Structural Defects Research Articles

STUDY THE ELECTRICAL PROPERTIES OF GRAPHENE OXIDE – NANOCELLULOSE COMPOSITE

This study investigates the electrical properties of a graphene oxide (GO) and nanocellulose (NC) composite using impedance spectroscopy, complemented by thorough characterization through Fourier-transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, and scanning electron microscopy (SEM). FTIR analysis revealed characteristic peaks corresponding to functional groups present in both GO and NC, providing insights into their chemical composition. XPS spectra exhibited distinctive peaks indicative of carbon and oxygen bonding states, elucidating the surface chemistry of the materials. Raman spectroscopy provided information on the structural order and defects within the samples, particularly highlighting the graphitic structure of GO. SEM images revealed the morphological features of the composite membrane, showcasing the distribution of NC particles and structural modifications induced by their incorporation. Impedance spectroscopy was utilized to investigate the electrical conductivity of the GO-NC composite. Results indicated a temperaturedependent behavior, with an increase in conductance observed as the temperature rose within the operational range of fuel cells. Remarkably, the addition of NC did not significantly alter the conductive behavior of the composite, suggesting compatibility and stability. In summary, this comprehensive characterization using multiple analytical techniques offers valuable insights into the electrical properties of the GO-NC composite. The findings suggest its potential for various applications requiring enhanced electrical conductivity, particularly in fuel cell technology.

Study on thermoelectric properties and atomic-scale mechanism of B-site molybdenum-modified La0.1Sr0.9TiO3

Extensive studies on strontium titanate thermoelectric materials have shown that their poor conductivity results in a low ZT value. However, elemental doping can effectively improve the thermoelectric properties of these materials. In this study, a two-step sintering process was applied, using physical mixing to introduce 1 % molybdenum powder as a modification to the lanthanum-doped strontium titanate solid powder (La0.1Sr0.9TiO3). The obtained sample exhibited a maximum conductivity of 7830 S/m, with a maximum ZT of 0.12. Furthermore, this study combined experimental data with first-principles simulation calculations to elucidate the mechanism at the atomic scale. The incorporation of Mo6+ in place of Ti4+ at the B-site by molybdenum (Mo) adds two free electrons, leading to an elevated carrier concentration. This change concurrently reduces the Fermi level of the material and improves mobility, collectively resulting in a substantial increase in electrical conductivity. Phonon simulation indicated that Mo doping increased structural defects, thereby reducing lattice thermal conductivity. This significant enhancement in electrical conductivity and decrease in lattice thermal conductivity collectively increased the ZT value of the material.

Structural defect and activated alumina of spheric α-Al2O3 improving alumina ceramics density from the industrial coarse gibbsite

The quality of alumina ceramics generally depends on alumina powder. High-density alumina ceramics were prepared from industrial coarse gibbsite. Near-spheric α-Al2O3 with particles smaller than 500 nm was produced via the synergy of B and F from NH4BF4. The near-spheric α-Al2O3 calcined at low temperature generated alumina ceramics with high density and low porosity. Meanwhile, the wet pretreatment yielded smaller particles with structural distortion and high microstrain and aluminum hydroxide, notably increasing the relative density of alumina ceramics. 99.18% relative density, 0.017% porosity, and 27.54 GPa Vickers hardness of alumina ceramics were achieved at 1650°C for 2 h without additives and pressed sintering. In addition, the early stage of sintering of alumina green body followed particle boundary diffusion with reduced activation energy in the sintering process. The close packing of the spheric α-Al2O3, high microstrain of α-Al2O3, structural defects with considerable AlO4 units calcined at low temperature, structural distortion in the alumina, and activated alumina on the α-Al2O3 surface collectively promoted the densification of alumina ceramics, achieving remarkable hardness, high density, and tiny porosity.

The effect of ultrasonic waves on the structure, morphology, and thermal conductivity of graphene oxide as nanofluids for direct absorption solar collector application

This research aims to explore how ultrasonic waves affect the structure and morphology of graphene oxide (GO) as a nanofluid, influencing its thermal conductivity (TC), stability, and photo-thermal conversion properties. GO was rapidly synthesized under ultrasonic bath irradiation using modified and improved Hummers' methods. Ultrasonic irradiation creates different structural and morphological defects in the GO that depend on the sonication time. The relationship between the exposure time to ultrasound and the creation of structural and morphological defects in graphene oxide nanosheets was investigated using UV–Vis, FTIR, Raman spectroscopies, AFM, and TEM analysis. The study examined how the structure and morphology of graphene oxide nanosheets affect the thermophysical and photo-thermal conversion properties of nanofluids by comparing heat transfer and stability. The simultaneous characterizing of the structure and morphology indicates that TC and stability are related to the sonication time. Indirect sonication with low intensity can carefully control the oxidation reaction of GO. Sonication for 30 min creates GO nanosheets that yield stable nanofluids with a 32.31 % enhancement in TC, with no extra treatment needed. This particular nanofluid has excellent photo-thermal conversion properties thanks to its high optical absorption, good stability, and thermal conductivity. This can increase the solar-thermal conversion efficiency (η) up to 72.5 %, making it a promising candidate for use as the working fluid in direct absorption solar collectors (DASCs)

YouTube as a Tool for Medical Education: Analyzing Content Quality and Reliability on Chiari Malformation

Chiari malformation is a structural defect in the brain, affecting the cerebellum, brainstem, upper cervical cord, and cranial base, with severe cases involving herniation through the foramen magnum. This condition can significantly impact the patient's quality of life. Given the elective nature of surgical treatment for Chiari 1malformations, many patients seek supplemental information on YouTube. This study aimed to evaluatethe quality, accuracy, reliability, and educational value of YouTube videos on Chiari malformation decompression surgery. We selected 77 videos for analysis based on specific criteria such as language, duration, and minimum view count. The selected videos were scored using modified DISCERN, Global Quality Score, and Journal of the American Medical Association criteria. Data regarding the video content and creators were collected. Statistical analysis was performed using the Kolmogorov-Smirnov test to assess data normality and the Mann-Whitney U test to determine statistical significance. The overall quality and reliability of YouTube videos on Chiari malformation decompression surgery were found to be moderate. Videos longer than 5 minutes and those featuring a physician had significantly higher scores across all metrics. This study highlights the need for improved regulation and the promotion of high-quality medical content on online platforms. Healthcare providers should guide patients toward reliable resources and consider collaborating with content creators to enhance the quality of educational materials available online.Improved oversight and quality control on platforms like YouTube can better support patient education and clinical decision-making.

Distribution characteristics of TiO2 NPs in Daihai lake and their stability regulated by abiotic factors

Accurate detection and stability analysis of titanium dioxide (TiO2 NPs) in surface water are critical for ecological risk assessment. Quantitative analysis of TiO2 NPs in water and sediment of Daihai Lake was performed and their occurrence forms was characterized by TEM, XRD and FTIR. Further investigation into the impact of pH, ionic strength (IS) and dissolved organic matter (DOM) on the stability of TiO2 NPs was carried out, along with a correlation analysis between abiotic factors and TiO2 NPs concentration. Results showed that TiO2 NPs in water and sediment are 1.01 × 105 and 5.66 × 105 particles/mL in July 2023, respectively. After transformed in water sample from Daihai Lake, the hydrodynamic particle (HDD) of TiO2 NPs reach 600–700 nm, with reduced crystallinity and observable characteristic peaks of NaCl, which is related to the high concentration of NaCl in Daihai Lake. Structural defects and changes in surface properties of TiO2 NPs are introduced due to the adsorption of organic matter, leading to higher aggregation and sedimentation rates. Specifically, Ca2+ promote the sedimentation of TiO2 NPs more than Na+. Conversely, A/A0 increased to 0.80–0.94 from 0.64 after humic acid (HA) and fulvic acid (FA) added. Hydroxyl and carboxyl groups of FA enhanced steric hindrance and inhibited TiO2 NPs sedimentation. While a strong promotion effect on the sedimentation of TiO2 NPs is detected when 10 mmol/L Ca2+ coexisted with 10 mg/L HA, with 70% of the TiO2 NPs settled within 120 min. Additionally, the concentration of TiO2 NPs in Daihai Lake is significantly positively correlated with dissolved organic carbon (DOC) and humification index, which might be relate to the enhancement of TiO2 NPs stability of aromatic organic matter. And the high concentration of DOC will also lead to the stable existence of TiO2 NPs in water and exacerbate aquatic toxicity.

Conduction mechanisms and dielectric relaxations in ternary ZnO/Zn2SiO4/SiO2 composites for energy storage systems

In this paper, ZnO-based composite (ZnO/Zn2SiO4/SiO2) powders were prepared and investigated as a function of SiO2 added amount. Indeed, the X-ray diffraction patterns (XRD) confirm the formation of ternary ZnO/Zn2SiO4/SiO2 composites. The structural defects are shown to increase with the SiO2 amount. In addition, the SEM observations reveal agglomerated and heterogenic grain shape distribution. Furthermore, dielectric properties were investigated as a function of SiO2 added amount. The Nyquist plots are simulated by an electric circuit formed by a parallel distribution of resistance (R), capacitance (C), and a constant phase element (CPE), in all composites. Moreover, using the Jonscher's law, we demonstrate a change in conduction mechanism as a function of SiO2 content. Indeed, for the 10% SiO2 doping, the conduction process is ensured by defects such as Zn interstitial and the oxygen vacancies, consistent with the Correlated Barrier Hopping (CBH) model. Whereas, for the 20% SiO2 doping, the conduction is dominated by grain boundaries contribution, according to the Non-Overlapping Small Polaron Tunneling (NSPT) model. Besides, the 10% SiO2-doped composite exhibits localized relaxation process, while the 20% SiO2-doped sample reveals simultaneously long-range and localized relaxations. These variations, caused by the increase of SiO2 percent, can be explained by the influence of the growth of Zn2SiO4 phase, and subsequently the development of further interfacial defects. Accordingly, the composites display capacitive behavior, high permittivity, and low dielectric losses, which make them good candidates for energy storage systems.

Effect of irradiation temperature on the mobility of structural and vacancy defects in the damaged layer of Li2ZrO3 ceramics

The paper presents the assessment results of the irradiation temperature effect on the change in the type of structural defects caused by irradiation with helium ions in the near-surface layer of Li2ZrO3 ceramics, as well as determining the nature of structural damage using the electron paramagnetic resonance method in the case of irradiation fluence variation. During characterization of the structural changes caused by helium ion irradiation, the main attention was paid to detailing the type of structural defects and radiolysis products arising during irradiation, alongside alterations in their concentration using the electron paramagnetic resonance method. During the experiments, it was determined that the observed effects of thermally stimulated mobility of vacancy defects in the damaged layer caused by irradiation with helium ions indicate a positive effect of thermal heating of samples during irradiation at low fluences. This effect consists in a decline in the number of oxygen vacancies in the damaged layer at low irradiation fluences (1015 – 1016 cm-2), the concentration of which was determined using the EPR method, and the observed structural changes at low irradiation fluences in the case of an elevation in irradiation temperatures are associated with deformation distortion of the crystalline structure of ceramics caused by transformation energy processes, and thermal expansion effects.

Influence of Temperature on the Performance of Metal Semiconductor Metal Photodetector Fabricated by Pure and Cationic Doped (Mg2+ and Cu2+) SnO2 Nanoparticles

Research based on various temperatures always provides beneficial awareness in the fabrication of a vital photodetector for significant applications. Increasing temperature and including dopants in photodetector materials will influence the functioning of the photodetector. This study included the influence of temperature on pure and doped SnO2 photodetectors. The crystal structure of stannic oxide has been modified by adding cationic dopants, namely Mg2+ and Cu2+, through co-precipitation techniques. Various characterization techniques were employed to examine the impact of Mg2+ and Cu2+ on the Sn4+ lattice. The electrical properties of the materials were studied at different temperatures using the Hall effect. Pure SnO2, Mg-doped SnO2, and Cu-doped SnO2 nanoparticles were synthesised separately and used as photodetectors using fluorine-doped tin oxide film as a conductive medium. The fabricated photodetectors are optimized by current-voltage characteristics at different temperatures. The effects of defects in crystal structure, oxygen vacancies, carrier concentration, and temperature on the photodetectors were studied. Comparative studies of pure and doped SnO2 photodetectors revealed that temperature and crystal defects play a significant role in photoconduction.

Mechanism of tetracycline sorption on carbon-bentonite

Antibiotics increased industrial production is the reason of their occurrence in wastewater, soils, groundwater, and drinking water. In this regard, treating the environment for pharmaceuticals is one of the urgent environmental challenges. Synthesis of adsorbents using different types of raw materials by the methods of mechanochemical activation makes it possible to significantly increase their sorption capacity due to the accumulation of various kinds of defects in the crystal structure of the adsorbent. We obtained the bentonite-carbon composite using roller-ring vibratory mill with coal-bentonite ratio of 30 : 70 and 50 : 50. However, the nature of the interaction between carbon and bentonite correlates with changes of surface area and porosity. The porous structure parameters of the samples show the mechanochemical activation of the mixture involves their components interactions. The authors studied the structural and chemical changes during the modification of bentonite with activated carbon by analysing the vibrational spectra of carbon, initial, and modified aluminosilicate samples. According to infrared spectroscopy of adsorbents, absorption bands characteristic of Si-O-C bond vibrations occurred. The paper investigates the sorption capacity of mechanochemically modified natural clay mineral Dash-Salakhli bentonite towards tetracycline hydrochloride. Research investigates the kinetics of the process and rapid sorption of tetracycline. The paper provides possible mechanisms of chemisorption due to donor-acceptor interaction and ion-exchange processes.

Multi-cation doped CuCrO[formula omitted] crystallite matrix: Exploring bandgap tunability through Ni-Zn and Ni-Zn-Mg doping for optoelectronic application

Bandgap tuning is a key approach to optimizing materials for advanced technologies, enabling the development of more efficient and specialized devices. In this study, we demonstrate the tunability of the bandgap of CuCrO2 from 2.38 to 4.37 eV via single cation-doping with Ni and Zn, and multi-cation doping with Ni-Zn and Ni-Zn-Mg. XRD analysis reveals structural changes due to lattice distortions by cationic substitution, while FESEM shows the impact of doping on particle size, surface morphology, and crystallinity. The lamellar structure observed with multi-cation doping in FESEM investigations indicates increased structural disorder and defects, causing tailing above the valence band and below the conduction band, significantly reducing the bandgap. The effect of Zn-Ni doping on the lattice is reversed with Mg2+ insertion due to p-p orbital interactions between Mg2+-O, replacing the d-p interaction in the Cr3＋-O bond, as confirmed by optical studies. UV–Vis and photoluminescence analyses reveal significant shifts in bandgaps and emission spectra, with Ni doping yielding a bandgap of 3.97 eV, Zn doping 3.16 eV, Zn-Ni doping expanding it to 4.37 eV, and Zn-Ni-Mg doping reducing it to 2.38 eV. The dopants also affect emission characteristics, including band edge and deep-level emissions. This study provides valuable insights into the relationship between cationic doping and material properties, guiding the design of CuCrO2-based materials with tailored functionalities.

Characteristics of deformation and defect of shield tunnel in coastal structured soil in China

Shield tunnel is a type of linear underground structure assembled by lining segments, characterized with long joint, weak stiffness, and strict deformation control requirement. The situation of the long-term deformation and defect of the shield tunnel in soft ground in coastal area of China is severe, mainly attributed to the tunneling-induced ground consolidation, frozen cross passage, groundwater pumping, cyclic train load, and nearby construction. Shield tunnel is buried in ground, and the above factors could result in underlying ground settlement, overlying ground loading/unloading, and at-side ground unloading. As a result, the tunnel could suffer from different types of structural deformation and defect. Based upon the aforementioned different reasons, this study investigates the characteristics of the tunnel deformation and defect corresponding to the different types of ground stress change and deformation. It is found that tunneling-induced ground consolidation, frozen cross passage, groundwater pumping, and cyclic train load mainly contribute to the longitudinal differential settlement but negligible transverse convergence, associated with water leakages at circumferential joints. In comparison, surface surcharge and at-side unloading not only cause significant longitudinal differential deformation but also increase transverse lining internal forces, resulting in water leakages at circumferential joints, longitudinal lining concrete cracks and water leakages. Finally, nearby construction could strongly disturb the ground and cause the generation of excess pore-water pressure, making the shield tunnel deformation develops continuously after the nearby construction is completed.

Multidimensional Engineering to Construct Ru/TiO2 Catalysts Enriched with Pores and Ti3+ Defects for Highly Efficient Selective Hydrogenation of Benzene

AbstractStructural engineering, coupled with crystalline phase engineering and surface engineering, serves as a practical and effective strategy for enhancing catalytic performance through the fine design of catalysts in terms of their structure, physical phases and surface defects. In this work, a set of strategies were employed for structural transformation and crystalline phase transition of Ru/TiO2 catalysts, utilizing multidimensional regulation. Ru nanoparticles loaded on a unique TiO2 nanosheet flowers (Ru/TSFs) enriched with pores and Ti3+ defects were prepared by solvothermal and impregnation‐chemical reduction methods. The Ru/TSFs exhibited an outstanding catalytic performance in the reaction of selective hydrogenation of benzene for the preparation of cyclohexene, with a selectivity of 79 % and a maximum yield of 52.8 % along with a benzene conversion of 45.9 % and a good stability. The excellent catalytic performance attributes to the distinctive structure of three‐dimensional nanosheet flowers, which offers a high specific surface area and improvs the effective contact between the catalyst and the reaction substrate. Meanwhile, the porous Ru/TSFs exhibit exceptional hydrophilicity and abundant Ti3+ defects on their surface, which is quite favorable for the desorption of cyclohexene from the reaction system, thus improving the selectivity of cyclohexene. The multidimensional engineering may provide an efficient approach for constructing high‐performance loaded catalysts for potential industrial applications.

Internal damage evolution of C/SiC composites in air at 1650 °C studied by in-situ synchrotron X-ray imaging

Carbon fibre reinforced silicon carbide (C/SiC) ceramic matrix composites have attracted considerable attention due to their exceptional properties and extensive potential applications as high-temperature structural materials. However, due to their complex structure and manufacturing defects, C/SiC composites exhibit intricate mechanical behaviour under thermal-mechanical-oxidative coupling environments. To date, systematic studies on the internal damage evolution and failure mechanisms of C/SiC composites under high-temperature oxidative environments are lacking. In this study, a combination of synchrotron X-ray micro-computed tomography (SR-μCT) and in-situ experiments under thermal-mechanical-oxidative coupling environments at room temperature and 1650 °C in air was used to characterize the internal microstructures and damage evolution processes of C/SiC composites at different loading levels. Additionally, the 3D strain fields during in-situ loading were quantitatively analysed using the Digital Volume Correlation (DVC) method. The findings underscore the substantial impact of oxidative damage on the mechanical response of C/SiC composites, particularly concerning tensile properties and fracture modes. At room temperature, severe delamination, fibre bundle pull-out and interfacial debonding occurred internally. Whereas, under high-temperature atmospheric conditions, severe fibre oxidation reactions occurred at the specimen edges, resulting in rapid porosity escalation. Crack initiation from surface defects followed by rapid inward propagation is observed. Moreover, while the strain distribution remains relatively uniform until fracture, a pronounced concentration of strain is evident near the fracture zones at room temperature, with an even greater concentration observed at 1650 °C. Notably, the region of concentrated strain within the 3D deformation field corresponds closely to the final fracture location, as revealed by quantitative DVC analysis.

Multi-scale modeling: Finite element analysis of the thermophysical properties of carbon/carbon composites considering manufacturing defects and porosity at high temperature

Carbon/carbon (C/C) composites have strict requirements for their thermal properties in extreme environments, especially at high temperature, where their properties are crucial for long-term life. The structure of C/C composites is exceptionally complex and exhibits multi-scale characteristics, and their thermophysical properties are closely related to temperature. Therefore, exploring their thermal response and heat transfer mechanisms through experimental method is relatively costly. This paper constructs a multi-scale finite element model to investigate the influence of structure and manufacturing defects on performance, and analyzes the thermophysical properties of the composites at High-temperature. By constructing a micro-representative volume element (Micro-RVE) that includes fibers, matrix, and pores, and using a steady-state heat transfer analysis method, the influence of material phase distribution on performance is studied. At the same time, a Meso-RVE reflecting the layering form, needle punching effect and manufacturing defects is established, and the transient heat transfer analysis method is used to investigate the influence of the structural form on performance. Finite element analysis shows that, the simulation values of the three C/C composites of unidirectional fiber bundles, short-chopped fiber felts, and needle punched C/C composites show good consistency with the experimental results in the published literature. This paper uses numerical methods to calculate the thermophysical properties of C/C composites from room temperature to 900°C and explores their variation with temperature. The constructed multi-scale model provides an accurate and effective method for predicting the thermophysical properties of C/C composites and also provides new perspectives and insights for thermal-mechanical coupling analysis and structural design.

Copper-induced lattice distortion in Na4Fe3(PO4)2(P2O7) cathode enabling high power density Na-ion batteries with good cycling stability

Na4Fe3(PO4)2P2O7 (NFPP) has attracted attention due to its high theoretical capacity, low cost, and good structure stability for Na-ion batteries. However, its practical application is limited by the low intrinsic electronic conductivity and sluggish ion diffusion kinetics. To tackle those problems, lattice strain engineering by heteroatom doping is applied to tune the local molecular structure and optimize the electrochemical properties of electrode materials. Copper cation (+2) with a smaller ionic radius was chosen to dope at Fe-site in NFPP, and the doping amount was also optimized, illustrating the optimized sample of Na4Fe2.7Cu0.3(PO4)2P2O7 (NFPP-0.3Cu) delivered a high capacity of 119.01 mAh g-1 at 1C (1 C = 129 mA g-1) and a high capacity retention of 82.76% after 3000 cycles at 20 C. Notably, full cells with NFPP-0.3Cu as cathode and hard carbon as anode delivered a high energy density of 230 Wh kg-1 and a power density of 2280 W kg-1. The exceptional electrochemical performances are attributed to the modulated electronic structure and abundant lattice defects by Cu-doping. Furthermore, in-situ X-ray diffraction technique and theoretical calculation have jointly proved that the lattice distortions originated from Cu-doping have reduced the band gap of the NFPP-0.3Cu and altered the coordination environment of Fe, shortening the Fe-O and Cu-O bond lengths, significantly enhancing the intrinsic ionic conductivity and the diffusion kinetics of Na+. This work provides new point of views on lattice strain engineering and reaction kinetics of cathode materials in promoting high energy and power density sodium-ion batteries.

Hollow CuO/Cu2O octahedrons for selective and stable detection of acetone gas

Acetone (C3H6O) is key member of the volatile organic compound family, which can cause health as well as environmental issues. The identification and sensing of acetone gas are important in many applications such as air quality control and biomarker-based diagnosis. Here, we synthesized hollow CuO/Cu2O octahedrons heterostructure composite through coprecipitation and subsequent heat treatment. The sensor manifested a response of 3.52 to 50 ppm acetone gas at 350 °C. Besides, it showed excellent stability in a 150-day test and excellent repeatability, with a response of 4.15. Also, exhaled gas sensing was carried out using standard method to estimate the acetone concentration in breath. The high sensing capability of the sensor was ascribed to the formation of p-p heterojunctions, the hollow morphology of octahedrons, and the presence of structural defects. The hollow CuO/Cu2O octahedron sensor with good performance may be employed for the detection and monitoring of acetone gas in real situations.

The influence of structural defects on the electrical and infrared emission properties of VO2 thin films

Defect engineering is widely used in the modification of transition metal oxides. In this study, defects are introduced into the polycrystalline VO2 film by the energetic Ar ion irradiation, and the influence of structural defects on the electrical and infrared emission properties of VO2 thin films have been investigated. The decrease in electrical switching ratio with the increase of defect ratio (displacement per atom (dpa)) can be described as R10°C/R90°C=2.032×(dpa+0.005)−1.8069, while the infrared modulation performance is Δε=−0.119×ln(dpa+0.061). The dpa thresholds of the electrical switching ratio and the infrared modulation performance are ηdpaRR = 0.005/atom and ηdpaΔε = 0.0426/atom, respectively, indicating that the electrical switching ratio of VO2 films is more responsive to defects than the infrared modulation performance. The relationship between transition temperature and defect ratio has be determined. Concerning electrical properties, the heating phase transition temperature can be described as TMITHeating=25.88−10.93×ln(dpa+0.01); while for infrared emission modulation, the heating phase transition temperature is given by Tε−MITHeating=31.65−8.18×ln(dpa+0.01). While reducing the phase transition temperature, the VO2 thin films still exhibit an electrical switching ratio of more than two orders of magnitude and obvious infrared modulation performance. It not only offers a viable solution for broadening the application scope of VO2 but also contributes to understanding the role of defects in VO2 thin films for further research.

Optimization of sodium-ion battery cathode performance by nickel-based Prussian blue epitaxial growth with iron-based Prussian blue core-shell structure

To address the structural defects and poor electrical conductivity of conventional Prussian blue analogues (PBAs) samples, in this study, nickel hexacyanoferrate (NiHCF) and nickel hexacyanoferrate epitaxially grown with iron hexacyanoferrate (Ni@FeHCF-X) series of samples were successfully synthesized by co-precipitation combined with epitaxial growth technique, and their structural and electrochemical properties were systematically characterized. X-ray powder diffractometer (XRD) results show that all the samples maintain a cubic crystal system structure, and the diffraction peaks of the (220) and (400) crystal planes are shifted to a lower angle with the epitaxial growth of ferric hexacyanoferrate (FeHCF). The successful embedding of Fe was confirmed by inductively coupled plasma (ICP) measurement data. Scanning electron microscope (SEM) images show that the samples are in a cubic morphology, and the surfaces gradually become rounded from sharp to rounded with the increase of the Fe content. High-resolution transmission electron microscope (HRTEM) and energy-dispersive spectrometer (EDS) analyses confirm the successful construction of the core-shell structure and the homogeneous distribution of the elements. Electrochemical testing showed that the Ni@FeHCF-X samples exhibited higher specific capacities and superior rate performance compared to NiHCF, particularly the Ni@FeHCF-4 sample, which delivered a high specific capacity of 73.4 mAh·g⁻¹ at a current density of 100 mA·g⁻¹, significantly outperforming the 38.2 mAh·g⁻¹ achieved by NiHCF. Additionally, the capacity retention rate of Ni@FeHCF-4 reached 42.16 %. Electrochemical impedance spectroscopy (EIS) further confirmed the reduced charge transfer resistance and enhanced reversibility of the electrochemical reactions in the Ni@FeHCF-X samples. These results demonstrate that Ni@FeHCF-4 significantly enhances the electrochemical performance of the samples in aqueous sodium-ion battery, providing new insights into the design of cathode materials for sodium-ion batteries.

Structural defect regulation in corundum-type medium-entropy oxides for enhanced infrared emissivity performance at high temperature

With the increasing demand in industry and hypersonic vehicles, advanced materials with high-performance infrared radiation need to be developed. Herein, two corundum-type medium-entropy oxide ceramics M3 (Al1/3Cr1/3Fe1/3)2O3 and M4 (Al0.25Cr0.25Fe0.25Ga0.25)2O3 were prepared by solid-state reaction method at different temperatures. Their chemical structure and infrared emissivity performance were analyzed through systematic experiments and theoretical analysis. Compared to the M3, M4 prepared at 1773 K possessed more preeminent emissivity performance, exhibiting emissivity values of 0.917, 0.912 and 0.90 in the wavelength of 0.2–0.78 μm, 0.78–2.50 μm and 2.5–14 μm, respectively. Meanwhile, the infrared emissivity of M4 still could exceed 0.85 at 800 °C in the wavelength of 1.5–25 μm, displaying excellent emissivity and stability under high temperature. As a consequence of lower bandgap and defects formation energy, more oxygen vacancy defects were generated in M4, resulting in better infrared emissivity performance. The results demonstrates that M4 as coating has great potential to be applied in energy-related and thermal protection of hypersonic vehicles.