Material Density Research Articles

The effect of lattice incorporation of Cu2+ in BaCe0.6Zr0.2-xY0.15Gd0.05CuxO3-δ proton conductor on its transport properties

In this paper, the introduction of Cu2+ into BaCe0.6Zr0.2-xY0.15Gd0.05CuxO3-δ (x = 0, 0.02, 0.04, 0.06; denoted as BCZYG, BCZYGCu0.02, BCZYGCu0.04 and BCZYGCu0.06, respectively)proton conductor materials. The effects of Cu doping strategy on the crystal structure, morphology and electrical properties of BCZYGCux proton conductor materials were systematically studied. The X-ray diffraction (XRD) results demonstrate that the synthesis of the BCZYGCux proton conductor material were successfully achieved through the solid-state reaction method. The scanning electron microscopy (SEM) analysis and relative density results indicate that an appropriate amount of Cu additions was conducive to lowering the sintering temperature and promoting the density of materials. A comprehensive analysis based on EIS and DRT was conducted to investigate the effects of temperature, testing atmosphere, and doping amount on the influence of conductivity on BCZYGCux proton conductor material. BCZYGCu0.02 has the largest total conductivity of 1.11×10-2 S·cm-1 at 700 ºC in the atmospheres of pO2=0.20 atm and pH2O=0.018 atm. The transference number of the BCZYGCux proton conductor material was calculated using a defect equilibrium model. The proton transference number of BCZYGCu0.02 is 0.97 at 500 °C. The BCZYGCu0.02 proton conductor has higher proton concentration and proton transference number in comparison to BCZYG. In conclusion, the Cu doping strategy has been demonstrated to be an effective method of improving the conductivity and proton transference number of BCZYGCux proton conductor materials. This provides a valuable insight into the optimisation of perovskite proton conductor performance.

Drag reduction in hypersonic flows with viscous compressible fluid–solid coupling: The role of elastic spikes and lateral jets

This article introduces a novel fluid–solid interaction (FSI) method designed for high-speed flow scenarios, which addresses the intricate interactions between viscous compressible fluids and elastic solids. The proposed method, grounded in the finite volume method, balances computational efficiency and stability while accurately capturing fluid dynamics and structural elasticity. Validation against experimental and numerical data from previous studies confirmed the algorithm's effectiveness. The validated FSI model is applied to study drag reduction in elastic spikes with lateral jets under hypersonic conditions, highlighting significant changes in flow characteristics due to structural deformation and lateral jets. The study extensively examined the effects of jet total pressure, jet orifice position, and spike material density on drag reduction, deformation, and flow field characteristics. Key findings include the influence of compressible FSI on temperature, pressure, and drag distribution, the benefits of increased jet pressure ratio for thermal protection, the impact of jet position on flow characteristics, and the relationship between spike deformation and material density. This study offers valuable perspectives and effective strategies for structure design and minimizing aerodynamic resistance in superspeed fluid situations. Nevertheless, there are still obstacles to overcome, such as non-linear deformation, thermal coupling, and computational precision, highlighting the necessity for further enhancement of FSI techniques.

Constructing unique dual-functional double-hollow architecture for enhanced high-voltage structural stability of layered oxide cathode

Elevating the working voltage has proven to be an effective strategy for enhancing the energy density of ternary layered cathode materials. However, the accelerated failure of secondary particle structure during high-voltage cycling hinders their practical application. Although some attempts have been exerted to address this issue by designing particle arrangement, these secondary structure modifications only provide the limited help to the structural failure problem. Herein, we focus on the cause and characteristic of secondary particle cracks, investigate their formation principle and development rule, and delicately propose a unique double-hollow secondary structure. The two hollow regions create an environment that facilitates the release of internal strain and reduces stress at grain boundaries, thus ensuring the homogeneous stress distribution within the secondary particles. Thereby, the formation of intergranular crack is effectively mitigated. Additionally, the hollow regions act as barrier layers to impede the crack propagation. The dual functions of this double-hollow structure efficiently maintain the tight connection among these primary particles, greatly boosting the high-voltage cycling stability. The designed material with double-hollow architecture exhibits an obvious capacity retention increase from 67.8 % (conventional structure) to 84.4 % at 1 C within 3.0-4.5 V after 300 cycles. This work demonstrates that the double-hollow structure can effectively address the key issues of crack occurrence and development, providing a novel structural design concept for the exploration of high-voltage cathode materials with superior stability.

Proposing novel body-centered cubic lattice core sandwich panels as satellite structure

In the present paper, a comparative study on the load-bearing as well as shielding performance against hypervelocity impact of space debris of sandwich panels with body-centered cubic lattice core is performed numerically in order to evaluate their eligibility to be utilized as the satellite structure. To this end, four types of body-centered cubic lattice structures, with similar areal densities which are assumed to be made of 5A06 aluminum alloy, including BCC, BCCz (BCC reinforced in Z direction), and also BCCz-I and BCCz-II were considered. Whipple shield structure of same material and areal density was also investigated in order to justify the necessity of lattice structures application, especially in protection field. The present study simulates hypervelocity impact of a spherical projectile with 2 mm diameter, represented the space debris, collides with the structures at the velocity range of 2–6 km/s. Current numerical simulation process accuracy and efficiency were verified through comparing its obtained data based on simulating a problem had been investigated at a valid experimental study to the data proposed by the mentioned research. BCCz-II structure which is newly proposed at this study provided outstanding shielding and load-bearing capabilities in comparison to other structures. Furthermore, the detailed effects of projectile impact location and a middle structure placed plate on the protection performance were investigated and the mentioned items were found to have crucial impact on the structure shielding performance.

Simplified, Infiltration-free Ceramic Matrix Composite Manufacturing

Manufacturing of ceramic matrix composites (CMCs) with carbon fiber and carbon matrix includes a time- and labor-intensive ceramic infiltration step that is responsible for more than half of the total manufacturing cost. To make CMCs cost-competitive in price-sensitive markets, like concentrated solar power, it is essential to develop a CMC manufacturing process that skips the ceramic infiltration process. In this work, we will show how a high-char-yield preceramic resin can eliminate the infiltration step while maintaining material density and evaluate the technoeconomic impact of our CMC manufacturing process. We monitor both morphology and porosity to determine the quality of CMCs made with different preceramic resins and evaluate the impact of polymer infiltration and pyrolyzing cycles.

Eco-friendly strain-hardening cementitious composites with recycled PET fine aggregate: Mechanical behavior and environmental benefits

The production of strain-hardening cementitious composites (SHCC) heavily relies on natural fine aggregates. This study employs recycled PET fine aggregates to prepare PET-modified SHCC (P-SHCC). The physical properties and mechanical behavior of P-SHCC with different PET volume replacement ratios (0 %, 25 %, 50 %, 75 %, and 100 %) are experimentally investigated. The microstructures were examined to analyze the impact of additional defects induced by the interfacial transition zone between recycled PET and cementitious matrix. The multiple cracking behavior was discussed based on the crack parameters. The results indicate that the incorporation of PET significantly enhances the ultimate strain and crack control capability of SHCC while reducing the material's density. Furthermore, energy consumption, carbon emission, and comprehensive environmental indexes were employed to analyze the environmental benefits. The findings demonstrate the feasibility of preparing SHCC with recycled PET fine aggregate, particularly in enhancing the strain capacity and environmental benefits.

Effect of the underlayer on the elastic parameters of the CoFeB/MgO heterostructures

We investigated the thermally induced surface acoustic waves in CoFeB/MgO heterostructures with different underlayer materials. Our results show a direct correlation between the density and elastic parameters of the underlayer materials and the surface phonon dispersion. Using finite element method-based simulations, we calculate the effective elastic parameters (such as elastic tensor, Young’s modulus, and Poisson’s ratio) for multilayers with different underlayer materials. The simulation results, either considering the elastic parameters of individual layers or considering the effective elastic parameters of whole stacks, exhibit good agreement with the experimental data. This study will help us deepen our understanding of phonon properties and their interactions with other quasiparticles or magnetic textures with the help of these estimated elastic properties.

Effect of raw material fineness on the properties of inorganic foam materials from solid waste

Solid waste inorganic lightweight materials not only compensate for the flammability of organic materials but also have a lower carbon footprint. They are environmentally safe and cost-effective compared with cement-based foaming materials, and they have good development prospects. This study aimed to improve the chemical foaming reaction kinetics by reducing the particle size of aluminum powder and alkaline solid waste, thereby increasing the expansion degree of solid waste slurry, to further reduce the absolute dry density of inorganic lightweight materials for solid waste and optimize their performance. The influence of the particle size of raw material on the absolute dry density, water absorption, and compressive strength of lightweight materials was investigated. The influence of the particle size of raw material on the macroscopic pore structure of foamed materials was analyzed through binarization of cross-sectional images of specimens. Furthermore, the hydration products and microstructure of materials were characterized using XRD, FTIR, TG-DTG, and SEM to provide a theoretical basis for related research. The experimental results showed that the smaller the particle size of the raw material, the easier it was to carbonize and the lower the flowability of the corresponding cementitious material slurry. Reducing the particle size of raw materials and aluminum powder increased the degree of slurry expansion, thereby reducing the absolute dry density of foaming materials. In addition, reducing the particle size of raw materials and using carbide slag wastewater instead of tap water increased the degree of foaming reaction and hydration reaction, which helped C-(A)-S-H gel formation and promoted the development of sample strength. Finally, the absolute dry density of inorganic lightweight materials was reduced to 0.35 g/cm3 at the minimum, and the corresponding 28-day compressive strength was 0.28 MPa, which met the requirements of the JG/T 266–2011 “foam concrete” specification.

Semi-analytical modeling of prompt redeposition in a steady-state plasma

Abstract A steady-state, 1D semi-analytical model for prompt redeposition based on the separation between redeposition caused by the electric field in the sheath and redeposition related to gyromotion is here described. The model allows for the estimation of not only the fraction of promptly redeposited flux but also the energy and angular distribution of the non-promptly redeposited population, along with their average charge state. Thus, the temperature and mean parallel-to-B velocity of the non-promptly redeposited flux are also available. The semi-analytical model was validated against equivalent Monte Carlo simulations across a broad range of input parameters. In this paper the eroded material under exam was tungsten (W) for which the code demonstrated consistent agreement with respect to numerical results, within its defined validity limits. The model can theoretically provide a solution for any material, temperature and electron density profile in the sheath, monotonic potential drop profile, and sputtered particles energy and angular distribution at the wall. As such, this code emerges as a potential tool for addressing the boundary redeposition phenomenon in fluid impurity transport simulations.

High-energy bimetallic substituted Na3V2(PO4)3 cathode for advanced sodium-ion batteries

NASICON-type cathodes have attracted great attention due to their open three-dimensional (3D) frame structure and excellent ion transport properties. Accordingly, how to improve the stability and energy density of materials is a hot topic of research. In this study, the significant effects of aluminum-zirconium bimetallic substitution on electrode kinetics and structural stability are reported. The designed Na2.9V1.8Al0.1Zr0.1(PO4)3 cathode exhibits a highly reversible capacity of 107 mAh g-1 at 1C and decent cyclic stability (75 mAh g-1 capacity after 2000 cycles at 20C). These excellent electrochemical properties can be attributed to expanding the lattice structure and activating part of V4+, which facilitates the migration of Na+ and increases the reversible capacity. The cyclic voltammetry, electrochemical impedance spectra and galvanostatic intermittent titration technique tests analyze the diffusion kinetics of sodium ions and confirm the desired sodium ion diffusion coefficients (DNa+). In situ X-ray diffraction reveals reversible structural changes during the electrochemical reaction, which confirms that the bimetallic doping strategy slows down material volume change. This work provides a new perspective for the construction of high-performance NASICON cathode materials.

Improving energy density of battery-type electrode material by growing β-Ni(OH)2 in situ on biochar for hybrid supercapacitors

The insufficient energy density of electrode materials has hindered the popularity and application of supercapacitors. The construction of hybrid supercapacitors offers an ideal solution by combining transition-metal hydroxides with high specific capacity and biochar with excellent conductivity. In this study, an electrode material (β-Ni(OH)2@AC22 composite) was created by in situ growth flower-like β-Ni(OH)2 nanosheets on biochar (AC) that extracted from the seed coat of Xanthoceras sorbifolium Bunge. This β-Ni(OH)2@AC22 composite exhibited a remarkable specific capacity of 617.5C g−1 (1 A g−1), nearly four times that of AC, and remarkable cycling stability (85.6 % retention after 5000 cycles). Using this composite as the positive electrode and biochar as the negative electrode, the assembled battery-type hybrid supercapacitors (HSCs) achieved a specific capacity of 92.75C g−1 (1 A g−1). The HSCs demonstrated a specific energy of 57.9 Wh kg−1, a specific power of 750.9 W kg−1, and even maintained 42.2 Wh kg−1 at a maximum specific power of 6049.4 W kg−1. The device maintained a specific capacity of about 78.7 % after 7000 charging/discharging cycles, demonstrating good practical performance. These results highlight the practical application potential of the prepared composites in supercapacitors, with biochar serving as a basis for enhancing the electrochemical performance of supercapacitors.

Study on Grouting Performance Optimization of Polymer Composite Materials Applied to Water Plugging and Reinforcement in Mines.

With the increasing drilling depth of mines, the cross-complexity of fissures in the rock body, and the frequent occurrence of sudden water surges, polymer slurry, with its advantages of good permeability and strong water plugging, is increasingly used in mine grouting projects. Additional research is needed in order to further improve the grouting performance of polymer slurry, ensure the safety of mining operations, and reduce the grouting cost. In this paper, a polymer composite grouting material was prepared with diphenyl methyl diisocyanate, polyether polyol, and fly ash, as the main raw materials, with coupling agent and catalyst as auxiliary reagents. The performance of the composite grouting material in terms of mechanical properties, thermal stability, hydrophobicity, and bonding was explored. This study's findings indicated that incorporating fly ash led to notable enhancements in the thermal stability and water resistance of the polymer slurry. Furthermore, the introduction of fly ash notably raised the starting degradation temperature of the polymer, boosted the water contact angle of the composite material, and reduced the density and reaction temperature of the composite material. In addition, the catalyst and coupling agent as auxiliary reagents affected the polymers in terms of mechanical properties; in this paper, dibutyltin dilaurate was used as the catalyst, and organosilanes were used as the coupling agent. The catalyst successfully sped up the polymer's gel time, however, an excessive quantity of catalyst compromised the polymer's mechanical characteristics. The addition of organosilanes has a positive effect on the dynamic mechanical properties of the composites, fracture toughness, compression, bending, and bond strength. The research can offer a theoretical direction for creating polymer mixtures in mine grouting projects.

Low-density, water-repellent, and thermally insulating cellulose-mycelium foams

This work explored whether partial cellulose bioconversion with fungal mycelium can improve the properties of cellulose fibre-based materials. We demonstrate an efficient approach for producing cellulose-mycelium composites utilizing several cellulosic matrices and show that these materials can match fossil-derived polymeric foams on water contact angle, compression strength, thermal conductivity, and exhibit selective antimicrobial properties. Fossil-based polymeric foams commonly used for these applications are highly carbon positive, persist in soils and water, and are challenging to recycle. Bio-based alternatives to synthetic polymers could reduce GHG emissions, store carbon, and decrease plastic pollution. We explored several fungal species for the biofabrication of three kinds of cellulosic-mycelium composites and characterized the resulting materials for density, microstructure, compression strength, thermal conductivity, water contact angle, and antimicrobial properties. Foamed mycelium-cellulose samples had low densities (0.058 – 0.077 g/cm3), low thermal conductivity (0.03 – 0.06 W/m∙K at + 10 °C), and high water contact angle (118 – 140°). The recovery from compression of all samples was not affected by the mycelium addition and varied between 70 and 85%. In addition, an antiviral property against active MS-2 viruses was observed. These findings show that the biofabrication process using mycelium can provide water repellency and antiviral properties to cellulose foam materials while retaining their low density and good thermal insulation properties.Graphical

Lexical Density of Reading Materials in An English Textbook: A Content Analysis

In reading, students are required to learn to comprehend the content of the text. Lexical density is one of the factors that influences students’ reading comprehension. Lexical density is a condition of words’ proportion in a text, which shows the ratio of content words (CW) and grammatical function words (GFW). This research used the “Passport to the World” English textbook for the 8th grade of junior high school to be analyzed. This study aims to find out the genres of reading materials offered by the curriculum 2013 found in the textbook and to examine the lexical density of the reading materials in the textbook. A qualitative approach was applied, while content analysis was used as the research design. Data were collected with document analysis. The findings showed that there are 3 genres of reading materials, among 5 genres offered by the curriculum 2013, included in the textbook such as descriptive, recount, and functional texts in the form of announcements. From those, it was found that two texts were categorized as low lexical density, 11 texts were categorized as medium lexical density, and four texts were labeled as high lexical density. In addition, the composition of this text did not reach the ideal ratio of 1:2:1 for index difficulty. However, this textbook can still be suggested to be used in the class with some usage modifications in the classroom.

Strong Covalent Metal-Ligand Interaction Enables a Fast Kinetic and Structurally Stable Na-Ion Layered Cathode.

Anionic redox chemistry has attracted increasing attention for the improvement in the reversible capacity and energy density of cathode materials in Li/Na-ion batteries. However, adverse electrochemical behaviors, such as voltage hysteresis and sluggish kinetics resulting from weak metal-ligand interactions, commonly occur with anionic redox reactions. Currently, the mechanistic investigation driving these issues still remains foggy. Here, we chemically designed Na0.8Fe0.4Ti0.6S2 and Na0.8Fe0.4Ti0.6O2 as model cathodes to explore the covalency effects on metal-ligand interactions during anionic redox process. Na0.8Fe0.4Ti0.6S2 with strengthened covalent interaction of metal-ligand bonds exhibits smaller voltage hysteresis and faster kinetics than Na0.8Fe0.4Ti0.6O2 during (de)sodiation process. Theoretical calculations suggest that Fe is the dominant redox-active center in Na0.8Fe0.4Ti0.6S2, whereas the redox-active center moves from Fe to O with the removal of Na+ in Na0.8Fe0.4Ti0.6O2. We attribute the above different redox behaviors between Na0.8Fe0.4Ti0.6S2 and Na0.8Fe0.4Ti0.6O2 to the charge transfer kinetics from ligand to metal. Moreover, the structural stability of Na0.8Fe0.4Ti0.6S2 is enhanced by increasing the cation migration barriers through strong metal-ligand bonds during desodiation. These insights into the originality of metal-ligand interactions provide guidance for the design of high-capacity and structurally stable cathode materials for Li/Na-ion batteries.

UV Resistance and Wetting of PLA Webs Obtained by Solution Blow Spinning.

In this work, the resistance of polylactide-based non-wovens produced by solution blow spinning to environmental factors was investigated. An average contact angle of up to 136° was achieved with an average fiber diameter of 340 nm at the optimal material density and nozzle-substrate distance. When exposed to ultraviolet (UV) radiation, the polylactide non-wovens rapidly lose their hydrophobic properties due to changes in surface morphology resulting from fiber melting. It was demonstrated that the influence of surface structural features on hydrophobicity is greater than that of the material itself. The stability of the wetting properties under UV irradiation was assessed using the derivative parameters of the Owens-Wendt technique, which can serve as an additional method for estimating surface polarity.

Effect of laser speed on neck formation in SS316L powder joining for LPBF

The objective of this study is to comprehend how changes in laser speed affect the behaviour and features of neck formation in SS316L during powder bed fusion. This study examines the impact of various laser speeds on the neck formation in the commonly used SS316L. Uniweld Laser 3000 was used for laser joining. A constant laser power of 15 W and laser scan speed of 25–150 mm/s were implemented, and powder joining within a single track was observed. Results show that neck size decreases with increasing laser scanning speed and no particle joining occurs at 150 mm/s scan speed, as it is considered too fast for sufficient heat absorption and melting. As laser speed decreases to 125 mm/s, neck starts to form because the particles absorb more heat, which facilitates melting and bonding. Surface diffusion occurs early at this stage because it requires only a small amount of energy to break atomic bonds on the surfaces of particles compared to those in the internal part. This process involves atoms moving along the surfaces of the particles, facilitating the initial stages of sintering by reducing surface energy and causing neck formation between particles. At 125 mm/s, the particle shape remains spherical, and the average neck size is 49 μm. At 100 μm, the powder average neck size is 62 μm. Moreover, the powder completely merges at 50 mm/s and 25 mm/s. The neck formed between particles considerably improves the product's mechanical strength by strengthening bonds between particles. Material density increases with neck quality, and stable neck growth can reduce the porosity of the final parts. Ensuring thermal stability in the laser powder bed fusion allows consistent heat to particles, ensuring even temperature in materials and ultimately facilitating stable neck growth. Thermal stability enables atoms in particles to migrate efficiently and prevents defects, such as bubbling, which increases porosity in printed parts. Therefore, a slow scanning speed allows particles to absorb more heat for melting, increasing the neck size of particles. This knowledge is useful for optimizing laser processing parameters in various industrial applications.

A phase-field gradient-based energy split for the modeling of brittle fracture under load reversal

In the phase-field modeling of fracture, the search for a physically reasonable and computationally feasible criterion to split the elastic energy density into fractions that may or may not contribute to crack propagation has been the subject of many recent studies. Within this context, we propose an energy split – or energy decomposition – aimed at accurately representing the evolution of a crack under load reversal. To this purpose, two key assumptions are made. First, the damage gradient direction is interpreted as being representative of the normal-to-crack direction, as already assumed in previous works in the literature. The second assumption consists of considering the sign of the projection of the stress tensor onto the damage gradient direction at a point as an indicator of whether this point should behave as an opening or as a closing crack. We associate the latter case (crack closing) to both (a) a complete recovery of elastic energy density of the intact material (i.e., perfectly rough crack surfaces) and (b) a zero crack driving force at that point. The first case (crack opening) is treated classically as a damageable material point at which damage can increase. The implementation of the proposed approach turns out to be remarkably simple and computationally robust. For the evaluation of the displacements and damage gradients at nodes, the classical Z2 technique is used, and a new effective and computationally convenient iterative strategy is implemented to guarantee convergence of the staggered scheme. Four examples are presented in order to assess the suitability of the present model by using both AT1 and AT2 regularization models. Results show the desired effect of limiting crack propagation to prevailing tensile states, as well as of recovering the initial intact stiffness upon load reversal, even when two of the most common energy splits fail.

High sulfur content cathode composites utilizing the Li(CB9H10)0.7(CB11H12)0.3 superionic conductor for all−solid−state Li−S batteries

Rechargeable batteries are encountering ever−growing demands for further improvements in energy density and safety. All−solid−state lithium−sulfur (Li−S) batteries have the potential to meet these demands, because they employ not only high−energy−density electrodes but also non−flammable inorganic solid electrolytes. However, the sluggish conducting nature of the S cathode results in high electric transfer barriers, making high S content in solid−state cathode composites difficult. In this study, we report the fabrication and reaction behavior of high S content cathode composites using a Li(CB9H10)0.7(CB11H12)0.3 superionic conductor. The lithium superionic conduction, high deformability, and low material density of Li(CB9H10)0.7(CB11H12)0.3 solid electrolyte facilitate intimate and favorable connections with sulfur and carbon, leading to facile electrical migrations within sulfur−Li(CB9H10)0.7(CB11H12)0.3−carbon (S−CH−C) composites. In battery tests, these close interconnections enable the fabrication of S−CH−C cathode composites through simple physical hand−mixing, allowing for reversible discharge−charge cycling of all−solid−state Li−S batteries engaging high energy density (>1,000 Wh kg−1cathode composite) S−CH−C cathode composites with a high S content of 50 wt%. In addition, a comparative investigation using various carbonaceous conductive materials suggests that simultaneously achieving high surface area, nanoparticle size, and non−spherical rough morphology is crucial for developing high S content S−CH−C composites with superior battery performances.

Prilling and Coating Strategy to Synthesize High-Performance Spherical NaNi0.4Fe0.2Mn0.4O2 Cathode Materials for Sodium Ion Batteries.

Low-cost sodium ion batteries are of great significance in large-scale energy storage applications. With its high energy density and simple synthesis process, layered transition-metal oxides have become one of the most likely sodium ion battery cathode materials to replace lithium ion batteries in the energy storage market. Here, we report a prilling and MoS2 coating strategy to prepare the spherical cathode material. The spherical micronano particles shorten the diffusion path of Na+, restrain the complexity phase transitions, and enhance the tap density of the materials. In addition, the MoS2 coating improves the electrical conductivity of the material and the structural stability of the cathode material in air. The initial specific discharge capacity is 148.4 mA h g-1 at 0.1 C, which can be maintained at 128.9 mA h g-1 after exposure to air for 10 days. This method dramatically improves the energy density and structural stability of the cathode material, which provides a new scheme for preparing high-performance sodium ion batteries.