Search Results (37)

Precise control over nanostructure evolution is critical for optimizing the electrochemical performance of pseudocapacitive materials. In this work, Nb₂O₅ nanostructures were synthesized via a time-engineered hydrothermal route by systematically varying the reaction duration (6, 12, and 18 h) to elucidate its influence on structural development, charge storage kinetics, and supercapacitor performance. Structural and surface analyses confirm the formation of phase-pure monoclinic Nb₂O₅ with a stable Nb⁵⁺ oxidation state. Morphological investigations reveal that a 12 h reaction time produces hierarchically organized Nb₂O₅ architectures composed of nanograin-assembled spherical aggregates with interconnected porosity, providing optimized ion diffusion pathways and enhanced electroactive surface exposure. Electrochemical evaluation demonstrates that the NbO-12 electrode delivers superior pseudocapacitive behavior dominated by diffusion-controlled Nb⁵⁺/Nb⁴⁺ redox reactions, exhibiting high areal capacitance (5.504 F cm⁻² at 8 mA cm⁻²), fast ion diffusion kinetics, low internal resistance, and excellent cycling stability with 85.73% capacitance retention over 12,000 cycles. Furthermore, an asymmetric pouch-type supercapacitor assembled using NbO-12 as the positive electrode and activated carbon as the negative electrode operates stably over a wide voltage window of 1.5 V, delivering an energy density of 0.101 mWh cm⁻² with outstanding durability. This study establishes hydrothermal reaction-time engineering as an effective strategy for tailoring Nb₂O₅ nanostructures and provides valuable insights for the rational design of high-performance pseudocapacitive electrodes for advanced energy storage systems. Full article

Metal oxide nanomaterials have emerged as transformative materials in the quest to enhance the energy density and overall performance of lithium-ion batteries (LIBs) and solid-state batteries (SSBs). Their unique properties—including their large surface areas and short ion diffusion pathways—make them ideal for next-generation energy storage technologies. In LIBs, the high surface-to-volume ratio of metal oxide nanomaterials significantly enlarges the active interfacial area and shortens the lithium-ion diffusion paths, leading to an improved high-rate performance and enhanced energy density. Transition metal oxides (TMOs) such as nickel oxide (NiO), copper oxide (CuO), and zinc oxide (ZnO) have demonstrated significant theoretical capacities, while binary systems like NiCuO offer further improvements in cycling stability and energy output. Additionally, layered lithium-based TMOs, particularly those incorporating nickel, cobalt, and manganese, have shown remarkable promise in achieving high specific capacities and long-term stability. The synergistic integration of metal oxides with carbon-based nanostructures, such as carbon nanotubes (CNTs), enhances the electrical conductivity and structural durability further, leading to a superior electrochemical performance in LIBs. In SSBs, the use of oxide-based solid electrolytes like garnet-type Li₇La₃Zr₂O₁₂ (LLZO) and sulfide-based electrolytes has facilitated the development of high-energy-density systems with excellent ionic conductivity and chemical stability. However, challenges such as high interfacial resistance at the electrode–electrolyte interface persist. Strategies like the application of lithium niobate (LiNbO₃) coatings have been employed to enhance interfacial stability and maintain electrochemical integrity. Furthermore, two-dimensional (2D) metal oxide nanomaterials, owing to their high active surface areas and rapid ion transport, have demonstrated considerable potential to boost the performance of SSBs. Despite these advancements, several challenges remain. Morphological optimization of nanomaterials, improved interface engineering to reduce the interfacial resistance, and solutions to address dendrite formation and mechanical degradation are critical to achieving the full potential of these materials. Full article

High-temperature proton exchange membrane fuel cells (HT-PEMFCs) offer distinct advantages over their low-temperature counterparts. However, their commercial viability is significantly hampered by durability challenges stemming from electrocatalyst support degradation in the corrosive phosphoric acid environment. This review provides a comprehensive analysis of advanced strategies to overcome this critical durability issue. Two main research directions are explored. The first involves engineering more robust carbon-based materials, including graphitized carbons, carbon nanostructures (nanotubes and graphene), and heteroatom-doped carbons, which enhance stability by modifying the carbon’s intrinsic structure and surface chemistry. The second direction focuses on replacing carbon entirely with intrinsically stable non-carbonaceous materials. These include metal oxides (e.g., TiO₂, SnO₂), transition metal carbides (e.g., WC, TiC), and nitrides (e.g., Nb₄N₅). For these non-carbon materials, a key focus is on overcoming their typically low electronic conductivity through strategies such as doping and the formation of multi-component composites. The analysis benchmarks the performance and durability of these advanced supports, concluding that rationally designed composite materials, which combine the strengths of different material classes, represent the most promising path toward developing next-generation, long-lasting catalysts for HT-PEMFCs. Full article

The Ti-6Al-4V alloy is widely used in orthopedic and dental implants due to its excellent mechanical, corrosion, and biological properties. However, it exhibits several limitations that can compromise its performance in clinical applications. Notably, the alloy suffers from a high coefficient of friction, which can lead to increased wear and reduced longevity of implants under relative movement conditions. Additionally, Ti-6Al-4V shows susceptibility to localized corrosion in physiological environments, particularly in the presence of bodily fluids that may result in the formation of pitting. These challenges underscore the need for surface modifications that can enhance the alloy’s tribological performance, thereby improving its overall efficacy and durability as a biomaterial in medical settings. In this context, the manuscript presents applied and innovative research that assesses the impact of implementing nanostructured Nb₂O₅ coatings through the reactive sputtering technique on the wear performance of Ti-6Al-4V alloy under both air and artificial saliva (AS) solution conditions using a Pin-on-Disk apparatus. The nanostructured Nb₂O₅ coating demonstrated the ability to reduce the wear rate and volume by up to 88% without inducing any modifications to the R_a and R_t of Ti-6Al-4V, a feature that is desirable for applications in implantable devices. The reduction in wear can be attributed to the shift from adhesive wear mechanisms on uncoated surfaces to abrasive mechanisms on coated surfaces. This research highlights the strategic advantage of utilizing Brazil’s abundant niobium resources to advance biomaterial technology and facilitate applications that benefit public health. Full article

Niobium pentoxide (Nb₂O₅) is a promising anode candidate for lithium-ion batteries due to its high theoretical capacity, excellent rate capability, and safe working potential. However, its inherent low conductivity limits its practical application in fast-charging scenarios. In this work, we develop an ultrathin carbon-coated two-dimensional T-Nb₂O₅ nanosheet composite (T-Nb₂O₅@UTC) through a facile solvothermal reaction and subsequent CVD acetylene decomposition. This unique design integrates a two-dimensional nanosheet structure with an ultrathin carbon layer, significantly enhancing electronic conductivity, reducing ion diffusion pathways, and preserving structural integrity during cycling. The T-Nb₂O₅@UTC electrode demonstrates an impressive specific capacity of 214.7 mAh g⁻¹ at a current density of 0.1 A g⁻¹, maintaining 117.9 mAh g⁻¹ at 5 A g⁻¹, much outperforming the bare T-Nb₂O₅ (179.6 mAh g⁻¹ at 0.1 A g⁻¹ and 62.9 mAh g⁻¹ at 5 A g⁻¹). It exhibits outstanding cyclic stability, retaining a capacity of 87.9% after 200 cycles at 0.1 A g⁻¹ and 83.7% after 1000 cycles at 1 A g⁻¹. In a full-cell configuration, the assembled T-Nb₂O₅@UTC||LiFePO₄ battery exhibits a desirable specific capacity of 186.2 mAh g⁻¹ at 0.1 A g⁻¹ and only a 1.5% capacity decay after 120 cycles. This work underscores a nanostructure engineering strategy for enhancing the electrochemical performance of Nb₂O₅-based anodes toward high-energy-density and fast-charging applications. Full article

Nanostructures based on flexible material are essential for modulating reflected colors by actively changing the unit structure. However, current nanostructures face challenges in achieving active and efficient modulation across a broader spectral range. Here, we propose a stretchable color management method. The structure consists of a polydimethylsiloxane (PDMS) flexible substrate and cross-shaped lithium niobate (LiNbO₃). This study achieves reflection color changes, continuous adjustment, and automatic switching of solar spectrum reflectance by optimizing the geometric structure. It shows that the spectral tuning range is larger, benefiting from the special nanostructures and the stretchability of PDMS, which result in a larger tunable period range and a maximum wavelength shift of nearly 180 nm. Moreover, this unique design has been effectively balanced and optimized to respond to different polarization waves. Finally, the sensing characteristics of the nanostructure are studied through its response to changes in the refractive index (RI). The results demonstrate a method with implications for flexible electronic devices, color generation, and biochemical sensing, contributing to progress in flexible wearable technology and green building. Full article

Graphene oxide (GO) and reduced graphene oxides (RGOs) show intrinsic electrocatalytic activity towards the electrocatalytic reduction of H₂O₂. Combining these materials with gold nanoparticles results in highly sensitive electrodes, with sensitivity in the nanomolar range because the electrocatalytic properties of GO and nanoparticles are synergistically enhanced. Understanding the factors influencing such synergy is crucial to designing novel catalytically active materials. In this contribution, we study gold nanostructures having shapes of nanospheres (AuNSs), nanourchins (AuNUs), and nanobowls (AuNBs) combined with GO or electrochemically reduced graphene oxide (ERGO). We investigate the amperometric responses of the hybrid layers to H₂O₂. The AuNUs show the highest sensitivity compared to AuNBs and AuNSs. All materials are characterized by electron microscopy and Raman spectroscopy. Raman spectra are deconvoluted by fitting them with five components in the 1000–1800 cm⁻¹ range (D*, D, D”, G, and D′). The interaction between nanoparticles and GO is visualized by the relative intensities of Raman bands (ID/IG) and other parameters in the Raman spectra, like various D”, D* band positions and intensities. The ID/IG parameter is linearly correlated with the sensitivity (R² = 0.97), suggesting that defects in the graphene structure are significant factors influencing the electrocatalytic H₂O₂ reduction. Full article

In this work, we report, for the first time, a comparative study on the effects of different solvents on the properties of LiNbO₃ (LN) nanostructures. The solvothermal synthesis method was successfully used with three different solvents: 1—water, 2—methanol, and 3—benzyl. The structural and optical properties of the as-prepared nanoparticles were studied using transmission electron microscopy (TEM), X-ray diffraction (XRD), UV-Vis absorbance, Raman spectroscopy, and photoluminescence (PL). Nanoparticles of a very small size, with an average size between 3 and 10 nm, were obtained for the first time. The photocatalytic activities of the three synthesized LiNbO₃ nanoparticles were studied in relation to the photodegradation of a complex and heavy reactive black 5 dye for a wastewater treatment application. The LiNbO₃ synthesized with deionized water showed a higher photocatalytic activity than those synthesized using other solvents, such as methanol or benzyl. Full article

Electrochromic materials enable the precise control of their optical properties, making them essential for energy-saving applications such as smart windows. This study focuses on the synthesis of molybdenum-doped niobium oxide (Mo-Nb₂O₅) thin films using a one-step hydrothermal method to investigate the effect of Mo doping on the material’s electrochromic performance. Mo incorporation led to distinct morphological changes and a transition from a compact granular structure to an anisotropic rod-like feature. Notably, the MN-3 (0.3% Mo) sample displayed an optimal electrochromic performance, achieving 77% optical modulation at 600 nm, a near-perfect reversibility of 99%, and a high coloration efficiency of 89 cm²/C. Additionally, MN-3 exhibited excellent cycling stability, with only 0.8% degradation over 5000 s. The MN-3 device also displayed impressive control over color switching, underscoring its potential for practical applications. These results highlight the significant impact of Mo doping on improving the structural and electrochromic properties of Nb₂O₅ thin films, offering improved ion intercalation and charge transport. This study underscores the potential of Mo-Nb₂O₅ for practical applications in energy-efficient technologies. Full article

Recently, the influence of Nb addition in the oxide solid solution of Sn and Ti was investigated with regard to the morphological, structural and electrical properties for the production of chemoresistive gas sensors. (Sn,Ti,Nb)_xO₂-based sensors showed promising features for ethanol monitoring in commercial or industrial settings characterized by frequent variation in relative humidity. Indeed, the three-metal solid solution highlighted a higher response level vs. ethanol than the most widely used SnO₂ and a remarkably low effect of relative humidity on the film resistance. Nevertheless, lack of knowledge still persists on the mechanisms of gas reaction occurring at the surface of these nanostructures. In this work, operando Diffuse Reflectance Infrared Fourier Transform spectroscopy was used on SnO₂- and on (Sn,Ti,Nb)_xO₂-based sensors to combine the investigations on the transduction function, i.e., the read-out of the device activity, with the investigations on the receptor function, i.e., compositional characterization of the active sensing element in real time and under operating conditions. The sensors performance was explained by probing the interaction of H₂O and ethanol molecules with the material surface sites. This information is fundamental for fine-tuning of material characteristics for any specific gas sensing applications. Full article

Herein, we describe the synthesis and evaluation of hierarchical mesoporous orthorhombic niobium oxide (T-Nb₂O₅) as an anode material for rechargeable lithium-ion batteries (LIB). The as-synthesized material addresses key challenges such as beneficial porous structure, poor rate capability, and cycling performance of the anode for Li-ion devices. The physicochemical characterization results reveal hierarchical porous nanostructure morphology with agglomerated particles and a 20 to 25 nm dimension range. Moreover, the sample has a high specific surface area (~65 m² g⁻¹) and pore volume (0.135 cm³ g⁻¹). As for the application in Li-ion devices, the T-Nb₂O₅ delivered an initial discharging capacity as high as 225 mAh g⁻¹ at 0.1 A g⁻¹ and higher rate capability as well as remarkable cycling features (~70% capacity retention after 300 cycles at 250 mA g⁻¹) with 98% average Coulombic efficiency (CE). Furthermore, the scan rate-dependent charge storage mechanism of the T-Nb₂O₅ electrode material was described, and the findings demonstrate that the electrode shows an evident and highly effective pseudocapacitive Li intercalation behaviour, which is crucial for understanding the electrode process kinetics. The origin of the improved performance of T-Nb₂O₅ results from the high surface area and mesoporous structure of the nanoparticles. Full article

An ammonia sensor based on a delay-line surface acoustic wave (SAW) device is developed in this study by coating the delay line area of the device with a nano-structured molybdenum disulfide (MoS₂) sensitive material. A SAW device of 122 MHz was designed and fabricated with a pair of interdigital transducers (IDTs) defined on a 128° y-cut LiNbO₃ substrate using photolithography technologies, and the aluminum IDT electrodes were deposited by a DC magnetron sputtering system. By adjusting the pH values of precursor solutions, molybdenum disulfide (MoS₂) nanospheres were prepared with various structures using a hydrothermal method. Finally, an NH₃ gas sensor with high sensitivity of 4878 Hz/ppm, operating at room temperature, was successfully obtained. The excellent sensitivity performance may be due to the efficient adsorption of NH₃ gas molecules on the surfaces of the nanoflower-like MoS₂, which has a larger specific surface area and provides more active sites, and results in a larger change in the resonant frequency of the device due to the mass loading effect. Full article

The High Speed High Pressure Torsion (HSHPT) is the severe plastic deformation method (SPD) designed for the grain refinement of hard-to-deform alloys, and it is able to produce large, rotationally complex shells. In this paper, the new bulk nanostructured Ti-Nb-Zr-Ta-Fe-O Gum metal was investigated using HSHPT. The biomaterial in the as-cast state was simultaneously compressed up to 1 GPa and torsion was applied with friction at a temperature that rose as a pulse in less than 15 s. The interaction between the compression, the torsion, and the intense friction that generates heat requires accurate 3D finite element simulation. Simufact Forming was employed to simulate severe plastic deformation of a shell blank for orthopedic implants using the advancing Patran Tetra elements and adaptable global meshing. The simulation was conducted by applying to the lower anvil a displacement of 4.2 mm in the z-direction and applying a rotational speed of 900 rpm to the upper anvil. The calculations show that the HSHPT accumulated a large plastic deformation strain in a very short time, leading to the desired shape and grain refinement. Full article

Stimulated Raman scattering in transparent glass-ceramics (TGCs) based on bulk nucleating phase Ba₂NaNb₅O₁₅ were investigated with the aim to explore the influence of micro- and nanoscale structural transformations on Raman gain. Nanostructured TGCs were synthesized, starting with 8BaO·15Na₂O·27Nb₂O₅·50SiO₂ (BaNaNS) glass, by proper nucleation and crystallization heat treatments. TGCs are composed of nanocrystals that are 10–15 nm in size, uniformly distributed in the residual glass matrix, with a crystallinity degree ranging from 30 up to 50% for samples subjected to different heat treatments. A significant Raman gain improvement for both BaNaNS glass and TGCs with respect to SiO₂ glass is demonstrated, which can be clearly related to the nanostructuring process. These findings show that the nonlinear optical functionalities of TGC materials can be modulated by controlling the structural transformations at the nanoscale rather than microscale. Full article

TiNb₂O₇ has been considered as a promising anode material for next-generation high power lithium ion batteries for its relatively high theoretical capacity, excellent safety and long cycle life. However, the unsatisfactory electrochemical kinetics resulting from the intrinsic sluggish electron transport and lithium ion diffusion of TiNb₂O₇ limit its wide application. Morphology controlling and carbon coating are two effective methods for improving the electrochemical performance of electrode materials. Herein, an ultrathin carbon-coated porous TiNb₂O₇ nanosheet (TNO@C) is successfully fabricated by a simple and effective approach. The distinctive sheet-like porous structure can shorten the transport path of ions/electrons and provide more active sites for electrochemical reaction. The introduction of nanolayer carbon can improve electronic conductivity and increase the specific surface area of the porous TiNb₂O₇ nanosheets. Based on the above synergistic effect, TiNb₂O₇@C delivers an initial discharge capacity of 250.6 mAh g⁻¹ under current density of 5C and can be maintained at 206.9 mAh g⁻¹ after 1000 cycles with a capacity retention of 82.6%, both of which are superior to that of pure TiNb₂O₇. These results well demonstrate that TiNb₂O₇@C is a promising anode material for lithium ion batteries. Full article