Search Results (107)

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

Titanium dioxide (TiO₂) is a wide-bandgap semiconductor material with broad application potential, known for its excellent photocatalytic performance, high chemical stability, low cost, and non-toxicity. These properties make it highly attractive for applications in photovoltaic energy, environmental remediation, and optoelectronic devices. For instance, TiO₂ is widely used as a photocatalyst for hydrogen production via water splitting and for degrading organic pollutants, thanks to its efficient photo-generated electron–hole separation. Additionally, TiO₂ exhibits remarkable performance in dye-sensitized solar cells and photodetectors, providing critical support for advancements in green energy and photoelectric conversion technologies. Boron-doped diamond (BDD) is renowned for its exceptional electrical conductivity, high hardness, wide electrochemical window, and outstanding chemical inertness. These unique characteristics enable its extensive use in fields such as electrochemical analysis, electrocatalysis, sensors, and biomedicine. For example, BDD electrodes exhibit high sensitivity and stability in detecting trace chemicals and pollutants, while also demonstrating excellent performance in electrocatalytic water splitting and industrial wastewater treatment. Its chemical stability and biocompatibility make it an ideal material for biosensors and implantable devices. Research indicates that the combination of TiO₂ nanostructures and BDD into heterostructures can exhibit unexpected optical and electrical performance and transport behavior, opening up new possibilities for photoluminescence and rectifier diode devices. However, applications based on this heterostructure still face challenges, particularly in terms of photodetector, photoelectric emitter, optical modulator, and optical fiber devices under high-temperature conditions. This article explores the potential and prospects of their combined heterostructures in the field of optoelectronic devices such as photodetector, light emitting diode (LED), memory, field effect transistor (FET) and sensing. TiO₂/BDD heterojunction can enhance photoresponsivity and extend the spectral detection range which enables stability in high-temperature and harsh environments due to BDD’s thermal conductivity. This article proposes future research directions and prospects to facilitate the development of TiO₂ nanostructured materials and BDD-based heterostructures, providing a foundation for enhancing photoresponsivity and extending the spectral detection range enables stability in high-temperature and high-frequency optoelectronic devices field. Further research and exploration of optoelectronic devices based on TiO₂-BDD heterostructures hold significant importance, offering new breakthroughs and innovations for the future development of optoelectronic technology. Full article

With the rapid growth of renewable energy, the need for efficient and stable energy storage systems has become increasingly urgent. Aqueous zinc-ion batteries (AZIBs) can offer high safety, abundant zinc supply, and promising electrochemical properties. However, their performance is limited by poor electronic conductivity, slow Zn²⁺ diffusion, and structural degradation of conventional cathode materials. To address these issues, an in situ polyaniline (PANI) intercalation strategy for vanadium oxide cathodes is introduced in this paper. The conductive PANI chains play three key roles: (1) expand and stabilize interlayer spacing, (2) enhance electronic conductivity, and (3) provide mechanical support to prevent structural collapse and zinc-dendrite formation. A flower-like PANI-V₂O₅ hybrid is synthesized via synchronous oxidative polymerization, forming a hierarchical architecture without inert intercalants. The resulting electrode achieves a high specific capacity of 450 mAh·g⁻¹ at 0.1 A·g⁻¹ and retains 96.7% of its capacity after 300 cycles at 1 A·g⁻¹, with excellent rate performance. These findings demonstrate that PANI intercalation enhances ion transport, electronic conductivity, and structural integrity, offering a promising design approach for next-generation AZIBs cathodes. Full article

This study successfully demonstrates the synthesis of foxtail millet carbon-activated (FMCA) materials using a two-step carbonization process from foxtail millet husk (FMH). The pre-carbonized biomass-derived millet husk was chemically activated with KOH at 500 °C and subsequently carbonized in an inert argon atmosphere at 800 °C in a tubular furnace. XRD analysis revealed a diffraction peak at 2θ = 23.67°, corresponding to the (002) plane, indicating the presence of graphitic structures. The Raman analysis of FMCA materials showed an intensity ratio (I_G/I_D) of 1.13, signifying enhanced graphitic ordering and structural stability. The as-prepared FMC and FMCA electrode materials demonstrate efficient charge storage electrochemical symmetric devices. Electrochemical analysis revealed the charge–discharge curves and a specific capacitance of Csp (FMC//FMC) 55.47 F/g and (FMCA//FMCA) 82.94 F/g at 0.5 A/g. Additionally, the FMCA//FMCA symmetric device exhibits superior performance with a higher capacity retention of 94.89% over 5000 cycles. The results confirm the suitability of FMCA for energy storage applications, particularly in electrochemical double-layer capacitors (EDLCs), making it a promising material for next-generation supercapacitors. Full article

The electrochemical carbon dioxide reduction reaction (CO₂RR) represents a promising approach for achieving CO₂ resource utilization. Carbon-based materials featuring single-atom transition metal-nitrogen coordination (M-N_x) have attracted considerable research attention due to their ability to maximize catalytic efficiency while minimizing metal atom usage. However, conventional synthesis methods often encounter challenges with metal particle agglomeration. In this study, we developed a Ni-doped polyvinylidene fluoride (PVDF) fiber membrane via electrospinning, subsequently transformed into a nitrogen-doped three-dimensional self-supporting single-atom Ni catalyst (Ni-N-CF) through controlled carbonization. PVDF was partially defluorinated and crosslinked, and the single carbon chain is changed into a reticulated structure, which ensured that the structure did not collapse during carbonization and effectively solved the problem of runaway M-Nx composite in the high-temperature pyrolysis process. Grounded in X-ray photoelectron spectroscopy (XPS) and X-ray absorption fine structure (XAFS), nitrogen coordinates with nickel atoms to form a Ni-N structure, which keeps nickel in a low oxidation state, thereby facilitating CO₂RR. When applied to CO₂RR, the Ni-N-CF catalyst demonstrated exceptional CO selectivity with a Faradaic efficiency (FE) of 92%. The unique self-supporting architecture effectively addressed traditional electrode instability issues caused by catalyst detachment. These results indicate that by tuning the local coordination structure of atomically dispersed Ni, the original inert reaction sites can be activated into efficient catalytic centers. This work can provide a new strategy for designing high-performance single-atom catalysts and structurally stable electrodes. Full article

The main method for large-scaled preparing powder superalloys in the production process is inert gas atomization, particularly vacuum-induced gas atomization (VIGA). A novel technique called electrode-induced gas atomization (EIGA) with a crucible-free electrode was proposed to prepare non-inclusion superalloy powders. In this study, a Ni-based superalloy of FGH4096 powder was prepared using both the VIGA and EIGA methods, while blanks were prepared through direct hot isostatic pressing (as-HIPed) near-net-forming method. The particle size, morphology, microstructure, and mechanical properties of the powders and blanks were compared via a laser particle size analyzer, SEM, TEM, and room-temperature and 650 °C tensile tests. The results indicated that EIGA-prepared powders exhibited a finer particle size and better surface quality than the one prepared via VIGA, which showed reduced satellite powders. However, the as-HIPed blank of EIGA-prepared powders had a lower secondary γ’ ratio and slightly reduced strength compared to the as-HIPed blank of VIGA-prepared powders due to its slightly lower secondary γ’ phase ratio and less effective inhibition of dislocation movement. Furthermore, the overall performance of the two samples did not differ significantly due to the similar microstructural characteristics of the powders. However, the variation in particle size affects heat conduction during the HIP process, resulting in slight differences in blanks’ properties. Full article

The paper focuses on material characterization and technology properties of a new Ti-12Al-42Nb spherical powder alloy for additive manufacturing of personal medical implants. The electrode induction melting inert gas atomization (EIGA) method was used to produce the powder alloy. The powder sphericity coefficient (PSC) was 1.02. Image J software was used to calculate the spherical degree by processing images sets from scanning electron microscopy (SEM) and optical microscopy (OM). SEM of particles cross-sections indicated internal thermal-induced porosity (TIP) with a 2.3 μm pore diameter. Particle size distribution was in the range from 15.72 μm (d10) to 64.48 μm (d100) as measured by laser particle analyzer. It was indicated that flowability and powder bulk density were 196 sec and 2.79 g/cm³, respectively. XRD analysis confirmed the beta phase of the powder alloy with no additional phases. X-ray fluorescence spectrometry confirmed the alloyed composition. Reducing and oxidative melting methods of analysis showed a slight amount of impurities: oxygen (0.0087 wt.%), nitrogen (0.03 wt.%), hydrogen (0.0012 wt.%), sulfur (0.0016 wt.%), and carbon (0.022 wt.%). Simultaneous thermal analysis (STA) was performed to indicate weight growth and losses and thermal effects in argon, nitrogen, and air as well as the oxidation of Al₂O₃, TiO₂, and Nb₂O₅ on the surface layer of Ti-12Al-42Nb powder alloy particles. Different phase transformations of γAl₂O₃ $\to$ θAl₂O₃ $\to$ αAl₂O₃ and TiO₂ rutile $\to$ TiO₂ anatase phase transformation were detected by STA in the oxidative layer. Full article

Intermetallic compounds from the Fe-Al system are attracting increasing attention due to their outstanding properties, including excellent mechanical performance, low density, corrosion, and oxidation resistance, as well as resistance to sulfidation, carburization, and wear at elevated temperatures. These unique characteristics make Fe-Al intermetallics promising candidates for high-temperature and harsh environmental applications. However, challenges such as brittleness and low plasticity have hindered their broader use. By exploring the impact of spray conditions on coating properties, this study contributes to enhancing the performance and functionality of Fe-Al coatings in industrial applications, where durability and resistance to extreme conditions are essential. This article presents the results of research on the production of composite coatings from the Fe-Al system with in situ fabricated intermetallic phases. For this purpose, arc spraying in an inert gas was used. The coating manufacturing process was carried out by simultaneously melting two different electrode filler wires, aluminum and steel, in a stream of argon. The obtained coatings were subjected to tests of roughness, adhesion to the substrate, and microstructure. It was shown that both the roughness and adhesion to the substrate of coatings sprayed in air are higher than those sprayed in argon. The increase in roughness results from the greater oxidation of coatings sprayed in air, while better adhesion is the result of the formation of coatings at a higher temperature. Metallographic studies have shown that during the spraying process, the in situ synthesis of intermetallic phases occurred. The results showed the local occurrence of intermetallic phases from the Fe-Al system. Among the two dominant phases, i.e., Al and the Fe alloy, there are also the following phases: FeAl₃, FeAl₂, and Fe₂Al₅. Furthermore, in layers sprayed in an inert atmosphere, the share of oxides is small. Full article

Cyclic voltammetry (CV) can be applied as a reliable method for the determination of chloride ions in a range from several to a couple hundred (about 200) ppm. Since the standard potential of chloride ion/gaseous chlorine is 1.36 V vs. normal hydrogen electrode (NHE), the efficient oxidation of Cl⁻ ion occurs at very positive electrode potentials, usually higher than +1.7 V vs. NHE. It is possible to observe this phenomenon only at noble-metal or inert carbon electrodes. Many other solutes, usually organic compounds, are often oxidized at this potential. This is the reason why the determination of Cl⁻ content directly from an increase in the oxidation current is not reliable and could lead to overestimated values. However, gaseous chlorine, generated at a positive potential dissolve in the analyzed solution, could be reduced in the reverse scan of a cyclic voltammetric curve. Optimization of the experimental procedure using statistical tools enables the development of an improved method for the direct quantification of chloride ions in acid copper electroplating baths. Under the proposed experimental conditions, the calibration curve (Cl₂ voltammetric reduction current vs. chloride ions concentration) is represented by the linear model for the concentration of chlorides ranging from 10 to 200 mg/dm³. The developed method for analyzing chloride ions in an acid sulfate electroplating copper bath has many unique properties. It is fast; the time of a single analysis is less than 20 min. In automatic mode, it can be repeated up to 50 times a day. The method does not require processing of the sample of the analyzed bath before measurement. As a result, no additional chemical reagents are used, and the test sample can be returned to the plating bath. Full article

Millions of electrostatically actuatable micromirror arrays have been arranged in between windowpanes in inert gas environments, enabling active daylighting in buildings for illumination and climatization. MEMS smart windows can reduce energy consumption significantly. However, to allow personalized light steering for arbitrary user positions with high flexibility, two main limitations must be overcome: first, limited tuning angle spans by MEMS pull-in effects; and second, the lack of a second orthogonal tuning angle, which is highly required. Firstly, design improvements of electrostatically actuatable micromirror arrays are reported by utilizing tailored bottom electrode structures for enlarging the tilt angle (Φ). Considerably larger tuning ranges are presented, significantly improving daylight steering into buildings. Secondly, 2D actuation means free movement of micromirrors via two angles—tilt (Φ) and torsion angle (θ)—while applying two corresponding voltages between the metallic micromirrors and corresponding FTO (fluorine-doped tin oxide) counters bottom electrode pads. In addition, a solution for a notorious problem in MEMS actuation is presented. Micromirror design modifications are necessary to eliminate possible crack formation on metallic structure due to stress concentration during the free movement of 2D actuatable micromirror arrays. The concept, design of micromirror arrays and bottom electrodes, as well as technological fabrication and experimental results are presented and discussed. Full article

Resource use is crucial for the sustainable growth of energy and green low-carbon applications since the improper handling of biomass waste would have a detrimental effect on the environment. This paper used nano-ZnO and ammonium persulfate ((NH₄)₂S₂O₈, APS) as a template agent and heteroatom dopant, respectively. Using a one-step carbonization process in an inert atmosphere, the biomass waste furfural residue (FR) was converted into porous carbon (PC), which was applied to the supercapacitor electrode. The impact of varying APS ratios and carbonization temperatures on the physicochemical properties and electrochemical properties of PC was studied. O, S, and N atoms were evenly distributed in the carbon skeleton, producing abundant heteroatomic functional groups. The sample with the largest specific surface area (SSA, 855.62 m² g⁻¹) was made at 900 °C without the addition of APS. With the increase in adding the ratio of APS, the SSA and pore volume of the sample were reduced, owing to the combination of APS and ZnO to form ZnS during the carbonization process, which inhibited the pore generation and activation effect of ZnO and damaged the pore structure of PC. At 0.5 A g⁻¹ current density, PC900-1 (FR: ZnO: APS ratio 1:1:1, prepared at 900 °C) exhibited the maximum specific capacitance of 153.03 F g⁻¹, whereas it had limited capacitance retention at high current density. PC900-0.1 displayed high specific capacitance (141.32 F g⁻¹ at 0.5 A g⁻¹), capacitance retention (80.7%), low equivalent series resistance (0.306 Ω), and charge transfer resistance (0.145 Ω) and showed good rate and energy characteristics depending on the synergistic effect of the double layer capacitance and pseudo-capacitance. In conclusion, the prepared FR-derived PC can meet the application of a supercapacitor energy storage field and realize the resource and functional utilization of biomass, which has a good application prospect. Full article

Polyhedron gold nanocrystals enclosed by high-index facets (HIF-Au NCs) are in high demand but are very difficult to prepare. To address this issue, we presented a simple, seedless method for synthesizing uniform HIF-Au NCs in an aqueous solution, which remarkably reduced the synthesis difficulty. Interestingly, the protonated N₂H₄ which served as both the reducing and capping agent played a crucial role in modulating the kinetic growth of the HIF-Au NCs. The resulting HIF-Au NCs exhibited distinct electronic oxidation inertness toward alcohol but demonstrated exceptional activity in the electrocatalytic oxidation of peroxides. To demonstrate their sensing capabilities, an electrode decorated with HIF-Au NCs was used to selectively detect benzoyl peroxide (BPO) in flour. BPO is a prohibited whitening agent that may be illegally added to flour and other products, posing potential health risks. The results demonstrate that this assay offers a promising method for the sensitive and selective detection of BPO. In conclusion, this research provides a straightforward pathway for obtaining HIF-Au NCs and further demonstrates their use in electronic sensing. It is expected that HIF-Au NCs will serve as a powerful tool in plasmon-enhanced spectroscopies, catalysis, and sensing applications. Full article

Carbon-based electrodes have recently been most widely used in P-MFC due to their desirable properties such as biocompatibility, chemical stability, affordable price, corrosion resistance, and ease of regeneration. In general, carbon-based electrodes, particularly graphite, are produced using a complex process based on petroleum derivatives at very high temperatures. This study aims to produce electrodes from bio-pitch and charcoal powder as an alternative to graphite electrodes. The carbons used to manufacture the electrodes were obtained by the carbonisation of Robinia pseudoacacia and Azadirachta indica wood. These carbons were pulverised, sieved to 50 µm, and used as the raw materials for electrode manufacturing. The binder used was bio-pitch derived from coconut shells as the raw materials. The density and coking value of the bio-pitch revealed its potential as a good alternative to coal-tar pitch for electrode manufacturing. The electrodes were made by mixing 66.50% of each carbon powder and 33.50% of bio-pitch. The resulting mixture was moulded into a cylindrical tube 8 mm in diameter and 80 mm in length. The raw electrodes obtained were subjected to heat treatment at 800 °C or 1000 °C in an inert medium. The electrical resistivity obtained by the four-point method showed that N1000 has an electrical resistivity at least five times lower than all the electrodes developed and two times higher than that of G. Fourier-transform infrared spectroscopy (FTIR) was used to determine the compositional features of the samples and their surface roughness was characterised by atomic force microscopy (AFM). Charge transfer was determined by electrical impedance spectroscopy (EIS). The FTIR of the electrodes showed that N1000 has a spectrum that is more similar to that of G compared to the others. The EIS showed the high ionic mobility of the ions and therefore that N1000 has a higher charge transfer compared to G and the others. AFM analysis revealed that N1000 had the highest surface roughness in this study. Full article

Carbon fiber is known for being lightweight and adaptable, making it useful for various current and future applications. However, to broaden the use of carbon fibers beyond niche applications, production costs must be lowered. A potential approach to achieving this is by using more affordable raw materials, such as lignin, which is renewable, cost-effective, and widely available compared with the materials commonly used in industry today. This study explores the impact of metal ions on the quality of carbon fiber derived from lignin, focusing on its mechanical and electrochemical properties and morphology. The effect of a specific metal ion (Ni(NO₃)₂·6H₂O) was examined by incorporating it into the spinning solution. The carbonization stage of the fiber was conducted at temperatures of 800, 900, and 1000 °C in an inert atmosphere. Scanning electron microscopy (SEM) analysis showed no defects or damage in any of the fibers. Therefore, it was concluded that moderate concentrations of Ni²⁺ ions in the fibers do not influence the stabilization or carbonization processes, thus leaving the mechanical properties of the final carbon fiber unchanged. These carbon nanofibers were also tested as a sustainable alternative to the non-renewable materials used in electrodes for energy storage and conversion devices, such as supercapacitors. Electrochemical performance was assessed in a 6 M KOH solution using a two-electrode cell configuration. Galvanostatic charge–discharge tests were performed at different current densities (0.1, 0.25, 0.5, 1.0, and 2.0 A g⁻¹). The specific capacitance of the carbon nanofibers was determined from CVA data at various scan rates: 5, 10, 20, 40, 80, and 160 mV s⁻¹. The results indicated that at 0.1 A g⁻¹, the capacitance reached 108 F g⁻¹, and at a scan rate of 5 mV s⁻¹, it was 91 F g⁻¹. The innovation of this work lies in its use of lignin, a renewable and widely available material, to produce carbon fibers, reducing costs compared with traditional methods. Additionally, the incorporation of nickel ions enhances the electrochemical properties of the fibers for supercapacitor applications without compromising their mechanical performance. Full article

The development of eco-friendly, cost-effective, and naturally abundant electrode materials for supercapacitors is gaining critical importance in current energy storage research. This study focuses on the synthesis of tin sulfide (SnSx) films via the eco-friendly successive ionic layer adsorption and reaction (SILAR) method, employing varying quantities of L-ascorbic acid (0.8 and 1.0 g) as a reducing agent. Tin sulfide films were deposited on fluorine-doped tin oxide (FTO) glass substrates and subsequently annealed in an inert atmosphere at temperatures ranging from 200 to 400 °C, resulting in thin films of varying thicknesses (100–420 nm). The structural and compositional characteristics of the films were thoroughly analyzed using Raman spectroscopy to confirm the purity and spectroscopic signatures of the sulfides. Further characterization was performed to assess the films’ morphology (scanning electron microscopy, SEM), phase composition (X-ray diffraction, XRD), surface chemical states (X-ray photoelectron spectroscopy, XPS), optical properties (UV–Vis spectroscopy), and electrical properties (Hall measurements). The gathered data were then used to evaluate the potential of tin sulfide films as electrode materials in supercapacitors, highlighting their suitability for sustainable energy storage applications. Full article