Facile Preparation Research Articles

Facile preparation of a highly efficient coin cell supercapacitor based on WO3 nanorods

Developing sustainable energy storage devices is challenging for the progress of energy storage applications. Here, nanotechnology represents a strategic route to reduce the amount of used critical materials, while continuing to take advantage of their properties, thanks to the high surface to volume ratio which characterizes nanostructures. WO3 nanostructures represent a promising active material for energy storage applications, thanks to their wide capability of small positive ions (H+ and Li+) intercalation and their high stability in acidic conditions. The coupling between WO3 nanorods and carbon black powder is studied to realize a highly efficient coin cell supercapacitor. The morphology of WO3 nanorods and carbon black is investigated by using a scanning electron microscope, and the energy storage performances were evaluated by performing cycling voltammetry and galvanostatic charge and discharge analysis, thus obtaining promising specific capacitance results (79 and 70 F/g at 5 mV/s and 0.5 A/g respectively). Moreover, the stability of the obtained coin cell was investigated, thus getting good capacity retention over 250 charge-discharge cycles. Energy and power densities were also calculated, obtaining the highest energy density of 39 Wh/kg at a power density of 500 W/kg. The WO3‑carbon black coin cells are used to power a red LED, so demonstrating the viability for practical applications.

Cholesterol-end-modified–PEG vesicle: DDS carrier with long-term stability to encapsulate a drug model by facile preparation

Abstract Vesicles such as liposomes are widely used as drug delivery system (DDS) carriers. On the other hand, they are complicated to prepare and have stability issues. In this study, we synthesized an amphiphile, Chol-U-Et-mPEG500, containing cholesterol and poly(ethylene glycol) (PEG) as a hydrophobic and hydrophilic block, respectively. Chol-U-Et-mPEG500 spontaneously formed a vesicle with a uniform particle size of about 90 nm just by dissolving its compound in water. The vesicle encapsulated sulforhodamine B as a drug model only by mixing with its solution.

Facile Preparation of Irradiated Poly(vinyl alcohol)/Cellulose Nanofiber Hydrogels with Ultrahigh Mechanical Properties for Artificial Joint Cartilage.

In this study, Poly(vinyl alcohol)/cellulose nanofiber (PVA/CNF) hydrogels have been successfully prepared using γ-ray irradiation, annealing, and rehydration processes. In addition, the effects of CNF content and annealing methods on the hydrogel properties, including gel fraction, micromorphology, crystallinity, swelling behavior, and tensile and friction properties, are investigated. Consequently, the results show that at an absorbed dose of 30 kGy, the increase in CNF content increases the gel fraction, tensile strength, and elongation at break of irradiated PVA/CNF hydrogels, but decreases the water absorption. In addition, the cross-linking density of the PVA/CNF hydrogels is significantly increased at an annealing temperature of 80 °C, which leads to the transition of the cross-sectional micromorphology from porous networks to smooth planes. For the PVA/CNF hydrogel with a CNF content of 0.6%, the crystallinity increases from 19.9% to 25.8% after tensile annealing of 30% compared to the original composite hydrogel. The tensile strength is substantially increased from 65.5 kPa to 21.2 MPa, and the modulus of elasticity reaches 4.2 MPa. Furthermore, it shows an extremely low coefficient of friction (0.075), which suggests that it has the potential to be applied as a material for artificial joint cartilage.

In Situ Synthesis of Hierarchical Co(CO3)0.5(OH)·0.11H2O@ZIF-67/WO3 With High Humidity Immunity and Response to H2S Sensing.

H2S gas sensors with facile preparation, low detection limits, and high selectivity are crucial for environmental and human health monitoring. However, it is difficult to maintain a high response of H2S gas sensors under high humidity in practical applications. To face this dilemma, a layer-by-layer growth method is applied to in situ prepare a nanostructured Co(CO3)0.5(OH)·0.11H2O/WO3 coated by a hydrophobic hierarchical ZIF-67 as the H2S sensor. This novel composite exhibits excellent humidity immunity without sacrificing the excellent sensitivity and selectivity of H2S. At a low operating temperature of 90°C, a remarkable response value of 1052.3 to 100ppm H2S has been achieved, which is 779 and 9.36 times higher than that of pure WO3 and Co(CO3)0.5(OH)·0.11H2O/WO3, respectively. More importantly, an 82.2% relative response value remains at a high humidity of 75%RH. The sensing mechanisms are investigated using gas chromatography-mass spectrometry (GC-MS), which revealed that the reaction products are H2O and SO2. The high humidity immunity and fast response of the Co(CO3)0.5(OH)·0.11H2O@ZIF-67/WO3 demonstrate the layer-by-layer in situ synthesis method holds the potential application for the development of high-performance WO3-based H2S sensors.

Facile Preparation of Smart Sponge Based on a Zeolitic Imidazolate Framework for the Efficient Separation of Oily Wastewater

The fabrication of durable materials with excellent oil-adsorption capacity and separation performance for the treatment of oily wastewater is meaningful based on the special property of smart responsiveness. Herein, a solvent-responsive melamine sponge (MS) was developed via silanization and the in situ growth of a zeolitic imidazolate framework-8 (ZIF-8). Detailed characterization of the resultant composite MS was conducted using scanning electron microscopy (SEM), energy-dispersive spectrometry (EDS), and X-ray diffraction (XRD). The multiscale hierarchical MS substrate exhibited highly hydrophobic properties in the pH range of 1–11, along with a satisfactory adsorption capacity in the range of 65.4–134.2 g/g for different oils. The modified surface transformed from superhydrophobic/superlipophilic to superhydrophilic/underwater superoleophobic upon ethanol wetting, reverting to its original superhydrophobic state upon drying. The separation flux of the MS substrate was above 1.5 × 104 L/m2h for both oil and water removal, and the separation efficiency was greater than 98.7%. The absence of obvious changes in separation performance after 50 successive immiscible oil−water separations indicated the excellent durability and robustness of the anchored ZIF-8 nanoparticles on the surface of the modified MS substrate. More importantly, oil-in-water emulsion separation was successfully carried out via the ZIF-8 MS composite, showing high separation efficiency (over 99.1%). The developed smart sponge, which had high oil-adsorption capacity, excellent chemical stability, and fire resistance, has a wide range of potential practical applications in the convenient treatment of oily wastewater.

Facile preparation of a novel core-shell fiber S-scheme C/CoS2@BiOBr heterojunction photocatalyst for efficient degradation of Congo red under visible light

Generally, it is of great scientific significance to improve the utilization of solar energy resources. However, it is still a huge challenge at present. For this reason, the construction of photocatalysts with heterostructures is an effective way. In this paper, a novel core-shell fiber-like C/CoS2@BiOBr S-scheme heterojunction with visible light response was rationally designed by in-situ reduction of MOF through anion exchange strategy. Density functional theory (DFT) calculation and characterization analysis show that the internal electric field is formed between C/CoS2 and BiOBr after contact. This is beneficial to charge transfer and separation, and the S-sheme transfer path endows the separated electrons and holes with large redox potential to participate in the reaction directly. Moreover, the addition of BiOBr significantly enhanced the visible light absorption of the composites and improved the photochemical properties. It is worth noting that C/CoS2@BiOBr has excellent catalytic ability, and the optimal value of photodegradation of Congo red (CR) reaches more than 99 % within 15 min of visible light irradiation. Consequently, the active species were •O2- and h+. •O2- play a dominant role in the photocatalytic process. The space charge transfer and possible separation mechanisms of the new heterostructures are further proposed. This study provides some new ideas for the preparation of efficient water purification photocatalysts.

An in situ gel electrolyte for the facile preparation of high‐safety Li‐S battery

AbstractLithium‐sulfur (Li‐S) battery shows promising development potential in secondary lithium‐ion batteries. However, the shuttle effect of polysulfides, uncontrollable lithium dendrite growth, and safety hazards in conventional liquid electrolytes limit the popularity of Li‐S batteries in the future commercial market. In this work, a high‐performance gel electrolyte (GPE) was prepared in situ by initiating the ring‐opening polymerization of 1,3‐dioxolane (DOL) with aluminum trifluoromethanesulfonate (Al(OTf)3) and using diethylene glycol dimethyl ether (DME) as a plasticizer, which can effectively improve the interfacial compatibility between sulfur cathode and the electrolyte, as well as the stability of lithium anode. The electrochemical performance of the poly‐DOL (PDOL) GPE was optimized by adjusting the concentration ratio of the initiator. When the concentration of Al(OTf)3 is 4 mM, the PDOL GPE has a high ionic conductivity up to 3.81 × 10−4 S cm−1 and a lithium ion migration number of 0.57. The assembled quasi‐solid‐state Li‐S batteries shows an initial discharge specific capacity of 908.1 mAh g−1 at 0.1 C with a capacity retention of 68% after 240 cycles, and its average Coulombic efficiency is maintained at 96.1%. This gel electrolyte design provides a feasible practical idea in quasi‐solid‐state Li‐S batteries.

Facile preparation of cubic metal organic framework sensor: Kinetics, mechanism analysis and sensitive detection of dopamine

Dopamine (DA) is one of the typical neurotransmitters, which plays an important role in early prevention of neurological diseases and clinical research. Rapid and sensitive detection of dopamine is crucial. In this work, a series Cu-metal organic framework material (Cu-MOF) with different raw material ratios were prepared by a one-step simple precipitation method. The as-prepared materials were characterized by scanning electron microscopy (SEM), High Resolution Transmission Electron Microscope (HRTEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and Fourier Transform Infrared Spectroscopy (FT-IR) techniques. The differential pulse voltammetry (DPV), cyclic voltammogram (CV) and electrochemical impedance spectroscopy (EIS) were applied for electrochemical characterization. The Cu-MOF-3 modification on the surface of glassy carbon electrodes (GCE) showed the strongest electrochemical signal and biggest peak current, which was superior to that of bare electrode and other prepared MOFs electrodes. The electrochemical reaction kinetics were investigated in detail, and the possible mechanism was proposed. Under optimized conditions, the enhanced peak currents represented the excellent analytical performance of detection of DA in the range of 10–100 μM, as well as good interference resistance and reproducibility. To further validate its possible application, the present electrochemical sensor was successfully applied to determine trace amount of DA with satisfactory recovery results (>99.5 %) in water sample. This work provides a simple and environment-friendly analysis method in DA detection, suggesting it as a promising low-cost, reliable platform for the DA detection application.

Aspartic acid/ thiourea − derived N and S − doped porous carbon as a metal-free electrocatalyst for oxygen and hydrogen evolution reactions

The preparation of high-efficiency electrocatalysts for the oxygen and hydrogen evolution process (OER and HER) using an easy, green, and facile preparation method is crucial for the effective and economical use of clean energy sources. Heteroatom-doped carbon nanomaterials are effective metal-free electrocatalysts for HER and OER reactions. Herein, N and S co-doped porous carbon nanocomposite (NS-PC) was constructed as a low-cost metal-free catalyst via pyrolysis of the Thiourea and L-aspartic acid. Doping heteroatoms (N and S) into the carbon structure can induce charge redistribution, expose many active sites, accelerate charge transfer, and thus effectively improve the catalytic activity. The NS-PC electrocatalyst demonstrates proper bifunctional electrocatalytic performance for HER and OER with long-term stability in KOH electrolytes. As a result, the NS-PC requires an overpotential of 139 mV and 315 mV in the current density of 10 mA cm– 2 and the Tafel slope of 59.6 and 69.8 mV dec−1 for HER and OER, respectively. As-papered NS-PC electrocatalyst offers the development of multi-functional electrocatalysts in the water splitting process using biological substances such as amino acids.

Balancing Graphitic Nanodomains and Heteroatom Doping in Hard Carbons Toward High Capacity and Durable Potassium‐Ion Battery Anodes

AbstractHard carbons (HCs) have emerged as promising candidates for commercial anodes in potassium‐ion batteries (PIBs). However, a thorny challenge remains in achieving high reversible capacities at high charge/discharge rates, which significantly hinders the development of HCs for PIBs. Here, a temperature‐controlled strategy is proposed to effectively balance graphitic nanodomains and heteroatom doping content in HCs, resulting in widened carbon layer spacing, high conductivity, and abundant K‐ion intercalation sites. The optimized NO‐HC600 electrode exhibits a high reversible capacity of 315.0 mAh g−1 at 0.2 A g−1, and exceptional cyclic stability (235.0 mAh g−1 after 1200 cycles at 2.0 A g−1 with a capacity retention rate of 98.82%). Furthermore, systematic in /ex situ experiments unveil a highly reversible “adsorption–intercalation” mechanism governing potassium‐ion storage, confirming the origin of the superior performance. This work offers valuable insights into the facile preparation of HC anodes with high reversible capacity and fast charge/discharge capability for PIBs.

Facile preparation and study of supramolecular architecture of an efficient nanocomposite LB film AHSM/SA based on azo-functionalized hockey stick-shaped mesogen at air-water and air-solid interface

Hockey stick-shaped mesogens are fascinating thermotropic liquid crystal systems owing to their exceptional supramolecular assembly properties and shape anisotropy compared to conventional rod-and bent-shaped mesogens. In this article, we present an investigation of the supramolecular organization of a new azo-functionalized hockey stick-shaped mesogen with stearic acid at the air-water interface and air-solid interfaces by applying the Langmuir-Blodgett film deposition method. The incorporation of stearic acid can change the molecular organization of azo-functionalized hockey stick-shaped mesogen at an aqueous interface through hydrophobic-hydrophobic interactions and form a supramolecular nanostructure at the solid interface. The interfacial nature of the Langmuir monolayer was studied by recording the isotherm (surface pressure area, π–A), which was further analyzed by using Brewster angle microscopy. The significant reduction in molecular area, increased surface pressure, and lower isotherm slope of the AHSM/SA composite mixture indicate the hybrid AHSM/SA monolayer's greater stability compared to pure AHSM. BAM images of the AHSM/SA composite signify nanostructure aggregates formed by the interaction of AHSM and SA molecules at the air-water interface. Field emission scanning electron microscopic analysis of composite films revealed the formation of supramolecular domains. The impact of changing the surface pressure and the number of depositions on the morphology of the composite film surface was monitored using field emission scanning electron microscopy. The supramolecular H-type aggregation of azo-functionalized hockey stick-shaped mesogen and stearic acid molecules in the composite LB film was characterized using UV–visible absorption and steady-state fluorescence spectroscopy. The adsorption of stearic acid onto azo-functionalized hockey stick-shaped mesogen via hydrophobic interactions was confirmed by Fourier transform infrared spectroscopy of the composite Langmuir Blodgett film. Further, Raman spectroscopy of the LB films of the AHSM/SA composites is distinct from the pristine film components due to the merging of signals at similar wave numbers for both SA and AHSM with a lack of typical packing pattern further supported by PXRD studies of the films.

Preparation and evaluation of a 1,1′-bi-2-naphthol-based chiral macrocycle bonded silica chiral stationary phase for high performance liquid chromatography

Macrocycles play vital roles in supramolecular chemistry and chromatography. 1,1′-Bi-2-naphthol (BINOL)-based chiral polyimine macrocycles are an emerging class of chiral macrocycles that can be constructed by one-step aldehyde-amine condensation of BINOL derivatives with other building blocks. These macrocycles exhibit good characteristics, such as facile preparation, rigid cyclic structures, multiple chiral centers, and defined molecular cavities, that make them good candidates as new chiral recognition materials for chromatographic enantioseparations. In this study, a BINOL-based [2+2] chiral polyimine macrocycle was synthesized by one-step condensation of enantiopure (S)-2,2′-dihydroxy-[1,1′-binaphthalene]-3,3′-dicarboxaldehyde with (1R,2R)-1,2-diaminocyclohexane. The product was modified with 5-bromo-1-pentene and then attached to thiolated silica using click chemistry to construct a new chiral stationary phase (CSP). The enantioselectivity of the new CSP was explored by separating various racemates under normal phase (NP) and reversed phase (RP) high performance liquid chromatography (HPLC). Thirteen racemates and eight racemates were enantioseparated under the two separation modes, respectively, including chiral alcohols, phenols, esters, ketones, amines, and organic acids. Among them, nine racemates achieved baseline separation under NP-HPLC and seven racemates achieved baseline separation under RP-HPLC. High resolution separation was observed with benzoin (Rs = 5.10), epinephrine (Rs = 4.98), 3-benzyloxy-1,2-propanediol (Rs = 4.42), and 4,4′-dimethylbenzoin (Rs = 4.52) in NP-HPLC, and with 4-methylbenzhydrol (Rs = 4.72), benzoin ethyl ether (Rs = 3.79), 1-phenyl-1-pentanol (Rs = 3.68), and 1-(3-bromophenyl)ethanol (Rs = 3.60) in RP-HPLC. Interestingly, the CSP complemented Chiralcel OD-H, Chiralpak AD-H, and CYCLOBOND I 2000 RSP columns for resolution of these test racemates, separating several racemic compounds that could not be well separated by the three commercially available columns. The influences of injected sample amount on separation were also evaluated. It was found that the column exhibited excellent stability and reproducibility after hundreds of injections, and the relative standard deviations (n = 5) of the retention time and resolution were less than 0.49% and 0.69%, respectively. This study indicates that the BINOL-based chiral macrocycle has great potential for HPLC enantioseparation.

Development of Bifunctional Electrocatalyst for Overall Water Electrolysis: Vanadium and Phosphorus Dual-Doping Strategy on Ni3S2 Nanoneedle

Along with the rapid consumption of fossil fuels and serious environmental pollution, the development of renewable and clean energy has been receiving a lot of attention recently. Among the various renewable energy sources, hydrogen (H2) is considered as most promising substance in future energy society owing to its high gravimetric energy density and environmental friendliness. Electrochemical water electrolysis system is powerful strategy for high-purity hydrogen production without emission of any pollutants. It consists of two electrocatalytic reactions: oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). However, the practical efficiency of water electrolysis is limited due to the intrinsically sluggish reaction kinetics of OER and HER. To date, the precious metal-based electrocatalysts such as RuO2 and Pt/C for OER and HER, respectively, were employed as state-of-the-art electrocatalyst to enhance the performance of water electrolysis. However, due to the high expense, mono-functionality, and unsatisfactory stability of the precious metal-based materials, research on bifunctional electrocatalysts with low cost and high activity has become an urgent topic. To date, numerous scientific endeavors have been dedicated to the advancement of highly efficient non-noble metal-based bifunctional electrocatalysts such as transition metal oxides, hydroxides, sulfides, carbides, nitrides, and phosphides. Among these, Ni3S2 has emerged as a particularly promising electrocatalyst for water splitting, garnering substantial attention owing to its high electric conductivity, rich redox property, abundance in the Earth's crust, and environmentally friendly characteristics. Nevertheless, the electrocatalytic activity of Ni3S2 lags behind that of noble metal counterparts. Therefore, elaborate modification of Ni3S2 catalyst should be conducted to further improve its intrinsic activity toward OER and HER. Among the various strategies, heteroatom doping into Ni3S2 structure could be adopted as powerful technique for enhancement of electrocatalytic performance. The homogeneously incorporated dopants not only generate lattice disorders but elaborately modulate the surface electronic property. Specifically, high-valent cation dopants such as vanadium and molybdenum can effectively mediate the change of chemical states of Ni active sites during the step-wise electrocatalytic procedure. Meanwhile, additionally introduced anion dopants, which have lower electronegativity compared with sulfur, can reduce the electron trapping phenomenon induced by excessive electron transfer from nickel to sulfur. Inspired by above features, we synthesized V and P co-doped Ni3S2 nanoneedles directly grown on nickel foam (V-Ni3S2-P/NF) through facile two-step preparation method. First, V doped Ni3S2 nanoneedles were homogeneously grown on NF (V-Ni3S2/NF) by hydrothermal process without use of nickel precursor. The vanadium ions promote the nucleation of Ni3S2 species and lead the preferential growth toward 1D direction during the hydrothermal reaction. After that, the V-Ni3S2/NF was annealed in the tube furnace with the NaH2PO2 as a phosphorus precursor under the Ar flow. Under the mild annealing condition, the PH3 gases generated from thermal decomposition of NaH2PO2 reacted with the V-Ni3S2 species. Consequently, the V-Ni3S2 was partially phosphidated into V-Ni3S2-P throughout anion exchange process. As a result, the V-Ni3S2-P/NF electrocatalyst exhibited excellent bifunctional activity toward both OER and HER compared with mono-doped and un-doped counterparts and precious metal-based electrocatalysts. Furthermore, the outstanding electrocatalytic performance of V-Ni3S2-P/NF was well-maintained over the 100 h of continuous operation under alkaline condition. This study will contribute to the development of efficient and cost-effective electrocatalysts for future energy conversion and storage technologies.

Advanced Nanostructured Textile Catalysts for Enhanced Hydrogen Production in PEM Water Electrolysis: An Overview and Recent Developments

As the global focus shifts towards a zero-emission society, hydrogen has emerged as a critical element in various industries, particularly in green hydrogen production. A promising method for this is Polymer Electrolyte Membrane Water Electrolysis (PEMWE), which uses pure water and electricity to produce high-purity hydrogen. However, the efficiency of PEMWE is highly dependent on the effectiveness of its catalysts, particularly in the context of the catalyst-coated membranes (CCMs) employed in these systems. Conventional preparation of these CCMs involves multiple steps, including synthesis and application of a catalyst ink, which often leads to catalyst agglomeration and requires high Ir (Iridium) loadings to maintain uniformity and performance.In our latest study, we have developed a novel approach using ultralight conductive IrO2 nanostructured textiles (NST) as a catalyst layer for PEMWE. This innovative method successfully circumvents the issue of electrically isolated inactive catalysts, a common problem with lower Ir amounts in traditional catalyst layers. By employing a process of sputtering IrO2 onto water-soluble polymer nanofibers, we have achieved facile CCM preparation and demonstrated unprecedented long-term hydrogen evolution with ultra-low Ir mass loadings at high rates. Our study revealed that the high performance of these CCMs is derived from their low resistivity and unique porous three-dimensional structure.The preparation of NST involves dissolving polyvinylpyrrolidone (PVP) in methanol, followed by electrospinning this solution onto a metal-foil collector. The resulting PVP nanofibers then undergo a sputtering process to deposit IrO2, forming the nanostructured textiles. This method eliminates the need for wet chemical routes and labor-intensive processes typically associated with conventional catalyst layer preparations, thus offering a more environmentally friendly and scalable alternative.Our performance evaluations of these NST CCMs, with varying Ir mass loadings, have shown significant advancements. The operational cell voltages of CCMs containing as little as 0.05 mg-Ir cm−2 were suppressed across all investigated current densities compared to conventional CCMs. Notably, operational voltages remained below 2 V even at the highest current density of 7 A cm−2. This level of performance is unprecedented for CCMs with such low catalyst amounts. Additionally, the long-term stability of these CCMs was remarkable, with operational times exceeding 1500 hours without significant increases in voltage, showcasing their potential for practical applications.An essential aspect of our study was the analysis of the electrical properties and the surface structure of the IrO2 NSTs. We observed that the electrical conductivity of these textiles was significantly higher than that of conventional catalyst layers. This high conductivity, coupled with the unique interconnected structure of the textiles, ensures efficient electrical contact between nano catalysts and the current collector, thus avoiding the formation of isolated catalysts. Our analyses revealed that the IrO2 NSTs have unique surface terminations and a high number of undercoordinated surface Ir atoms, contributing to their high intrinsic catalytic activity.Further insights were gained through operando X-ray absorption spectroscopy (XAS) measurements, which showed that the IrO2-nanostructured textiles possess a large number of D-band holes and are intrinsically highly active. This finding is crucial as it links the unique chemical state of the textiles to their high activity in oxygen evolution reactions (OER), a key process in PEMWE.Our recent developments in nanostructured textile catalysts for PEMWE mark a significant leap in hydrogen production technology. By demonstrating high-rate hydrogen production at low operational voltages and with significantly lower Ir mass loadings compared to conventional CCMs, we have addressed major challenges in the field. These advancements not only enhance the efficiency and sustainability of hydrogen production but also open avenues for applying this technology to other electrochemical conversion cells, paving the way for broader applications and further research. In this talk, we discuss the latest activity on NST, and highlight the challenges and opportunities for hydrogen production.

Facile and scalable preparation of gradient multilayer nanocomposite structure with preeminent microwave absorption and radar cross section reduction capability

The pressing need for the enhancement of stealth materials that are harmonious with state-of-the-art military equipment is critical, as it plays a pivotal role in bolstering the survivability and operational capabilities of advanced military technology. This research offers a straightforward approach for fabricating a gradient triple-layer absorber utilizing a Cu2O/h-BN nanocomposite and FeCoNi magnetic compounds, characterized by reduced thickness, designed for X-band wave spectrum attenuation purposes. The primary objective of this study is to examine the electromagnetic wave absorption characteristics of single-layer samples and subsequently develop a triple-layer gradient sample with distinct electromagnetic wave stealth features based on the findings. Optimal performance was observed in the gradient sample, where Cu2O/h-BN nanocomposite with 20 and 10 wt% was incorporated as a matching layer with thicknesses of 0.5 and 0.5 mm, respectively, and FeCoNi with 20 wt% was employed as an absorbing layer with a 0.4 mm thickness, surpassing the performance of the other samples. The optimal sample achieves a dissipation loss of −45.6 dB and a bandwidth of 2.9 GHz, all while maintaining a total thickness of just 1.4 mm. Facilitating multiple heterogeneous interfaces among layers, substances, and the synergistic interaction between constituent elements and layers’ thickness and arrangement enable this gradient configuration to demonstrate exceptional performance in radar stealth compatibility.

In-Situ Ionothermal Synthesis of Nanoporous Carbon/Oxide Composites: A New Key to Functional Separators for Stable Lithium-Sulfur Batteries

Lithium–sulfur batteries (LSBs) are promising high-energy energy storage systems. However, conventional polypropylene-based separator cannot avoid polysulfides shuttling and thus dramatically impedes the practical LSBs. Herein, a novel in-situ ionothermal synthesis strategy that concurrently applies ionic liquid as the solvent, template and high-yield carbon source is proposed for facile preparation of nanoporous carbon/oxides composites. Theoretical and experimental studies suggests that the composites exhibit features of high polarity, Ti3+ doping, oxygen vacancy, heteroatom doping, abundant defects and high electronic conductivity for fast trapping and conversion of polysulfides in LSBs. As functional materials towards separator modification, the assembled high-loading LSBs deliver enhanced performance due to the suppression of shuttle effects. Furthermore, the proposed strategy exhibits excellent versatility and good practicality.

Facile preparation and characterization of biodegradable and biocompatible UV shielding transdermal patches based on natural rubber latex- dextrin blends

The physico-chemical and biological properties of natural rubber latex (NRL), entailing its biodegradability and biocompatibility, render it a promising material for various biomedical applications. This research explores the facile blending of NRL with dextrin in different compositions to investigate its potential as a prospective UV shielding transdermal patch for biomedical applications. The superior compatibility between the polymers after blending and the improved thermal stability have been established through FTIR, DSC, and TGA examinations, respectively. Optimization of blended polymers for compatibility, wettability, crystallinity, and static mechanical properties has been performed. Morphology characterization conducted via SEM and AFM techniques suggests a uniform morphology for the optimized blend system. The UV shielding ability of the blend has been confirmed by the evaluation of in-vitro UV shielding performance, UV protection factor (UPF), and the superior protection of the optimized system on living cells upon UV irradiation. The observed cell viability, swelling, erosion, porosity, hemocompatibility, and soil degradation properties suggest the NRL-DXT combination for the possible development of high-quality transdermal patches.

Facile preparation and performance of flexible sensors based on polyacrylamide/carboxymethylchitosan/tannin acid hydrogels

AbstractHydrogel flexible sensors are gaining significant interest due to their distinct biocompatibility, flexibility, and unique features of being adjustable and injectable, but there are still problems of poor self‐healing performance and low conductivity in the current stage of research. In this work, a prefabricated blending method was used to construct a dual‐network system using polyacrylamide (PAM), carboxymethyl chitosan (CMCS), and tannin acid (TA), and ferric ions (Fe3+) were introduced to apply ionically conductive organic hydrogels to flexible sensors. The PAM/CMCS‐Fe3+/TA hydrogels have good fatigue resistance and self‐healing properties, and their conductivity is as high as 6.42 S/m. This hydrogel‐based sensor for strain sensing purpose offers a lot of promise for flexible sensor applications since it can provide steady, dependable, and repeatable electrical impulses.

Controlled Radical Copolymerization toward Tailored F/N Hybrid Polymers by Using Light‐Driven Organocatalysis

AbstractControlled radical copolymerizations present attractive avenues to obtain polymers with complicated compositions and sequences. In this work, we report the development of a visible‐light‐driven organocatalyzed controlled copolymerization of fluoroalkenes and acyclic N‐vinylamides for the first time. The approach enables the on‐demand synthesis of a broad scope of amide‐functionalized main‐chain fluoropolymers via novel fluorinated thiocarbamates, facilitating regulations over chemical compositions and alternating fractions by rationally selecting comonomer pairs and ratios. This method allows temporally controlled chain‐growth by external light, and maintains high chain‐end fidelity that promotes facile preparation of block sequences. Notably, the obtained F/N hybrid polymers, upon hydrolysis, afford free amino‐substituted fluoropolymers versatile for post modifications toward various functionalities (e.g., amide, sulfonamide, carbamide, thiocarbamide). We further demonstrate the in situ formation of polymer networks with desirable properties as protective layers on lithium metal anodes, presenting a promising avenue for advancing lithium metal batteries.

Controlled Radical Copolymerization toward Tailored F/N Hybrid Polymers by Using Light-Driven Organocatalysis.

Controlled radical copolymerizations present attractive avenues to obtain polymers with complicated compositions and sequences. In this work, we report the development of a visible-light-driven organocatalyzed controlled copolymerization of fluoroalkenes and acyclic N-vinylamides for the first time. The approach enables the on-demand synthesis of a broad scope of amide-functionalized main-chain fluoropolymers via novel fluorinated thiocarbamates, facilitating regulations over chemical compositions and alternating fractions by rationally selecting comonomer pairs and ratios. This method allows temporally controlled chain-growth by external light, and maintains high chain-end fidelity that promotes facile preparation of block sequences. Notably, the obtained F/N hybrid polymers, upon hydrolysis, afford free amino-substituted fluoropolymers versatile for post modifications toward various functionalities (e.g., amide, sulfonamide, carbamide, thiocarbamide). We further demonstrate the in situ formation of polymer networks with desirable properties as protective layers on lithium metal anodes, presenting a promising avenue for advancing lithium metal batteries.