High Durability Research Articles

Transfunctional Optical Thin Films via Bioinspired Engineering.

Advanced multifunctional optical films or substrates have continued to develop as essential components in the diverse optical industry. Several functions, including high transparency, self-cleaning ability, structural color, flexibility, and durability, are required to obtain versatile and practical optical films. Herein, we introduce a cicada-wing-inspired transfunctional optical thin film (CITOTF) with nanostructures on both surface nanostructures inspired by the cicada-wings. CITOTFs made of perfluoropolyether (PFPE), which has a low refractive index, low surface energy, and high robustness as a substrate material, are obtained by a well-designed sandwich lithography method. We fabricated two types of CITOTFs depending on the size (300 and 1000 nm) of the surface nanostructure. 300-CITOTF and 1000-CITOTF exhibit high transparency and structural color effects, respectively. Both samples demonstrate self-cleaning ability, flexibility, and long-term stability. The bioinspired transfunctional optical films developed in this study can be used in various optical applications.

Optimization of hydrogen production via electrocatalysis using NiCoMo-modified electrodes: An RSM approach

ABSTRACT The depletion of fossil fuels and the environmental impact of their combustion have increased the demand for sustainable energy alternatives, with hydrogen appearing as an appropriate option due to its clean energy potential. This study focuses on developing a laboratory-scale alkaline electrolysis system for hydrogen production. Platinum, known for its high catalytic activity and durability, was employed as the anode, while graphite was selected as the cathode for its cost-effectiveness. To enhance catalytic performance, the graphite electrodes were modified with nickel-cobalt-molybdenum (NiCoMo) using a galvanostatic method. The electrode voltage and molarity were chosen as independent variables to evaluate their effect on hydrogen production. Using the Design-Expert software, the optimal conditions were identified at 3 V and 1.5 mol/l, yielding 10.67 ml of hydrogen. The coefficient of determination (R2) values 98.81% for R2, 97.96% for adjusted R2, and 91.63% for predicted R2 indicate suitable model accuracy. The error margin between experimental and optimized results was only 1.7%, confirming the reliability of the method. This study highlights the potential of NiCoMo-modified electrodes to enhance hydrogen production efficiency. Future research could explore scaling up the system and integrating it with renewable energy sources, positioning this method as a viable pathway toward sustainable hydrogen production.

Development of Novel Frontsheets With Protective Coatings to Increase the Durability and Reliability of Glass‐Free Lightweight PV Modules

ABSTRACTIn this work, novel PET‐based frontsheet materials with UV‐cured coatings were developed and investigated. UV‐curing urethane acrylates were selected as innovative, fluorine‐free coating systems. Polyurethane coatings exhibit excellent UV resistance, chemical and moisture resistance and, thus, high durability in outdoor applications. A homogeneous application without coating defects such as bubbles, voids or detachments was achieved. Material tests with cross‐cut tests showed no separation from the PET substrate. The water vapor transmission rates and the physical (optical and thermal) and chemical properties of the novel polymeric frontsheets were measured and compared with uncoated reference systems and products already on the market. The aging‐related changes after irradiation and humid heat storage were investigated and described in detail. Based on this comprehensive study, the newly developed frontsheets can be considered a suitable alternative to polymeric frontsheets with fluorine‐containing top layers.

The Reduced Barrier for the Photogenerated Charge Migration on Covalent Triazine‐Based Frameworks for Boosting Photocatalytic CO2 Reduction Into Syngas

AbstractPhotocatalytic CO2 reduction together with hydrogen generation is a promising approach to generate syngas, the photogenerated electron migration from photosensitizers to the catalytic active sites is the rate‐determining step. Herein, an integrative strategy is presented by covalently grafting metal complexes into donor–acceptor covalent triazine‐based frameworks. The catalytic active sites are integrated with the photosensitizer units by covalent linkages to form an extended π‐conjugated framework, which significantly reduces the energy barrier for the migration of the photogenerated charge carriers, resulting in high activity and durability in photocatalytic CO2 reduction into syngas under visible light irradiation. The CO and H2 evolution amounts in 1.5 h are 1086 and 1042 µmol g−1, respectively, which greatly surpass those in the host‐guest counterparts. Furthermore, selective adsorption for CO2 over N2 renders this photocatalytic system to be effective for syngas production from the simulated flue gas. This study provides new approaches to construct the integrative photocatalytic systems for solar‐to‐chemical energy conversion.

State-of-the-Art Review of Microcapsule Self-Repairing Concrete: Principles, Applications, Test Methods, Prospects

Cement-based materials are widely used in construction worldwide, but they are vulnerable to environmental stressors and thermal fluctuations, leading to the formation of internal cracks that compromise structural integrity and durability. Traditional repair methods such as surface coatings, grouting, and groove filling are often costly and labor-intensive. In response, self-repairing technologies for cement-based materials have emerged as an innovative and promising solution, offering the potential to significantly extend the lifespan of structures and reduce maintenance costs. A particularly novel approach is the development of microcapsule-based self-repairing concrete. In this system, repair agents are encapsulated within microcapsules and combined with curing agents in the concrete matrix. When cracks form, the microcapsules rupture, releasing the repair agents to autonomously heal the damage. This self-repairing mechanism is characterized by its high efficiency, durability, environmental sustainability, and versatility, making it a promising alternative to traditional repair methods. Recent research has focused on the development of microcapsules with various core materials, such as TDI (toluene diisocyanate), IPDI (isophorone diisocyanate), or epoxy resin, as well as composite shell materials including paraffin wax, PE (polyethylene) wax, nano-SiO2, and nano-CaCO3. A novel advancement in this area involves the enhancement of microcapsules through the incorporation of magnetic nanomaterials into the shell, providing new possibilities for self-repairing systems that address cracks in cement-based materials.

Composite Gel Polymer Electrolyte for High-Performance Flexible Zinc-Air Batteries.

Enhancing ionic conductivity and electrolyte uptake is of significance for gel polymer electrolytes (GPEs) for flexible zinc-air batteries (FZABs). Herein, a composite mesoporous silica/polyacrylamide (5 wt.% mPAM) GPE is constructed with comparable ionic conductivity to aqueous electrolytes, where the ionic conductivity is up to 337 mS cm-1, and the weight loss after exposing in air 72h is less than 18%, owing to the excellent electrolyte uptake and continuous ion migration network provided by the mesoporous silica fillers. When used as a quasi-solid-electrolyte, the rechargeable FZAB exhibited high electrochemical performance and structural stability, where the peak power density is up to 162.8mW cm-2, and the initial charge-discharge potential gap is as low as 0.62V, resulting in a long lifespan exceeding 110h, showcasing the combination of high durability, cost-effectiveness and easy production for practical applications.

Developing Sustainable Wood Preservatives: The Antifungal Efficiency of Afzelia quanzensis Welv. and Androstachys johnsonii Prain Sawdust Extracts from Mozambique

This study aimed to both develop and assess the antifungal efficacy of extractives derived from different sets of sawdust originating from two hardwood species, namely chanfuta (Afzelia quanzensis Welv.) and mecrusse (Androstachys johnsonnii Prain). These hardwood species possess inherent characteristics of high natural durability. The primary objective was to use these extractives to impregnate perishable wood species, enhancing their durability and augmenting their commercial value. Collected wood sawdust was initially sieved to remove residues and unwanted materials and conditioned until 12% moisture content. Subsequently, the sawdust was Soxhlet-extracted using a mixture of organic solvents, including acetone, ethanol, and toluene. After evaporating the solvents, the resulting extractives were used to prepare a preservative solution with ethanol and acetone. The extractive solutions from each wood species were mixed with malt extract agar and then diluted to various concentrations: 0.125 mg/mL, 0.25 mg/mL, 0.5 mg/mL, 1.25 mg/mL, 2.0 mg/mL, and 2.5 mg/mL. For each concentration, fungal plugs from the periphery of actively growing cultures were moved to the centre of Petri dishes and placed in controlled laboratory conditions for incubation. The antifungal efficacy was assessed against specific wood-decaying fungi, including brown rot fungi (Coniophora puteana, Postia placenta, Lentinus lapideus) and white rot (Trametes versicolor). The evaluation involved daily monitoring of the linear expansion along two perpendicular radii for each fungus expressed as a percentage of the empty Petri dish area. The results indicated that the chanfuta extractives inhibited the growth of brown rot fungi at a concentration of 0.25 mg/mL and white rot fungi at 2.0 mg/mL. Similarly, the mecrusse extractives inhibit brown rot at 0.5 mg/mL and white rot at 2.0 mg/mL. The fatty acids Oleic (C18:1) present in the chanfuta extractives solution and linoleic (C18:2) in mecrusse extractives contributed to restraining the fungal growth. These results suggest that sawdust extractives from both wood species exhibit promising potential for creating environmentally friendly wood preservatives, which, with effective treatments, could extend the lifespan of perishable wood species

Luminescence Patterns on Multimillimeter Single-Crystal MAPbBr3 Microplatelets via Thermal Ablation Effects.

The single crystal distinguishes itself as the most outstanding representative of excellent optoelectronic performance among perovskite semiconductors due to its exceptional charge carrier properties, extraordinary optophysics, precise structural geometries, and superior material stabilities. However, it exhibits mediocre performance in light emission, which can be attributed to its excessive carrier diffusion lengths and extremely low recombination rates. To address this challenge, this study puts forward a controllable high-temperature annealing treatment strategy concentrating on multimillimeter-scale MAPbBr3 micrometer-thick platelet single crystals (MPSCs). Through the utilization of thermal ablation effects to convert the surface monocrystalline lattices into polycrystalline perovskite nanocrystals (PNCs) with a remarkably increased specific surface area, the fluorescence intensity arising from the rapid recombination of free carriers on the PNC surface is enhanced by 320 times compared to the pristine MPSC surface. These PNCs produced through surface annealing, with the characteristic of loose adhesion to surfaces, can be mechanically wiped away and regenerated in situ via reannealing the residual MAPbBr3 MPSCs, guaranteeing high intensity, durability, and standard geometric fluorescence. Moreover, by regulating the surface distributions of thermal ablation effects and carrying out embossing annealing treatment or laser direct writing, we can design and fabricate relatively complex, high-contrast (255×), and clearly resolved fluorescence patterns on MPSC surfaces.

Roles of Divinylbenzene Co‐Cross‐Linker in a Threefold Cross‐Linked Polystyrene–Phosphine Hybrid Monolith: Impact of Cross‐linking Degree on Catalytic Performance

AbstractContinuous‐flow organic transformations using immobilized catalysts are crucial for green and sustainable chemistry. Cross‐linked polymer ligands offer high stability, ease of recovery through filtration, and thus enhance performance in continuous‐flow reactions via transition‐metal catalysis. Additionally, the cross‐linking structure of the polymer support creates a unique reaction platform that controls the coordination behavior of the supported ligands and stabilizes the metal catalysts. However, insights into the material‐based design for preparing highly active and durable immobilized metal catalysts are still limited. In this report, we propose a straightforward approach to boost both selective mono‐coordination and effective stabilization of metal complexes. We developed threefold cross‐linked polystyrene‐triphenylphosphine hybrid monoliths with cross‐linking structures adjusted by varying the content of divinylbenzene as co‐cross‐linker. The coordination behaviors and metal‐support interactions of these monoliths were evaluated, highlighting the importance of co‐cross‐linker content in site‐isolating phosphine units and stabilizing metal centers via arene‐metal interactions on the polystyrene network. By optimizing the cross‐linking structure, the monolith catalysts demonstrated exceptionally high catalytic activity and durability in Pd‐catalyzed C−Cl transformations, such as Suzuki–Miyaura cross‐couplings and Buchwald‐Hartwig aminations in continuous flow. This underscores the utility of our monolith system in challenging transition‐metal catalysis.

Photothermal Induced Dual-Interface: Accelerating Sustainable Hydrogen Evolution from Formic Acid.

Formic acid (FA), a liquid hydrogen storage carrier, can release hydrogen via photothermal catalysis, providing a clean and sustainable solution toward a carbon-neutral energy cycle. Despite recent advances in the design of efficient catalysts, the development of advanced systems with high H2 yield, stability, and durability remains challenging due to the inefficient photothermal conversion and mass transfer in the traditional liquid-solid bulk system, as well as the trade-off between hydrogen storage density and dehydrogenation rate. Here, we address these challenges by creating a photothermal-induced dual-interface characterized by high spectral absorption and low heat loss, a facile supply of FA, and vaporization of FA to minimize the energy barrier of the reaction. As a result, a record hydrogen evolution rate (200.9 mmol g-1 h-1) is achieved in a high concentration (26 M) of FA, which is about 15 times higher than the liquid-solid bulk system. In addition, it can be operated continuously for more than 192 h without additive addition and energy consumption, providing a strategy for accelerating interfacial mass transfer to improve catalytic activity, and also presents a reference for sustainable hydrogen production.

Fabrication of high-efficiency perovskite solar cells using benzodithiophene-based random copolymeric hole transport material

The design of donor-acceptor (D-A)-based random copolymers-type hole transporting materials (HTMs) are important for achieving superior performance of perovskite solar cells (PSCs) with high durability. In this work, a 2-alkylthienyl-substituted benzodithiophene (BDTT)-based random copolymer (denoted as RCP-BDTTPD), containing 2-ethylhexylthiophene-substituted benzo[1,2-b:4,5-b′]dithiophene (BDTT as an electron-donor; M1) and two different side-chain functionalized thieno[3,4-c]-pyrrole-4,6‑dione as the electron-acceptors (M2 and M3), is prepared and applied as an efficient interfacial HTM for PSCs. The optical, electrochemical, and electronic properties of RCP-BDTTPD are shown to be structurally and energetically viable to serve as HTM for PSCs. The RCP-BDTTPD has deeper highest occupied molecular orbitals (HOMO; −5.53 eV) and lowest unoccupied molecular orbitals (LUMO; −3.57 eV) energy levels. This is shown to be energetically suitable for realizing better compatibility with Cs-containing formamidinium/methylammonium (FAMA) mixed-cation perovskite as light absorber having HOMO energy level (−5.85 eV). The RCP-BDTTPD possessing gradient band alignment with perovskite, which is shown to be highly significant for the extraction of charge carriers, resulting in higher hole mobility of PSCs. RCP-BDTTPD delivered a reasonably good Voc of 1.10 V and higher Jsc of 19.01 mAcm−2 and, champion power conversion efficiency (PCE) up to 15.30 % with hole mobility (1.34×10−3 cm2V−1s−1) and high durability (Encapsulated cell retention of its PCE about 98 % over 16 h under harsh environment: Temp. ∼85 °C, RH∼85 %). This work demonstrating a potential application of RCP-BDTTPD based HTMs for the fabrication of high-performance PSCs with high durability as well as low cost.

Silver Nanoparticles Formed Directly on a Screen-Printed Electrode/Graphene Oxide: A One-Step Electrochemical Synthesis and an Effective 2,4,6-Trichlorophenol Electrochemical Sensor

Abstract A graphene oxide/silver nanoparticles (GO/AgNPs) nanocomposite was synthesized directly onto a screen-printed electrode (SPE) using a one-step electrochemical synthesis process. The obtained result is that the SPE electrode was modified by AgNPs with an average diameter of 11.5 nm which distributed evenly on GO sheets. A 0.01 M AgNO3 solution dropped onto the SPE/GO electrode and a chronoamperometry (CA) method with a potential of −1.2 V and a time period of 10 seconds were the optimal synthesis conditions. Then, the SPE/GO/AgNPs electrode was applied in developing an electrochemical sensor to detect 2,4,6-trichlorophenol (2,4,6-TCP) using a square wave voltammetry method. A reasonable cost, a wide linear range (0.05–1.0 mM), a low detection limit (0.85 μM), a high repeatability, a good selectivity, a high durability, and especially, a rapid detection time (< 1 minute) thanks to the ability to directly detect 2,4,6-TCP were the outstanding advantages of the fabricated electrochemical sensor. Moreover, the electrochemical sensor based on the SPE/GO/AgNPs electrode was also applied to detect 2,4,6-TCP in a tap water sample using a standard addition method.

Recyclable VOCs-free eutectic adhesive based on hydrogen bond fusion strategy with robust adhesion, flame retardancy, transparency, high durability, and low-temperature resistance

Although emerging supramolecular adhesives have addressed the challenge of traditional adhesives in terms of de-bonding through non-covalent interactions, they still face issues such as high synthetic difficulty, elevated costs, and inadequate adhesion strength, particularly under low temperatures. Additionally, achieving robust adhesion to low-energy hydrophobic surfaces remains a persistent challenge. This paper proposes a novel hydrogen bond fusion strategy to address these challenges, presenting the synthesis of a new HCX eutectogel, containing intramolecular fused hydrogen bonds and intermolecular hydrogen bonds. This approach enables the attainment of high-strength adhesion on both hydrophilic (up to 10.61 MPa) and hydrophobic (up to 4.87 MPa) substrates. Notably, the HCX eutectogel stands out for its ability to maintain stable adhesion performance at low temperatures (−80 °C & liquid nitrogen) and its extraordinary flame retardancy and recyclability. These findings contribute novel insights into the development of high-performance adhesives with multifunctionality, promising advancements in diverse applications.

Humidity tolerant enhanced hydrogen gas sensing using MoSe[formula omitted]-WSe[formula omitted] heterostructures: An experimental and computational insights

In recent times, air pollution’s threat to humanity highlights the urgent need for advanced sensors to monitor harmful gases, essential for industrial regulation, gas leak detection, and air quality surveillance. Two-dimensional transition metal dichalcogenides (TMDCs) has garnered noteworthy attention as potential materials for gas sensing. This paper investigates the synthesis and characterization of a heterostructure composed of molybdenum diselenide with tungsten diselenide (MoSe2-WSe2) nanomaterials using a liquid phase exfoliation technique and it’s H2 sensing performance. The material characterisations confirmed the successful exfoliation into a hexagonal sheet-like, nanocrystalline MoSe2-WSe2 nanostructure. The study further assessed the sensor’s response to H2 gas, for concentrations of 5–25 ppm at room temperature, comparing the performance of MoSe2-WSe2 sensor with a pristine WSe2 sensor. The MoSe2-WSe2 sensor outperformed the pristine WSe2 sensor with a response of 59.57%, rapid response times and recovery times (16 s and 30 s respectively), low detection limit of 5.55 ppm, good repeatability, and high durability (30 days). Additionally, the impact of humidity was evaluated at 25 ppm H2 (at relative-humidity from 40% to 90%). The hydrophobic nature of MoSe2-WSe2 (CA = 141.4°) aligns with the first principle studies, showing almost no change in bandgap when exposed to humidity. These findings emphasize the potential of MoSe2-WSe2 heterostructure sensors for detecting H2 in humid conditions, filling a gap in research and advancing gas sensing technology for environmental safety.

N-Type Nanocomposite Films Combining SWCNTs, Bi2Te3 Nanoplates, and Cationic Surfactant for Pn-Junction Thermoelectric Generators with Self-Generated Temperature Gradient Under Uniform Sunlight Irradiation.

Flexible thermoelectric generators (TEGs) with pn-junction single-walled carbon nanotube (SWCNT) films on a polyimide substrate have attracted considerable attention for energy harvesting. This is because they generate electricity through the photo-thermoelectric effect by self-generated temperature gradient under uniform sunlight irradiation. To increase the performance and durability of the pn-junction TEGs, n-type films need to be improved as a priority. In this study, bismuth telluride (Bi2Te3) nanoplates synthesized by the solvothermal method were added to the n-type SWCNT films, including a cationic surfactant to form the nanocomposite films because Bi2Te3 has high n-type thermoelectric properties and high durability. The performances of the pn-junction TEGs were investigated by varying the heat treatment times. When the artificial sunlight was uniformly irradiated to the pn-junction TEGs, a stable output voltage of 0.47 mV was observed in the TEG with nanocomposite films heat-treated at 1 h. The output voltage decreased with increasing heat treatment time due to the decrease in the p-type region. The output voltage of TEG at 1 h is higher than that of the TEGs without Bi2Te3 nanoplates under the same conditions. Therefore, the addition of Bi2Te3 nanoplates was found to improve the performance of the pn-junction TEGs. These findings may aid in the development of facile and flexible optical devices, including photodetectors and hybrid devices integrating solar cells.

Modulating the energy harvesting with tunable hardness from mildly functionalized graphite nanoplatelets-based composites for wearable applications

It is challenging to obtain balanced properties with good stretchability, mechanical stability, small response time, high output voltage, and finally optimum mechanical hardness. Thus, the present work supports that balanced properties can be obtained with good interfacial interactions during composite fabrication. Here, the ingredients involve the addition of mild functionalized graphite nanoplatelets (mf-GNP), silicone oil, and vulcanizing agents into the silicone rubber (SR) as a rubber matrix. The justification for the “mild” functionalization of GNP was validated through spectroscopic studies in this work. Robust functional groups like carboxyl (O-H), carbonyl (C=O), epoxy, and alkoxy (C-O) on the surface of mf-GNP expect improved interactions with the SR matrix. Moreover, results show that adding 5 per hundred parts of rubber (phr) of mf-GNP in the SR matrix increases compressive modulus, hardness, and stretchability. However, the addition of a different content of thinner lowers the hardness making the composites mechanically soft and ultrasoft. For example, the hardness was 25 (control sample), 27 (5 phr of mf-GNP filled sample)., 24 with 10 phr thinner (T10 sample), and finally 16 with 30 phr of thinner (T30 sample). The results further insight the stretchability was increased with different contents of mf-GNP or thinner in the SR matrix. For example, stretchability was 111% (control sample), 144% (5 phr of mf-GNP filled sample), 156% (T10 sample), and finally 129% (T30 sample). Also, the energy harvested tests were performed to obtain output voltage and response time for industrial applications of this work. For example, the response time at 30% compressive strain was 154 milliseconds (ms) (5 phr of mf-GNP filled sample), 184 ms (T10 sample), and finally 225 ms (T30 sample). The power density was ~2.65 nanowatt per centimeter square (nW/cm2) (mf-GNP sample), ~8.34 nW/cm2 (T10 sample), and finally ~1.69 nW/cm2 (T30 sample). Moreover, the piezoelectric coefficient was 14.5 picocoulomb per Newton (pC/N) (mf-GNP sample), 66.2 pC/N (T10 sample), and finally 19.37 pC/N (T30 sample). Finally, the results support the T10 sample as best with the balance of good stretchability, relatively optimum response time, higher durability, and finally good output voltage.

Intermittent polarity inversion of stainless-steel paired electrodes for efficient and durable water electrolysis

Designing robust and cost-effective catalysts through straightforward and replicable techniques is crucial for advancing water electrolysis. In this study, we introduce a dynamic polarization control method for the continuous activation of stainless steel (SS) substrates to achieve high water-splitting performance and durability. By applying periodic inverted current density during high-current–density operation (0.5 or 1 A cm−2) on bare SS adopted as both cathode and anode substrates, a NiFe-based oxide structure favorable for the hydrogen evolution reaction is formed at the cathode, while a Fe-incorporated NiOOH structure with high efficacy for the oxygen evolution reaction develops at the anode. Implemented in an anion exchange membrane water electrolysis system, this inverted polarization approach applied for the SS paired electrolyzer system successfully maintains a cell voltage of approximately 1.9 V for 500 h at a current density of 1 A cm−2 using bare SS for both electrodes.

High Energy Conversion Efficiency and Cycle Durability of Solar-Powered Self-Sustaining Light-Assisted Rechargeable Zinc–Air Batteries System

The issue of energy supply in outdoor and remote areas has become a significant challenge. Solar-powered self-sustaining rechargeable zinc-air batteries (RZABs) offer a viable energy solution for off-grid regions. However, there has been no specific study on the technical compatibility and adaptability of the solar power generation system and RZABs system, as well as the efficiency of energy conversion and storage in such solar-powered RZABs systems. To address these challenges, this study developed a solar-powered self-sustaining photo-assisted RZABs system based on a photo-responsive polyterthiophene (pTTh) cathode. This system employs pTTh with photo-responsive properties as the cathode catalyst for RZABs, which not only significantly reduces the overpotential of the cathode but also enhances the performance of the RZABs and the overall energy conversion efficiency (reaching 16.2%). In practical applications, the system exhibits excellent stability, operating continuously within a wide temperature range of -15 to 40°C, and demonstrating a stable cycling operation capability of up to 33 days. It provides reliable, low-cost power support for electronic devices such as mobile phones, flashlights, GPS units, and small pollutant detection systems, greatly improving the practicality of these devices in off-grid areas.

Bioinspired multi-functional modified PVDF membrane for efficient oil-water separation

The pervasive issue of oily wastewater presents a critical environmental challenge, necessitating the development of advanced membranes that offer high purification efficiency, durability, and versatility. In this study, we introduce a novel bioinspired multifunctional membrane, synthesized by modifying polyvinylidene fluoride (PVDF) with fibrous two-dimensional carbides and nitrides (MXene) and silica (SiO2) nanoparticles, drawing inspiration from the complex structure of coral stones. The membrane was fabricated using the phase inversion technique, producing a robust material that achieves over 99% separation efficiency for oil–water mixtures. Beyond oil–water separation, the membrane exhibited exceptional performance in removing various contaminants from complex oily wastewater, including heavy metals, dyes, and phenol. Remarkably, the membrane maintained its high purification efficiency even after 5 consecutive cycles of oil–water separation and pollutant adsorption. This bioinspired multifunctional modified PVDF (MMP) membrane represents a major advancement in wastewater treatment technology, with significant potential for widespread application in the purification of complex oily wastewater.

K-Mn3O4-NCs@PANI nanochains for high-rate and stable aqueous zinc-ion batteries: A doping and morphology-tailored synthesis strategy

Aqueous zinc ion batteries (AZIBs) are promising energy storage solutions due to their high energy density and safety. However, developing cathode materials that offer both high energy density and durability for Zn2+ ions storage remains challenging. Manganese (Mn) oxide-based cathodes have been developed for AZIBs due to their high discharge voltage and desirable capacity, but face challenges like poor conductivity, slow reaction kinetics, and dissolution during cycling. Doping, morphology/structure design, and protective layers are effective for enhancing the structure, conductivity, and electronic properties of Mn-based oxides. A synthetic strategy combining these methods for Mn3O4 cathodes is proposed for AZIBs. K+ ions doping in Mn3O4 (K-Mn3O4) can regulate local electronic structure, induce oxygen vacancies, improve conductivity, and provide more active sites for Zn2+ ions diffusion. Additionally, K-Mn3O4 nanochain (K-Mn3O4-NCs), with a unique chain-like nanostructure (NCs) and high aspect ratio, synthesized via Mn2+ ions chelation with nitrilotriacetic acid (NTA) and calcination, show reduced interparticle contact resistance, shorter Zn2+ ions diffusion length, and faster reaction kinetics. Meanwhile, the in-situ polymerized polyaniline (PANI) layer on K-Mn3O4-NCs shields against corrosion (K-Mn3O4-NCs@PANI), connects 1D K-Mn3O4-NCs into a continuous conductive network, suppresses volume expansion, and improves stability. Electrochemical analysis shows that K-Mn3O4-NCs@PANI exhibits higher stability and faster reaction kinetics due to a reduced bandgap, increased oxygen defects, and less coulombic repulsion between Zn2+ ions and Mn oxide hosts. The K-Mn3O4-NCs@PANI cathode achieved a high capacity of 510mAh/g at 0.1 A/g and excellent rate capacity of 203.2mAh/g at 5 A/g. After 20,000 cycles, it maintained a capacity of 90.3mAh/g at 5 A/g, showing exceptional long-term stability with a minimal decay rate of 0.026 ‰ per cycle.