Search Results (28)

Tantalum metal and tantalum oxide thin films are commonly used in semiconductor devices, protective coatings, and biomedical implants. However, there is limited information on their nanotribological behavior and small-scale mechanical properties. This study characterized the chemical, mechanical, and tribological properties of as-deposited and 400 °C annealed β-Ta thin films using nanoindentation and atomic force microscope (AFM)-based nanoscale friction and wear tests. X-ray photoelectron spectroscopy (XPS) results revealed that a thermally grown Ta oxide layer forms on the surface of Ta film after being annealed at 400 °C. The nanoindentation data indicated an increase in both the hardness and elastic modulus in the heat-treated sample compared to the as-deposited Ta film (13.1 ± 1.3 GPa vs. 12.0 ± 1.4 GPa for hardness) and (213.1 ± 12.7 GPa vs. 175.2 ± 12.3 GPa for elastic modulus). Our nanotribological results show that the friction increased and wear resistance decreased on the surface of the annealed sample compared to the as-deposited Ta film. This discrepancy may be caused by the oxidation of Ta on the film surface, which induces residual compressive stresses in the film and degrades its wear resistance. Our results highlight the influence of thermal annealing and oxidation on nanotribological behavior and small-scale mechanical properties of Ta thin films. Full article

The ever-increasing global energy demand necessitates the development of efficient, sustainable, and high-performance energy storage systems. Nanotechnology, through the manipulation of materials at the nanoscale, offers significant potential for enhancing the performance of energy storage devices due to unique properties such as increased surface area and improved conductivity. This review paper investigates the crucial role of nanotechnology in advancing energy storage technologies, with a specific focus on capacitors and batteries, including lithium-ion, sodium–sulfur, and redox flow. We explore the diverse applications of nanomaterials in batteries, encompassing electrode materials (e.g., carbon nanotubes, metal oxides), electrolytes, and separators. To address challenges like interfacial side reactions, advanced nanostructured materials are being developed. We also delve into various manufacturing methods for nanomaterials, including top–down (e.g., ball milling), bottom–up (e.g., chemical vapor deposition), and hybrid approaches, highlighting their scalability considerations. While challenges such as cost-effectiveness and environmental concerns persist, the outlook for nanotechnology in energy storage remains promising, with emerging trends including solid-state batteries and the integration of nanomaterials with artificial intelligence for optimized energy storage. Full article

This study introduces a novel approach for fabricating ZnS/Al₂O₃/TaSe₂ heterostructured core/shell nanowires (NWs) through the selenization of a metallic Ta thin film precursor. The synthesis process involves a meticulously designed four-step protocol: (1) generating ZnS NWs on an oxidized silicon substrate, (2) encapsulating these NWs with a precisely controlled thin Al₂O₃ layer via atomic layer deposition (ALD), (3) applying a Ta precursor layer by magnetron sputtering, and (4) annealing in a Se-rich environment in a vacuum-sealed quartz ampoule to transform the Ta layer into TaSe₂, resulting in the final core/shell structure. The characterization of the newly produced NWs using scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) was validated using the integrity and composition of the heterostructures. Our method not only establishes a new pathway for the synthesis of TaSe₂-based core/shell NWs but also extends the potential for creating a variety of core/shell NW systems with chalcogenide shells by adapting the thin film metal precursor approach. This versatility opens the way for future advancements in nanoscale material applications, particularly in electronics and optoelectronics where core/shell geometries are increasingly important. Full article

Addressing the challenges associated with the highly exothermic nature of CO₂ methanation, there is considerable interest in innovative catalyst designs on structural metallic supports. One promising solution in this regard involves thin films containing cobalt oxide within a carbon matrix, fabricated using the cold plasma deposition method (PECVD). The objective of this study was to search for a relationship between the molecular structure, nanostructure, and electronic structure of such films and their catalytic activity. The investigations employed various techniques, including X-ray photoelectron spectroscopy (XPS), ultraviolet photoelectron spectroscopy (UPS), X-ray diffraction (XRD), UV-VIS absorption, and catalytic tests in the CO₂ methanation process. Three types of films were tested: untreated as-deposited (ad-CoO), thermally post-treated (TT-CoO), and argon plasma post-treated (PT-CoO) films. Among these, TT-CoO exhibited the most favorable catalytic properties, demonstrating a CO₂ conversion rate of 83%, CH₄ selectivity of 98% at 400 °C, and stability during the catalytic process. This superior performance was attributed to the formation of nanoscale heterojunctions in the TT-CoO film, where p-type CoO nanocrystallites interacted with the n-type carbon matrix. This work provides compelling evidence highlighting the key role of nanoscale heterojunctions in shaping the properties of nanocatalysts in thermal catalysis. These findings suggest promising prospects for designing new catalytic systems by manipulating interactions at the nanoscale. Full article

Tin oxide (SnO₂) and titanium dioxide (TiO₂) are recognized as attractive energy materials applicable for lead halide perovskite solar cells (PSCs). Sintering is one of the effective strategies for improving the carrier transport of semiconductor nanomaterials. Using the alternative metal-oxide-based ETL, nanoparticles are often used in a way that they are dispersed in a precursor liquid prior to their thin-film deposition. Currently, the creation of PSCs using nanostructured Sn/Ti oxide thin-film ETL is one of the topical issues for the development of high-efficiency PSCs. Here, we demonstrate the preparation of terpineol/PEG-based fluid containing both tin and titanium compounds that can be utilized for the formation of a hybrid Sn/Ti oxide ETL on a conductive substrate (F-doped SnO₂ glass substrate: FTO). We also pay attention to the structural analysis of the Sn/Ti metal oxide formation at the nanoscale using a high-resolution transmission electron microscope (HR-TEM). The variation of the nanofluid composition, i.e., the concentration of tin and titanium sources, was examined to obtain a uniform transparent thin film by spin-coating and sintering processes. The maximum power conversion efficiency was obtained for the concentration condition of [SnCl₂·2H₂O]/[titanium tetraisopropoxide (TTIP)] = 25:75 in the terpineol/PEG-based precursor solution. Our method for preparing the ETL nanomaterials provides useful guidance for the creation of high-performance PSCs using the sintering method. Full article

The developing field of plasmonics has led to the possibility of creating a new type of high-speed, highly sensitive optical sensors for the analysis of chemical and biological media. The functional conducting layers of surface plasmon resonance (SPR) optical sensors are almost always nanoscale thin films of noble metals. To enhance the plasmon resonance, nanostructured films of transparent conductive oxides are introduced into the optical sensors. However, such modified optical sensors operate in the infrared region of the spectrum. In this work, we demonstrate that the use of indium tin oxide (ITO) films with a high concentration of charge carriers makes it possible to shift the surface plasmon resonance into the visible radiation region. The work presents the results of the development of magnetron deposition technology for ITO thin films, with optimal parameters for optical sensors based on surface plasmon resonance operating in the visible range of the spectrum. Their optical and electrical characteristics are investigated. Excitation of the surface and volume plasmon resonance at the dielectric-ITO film interface, using the Kretschman configuration, is studied. It is shown that SPR is excited in the investigated ITO films with a concentration of free charge carriers of the order of 10²¹–10²² cm⁻³, when irradiated with a beam of light with TM polarization in the wavelength range of 350–950 nm. At the same time, the addition of various analytes to the surface of an ITO film changes the excitation wavelength of the SPR. Full article

The development and improvement of methods for the synthesis of environmentally friendly catalysts based on base metals is currently an urgent and promising task of modern catalysis. Catalysts based on nanoscale magnetite and maghemite have fast adsorption–desorption kinetics and high chemical activity. The purpose of this work is to obtain magnetic composites, determine their physicochemical characteristics and verify their activity in the process of liquid-phase oxidation of phenol with oxygen. Magnetic nanocomposites were obtained by chemical co-deposition of salts of ferrous and trivalent iron. The synthesized magnetic composites were studied by X-ray diffractometry, energy dispersive X-ray fluorescence and Mössbauer spectroscopy, IR-Fourier spectroscopy and elemental analysis. To increase the catalytic activity in oxidative processes, the magnetite surfaces were modified using cobalt nitrate salt. Further, CoFe₂O₄ was stabilized by adding polyethylenimine (PEI) as a surfactant. Preliminary studies of the oxidation of phenol with oxygen, as the most typical environmental pollutant were carried out on the obtained Fe₃O₄, CoFe₂O₄, CoFe₂O₄/PEI catalysts. The spectrum of the reaction product shows the presence of CH in the aromatic ring and double C=C bonds, stretching vibrations of the C=O groups of carbonyl compounds; the band at 3059 cm⁻¹ corresponds to the presence of double C=C bonds and the band at 3424 cm⁻¹ to hydroquinone compounds. The band at 1678 cm⁻¹ and the intense band at 1646 cm⁻¹ refer to vibrations of the C=O bonds of the carbonyl group of benzoquinone. Peaks at 1366 cm⁻¹ and 1310 cm⁻¹ can be related to the vibrations of C–H and C–C bonds of the quinone ring. Thus, it was demonstrated that produced magnetic composites based on iron oxide are quite effective in the oxidation of phenol with oxygen. Full article

Composite inorganic nanoarchitectures, based on combinations of distinct materials, represent advanced solid-state constructs, where coexistence and synergistic interactions among nonhomologous optical, magnetic, chemical, and catalytic properties lay a basis for the engineering of enhanced or even unconventional functionalities. Such systems thus hold relevance for both theoretical and applied nanotechnology-based research in diverse areas, spanning optics, electronics, energy management, (photo)catalysis, biomedicine, and environmental remediation. Wet-chemical colloidal synthetic techniques have now been refined to the point of allowing the fabrication of solution free-standing and easily processable multicomponent nanocrystals with sophisticated modular heterostructure, built upon a programmed spatial distribution of the crystal phase, composition, and anchored surface moieties. Such last-generation breeds of nanocrystals are thus composed of nanoscale domains of different materials, assembled controllably into core/shell or heteromer-type configurations through bonding epitaxial heterojunctions. This review offers a critical overview of achievements made in the design and synthetic elaboration of colloidal nanocrystal heterostructures based on diverse associations of transition metals (with emphasis on plasmonic metals) and transition-metal oxides. Synthetic strategies, all leveraging on the basic seed-mediated approach, are described and discussed with reference to the most credited mechanisms underpinning regioselective heteroepitaxial deposition. The unique properties and advanced applications allowed by such brand-new nanomaterials are also mentioned. Full article

Powder bed fusion using a laser beam (PBF-LB) is a commonly used additive manufacturing (3D printing) process for the fabrication of various parts from pure metals and their alloys. This work shows for the first time the possibility of using PBF-LB technology for the production of 3D titanium substrates (Ti 3D) for surface-enhanced Raman scattering (SERS) measurements. Thanks to the specific development of the 3D titanium surface and its nanoscale modification by the formation of TiO₂ nanotubes with a diameter of ~80 nm by the anodic oxidation process, very efficient SERS substrates were obtained after deposition of silver nanoparticles (0.02 mg/cm², magnetron sputtering). The average SERS enhancement factor equal to 1.26 × 10⁶ was determined for pyridine (0.05 M + 0.1 M KCl), as a model adsorbate. The estimated enhancement factor is comparable with the data in the literature, and the substrate produced in this way is characterized by the high stability and repeatability of SERS measurements. The combination of the use of a printed metal substrate with nanofunctionalization opens a new path in the design of SERS substrates for applications in analytical chemistry. Methods such as SEM scanning microscopy, photoelectron spectroscopy (XPS) and X-ray diffraction analysis (XRD) were used to determine the morphology, structure and chemical composition of the fabricated materials. Full article

Copper(II) carboxylate compounds with ethylamine and isopropylamine of the general formula [Cu₂(RNH₂)₂(µ-O₂CR_f)₄], where R = Et, ⁱPr, and R_f = C_nF_2n+1, n = 1–6, were characterised in the condensed and gas phases by electron impact mass spectrometry (EI MS), IR spectroscopy, and thermal analysis. A mass spectra analysis confirmed the presence of metallated species in the gas phase. Among the observed fragments, the pseudomolecular ions [Cu₂(RNH₂)₂(µ-O₂CR_f)₃]⁺ were found, which suggests the dimeric structure of the studied complexes with axially N-coordinated ethyl- or isopropylamine molecules and bridging perfluorinated carboxylates. TGA studies demonstrated that copper transfer to the gas phase occurs even under atmospheric pressure. The temperature range of the [Cu₂(RNH₂)₂(µ-O₂CR_f)₄] and other copper carriers detection, observed in variable temperature infrared spectra, depends on the type of amine. The possible mechanisms of the decomposition of the tested compounds are proposed. The copper films were produced without additional reducing agents despite using Cu(II) CVD precursors in the chemical vapor deposition experiments. The layers of the gel-like complexes were fabricated in both spin- and dip-coating experiments, resulting in copper or copper oxide materials when heated. Dinuclear copper(II) carboxylate complexes with ethyl- and isopropylamine [Cu₂(RNH₂)₂(µ-O₂CR_f)₄] can be applied for the formation of metal or metal oxide materials, also in the nanoscale, by vapour and ‘wet’ deposition methods. Full article

Doping process is widely used to improving emission performance of MgO films thicker than 10 nm via assisting the surface recharge and changing in electron structure. The present paper briefly reviews this strategy in a search for the new materials and structures being effective for secondary electron emission (SEE) and their diagnostics. Then, Metal-Organic Chemical Vapor Deposition (MOCVD) coupled with the specially selected precursor is suggested here as a new technique that transforms the refractory oxides to nanoscale, defect-disordered materials able to solid-solid interaction at 450 °C. Primary experiments have been performed for demanded mixed films based on MgO with ZrO₂ and CeO₂ additions. A dopant impact on facilitating the formation of oxygen vacancies in the host oxide and on the features of new mixed phases have been studied by new diagnostic means, based primarily on chemical method of differential dissolution. The method brought out the effective solvents that were the probes for identifying the nanoscale and amorphous phases possessing by the different defects on the surface of MgO films and determining contents of these phases. This approach allowed us to explain the origin of mixed phases and to estimate contribution of each from them in the macroscopic SEE properties. Full article

An important direction in the development of energy saving policy is harvesting and conversion into electricity of low-grade waste heat. The present paper is devoted to the improvement of the efficiency of thermo-electrochemical cells based on carbon fiber electrodes and potassium ferri-/ferrocyanide redox electrolyte. The influence of the carbon fiber electrode surface modification (magnetron deposition of silver and titanium or infiltration implantation of nanoscale titanium oxide) on the output power and parameters of the impedance equivalent scheme of a thermo-electrochemical cell has been studied. Two kinds of cell designs (a conventional electrochemical cell with a salt bridge and a coin cell-type body) were investigated. It was found that the nature of the surface modification of electrodes can change the internal resistance of the cell by three orders of magnitude. The dependence of the equivalent scheme parameters and output power density of the thermoelectric cell on the type of electrode materials was presented. It was observed that the maximum power for carbon fiber modified with titanium metal and titanium oxide was 25.2 mW/m² and the efficiency was 1.37%. Full article

Graphite felt (GF) is a multi-functional material and is widely used as electrodes of electrochemical devices for energy and environmental applications. However, due to the inherent hydrophobicity of graphite felt, it must be hydrophilically pretreated to obtain good electrochemical activity. Metal oxides coating is one of the feasible methods to modify the surface of GF, and in order to ensure that the metal oxides have a better conductivity for obtaining higher electrochemical activity, a subsequent H₂ heat-treatment process is usually adopted. In this study, atomic layer deposition (ALD) is used to deposit TiO₂ nanocoating on graphite felt (GF) for surface modification without any H₂ thermal post-treatment. The results show that the ALD-TiO₂-modified GF (ALD-TiO₂/GF) owns excellent hydrophilicity. Moreover, the ALD-TiO₂/GF exhibits excellent electrochemical properties of low equivalent series resistance (R_s), low charge-transfer resistance (R_ct), and high electrochemical activity. It demonstrates that ALD is an applicable technique for modifying the GF surface. In addition, it can be reasonably imagined that not only TiO₂ film can effectively modify the GF surface, but also other metal oxides grown by ALD with nanoscale-thickness can also obtain the same benefits. We anticipate this work to be a starting point for modifying GF surface by using ALD with metal oxides nanocoating. Full article

Energy-efficient computing paradigms beyond conventional von-Neumann architecture, such as neuromorphic computing, require novel devices that enable information storage at nanoscale in an analogue way and in-memory computing. Memristive devices with long-/short-term synaptic plasticity are expected to provide a more capable neuromorphic system compared to traditional Si-based complementary metal-oxide-semiconductor circuits. Here, compositionally graded oxide films of Al-doped Mg_xZn_1−xO (g-Al:MgZnO) are studied to fabricate a memristive device, in which the composition of the film changes continuously through the film thickness. Compositional grading in the films should give rise to asymmetry of Schottky barrier heights at the film-electrode interfaces. The g-Al:MgZnO films are grown by using aerosol-assisted chemical vapor deposition. The current-voltage (I-V) and capacitance-voltage (C-V) characteristics of the films show self-rectifying memristive behaviors which are dependent on maximum applied voltage and repeated application of electrical pulses. Endurance and retention performance tests of the device show stable bipolar resistance switching (BRS) with a short-term memory effect. The short-term memory effects are ascribed to the thermally activated release of the trapped electrons near/at the g-Al:MgZnO film-electrode interface of the device. The volatile resistive switching can be used as a potential selector device in a crossbar memory array and a short-term synapse in neuromorphic computing. Full article

Carbon monoxide (CO) gas is an odorless toxic combustion product that rapidly accumulates inside ordinary places, causing serious risks to human health. Hence, the quick detection of CO generation is of great interest. To meet this need, high-performance sensing units have been developed and are commercially available, with the vast majority making use of semiconductor transduction media. In this paper, we demonstrate for the first time a fabrication protocol for arrays of printed flexible CO sensors based on a printable semiconductor catalyst-decorated reduced graphene oxide sensor media. These sensors operate at room temperature with a fast response and are deposited using high-throughput printing and coating methods on thin flexible substrates. With the use of a modified solvothermal aerogel process, reduced graphene oxide (rGO) sheets were decorated with tin dioxide (SnO₂) nanoscale deposits. X-ray diffraction data were used to show the composition of the material, and high-resolution X-ray photoelectron spectroscopy (XPS) characterization showed the bonding status of the sensing material. Moreover, a very uniform distribution of particles was observed in scanning (SEM) and transmission electron microscopy (TEM) images. For the fabrication of the sensors, silver (Ag) interdigitated electrodes were inkjet-printed from nanoparticle inks on plastic substrates with 100 µm linewidths and then coated with the SnO₂-rGO nanocomposite by inkjet or slot-die coating, followed by a thermal treatment to further reduce the rGO. The detection of 50 ppm of CO in nitrogen was demonstrated for the devices with a slot-die coated active layer. A response of 15%, response time of 4.5 s, and recovery time of 12 s were recorded for these printed sensors, which is superior to other previously reported sensors operating at room temperature. Full article