Search Results (134)

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 work presents a high-performance novel photodetector based on two-dimensional boron nitride (BN) nanosheets functionalized with gold nanoparticles (Au NPs), offering ultra-broadband photoresponse from 0.25 to 5.9 μm. Operating in both photovoltaic and photoconductive modes, the device features rapid response times (<0.5 ms), high responsivity (up to 1015 mA/W at 250 nm and 2.5 V bias), and thermal stability up to 100 °C. The synthesis process involved CO₂ laser exfoliation of hexagonal boron nitride, followed by gold NP deposition via RF sputtering and thermal annealing. Structural and compositional analyses confirmed the formation of a three-dimensional network of atomically thin BN nanosheets decorated with uniformly distributed gold nanoparticles. This architecture facilitates plasmon-enhanced absorption and efficient charge separation via heterojunction interfaces, significantly boosting photocurrent generation across the deep ultraviolet (DUV), visible, near-infrared (NIR), and mid-infrared (MIR) spectral regions. First-principles calculations support the observed broadband response, confirming bandgap narrowing induced by defects in h-BN and functionalization by gold nanoparticles. The device’s self-driven operation, wide spectral response, and durability under elevated temperatures underscore its strong potential for next-generation broadband, self-powered, and wearable sensing and optoelectronic applications. Full article

Using novel SiO₂ surface passivation and ultraviolet (UV) light anneal, a 12 nm thick SnO p-type FET (pFET) shows hole effective mobilities (µ_eff) of more than 100 cm²/V·s and 31.1 cm²/V·s at hole densities (Q_h) of 1 × 10¹¹ and 5 × 10¹² cm⁻², respectively. To further improve the on-current/off-current (I_ON/I_OFF), an ultra-thin 7 nm thick SnO nanosheet pFET shows a record-breaking I_ON/I_OFF of 6.9 × 10⁶ and remarkable µ_eff values of ~70 cm²/V·s and 20.7 cm²/V·s at Q_h of 1 × 10¹¹ cm⁻² and 5 × 10¹² cm⁻², respectively. This is the first report of an oxide semiconductor transistor achieving a hole effective mobility µ_eff that reaches 20% of that in single-crystal Si pFETs at an ultra-thin body thickness of 7 nm. In sharp contrast, the control SnO nanosheet pFET without surface passivation or UV anneal exhibits a small I_ON/I_OFF of 1.8 × 10⁴ and a µ_eff of only 6.1 cm²/V·s at 5 × 10¹² cm⁻² Q_h. The enhanced SnO pFET performance is attributed to reduced defects and improved quality in the SnO channel, as confirmed by decreased charges related to sub-threshold swing (SS) and threshold voltage (Vth) shift. Such a large improvement is further supported by the increased Sn²⁺ after passivation and UV anneal, as evidenced by X-ray photoelectron spectroscopy (XPS) analysis. The I_ON/I_OFF ratio exceeding six orders of magnitude, remarkably high hole µ_eff, and excellent two-month stability demonstrate that this pFET is a strong candidate for integration with SnON nFETs in next-generation ultra-high-definition displays and monolithic three-dimensional integrated circuits (3D ICs). Full article

In the current study, the Prussian blue analog decorated with zinc oxide (PBA@ZnO) was produced using a simple chemical co-precipitation method. The nanohybrid was examined using XRD, EDX, SEM, and TEM techniques, where it exhibited a polycrystalline structure with highly intense broadening peaks. The surface morphology was observed as thin nanosheets decorated with tiny spheres. Following excitation at 360 nm, the fluorescence spectra of PBA@ZnO showed fluorescence emission at 455 nm. The developed PBA@ZnO was used to qualitatively and quantitatively assess sunset yellow (SY), where its native fluorescence was selectively quenched as SY concentrations increased. For the first time, PBA@ZnO was used as a turn-off nano-sensor for the spectrofluorimetric measurement of SY. The method’s markable sensitivity was demonstrated within an SY linearity range of 50–500 ng/mL, where the limit of detection was calculated as 9.77 ng/mL. Real sample analysis in the food industry, including samples from real food, soft drinks, and sun cream, was made possible by the detection of tiny amounts of SY. Analytical Greenness (AGREE), AGREEprep, and the complementing Green Analytical Procedure Index (Complex MoGAPI) were used to illustrate the new approach’s exceptional eco-friendliness and greenness. The RGB 12 algorithm worked to demonstrate that the suggested approach is less costly, more environmentally friendly, more sustainable, analytically sound, and whiter than the ones that were previously published. In accordance with ICH principles, the suggested method was validated. This approach offers a promising way to rapidly and accurately identify and measure SY in the food industry, helping to guarantee food safety and maintain the health of customers. Full article

Aluminum ion batteries (AIBs) exhibit a promising development prospect due to their advantages such as high theoretical specific capacity, high safety, low cost, and sufficient raw material sources. In this work, nanosheet tin disulfide (SnS₂) was successfully prepared using the hydrothermal method and then used as a cathode material for AIBs. The synthesized nano-flake SnS₂ has a large size and thin thickness, with a size of about 900 nm and a thickness of about 150 nm. This electrode material effectively enhances the contact interface with the electrolyte and shortens the depth and travel distance of ion deintercalation. As an electrode, the battery obtained a residual discharge specific capacity of about 55 mAh g⁻¹ and a coulombic efficiency of about 83% after 600 cycles. Furthermore, the first-principles calculation results show that the energy storage mechanism is the deintercalation behavior of Al³⁺. Based on model analysis and calculation results, it can be seen that compared with the position between two sulfur atoms, Al³⁺ is more inclined to be deintercalated directly above the sulfur atom. This study provides fundamental data for the large-scale preparation of AIBs using SnS₂ as an electrode material and the application research of AIBs. Full article

We report a gas-phase precursor modulation strategy for the controlled synthesis of 1T-phase vanadium diselenide (VSe₂) from vanadium pentoxide (V₂O₅) nanosheets by systematically adjusting the vapor pressure of selenium. By controlling the selenium vapor pressure, selenium-free vapor transport of vanadium dioxide led to the spontaneous oxidation and formation of tens-of-micrometer-sized rectangular V₂O₅ crystals, while moderate selenium introduction produced intermediate oxygen-rich phases with trapezoidal crystal facets, and a highly selenium-rich environment yielded trigonal VSe₂ crystals. Raman scattering measurements confirmed the stepwise transformation from V₂O₅ to VSe₂, and atomic force microscopy revealed well-defined layered morphologies and distinct conformation within an atomically thin regime. Additionally, high-resolution transmission electron microscopy validated the orthorhombic and trigonal crystal structures of V₂O₅ and VSe₂, respectively. This work demonstrates the versatility of fine-tuned vapor-phase growth conditions in vanadium-based layered compounds, providing useful platforms to optimize structural composition with atomic precision. Full article

The use of solar energy to convert CO₂ into value-added chemicals is a promising sustainable development strategy. In this study, a black graphitic carbon nitride (CN-B) photocatalyst was fabricated through a single-step calcination process, employing phloxine B and urea as the precursor materials. The catalysts were characterized using TEM, XRD, FTIR, XPS and so on. The amount of prepolymer phloxine B was 25 mg, 35 mg and 45 mg, respectively, and the obtained samples were CN-B-0.025, CN-B-0.035 and CN-B-0.045. All samples were used for visible-catalyzed CO₂ reduction. The experimental findings indicate that the CO evolution rate of the optimal photocatalyst CN-B-0.035 reaches 27.56 μmol g_cat.⁻¹ h⁻¹. This value is nine-fold higher than that of pure CN, which has a CO evolution rate of 3.22 μmol g_cat.⁻¹ h⁻¹. The excellent photocatalytic reduction performance is due to the following factors: Firstly, the exceedingly thin nanosheet structure of the catalyst enhances the velocity of the charge transfer, and transmission electron microscopy (TEM) analysis shows that the nanosheet thickness of the catalyst CN-B is significantly thinner. Secondly, the light absorption capacity of the catalyst is enhanced. The absorbance of CN-B increases significantly in the ultraviolet region and extends to the near-infrared region, as shown with UV diffuse reflection spectroscopy. Finally, the photothermal effect of CN-B causes the catalyst temperature to rise rapidly from 20 °C to 131 °C within 120 s, which further promotes photogenerated carrier separation. This research offers a novel approach to the development of photocatalysts aimed at the photothermal-assisted photocatalytic conversion of CO₂. Full article

Electroconductive textiles (e-Textiles) are vital in developing wearable sensors that preserve the comfort and characteristics of textiles. Among two-dimensional (2D) transition metal dichalcogenides (TMDs), considered a promising option for sensor applications, tungsten di-selenide (WSe₂) homostructures have been used as humidity- and temperature-sensing materials for developing e-textiles, as mentioned in a first-of-its-kind report. Exfoliated chemical vapor deposition (CVD)-grown 2H-WSe₂ nanosheets were dispersed in hydroalcoholic solutions using an amino-functionalized silane to improve dispersion. Acrylic thickener was added to create 2H-WSe₂-based pastes, which were applied onto cotton using the knife-over-roll technique to obtain thin, flexible electroconductive coatings on textiles. Various characterization techniques confirmed the even distribution of 2D-WSe₂-based coatings on fabrics and the maintenance of textile comfort and wearability. The conductivity of coated fabrics was measured at room temperature and ranged between 2.9 × 10⁸ and 1.6 × 10⁹ Ω sq⁻¹. The WSe₂-based textile sensors functioned well as resistance humidity detectors within 30–90% relative humidity (RH), revealing good repeatability and sensitivity after multiple exposure cycles. To a lesser extent, WSe₂-based textile sensors act as temperature detectors within 20–60 °C with limited repeatability. The 2D-based textiles exhibited a quadratic dependence of resistance on temperature and a characteristic thermal hysteresis. This proposed strategy marks a significant milestone in developing scalable and flexible 2D TMD-based detectors with great potential for wearable sensing devices. Full article

In the presented work, erbium fiber lasers operating in the pulsed mode with a nonlinear element containing a vanadium oxide saturable absorber are demonstrated. The structure of the saturable absorber is based on a segment of thinned silica fiber coated with a thin-film vanadium oxide by the method of metalorganic chemical vapor deposition. A fiber laser scheme is demonstrated that allows controlling the transmission of the internal cavity of the resonator during laser generation and deposition of a thin film. We have demonstrated a method for obtaining and annealing nanocoatings with laser generation control. We controlled the laser output parameters directly during the synthesis of the saturable absorber material. Vanadium oxides obtained in the work demonstrated the Mott–Paierls phase transition practically at room temperature. In this work, the optical characteristics of the output radiation of a fiber laser with a saturable absorber were measured. At temperatures above 70 °C, the coatings demonstrate a passive Q-switch with a repetition rate of 38 kHz and a pulse duration of 3.8 μs. At temperatures below the phase transition, a short-term mode-locking mode occurs. The transmission jump at a wavelength of about 1350 nm during structural rearrangement was 24%. For comparison, VO₂ nanopowder in a polydimethylsiloxane elastomer matrix was used as a saturable absorber material. The nanopowder modulator made it possible to obtain pulses with a frequency of 27 kHz and a duration of about 7.2 μs. Full article

The development of functional materials and the use of nanotechnology are ongoing projects. These fields are closely linked, but there is a need to combine them more actively. Nanoarchitectonics, a concept that comes after nanotechnology, is ready to do this. Among the related research efforts, research into creating functional materials through the formation of thin layers on surfaces, molecular membranes, and multilayer structures of these materials have a lot of implications. Layered structures are especially important as a key part of nanoarchitectonics. The diversity of the components and materials used in layer-by-layer (LbL) assemblies is a notable feature. Examples of LbL assemblies introduced in this review article include quantum dots, nanoparticles, nanocrystals, nanowires, nanotubes, g-C₃N₄, graphene oxide, MXene, nanosheets, zeolites, nanoporous materials, sol–gel materials, layered double hydroxides, metal–organic frameworks, covalent organic frameworks, conducting polymers, dyes, DNAs, polysaccharides, nanocelluloses, peptides, proteins, lipid bilayers, photosystems, viruses, living cells, and tissues. These examples of LbL assembly show how useful and versatile it is. Finally, this review will consider future challenges in layer-by-layer nanoarchitectonics. Full article

TiO₂ has broad prospects in reducing the safety risks posed by emerging pollutants in water environments. However, the high recombination rate of photogenerated carriers limits the activity and photon utilization efficiency of TiO₂. In this study, mesoporous TiO₂ (m-TiO₂) and ultra-thin g-C₃N₄ nanosheets were composited using a hydrothermal method, with the m-TiO₂ tightly and uniformly wrapped by g-C₃N₄. The chemical structure, elemental composition, and optical properties of the heterojunction were analyzed by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR), and ultraviolet-visible diffuse reflectance spectroscopy (UV-vis-DRS). The activity of the m-TiO₂@g-C₃N₄ was evaluated by the degradation of tetracycline hydrochloride (TCH). Results showed that the heterojunction exhibited significantly enhanced reactivity compared to pure m-TiO₂ and g-C₃N₄, with kinetic rates of TCH being 1.48 and 6.84 times that of pure m-TiO₂ and g-C₃N₄, respectively. The TCH degradation kinetic rate varied from 0.194 min⁻¹ to 0.026 min⁻¹ and then decreased to 0.015 min⁻¹ on the scale of the bandgap and the number of absorbed photons in m-TiO₂@g-C₃N₄. Concurrently, a 10wt% doping amount of g-C₃N₄ significantly increased the reaction rate of photogenerated carriers in the system compared to the recombination rate, corresponding to excellent photon efficiency. Reproducibility was evaluated, and a possible degradation mechanism is proposed. This study opens new perspectives for the optimization of catalyst preparation processes aimed at enhancing photon efficiency. Full article

The selective depolymerization of β-O-4 lignin models into high-value aromatic monomers using photocatalysis presents both significant opportunities and challenges. Photocatalysts often face issues such as high photogenerated carrier recombination rates and limited operational lifetimes. This study introduces S doping to modulate the surface interface of Bi₃O₄Cl (BOC) nanosheets, enhancing C-O bond cleavage efficiency in β-O-4 lignin models under visible light at ambient temperatures. Comprehensive characterization, including atomic force microscopy (AFM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), electron spin resonance (ESR), and density functional theory (DFT) analysis, revealed that S doping reduces BOC nanosheet thickness to 1.51 nm and promotes charge carrier separation, thereby generating greater concentrations of reactive species, specifically •O₂⁻ and •OH. Photocatalytic depolymerization experiments demonstrated that S-doped BOC achieved a C-O bond cleavage selectivity of 93% and an aromatic monomer yield of 629.03 μmol/g/h (i.e., 1.5 times higher than that of undoped BOC). This work provides a strategic approach to designing photocatalysts with enhanced selectivity and efficiency for lignin depolymerization. Full article

Based on the minimum conduction band edge caused by the minimum channel potential resulting from the quasi-3D scaling theory and the 3D density of state (DOS) accompanied by the Fermi–Dirac distribution function on the source and drain sides, a unified semiconductor-device-physics-based ballistic model is developed for the threshold voltage of modern multiple-gate (MG) transistors, including FinFET, Ω-gate MOSFET, and nanosheet (NS) MOSFET. It is shown that the thin silicon, thin gate oxide, and high work function will alleviate ballistic effects and resist threshold voltage degradation. In addition, as the device dimension is further reduced to give rise to the 2D/1D DOS, the lowest conduction band edge is increased to resist threshold voltage degradation. The nanosheet MOSFET exhibits the largest threshold voltage among the three transistors due to the smallest minimum conduction band edge caused by the quasi-3D minimum channel potential. When the n-type MOSFET (N-FET) is compared to the P-type MOSFET (P-FET), the P-FET shows more threshold voltage because the hole has a more effective mass than the electron. Full article

Urea shows promise as an alternative substrate to water oxidation in electrolyzers, and replacing OER with the Urea Oxidation Reaction (UOR, theoretical potential of 0.37 V vs. RHE) can significantly increase hydrogen production efficiency. Additionally, the decomposition of urea can help reduce environmental pollution. This paper improves the inherent activity of catalytic materials through morphology and electronic modulation by incorporating tungsten (W), which accelerates electron transfer, enhances the electronic structure of neighboring atoms to create a synergistic effect, and regulates the adsorption process of active sites and intermediates. NiCoW catalytic materials with an ultra-thin nanosheet structure were prepared using an ultrasonic-assisted NaBH₄ reduction method. The results show that during the OER process, NiCoW catalytic materials have a potential of only 1.53 V at a current density of 10 mA/cm², while the UOR process under the same conditions requires a lower potential of 1.31 V, demonstrating superior catalytic performance. In a mixed electrolyte of 1 M KOH and 0.5 M urea, overall water splitting also shows excellent performance. Therefore, the designed NiCoW electrocatalyst, with its high catalytic activity, provides valuable insights for enhancing the efficiency of water electrolysis for hydrogen production and holds practical research significance. Full article

Highly solar light-absorbing poly(vinyl alcohol) (PVA) nanocomposite films have garnered wide attention in fields such as flexible optoelectronics, solar energy harvesting, and photothermal therapy. However, fabricating PVA nanocomposite films with a broad spectrum of solar absorption using cost-effective and non-toxic nanofillers remains challenging. Herein, nanocomposite films of PVA incorporating various concentrations of mixed-phase 2D MoSe₂ nanosheets (i.e., a combination of the 2H and 1T phase) were prepared using a solution casting technique. Scanning electron microscopy (SEM) shows homogenous dispersion of MoSe₂ nanosheets in the PVA matrix even at higher concentrations, while atomic force microscopy (AFM) reveals increasing surface roughness with increasing MoSe₂ content, reaching a plateau after 20 wt%. With the increase in the concentration of MoSe₂, the nanocomposite films exhibit interesting light absorption characteristics reaching their highest absorption (average 94.9%) at 40 wt% MoSe₂. The incorporated mixed-phase MoSe₂ nanosheets induce a significant change in the energy levels of the PVA matrix, which is reflected in the reduced optical band gap energy (2.63 eV) at 40 wt% MoSe₂ against pure PVA (5.28 eV). The excellent light absorption of PVA nanocomposite films across the entire range from 250 nm to 2500 nm is attributed to the thin 2D structure of MoSe₂ and the presence of its mixed phase. Full article