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The dynamics of residual stress (RS) within glass-to-metal (GTM) seals play a crucial role in their operational efficacy, with the progression of RS in response to temperature variations being a critical aspect in engineering applications. This research utilizes fiber Bragg grating sensors and temperature-calibrated photoluminescence spectroscopy techniques for the in situ monitoring of RS changes within GTM seals during heating. Initially, the glass body exhibited a compressive stress of −203 MPa, while the stress in the glass close to the interface was −367 MPa at room temperature. With increasing temperature, RS within both the glass body and in the glass close to the interface transitions through three distinct phases: a near-linear decrease, a rapid decrease, and a shift from compressive to tensile stress. By 540 °C, tensile stresses of approximately 11 MPa within the glass body and 36 MPa in the glass close to the interface were observed. The study elucidates that RS evolution is intricately linked not only to the thermal expansion properties of the constituent materials but also to the β-relaxation phenomenon within the glass structure and the presence of an oxide layer at the interface. Finite-element analysis simulations were conducted to corroborate the experimental findings, illustrating a congruent RS evolution pattern and delineating the transition from a compressive to a tensile state. This investigation provides empirical data and analytical insights concerning the management of RS in GTM seals, underscoring the significance of RS control in maintaining seal integrity. [ABSTRACT FROM AUTHOR]

Flexible electronic devices with skin-like properties are hailed as revolutionary for the development of next-generation electronic devices, such as electric-skin and humanoid robotics. Graphene is intrinsically flexible due to its structural thinness in nature and are considered next-generation materials for wearable electronics. These devices usually experience a large mechanical deformation in use so as to achieve intimate conformal contact with human skin and to coordinate complex human motions, while heat dissipation has been a major limitation when the device is under a large mechanical strain. Unlike the small deformation (<1%) induced by intrinsic material factors such as lattice mismatch between material components in devices, a large mechanical deformation (>1%) by an external loading condition could lead to apparent changes to global geometric shapes and significantly impact thermal transport. In this study, we investigated the thermal conductivities of graphene under several large mechanical strains: 2.9%, 4.3%, and 6.1%. We used a refined opto-thermal Raman technique to characterize the thermal transport properties and discovered the thermal conductivities to be 2092 ± 502, 972 ± 87, 348 ± 52, and 97 ± 13 W/(m K) for the relaxed state, 2.9%, 4.3%, and 6.1% tensile strain, respectively. Our results showed a significant decreasing trend in thermal conductivities with an increasing mechanical strain. The findings in this study reveal new thermal transport mechanisms in 2D materials and shed light on building novel flexible nanoelectronic devices with enhanced thermal management. [ABSTRACT FROM AUTHOR]

An accurate and efficient heat bath method plays a key role in atomic simulations of the thermal and mechanical properties of single-crystal silicon. Here, focusing on the single-crystal silicon (111) layer, which is a crucial lattice structure commonly employed as a substrate for chips, we propose a heat jet approach for finite temperature atomic simulations of silicon layers. First, we formulate the linearized dynamic equations for the silicon atoms and calculate the dispersion relation and lattice wave solutions. Then, an appropriate matching boundary condition is chosen for designing the two-way boundary condition, which allows incoming waves to inject into the lattice system while eliminating boundary reflections. Combining the two-way boundary condition and phonon heat source, the heat jet approach for the silicon (111) layer is proposed. Numerical tests illustrate the accuracy and effectiveness of the heat jet approach in simultaneously resolving thermal fluctuations and controlling temperature. Furthermore, we simulate the propagation of a Gaussian hump at a given temperature with the heat jet approach compared to the Nosé–Hoover heat bath. Numerical results demonstrate that the heat jet approach can well describe the movement of large structural deformations among thermal fluctuations without boundary reflections. [ABSTRACT FROM AUTHOR]

Bond line thickness (BLT) is an essential parameter of thermal conductive composite gels as the thermal interface material (TIM). Extensive research has been performed on designing next-generation TIMs with high thermal conductivity; however, it remains elusive how to link laboratory measurements and the theoretically predicted BLT. Here, we propose a new model to estimate BLT based on a rheological property, in which the TIM is assumed to be a simple power law fluid. To avoid the unrealistic situation of the BLT tending to zero, we introduce a decaying exponential function to describe the influence from fillers during the lid attach process and rebuild the force balance equation. Compared with previously reported models, the theoretical prediction BLT based on the proposed model is in good agreement with the experimental data. Our model has a guiding significance in predicting the BLT, which may help to optimize the thermal performance of TIMs. [ABSTRACT FROM AUTHOR]

The two-dimensional laser-based Ångstrom method measures the in-plane thermal properties for anisotropic film-like materials. It involves periodic laser heating at the center of a suspended film sample and records its transient thermal response by infrared imaging. These spatiotemporal temperature data must be analyzed to extract the unknown thermal conductivity values in the orthotropic directions, an inverse parameter fitting problem. Previous demonstration of the metrology technique used a least-squares fitting method that relies on numerical differentiation to evaluate the second-order partial derivatives in the differential equation describing transient conduction in the physical system. This fitting approach is susceptible to measurement noise, introducing high uncertainty in the extracted properties when working with noisy data. For example, when noise of a signal-to-noise ratio of 10 is added to simulated amplitude and phase data, the error in the extracted thermal conductivity can exceed 80%. In this work, we introduce a new alternative inverse parameter fitting approach using physics-informed neural networks (PINNs) to increase the robustness of the measurement technique for noisy temperature data. We demonstrate the effectiveness of this approach even for scenarios with extreme levels of noise in the data. Specifically, the PINN-approach accurately extracts the properties to within 5% of the true values even for high noise levels (a signal-to-noise ratio of 1). This offers a promising avenue for improving the robustness and accuracy of advanced thermal metrology tools that rely on inverse parameter fitting of temperature data to extract thermal properties. [ABSTRACT FROM AUTHOR]

Cobalt oxides are known for their excellent heat transfer properties. The main component of cobalt oxides is the CoO2 monolayer, which exhibits high-temperature superconductivity caused by strong electron–phonon coupling (EPC). We here systematically investigate the structural stability, electronic structure, and magnetism of the CoO2 monolayer using first-principles and Monte Carlo simulations. On this basis, we further study the changes in the spin energy gap, magnetic axis direction, and other properties of the CoO2 monolayer with the changes in carrier concentration. By appropriately doping the CoO2 monolayer with holes, the magnetic axis direction of the CoO2 monolayer can be reversed, thereby enhancing its potential application in the field of spin electronic devices. Monte Carlo simulation is used to study the regulation of different factors on the magnetothermal properties of the CoO2 monolayer. Through the analysis of physical parameters such as Curie temperature (TC) and bandgap, we find that the appropriate carrier concentration and magnetic field can not only regulate the magnetothermal properties of materials but also further improve the efficiency of materials in low-temperature environments. [ABSTRACT FROM AUTHOR]

Thermal transport plays a pivotal role across diverse disciplines, yet the intricate relationship between amorphous network structures and thermal conductance properties remains elusive due to the absence of a reliable and comprehensive network's dataset to be investigated. In this study, we have created a dataset comprising multiple amorphous network structures of varying sizes, generated through a combination of the node disturbance method and Delaunay triangulation, to fine-tune an initially random network toward both increased and decreased thermal conductance C. The tuning process is guided by the simulated annealing algorithm. Our findings unveil that C is inversely dependent on the normalized average shortest distance L n o r m connecting heat source nodes and sink nodes, which is determined by the network topological structure. Intuitively, the amorphous network with increased C is associated with an increased number of bonds oriented along the thermal transport direction, which shortens the heat transfer distance from the source to sink node. Conversely, thermal transport encounters impedance with an augmented number of bonds oriented perpendicular to the thermal transport direction, which is demonstrated by the increased L n o r m . This relationship can be described by a power law C = L n o r m α , applicable to the diverse-sized amorphous networks we have investigated. [ABSTRACT FROM AUTHOR]

We here report the electronic structure calculation of GaInSe3 and GaInTe3 monolayers with the P3m1 (no. 156) space group. The electronic structure and thermoelectric properties of the monolayers are calculated through the Vienna Ab initio Simulation Package and BoltzTraP2 codes. The dynamic and thermodynamic stabilities were verified by calculating their phonon spectra and simulating ab initio molecular dynamics. The monolayers were found to have a direct bandgap, with both PBE + SOC and HSE06 + SOC potentials. The lattice thermal conductivity of GaInTe3 monolayer calculated using Phono3py code shows ultra-low values due to enhanced phonon–phonon scattering. Combining electrical and thermal transport, the values have been evaluated. Importantly, the p-type GaInTe3 has excellent thermoelectric properties at 700 K, with a z T value of 2, indicating that the p-type GaInTe3 has potential application in the field of thermoelectricity. [ABSTRACT FROM AUTHOR]

The binary high-pressure phase diagram of the Ta–Sb system was constructed for the first time in this study, utilizing the evolutionary algorithm USPEX and density functional theory (DFT). Ten pressurized dynamically and mechanically stable or metastable novel phases of Ta–Sb were discovered, including I4/mmm-TaSb2, P4/nmm-TaSb, P-3-Ta2Sb7, I4/mmm-Ta2Sb3, P-4m2-Ta7Sb, Pm-3-Ta7Sb, Pmm2-Ta15Sb, P4/nmm-TaSb3, I4/mmm-Ta3Sb4, and I4/mmm-Ta2Sb5. The compounds P-4m2-Ta7Sb and Pmm2-Ta15Sb exhibit promising characteristics as non-centrosymmetric superconductors (NCSs), with their superconducting critical temperature (TC) being 3.831 and 3.221 K, respectively. The application of pressure tuning is predicted to transform the topological characteristics of P4/nmm-TaSb, causing it to transition from a topological insulator state to a Dirac semimetal state and ultimately reverting back to a topological insulator state. Therefore, the P4/nmm-TaSb compound is considered a promising candidate to investigate topological and superconducting excitations. Moreover, the mechanical and thermal properties of Ta–Sb binary phases were also investigated. The thermal conductivity of I4/mmm-TaSb2, P4/nmm-TaSb, and P4/nmm-TaSb3 all surpasses 20 W m−1 K−1 at 1000 K, showcasing their excellent thermal conductivity properties. The present study addresses the research gap concerning high-pressure structures in the Ta–Sb binary system, thereby offering valuable insights for the design and development of intermetallic compounds within this binary system. [ABSTRACT FROM AUTHOR]

Owing to the unique asymmetric geometry, Janus monolayer compounds exhibit various exotic thermal properties and have promising applications in thermal management. In this study, we combine machine learning potentials and the phonon Boltzmann transport equation to perform a comparative study of the thermal transport properties in Janus XBAlY (X = Se, S, Te; Y = S, Se, O; X ≠ Y) monolayers. Our findings unveil a thermal conductivity (κ p) ranking as SeBAlS > TeBAlO > SBAlSe, contradicting the conventional expectation that a higher κ p is typically observed when the average atomic mass is smaller. At room temperature, the κ p of SeBAlS is 174 Wm−1 K−1, which is 4.8 times that of SBAlSe when considering three-phonon scattering processes. Moreover, the consideration of four-phonon scatterings does not alter such ranking. The anomalous κ p phenomenon was explained through a detailed analysis of the phonon–phonon scattering mechanism, phonon bandgap, phonon anharmonicity, and chemical bond strength. This study highlights the intricate relationship between atomic mass, bonding characteristics, and thermal properties, offering insights for designing Janus materials with tailored thermal conductivity. [ABSTRACT FROM AUTHOR]

Hafnia (HfO2) is a potential candidate for the high-k gate dielectrics in next-generation high-power electronics. Its thermal transport properties, which determine the performance of these related high-power electronics, are critical while rarely investigated. Here, the thermal transport properties of HfO2 in a wide temperature range of 300–2000 K with a phase transition between monoclinic and tetragonal phases at ∼1765 K, are systematically studied based on the temperature-dependent effective potential landscapes with both propagating and coherence thermal transport considered. It is found that the cage-like structure of monoclinic HfO2 results in the avoid crossing in the phonon band structures, which increases the three-phonon scattering largely. Some phonon modes with significant scattering matrix can have relatively larger 3ph and 4ph scattering rates in tetragonal HfO2. Consequently, the thermal conductivity of HfO2 is only 11.95–1.72 W/mK at 300–2000 K. Our results further show that propagating phonon channels dominate the thermal transport in HfO2 and contribute at least 70% to the total thermal conductivity. The rest of the thermal conductivity of HfO2 results from the coherence thermal transport channels, which is caused by the overlap of phonons. Four-phonon scatterings are found to be significant for the thermal transport in tetragonal HfO2, which can result in a thermal conductivity reduction of ∼50%. Our results here advance the understanding of the thermal transport in HfO2, which may benefit the performance optimization of HfO2-related electronics. [ABSTRACT FROM AUTHOR]

Thermal transport in wurtzite aluminum nitride (w-AlN) significantly affects the performance and reliability of corresponding electronic devices, particularly when lattice strains inevitably impact the thermal properties of w-AlN in practical applications. To accurately model the thermal properties of w-AlN with high efficiency, we develop a machine learning interatomic potential based on the atomic cluster expansion (ACE) framework. The predictive power of the ACE potential against density functional theory (DFT) is demonstrated across a broad range of properties of w-AlN, including ground-state lattice parameters, specific heat capacity, coefficients of thermal expansion, bulk modulus, and harmonic phonon dispersions. Validation of lattice thermal conductivity is further carried out by comparing the ACE-predicted values to the DFT calculations and experiments, exhibiting the overall capability of our ACE potential in sufficiently describing anharmonic phonon interactions. As a practical application, we perform a lattice dynamics analysis using the potential to unravel the effects of biaxial strains on thermal conductivity and phonon properties of w-AlN, which is identified as a significant tuning factor for near-junction thermal design of w-AlN-based electronics. [ABSTRACT FROM AUTHOR]

The lattice thermal conductivity (LTC) of Ga 2 O 3 is an important property due to the challenge in the thermal management of high-power devices. In this work, we develop machine-learned neuroevolution potentials (NEPs) for single-crystalline β - Ga 2 O 3 and κ - Ga 2 O 3 and demonstrate their accuracy in modeling thermal transport properties. Combining NEP-driven homogeneous non-equilibrium molecular dynamics simulations with tensor analysis, we determine the spatial distributions of LTCs for two Ga 2 O 3 crystals, showing dissimilar thermal behaviors. Specifically, β - Ga 2 O 3 shows isotropic thermal transport properties, with the LTCs along [100], [010], and [001] directions being predicted to be 10.3 ± 0.2 , 19.9 ± 0.2 , and 12.6 ± 0.2 W/(m K), respectively, consistent with previous experimental measurements. For κ - Ga 2 O 3 , our predictions suggest nearly isotropic thermal transport properties, with the LTCs along [100], [010], and [001] being estimated to be 4.5 ± 0.1 , 3.9 ± 0.1 , and 4.0 ± 0.1 W/(m K). The reduced LTC of κ -Ga 2 O 3 vs β -Ga 2 O 3 stems from its restricted low-frequency phonons up to 5 THz. Furthermore, we find that the β phase exhibits a typical temperature dependence slightly stronger than ∼ T − 1 , whereas the κ phase shows a weaker temperature dependence, ranging from ∼ T − 0.5 to ∼ T − 0.7 . [ABSTRACT FROM AUTHOR]

We present results of resonant ultrasound spectroscopy (RUS) measurements applied to granular high explosive materials at different bulk pressing densities and degree of thermal conditioning. The material chosen in this study is a ubiquitously used explosive material known as pentaerythritol tetranitrate (PETN), which is used commercially in civil and defense applications both as a binderized plastic bonded explosive material and an unbinderized neat material. However, changes in granular PETN bulk elastic properties due to thermal conditioning, which could have implications for better understanding environmental aging-related effects, have not been well studied even though it is believed that elasticity may play an important role in explosive material initiation mechanisms. Furthermore, monitoring elastic property changes in granular explosive pressings has not yet been demonstrated using RUS, which is an appealing non-destructive characterization tool that requires only dry point contact with the explosive material. To this end, we report the first study using RUS to quantify the elastic properties of binderized and neat PETN pressings as well as to quantify changes in elastic properties as a function of both thermal conditioning and bulk pressing density. Elastic stiffness coefficients, sometimes more commonly referred to as elastic constants, calculated from the RUS measurements on the different PETN-based materials show a significant increase for the post-conditioned samples compared to the pre-conditioned samples. This trend of increasing elastic properties with thermal conditioning was consistent for different density pressings, different thermal exposure conditions, and even different neat PETN pressings of differing average crystal sizes and/or specific surface areas. [ABSTRACT FROM AUTHOR]

The crystallization thermal stability plays an essential role in affecting thermal stress of glass-ceramic sealant for long-term planar-type solid oxide fuel cells (SOFC) to prevent fuel leakage during operation. Due to the lack of systematic research on regulating the stable performance of glass-based sealant with the working time at operation temperature, herein, the effect of MgO on crystallization kinetics, phase stability, and thermal and mechanical properties of MgO–BaO–CaO–Al 2 O 3 –B 2 O 3 –SiO 2 (MBCABS) glass-ceramic has been firstly analyzed at heat-treatment of 750 °C with working time of 1∼1000h in this work. Subsequently, the relationship evolution of crystallization thermal stability-coefficient of thermal expansion (CTE) match-thermal stress was established by Finite Element Method (FEM). The main reasons for the decrease of CTE of MBCABS glass-ceramics with low-content MgO are the precipitation of hexagonal BaAl 2 Si 2 O 8 phase and the transformation of hexagonal BaAl 2 Si 2 O 8 to low-CTE monoclinic BaAl 2 Si 2 O 8 phase, bring about that the Von Mises thermal stress of sealant itself and interface having tripled at 1000h (more than 200 MPa) according to FEM simulation results. The thermal stable and high-CTE BaMgSiO 4 , Ba 8 Mg 16 Si 16 O 56 , and BaCa 2 Mg(SiO 4) 2 phases crystallized in MBCABS glass-ceramics with high-content MgO, therefore the maximum stress at all time parameters was below 100 MPa for 1∼1000h. This study was useful for identifying the optimal phase option and CTE matching of glass-based sealant for efficient and stable long-term operation of solid oxide fuel cells. [ABSTRACT FROM AUTHOR]

Cordierite-mullite composite ceramics were prepared by solid-state method using Panzhihua low-grade Ti-rich clay, talc, and alumina. Influences of cordierite/mullite ratio, sintering temperature, and the chemical composition of clay on the phase composition, microstructure, physical properties, and thermal properties were investigated in detail. The results showed that the impurity oxides inside the Ti-rich clay had a great ability of forming liquid. Above 1300 °C, the reaction between TiO 2 of the clay and Al 2 O 3 produced stable Al 2 TiO 5 , which was conducive to decreasing the coefficient of thermal expansion (CTE). At 1300–1350 °C, the secondary mullitization caused the volumetric expansion, decreasing the bending strength and increasing the CTE. The optimum ratio of cordierite to mullite ranged from 90:10 to 80:20, and the sample fired at 1400 °C exhibited the lowest water absorption and porosity (0.64 % and 1.56 %, respectively), optimal bulk density, and bending strength (2.59 g cm−3 and 87.79 MPa), as well as better CTE, thermal conductivity, and thermal storage density (2.91 × 10−6 °C−1, 4.11 W/(m⋅K) (30 °C), and 1181 kJ kg−1, respectively). Compared with the reported values of cordierite-based thermal storage ceramics prepared by using the high-grade clay or minerals, the obtained samples showed the advantages such as lower costs for raw materials, higher bending strength, higher thermal conductivity (1.63–2 times higher), low CTE, and high thermal storage density. This study demonstrated that the low-grade Ti/Fe-rich clay has excellent cost-effective potential for the preparation of thermal storage ceramics. [ABSTRACT FROM AUTHOR]

In the domain of personal thermal protection, there is a growing demand for lightweight and efficient ceramic thermal insulation materials. However, conventional ceramic membranes face challenges such as brittleness, structural collapse, and pulverization, hindering their practical application. To address this issue, aluminum hydroxide-enhanced silica-zirconia ceramic membranes (SZ@ANFMs) have been successfully fabricated using electrospinning followed by subsequent calcination processes, and their properties have been comprehensively evaluated. The results demonstrate that SZ@ANFMs exhibit outstanding high-temperature resistance under an alcohol lamp, along with an extremely low thermal conductivity (only 0.041 W/m·K), excellent tensile strength (2.3 MPa), and flexible characteristics. This makes them highly promising in the domain of personal thermal protection. The study builds upon existing research in lightweight and efficient thermal insulation materials, offering improvements and robust support for the further development of personal thermal protection technology. [ABSTRACT FROM AUTHOR]

The present research article demonstrates the dispersion of boehmite (BHM) nanoparticles into sericin (SER) from silk industry waste with polyvinyl alcohol (PVA) to enhance the optical, mechanical, thermal and electrical characteristics of PVA/SER blend nanocomposites prepared by a simple green synthesis. Techniques such as Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), UV visible spectroscopy, field emission scanning electron microscopy (FE-SEM), high-resolution transmission electron microscopy (HR-TEM), differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) were carried out for the characterization of the prepared composites. XRD revealed the increased crystallinity of the polymer blend by the reinforcement of BHM. The existence of intermolecular interactions in the blend composite was confirmed by FTIR and UV spectroscopy. The optical bandgap energy of the biopolymer blend decreases with the inclusion of BHM. The SEM and HR-TEM confirmed the homogeneous dispersion of BHM in the blend at 5 wt% loading. The glass transition temperature and thermal stability of the blend nanocomposites were significantly improved by the inclusion of BHM was deduced from DSC and TGA. The dielectric constant and AC conductivity were remarkably increased with the reinforcement of nanoparticles. The activation energy obtained from AC conductivity decreased with temperature. The mechanical properties of the blend nanocomposites (hardness, tensile strength and Young's modulus) were greatly increased in presence of BHM. The 5 wt% sample has the highest tensile strength, Young's modulus, dielectric constant, AC conductivity and optical properties, allowing it to be used to make optoelectronic devices with better charge-storing capacity and flexible-type electrochemical gadgets. [ABSTRACT FROM AUTHOR]

In this study, composite phase change materials (CPCMs) comprising hexadecylamine (HDA) (C 16 H 35 N), disodium hydrogen phosphate dodecahydrate (DHPD) (Na 2 HPO 4 ·12H 2 O), and expanded graphite (EG) were prepared using the demulsification method. These CPCMs exhibit high latent heat and stable thermal properties. This approach effectively mitigates the issues of substantial supercooling and poor thermal conductivity commonly associated with DHPD and HDA. Additionally, the inclusion of EG imparts superior morphological stability to the CPCMs. The HDA/DHPD/EG CPCMs demonstrated robust thermal and morphological stability at temperatures below 100 °C. Their latent heat reached up to 221 J/g and remained stable at this value even after 50 cold-heat cycles, thereby indicating excellent cycling stability. When EG was incorporated at 2 wt%, the thermal conductivity of the HDA/DHPD/EG CPCMs increased to 0.751 W/(m·K), indicating that the three-dimensional network structure of EG facilitates heat conduction and offers exceptional photothermal conversion capabilities, with a photothermal conversion efficiency of up to 97.1 %. The aforementioned results highlight the promising potential of the prepared CPCMs for applications in low-temperature waste heat recovery. [ABSTRACT FROM AUTHOR]

One of the challenges facing our current and future generations is the effective management of energy and its acquisition through more sustainable means. One solution is using materials capable of generating energy from temperature differences. Construction materials could be the answer, as they are already integrated into structures and have good thermoelectric properties. Geopolymers, emerge as a promising candidate due to their enhanced sustainability compared to alternative materials. Our research explored the use of geopolymers for electricity generation from heat. To minimize the usage of kaolin, we incorporated 50 % of two mining residues obtained from old mines located in Portugal. This approach optimizes the utilization of mineral resources and mitigates the environmental impact. Various methods were used to characterize this material, such as X-ray diffraction, simple compressive strength tests and evaluation of thermoelectric properties, such as the Seebeck coefficient and figure of merit. The geopolymers tested exhibit semiconductor characteristics, demonstrating poor heat conduction due to their low thermal conductivity. Regarding thermoelectric properties, these materials display N-type behavior, with a Seebeck Coefficient between −643 μV/°C and −2760 μV/°C. These findings underscore the advantages of utilizing this sustainable material for the widespread implementation of energy management in buildings on a large scale. [ABSTRACT FROM AUTHOR]

BiCuSeO, an oxide thermoelectric material with a superlattice structure, presents the advantages of affordability, low toxicity, and environmental friendliness. However, its intrinsic low electrical conductivity has impeded its possible applications. To address this challenge, we put tiny PbZr 0.52 Ti 0.48 O 3 (PZT) with varying weight percentages (x = 0, 5, 7, 9, 11) into BiCuSeO (BCSO) to fabricate thermoelectric nanocomposites. Through the spark plasma sintering process, PZT particles underwent in-situ decomposition, generating nano-sized second phases such as PbO 2 , TiO 2 , and PbZrO 3 , which are homogenously distributed within BCSO matrix (validated by XRD and TEM). The introduced PbO 2 , TiO 2 , and PbZrO 3 second phases served a dual purpose: inhibiting the grain growth of BCSO and introducing additional nano-grain boundaries. This resulted in more effective phonon scattering sites, thereby reducing lattice thermal conductivity. Simultaneously, the Pb element derived from PZT decomposition was doped into the Bi site of the BCSO matrix, causing a reduction in the band gap of BCSO from 0.49 eV to 0.388 eV and a significant increase in carrier concentration. Consequently, this doping enhanced the electrical conductivity of BCSO-based composites, with the composite with 11 wt% PZT additive amount exhibiting a remarkable 318-fold increase, reaching 550 S/cm compared to pristine BCSO. Notably, the composite with 7 wt% PZT additive amount achieved an exceptionally low lattice thermal conductivity of 0.333 W m−1 K−1 at 823 K. Through the synergistic optimization of electrical and thermal transport properties, the BCSO-based composite with 7 wt% PZT additive amount obtained a ZT value of ∼0.9 at 873 K, representing a 2.45-fold increase compared to pristine BiCuSeO. This straightforward method presents a cost-effective and scalable approach to enhance the thermoelectric performance of various materials, opening new avenues for potential commercial applications. [ABSTRACT FROM AUTHOR]

The current market's imperative demand necessitates the research and development of advanced polymer composites, especially those incorporating nanofillers. Carbon nanotubes, in particular, have attracted significant attention within research and development for their potential in creating multifunctional composites. This study aims to evaluate the impact of incorporating carbon nanotube buckypapers (BP) on the thermal and electrical properties of poly (aryl ether ketone) (PAEK)/glass fiber (GF) composites. The BP was prepared through vacuum filtration and integrated into PAEK/GF composites with varying stacking sequences, followed by hot compression processing. The degradation behavior of the laminates was investigated using thermogravimetric analysis (TGA). The viscoelastic properties, evaluated by dynamic mechanical analysis (DMA), suggested an increase in stiffness with the inclusion of BP in two of the analyzed stacking sequences. Thermal conductivity, measured via the pulse laser method, showed results comparable to the base laminate (0.153 W/m·K). Meanwhile, electrical conductivity, assessed using the four‐point probe method in the in‐plane direction, revealed semiconductor properties, achieving a mean value of 3.162 S/cm for one of the samples, indicating electrical anisotropy within the multifunctional composite material. [ABSTRACT FROM AUTHOR]

Sulfatotungstates constitute a rather new host structure materials that may exhibit interesting optical properties. The compounds M2[W2O3(SO4)6], with M = Y, Eu, Tb, Lu, and Bi, were synthesised as phase pure materials under solvothermal conditions in oleum. They crystallise isotypic to each other in the monoclinic space group C2/c (no. 15) with Z = 4, determined by single-crystal X-ray diffraction. Their structures feature corner-connected sulfate and tungstate units, the latter showing a disorder of the tungstate cations with a thread-like arrangement along the b-axis. The metal cations M are eight-fold-coordinated and show typical red (M = Eu) or green (M = Tb) luminescence in fluorescence spectra due to their f–f transitions. The f–d transition of Tb3+ reveals rather weak coordination behaviour of the host structure. Thermal analysis showed relatively high temperature stabilities of the compounds, increasing as the ionic radii of the metal cations decrease. Additionally, the compounds were characterised by FT-IR and UV-vis measurements while using Tauc plots to determine their band gaps. The lone-pair activity of the bismuth compound was elucidated by geometrical calculations based on the structural data. [ABSTRACT FROM AUTHOR]

In this study, poly(butylene adipate‐co‐terephthalate) (PBAT) biocomposites were generated from spent coffee grounds (SCGs) or torrefied SCG (TSCGs) using a melt compounding process. TSCGs were obtained at torrefaction temperatures of 230, 245, 260, 275, or 290°C for a duration of 60 min. Torrefaction enhanced the hydrophobicity, grindability, and biomass stability of the resulting composites by eliminating hemicellulose. Various concentrations of SCGs (10 and 20 wt.%) and TSCGs (10, 20, and 30 wt.%) were compounded into PBAT. The thermal, mechanical, and degradation properties of PBAT biocomposites were investigated. As SCGs and TSCGs were introduced, the crystallization temperature drastically increased. Compared with PBAT biocomposites with SCGs, PBAT biocomposites with TSCGs exhibited higher thermal stability and hydrophobicity, and improved mechanical properties. Further, alkaline hydrolysis occurred at a faster rate for biocomposites with biofillers than for neat PBAT. Therefore, this study demonstrated the improved compatibility between SCGs and PBAT by torrefaction. [ABSTRACT FROM AUTHOR]

The widespread use of traditional petroleum‐based plastics is causing significant environmental pollution for example microplastics issues, due to its non‐biodegradability. Poly (lactic acid) (PLA) as a representative biodegradable polymer is a promising candidate to replace petroleum‐based plastics in some fields of disposable packaging materials and tableware. In this work, in order to improve the poor crystallization, mechanical and heat resistance performances of PLA, styrene–acrylonitrile‐glycidyl methacrylate (SAG) as a chain extender and octamethylenedicarboxylic dibenzoylhydrazide (ST‐NAB3) as a heterogeneous nucleating agent (HNA) were added simultaneously into PLA matrix. The chain‐extended PLA (CPLA) with branch structures had smaller crystal sizes and higher crystal density, compared with those of pure PLA. In addition, thanks to the nucleation effect of ST‐NAB3 and the development of "shish‐kebab", this tendency became more pronounced in CPLA/HNA systems. It was worth mentioning that, CPLA with the ST‐NAB3 content of 1 wt% (CPLA‐1) possessed the highest crystallinity of 43.6%. Meanwhile, CPLA‐1 had the best impact strength and heat deformation temperature of 38.9 kJ/m2 and 91.3°C respectively, which had increased by 11.3 kJ/m2 and 32.4°C contrast to pure PLA. On the whole, this study proposed a simple and effective method, which provided a new possibility for PLA modification research. [ABSTRACT FROM AUTHOR]

This study investigates the synthesis and characterization of new diamines with carbazole and imidazole pendant groups, leading to the development of polyamides and polyimides. The polyamides were synthesized by reacting diamines with carboxylic acids using polyamidation and phosphorylation techniques, while polyimides were prepared by combining diamines and dianhydrides. FT–IR and 1H-NMR analyses were used for comprehensive structural elucidation of diamine, polyamides, and polyimides. The polyamides and polyimides with inherent viscosities ranging from 0.48 to 0.64 dL/g showed notable thermal stability. The T10% weight loss values were between 287 and 340 °C for polyamides and 321–381 °C for polyimides. The percentage of char residue varied between 33 and 56% at 700 °C. Additionally, the maximum emission wavelengths of polymers ranged from 410 to 436 nm. The presence of bulky carbazole and imidazole pendant groups facilitated the good solubility of the polymers in common organic solvents. The antibacterial properties of synthesized polyamides and polyimides against both Gram-negative and Gram-positive bacteria and fungi were investigated. [ABSTRACT FROM AUTHOR]

The list of standard abbreviations for JDS is available at adsa.org/jds-abbreviations-24. Nonstandard abbreviations are available in the Notes. The aim of the study was to investigate the effect of potassium-based emulsifying salts (ES; 2% wt/wt concentration) with different phosphate chain lengths (dipotassium hydrogenphosphate [K 2 HPO 4 ; DKP], tetrapotassium diphosphate [K 4 P 2 O 7 ; KTPP], pentapotassium triphosphate [K 5 P 3 O 10 ; TKPP]) on the physicochemical, viscoelastic, textural, tribological, thermal, and sensory properties of processed cheese (PC; 40% wt/wt DM, 50% wt/wt fat in DM) during a 60d storage period (6°C ± 2°C). On the whole, the hardness of all PC samples increased with the increasing chain length of ES (DKP < TKPP < KTPP) and the prolonging storage period. Moreover, the hardness results were in accordance with those of the rheological analysis. All PC samples exhibited a more elastic character (G′ > G″; tan δ < 1). The type of potassium-based ES affected the binding of water into the structure of the PC. Furthermore, the study confirmed that the manufactured PC received optimal sensory scores, without any excessive bitterness. It could be concluded that the type of applied ES and storage length affected the functional properties of PC. Finally, the information provided in this study could serve as a tool for the dairy industry to help appropriately select potassium-based ES for PC manufacture with desired properties. [ABSTRACT FROM AUTHOR]

Summary: The plant cuticle is located at the interface of the plant with the environment, thus acting as a protective barrier against biotic and abiotic external stress factors, and regulating water loss. Additionally, it modulates mechanical stresses derived from internal tissues and also from the environment. Recent advances in the understanding of the hydric, mechanical, thermal, and, to a lower extent, optical and electric properties of the cuticle, as well as their phenomenological connections and relationships are reviewed. An equilibrium based on the interaction among the different biophysical properties is essential to ensure plant growth and development. The notable variability reported in cuticle geometry, surface topography, and microchemistry affects the analysis of some biophysical properties of the cuticle. This review aimed to provide an updated view of the plant cuticle, understood as a modification of the cell wall, in order to establish the state‐of‐the‐art biophysics of the plant cuticle, and to serve as an inspiration for future research in the field. [ABSTRACT FROM AUTHOR]

Glass and glass ceramics are very functional materials, albeit their structural complexity. Their relevance ranges from fundamental science problems in the fields of physics, chemistry, and geoscience, to applications in health areas, engineering, or technological matters that require high performance. Enhancing our understanding of these materials' performance and refining sample preparation methods remains paramount in this field. Synchrotron facilities offer a suite of powerful techniques for the detailed characterization of glasses and glass ceramics. These methods provide valuable insights into their atomic and molecular structure, phase transformations, mechanical behavior, and thermal properties, ultimately contributing to the development of improved materials for a wide range of applications. In‐depth investigations conducted under extreme conditions of pressure and temperature have yielded pivotal insights into densification mechanisms, phase transitions, crystallization kinetics, and their consequential macroscopic properties. The emergence of fourth‐generation synchrotrons brings in a wave of novel experimental possibilities that may exert a profound influence on this field in the coming decade. In this study, we unveil a selection of the remarkable capabilities now accessible to researchers at the Brazilian Synchrotron Light Source—Sirius, within the realm of extreme methods of analysis (EMA) beamline for investigating vitreous systems under extreme conditions. [ABSTRACT FROM AUTHOR]

[Display omitted] • New powder reuse schema in powder bed fusion of polymers was demonstrated. • The characteristics of the recycled PA12 powder were investigated. • Recycled PA12 allowed to produce components with satisfactory properties. The laser-based powder bed fusion of polymers (PBF-LB/P) process often utilizes a blend of powders with varying degrees of degradation. Specifically, for polyamide 12, the traditional reuse schema involves mixing post-processed powder with virgin powder at a predetermined ratio before reintroducing it to the process. Given that only about 15% of the powder is utilized in part production, and powders are refreshed in equal proportions, there arises a challenge with the incremental accumulation of material across build cycles. To mitigate the consumption of fresh powder relative to the actual material usage, this study introduces the incorporation of recycled material into the PBF-LB/P process. This new powder reuse schema is presented for the first time, focusing on the laser sintering process. The characteristics of the recycled powder were evaluated through scanning electron microscopy, differential scanning calorimetry, X-ray diffraction, particle size distribution, and dynamic powder flowability assessments. The findings reveal that waste powders can be effectively reused in PBF-LB/P to produce components with satisfactory mechanical properties, porosity levels, dimensional accuracy, and surface quality. [ABSTRACT FROM AUTHOR]

The combination of the best properties of Polycarbonate (PC) and Acrylonitrile-butadiene-styrene (ABS) has resulted in the development of commercially available PC/ABS blends that have been found to be useful in many molding applications. PC has excellent mechanical and optical properties, but predominant use of bisphenol A in PC synthesis raises concerns regarding its potential environmental harm. In this study, we have studied the alternative for the PC/ABS blend by replacing PC with the bio-based PC and ABS with the Acrylonitrile-styrene-acrylate (ASA). A blend of bio-based PC and ASA was prepared by the melt blending techniques and investigated mechanical, thermal, and degradation (hydrolytic and soil burial degradation) properties. [ABSTRACT FROM AUTHOR]

To date, the thermal and electrical properties of three‐phase ceramics containing a boride phase, silicon carbide, and boron carbide have not been studied in detail. Further, the effect of the source of the boride powder has also not been investigated. This study produced three‐phase ceramics containing titanium diboride, silicon carbide, and boron carbide using three different TiB2 sources: commercial powder, TiB2 synthesized by boro/carbothermal reduction, or (Ti,Cr)B2 synthesized by boro/carbothermal reduction to address the effect of the TiB2 source. Ceramics containing synthesized TiB2 or (Ti,Cr)B2 reached >99% relative density, while the ceramic produced from commercial powder reached ∼93% relative density. The addition of Cr reduced both the thermal and electrical conductivities, but had little effect on the Vickers hardness. The (Ti,Cr)B2–SiC–B4C ceramic had a thermal conductivity of ∼33 W/m K, an electrical conductivity of ∼105 S/m, and a hardness of ∼61 GPa at 0.49 N. The highest hardness of ∼66 GPa at a load of 0.49 N was for the TiB2–SiC–B4C ceramic made with synthesized TiB2 powder. [ABSTRACT FROM AUTHOR]

Glass foams and glass-ceramic foams exhibit great potential in thermal insulation of buildings, consequently reducing the necessity for heating or cooling, and ultimately contributing to energy saving. In this study, we prepared glass-ceramic foams utilizing silicate glass as starting material and CaCO 3 as foaming agent through a thermochemical process. Foams with varying degrees of relative crystallinity were produced by controlling temperature and duration of isothermal heat treatment. The foaming mechanism in the glass-ceramics was discussed by analyzing how the heat flow, mass, and volume evolve within the powder mixture during dynamic heating. The crystallization in glass did not show any clear trend on the compressive strength of glass foams. On the other hand, the thermal conductivity of the glass-ceramic foams increases with increasing relative crystallinity. The calculated solid thermal conductivity exhibited a minimum at low relative crystallinity (<20 %). These findings are crucial for designing high performance glass-ceramic foams for thermal insulation, potentially also for fabricating glass-ceramic foams using waste glasses. [ABSTRACT FROM AUTHOR]

Thermal protection was always a prominent issue in the aerospace industry. For vehicle safety, reliability and payload requirements, thermal protection materials were usually expected to possess low density, superior mechanical and thermal insulation properties. Here, lightweight and high-strength porous mullite-silica ceramics were manufactured using particle-stabilized foaming technique. The strength and thermal insulation properties of porous ceramics modified with hollow silica spheres were significantly enhanced. A 10 wt% hollow spheres addition achieved a 28.9 % increase in strength and a 33.4 % decrease in thermal conductivity with almost constant porosity (from 86.39 % to 87.04 %). Considering the characteristics of light weight, high compression strength and superior thermal insulation performance, porous ceramics could be applied as thermal protection materials in the aerospace sector. [ABSTRACT FROM AUTHOR]

Porous high-entropy transition metal compounds, an important type of ultra-high temperature material, have attracted increasing attention in the applications of extreme environments due to their low density, good thermal insulation and stable chemical properties. A robust, flame-retardant and high-temperature resistant high-entropy carbonitride (Ti 1/5 V 1/5 Mo 1/5 Nb 1/5 Ta 1/5)(C 0.55 N 0.45) (HECN) porous ceramic was synthesized and thoroughly characterized. It exhibited a porosity of 93.5 %, a compressive strength of 1.3 MPa and a good high-temperature stability up to 1673 K, which, along with its outstanding fire-retardancy, and low thermal conductivity (as low as 0.150 W m−1 K−1 at 298 K), made it a good candidate material for thermal insulation applications in ultra-high temperature environments. Moreover, the Density functional theory (DFT) calculations predict that the [N]/([C]+[N]) ratio in HECN foam affects its lattice thermal conductivity which is decreased by 67 % upon increasing the ratio from 0 to 1/2. [ABSTRACT FROM AUTHOR]

The preparation and characterization of composite materials composed of polypropylene (PP) as the base mixed with halloysite nanotubes (HNT) at various weight percentages (0.5, 1.5, and 3 wt.%) using a melt extrusion method operated at a temperature between 190 °C and 200 °C is described. The impact of the addition of the HNT filler on the PP nanocomposites was investigated based on the thermal and mechanical properties. The thermal characterization was conducted by differential scanning calorimetry (DSC). Significant increases in the rheological properties were observed with the addition of a high content of HNTs. The water absorption decreased with increasing HNT. The SEM micrographs showed that the HNT fillers were homogeneously dispersed throughout the entire PP matrix. [ABSTRACT FROM AUTHOR]

Natural fibers and nanomaterials are currently receiving more attention in the construction sector for two reasons. One reason is to use natural fibers instead of synthetic ones in fiber-reinforced concrete to create environmentally friendly products. In this study, sisal fiber (SF) and Cloisite 30B nanoclay particles were used to manufacture cement nano concrete. The cement nano concrete was reinforced with 3 wt% 10 mm sisal fiber and varying levels of Cloisite 30B nanoclay (0%, 0.5%, 1%, 1.5%, and 2%). Comprehensive research was conducted to evaluate the physical, mechanical, thermal, and water absorption properties of the concrete. The results indicate that the incorporation of nanoclay enhances these qualities. The results of the experiments indicated above demonstrate that the 3 wt% SF and 1.5% nanoclay concrete has superior mechanical qualities to other nanoclay concrete in terms of compressive strength (7.12 MPa) and flexural strength (9.6 MPa). Additionally, testing was performed on the concrete's morphology, physical properties, and water absorption. [ABSTRACT FROM AUTHOR]

This work aims to convert the bio-waste material into a fruitful product. This prepared product can be a solution for environmentally hazardous materials like polymer bags and plastic food wrappers. The prepared material is composed of bio-waste pomegranate peel powder and environmentally friendly polyvinyl alcohol. To extend its functionality in food wrappers, the silver nitrate solution is incorporated. The prepared samples were undergone various performance studies. The prepared films show high thermal with standing capacity and tensile properties and especially show better results in biodegradability as well as antibacterial activity. Among the fabricated films, the 5 mM AgNO3-fabricated film shows that the thermal stability up to 331 °C also possesses higher tensile strength of 25.7 MPa. These results make the possibilities of the fabricated PP/PVA/5 mM AgNPs film as an alternative for conventionally used plastic-based food wrappers. [ABSTRACT FROM AUTHOR]

Bio‐based materials as crosslinkers for composites have gained attention for their nontoxic, cost‐effective benefits. Using eco‐friendly crosslinkers enhances the properties of the composites and promotes sustainable manufacturing practices too. This study aimed to compare the efficacy of citric acid (CA), itaconic acid (IA), and tannic acid (TA), derived from plant‐based sources, as crosslinkers in the creation of green composites. In this work, compression molding technique was employed for producing composites using coconut fiber as the reinforcing agent and methacrylic anhydride modified epoxidized linseed soybean oil (MAELSO) as the resin. The amount of crosslinkers was varied between 5, 10, and 15 (wt%) to achieve this. Nuclear magnetic resonance spectroscopy confirmed the successful modification of the resin. Fourier transform infrared spectroscopy revealed interactions between components of the composites. Biocomposites loaded with 5 wt% of CA showed 1268 and 92% increase in tensile strength and 1098 and 49% increase in flexural strength compared to those of similar wt% of TA‐ and IA‐based composites respectively. Similarly, the impact strength for CA‐based composite was 84.94 J/m against 168.74 J/m for IA and 330.85 J/m for TA‐based composites. Additionally, composites containing 5 wt% CA exhibited the highest levels of chemical resistance, flame retardancy, and thermal stability. Thus the results suggest that citric acid can serve as an effective crosslinker to fabricate environmentally acceptable composite materials that are suitable for long‐term use. This is noteworthy as it can pave the way for the production of sustainable and eco‐friendly materials, which can be used in various industrial and commercial applications. [ABSTRACT FROM AUTHOR]

Highlights Microfibrillated cellulose (MFC) was uniformly dispersed in high‐density polyethylene (HDPE) using a large amount of surfactant, and composites were prepared after removing the surfactant at different contents. The structural, morphological, thermal, and tensile properties of these composites were systematically investigated. The results demonstrated an asymptotic relationship between the amount of surfactant removed and the number of removal cycles. A negative linear correlation was observed between the surfactant content and the tensile strength, tensile modulus, and storage modulus at −20 °C of the composites, while a positive linear correlation was found with the loss modulus at −20 °C. Excessive surfactant adversely affected the dispersion of MFC, as well as the mechanical properties and thermal stability of the composites. However, when the surfactant content was below 2.8%, its impact on the composite properties was minimal, and the tensile strength, modulus, and thermal stability of the composites were significantly improved compared to neat HDPE. These findings indicate that surfactant pretreatment is an effective strategy for dispersing MFC in non‐polar polymers, and controlling the surfactant content in the final product can effectively tailor the properties of the resulting composites. Confirms the relationship between surfactant content and MFC/HDPE composite properties. Surfactant content showed an asymptotic relationship with removal cycles. Surfactant content and mechanical properties exhibited a negative linear correlation. Surfactant content and thermal stability exhibited a negative relationship. Surfactant content had minor impact when below 2.8%. [ABSTRACT FROM AUTHOR]

Comprehensive Summary Post‐polymerization modification provides an important approach to tuning the material properties of obtained polymers. In this work, we demonstrated a rational design of novel vinylcyclopropane monomer bearing a pendant N‐hydroxylphthalimide redox ester, and explored its radical ring‐opening polymerization behavior under visible‐light conditions. Photochemical decarboxylation of resulted polymer provided unique access to poly(vinylcyclopropane) bearing single ester group in each repeating unit. This decarboxylative modification has greatly reshaped the thermal and mechanical properties, converting a glassy polymer into a soft, ductile, and rubber‐like material. [ABSTRACT FROM AUTHOR]

Amino acid‐based poly(ester urea)s are an attractive class of polymers that are of interest for a variety of biomedical applications. Generally, amino acid‐based poly(ester urea)s are prepared by polymerization of diamines, which are obtained from the corresponding amino acids and aliphatic diols. This article presents an alternative synthetic strategy that uses diamine monomers obtained from aromatic, 4‐hydroxycinnamic acid‐derived diols. A library of structurally related diamine monomers has been prepared by coupling l‐leucine to 4‐hydroxycinnamic acid‐based diols that incorporate alkyl spacers of different lengths. The exploration of 4‐hydroxycinnamic acid as a building block is interesting as it can be obtained from various biological resources, such as for example lignin, and thus provides an opportunity to take advantage of (under‐utilized) bio‐based renewables for the design of new polymer materials. These diamine monomers can be copolymerized in a solvent‐free, one‐pot, two‐step process using dimethyl carbonate as an environmentally sustainable reagent to afford amino acid‐based aromatic poly(ester urea) homo‐ and copolymers with thermal properties that can be tuned by varying the chemical structure of the diamine monomer, or via copolymerization of two different monomers. [ABSTRACT FROM AUTHOR]

ABSTRACT Low‐temperature densification of alumina using calcium vanadate (CaV2O6, CV) having a similar dielectric constant as a liquid‐forming additive has been studied. The alumina‒CV composites containing 20‒40 vol.% CV achieve ∼94% of theoretical density at low temperatures of 1100°C‒900°C by liquid‐phase sintering. A reduction in the average size of grains from .87 to .42 µm with a surge in CV amount from 20 to 40 vol.% is observed. The permittivity decreases from 9.2 to 8.90, and the dielectric loss increases from 2.154 × 10‒3 to 4.761 × 10‒3 when the amount of CV in the alumina‒CV composite rises from 20 to 40 vol.%. The temperature coefficient of resonance frequency, thermal expansion coefficient, and thermal conductivity of the alumina‒CV composites are observed in the ranges of ‒54 to ‒72 ppm °C‒1, 6.94‒7.32 ppm °C‒1, and 13.78‒8.02 W m‒1 K‒1, respectively. The compatibility of the composites with Ag for low‐temperature co‐fired ceramics (LTCC) application is established through co‐sintering and energy‐Dispersive X‐ray spectroscopy line spectra analysis. The low‐temperature densification, acceptable range of dielectric and thermal properties, and silver compatibility make the alumina‒CV composite a candidate for LTCC application. [ABSTRACT FROM AUTHOR]

The high production cost and extremely weak mechanical properties of SiO 2 aerogels have been two major challenges hindering its widespread application. Atmospheric pressure drying (APD) has always been regarded as the optimal process to reduce costs. However, traditional APD is cumbersome, still uses a large amount of expensive raw materials, and is extremely immature. In this study, a novel APD was developed, inspired by the wing changes during adult damselfly process. Inorganic silica source/water was used as the raw material, and CO 2 was used instead of low surface tension solvent to stabilize the aerogel skeleton structure in situ, and ultimately aerogel material was obtained. The thermal conductivity of pure aerogels was as low as 0.0264 W/(m·K), the porosity reached 94.7 %, and the preparation cycle was only 28.5 h. The thermal stability of the skeleton structure and the chemical stability of surface were investigated and showed the hydrophobicity to withstand temperatures up to 400 °C. Aerogel composites feature low thermal conductivity of 0.0283 W/(m·K), and prominent thermal insulation properties over a wide temperature range of 50–300 °C. For traditional APD, this method shortens preparation cycle by 1–6 times. Compared with the commercial aerogel, the cost is reduced by 38.2 %, and the process is simple and environmentally friendly under the premise of ensuring excellent performance. [Display omitted] • A novel atmospheric pressure drying of aerogels preparation inspired by biology. • Stabilization of aerogel structures with CO 2 instead of low surface tension solvents. • The preparation cycle time is shortened by 1–6 times, the cost is reduced by 38.2 %. • Thermal conductivity of 0.0264 W/(m·K) and hydrophobic temperature resistance of 400 °C. • Aerogel composites have outstanding thermal insulation and moisture resistance. [ABSTRACT FROM AUTHOR]

Dy3+, Eu3+ co-doped glass ceramics (GCs) containing SrMoO 4 crystalline phase were prepared by melt-curing-crystallization method. The most favorable heat treatment conditions for the glass ceramics were found to be 610 °C/2 h by differential scanning calorimetry (DSC), ultraviolet spectrophotometer (UV–Vis), X-ray diffraction (XRD) and scanning electron microscopy (SEM). The best doping concentrations of Dy3+ and Eu3+ in this glass ceramic were 0.8 % and 0.6 %, concentration quenching caused by dipole-dipole interactions occurs when the content of rare earth ions in GCs continues to increase. The chromaticity coordinates of the Dy3+- Eu3+ co-doped glass ceramics changed from cool white light to warm white light with the addition of Eu3+ concentration. At the optimal doping concentration (0.8 % Dy3+-0.6 % Eu3+), the chromaticity coordinate of glass ceramics is (0.3972, 0.3331), and the related color temperature is 3047 K. The luminescence intensity can still reach about 80 % of room temperature at 180 °C, and its thermal quenching activation energy is 0.233 eV. This suggests that glass ceramics have excellent thermal stability. After adding an appropriate amount of Li+, the crystalline phase of the glass ceramics remained unchanged and the luminous intensity of the glass ceramics increased by a factor of about 1.4 in the same environment. The thermal quenching activation energy of the glass ceramic doped with 0.2 % Li+-0.8 % Dy3+-0.6 % Eu3+ was 0.344 eV. The experimental results indicate that GCs has potential application prospects in the field of solid-state lighting. [ABSTRACT FROM AUTHOR]

This study describes the preparation of bimodal reinforced Cu/Ti 3 SiC 2 /C laminated-like composites using flake powder metallurgy and vacuum hot-press sintering process. The objective was to accurately modulate the formation of oriented reinforcement network in two-dimensional carbon materials. The powders used in the five designed composites were flake Cu powder (45–60 μm), Ti 3 SiC 2 (1–5 μm), graphite flakes (GFs, 120 μm) and graphene nanoplatelets (GNPs, 15 μm). Among them, the proportions of Ti 3 SiC 2 (10 wt %) and GFs (3 wt %) remained unchanged, GNPs accounted for 0 wt %, 0.5 wt %, 1.0 wt %, and 1.5 wt %, and Cu powder accounted for a decreasing proportion. Formation mechanisms of GFs and GNPs in oriented networks were quantitatively analyzed using the alignment model. Additionally, the related strengthening and failure mechanisms were investigated. According to the study, the bimodal laminated-like Cu/Ti 3 SiC 2 /C composites with 0.5 wt% GNPs added showed the best overall performance. Specifically, it exhibited a hardness of 125.7 HV, tensile strength of 276.3 MPa, thermal conductivity of 207.8 W m−1 K−1, and electrical conductivity of 23.6 MS/m. The network enhanced by the two-dimensional carbon material achieves efficient and orderly load transfer and dissipation mechanisms, optimizing stress distribution and enhancing fracture resistance, resulting in improved mechanical properties. In addition, the formation of the oriented reinforcement network optimizes the orientation arrangement of the reinforcing particles, which somewhat mitigates the scattering of thermoelectric carriers by structural defects in the composites, and the enlarged mean free-range improves the migration efficiency of electrons and phonons. Therefore, the erection of bimodal laminated-like structure achieves the goal of optimizing the properties of the composites. [ABSTRACT FROM AUTHOR]

Inspired by the significant catalytic charring effect of metal–organic frameworks (MOFs), Cu‐MOF decorated ammonium polyphosphate (APP@Cu‐MOF) was prepared by coupling agents to improve the fire safety of epoxy resin (EP). After adding 9 wt% APP@Cu‐MOF, the fire performance of EP is significantly improved with limiting oxide index (LOI) value of 29.4 and UL‐94 V‐0 rating. The peak heat release rate (PHRR), total smoke production (TSP), CO production, and CO2 production of EP composite samples decreased by 34.6%, 54.7%, 24.6% and 30.0%, respectively. It is proposed that the synergistic effect among Cu‐MOF and APP promoted the char formation of EP. The dense carbon layers formed a barrier that prevented the transfer of heat and inhibited the release of toxic gases, thus acting as a flame retardant. This work provides a new strategy to develop a high‐efficient MOF‐decorated flame retardant with smoke inhibition, toxicity reduction, and catalytic carbonization effect. [ABSTRACT FROM AUTHOR]

The escalating threat of bacterial infections to human health necessitates innovative antibacterial strategies and materials. Despite this need, there is still a significant demand for materials that combine high mechanical and thermal properties with biocompatibility. To address these urgent issues, our study investigates the development of poly(vinyl alcohol) (PVA) composite with graphene flakes (GF) as fillers. The aim is to strengthen the unique properties of graphene to enhance antibacterial activity. Graphene oxide (GO) was used as a surfactant to achieve stable graphene dispersion in water, preserving its inherent properties while avoiding the drawbacks associated with common surfactants, such as property reduction and complex removal processes. In this study, the mechanical and thermal properties of PVA composites containing GO and GF are superior to those of pristine PVA. Especially, the PVA‐2 composite exhibited a notable enhancement in both tensile strength and elongation at break compared with the PVA composite, with increases of 7.8% and 15% respectively. Moreover, PVA‐2, 4, and 6 composites exhibit significant antibacterial efficacy, achieving 4.8 and 4.9 log CFU/cm2 for Staphylococcus aureus and Escherichia coli, respectively. These results indicate that the enhanced oxidative stress induced by GO as a surfactant, combined with the physical damage caused by the increased GF nanostructures. This study highlights the potential of PVA/GF/GO composites in biomedical and tissue engineering applications, providing a promising pathway for the development of new antibacterial materials. [ABSTRACT FROM AUTHOR]