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As a common smart hydrogel, thermo‐sensitive hydrogel exhibits significant potential applications in the field of biological engineering due to its unique property of undergoing a substantial volume transition in response to temperature changes. For numerical implementation of thermo‐sensitive hydrogel, many approaches have been developed to simulate the transient deformation during fluid diffusion or heat conduction process. However, the numerical approach for the transient deformation during both fluid diffusion and heat conduction processes is still lacking. To this end, we develop a three‐field coupled finite element framework that can be used to simulate the transient deformation behavior of thermo‐sensitive hydrogel involving large deformation, fluid diffusion, and heat conduction. In the proposed framework, there exist three processes that deal with displacement, concentration, and temperature fields, separately. To realize the coupling of three fields, the separated solving processes are assembled together by using a two‐way coupled approach. Based on the developed finite element framework, the coupling effects between the concentration and temperature can be realized by defining a body flux and a temperature‐dependent diffusion coefficient without solving the complex coupling equations. The finite element framework is implemented in ABAQUS by utilizing several user subroutines. The numerical implementation is validated by comparing the numerical results of a hydrogel disk with experimental results. Furthermore, various numerical examples are simulated to investigate the applicability of the proposed finite element framework under different multi‐field coupling conditions. The proposed finite element scheme is proved to be an efficient and stable tool for numerically simulating the transient behavior of thermo‐sensitive hydrogel incorporating the phase transition effect. [ABSTRACT FROM AUTHOR]

4D printing has attracted widespread attention due to its ability to fabricate complex structures capable of responding to specific stimuli. However, existing smart materials used for 4D printing, such as conventional hydrogels, liquid crystal elastomers, and shape‐memory polymers, are constrained in their ability to fulfill both mechanical ultrastrength and ultrastretchability requirements simultaneously due to their water saturation or uneven network structures. This study presents 4D printing of liquid‐free ionic elastomers (LFIEs) that is achieved through photopolymerization of the acrylic acid‐tetramethylammonium chloride‐polymerizable deep eutectic solvent. The transition temperature (Tt) of the high‐fracture‐strength LFIEs is adjusted by introducing phenylphosphoric acid, harboring multiple hydrogen‐bonds, leading to improved molecular chain mobility through softening of the chains. Consequently, the 4D‐printed LFIEs retain their high strength while achieving ultrastretchable properties even under elevated temperatures during heating. Moreover, the 4D‐printed LFIEs demonstrate both a swift response time and a high fixation rate even after undergoing repeated transformation cycles. These outstanding capabilities exhibit by LFIEs present a reliable strategy for advancing their applications in diverse fields, such as smart furniture, robotics, and intelligent manufacturing with remote monitoring, and beyond. [ABSTRACT FROM AUTHOR]

Magnetocaloric materials have the ability to undergo temperature changes when subjected to varying magnetic fields. These materials are of interest due to their potential for innovative cooling applications. This review article summarizes materials that exhibit magnetic ordering within the temperature range required for gas liquefaction and explores their potential applications through the magnetocaloric effect (MCE). The gas liquefaction temperature range is typically assumed to be 20–77 K, however, this study specifically summarizes materials that have a transition temperature near to the hydrogen liquefaction temperature (≈20K). This review article aims to showcase ongoing research on magnetic materials for hydrogen liquefaction. Driven by the depletion of natural resources and environmental concerns, the search for environmentally sustainable fuels has intensified, making hydrogen a promising alternative. However, the liquefaction of hydrogen is highly energy‐intensive. The investigation focuses on identifying and understanding these materials and assessing their suitability for environmentally friendly and sustainable cooling technologies. By harnessing the magnetocaloric effect, these materials exhibit temperature changes in response to an applied magnetic field, offering advantages over traditional cooling methods that are 20–50% more efficient. The review aims to furnish researchers with essential information that can help modify magnetocaloric effect (MCE) materials, enabling them to achieve the desired magnetic ordering temperature conducive to the liquefaction of hydrogen. [ABSTRACT FROM AUTHOR]

Alkaline earth halides garnered interest in spintronics research due to their longer spin relaxation time. Employing first principles calculations, 3d transition metal (TM)-substituted magnesium bromide (MgBr2) monolayers have been reported for the first time for potential spintronics applicability. Among these systems, Cr-, Cu- and Fe-substituted MgBr2 monolayers showed half-metallicity that can be used in ultra-fast spintronics because of high spin polarization. Bipolar magnetic semiconducting (BMS) nature was observed in Mn-substituted monolayer that enables spin control and manipulation by external bias voltage. The formation energy of TM dopants under Br-rich condition showed the feasibility of TM substitution. The half-metallic TM-substituted systems showed a large spin channel gap which inhibits spin leakage. The spin flip gap in BMS monolayer was feasible for practical device operation. Additionally, significant magnetic anisotropy energy per dopant has been observed with a ferromagnetic coupling in Cr-, Cu- and Fe-substituted systems, while antiferromagnetic coupling was shown by Mn- and V-substituted monolayers. Monte Carlo (MC) simulation revealed a near room temperature magnetic phase transition temperature. Robustness of the half-metallicity and BMS spin flip gap was ascertained with strain-mediated density of states which is of importance while fabrication upon a lattice mismatch between substrate. The magnetic transition temperature tuned by applied either compressive or tensile strain is also performed. Hence, electronic and magnetic studies revealed 3d TM element-substituted monolayer MgBr2 to be a potential system in spintronics applications. [ABSTRACT FROM AUTHOR]

Spin crossover (SCO) has long been a hot topic in the field of molecular magnetism owing to its unique bistability character. Rational control of thermal hysteresis and transition temperature (T1/2) is crucial for their practical applications, which rely on precise manipulation of the substituents of SCO coordinating ligands and molecular packing interactions. In this study, we designed two different bridging ligands (2-FDPB: 4,4'-(2-fluoro-1,4-phenylene)dipyridine; 2,3-FDPB: 4,4'-(2,3-difluoro-1,4-phenylene)dipyridine) featuring one and two fluoro substitution on the central benzene ring and applied a Schiff base-like equatorial tetradentate ligand {diethyl(E,E)-2,2'-[4,5-difluoro-1,2-phenyl-bis(iminomethylidyne)]bis(3-oxobutanoate)-(2-)-N,N',O3,O3'} (H2L) to coordinate with the FeII ion. Two FeII-coordination chain polymers [FeII(L)(2,3-FDPB)]·0.25CH2Cl2 (1) and [FeII(L)(2-FDPB)]·0.5CH3OH (2) were obtained. 1 crystallizes in the monoclinic P21/n space group with only one FeII center, while 2 crystallizes in the triclinic P1 space group with two independent FeII centers. Unlike the identical 2D layer stacking in 1, 2 exhibited alternating stacking of the extending 2D layers and meshed chains. Magnetic measurements revealed the typical thermally induced spin crossover behavior (SCO): 1 exhibited a 41 K-wide thermal hysteresis with transition temperatures of T1/2↑ = 245 K and T1/2↓ = 204 K, while 2 showed a higher transition temperature (T1/2 = 330 K) with no thermal hysteresis. Magneto-structural correlation studies suggest that the electron-withdrawing effect present in the fluoro substituents does not have a significant impact on the SCO behaviors. Despite the fluoro substituents having a similar atomic radius of hydrogen atoms, variations in the number of these substituents can alter the crystallization behavior of these complexes, which in turn affects the solvents, molecular stacking patterns, and intermolecular interactions, ultimately influencing the SCO behaviors. [ABSTRACT FROM AUTHOR]

A computational study on the interplay between ligand functionalization and guest effects on the transition temperature (T1/2) in the [Fe2(L1R)3]@X (L1 = 1,3-bis-(3-(pyridin-2-yl)-1H-pyrazol-5-yl)benzene, X = H-, F-, Cl-, Br-, I- and [BF4]-, R = H, F, or CH3) family of metal-organic cages (MOCs) is presented. Our results indicate that ligand functionalization with electron-donating or electron-withdrawing groups can significantly impact the T1/2 as expected, while the guest effect in lowering the T1/2 has a linear correlation with the increasing guest size. More importantly, small guests can move away from the center of the cavity, thus enhancing the two-step characteristic of the transition. All the data can be understood by analyzing the underlying electronic structure of the studied systems in terms of the relevant d-based molecular orbitals. These results can help in the rational design of new MOCs that can operate as sensors at specific temperatures, thus accelerating the discovery of new SCO devices with tailored properties. [ABSTRACT FROM AUTHOR]

The multiferroics with remarkable magnetoelectric (ME) coupling and technological application have drawn significant attention. Here, we report a chemical doping tunable effect on the magnetic, ferroelectric, and dielectric properties in type-II multiferroic Gd 2 BaCuO 5. The magnetic measurement results show that a long-range antiferromagnetic ordering forms at the Néel temperature (T N1) of ∼12.1 K, and a second magnetization anomaly occurs at a lock-in transition temperature (T N2) of ∼6.4 K. Sharp peaks in the pyroelectric and dielectric curves are observed at the magnetic transition temperatures, indicating intrinsic coupling between magnetic and ferroelectric orderings. The doping of Zn2+ results in a gradual enhancement of magnetization due to the increase of uncompensated spins, and large magnetodielectric (MD) coupling parameter up to ∼7.65 % is obtained in Gd 2 BaCu 0.7 Zn 0.3 O 5 because of strong spin-phonon coupling. The ferroelectric property is weakened in Zn2+ doped samples, suggesting the critical role of the 4 f -3 d magnetic interactions in determining the ME coupling effect. Moreover, an effective manipulation of electric field on magnetization is observed in Gd 2 BaCuO 5. This work helps understand the importance of 4 f -3 d magnetic interactions in inducing ferroelectricity and explore the ME and MD coupling effects with multiple magnetic orderings. [ABSTRACT FROM AUTHOR]

To decipher the effects of replacing alkali with zinc on thermo-mechanical properties, a series of borosilicate glasses with the molar compositions of 70.65SiO 2 ·21.09B 2 O 3 ·1.88Al 2 O 3 ·1Li 2 O·(5.38- x)R 2 O· x ZnO (x = 0, 0.34, 0.67, 1, 1.34, 2.69, 4.04, and 5.38) were prepared. Upon adding a slight quantity of ZnO, a local extreme point for glass transition temperature (T g) appears. This behavior is deciphered to be originated from two opposite factors. On one hand, T g reduces as a characteristic of the colligative properties for a dilute solution; in addition, T g rises due to the higher field strength, bond energy and covalent characteristic of zinc cations compared to that of alkali ions. Otherwise, based on the evolution of intermediate-range clusters revealed by infrared, Raman and NMR spectra, we elucidate the atomic-scale structural origin, which leads to the nonlinear evolution of elastic moduli and coefficient of thermal expansion with the molar ratio of [ZnO]/([R 2 O]+[ZnO]). [ABSTRACT FROM AUTHOR]

Ni–Zn–Mg ferrites having the chemical composition Ni0.7-xZnxMg0.3Fe2O4 (x = 0.1, 0.2, 0.3, 0.4, 0.5) were synthesized using easy and low cost-effective sol–gel autocombustion method. Thermogravimetric and differential thermal analysis (TGA–DTA), X-ray diffraction (XRD), Scanning electron microscopy (SEM), and Transmission electron microscopy (TEM) characterization techniques were used to characterize the synthesized samples. Structural and morphological properties of samples calcined at 500 °C, 600 °C, and 700 °C for 8 h were studied from XRD analysis and SEM analysis. Pure cubic phase along with proper grain growth was observed at calcined temperature 700 °C for 8 h. From TEM study of Ni0.4Zn0.3Mg0.3Fe2O4 average grain size is observed to be in range 50–55 nm that revealed the formation of nanosized particles. Thermoelectric power measurement (TEP) shows the p-type behavior at low temperature and n-type behavior at high temperature. p–n transition temperature for Ni–Zn–Mg ferrite system under investigation lies in the temperature range 90–135 °C. Gas sensing properties of Ni–Zn–Mg ferrite thick films toward NO2 and NH3 gases revealed Ni0.6Zn0.1Mg0.3Fe2O4 ferrite thick film shows good response along with quick response and recovery time as compared to other compositions under investigation. [ABSTRACT FROM AUTHOR]

Asymmetric carbon molecular sieve (CMS) hollow fiber membranes with tunable micro‐ and macro‐structural morphologies for energy efficient propylene‐propane separation are reported here. A sub‐glass transition temperature (sub‐Tg) thermal oxidative crosslinking strategy enables simultaneous optimization of the intrinsic molecular sieving properties while also reducing the thickness of the CMS “skin” derived from the 6FDA : BPDA/DAM polyimide precursors. Such synergistic tuning of CMS microstructure and macroscopic morphology of CMS hollow fibers enables significantly increased propylene permeance (reaching 186.5 GPU) while maintaining an appealing propylene/propane selectivity of 13.3 for 50/50 propylene/propane mixed gas feeds. Our findings reveal a more refined and versatile tool than available with previous O2‐doping pretreatments. The advanced approach here should be broadly useful to other polyimide precursors and diverse gas pairs. [ABSTRACT FROM AUTHOR]

Objective Methods Results Conclusion Hair fibres possess an inherently porous structure, which is affected by physical and chemical agents from the environment, as well as those from cosmetic treatments. The present work aims to investigate the potential of a calorimetric method for evaluating the changes of hair porosity, in terms of pore size and size distribution.The temperature of the phase transition from solid to liquid is known to be depressed if the liquid is confined within a pore. This shift in temperature can be measured by a calorimetric method like differential scanning calorimetry, DSC. This method is termed thermoporometry and it is the tool used for investigating hair porosity in this work.Virgin and bleached hair fibres are measured by DSC and, by using the equations developed for water behaviour confined in pores of a solid, the size and size distribution of the hair pores are evaluated, and the influence of the cosmetic treatment on the pores is discussed.Thermoporometry measurements of hair produced results in good agreement with those obtained by other methods for measuring hair porosity. The analysis of the data suggests that the fibre pores are mostly of a radius of 4 nm, and that the bleaching process increases the total volume of pores through the addition of smaller pores. A prolonged bleaching process appears to reduce the amount of fine pores produced by the first short process, resulting in fewer, but larger, cavities, most likely through a process of pore‐merging. [ABSTRACT FROM AUTHOR]

The crystallographic, microstructural, and dielectric properties of Sr 2.1 Na 0.8-x Ca x Nb 5-x Sn x O 15 (x = 0.00, 0.01, 0.05, 0.10) polycrystalline ceramics have been studied by X-ray diffraction, scanning electron microscopy, dielectric spectroscopy (DS) and impedance spectroscopy (IS). For x = 0.00, 0.05, and 0.10, samples are single phase with P 4 bm symmetry at room temperature with x = 0.01 showing a small quantity of secondary phase(s). All compositions show typical ceramic microstructures and d 50 grain sizes ranging from 5.1 to 26.6 μm. DS shows a clear trend in the high temperature ferroelectric-paraelectric transition with the Curie temperature, T 0 , decreasing from ∼ 160 to ∼ 110 °C, and an additional relaxation at approximately 120 °C with increasing CaSnO 3. IS reveals all samples have a homogeneous electrical microstructure with predominantly electronic conduction. The activation energy of conduction calculated from Arrhenius plots of the conductivity increases with CaSnO 3 content from 1.27 to 1.38 eV likely due to the expansion of the band gap. [ABSTRACT FROM AUTHOR]

Unconventional 1T′ phase transition metal dichalcogenides (TMDs) show great potential for hydrogen evolution reaction (HER). However, they are susceptible to transitioning into the stable 2H phase, which reduces their catalytic activity and stability. Herein, we present a scalable approach for designing thermally stable 1T′‐TMDs hollow structures (HSs) by etching Cu1.94S templates from pre‐synthesized Cu1.94S@TMDs heterostructures, including 1T′‐MoS2, MoSe2, WS2, and WSe2 HSs. Furthermore, taking 1T′‐MoS2 HSs as an example, the etched Cu ions can be firmly adsorbed on their surface in the form of single atoms (SAs) through Cu−S bonds, thereby elevating the phase transition temperature from 149 °C to 373 °C. Due to the advantages conferred by the 1T′ phase, hollow structure, and synergistic effect between Cu SAs and 1T′‐MoS2 supports, the fabricated 1T′‐MoS2 HSs demonstrate superior HER performance. Notably, their high‐phase stability enables continuous operation of designed 1T′‐MoS2 HSs for up to 200 hours at an ampere‐level current density without significant activity decay. This work provides a universal method for synthesizing highly stable 1T′‐TMDs electrocatalysts, with a particular focus on the relationship between their phase and catalytic stability. [ABSTRACT FROM AUTHOR]

Topological semimetals, possessing topologically non-trivial band structures, serve as excellent platforms for realizing topological superconductivity through hard point-contact experiments. In this study, we successfully induce superconductivity in the three-dimensional Dirac semimetal, cubic PtBi2, using ferromagnetic and paramagnetic tips in hard point contact experiments. The induced superconductivity is proven to be insensitive to ferromagnetism and exhibits unconventional features in the point-contact spectra. The highest superconducting transition temperature ( T c ) reaches approximately 5.1 K, and the T c values are proven to have a positive correlation with the coupling between the tip and the sample. Furthermore, we extend our point-contact experiments to trigonal PtBi2, a material possessing a type-I Weyl semimetal band structure and triply degenerate points proximate to the Fermi level. Utilizing both ferromagnetic Ni tips and paramagnetic Ag tips, we successfully enhance superconductivity with a T c of up to 3.0 K in this material. The findings from point-contact measurements reveal that the enhanced superconductivity is compatible with ferromagnetism and the magnetism of the tip can affect the symmetry of the enhanced superconducting state. Given that the lattice structure remains stable under pressure up to 51.2 GPa for cubic PtBi2 and 12.9 GPa for trigonal PtBi2, the emergent superconducting states observed in these two PtBi2 materials could inherit their topological nontrivial nature and be promising candidates for topological superconductor. [ABSTRACT FROM AUTHOR]

Smart, stimuli‐responsive materials that are also environmentally friendly are highly desired in the fashion and textile industry. For example, thermoresponsive properties show potential in creating dynamic comfort by improving moisture wicking and breathability at high temperatures. Additionally, color change properties provide aesthetic appeal and can be used as flexible sensors for physiological or environmental monitoring. Herein, the integration of bioproduced, thermoresponsive polymers into textiles as coatings that can also deliver pH‐responsive color change is explored. Elastin‐like polypeptides (ELPs) are recombinant protein biopolymers that exhibit an inverse phase transition when temperature is raised above a tunable transition temperature. To incorporate these into cotton textiles, amino acid residues with functional groups are genetically introduced. These are covalently coupled to oxidized cotton fabric, as well as a pH indicator dye, and copper‐free “click” conjugation handles. Thus, a facile layer‐by‐layer assembly process is used to assemble coatings with tunable thickness. The chemical derivatization of ELPs is shown and how these modifications influence thermoresponsive properties in solution is demonstrated. Cotton fabric is oxidized to introduce carboxylic acid chemical handles and up to ten coats of ELP is layered onto the modified cotton. The coating demonstrates spatiotemporal pH responsive color change. [ABSTRACT FROM AUTHOR]

Time-dependent thermoremanent magnetization (TRM) studies have been instrumental in probing energy dynamics within the spin glass phase. In this paper, we review the evolution of the TRM experiment over the last half century and discuss some aspects related to how it has been used in the understanding of spin glasses. We also report on recent experiments using high-resolution DC SQUID magnetometry to probe the TRM at temperatures less than but nearto the transition temperature Tc. These experiments have been performed as a function of waiting time, temperature, and five different magnetic fields. We find that as the transition temperature is approached from below, the characteristic time scale of TRM is suppressed up to several orders of magnitude in time. In the highest-temperature region, we find that the waiting time effect subsides, and a waiting time-independent crossover line is reached. We also find that increasing the magnetic field further suppresses the crossover line. Using a first-principles energy argument across the crossover line, we derive an equation that is an excellent fit to the crossover lines for all magnetic fields probed. The data show strong evidence for critical slowing down and an H = 0 Oe phase transition. [ABSTRACT FROM AUTHOR]

During last decades, significant advances have been made in iron-based spin crossover (SCO) complexes, with a particular emphasis on achieving reversible and reproducible thermal hysteresis at room temperature (RT). This pursuit represents a pivotal goal within the field of molecular magnetism, aiming to create molecular devices capable of operating in ambient conditions. Here, we summarize the recent progress of iron complexes with spin transition near RT based on nitrogen ligands containing aromatic rings from molecular design to functional devices. Specifically, we discuss the various factors, including supramolecular interactions, crystal packing, guest molecules and pressure effects, that could influence its cooperativity and the spin transition temperature. Furthermore, the most recent advances in their implementation as mechanical actuators, switching/memories, sensors, and other devices, have been introduced as well. Finally, we give a perspective on current challenges and future directions in SCO community. [ABSTRACT FROM AUTHOR]

A new hydrophobic deep eutectic solvent was designed by combining menthol and salicylaldoxime. The mixture has low temperature of glass transition and, additionally, structural reorganization with abnormally long lifetime. The properties of this ligand-containing mixture allow it to be used as an extraction system for metal ions, which was tested with Cu(II). [ABSTRACT FROM AUTHOR]

We present a theory for charge-4e superconductivity as a leading low-temperature instability with a nontrivial d-wave symmetry. We show that in several microscopic models for the pair-density-wave (PDW) state, when the PDW wave vectors connect special parts of the Fermi surface, the predominant interaction is in the bosonic pairing channel mediated by exchanging low-energy fermions. This bosonic pairing interaction is repulsive in the s-wave channel but attractive in the d-wave one, leading to a d-wave charge-4e superconductor. By analyzing the Ginzburg-Landau free energy including higher-order fluctuation effects of PDW, we find that the charge-4e superconductivity emerges as a vestigial order of PDW, and sets in via a first-order transition. Both the gap amplitude and the transition temperature decay monotonically with increasing superfluid stiffness of the PDW order. Our work provides a microscopic mechanism of higher-charge condensates with unconventional ordering symmetry in strongly-correlated materials. [ABSTRACT FROM AUTHOR]

Materials with electrocaloric effect (ECE) and/or thermal switching ratio λ are desirable for developing various heat management devices, but developing high-performance candidates, especially those that simultaneously possess large near room-temperature ECE and λ is actually absent. The Zr-rich PbZr1−xTixO3 (PZT) displays a composition-induced antiferroelectric-ferroelectric (AFE-FE) phase boundary, where an unusual negative ECE is expected. Meanwhile, the electric field-sensitive dipole orientation during the AFE-FE phase transition can be employed to modulate λ. In this work, the Zr-rich PZT with coexisting AFE and FE phases was developed and the AFE-FE phase transition temperature is tuned toward room temperature by changing the Ti content to achieve large negative ECE and λ. A large adiabatic temperature change ΔT of −3.3 K accompanied by a giant λ of 1.84 near 60 °C is captured in optimal PbZr0.95Ti0.05O3 ceramics, demonstrating a prominent application prospect in solid-state refrigeration. [ABSTRACT FROM AUTHOR]

As part of obtaining excellent properties that can be used as lead-free hybrid solar cells, the crystal growth, crystal structure, phase transition temperature, and thermal properties for [NH3(CH2)2NH3]CuBr4 were discussed. The crystal structure at 300 K was determined to be monoclinic by single-crystal X-ray diffraction (XRD) analysis. The phase transition temperatures were determined to be 447 and 473 K, and the results were consistent with the powder XRD patterns. Thermogravimetric analysis revealed thermal stability up to ~ 460 K. The continuous changes in the 1H and 13C chemical shifts and 14N static resonance frequency with increasing temperature are related to variations in the local environment and coordination geometry. The significant differences in activation energies obtained from the 1H and 13C spin–lattice relaxation times (t1ρ) at low and high temperatures were discussed. The activation energy results suggested that the energy barrier at low temperatures was related to the reorientation of the NH3 and CH2 groups around the three-fold symmetry axis, and the energy barrier at high temperatures was related to the reorientation of the [NH3(CH2)2NH3] cation. These physical properties will be provide important insights or potential applications of this crystal.Please check and confirm that the corresponding author and their respective corresponding affiliation have been correctly identified and amend if necessary.OK ! [ABSTRACT FROM AUTHOR]

As part of obtaining excellent properties that can be used as lead-free hybrid solar cells, the crystal growth, crystal structure, phase transition temperature, and thermal properties for [NH3(CH2)2NH3]CuBr4 were discussed. The crystal structure at 300 K was determined to be monoclinic by single-crystal X-ray diffraction (XRD) analysis. The phase transition temperatures were determined to be 447 and 473 K, and the results were consistent with the powder XRD patterns. Thermogravimetric analysis revealed thermal stability up to ~ 460 K. The continuous changes in the 1H and 13C chemical shifts and 14N static resonance frequency with increasing temperature are related to variations in the local environment and coordination geometry. The significant differences in activation energies obtained from the 1H and 13C spin–lattice relaxation times (t1ρ) at low and high temperatures were discussed. The activation energy results suggested that the energy barrier at low temperatures was related to the reorientation of the NH3 and CH2 groups around the three-fold symmetry axis, and the energy barrier at high temperatures was related to the reorientation of the [NH3(CH2)2NH3] cation. These physical properties will be provide important insights or potential applications of this crystal.Please check and confirm that the corresponding author and their respective corresponding affiliation have been correctly identified and amend if necessary.OK ! [ABSTRACT FROM AUTHOR]

2D transition metal oxides have created revolution in the field of supercapacitors due to their fabulous electrochemical performance and stability. Molybdenum trioxides (MoO3) are one of the most prominent solid-state materials employed in energy storage applications. In this present work, we report a non-laborious physical vapor deposition (PVD) and ultrasonic extraction (USE) followed by vacuum assisted solvothermal treatment (VST) route (DEST), to produce 2D MoO3 nanosheets, without any complex equipment requirements. Phase transition in MoO3 is often achieved at very high temperatures by other reported works. But our well-thought-out, robust approach led to a phase transition from one phase to another phase, for e.g., hexagonal (h-MoO3) to orthorhombic (α-MoO3) structure at very low temperature (90 °C), using a green solvent (H2O) and renewable energy. This was achieved by implementing the concept of oxygen vacancy defects and solvolysis. The synthesized 2D nanomaterials were investigated for electrochemical performance as supercapacitor electrode materials. The α-MoO3 electrode material has shown supreme capacitance (256 Fg−1) than its counterpart h-MoO3 and mixed phases (h and α) of MoO3 (< 50 Fg−1). Thus, this work opens up a new possibility to synthesize electrocapacitive 2D MoO3 nanosheets in an eco-friendly and energy efficient way; hence can contribute in renewable circular economy. [ABSTRACT FROM AUTHOR]

As part of obtaining excellent properties that can be used as lead-free hybrid solar cells, the crystal growth, crystal structure, phase transition temperature, and thermal properties for [NH3(CH2)2NH3]CuBr4 were discussed. The crystal structure at 300 K was determined to be monoclinic by single-crystal X-ray diffraction (XRD) analysis. The phase transition temperatures were determined to be 447 and 473 K, and the results were consistent with the powder XRD patterns. Thermogravimetric analysis revealed thermal stability up to ~ 460 K. The continuous changes in the 1H and 13C chemical shifts and 14N static resonance frequency with increasing temperature are related to variations in the local environment and coordination geometry. The significant differences in activation energies obtained from the 1H and 13C spin–lattice relaxation times (t1ρ) at low and high temperatures were discussed. The activation energy results suggested that the energy barrier at low temperatures was related to the reorientation of the NH3 and CH2 groups around the three-fold symmetry axis, and the energy barrier at high temperatures was related to the reorientation of the [NH3(CH2)2NH3] cation. These physical properties will be provide important insights or potential applications of this crystal.Please check and confirm that the corresponding author and their respective corresponding affiliation have been correctly identified and amend if necessary.OK ! [ABSTRACT FROM AUTHOR]

As part of obtaining excellent properties that can be used as lead-free hybrid solar cells, the crystal growth, crystal structure, phase transition temperature, and thermal properties for [NH3(CH2)2NH3]CuBr4 were discussed. The crystal structure at 300 K was determined to be monoclinic by single-crystal X-ray diffraction (XRD) analysis. The phase transition temperatures were determined to be 447 and 473 K, and the results were consistent with the powder XRD patterns. Thermogravimetric analysis revealed thermal stability up to ~ 460 K. The continuous changes in the 1H and 13C chemical shifts and 14N static resonance frequency with increasing temperature are related to variations in the local environment and coordination geometry. The significant differences in activation energies obtained from the 1H and 13C spin–lattice relaxation times (t1ρ) at low and high temperatures were discussed. The activation energy results suggested that the energy barrier at low temperatures was related to the reorientation of the NH3 and CH2 groups around the three-fold symmetry axis, and the energy barrier at high temperatures was related to the reorientation of the [NH3(CH2)2NH3] cation. These physical properties will be provide important insights or potential applications of this crystal.Please check and confirm that the corresponding author and their respective corresponding affiliation have been correctly identified and amend if necessary.OK ! [ABSTRACT FROM AUTHOR]

A series of new oligoimides based on 4,4- and 3,4-oxydianiline and 2,2-bis[(3,4-dicarboxyphenoxy)phenyl]propane dianhydride, possessing different average chain lengths, and containing terminal propargyl groups were synthesized according to an efficient single-step high-temperature polycyclocondensation method. Their molecular weight characteristics, solubility in organic solvents, thermal (DSC, TMA, and TGA), and rheological properties were studied. The synthesized oligoimides exhibited a significantly lower exothermic effect upon curing due to their elongated chain as compared to diimides. The oligoimides upon increasing the temperature enter into a viscous fluid state, in which they remain up to the curing onset temperature of 270–320 °C. The symmetry of structure of the diamine moiety (4,4-ODA or 3,4-ODA) and the molecular weight of oligoimides affect the temperature of transition to the viscous fluid state. [ABSTRACT FROM AUTHOR]

Exact solutions have been constructed for some problems on thawing frozen soil in the process of water seeping into it as a result of the melting of underground ice and the associated violation of the mechanical integrity of the soil (thermokarst). Factors of thermokarst in frozen soil, determined by the specifics of heat and mass transfer in it, have been identified. The influence of the porosity of rocks, which changes during their melting, on the course of the thermokarst formation as a whole has been studied. An analytical solution to the problem of thermokarst is constructed. An expression was obtained for the rate of thermokarst formation in frozen soil. [ABSTRACT FROM AUTHOR]

The scientific strategies reported in the literature for developing biobased epoxy vitrimers are summarized. Biomass resources such as lignin, cellulose, or different vegetable oils can be exploited as biobased building blocks for epoxy thermosets as an alternative to the bisphenol‐A‐based ones. Biorenewable resources have been synthesized introducing dynamic covalent bonds in the cross‐linked networks. This combination allows to achieve cross‐linked biobased epoxy networks with thermoset‐like properties at a temperature of use, but showing (re)processability, recyclability, and self‐healing properties above a well‐defined temperature named topology freezing transition temperature (Tv). [ABSTRACT FROM AUTHOR]

Thermochromic luminescent materials (TLMs) with spectral responsiveness to thermal stimuli have received broad attention due to the forefront applications in temperature visualization and sensing technologies. Herein, a phase diagram‐driven strategy for designing TLMs in Cs–Cd–Br ternary system is presented. The room temperature stable Cs7Cd3Br13 crystal is first obtained by utilizing a facile hydrothermal method, and the self‐trapped exciton (STE) luminescence is improved by breaking local symmetry via Mg2+ doping. Then thermochromic luminescence is further realized in Mn2+ co‐doped Cs7Cd3Br13 on the basis of reversible structural transition to metastable Cs2CdBr4 under thermal stimuli. The emission color change from bright yellow to green benefits from the variation of crystal fields around Mn2+, which can be switched by heating and cooling circulations. Finally, the resulting material is used as a demo to visualize the temperature of a homemade high‐frequency induction heating sintering platform. [ABSTRACT FROM AUTHOR]

Lamellae forming polystyrene‐b‐poly‐2‐vinylpyridine diblock copolymer melts are investigated with linear shear rheology and Fourier transformation rheology (FT rheology) to quantify their nonlinear behavior under oscillatory shear via mechanical higher harmonic contributions such as I3/1(ω1, γ0). The determination of the zero‐shear nonlinearity (3Q0(ω)≡limγ0→0I3/1/γ02$^3Q_0(\omega)\equiv \lim _{\gamma _0 \rightarrow 0}I_{3/1}/\gamma _0^2$) by a variation of γ0 is hindered by the increasing domain alignment at increasing γ0. Thus, an approach for determining 3Q0(T) by a variation of the temperature is developed and used. This approach allows obtaining insights on the nonlinear behavior directly at temperature‐dependent phase transitions, such as at the order‐disorder transition temperature TODT of block copolymers. The maximum of 3Q0 is found to be close to TODT. The nonlinearity originating from the connection of the unequal polymer blocks is shown to dominate the overall nonlinearity, and the maximum of 3Q0(T) correlates to domain alignment for T < TODT. [ABSTRACT FROM AUTHOR]

Here, we have developed a more temperature-tolerant emitter with a gradient emittance, which can enable adaptation to changing environmental conditions. Such a thermal emitter is mainly constructed by multilayered films composed of nitrogen (N)-doped Ge2Sb2Te5 (N-GST) and an underlying metal film. The proposed device not only possesses special wavelength selectivity in the middle infrared range but can also dynamically adjust average emissivity (from 0.13 to 0.83) through the degree of crystallization. Besides, N doping can elevate the phase transition temperature of GST and enhance its thermal resistance, which renders it particularly well-suited for applications in higher temperature environments than pure GST. This emitter also shows strong adhesion capability and high flexibility against bending, enabling more practical and widespread situations. By using a multi-layer structure, we combined the more temperature-tolerant and dynamically modulating N-GST emitter with an optical thin film, successfully achieving dual camouflage for both infrared and visible light. The element doping technology and multi-layer stacking approach presented in this research will provide valuable insight for the development of dynamic emissive materials in multi-spectral camouflage scenarios. [ABSTRACT FROM AUTHOR]

Experiments were conducted to characterize the mechanical behavior of Divinycell PVC foams over a wide range of environmental temperatures, from −60 to +80°C. Transversely isotropic properties of the foams, including modulus, strength, and ductility, were found to vary with temperatures between the ductile-to-brittle transition temperature (−60 to −50°C) and just under the glass transition temperature (95 to 100°C). The elastic modulus and yield strength decreased linearly as the temperature increased from −60 to +80°C. Compressive strength also decreased steadily with increasing temperature over the entire temperature range. In contrast, tensile and shear strengths only showed a significant decrease in values as the temperature rose above 23°C (room temperature). Below 23°C, there was a minor change in tensile and shear strengths. Tensile and shear ductility decreased sharply as the temperature decreased from +80°C to −40°C and stabilized between −60 and −40°C, which is close to the ductile-to-brittle transition region. Fractography of the tensile and shear fracture surfaces confirmed brittle fracture at −60°C and ductile tearing at +60°C. Equations were derived to predict modulus, yield strength, compressive, tensile and shear strengths, and ductility at any temperature in terms of room temperature values. [ABSTRACT FROM AUTHOR]

Aqueous fluids are extensively present in the middle to lower crust, as revealed by seismic and magnetotelluric soundings. The α−β quartz phase transition significantly affects many physical properties and leads to substantial microcracks that can provide pathways for the migration of crustal fluids. A systematic investigation of macroscopic physical properties and microstructure of quartz is crucial to elucidate their correlation. In the present study, the effects of water content, trace elements, orientations, and phase transition on the electrical conductivity of quartz were thoroughly evaluated at 400−900°C and 1 GPa. Individual annealing experiments were simultaneously conducted on quartz single crystals at different peak temperatures and 1 GPa to investigate the evolution and spatial distribution of microcracks using X‐ray microtomography (CT) and backscattered electron imaging. We found that trace element content and orientations, rather than H2O, are the dominant factors controlling the conductivity of quartz. The distinct changes in conductivity of single crystals at around α−β phase transition temperature are attributed to the transformation of microcracks from isolated to interconnected networks, as confirmed by two‐dimensional (2‐D) and three‐dimensional (3‐D) microstructure images. Based on the variation in electrical conductivity and microstructure across the transition, it thus is proposed that the intragranular microcracks caused by quartz phase transition can serve as fluid or melt pathways within highly conductive zones present in the middle to lower crust, while α‐quartz acts as an impermeable cap. Plain Language Summary: Numerous geophysical observations have disclosed the widespread presence of aqueous fluids in the middle to lower crust. It has been demonstrated that the α−β quartz phase transition not only causes drastic changes in many physical properties, but also play an important role in fluid storage in crust due to the generation of microcracks. An integrated study on electrical conductivity, X‐ray tomography and backscattered electron images can unravel the correlation of macroscopic physical properties and microstructure of quartz. Our results indicated that orientations and trace element content have predominant influences on the electrical conductivity compared to water content. Additionally, a marked change in the conductivity of quartz single crystals occurred at temperature around the α−β phase transition, which is ascribed to the formation of interconnected microcracks confirmed by 2‐D and 3‐D high‐resolution microstructure images. These intragranular microcracks in quartz can promote porosity and permeability, facilitating the interconnection of fluid or melt required for the highly conductive anomaly in the middle to lower crust, while the α‐quartz above it may serve as a permeability barrier. Key Points: The effects of temperature, trace elements, and orientations on electrical conductivity of quartz were quantitatively evaluatedThe interconnected microcracks formed at α−β quartz phase transition were confirmed by electrical conductivity, 2‐D and 3‐D imagesThe transition‐induced microcracks provide fluid pathways for high conductivity zones in the middle to lower crust [ABSTRACT FROM AUTHOR]

Two-dimensional (2D) computational fluid dynamics (CFD) simulations of water-based microencapsulated phase change material suspension (MPCMS) on the flow boiling in a gas–liquid–solid flow system was performed with volume of fluid (VOF) method and discrete particle model (DPM). The Lagrangian particles were linked to the Eulerian phases through the interchange terms such as the drag force in the respective momentum equations. Influences of particle properties including mass fraction and core phase transition temperature, fluid properties including liquid surface tension force and viscosity, detachment time and rise velocity of gas bubbles and particle entrainment in the gas–liquid–solid flow under ambient conditions were numerically investigated. The effects of particles on bubble nucleation, growth and rupture during boiling were studied by visualization. The results show that MPCM can enhance the boiling heat transfer ability of the base liquid. The maximum heat transfer enhancement rate of MPCMS (28 °C) is 4.8%, the maximum heat transfer enhancement rate of MPCMS (90 °C) is 5.1%, the maximum heat transfer enhancement rate of MPCMS (110 °C) can reach 6.7%. MPCM can promote the formation of new bubbles and the rupture of large bubbles, reduce the departure diameter of bubbles, and enhance the boiling heat transfer capacity of the base liquid. The MPCM with core phase change temperature higher than the boiling temperature of base fluid has the best enhancement effect. Through the combination of numerical simulation methods such as VOF and DPM, the complex phase transition heat transfer process of gas-liquid-solid particle coupling of latent thermal functional thermal fluid can be accurately simulated. The work lays a foundation for further explorations on the gas–liquid–solid flows and possible industry applications. [ABSTRACT FROM AUTHOR]

Rare earth niobate Re 3 NbO 7 (Re=Rare earth element) possesses ultra-low thermal conductivity for application as thermal barrier coatings (TBCs). However, Re 3 NbO 7 with large rare earth ion radius (Re La, Nd, Sm) exhibits both low temperature phase transition and poor facture toughness which is detrimental to the durability of the coatings. In this work, an effective method was proposed to solve those problems by doping. Considering the low-temperature phase transition at about 340K, La 3 NbO 7 is selected as representative material. In order to suppress phase transition, Y3+ with relatively smaller ionic radius is used as a doped ion, and (La 1- x Y x) 3 NbO 7 (x = 0.0,0.1,0.3,0.5) were prepared and investigated. It is shown that, low temperature phase transition of La 3 NbO 7 is effectively suppressed due to Y3+ doped. Facture toughness is increased significantly from 0.5 to 2.3 MPa m1/2 with the increase of doping concentration. Furthermore, the Vickers hardness is also improved by doping. Considering the phase stability and ultra-low thermal conductivity, (La 1- x Y x) 3 NbO 7 solid solution (x = 0.5) maybe promising candidates for high temperature thermal insulation materials such as TBCs, thermoelectric materials, etc. [ABSTRACT FROM AUTHOR]

In the study, we synthesized the (BiO 1.5) 0.88 (ErO 1.5) 0.08 (HoO 1.5) 0.04 and (BiO 1.5) 0.88 (ErO 1.5) 0.04 (HoO 1.5) 0.08 ternary compositions using the solid–state reactions in an atmosphere of air. All compositions were then heated to 650, 700, 750, and 800 °C to observe how the calcination temperature impacts phase stability and conductivity. All XRD patterns suggested that the cubic δ–phase, a high–ion conductor, became stable at room temperature. Depending on the temperature, the DTA curves revealed that some compositions had an endothermic peak at around 600 °C, indicating an order–disorder transition wholly related to anion sublattice arrangement without a phase transition. At 700 °C, the highest conductivity was found to be 0.482 S/cm for the (BiO 1.5) 0.88 (ErO 1.5) 0.04 (HoO 1.5) 0.08 composition calcined at 800 °C, and this conductivity is greater than that of a single–doped (BiO 1.5) 0.80 (ErO 1.5) 0.20 system. The FE–SEM images indicated that calcination at 650 °C and 700 °C, which are below the phase transition temperature (729 °C) from α–phase to cubic δ–phase, results in atom aggregation and porosity on the surface. Besides, the calcination temperature was shown to significantly impact grain sizes, with compositions produced with a calcination at 800 °C exhibiting bigger grains than lower ones. [ABSTRACT FROM AUTHOR]

Sol–gel synthesis method was employed to fabricate nanocomposites of (Dy, Hf) co-doped 0.8BiFeO3–0.2CaTiO3 (Bi0.75Dy0.05Fe0.80O3–Ca0.20Ti0.18Hf0.02O3/BDyFO–CTHfO composite). Structural analysis, utilizing X-ray diffraction and Rietveld refinement with Fullprof software, confirmed a rhombohedral structure with space group R3c and an orthorhombic structure with Pnma space group. Particle size determined through Scherrer's formula was ~15 nm. FESEM studies revealed irregular and slightly dense inhomogeneous grains. Dielectric permittivity (ε) and tangent loss (tan δ) were investigated as functions of frequency from 100 Hz to 1 MHz at different temperatures ranging from 303 to 663 K. The dielectric dispersion behaviour was attributed to Maxwell–Wagner-type polarization, with a notable anomaly in dielectric permittivity observed near the magnetic phase transition temperature (TN ~ 643 K) of BiFeO3. Frequency-dependent ac conductivity exhibited low-frequency dispersion following Jonscher's power law. Presence of ferroelectricity was confirmed by the polarization–electric field (PE) loop. Magneto-dielectric characteristics were assessed in a frequency range of 100 Hz–1 MHz under a magnetic field of 0–2 Tesla. Impedance spectroscopy highlighted electrical properties, distinguishing grain and grain boundary contributions via Nyquist plot with respect to the magnetic field. The BDyFO–CTHfO composite demonstrated significant absorption and ~ 25% transmittance in the visible spectrum. The material exhibited a band gap (Eg) of 1.97 eV, suggesting potential applications in ultrafast optoelectronic devices. [ABSTRACT FROM AUTHOR]

In this study, we demonstrate the high luminous efficacy of 118 lm/W and the high reliability of white LEDs (WLEDs) through 450 °C thermal aging, utilizing four-inch YAG: Ce3+ phosphor-in-glass (PiG) plates designed for vehicle headlights. The sintering process of mixing glass and phosphor typically generates pores, which can scatter light and reduce the luminous efficacy of the fabricated PiG. In this study, we produced four-inch PiG plates under four different fabrication conditions to evaluate their luminous efficacy. Our results revealed that the PiG plate with a thin thickness of 0.08 mm exhibited a 16.83% increase in luminous efficacy compared to the 0.15 mm plate, attributed to reduced light interaction with the pores. Unlike silicone-based phosphor WLEDs, which offer high performance but lower reliability due to the silicone resin's low transition temperature (150 °C), our novel thin PiG plate achieves high performance and reliability. This advancement suggests that the proposed thin PiG plate could replace traditional silicone-based phosphors, enabling the development of high-quality WLEDs for vehicle headlights in automotive applications. [ABSTRACT FROM AUTHOR]

To realize large-scale micro/nanofabrication process in superconducting devices, the nano laser direct writing (NLDW) as a potential tool was implemented. In this paper, thermal effect induced laser-matter (superconducting film) interaction based on laser direct writing on Nb films and laser exposure on photoresist were investigated by simulation and experiment. To avoid nanoscale thermal effect on superconducting films, large-scale superconducting nanoarrays with the area up to 100 µm × 100 µm based on laser exposure on photoresist were fabricated. Compared with laser direct writing on superconducting films, which lead to the degradation of superconducting performance such as critical current, transition temperature, the superconducting nanoarrays based on laser exposure on photoresist maintain excellent superconducting performance without degradation. Besides that, by further optimizing the process parameters and the thickness of photoresist, the nanowires with the width down to nanometers are plausible. Compared with the traditional electron beam and ion beam process, to some extent, the nanowires fabrication process based on NLDW provides a more efficient and cost-effective path for the fabrication of large-area superconducting devices/circuits. [ABSTRACT FROM AUTHOR]

The dielectric properties of a mixed Zethrene-inspired nanoscale system ( S i Z -1, σ k Z -5/2) have been analyzed in detail using the Monte Carlo approach (MCa) in this study. First, the most stable configurations in different planes were investigated. Then, the influences of the physical factors, namely the coupling interaction factor, on the thermal behaviors of the polarization and the susceptibility of the studied nanostructure have been examined for nonzero temperatures and fixed external electric field values. It was found that the obtained transition temperature point relies weakly on the coupling interaction. Finally, the effects of the physical factors on the electric hysteresis cycles were discussed. [ABSTRACT FROM AUTHOR]

In this study, Monte Carlo investigation delves into the dielectric features of silicene–germanene nanosystem with junction connection. We emphasized the profound influence of physical parameters, coupling between Si–Si and Ge–Ge atoms and temperature, on these dielectric features. Our results highlight the pivotal role of the coupling parameter between Ge atoms in influencing blocking temperatures, underlining the significance of high values for spin and coupling parameters for achieving a high blocking temperature and delaying transitions. Furthermore, our analysis of electric hysteresis loops demonstrates their sensitivity to parameter variations, which can offer valuable insights for nanoelectronics and materials science applications. [ABSTRACT FROM AUTHOR]

Smart windows have the potential to respond dynamically and passively to external stimuli, controlling the amount of light passing through the window. When a smart window switches from a clear to a translucent state, energy flow through the window is partially attenuated, allowing a room to cool down passively, thereby reducing the energy and fossil fuel consumption for air conditioning. The smart window demonstrated here consists of a thermoresponsive liquid consisting of Tergitol 15‐S‐7, which can dynamically and passively switch the window's transmittance when a temperature of 39 °C is reached. It is also demonstrated how the transition temperature can be lowered by adding salts. Outdoor experiments in realistic environments show that the temperature of a model house built with a thermo‐responsive window can achieve an indoor temperature of 7 °C less than a control house with an ordinary window. This study quantifies the energy savings possible using such windows at the building scale for cooling and heating in different climates and times of the year. [ABSTRACT FROM AUTHOR]

This study investigates corner solidification in a closed cavity in which the left and bottom walls are kept at a temperature lower than its initial temperature. The liquid material in the cavity initially lies at its phase transition temperature and, due to cold boundary conditions at the left–bottom walls, solidification starts. The simulation of corner solidification was performed using a kinetic-based lattice Boltzmann method (LBM), and the tracking of the solid–liquid interface was captured through the evaluation of time. The present investigation addresses the effect of natural convection over conduction across a wide range of higher Rayleigh numbers, from 106 to 108. The total-enthalpy-based lattice Boltzmann method (ELBM) was used to observe the thermal profiles in the entire cavity with a two-phase interface. The isotherms reveal the relative dominance of natural convection over conduction, and the pattern of interface reveals the effective growth of the solidified layer in the cavity. To quantify the uniformity of cooling, a coefficient of variation (COV) for the thermal field was calculated in the effective solidified zone at a wide range of Ra. The results show that the value of COV increases with Ra and reduces with time. The thermal instability in the flow field is also quantified through FFT analyses. [ABSTRACT FROM AUTHOR]

Textiles are promising candidates for use in soft robots and wearable devices due to their inherent compliance, high versatility, and skin comfort. Planar fluidic textile‐based actuators exhibit low profile and high conformability, and can seamlessly integrate additional components (e.g., soft sensors or variable stiffness structures [VSSs]) to create advanced, multifunctional smart textile actuators. In this article, a new class of programmable, fluidic soft textile muscles (STMs) that incorporate multilayered silicone sheets with embedded fluidic channels is introduced. The STMs are scalable and fabricated by apparel engineering techniques, offering a fabrication approach able to create large‐scaled multilayered structures that can be challenging for current microfluidic bonding methods. They are also highly automation compatible due to no manual insertion of elastic tubes/bladders into textile structures. Liquid metal is employed for creating fluidic channels. It is not only used for actuation but also used as channels for additional features such as soft piezoresistive sensors with enhanced sensitivity to STMs' pressure‐induced elongation, or VSSs of either low‐melting‐point alloys or a new thermo‐responsive epoxy with low viscosity and transition temperature. The STMs hold promising prospects for soft robotic and wearable applications, which is demonstrated by an example of a textile‐based wearable 3D skin‐stretch haptic interface. [ABSTRACT FROM AUTHOR]

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Multi-component thermal luid technology optimizes development effects and has a strong adaptability, providing a new choice for the efficient development of heavy oil reservoirs. However, due to the significant differences between the phase behavior of multi-component thermal-fluid-heavy oil systems and conventional systems, and the lack of targeted and large-scale research, key issues such as the phase behavior of these systems are unclear. This research studies the phase behavior and influencing factors of emulsions and foamy oil in a multi-component thermal-fluid-heavy oil system through high-temperature and high-pressure PVT experiments, revealing the characteristics of the system's special phase behavior. In the heavy oil emulsion system, the water content directly affects changes in the system's phase state. The higher the temperature, the larger the phase transition point, and the two are positively correlated. As the stirring speed increases, the phase transition point first increases and then decreases. The amount of dissolved gas is negatively correlated with the size of the phase transition point, and dissolution can form foamy oil. In the heavy oil–foamy oil system, the dissolution capacity of CO2 is greater than that of multi-component gases, which is greater than that of N2. A high water content and high temperature are not conducive to the dissolution of multi-component gases. While an increase in stirring speed is beneficial for the dissolution of gases, there are limitations to its enhancement ability. Therefore, the development of multi-component thermal fluids should avoid the phase transition point of emulsions and promote the dissolution of multi-component gases. [ABSTRACT FROM AUTHOR]

We report an isothermal electric field-induced first-order phase transition from a Mott insulator to the metallic state in the epitaxial thin film of V 2 O 3 in the temperature regime below its Mott transition temperature of ≈ 180 K. This isothermal electric field-induced transition is accompanied by interesting electrothermal history effects, which depend on the measurement paths followed in the electric field–temperature phase space. These interesting properties result in tuneable resistive switching and distinct memristive behaviour in V 2 O 3 . A generalized framework of disorder-influenced first-order phase transition in combination with a resistor network model has been used to explain the observed experimental features. These findings promise possibilities for Mott insulators to be used as highly energy-efficient switches in novel technologies such as neuromorphic computing. [ABSTRACT FROM AUTHOR]

Lead-free 0.96(K0.48Na0.52)(Nb0.965Sb0.035−xErx)O3-0.04(Bi0.5Na0.5)ZrO3 (KNNS0.035−xEx-BNZ) multifunctional ceramics were prepared by the conventional solid-state reaction method combined with the two-step sintering method. The results show that the ceramics doped with a moderate amount of Er3+ show good piezoelectric properties and excellent temperature stability, while displaying bright up-conversion photoluminescence. Er3+-doping shifts the orthorhombic–tetragonal phase transition temperature (TO-T) down to below room temperature and enhances the temperature stability of the ceramics. For a 0.2 mol%Er3+-doped sample, the room-temperature piezoelectric constant d33 reached 343 pC/N. The sample shows good resistance to thermal depoling as noted that the d33 value remaining at more than 95% of that at room temperature when the temperature was increased to 230 °C. Relying on the luminescence behavior of rare earth Er3+ ions, Er3+-doped samples exhibit a strong photoluminescence with a bright green up-conversion emission under excitation at 980 nm. Two green emissions, at 525 nm and 550 nm, corresponded to the transitions from 2H11/2 → 4I15/2 to 4S3/2 → 4I15/2, and a weak red emission at 660 nm was assigned to the 4F9/2 → 4I15/2 transition obtained under the excitation of a 980-nm laser. The multifunctional properties in the Er-doped samples make them promising for multifunctional device applications. [ABSTRACT FROM AUTHOR]

Laser powder bed fusion (LPBF) presents both opportunities and challenges with regard to the customisation of NiTi alloy properties. This paper presents a systematic study of the influence of process parameters on the superelasticity of LPBF Ni-rich Ni51.3Ti48.7 shape memory alloy. The findings demonstrate that NiTi alloys produced through disparate process parameters exhibit disparate phase transformation behaviours and microstructures, which in turn result in varying degrees of superelasticity. At an energy density of 166.7 to 233.3 J/mm3, LPBFed Ni-rich Ni51.3Ti48.7 is predominantly in the martensite phase at room temperature due to the high phase transition temperature caused by a large amount of Ni evaporation loss, and exhibits almost no superelasticity. At an energy density of 66.7 to 116.7 J/mm3, LPBFed Ni-rich Ni51.3Ti48.7 has less Ni evaporation loss and lower phase transition temperature. It is primarily austenite phase at room temperature, and contains nano-precipitated phases internally, thereby exhibiting excellent superelasticity. The recovery rate is in excess of 5.5% at the initial compression (up to 5.7%) and in excess of 5.0% following ten cycles (up to 5.3%). Furthermore, the lower the energy density, the smaller the stress–strain hysteresis of LPBFed Ni-rich Ni51.3Ti48.7, with a variation range of 1.8–3.9 mJ/mm3. [ABSTRACT FROM AUTHOR]

In dairy-based imitation mozzarella cheese (IMC) formulations, intact casein is critical and imparts IMC with a firm and elastic, stringy, melted texture. Rennet casein (RCN) is the desired ingredient to provide intact casein in IMC and is preferred over milk protein concentrate (MPC) and micellar casein concentrate (MCC). Transglutaminase (TGase), a crosslinking enzyme, alters the physical properties of MPC or MCC and may change IMC functionality. The objective of this study was to determine the effect of TGase-crosslinked MPC and MCC powders on the functionality of IMCs. The TGase treatment included TGase at 0.3 (L) and 3.0 (H) units/g of protein and a control (C) with no TGase addition. Each IMC formulation was balanced for constituents and was produced in a Rapid Visco Analyzer (RVA). The MCC or MPC powder with high TGase enzyme in IMC formulation did not form an emulsion. The IMC containing TGase-treated powders had a significantly (p ≤ 0.05) higher RVA-viscosity during manufacture and transition temperature (TT), and a significantly (p ≤ 0.05) lower Schreiber melt test area. The IMC made from MPC (with or without TGase) had lower TT values and Schreiber melt test area as compared with that made from MCC. The TGase-treated MPC and MCC, when used for IMC manufacture, were comparable to IMC manufactured with RCN in texture and some measured melted characteristics. In conclusion, TGase treatment alters the melt characteristics of MCC and MPC in IMC applications. [ABSTRACT FROM AUTHOR]