Oxide Layer Research Articles

Effect of Surface Oxidation and Crystal Thickness on the Magnetic Properties and Magnetic Domain Structures of Cr2Ge2Te6.

van der Waals (vdW) magnetic materials, such as Cr2Ge2Te6 (CGT), show promise for memory and logic applications. This is due to their broadly tunable magnetic properties and the presence of topological magnetic features such as skyrmionic bubbles. A systematic study of thickness and oxidation effects on magnetic domain structures is important for designing devices and vdW heterostructures for practical applications. Here, we investigate thickness effects on magnetic properties, magnetic domains, and bubbles in oxidation-controlled CGT crystals. We find that CGT exposed to ambient conditions for 5 days forms an oxide layer approximately 5 nm thick. This oxidation leads to a significant increase in the oxidation state of the Cr ions, indicating a change in local magnetic properties. This is supported by real-space magnetic texture imaging through Lorentz transmission electron microscopy. By comparing the thickness-dependent saturation field of oxidized and pristine crystals, we find that oxidation leads to a nonmagnetic surface layer that is thicker than the oxide layer alone. We also find that the stripe domain width and skyrmionic bubble size are strongly affected by the crystal thickness in pristine crystals. These findings underscore the impact of thickness and surface oxidation on the properties of CGT, such as saturation field and domain/skyrmionic bubble size, and suggest a pathway for manipulating magnetic properties through a controlled oxidation process.

One-step chemical vapor deposition synthesis of Si NWs@C core/shell anodes without additional catalysts by the oxide-assisted growth mechanism for lithium-ion batteries.

Si NWs@C core/shell anodes for lithium-ion batteries were synthesized via a one-step environmental-pressure chemical vapor deposition (CVD) process utilizing nano-silicon and methane as raw materials. In this structure, the silicon nanowire core is obtained by controlling the temperature above 900 °C to catalyze the growth of nano-silicon particles coated with a natural oxide layer according to the oxide-assisted growth (OAG) mechanism, while the carbon as a protective coating shell is derived from methane cracking. In contrast to the conventional nanowire catalytic approach, this method obviates the addition of metal catalysts while ensuring a straightforward and scalable process. This Si NWs@C electrode displayed excellent electrochemical performance, exhibiting high reversible capacity (745.8 mA h g-1) and excellent cycling stability (91.3% after 100 cycles at 0.5 A g-1).

Early-phase core degradation interpretation by interaction between fuel cladding and fuel components in Fukushima Daiichi nuclear power plant Unit 2

ABSTRACT The early phase of the core degradation at the Fukushima Daiichi Nuclear Power Station Unit 2 was investigated in terms of a fuel-component degradation by materials interaction by carrying out the accident analysis, evaluation of chemical conditions and experimental works. First, the accident scenario was evaluated to specify a target period (from 18:40 to 22:40 on NaN Invalid Date NaN), and then the temperature and H2/H2O pressure ratio in the core region during this period were calculated based on plant parameters. Subsequently, semi-integral experiments were performed using the mocked-up fuel components of a boiling water reactor (BWR). Furthermore, separate-effects tests using Ni-alloy/Zircaloy4 were also performed to understand the phenomenon observed in the semi-integral experiments, where the Ni-Zr reaction occurred even with the oxide layer on the Zr-based alloy. Consequently, it was estimated that the Zr-Ni eutectic melting reaction above 1100°C under steam-starved conditions resulted in a fuel failure at 19:08, melting of spacer locations at 19:37, and upper-tie-plate at 21:26. The first and second degradations could have caused the release of radioactive elements or particles leading to the neutron detection at 21:00 in front of the main gate, and the third degradation could have resulted in the separation of the upper-tie-plate.

Effect of high-energy shot peening process on the oxidation behaviour of AISI 321 stainless steel at 900 °C

ABSTRACT The present work comparatively investigates the oxidation behaviour of AISI 321 austenitic stainless steel at 900 °C in Ar-21vol.%O2 in two conditions of solution annealed (SAed) and after a high-energy shot peening process (HESPed). Kinetic observations indicated that during the initial 25 h of oxidation, the HESPed sample exhibits higher oxidation kinetics. However, as oxidation progresses, the kinetics of the SAed sample surpasses in a way that after 150 h, the weight gain for SAed is 0.93 mg/cm2, and for HESPed, it is 0.71 mg/cm2. GI-XRD results after 150 h of oxidation revealed similar oxide phases on both samples, including (Cr,Fe)2O3, Mn(Fe,Cr)2O4, and Fe2O3. An important point is that the oxide formed on the surface of the SAed sample, unlike HESPed, undergoes severe spallation and cracking after 150 h, leading to sub-surface oxidation and the formation of Ni-rich oxide phases such as Ni(Fe,Cr)2O4. The enhancement observed in the oxidation performance of the HESPed sample can be ascribed to the augmented density of high-diffusivity paths, a consequence of the high-energy shot peening process, and the prompt development of uniform inner Si-rich and intermediate Cr-rich oxide layers.

ADJUSTABLE NITROOXIDATION TECHNOLOGY FOR LOW ALLOY STEEL

The article discusses the production of a surface diffusion nitride-oxide layer on low-alloy structural steel with specified structures and properties. To develop a controlled technology for nitro-oxidation of low-alloy carbon steel, the dependences of the composition and structure of the nitrided and oxide layer on the chemical composition of the steel and the technological parameters of the process were studied. Technical iron was used as a model alloy and samples of industrial steel grades 40X, P6M5 and steel 45 were processed. Saturation temperatures were studied in the ranges above and below the eutectoid temperature for the “Fe-N” system and, accordingly, for the “Fe-O” system and it was found that the best structures are at saturation temperatures below the eutectoid

A novel double-gate trench SOI LDMOS with double-dielectric material by TCAD Simulation Study

Abstract In this paper, a novel double-gate trench silicon-on-insulator (SOI) lateral double-diffused metal oxide semiconductor field-effect transistor (LDMOS) with double-dielectric material (DGDK-LDMOS) is proposed. DGDK-LDMOS has two dielectric materials: a reverse-L-shaped high-k (HK) thin film and an low-k (LK) buried oxide layer. The HK thin film optimizes the electric field distribution on the drift region surface, attracting electric flux, and the excellent withstand voltage of the LK buried oxide layer can significantly improve the breakdown voltage (BV) and reduce specific on-resistance (Ron,sp) of the device. The modulation mechanism of LDMOS by HK thin film and LK buried oxide layer is analyzed. The results show that compared with conventional LDMOS (C-LDMOS), when the permittivity of HK thin film is 25 and the permittivity of LK buried oxide is 3, the BV of DGDK-LDMOS is increased by 89.6%, the Ron,sp is decreased by 26.4%, and the figure of merit (FOM, FOM = BV2/Ron,sp) is increased by 397.2% from 3.6 MW·cm−2 to 17.9 MW·cm−2. Meanwhile, the output characteristics, transfer characteristics, lattice temperature, AC characteristics and switching characteristics of DGDK-LDMOS are also discussed and compared.

Optimizing the preparation of polymer nanocoatings by self-assembly and gamma irradiation of elaidic acid on copper surfaces

Self-assembling molecular layers (SAMs) can serve as a densely packed film of monomers that can be easily crosslinked to form nanometer-thick polymer coatings with high protective properties. However, the properties of the resulting coatings are highly dependent on the preparation method used to apply the SAM to the surface.In this work, the influence of different SAM preparation steps (preparation of the oxide layer, self-assembly and drying) on the corrosion resistance of the coated samples, as well as the method of applying the molecules to the surface (immersion, spraying, brush application), was investigated. Elaidic acid, an unsaturated trans fatty acid, was applied to copper and crosslinked with gamma radiation. The properties of the coatings were studied by electrochemical methods, contact angle measurements, XPS, AFM and FTIR. The results show that the oxidation step is crucial for obtaining proper coatings, while the drying at elevated temperatures is not required. It has also been shown that the immersion of samples results in coatings with the best protective properties, while the application by brush can be an alternative method of application. On the other hand, spraying the elaidic acid results in a less uniform coating.

Long-term oxidation of Ti3Al0.8Sn0.2C2 in air at 1200 °C

The addition of Sn into the raw materials is currently one of the most widely used methods to improve the purity and mechanical properties of Ti3AlC2. It follows in this work to investigate the oxidation behavior of the resulting Ti3Al0.8Sn0.2C2 at 1200 °C with the oxidation time up to 500 h. The oxidation kinetics shows that its oxidation resistance is much worse than that of common MAX phases including Ti3AlC2, Ti2AlC, and Cr2AlC. The oxide layer mainly consists of TiO2 and Al2O3, with only a small amount of SnO2 at the beginning of the oxidation stage. Cracks induced by the internal thermal stress penetrate through the entire oxide layer after only 1 h, which is an important reason for the rapid oxidation of the internal substrate layer. This work is expected to provide some inspiration and reference for Ti3Al0.8Sn0.2C2 used as the potential high-temperature structural material.

Mitigating waveguide loss in Ge–Sb–Se chalcogenide glass photonics

Minimizing propagation loss within waveguides remains a central objective across diverse photonic platforms, impacting both linear lightwave transmission and nonlinear wavelength conversion efficiencies. Here, we present a method to mitigate waveguide loss in Ge28Sb12Se60 chalcogenide glass, a material known for its high nonlinearity, broad mid-infrared transparency, and significant potential for mid-IR photonics applications. By applying a sacrifical oxide layer to eliminate etching residues and a subsequent waveguide thermal reflow to smooth lithography-induced line edge roughness, we successfully reduced the waveguide loss down to 0.8 dB cm−1 at 1550 nm wavelength. This represents the best result in small-core and high-index-contrast Ge28Sb12Se60 channel waveguides. Our approach paves the way for low-loss, on-chip chalcogenide photonic devices.

CIGS bifacial solar cells with novel rear architectures: Simulation point of view and the creation of a digital twin

The performance of bifacial Cu(In,Ga)Se2 (CIGS) cells does not yet reach the one of monofacial cells, with standard Mo rear contacts. By exploring optoelectronic simulations, this study addresses the impact of a transparent conducting oxide layer used as rear contact in CIGS solar cells. These simulations, which aim to create a digital twin of bifacial CIGS solar cells, offer insight into the impact of novel rear contact architectures. It was observed that with an indium tin oxide (ITO) rear contact the CIGS cell performance lacks in comparison to a Mo one due to an electrical barrier, under rear side illumination these devices may only reach 3.9 % in conversion efficiency. The implementation of dielectric rear passivation schemes have great performance benefits in cells with Mo rear contacts. Therefore, the same passivation strategy in ITO contacts is discussed and additional novel architectures are proposed, from which a design of alternated lines between dielectric and 15 nm Mo layers on ITO showed promising results. Such rear architectures aim to achieve i) a highly transparent rear contact, ii) an ohmic-like behaviour with CIGS, and iii) a low defective interface with rear passivation. The selenization of the complete 15 nm Mo in the proposed novel architecture during the CIGS growth was considered, resulting in transmittance values above 70 % and, notably, reaching the transparency of bare ITO in the infrared range. Such rear architecture may provide for bifacial CIGS solar cells with conversion efficiency values surpassing 20 and 15 % for front and rear side illumination, respectively, allowing to fully exploit bifaciality.

Self-Ordered Anodic Porous Oxide Layers as a High Performance Electrocatalyst for Water Oxidation

Self-Ordered Anodic Porous Oxide Layers as a High Performance Electrocatalyst for Water Oxidation

Non-destructive characterization of silicon nanowires and nanowire coatings using mid-infrared spectroscopy

Silicon nanowires (SiNWs) have attracted much attention owing to their potential applications in electronics and photonics, while remaining as a cost-effective material platform. Key material properties in engineering SiNWs for different applications include their length, density, and presence of oxides or other chemicals on the surface. However, monitoring these properties is challenging, as scanning electron microscopy and atomic force microscopy (AFM), which directly image the wires, require destructive cleaving of the sample. This paper uses polarized, variable-angle Fourier Transform IR reflectance spectroscopy as a nondestructive technique to characterize the areal density and length of metal-assisted chemically etched SiNW arrays. In addition to the ability to characterize “as-etched” wires, we show that IR spectroscopy can also measure few-nanometer thick layers of aluminum oxide (AlOx) grown radially around the length of the SiNWs utilizing atomic layer deposition. Despite sample inhomogeneities, an effective medium theory (EMT) model can determine the length and density of the NWs for a range of lengths between 3 and 14 μm. The EMT can also reproduce the experimentally measured vibrational bands for coated NWs, demonstrating that IR spectroscopy can also evaluate the presence of molecular contaminants on the wires.

Evaluation of the Combustion Properties and Catalytic Activity of MgAlB Energetic Ternary Particles

ABSTRACT Boron powder possesses significant potential for use as a combustible agent in energetic materials, owing to its superior combustion thermodynamic properties. However, the powder’s tendency to form an oxide layer on its surface results in delayed ignition, reduced combustion efficiency, and compromised energy advantage. To enhance the ignition and combustion properties of boron powder, we prepared boron-based energetic composites containing flammable metals (MgxAl1-xB2) through high-temperature sintering. These were then characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), energy dispersive spectroscopy (EDS). The combustion heat of these alloy powders were measured using an oxygen bomb calorimeter, while their catalytic performance on the thermal decomposition of ammonium perchlorate (AP) was analyzed using differential scanning calorimetry (DSC) and differential thermal analysis (DTA). The results indicate that compared with boron, the MgxAl1-xB2 powders are more flammable, require less oxygen, exhibit a higher combustion efficiency and exothermic advantage. Especially, the Mg0.9Al0.1B2 and MgB2 alloy exhibit optimal combustion heat values of 39,094.92 and 37,693.90 J·g−1, respectively. They significantly enhance the thermal decomposition of AP and reduce the activation energy by over 20%.

Mechanism for Control of Laser‐Induced Stainless Steel Oxidation

AbstractThis paper presents the development of a model for Nd:YAG laser surface oxidation of 316L stainless steel. A full factorial design of experiments (DOE) are implemented to produce a model for the prediction of elemental composition and color. The elemental composition of the films produced where measured using an X‐ray photoelectron spectroscopic (XPS) and the color is measured using optical reflectance spectroscopy. Oxide layers produced have a Cr/Fe ratio in the range of 0.13–2.09, and highly controllable color variation via single‐pass laser process. The effect of the process parameters used such as power, frequency, and scan speed on laser‐induced oxides is examined with an aim to produce a model suitable for predictive control of the elemental composition and color of the oxide film. Surface morphology control via alteration of the laser power is an important factor for defining the resulting coloration. A new finding from this work is the discovery that within the range of laser surface processing parameters investigated, the molybdenum concentration is inversely proportional to the chromium concentration. This paper provides data required for control of 316L‐SS surface chemistry, and for the expansion of the current thermokinetic model to incorporate the mechanistic effect of molybdenum.

Thermo-Compression Sinter-Bonding in Air Using Cu Formate/Cu Particles Mixed During Reduction of Cu<sub>2</sub>O

A Cu-based paste containing Cu formate and Cu particles was prepared for the compressionassisted sinter-bonding of Cu-finished wide-bandgap power devices onto a Cu-finished substrate at a relatively low bonding temperature of 250 oC in air. A mixture of Cu formate and Cu particles was designed to mitigate the tremendous volume shrinkage during reduction of Cu formate, which approaches approximately 90%, and could be a significant obstacle in the formation of a high-density bond-line. The mixture was spontaneously formed during the 15-min reduction of the initial Cu<sub>2</sub>O particles by a simple wet process using formic acid. In the bonding, pure Cu generated in situ from the Cu formate at a temperature exceeding 200 °C exhibited significant sinterability, and the generated hydrogen reduced oxide layers on the Cu finishes. Furthermore, the mixed particles resulted in low volume shrinkage in the bond-line during bonding, compared to the use of Cu formate particles alone. Consequently, a robust die shear strength of 22.2 MPa was achieved by sinterbonding for even 10 min at low temperature and the compression of 10 MPa, even though Cu oxide shells were formed in the bond-line because of the long sintering in air. The simple wet process provided an efficient preparation of an effective filler system before the paste formulation for the sinter-bonding.

The Effects of Irradiation on the Improvement in Oxidation Behavior of MX-ODS Steel in Liquid Pb.

Lead-cooled fast reactors exhibit strong inherent safety performance and good economic features, while material degradation due to corrosion and irradiation is still challenging. Oxide dispersion-strengthened steels are one of the promising candidates for fuel cladding materials. The effects of both irradiation and corrosion on ODS steel need to be further studied. In this work, MX-ODS steel was irradiated by Fe ions at 500 °C up to 46 dpa. Later, the as-received specimen and the irradiated specimen were used to conduct corrosion tests in oxygen-saturated Pb at 550 °C for 1 h. In the as-received specimen, discontinuous oxides penetrated by Pb and Pb in contact with steel matrix were observed, demonstrating unsatisfactory corrosion resistance of the material. However, in the irradiated specimen after corrosion experiment, a protective oxide layer formed and prevented Pb attack. The oxidation behavior differences between the two specimens can be attributed to the defects produced by irradiation and the structural discrepancy in oxides caused by the formation process. A possible mechanism of irradiation on the corrosion is discussed. In the as-received specimen, Fe atoms loss led to voids in the oxides, and lead penetrated the oxides through these voids. In the irradiated specimen, defects left by previous irradiation helped to form a more uniform oxide layer. The adhesive outer magnetite oxide and the Fe ions generated from where grain boundary oxidation developed retarded the presence of voids and made the oxide layer protective.

Corrosion kinetics of T91 steel under low oxygen conditions (10−7 wt% O) in lead-bismuth eutectic at 500 °C

Among the advanced reactor designs of the fourth generation, the Lead-cooled Fast Reactor (LFR) stands out as one of six distinct types. The corrosion caused by the liquid Lead-Bismuth Eutectic (LBE) on structural materials is recognized as a significant obstacle hindering the development of LFR. The corrosion kinetics of T91 steel in static LBE with 10−7 wt% oxygen at 500 ºC is analyzed in this study. The formed oxide scale consists of an outer (Fe, Cr)3O4 layer with a Fe-Cr spinel structure and an inner internal oxidation zone (IOZ). The thickness evolution of the oxide layers follows a parabolic rule, with rate constants determined for different layers. The dissolution rate of metals into the LBE decreases over time, indicating diminishing the concentration gradient of Fe across the oxide layer-LBE interface. The observed deviations from expected norms may be attributed to dynamic flow conditions and non-isothermal loop experiments, which accelerate Fe diffusion into LBE.

Enhanced interaction of CO2 with TCNQ-modified CuO nanoparticle-infused PEO matrix: A novel approach in gas transport technology

We developed a composite membrane based on polyethylene oxide (PEO), achieving high CO2 selectivity, by incorporating 7,7,8,8-tetracyanoquinodimethane (TCNQ)-modified CuO nanoparticles into the PEO matrix. The addition of TCNQ helps in evenly distributing the CuO nanoparticles throughout the membrane, preventing them from clumping together. This treatment not only enhances the dispersion of CuO particles but also imparts a positive charge to their surface, which is beneficial for increasing the selectivity for CO2 over N2. The extent of this surface charge modification on the CuO nanoparticles was evaluated using X-ray photoelectron spectroscopy (XPS), while the synergy between the polymer and the additives was verified through Fourier-transform infrared (FT-IR) spectroscopy studies. The combination of CuO nanoparticles in the membrane contributes to both barrier and carrier effects, enhancing the gas selectivity. This is further aided by the intrinsic properties of PEO, a rubber-like polymer known for its good gas permeance. As a result of these combined effects, the PEO/CuO/TCNQ membrane exhibited a remarkable CO2 selectivity of 393 and a CO2 permeance of 3.9 gas permeation unit (GPU). The superior separation performance of this membrane can be ascribed to three main factors: enhanced solubility due to the oxide layer on the particle surfaces and in the polymer matrix, improved transport efficiency via reversible interactions thanks to the positively charged surface, and the effective barrier provided by the nanoparticles against N2 transport. These findings are expected to contribute significantly to future studies on the surface modification of metal nanoparticles and in the field of gas separation membranes.

Evidence of disordered local structure of ZnO buffered MgB2 films via polarized extended X-ray absorption fine structure analysis

Herein, we investigated the mechanism by which the critical temperature (Tc) of a magnesium diboride (MgB2) superconductor is altered by the buffer layer. Zinc oxide (ZnO) layers with different thicknesses (28, 80, and 134 nm) were deposited epitaxially on a Hastelloy substrate beneath a ∼ 1 μm MgB2 film. To measure the local structural distortion of the boron plane, three different angle polarizations (0°, 45°, and 90° parallel to the ab-axis) on the Mg K-edge, extended X-ray absorption fine structure (EXAFS) measurements were performed. The EXAFS analyses revealed that the ZnO buffer layer caused the boron layer to disorient, leading to buckling between the Mg and B layers, which affected the charge transfer capability in the intra-layer structure. Furthermore, the uneven distribution of B atoms amid the surrounding Mg atoms resulted in an asymmetric crystal structure, which leads to Tc fluctuation. This study reveals the relationship between modifications made to the boron plane condition of MgB2 by the ZnO buffer layer and the superconducting Tc behavior of MgB2.

Development of Superior Nickel Oxide Layer for Boosted Hole‐Transport Performance in Perovskite Solar Cells

Although revolutionary power conversion efficiency progress has been realized for inverted perovskite solar cells (PSCs), the selection and optimization of the hole‐transporting materials (HTMs) are still crucial for fabricating high‐efficiency, stable, and low‐cost PSCs. Nickel oxide (NiOx) is widely used in the PSCs community for material design and modification. However, various NiOx synthesis processes lead to kinds of NiOx, and it is difficult to determine which NiOx is suitable for application in PSCs. Herein, two kinds of NiOx HTMs are synthesized using sol–gel processed and chemical‐calcination‐processed (CCP) routes for the preparation of PSCs. Based on the physical properties of two kinds of NiOx HTMs as well as the corresponding photovoltaic parameters of PSCs, it is demonstrated that superior NiOx HTMs is obtained by the CCP method with the following properties: high transmittance to ensure sufficient sunlight capture of perovskite, appropriate energy levels to promote hole extraction and transfer, high conductivity to support charge transfer, and a good wetting surface to boost perovskite spreading and film formation. Thus, in this study, the direction for the reasonable selection of HTMs is pointed out to prepare efficient PSCs.