Wide Temperature Research Articles

Evaluating Plant Growth-Promoting Rhizobacteria to Improve the Productivity of Forage Pearl Millet.

India's livestock industry is grappling with a shortage of green fodder, necessitating concerted efforts to boost organized production and ensure a sufficient supply of high-quality forages, crucial for formulating nutritionally balanced, cost-effective, and rumen-healthy animal diets. Hence, this study was conducted to assess the plant growth-promoting characteristics of liquid microbial inoculants and their impact on the yield of forage pearl millet. The bacterial cultures utilized included Sphingobacterium sp., Stenotrophomonas maltophilia, and an isolate from vegetable cowpea, subsequently identified as Burkholderia seminalis. These cultures were initially characterized for their plant growth-promoting traits at different temperature and physiological conditions. All the bacterial cultures were found promising for PGPR traits over varied temperature conditions and the optimum activity was recorded at 40°C, with tolerance to saline and drought stresses as well as wide pH and temperature ranges. A field experiment was conducted during kharif 2020 at Punjab Agricultural University, Ludhiana and Punjab Agricultural University, Regional Research Station, Bathinda, involving combinations of liquid microbial inoculants along with 100% Recommended Dose of Fertilizer (RDF). It was observed that the treatment including B. seminalis + S. maltophilia along with RDF yielded the highest green fodder and dry matter yield, In conclusion, it is evident that the utilization of these liquid microbial inoculants holds significant potential for playing a pivotal role in the integrated nutrient management of forage pearl millet, thereby contributing to heightened productivity and sustained soil health.

Exploring the low-temperature polarization and the multifield-manipulated dielectric tunability behavior of NiMn2O4

Manganese oxides with spinel structure could exhibit abundant physical effects due to the complex sublattice structure, variable valence states and the intricate roles of manganese cations in magnetic interaction. In this work, NiMn2O4 ceramic with space group of Fd3‾m is synthesized. The low-temperature polarization behavior is investigated accompanied by revealing the multi-stage dielectric relaxation. Moreover, the relaxation mechanism is confirmed through microstructure characterization, multiple-condition pyroelectric measurement and the dielectric tunability properties under electric/magnetic fields. With increasing measuring temperature, different relaxation phenomena are respectively induced by lattice distortion because of the competition among magnetic coupling interactions (below ∼135 K), electron hopping relating to the coexistence of different valence states of manganese ions (∼135–230 K), and the synergistic contribution of oxygen vacancies and domain wall effect (above ∼230 K). These results provide additional evidence for comprehensive understanding the low-temperature polarization in NiMn2O4, guiding the method design for exploring the physical origin within a wide temperature range.

Observation of Hydrostatic‐Pressure‐Modulated Giant Caloric Effect and Electronic Topological Transition

AbstractPhase transition is a fundamental phenomenon in condensed matter physics, in which states of matter transform to each other with various critical behaviors under different conditions. The magnetic martensitic transformation features significant multi‐caloric effects that benefit the solid‐state cooling or heat pumping. Meanwhile, the electronic topological transition (ETT) driven by pressure has been rarely reported in martensitic systems. Here, the modulation effects of hydrostatic pressure on phase transitions in a magnetic martensitic alloy are reported. Owing to the huge volume expansion during the transition, the martensitic transition temperature is driven from 339 to 273 K by pressure within 1 GPa, resulting in highly tunable giant baro‐ and magneto‐caloric effects (BCE and MCE) in a wide working temperature range. Interestingly, an ETT is further induced by pressure in the martensite phase, with a sudden drop of the measured saturation magnetization around 0.6 GPa. First‐principles calculations reveal a sharp change in the density of states (DOS) due to the orbit shift around the Fermi level at the same pressure and reproduce the experimental observation of magnetization. Besides, the ETT is accompanied by remarkable changes in the lattice parameters and the unit‐cell orthorhombicity. The study provides insight into pressure‐modulated exotic phase‐transition phenomena in magnetic martensitic systems.

Carbon Dots-Inked Paper with Single/Two-Photon Excited Dual-Mode Thermochromic Afterglow for Advanced Dynamic Information Encryption.

Achieving thermochromic afterglow (TCAG) in a single material for advanced information encryption remains a significant challenge. Herein, TCAG in carbon dots (CDs)-inked paper (CDs@Paper) was achieved by tuning the temperature-dependent dual-mode afterglow of room-temperature phosphorescence (RTP) and thermally activated delayed fluorescence (TADF). The CDs were synthesized through thermal treatment of levofloxacin in melting boric acid with post-purification via dialysis. CDs@Paper exhibited TCAG and excitation-dependent afterglow color properties. The TCAG of CDs@Paper exhibited dynamic color changes from blue at high temperatures to yellow at low temperatures by adjusting the proportion of the temperature-dependent TADF and phosphorescence. Notably, two-photon afterglow in CDs-based afterglow materials and time-dependent two-photon afterglow colors were achieved for the first time. Moreover, leveraging the opposite emission responses of phosphorescence and TADF to temperature, CDs@Paper demonstrated TCAG with temperature-sensing capabilities across a wide temperature range. Furthermore, a CDs@Paper-based 3D code containing color and temperature information was successfully developed for advanced dynamic information encryption. This article is protected by copyright. All rights reserved.

Smart Building Material with Near‐Infrared‐Triggered Reversible Color Switching

Smart materials and devices play an increasingly important role in improving modern life due to their richer functions, enhanced controllability, and improved biocompatibility. Herein, calcium silicate hydration (C–S–H) is integrated with layered [Co(NCS)2(pyrazine)2]n metal–organic frameworks (Co–MOF) and polymeric skeleton to fabricate the smart building material (M–C–S–H). C–S–H was anchored on the polymeric skeleton to reinforce the network structure for enhanced mechanical strength and toughness. Simultaneously, the highly porous skeleton structure enables the uniform distribution of layered Co–MOF, which could maintain its molecular form to endow the M–C–S–H with the photoresponsive color‐switching performance. The M–C–S–H as a smart building material exhibits the color change between light blue and black blue upon near‐infrared illumination on/off within a wide temperature range to achieve personalized wall and building decoration. Taking advantage of the low cost, rapid response, outstanding reversibility, and good color stability, M–C–S–H could provide lively, dynamic, and changeable decorating effects for walls and buildings.

ПРОБЛЕМЫ И МЕТОДЫ СОВЕРШЕНСТВОВАНИЯ АВТОСЦЕПНОГО УСТРОЙСТВА ГРУЗОВЫХ ВАГОНОВ С УЧЕТОМ ОСОБЕННОСТЕЙ ЭКСПЛУАТАЦИИ

The problems to operate the automatic coupling device are considered, taking into account significant changes in the operating conditions of freight cars. The operation experience of freight car automatic coupling devices of domestic railways and the United States of America is analyzed; common problematic issues are identified. Approaches to the study of modes of longitudinal-dynamic impact of cars are defined, a simplified model is given. There is a need to change the design of the automatic coupling device of freight cars by using two sequentially arranged blocks with working elements, as well as improving the properties of the working material of absorbing devices, especially in operating conditions over a wide temperature range.

High-performance and low-power consumption deep UV photodetectors based on MOCVD-grown ZnGa2O4epilayers with high temperature functionality

This work reports on the fabrication of excellent quality deep ultraviolet photodetectors (DUV PDs) based on metalorganic chemical vapor deposition (MOCVD) grown spinel ZnGa2O4 thin films on c-plane sapphire. Herein, The DUV PDs by exhibiting an ultra-low dark current of 6.69 fA and a high photo-to-dark-current ratio (PDCR) of >108 at a low-power operation of 0.2 V. While PDCR reached more than 109 on applied bias of 10 V having extremely low dark current of 37 fA. The detector revealed an ultra-high responsivity of 185 and 3.53 A/W under the exposure of 107 μW/cm2 of 245 nm wavelength at room temperature (RT) and applied bias of 10 and 0.2 V, respectively, and exhibited the record-high detectivity of the order of 1017 Jones. The temperature-dependent operation remained stable across a wide temperature range, from 27 °C to 125 °C, maintaining ultra-low dark current. The nearly constant growth and decay time of DUV PDs throughout the temperature range emphasizes the robustness and reliability of PD. The ideality factor in both DUV and dark conditions nearing unity proves the dominance of the thermionic emission mechanism. Also shows the stable and slight improved performance after a year. Therefore, these findings suggest that ZnGa2O4 is a strong contender for deep UV detection that shows robustness even at high temperatures.

Strain rate-temperature effects and constitutive models for Q690D QT steel

This paper investigates the mechanical properties of the high-strength structural steel Q690D QT (Quenched and Tempered) over a wide temperature range and a wide strain rate range. Firstly, a series of quasi-static and dynamic tests adopting the universal testing machine and Split Hopkinson Pressure Bar were carried out to investigate the mechanical properties at strain rates from 0.00025 s−1 to 5000 s−1 and temperatures from room temperature (20 °C) to 700 °C. Stress-strain curves and dynamic yield strength increase factors were extracted and investigated. Test results show that Q690D QT exhibits different strain rate effects at different temperatures, more significant at the temperatures of 600 and 700 °C, as well as the high-temperature softening effect. Dynamic strain aging effect is identified at temperatures between 300 − 600 °C for plastic strain rates of 800 s−1 and 2300 s−1, nevertheless, this effect is observed at a higher temperature range of 500–700 °C for higher plastic strain rates of 4000 s−1 and 6400 s−1. From the analysis, the adiabatic thermosoftening effect cannot be ignored when the plastic strain rates reach 4000 s−1. Finally, an improved form of the Johnson-Cook model is proposed for capturing the adiabatic temperature effects at different temperatures and validated by the test data. A parameter dynamic temperature factor is proposed to describe the comprehensive effect of strain rate, test temperature, and adiabatic thermosoftening.

Atomistic modeling of nucleation kinetics of Guinier–Preston zones in Al–Cu alloys: Two formation scenarios and prediction of the time-temperature-transformation diagram

Metastable precipitates of solute atoms, known as Guinier–Preston (GP) zones, play a significant role in the age hardening of Al–Cu alloys. In this study, we utilized the classical nucleation theory (CNT) to obtain time-temperature-transformation (TTT) diagrams for steady-state nucleation over a wide temperature range. The CNT model, which is based on atomistic simulations using artificial neural network potentials, was constructed to predict the nucleation kinetics of GP zones in the Al–Cu system with solute concentrations ranging from 1.3 to 2.5 at% (3.0 to 5.7 wt%). The nose temperature at which the steady-state nucleation time for GP zone formation is the shortest was calculated. The nose temperature increased and the minimum nucleation time decreased as the solute concentration increased. These predictions are comparable to previous theoretical results and are in good qualitative agreement with experimental observations. Furthermore, two formation scenarios of double-layer GP (GP2) zones, considering synchronous and asynchronous attachments of solute atoms to clusters, were compared in terms of nucleation efficiency. This provides new insights into the nucleation pathways of the GP2 zone in Al–Cu alloys.

A 1.65‐nW 11.14‐ppm/°C self‐biased subthreshold CMOS voltage reference with temperature compensation circuit

SummaryThis paper presents a subthreshold CMOS voltage reference (VR) that utilizes self‐biased circuits. This voltage reference includes temperature compensation circuits to expand its operating temperature range and reduce its temperature coefficient. The proposed CMOS voltage reference is designed using a standard 0.18‐μm CMOS process and has a small area of only 0.005 mm2. Post‐layout simulation results demonstrate that the power consumption of the circuit at room temperature (25°C) is only 1.65 nW at a power supply voltage of 1 V. In this case, the voltage reference output is 316.56 mV, with an average temperature coefficient (TC) of 11.14 ppm/°C in a wide temperature range from −40°C to 140°C. Furthermore, the line sensitivity (LS) of the circuit is 0.024%/V, and the power supply rejection ratio (PSRR) of the circuit is −86.5 dB at 10 Hz. In summary, the subthreshold CMOS voltage reference structure proposed in this paper demonstrates excellent performance characteristics, such as low power consumption, a small area, and high‐temperature stability. These features make it a promising candidate for voltage reference for low‐power applications with significant changes in environmental temperature.

Temperature Evolution of Composition, Thermal, Electrical and Magnetic Properties of Ti3C2Tx-MXene

MXenes are a family of two-dimensional nanomaterials. Titanium carbide MXene (Ti3C2Tx-MXene), reported in 2011, is the first inorganic compound reported among the MXene family. In the present work, we report on the study of the composition and various physical properties of Ti3C2Tx-MXene nanomaterial, as well as their temperature evolution, to consider MXenes for space applications. X-ray diffraction, thermal analysis and mass spectroscopy measurements confirmed the structure and terminating groups of the MXene surface, revealing a predominant single OH layer character. The temperature dependence of the specific heat shows a Debye-like character in the measured range of 2 K–300 K with a linear part below 10 K, characteristic of conduction electrons of metallic materials. The electron density of states (DOS) calculations for Ti3C2OH-MXene reveal a significant DOS value at the Fermi level, with a large slope, confirming its metallic character, which is consistent with the experimental findings. The temperature dependence of electrical resistivity of the MXene samples was tested for a wide temperature range (3 K–350 K) and shows a decrease on lowering temperature with an upturn at low temperatures, where negative magnetoresistance is observed. The magnetoresistance versus field is approximately linear and increases its magnitude with decreasing temperature. The magnetization curves are straight lines with temperature-independent positive slopes, indicating Pauli paramagnetism due to conduction electrons.

Air-Stable and Low-Cost High-Voltage Hydrated Eutectic Electrolyte for High-Performance Aqueous Aluminum-Ion Rechargeable Battery with Wide-Temperature Range.

Aqueous aluminum-ion batteries (AAIBs) are considered as a promising alternative to lithium-ion batteries due to their large theoretical capacity, high safety, and low cost. However, the uneven deposition, hydrogen evolution reaction (HER), and corrosion during cycling impede the development of AAIBs, especially under a harsh environment. Here, a hydrated eutectic electrolyte (AATH40) composed of Al(OTf)3, acetonitrile (AN), triethyl phosphate (TEP), and H2O was designed to improve the electrochemical performance of AAIBs in a wide temperature range. The combination of molecular dynamics simulations and spectroscopy analysis reveals that AATH40 has a less-water-solvated structure [Al(AN)2(TEP)(OTf)2(H2O)]3+, which effectively inhibits side reactions, decreases the freezing point, and extends the electrochemical window of the electrolyte. Furthermore, the formation of a solid electrolyte interface, which effectively inhibits HER and corrosion, has been demonstrated by X-ray photoelectron spectroscopy, X-ray diffraction tests, and in situ differential electrochemical mass spectrometry. Additionally, operando synchrotron Fourier transform infrared spectroscopy and electrochemical quartz crystal microbalance with dissipation monitoring reveal a three-electron storage mechanism for the Al//polyaniline full cells. Consequently, AAIBs with this electrolyte exhibit improved cycling stability within the temperature range of -10-50 °C. This present study introduces a promising methodology for designing electrolytes suitable for low-cost, safe, and stable AAIBs over a wide temperature range.

First-principles study on the structural, elastic, electronic, optical and thermophysical properties of NaNO3 and K-doped NaNO3

Abstract The present work represents the structural, electronic, elastic, and thermophysical properties of pure and K-doped NaNO3 obtained using DFT calculations. The estimated structural properties of NaNO3 correspond well with the existing reported values. Electronic characteristics such as band structure and density of statesof pure and doped NaNO3 are analyzed where the calculated band gaps for pure and K-doped NaNO3 are found to be 3.05 eV and 2.90 eV, respectively. The Berry–phase calculations carried out on both systems showed the existence of ferroelectric polarization, where an enhanced spontaneous polarization value of 36 μC/cm2 for K-doped NaNO3, as compared to 20 μC/cm2 for intrinsic NaNO3. The thermophysical properties such as bulk modulus (B0), Debye temperature (θD), and specific heat capacity (Cv) were calculated over a wide temperature range from 0K to 800 K. The linear optical properties namely the dielectric constant, refractive index, absorption coefficient, extinction coefficient and electron energy loss function are calculated in wide energy range from 0 to 30 eV and discussed in detail.

Highly Reliable Magnetic Memory-Based Physical Unclonable Functions.

Magnetic random-access memory (MRAM), which stores information through control of the magnetization direction, offers promising features as a viable nonvolatile memory alternative, including high endurance and successful large-scale commercialization. Recently, MRAM applications have extended beyond traditional memories, finding utility in emerging computing architectures such as in-memory computing and probabilistic bits. In this work, we report highly reliable MRAM-based security devices, known as physical unclonable functions (PUFs), achieved by exploiting nanoscale perpendicular magnetic tunnel junctions (MTJs). By intentionally randomizing the magnetization direction of the antiferromagnetically coupled reference layer of the MTJs, we successfully create an MRAM-PUF. The proposed PUF shows ideal uniformity and uniqueness and, in particular, maintains performance over a wide temperature range from -40 to +150 °C. Moreover, rigorous testing with more than 1584 challenge-response pairs of 64 bits each confirms resilience against machine learning attacks. These results, combined with the merits of commercialized MRAM technology, would facilitate the implementation of MRAM-PUFs.

Modeling self‐diffusion coefficients of ionic liquids using ePC‐SAFT and FVT combined with Einstein relation

AbstractThe electrolyte perturbed‐chain statistical associating fluids theory (ePC‐SAFT) coupled with free volume theory (FVT) was combined with Einstein relation, that is, ePC‐SAFT‐FVT‐E, to describe self‐diffusion coefficients (SDCs) of ionic liquids (ILs). In modeling, ePC‐SAFT was used to calculate density, while FVT parameters, determined from viscosity data, were utilized to calculate the summation of ionic SDCs through the Einstein relation with one parameter. Two strategies were employed to determine this parameter: fitting experimental data for each IL or estimating a universal parameter from van der Waals volume. Comparative analysis reveals good agreement with experimental data, with average absolute relative deviations (ARDs) of 8.14% (strategy 1) and 10.29% (strategy 2). Subsequently, cationic and anionic SDCs were reliably determined from the summation of ionic SDCs, with average ARDs of 10.80% and 10.21%, respectively. This study indicates the ePC‐SAFT‐FVT‐E model, employing viscosity‐derived parameters and three universal parameters, reliably predicts SDCs of ILs in wide temperature and pressure ranges.

Calculation of the parameters of an axial flux motor as an actuator of automotive systems

Problem. Axial flux electric motors offer several significant advantages compared to electric motors of traditional design. Currently, scientific periodicals contain numerous publications regarding the development and use of axial flux electric motors with printed windings across various fields. These include applications such as HDD-drives in computer technology, fans and pumps of various capacities, propulsion systems for bicycles and motorcycles, including in-wheel motors, manipulator drives for machine tools and industrial robots, and even within space technologies. Research confirms the high efficiency and size-to-weight ratios of axial flux motors when modern technologies are employed. However, there is little information available regarding the application of such motors in automotive electromechanical equipment. A distinctive feature of automotive electrical systems is their predominantly 12 V onboard power supply, along with high demands on size-to-weight ratios and reliability in conditions of elevated vibrations and wide temperature ranges. In this context, the development of an axial flux motor for automotive applications becomes relevant, particularly as an actuating mechanism for auxiliary systems such as window lifters, windshield wipers, air conditioning, and cooling fans, etc. Goal. The goal of the article is to determine the feasibility of using an axial flux electric motor as an actuator for automotive auxiliary systems by comparing its calculated parameters with the parameters of motors of traditional design using modern technologies and materials. Methodology. The methods and algorithms used for the calculation of electric machines take into account the characteristics and physical processes specific to axial flux machines with printed windings and permanent magnet arrays. Results. A comparison of the obtained characteristics of the designed motor with the characteristics of a modern prototype of traditional design was conducted. Based on the comparison, it was determined that the designed motor has better size-to-weight ratios while maintaining energy performance. Consequently, a conclusion was drawn about the feasibility of using electric motors with axial flux as actuators for automotive auxiliary systems. Originality. The prototype of the designed motor is considered to be a 250 W DC motor with a supply voltage of 12 V. The imposed constraint on the external diameter of the designed motor is set to 100 mm. Practical value. At the same output power and nearly identical torque, the calculated motor exhibits higher size-to-weight ratios. The weight of the calculated motor is 46% of the weight of the prototype. With an external diameter 54% larger than the prototype, the axial length of the calculated motor is 73% smaller. The mass of the calculated motor is 2.34 times smaller than the mass of the prototype.

Nonflammable Succinonitrile-Based Deep Eutectic Electrolyte for Intrinsically Safe High-Voltage Sodium-Ion Batteries.

Intrinsically safe sodium-ion batteries are considered as a promising candidate for large-scale energy storage systems. However, the high flammability of conventional electrolytes may pose serious safety threats and even explosions. Herein, a strategy of constructing a deep eutectic electrolyte is proposed to boost the safety and electrochemical performance of succinonitrile (SN)-based electrolyte. The strong hydrogen bond between S═O of 1,3,2-dioxathiolane-2,2-dioxide (DTD) and the α-H of SN endows the enhanced safety and compatibility of SN with Lewis bases. Meanwhile, the DTD participates in the inner Na+ sheath and weakens the coordination number of SN. The unique solvation configuration promotes the formation of robust gradient inorganic-rich electrode-electrolyte interphase, and merits stable cycling of half-cells in a wide temperature range, with a capacity retention of 82.8% after 800 cycles (25°C) and 86.3% after 100 cycles (60°C). Correspondingly, the full cells deliver tremendous improvement in cycling stability and rate performance.

Turning Ultra-Low Coercivity and Ultra-High Temperature Stability Within 897 K via Continuous Crystal Ordering Fluctuations.

High-performance soft magnetic materials are important for energy conservation and emission reduction. One challenge is achieving a combination of reliable temperature stability, high resistivity, high Curie temperature, and high saturation magnetization in a single material, which often comes at the expense of intrinsic coercivity-a typical trade-off in the family of soft magnetic materials with homogeneous microstructures. Herein, a nanostructured FeCoNiSiAl complex concentrated alloy is developed through a hierarchical structure strategy. This alloy exhibits superior soft magnetic properties up to 897K, maintaining an ultra-low intrinsic coercivity (13.6 A m-1 at 297 K) over a wide temperature range, a high resistivity (138.08µΩcm-1 at 297K) and the saturation magnetization with only a 16.7% attenuation at 897 K. These unusual property combinations are attributed to the dual-magnetic-state nature with exchange softening due to continuous crystal ordering fluctuations at the atomic scale. By deliberately controlling the microstructure, the comprehensive performance of the alloy can be tuned and controlled. The research provides valuable guidance for the development of soft magnetic materials for high-temperature applications and expands the potential applications of related functional materials in the field of sustainable energy.

Direct Observation of Covalently Bound Clusters in Resonantly Stabilized Radical Reactions and Implications for Carbonaceous Particle Growth.

Based on quantum mechanically guided experiments that observed elusive intermediates in the domain of inception that lies between large molecules and soot particles, we provide a new mechanism for the formation of carbonaceous particles from gas-phase molecular precursors. We investigated the clustering behavior of resonantly stabilized radicals (RSRs) and their interactions with unsaturated hydrocarbons through a combination of gas-phase reaction experiments and theoretical calculations. Our research directly observed a sequence of covalently bound clusters (CBCs) as key intermediates in the evolution from small RSRs, such as benzyl (C7H7), indenyl (C9H7), 1-methylnaphthyl (1-C11H9), and 2-methylnaphthyl (2-C11H9), to large polycyclic aromatic hydrocarbons (PAHs) consisting of 28 to 55 carbons. We found that hydrogen abstraction and RSR addition drive the formation and growth of CBCs, leading to progressive H-losses, the generation of large PAHs and PAH radicals, and the formation of white smoke (incipient carbonaceous particles). This mechanism of progressive H-losses from CBCs (PHLCBC) elucidates the crucial relationship among RSRs, CBCs, and PAHs, and this study provides an unprecedentedly seamless path of observed assembly from small RSRs to large nanoparticles. Understanding the PHLCBC mechanism over a wide temperature range may enhance the accuracy of multiscale models of soot formation, guide the synthesis of carbonaceous nanomaterials, and deepen our understanding of the origin and evolution of carbon within our galaxy.

Regulation of Dipolar‐Dipolar and Ion‐Dipolar Interactions Simultaneously in Strong Solvating Electrolytes for All‐Temperature Zinc‐Ion Batteries

Regulation of Dipolar‐Dipolar and Ion‐Dipolar Interactions Simultaneously in Strong Solvating Electrolytes for All‐Temperature Zinc‐Ion Batteries