Search Results (535)

Ecotribology focuses on both saving energy resources and reducing environmental pollution. Considering environmental concerns, water-based nanolubricants have gained significant attention over conventional oil-based ones. Non-ecotoxic and highly environmentally friendly nanoadditives were chosen for nanolubricant synthesis, especially considering their use at elevated temperatures. In this study, hexagonal boron nitride nanosheets (hBNNSs) and titanium dioxide nanoparticles (TiO₂ NPs) were used to prepare water-based lubricants with glycerol and surfactant sodium dodecyl benzene sulfonate (SDBS) in water under ultrasonication. An Rtec ball-on-disk tribometer was used to investigate the tribological performance of the synthesised water-based lubricants containing different nano-hBN/TiO₂ concentrations, with dry and water conditions used as benchmarks. The results indicated that the water-based nanolubricant containing 0.5 wt% hBN and 0.5 wt% TiO₂ exhibited the best tribological performance at both ambient (25 °C) and elevated (500 °C) temperatures. This optimal concentration leads to a reduction in the coefficient of friction (COF) by 72.9% and 37.5%, wear of disk by 62.5% and 49%, and wear of ball by 74% and 69% at ambient and elevated temperatures, respectively, compared to that of distilled water. Lubrication mechanisms were attributed to the rolling, mending, tribofilm, solid layer formation, and synergistic effects of hBNNSs and TiO₂ NPs. Full article

The development of lightweight composites with superior mechanical properties and electromagnetic interference (EMI) shielding performance is essential for various structural and functional applications. This study investigates the effect of hybrid nanocarbon (graphene nanosheet (GNS) and carbon nanotube (CNT)) reinforcements on the properties of magnesium (Mg) matrix composites. Specifically, the GNS-CNT hybrid, which forms a three-dimensional interconnected network structure, was analyzed and compared to composites reinforced with only GNSs or CNTs. The objective was to determine the benefits of hybrid reinforcements on the mechanical strength and EMI shielding capability of the composites. The results indicated that the GNS-CNT/Mg composite, at a nanocarbon content of 0.5 wt.% and a GNS-CNT ratio of 1:2, achieved optimal performance, with a 55% increase in tensile strength and an EMI shielding effectiveness of 70 dB. The observed enhancements can be attributed to several key mechanisms: effective load transfer, which promotes tensile twinning, along with improved impedance matching and multiple internal reflections within the GNS-CNT network, which enhance absorption loss. These significant improvements position the composite as a promising candidate for advanced applications requiring high strength, toughness, and efficient electromagnetic shielding, providing valuable insights into the design of high-performance lightweight materials. Full article

The electrocatalytic CO₂ reduction reaction (CO₂RR) offers an energy-saving and environmentally friendly approach to producing hydrocarbon fuels. The use of a gas diffusion electrode (GDE) flow cell has generally improved the rate of CO₂RR, while the gas diffusion layer (GDL) remains a significant challenge. In this study, we successfully engineered a novel metal–organic framework (MOF) heterojunction through the controlled coating of zeolitic imidazolate framework (ZIF-L) on ultrathin nickel—metal–organic framework (Ni-MOF) nanosheets. This innovative architecture simultaneously integrates GDL functionality and exposes abundant solid–liquid–gas triple-phase boundaries. The resulting Ni-MOF@ZIF-L heterostructure demonstrates exceptional performance, achieving a formate Faradaic efficiency of 92.4% while suppressing the hydrogen evolution reaction (HER) to 6.7%. Through computational modeling of the optimized heterojunction configuration, we further elucidated its competitive adsorption behavior and electronic modulation effects. The experimental and theoretical results demonstrate an improvement in electrochemical CO₂ reduction activity with suppressed hydrogen evolution for the heterojunction because of its hydrophobic interface, good electron transfer capability, and high CO₂ adsorption at the catalyst interface. This work provides a new insight into the rational design of porous crystalline materials in electrocatalytic CO₂RR. Full article

In this paper, a series of polyaniline (PANI)/Ti₃C₂ MXene composites (PMCs) with a biomimetic structure were prepared and employed as an anticorrosion coating application. First, the PANI was synthesized by oxidative polymerization with ammonium persulfate as the oxidant. Then, 2D Ti₃C₂ MXene nanosheets were prepared by treating the Ti₃AlC₂ using the optimized minimally intensive layer delamination (MILD) method, followed by characterization via XRD and SEM. Subsequently, the PMC was prepared by the oxidative polymerization of aniline monomers in the presence of Ti₃C₂ MXene nanosheets, followed by characterization via FTIR, XRD, SEM, TEM, CV, and UV–Visible. Eventually, the PMC coatings with the artificial biomimetic surface structure of a macaw feather were prepared by the nano-casting technique. The corrosion resistance of the PMC coatings, evaluated via Tafel polarization and Nyquist impedance measurements, shows that increasing the MXene loading up to 5 wt % shifts the corrosion potential (E_corr) on steel from −588 mV to −356 mV vs. SCE, reduces the corrosion current density (I_corr) from 1.09 µA/cm² to 0.035 µA/cm², and raises the impedance modulus at 0.01 Hz from 67 kΩ to 3794 kΩ. When structured with the hierarchical feather topography, the PMC coating (Bio-PA-MX-5) further advances the E_corr to +103.6 mV, lowers the I_corr to 7.22 × 10⁻⁴ µA/cm², and boosts the impedance to 96,875 kΩ. Compared to neat coatings without biomimetic structuring, those with engineered biomimetic surfaces showed significantly improved corrosion protection performance. These enhancements arise from three synergistic mechanisms: (i) polyaniline’s redox catalysis accelerates the formation of a dense passive oxide layer; (ii) MXene nanosheets create a tortuous gas barrier that cuts the oxygen permeability from 11.3 Barrer to 0.9 Barrer; and (iii) the biomimetic surface traps air pockets, raising the water contact angle from 87° to 135°. This integrated approach delivers one of the highest combined corrosion potentials and impedance values reported for thin-film coatings, pointing to a general strategy for durable steel protection. Full article

This study reported covalent organic frameworks (COFs) and their hybrid composites with two-dimensional materials, graphene oxide (GO), graphitic carbon nitride (g-C₃N₄), and boron nitride (BN), to examine their structural, textural, and gas adsorption properties. Material characterization confirmed the crystallinity of COF-1 and the preservation of framework integrity after integrating the 2D nanomaterials. FT-IR spectra exhibited pronounced vibrational fingerprints of imine linkages and validated the functional groups from the COF and the integrated nanomaterials. TEM images revealed the integration of the two components, porous, layered structures with indications of interfacial interactions between COF and 2D nanosheets. Nitrogen adsorption–desorption isotherms revealed the microporous characteristics of the COFs, with hysteresis loops evident, indicating the development of supplementary mesopores at the interface between COF-1 and the 2D materials. The BET surface area of pristine COF-1 was maximal at 437 m²/g, accompanied by significant micropore and Langmuir surface areas of 348 and 1290 m²/g, respectively, offering enhanced average pore widths and hierarchical porous strcuture. CO₂ adsorption tests were investigated showing maximum adsorption capacitiy of 1.47 mmol/g, for COF-1, closely followed by COF@BN at 1.40 mmol/g, underscoring the preserved sorption capabilities of these materials. These findings demonstrate the promise of designed COF-based hybrids for gas capture, separation, and environmental remediation applications. Full article

Owing to high electrical conductivity, layered structure, and abundant surface functional groups, transition metal carbides/nitrides (MXenes) have received enormous interest in the field of gas sensors at room temperature. In this work, we synthesize a heterostructured nanocomposite with indium oxide (In₂O₃) decorated on titanium carbide (Ti₃C₂T_x) nanosheets by electrostatic self-assembly and develop it for high-selectivity NO₂ gas sensing at room temperature. Self-assembly formation of multiple heterojunctions in the In₂O₃/Ti₃C₂T_x composite provide abundant NO₂ gas adsorption sites and high electron transfer activity, which is conducive to improving the gas-sensing response of the In₂O₃/Ti₃C₂T_x gas sensor. Assisted by rich adsorption sites and hetero interface, the as-fabricated In₂O₃/Ti₃C₂T_x gas sensor exhibits the highest response to NO₂ among various interference gases. Meanwhile, a detection limit of 0.3 ppm, and response/recovery time (197.62/93.84 s) is displayed at room temperature. Finally, a NO₂ sensing mechanism of In₂O₃/Ti₃C₂T_x gas sensor is constructed based on PN heterojunction enhancement and molecular adsorption. This work not only expands the gas-sensing application of MXenes, but also demonstrates an avenue for the rational design and construction of NO₂-sensing materials. Full article

Two-dimensional (2D) material-based resistive random-access memory (RRAM) has emerged as a promising solution for neuromorphic computing and computing-in-memory architectures. Compared to conventional metal-oxide-based RRAM, the novel 2D material-based RRAM devices demonstrate lower power consumption, higher integration density, and reduced performance variability, benefiting from their atomic-scale thickness and ultra-flat surfaces. Remarkably, 2D layered metal oxides retain these advantages while preserving the merits of traditional metal oxides, including their low cost and high environmental stability. Through a multi-step dry transfer process, we fabricated a Pd-MoO₃-Ag RRAM device featuring 2D α-MoO₃ as the resistive switching layer, with Pd and Ag serving as inert and active electrodes, respectively. Resistive switching tests revealed an excellent operational stability, low write voltage (~0.5 V), high switching ratio (>10⁶), and multi-bit storage capability (≥3 bits). Nevertheless, the device exhibited a limited retention time (~2000 s). To overcome this limitation, we developed a Gr-MoO₃-Ag heterostructure by substituting the Pd electrode with graphene (Gr). This modification achieved a fivefold improvement in the retention time (>10⁴ s). These findings demonstrate that by controlling the type and thickness of 2D materials and resistive switching layers, RRAM devices with both high On/Off ratios and long-term data retention may be developed. Full article

In this paper, we use the facile approach for preparing novel, low-cost, efficient electrocatalysts for electrocatalytic water splitting. Interfacial engineering can significantly enhance the intrinsic performance of electrocatalysts. Herein, self-supporting FeOOH/NiFe-layered double hydroxide (LDH) nanosheet arrays were synthesized via hydrothermal and impregnation methods. The resulting FeOOH/NiFe-LDH can provide more active regions, which provide more active regions for co-reaction to proceed and accelerates electron transmit processes. Additionally, the amorphous FeOOH provides abundant active sites with low coordination, leading to excellent activity. The FeOOH/NiFe-LDH demonstrates remarkable two half-reaction electrocatalytic activity, along with excellent overpotentials of 168 mV (OER) and 155 mV (HER). This research introduces a sophisticated and scalable methodology for the creation of remarkably efficient and resilient alkaline conditions specifically designed for the HER and OER. Full article

Transition metal oxides (TMOs) are considered to be highly promising materials for supercapacitor electrodes due to their low cost, multiple convertible valence states, and excellent electrochemical properties. However, inherent limitations, including restricted specific surface area and low electrical conductivity, have largely restricted their application in supercapacitors. In this paper, core–shell heterostructures of nickel–iron layered double hydroxide (NiFe-LDH) nanosheets uniformly grown on CuCo₂O₄ nanoneedles were synthesized by hydrothermal and calcination methods. It is found that the novel core–shell structure of CuCo₂O₄@NiFe-LDH improves the electrical conductivity of the electrode materials and optimizes the charge transport path. Under the synergistic effect of the two components and the core–shell heterostructure, the CuCo₂O₄@NiFe-LDH electrode achieves an ultra-high specific capacity of 323.4 mAh g⁻¹ at 1 A g⁻¹. And the capacity retention after 10,000 cycles at 10 A g⁻¹ is 90.66%. In addition, the assembled CuCo₂O₄@NiFe-LDH//RGO asymmetric supercapacitor device achieved a considerable energy density (68.7 Wh kg⁻¹ at 856.3 W kg⁻¹). It also has 89.36% capacity retention after 10,000 cycles at 10 A g⁻¹. These properties indicate the great potential application of CuCo₂O₄@NiFe-LDH in the field of high-performance supercapacitors. Full article

The textile industry encounters serious environmental challenges from wastewater with persistent organic pollutants, demanding sustainable solutions for remediation. Herein, we report a novel green synthesis of flexible BiOBr@PZT nanocomposite membranes via electrospinning and successive ionic layer adsorption and reaction (SILAR) for visible-light-driven photocatalytic degradation. The hierarchical structure integrates leaf-like BiOBr nanosheets with PAN/ZnO/TiO₂ (PZT) nanofibers, forming a Z-scheme heterojunction. This enhances the separation of photogenerated carriers while preserving mechanical integrity. SILAR-enabled low temperature deposition ensures eco-friendly fabrication by avoiding toxic precursors and cutting energy use. Optimized BiOBr@PZT-5 shows exceptional photocatalytic performance, achieving 97.6% tetracycline hydrochloride (TCH) degradation under visible light in 120 min. It also has strong tensile strength (4.29 MPa) and cycling stability. Mechanistic studies show efficient generation of O₂⁻ and OH radicals through synergistic light absorption, charge transfer, and turbulence-enhanced mass diffusion. The material’s flexibility allows reusable turbulent flow applications, overcoming rigid catalyst limitations. Aligning with green chemistry and UN SDGs, this work advances multifunctional photocatalytic systems for scalable, energy-efficient wastewater treatment, offering a paradigm that integrates environmental remediation with industrial adaptability. Full article

The preparation of stable dispersions of MoS₂ by ultrasonic aqueous and/or organic media containing amphiphilic molecules is an attractive and widely applicable method to form MoS₂ fine particles while suppressing its aggregation. In this study, we developed a series of polymers with pendant sulfide moieties as a new dispersant, under the hypothesis that it would interact with sulfur atoms on MoS₂ surfaces. First, we designed a sulfide group-substituted methacrylate derivative (ESMA) with the hypothesis that it would interact with the MoS₂ surface through sulfur-sulfur interactions. Then, we synthesized well-defined polymers with pendant sulfide groups by living radical polymerization (ATRP). Next, 0.5 wt% MoS₂ was added to a DMSO solution containing 1 wt% of the obtained polymer (polyESMA), and the mixture was treated with a bath-type ultrasonicator for 3 h to obtain a MoS₂ dispersion. We found that stable dispersions of MoS₂ in a fine particle state, although not in the form of single-layer or few-layer nanosheets, could be readily formed in DMSO using polyESMA as a polymeric dispersant. Furthermore, we synthesized polymeric dispersants with different molecular weights and investigated the relationship between the structure of the dispersant and the dispersion stability. Full article

Excessive Zn(II) ions in aquatic environments pose significant risks to both human health and ecological systems due to their toxic effects, bioaccumulation potential, and interference with essential biological processes. To address this issue, a novel analcime@calcium aluminate@polyethylene glycol 400 (ACP) nanocomposite was fabricated using the hydrothermal technique, alongside an analcime@calcium aluminate (AC) nanocomposite for the efficient elimination of Zn(II) ions from aqueous media. X-ray diffraction (XRD) analysis affirmed the successful formation of crystalline phases, revealing average crystallite sizes of 72.93 nm for AC and 63.60 nm for ACP. Energy-dispersive X-ray spectroscopy (EDX) confirmed the elemental composition of the nanocomposites, showing that AC primarily contained oxygen, sodium, aluminum, silicon, and calcium, whereas ACP incorporated 19.3% carbon due to the polyethylene glycol 400. Field emission scanning electron microscopy (FE-SEM) revealed that AC exhibited hexagonal and platelet-like structures, whereas ACP displayed more dispersed and layered morphologies. High-resolution transmission electron microscopy (HR-TEM) confirmed the presence of stacked platelet-like structures in AC and more defined, separated nanosheets in ACP. The maximum adsorption capacities of AC and ACP were 149.93 and 230.95 mg/g, respectively. The adsorption pathway of Zn(II) ions onto ACP nanocomposite involved three primary interactions: electrostatic attraction facilitated by calcium aluminate, ion exchange provided by analcime, and complexation promoted by polyethylene glycol 400. Thermodynamic analysis indicated that the adsorption process was exothermic, spontaneous, and primarily chemical in nature. Kinetic modeling confirmed that adsorption followed the pseudo-second-order model, while isotherm studies demonstrated adherence to the Langmuir model, indicating monolayer adsorption on homogeneous sites. Full article

Two-dimensional transition metal dichalcogenides have attracted considerable attention in electrocatalytic hydrogen evolution due to their unique layered structures and tunable electronic properties. However, prior research has predominantly focused on the intrinsic catalytic activity of planar few-layer structures, which offer limited exposure of edge-active sites due to their restricted two-dimensional geometry. Moreover, van der Waals interactions between layers impose substantial barriers to electron transport, significantly hindering charge transfer efficiency. To overcome these limitations, this study presents the innovative synthesis of high-quality single-screw WS₂ with a 5° dislocation angle via physical vapor deposition. Second harmonic generation measurements revealed a pronounced asymmetric polarization response, while the selected area electron diffractionand atomic force microscopy elucidated the material’s distinctive screwed dislocation configuration. In contrast to planar monolayer WS₂, the conical/screw-structured WS₂—formed through screw-dislocation-mediated growth—exhibits a higher density of exposed edge-active catalytic sites and enhanced electron transport capabilities. Electrochemical performance tests revealed that in an alkaline medium, the screwed WS₂ nanosheets exhibited an overpotential of 310 mV at a current density of −10 mA/cm², with a Tafel slope of 204 mV/dec. Additionally, under a current density of 18 mA/cm², the screwed WS₂ can sustain this current density for at least 30 h. These findings offer valuable insights into the design of low-cost, high-efficiency, non-precious metal catalysts for hydrogen evolution reactions. Full article

The search for effective and reliable methods of photosensitization of oxide-based semiconductor materials is of great significance for their use in photocatalytic reactions of hydrogen production and environmental remediation under natural sunlight. The present study is focused on partial substitution of titanium with manganese in the structure of layered perovskite-like titanate Na₂La₂Ti₃O₁₀, which was employed to yield a series of photocatalytically active materials, Na₂La₂Mn_xTi_3−xO₁₀ (x = 0.002–1.0), as well as their protonated forms H₂La₂Mn_xTi_3−xO₁₀ and nanosheets. It was established that the manganese cations Mn⁴⁺ are embedded in the middle sublayer of oxygen octahedra in the perovskite slabs La₂Mn_xTi_3−xO₁₀²⁻ and that the maximum achievable manganese content x in the products is ≈0.9. The partial cationic substitution in the perovskite sublattice led to a pronounced contraction of the optical band gap from 3.20 to 1.35 eV (depending on x) and, therefore, allowed the corresponding photocatalysts to utilize not only ultraviolet, but also visible and near-infrared light with wavelengths up to ≈920 nm. The materials obtained were tested as photocatalysts of hydrogen evolution from aqueous methanol, and the greatest activity in this reaction was demonstrated by the samples with low manganese contents (x = 0.002–0.01). However, the materials with greater substitution degrees may be of high interest for use in other photocatalytic processes and, especially, in thermophotocatalysis due to their improved ability to absorb the near-infrared part of solar radiation. Full article

The rapidly evolving field of functional yarns has garnered substantial research attention due to their exceptional potential in enabling next-generation electronic textiles for wearable health monitoring, human–machine interfaces, and soft robotics. Despite notable advancements, the development of yarn-based strain sensors that simultaneously achieve high flexibility, stretchability, superior comfort, extended operational stability, and exceptional electrical performance remains a critical challenge, hindered by material limitations and structural design constraints. Here, we present a bioinspired, hierarchically structured core-sheath yarn sensor (CSSYS) engineered through an efficient dip-coating process, which synergistically integrates the two-dimensional conductive MXene nanosheets and one-dimensional silver nanowires (AgNWs). Furthermore, the sensor is encapsulated using a yarn-based protective layer, which not only preserves its inherent flexibility and wearability but also effectively mitigates oxidative degradation of the sensitive materials, thereby significantly enhancing long-term durability. Drawing inspiration from the natural architecture of plant stems—where the inner core provides structural integrity while a flexible outer sheath ensures adaptive protection—the CSSYS exhibits outstanding mechanical and electrical performance, including an ultralow strain detection limit (0.05%), an ultrahigh gauge factor (up to 744.45), rapid response kinetics (80 ms), a broad sensing range (0–230% strain), and exceptional cyclic stability (>20,000 cycles). These remarkable characteristics enable the CSSYS to precisely capture a broad spectrum of physiological signals, ranging from subtle arterial pulsations and respiratory rhythms to large-scale joint movements, demonstrating its immense potential for next-generation wearable health monitoring systems. Full article