Magnetron Sputtering Deposition Technique Research Articles

Artificial synapses based on HfOx/TiOy memristor devices for neuromorphic applications

As a result of enormous progress in nanoscale electronics, interest in artificial intelligence (AI) supported systems has also increased greatly. These systems are typically designed to process computationally intensive data. Parallel processing neural network architectures are particularly noteworthy for their ability to process dense data at high speeds, making them suitable candidates for AI algorithms. Due to their ability to combine processing and memory functions in a single device, memristors offer a significant advantage over other electronic platforms in terms of area scaling efficiency and energy savings. In this study, single-layer and bilayer metal-oxide HfOxand TiOymemristor devices inspired by biological synapses were fabricated by pulsed laser and magnetron sputtering deposition techniques in high vacuum with different oxide thicknesses. The structural and electrical properties of the fabricated devices were analysed using x-ray reflectivity, x-ray photoelectron spectroscopy, and standard two-probe electrical characterization measurements. The stoichiometry and degree of oxidation of the elements in the oxide material for each thin film were determined. Moreover, the switching characteristics of the metal oxide upper layer in bilayer devices indicated its potential as a selective layer for synapse. The devices successfully maintained the previous conductivity values, and the conductivity increased after each pulse and reached its maximum value. Furthermore, the study successfully observed synaptic behaviours with long-term potentiation, long-term depression (LTD), paired-pulse facilitation, and spike-timing-dependent plasticity, showcasing potential of the devices for neuromorphic computing applications.

Tailored nanocones arrays on cellulose fiber: A higher-performance flexible SERS substrate for trace chemical detection

This study presents the successful fabrication of silver nanocone surface-enhanced Raman spectroscopy (SERS) substrate on flexible 70 GSM paper using the Direct Current (DC) magnetron sputter deposition technique. XRD analysis confirmed the crystalline nature and face-centered cubic structure of the Silver Nanocone (AgNC) substrate. SEM analysis revealed the fabricated AgNC substrate shows nanocones arrayed on the cellulose fibers. UV–visible spectral analysis validates the surface plasmon resonance peak of the AgNC substrate at 406 nm. Furthermore, SERS spectral analysis showed excellent detection abilities by accurately identifying rhodamine 6G and methylene blue dyes and fipronil pesticides at concentrations of 10−9 M, 10−8 M, and 10−6 M respectively. In addition, the substrate detects fipronil (pesticide) sprayed on tomatoes and nicotine (energy booster) mixed with tea for commercial applications. The substrate exhibits enhancement factor values for rhodamine 6G, methylene blue, fipronil, and nicotine as 1.3 × 107, 1.2 × 106, 2.6 × 105, and 5.8 × 104, respectively. Theoretical validation using density functional theory confirms the experimental Raman and SERS peaks show good similarity. Considering that the charge transfer mechanism shown in the study of the frontier molecular orbitals allowed for the identification of the interaction between the analyte molecules and silver cluster. The fabricated SERS substrate exhibited remarkable stability and reproducibility.

Facile Fabrication of Large-Area CuO Flakes for Sodium-Ion Energy Storage Applications.

CuO is recognized as a promising anode material for sodium-ion batteries because of its impressive theoretical capacity of 674 mAh g-1, derived from its multiple electron transfer capabilities. However, its practical application is hindered by slow reaction kinetics and rapid capacity loss caused by side reactions during discharge/charge cycles. In this work, we introduce an innovative approach to fabricating large-area CuO and CuO@Al2O3 flakes through a combination of magnetron sputtering, thermal oxidation, and atomic layer deposition techniques. The resultant 2D CuO flakes demonstrate excellent electrochemical properties with a high initial reversible specific capacity of 487 mAh g-1 and good cycling stability, which are attributable to their unique architectures and superior structural durability. Furthermore, when these CuO flakes are coated with an ultrathin Al2O3 layer, the integration of the 2D structures with outer nanocoating leads to significantly enhanced electrochemical properties. Notably, even after 70 rate testing cycles, the CuO@Al2O3 materials maintain a high capacity of 525 mAh g-1 at a current density of 50 mA g-1. Remarkably, at a higher current density of 2000 mA g-1, these materials still achieve a capacity of 220 mAh g-1. Moreover, after 200 cycles at a current density of 200 mA g-1, a high charge capacity of 319 mAh g-1 is sustained. In addition, a full cell consisting of a CuO@Al2O3 anode and a NaNi1/3Fe1/3Mn1/3O2 cathode is investigated, showcasing remarkable cycling performance. Our findings underscore the potential of these innovative flake-like architectures as electrode materials in high-performance sodium-ion batteries, paving the way for advancements in energy storage technologies.

Investigation of crystalline and band alignment properties of NiO/GaN and Ni0.5Co0.5O/GaN heterojunctions using synchrotron radiation based techniques

Epitaxial layers of NiO and Ni0.5Co0.5O have been deposited on GaN templates using RF magnetron sputtering deposition technique. The epitaxial relationship in out-of-plane and in-plane directions for NiO and Ni0.5Co0.5O layers with respect to GaN is [111]NiO(Ni0.5Co0.5O)∥[0001]GaN and [1̅10]NiO(Ni0.5Co0.5O)∥[1̅21̅0]GaN, respectively. The epi-layers are found to have two triangular domain structures oriented along [111] direction with an in-plane rotation of 60° with respect to each other. Photoelectron spectroscopy (PES) has been used to determine the valence band offset (∆EV) and the band alignment at the heterojunctions (HJs). The ∆EV at NiO/GaN and Ni0.5Co0.5O/GaN HJs are 1.2 ± 0.2 eV and 1.8 ± 0.2 eV, respectively. The conduction band offsets (∆EC) have also been estimated using the determined values of optical band gap (NiO: Eg = ∼ 3.5 eV; Ni0.5Co0.5O: Eg = ∼ 3.3 eV) from optical transmission measurements. The values of ∆EC are found to be 1.5 ± 0.2 eV and 1.9 ± 0.2 eV at NiO/GaN and Ni0.5Co0.5O/GaN HJs, respectively. A type-II band alignment is observed at both the HJs. Higher values of valence band and conduction band offsets are observed at Ni0.5Co0.5O/GaN HJ in comparison to NiO/GaN. These experimentally determined values of band offsets can be used to design wide band gap HJ based devices like photodetectors, where higher values of band off-set at the Ni0.5Co0.5O/GaN HJ can be utilized to confine the carriers.

Enhanced corrosion resistance of graphite-like carbon coatings via dense ta-C interlayer encapsulating

Taking the combination of atomic bond density, in this work, the tetrahedral amorphous carbon (ta-C) layer with high sp3 bond were especially introduced into the sp2-riched graphite-like carbon (GLC) coatings, using a hybrid filtering cathodic arc and magnetron sputtering deposition technique. The focus was elaborated on the electrochemical behavior of coatings against the stimulated chloride solutions for marine applications. Results showed that inserting dense ta-C layer significantly encapsulated the intrinsic pore defects within GLC growth, thereafter enhancing the corrosion resistance remarkably. In particular, the coating porosity was reduced from 10.84 % for pristine GLC system to 3.19 % for GLC with ta-C sealing layer, accompanying with a reduction in corrosion current to 7.8 × 10−9 A/cm2 and an increment in protective efficiency to maximum value of 95.49 %. The small angle X-ray scattering (SAXS) analysis evidenced qualitatively that the coating porosity was suppressed greatly, which were well consisted with the enhanced corrosion resistance of GLC coating with ta-C sealing layer. Furthermore, the balance between pores sealing and interfacial matching could be tailored by controlling the thickness ratio of ta-C and GLC layers, enabling the achievement of both the compact structure and the superior corrosion resistance. These observations offer a new promising strategy to develop the protective coatings for harsh marine environment that required both excellent capability against corrosion and friction with long lifetime.

Nanovoid formation mechanism in nanotwinned Cu

Nanotwinned metals have been intensely investigated due to their unique microstructures and superior properties. This work aims to investigate the nanovoid formation mechanism in sputter-deposited nanotwinned Cu. Three different types of epitaxial or polycrystalline Cu films are fabricated by magnetron sputtering deposition technique. In the epitaxial Cu (111) films deposited on Si (110) substrates, high fractions of nanovoids and nanotwins are formed. The void size and density can be tailored by varying deposition parameters, including argon pressure, deposition rate, and film thickness. Interestingly, nanovoids become absent in the polycrystalline Cu film deposited on Si (111) substrate, but they can be regained in the epitaxial nanotwinned Cu (111) when deposited on Si (111) substrate with an Ag seed layer. The nanovoid formation seems to be closely associated with twin nucleation and film texture. Based on the comparative studies between void-free polycrystalline Cu films and epitaxial nanotwinned Cu films with nanovoids, the underlying mechanisms for the formation of nanovoids are discussed within the framework of island coalescence model.Graphical abstract

Highly sensitive self-powered solar-blind ultraviolet photodetectors based on n-Zn1-xFexO/p-Si heterojunctions

The pristine and iron-doped ZnO thin films were fabricated on p-type silicon and glass substrates using the radio-frequency magnetron sputter deposition technique. The structural, morphological, and electrical properties of the deposited thin films were analyzed using X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscope (SEM), and I-V characteristics. XRD analysis revealed the preferential growth of ZnO along the c-axis, with lattice parameter (c) values of 5.216, 5.234, and 5.241 Å for the pristine ZnO, Zn0.97Fe0.03O, and Zn0.95Fe0.05O thin films, respectively. The crystallite sizes were measured to be 13.2 nm, 16.2 nm, and 18.3 nm for the respective films. The elemental analysis of the deposited films was done under X-ray photoelectron spectroscopy (XPS), which revealed the concentrations of iron Zn0.97Fe0.03O, and Zn0.95Fe0.05O thin films were 2.93 at% and 5.14 at%, respectively. Raman spectroscopy confirmed the presence of the hexagonal wurtzite structural form in the deposited films. The I-V characteristics of the deposited films confirmed the formation of a heterojunction between the film and the silicon substrate. Furthermore, the constructed heterojunction devices were evaluated for their ability to detect ultraviolet (UV) radiations of wavelengths 365 nm and 254 nm. The devices exhibited response and recovery times of less than 1 s. The detectivity values were found to be 0.321 ×1011, 1.051 ×1011, and 2.992 ×1011 Jones for the ZnO/p-Si, Zn0.97Fe0.03O/p-Si, and Zn0.95Fe0.05O/p-Si devices, respectively, under a fixed illumination intensity of 0.812 mW/cm2 for a UVA source with a wavelength of 365 nm. These results confirm the excellent photodetection ability of the constructed devices. The mechanism of UV radiation detection by the devices has also been extensively discussed.

Direct Growth of Low Thermal Conductivity WTe2 Nanocrystalline Films on W Films.

WTe2 has attracted much attention because of its layered structure and special electronic energy band structure. However, due to the difficulty of evaporating the W element itself and the inactivity of the Te element, the obtained large-area WTe2 thin films are usually accompanied by many defects. In this paper, WTe2 nanocrystalline films were successfully prepared on quartz substrates using magnetron sputtering and chemical vapor deposition techniques. Various analytical techniques such as X-ray Diffraction, Raman spectra, X-ray Photoelectron Spectroscopy, Scanning Electron Microscope, and photoluminescence spectra are employed to analyze the crystal structure, composition, and morphology. The effects of different tellurization temperatures and tellurization times on the properties of WTe2 thin films were investigated. WTe2 nanocrystalline films with good crystallinity were obtained at 600 °C for 30 min. The thermal conductivity of the WTe2 films prepared under this condition was 1.173 Wm-1K-1 at 300 K, which is significantly higher than that of samples prepared using other methods.

Study of optical and structural properties of CZTS thin films using copper capping layer and sulfurization to correct stoichiometry

Non-toxic, environment friendly and low cost Cu2ZnSnS4 (CZTS) thin films were deposited on sodalime glass substrates by radio frequency magnetron sputter deposition technique. Stoichiometry analysis revealed that the as-deposited films were Cu deficient. Hence, Cu capping layer was deposited, to study its’ effect on optical and structural properties of the films. These films were subsequently sulfurized in a quartz setup. Ultimately, stoichiometric CZTS films with improved Cu content up to 27.4% were obtained. The kesterite CZTS phase was identified in the samples using x-ray diffraction measurements. The morphological studies revealed that, grain size varies as a function of the thickness of Cu capping layer. The formation of undesired Cu2S and ZnS phases were also observed in the film with Cu content above and below the optimum range. Optical bandgap (Eg) of the films could also be optimized by controlling the Cu content in the film. An optimal Cu content between 24% and 26% was found to be appropriate for achieving a desired bandgap within a range of 1.55 to 1.4 eV, suitable for application in thin film solar cells. The CZTS films with corrected stoichiometry have a charge carrier density in the rage of ∼1021 cm−3, which are much better than values reported so far in the literature.

Corrosion-Resistant and Electrically Conductive Oxide Coatings for Metal Bipolar Plates for PEM Electrolyzers

The PEM electrolyzers are considered a promising alternative to alkaline water electrolyzers, as the advantages of PEM technology are high efficiency, high power density, a wide range of power inputs, low operating temperatures, relatively quick start-up, and easy scale-up. The ability of PEM electrolyzers to function dynamically makes them particularly appealing in energy capture and storage systems where electrical energy is derived from renewable sources such as solar and wind power. The bipolar plates (BPPs) are essential components of the PEM electrolyzer stacks and account for the main fraction of the total weight and cost. The BPPs must be electrically conductive, highly corrosion-resistant, and maintain a low interface contact electrical resistance (ICR). The root causes of the BPPs corrosion issues are non-conductive oxides formation increasing electrical resistance, and metal ions out-diffusion poisoning the catalyst and electrolyte membrane. The US Department of Energy has set targets for bipolar plates in fuel cells, including corrosion current densities < 1 µA/cm2 and ICR < 10 mΩ·cm2. Even though these targets do not apply to BPPs in PEM electrolyzers, they provide an indication of acceptable values. The problems outlined above are being overcome or minimized by applying corrosion-resistant and simultaneously electrically conductive coatings.This work, therefore, investigates various corrosion-resistant and electrically conductive oxide coatings prepared by reactive high-power impulse magnetron sputtering (HiPIMS) on SS316L substrates. Reactive HiPIMS is an advanced and progressive magnetron sputter deposition technique suitable for preparing high-quality oxide coatings. The main advantage of HiPIMS is a high degree of ionization of sputtered particles in the discharge plasma and the associated high ion-to-atom ratio in particle flux toward the substrate. This allows one to achieve coating densification and crystallinity at low substrate temperature and without applying a substrate bias voltage. In our case, the native oxide on the SS316L substrate surface was removed by employing plasma etching prior to the coating deposition utilizing HiPIMS-generated ions accelerated towards the substrate by an applied bias voltage. The oxide coatings were deposited using an unbalanced magnetron with a directly water-cooled planar target with a diameter of 100 mm in argon-oxygen gas mixtures at the argon pressure of 1 Pa in an ultra-high vacuum chamber. The oxygen partial pressure was controlled by a PID regulator at a given power density in a pulse. This allowed the deposition of the coatings with different stoichiometries and, thus, different electrical conductivity and corrosion resistance.The electrical resistivity of oxide coatings was measured by a four-point probe system on a non-conductive glass substrate. The compaction pressure dependence of ICR between the test plate and a gas diffusion layer (GDL) was measured in a range from 0.3 to 2.0 MPa on a custom-designed device using gold-coated cylindrical copper electrodes. All electrochemical measurements were performed in an H2SO4 electrolyte solution with an acidity of pH 5.5, fluorine ions concentration of 5 ppm, and a temperature of 60 ℃ to simulate the PEM electrolyzer environment. Accelerated corrosion tests were carried out in extreme anodic conditions of the PEM electrolyzer via potentiostatic polarization at a potential of 2 V vs SHE. Open circuit potential, corrosion current, Tafel slopes, and polarization resistance were determined from potentiodynamic polarization curves measured from 0 to 2 V vs SHE recorded at a scan rate of 1 mV/s, this range should cover most of the potentials experienced inside a PEM electrolyzer. Potentiodynamic polarization and ICR versus compaction pressure were measured before and after the accelerated corrosion test.

Effect of Film Thickness on Microstructural and Magnetic Properties of Lithium Ferrite Films Prepared on Strontium Titanate (001) Substrates

Epitaxial lithium ferrite (LiFe5O8) films with different thicknesses were successfully fabricated on strontium titanate (SrTiO3) (001) substrates using the magnetron sputtering deposition technique. The microstructural and magnetic properties of the films were characterized by an advanced transmission electron microscope and a magnetic measurement device. It was found that the formation of structural defects can be influenced by the thickness of the film. In addition to misfit dislocations, orientation domains form in thinner films and twin boundaries appear in thicker films, respectively, contributing to the misfit strain relaxation in the heterosystem. The magnetic measurement showed that the thinner films have enhanced magnetization and a relatively lower coercive field compared with the thicker films containing antiferromagnetic twin boundaries. Our results provide a way of tuning the microstructure and magnetic properties of lithium ferrite films by changing the film thickness.

3D binder-free nanoarchitecture design of porous silicon/graphene fibers for ultrastable lithium storage

Enhancing the stability and fast-charging capability of battery electrodes is of paramount importance in the field of battery technology. Silicon (Si), renowned for its high specific capacity, has emerged as a promising candidate for anodes. However, the limited structural stability and electron/ion conductivity of silicon-based anodes have raised significant concerns, including fractures and the continuous formation of unstable solid-electrolyte interphase (SEI) layers, leading to rapid capacity decay. In this study, we introduce a comprehensive approach to fabricating a binder-free and free-standing anode electrode paper using a combination technique of employing electrospinning, magnetron sputtering, and chemical vapor deposition (CVD) techniques. This developed paper electrode incorporates a 3D interconnected network of nitrogen-doped vertical graphene nanosheets (VGs) that connect porous carbon fibers (PCFs) with uniformly distributed Si nanoparticles (VGs@Si@PCFs). The as-fabricated VGs@Si@PCFs paper effectively addresses the mechanical and chemical stability issues commonly associated with Si anodes. The VGs@Si@PCFs anode demonstrates a remarkable reversible capacity of 2205 mAh g-1 at 0.1 A g-1 and exhibits exceptional cycling performance with 83.5% capacity retention at 1.0 A g-1 after 3000 cycles. This design leverages the nanoporous carbon fibers and nitrogen-doped vertical graphene nanosheets as flexible and conductive supports, enhancing the robustness and flexibility of the electrode. Additionally, mechanical modeling reveals that the overall Mises strain in the porous VGs@Si@PCFs structure is significantly lower compared to nonporous cases, potentially minimizing low-cycle fatigue. Our free-standing Si/C composite anode introduces a new class of low-strain Si-based materials, showcasing significantly improved stabilities and fast-charging capabilities.

Enhancement of the efficiency of solar collector by SiO2, TiO2, and ZnO thin films layers

Most scientific researchers are motivated to develop alternative energy applications and raise their efficiency as a result of rising global warming and pollution from traditional energy sources. In this study, Nanocoating thin films of ` have been prepared on different substrates (stainless steel 316 L, commercially pure Ti, Si-Wafer(100) and glass). Magnetron sputtering deposition technique at 2.8 × 10–7 Torr vacuum has been used to synthesize the nanocoated thin films. Scanning electron microscope (SEM), X-ray diffraction (XRD), X-ray fluorescence (XRF), Atomic Force Microscopy (AFM), and UV–visible radiation tests have been used to characterize the thin films deposited. The investigation results showed that the thin films deposited do not have microcracks or defects with a uniform and homogenous structure at 400 nm magnification. It has a nanoparticle grain size of 60–90 nm with a crystal structure for TiO2, SiO2, and ZnO films. ZnO films have coarser grain and more aggregation than the other films. The highest efficiency of the collector was recorded for a collector integrated with ZnO thin-film. The efficiency of the ZnO-coated collector was about 66 % at midday compared to the conventional system (no thin film), which was 39 %.

Low-cycle fatigue behavior of zirconium fuel cladding with Cr coatings deposited by High-power Impulse Magnetron Sputtering

In this paper, the work reports on finding of an experimental investigation of the low cycle fatigue performance of Cr-coated zirconium fuel cladding. Cr coatings were fabricated by utilizing High-power Impulse Magnetron Sputtering (HiPIMS) and Direct Current Magnetron Sputtering (DCMS) deposition techniques, respectively. The experimental results have indicated that, due to the different discharge characteristics of DCMS and HiPIMS, the microstructure and mechanical performances of the deposited Cr coating are significantly different. The film morphology alter from columnar for DCMS-Cr coating to dense for HiPIMS-Cr coating, and the hardness of HiPIMS-Cr coating is higher than the values of DCMS-Cr coating. The low cycle fatigue performance of HiPIMS-Cr coated zirconium fuel cladding is better than that of DCMS-Cr coated ones, which revealed that the dense Cr coating benefitted the low-cycle fatigue life of the zirconium alloy cladding tube.

Structure and Void Connectivity in Nanocolumnar Thin Films Grown by Magnetron Sputtering at Oblique Angles

The morphology and void connectivity of thin films grown by a magnetron sputtering deposition technique at oblique geometries were studied in this paper. A well-tested thin film growth model was employed to assess the features of these layers along with experimental data taken from the literature. A strong variation in the film morphology and pore topology was found as a function of the growth conditions, which have been linked to the different collisional transport of sputtered species in the plasma gas. Four different characteristic film morphologies were identified, such as (i) highly dense and compact, (ii) compact with large, tilted mesopores, (iii) nanocolumns separated by large mesopores, and (iv) vertically aligned sponge-like coalescent nanostructures. Attending to the topology and connectivity of the voids in the film, the nanocolumnar morphology was shown to present a high pore volume and area connected with the outside by means of mesopores, with a diameter above 2 nm, while the sponge-like nanostructure presented a high pore volume and area, as well as a dense network connectivity by means of micropores, with a diameter below 2 nm. The obtained results describe the different features of the porous network in these films and explain the different performances as gas or liquid sensors in electrochromic applications or for infiltration with nanoparticles or large molecules.

Crystallization discrepancies in Mg65Zn30Ca5 metallic glass ribbon and thin film revealed by nanocalorimetry

In this study, ribbons and thin films of Mg65Zn30Ca5 (at.%) metallic glass were prepared by melt-spinning and magnetron sputtering deposition techniques, respectively. With nanocalorimetry and structural characterization, the rapid crystallization mechanisms of the Mg65Zn30Ca5 ribbon and thin film were evaluated comparatively. The metallic glass thin film has a lower crystallization temperature but a higher apparent activation energy compared to the ribbon. The granular and hierarchical surface of the film promotes heterogeneous nucleation, leading to a lower crystallization temperature. The crystal nucleation and growth processes are analyzed using the Johnson-Mehl-Avrami equation. Compared with the ribbon, whose crystallization is dominated by the growth of pre-existing nuclei, both nucleation and crystal growth occur during the crystallization of the thin film, leading to a higher activation energy. With respect to the ribbon, the crystal growth rate of the thin film is exceptionally higher because of the formation of ordered microstructures inside the film.

Environmentally adaptive lubrication enabled by gradient structure design of TiN-MoS2/Ti

Molybdenum disulfide (MoS2) films have been widely employed as lubricants for mechanical components but continue to face significant engineering challenges including their low hardness, high humidity sensitivity and weak adhesion to substrates. Although the co-deposition of MoS2 with additives provides enhanced functionality in some cases, the weak adhesion of MoS2 to the substrate is the key to the localized delamination or even early failure of the film. Herein, a novel MoS2-based film is designed and fabricated by magnetron sputtering deposition technique, which consists of Ti bonding layer, TiN load-carrying layer, TiN/Ti/MoS2 gradient layer, and top layer of Ti-doped MoS2 lubricating film. Results demonstrate that the rationally gradient design not only improves the adhesion strength between MoS2 and substrate, but also promotes the preferential growth of MoS2 along [001] zone axis perpendicular to the (002) crystal plane. The 3.2 at.% Ti-doped MoS2 film exhibits a low friction coefficient and wear rate before and after salt spray test, which is ascribed to the formation of a continuous and dense MoS2 tribofilm. Additionally, Ti additive can preferentially absorb oxygen in air, thereby preserving the self-lubricating ability of MoS2. This novel structure design provides an example for obtaining functional lubricants with good mechanical properties and environmental adaptability.

Bi-Substituted Ferrite Garnet Type Magneto-Optic Materials Studied at ESRI Nano-Fabrication Laboratories, ECU, Australia

Since 2007, at the Electron Science Research Institute (ESRI) nano-fabrication laboratories, Edith Cowan University, Australia, we have devoted research efforts to the synthesis and characterization of bismuth-containing ferrite-garnet-type thin-film magneto-optic (MO) materials of different compositions. We report on the growth and characteristics of radio frequency (RF) magnetron sputtered bismuth-substituted iron-garnet thin films. We study the process parameters associated with the RF magnetron sputter deposition technique and investigate the results of optimizing process parameters. To achieve the best MO properties, we employ a few unique techniques, such as co-sputtered nanocomposite films and all-garnet multilayer structures, as well as the application of oxygen plasma treatment to amorphous garnet layers immediately following the deposition process. We demonstrated a remarkable enhancement in the MO properties of Bi-containing ferrite-type garnet thin-film materials, including record-high MO figures of merit and improved conventional and unconventional hysteresis loops of Faraday rotation. Previously unpublished research results on the forward-looking applications of magnetic garnet coatings applied to microparticles of advanced luminescent materials are reported. In the context of developing the next-generation ultra-fast optoelectronic devices, such as light intensity switches and modulators, high-speed flat panel displays, and high-sensitivity sensors, it is important to consider the desirable optical, magnetic, and magneto-optic properties that are found in highly bismuth-substituted iron garnet thin-film materials of various composition types.

Investigation of the wear and corrosion behaviors of CrN films onto oxynitriding-treated AISI H13 alloy steel by the direct current magnetron sputtering process

• The optimal deposition time of CrN films onto oxynitriding-treated samples was 2.5 h. • Study confirmed that the 2.5 h specimen had the smaller surface roughness (20.5 nm). • 2.5 h specimen possessed the most stable columnar crystal structure of CrN films. • CrN/oxynitriding treated had the relatively lowest wear volume loss (5.38 × 10 −6 mm 3 ). • Duplex surface treatment possesses the lowest corrosion current (4.30 × 10 −5 A·cm −2 ). In the research reported herein, CrN films were coated onto oxynitriding-treated AISI H13 alloy steel using direct current magnetron sputtering deposition technique. The AISI H13 substrate has a 50-µm oxynitrided top layer with a hardness of 1000 HV 0.05 . The duration of the CrN film deposition were varied while the sputtering parameters were kept constant with constant bias of -25 V, power of 100 W, Ar and N 2 gas flow rate of 45 and 30 sccm, respectively, and deposition temperature of 300 °C. The duplex oxynitride/CrN coating exhibited optimal properties when the CrN film was 3.35 µm thick after 2.5 h deposition. This sample showed good adhesion to the oxynitrided layer. It also had the best wear resistance with wear loss volume and specific wear rate was 5.38 × 10 −6 mm 3 and 1.35 × 10 −6 mm 3 ·m − 1 ·N −1 , and good corrosion resistance with a corrosion current of 4.30 × 10 −5 A·cm −2 and polarization resistance of 604.66 Ω·cm 2 . Overall, the CrN/oxynitriding duplex surface treatment is effective in improving the properties of oxynitrided AISI H13 alloy steel.

Magnetic Properties of FeNi Films Prepared by Oblique Deposition at Different Growth Conditions

FeNi films were prepared by oblique deposition onto glass substrate using magnetron sputtering deposition technique. The deposition was carried out on a rotating or nonrotating substrate with or without a constant magnetic field applied parallel to the substrate plane. The magnetic properties of the samples were measured by a magneto-optical Kerr effect at room temperature. All films had in-plane uniaxial magnetic anisotropy. The presence of in-plane magnetic anisotropy was also confirmed by the features of the domain structure. The main factor determining the orientation of the induced anisotropy axis of films was the magnetic field applied during deposition.