium copolymer coating. Furthermore, the coagulation time, platelet adhesion, and hemolysis tests revealed that the hemocompatibility of the copolymer coating improved with the addition of the anionic group. The mixed-charged copolymer combined both bactericidal property and hemocompatibility and has a promising potential in blood-contacting antibacterial devices and implants.