Near-room Temperature Research Articles

Pressureless joining of soda lime silicate glass using polysilazane-derived silica at near-room temperature

Perhydropolysilazane (PHPS) pre-ceramic polymer was used to join soda lime silicate glass at temperatures below 200°C under pressureless conditions. The results show that: (i) the junction material is largely converted to silica at 100°C and fully converted to glass at 150°C; (ii) the samples treated at room temperature and 100°C show a perfectly dense and clean bond, whereas porosity develops starting from 150°C as a result of the hydrolysis reactions and solvent evaporation; (iii) a maximum tensile bond strength of about 5-6 MPa is obtained after treatments at 100°C. Remarkably, after treatment at 500°C, the junction remains intact. These preliminary findings provide the first successful attempt regarding the use of PHPS as a joining material to produce inorganic and transparent bonds for glass at relatively low temperatures.

SURG-58. COLD ATMOSPHERIC PLASMA (CAP) CAUSES SELECTIVE TUMOR CELL DEATH VIA APOPTOSIS AND FERROPTOSIS IN MALIGNANT GLIOMA CELLS

Abstract BACKGROUND High-grade gliomas (HGGs) are primary brain tumors associated with significant morbidity and mortality, and despite advances in neuro-oncology, the prognosis remains poor. Cold atmospheric plasma, a novel experimental anti-cancer therapeutic tool, is a near-room temperature ionized gas generated at atmospheric pressure. It has many promising results in vitro and in vivo with a variety of cancers. CAP cytotoxicity appears to be selective to cancer cells without significant damage to surrounding healthy tissues. We aim to evaluate the efficacy of CAP in generating tumor-selective cytotoxicity against high-grade glioma. METHODS B16, U87, GL261, patient derived high grade glioma, human neural stem cells (LM-NSC008) and astrocytes (NHA hTERT) were treated with CAP. Proliferation and propidium iodide (PI)/annexin V flow cytometry assays were employed to quantify cytotoxicity, cell cycle phases and apoptosis. Cells were pre-treated with ferroptosis inhibitors Ferrostatin-1 and Deferoxamine (DFO) in rescue assays. Cerebral organoids were transplanted with fluorescent tumor cell lines and stained with cleaved caspase-3, ki67 and transferrin receptor. RESULTS CAP induces dose dependent cell death in all glioma cell lines tested. CAP induces an accumulation of intracellular ROS, most prominent in glioma cells. CAP-mediated cell death involves apoptosis and ferroptosis. CAP selectively leads to apoptosis in tumor implanted organoids and leads to decreased proliferation in malignant and non-malignant cells. CAP leads to a shift into G0 phase of all treated cells, malignant and non-malignant. CONCLUSIONS CAP treatment induces dose-dependent increases in ROS and apoptosis in HGG lines tested more significantly than in NHAs and hNSCs. CAP induces decreased proliferation and G0 phase cell cycle arrest in all CAP-treated cells. CAP-mediated cytotoxicity was significantly mitigated with DFO pre-treatment in HGG cells, suggesting that ferroptosis plays a critical role in the mechanism of CAP treatment in HGG. CAP led to selective glioma cell death in tumor implanted cerebral organoids.

Selective Hydrogenation of Furfural Under Mild Conditions Over Single-Atom Pd1/α-MoC Catalyst.

The selective activation of C=O bonds was the key challenge in the field of biomass utilization. Researchers worked on this purpose by developing high-active and high-selective catalysts. In this study, a Pd1/α-MoC single-atom catalyst was synthesized and applied in selective hydrogenation of biomass-derived furfural with 96.7 % conversion and 92.4 % selectivity under a near-room temperature. With various characterizations, the formation of Pd single-atom sites over the surface of α-MoC was confirmed. Then, the dominant structure of Pd single-atom site and the reaction pathway were proposed with experimental and Density Functional Theory (DFT) studies. Compared with undecorated α-MoC, the introduction of Pd single-atom species significantly altered the reaction mechanism from Meerwein-Ponndorf-Verley (MPV) process. Moreover, the Pd single-atoms loading on α-MoC(111) surface notably reduced the energy barriers of H2 activation and C=O bond hydrogenation, which may lead to the improving catalytic performance of α-MoC based catalyst. Hence, this investigation could provide a new strategy and understanding for the development of high-active and low-cost catalysts.

Large Room-Temperature Electrocaloric Effect in Lead-Free Relaxor Ferroelectric Ceramics with Wide Operation Temperature Range.

In order to obtain large room-temperature electrocaloric effect (ECE) and wide operation temperature range simultaneously in lead-free ceramics, we proposed designing a relaxor ferroelectric with a Tm (the temperature at which the maximum dielectric permittivity is achieved) near-room temperature and glass addition. Based on this strategy, we designed and fabricated lead-free 0.76NaNbO3-0.24BaTiO3 (NN-24BT) ceramics with 1wt.% BaO-B2O3-SiO2 glass addition, which showed distinct relaxor ferroelectric characteristics with strongly diffused phase transition and a Tm near-room temperature. Based on a direct measurement method, a large ΔT (adiabatic temperature change) of 1.3 K was obtained at room temperature under a high field of 11.0 kV mm-1. Additionally, large ECE can be maintained (>0.6 K@6.1 kV mm-1) over a broad temperature range from 23 °C to 69 °C. Moreover, the ECE displayed excellent cyclic stability with a variation in ΔT below ±7% within 100 test cycles. The comprehensive ECE performance is significantly better than other lead-free ceramics. Our work provides a general and effective approach to designing lead-free, high-performance ECE ceramics, and the approach possesses the potential to be utilized to improve the ECE performance of other lead-free ferroelectric ceramic systems.

6-Hydroxy Picolinohydrazides Promoted Cu(I)-Catalyzed Hydroxylation Reaction in Water: Machine-Learning Accelerated Ligands Design and Reaction Optimization.

Hydroxylated (hetero)arenes are privileged motifs in natural products, materials, small-molecule pharmaceuticals and serve as versatile intermediates in synthetic organic chemistry. Herein, we report an efficient Cu(I)/6-hydroxy picolinohydrazide-catalyzed hydroxylation reaction of (hetero)aryl halides (Br, Cl) in water. By establishing machine learning (ML) models, the design of ligands and optimization of reaction conditions were effectively accelerated. The N-(1,3-dimethyl-9H- carbazol-9-yl)-6-hydroxypicolinamide (L32, 6-HPA-DMCA) demonstrated high efficiency for (hetero)aryl bromides, promoting hydroxylation reactions with a minimal catalyst loading of 0.01 mol % (100 ppm) at 80 °C to reach 10000 TON; for substrates containing sensitive functional groups, the catalyst loading needs to be increased to 3.0 mol % under near-room temperature conditions. N-(2,7-Di-tert-butyl-9H-carbazol-9-yl)-6-hydroxypicolinamide (L42, 6-HPA-DTBCA) displayed superior reaction activity for chloride substrates, enabling hydroxylation reactions at 100 °C with 2-3 mol % catalyst loading. These represent the state of art for both lowest catalyst loading and temperature in the copper-catalyzed hydroxylation reactions. Furthermore, this method features a sustainable and environmentally friendly solvent system, accommodates a wide range of substrates, and shows potential for developing robust and scalable synthesis processes for key pharmaceutical intermediates.

Novel screen-printed ceramic MEMS microhotplate for MOS sensors

We developed a new approach to the fabrication of MEMS substrates for MOS gas sensors. This full screen-printing process is based on the application of sacrificial material, which is solid at the near-room temperature of printing and turns to powder after the firing of the elements of the sensor. Therefore, this sacrificial material can be removed from under the suspended elements of the MEMS structure in ultrasonic bath. The glass-ceramic MEMS is a cantilever structure equipped with a Pt-based microheater made of Pt resistive material with sheet resistance of about 4 Ohm/square fabricated using core-shell technology. It is located at the end edge of the cantilever and is isolated from the contacts to the sensing layer by glass-ceramic insulation. Screen-printing provides cheap fabrication, robustness and low power (∼120 mW@450°C) of the sensing element. The functionality of the microhotplate was checked using ZnO nanomaterial deposited by microextruder, it demonstrated high response and selectivity of ZnO material to NO2 (response 41.6 at 200°C for 10 ppm).

Machine learning-aided design of LaCe(Fe,Mn,Si)13H-type magnetocaloric materials for room-temperature applications

La(Fe,Si)13 magnetocaloric materials have attracted extensive attention in recent years due to their excellent magnetocaloric properties and low price. In this study, we established and compared several machine models and used a support vector machine for predicting the influences of different element contents on the Curie temperature. Based on the results predicted by the machine learning model, a series of fully hydrogenated materials (La1.1-xCexFe13-y-zMnySizHF, y≈0.3–0.5x, z=1.1, 1.3, 1.5) with Curie temperatures between 290 and 310 K were designed. After material screening, a material with an element composition of La0.66Ce0.44Fe11.4Mn0.1Si1.5HF was proven to have good room temperature magnetocaloric properties, with a Curie temperature of 301 K, magnetic entropy change of 11.3 J/kgK under a 0–2 T magnetic field, and a relative cooling power of 119.3 J/kg, which performs well in the existing La(Fe,Si)13-type materials that can be applied near room temperature. This work not only deepens researchers' understanding of machine learning-aided design of materials with specific application environment restrictions but also greatly accelerates the design of near-room temperature La(Fe,Si)13 magnetocaloric materials.

Self-aligned shadow masking for antimony telluride growth: Novel advancements in single-leg thermoelectric array design

In the present study, a fabrication technique using self-aligned shadow masking was employed to create a state-of-art thermoelectric single-leg array of Antimony telluride (Sb2Te3) thin film via thermal evaporation technique. The thermoelectric (TE) performance of the array was evaluated using an in-house developed measurement setup. The TE characteristics of the developed p-type Sb2Te3 based TEGs with single-leg configurations, having 5-TE legs, exhibits a highest Power factor (PF) of ∼5173 μW/mK2 at RT along with thermoelectric voltage generation of 70 mV. As compared to planar configuration these segmented single-leg array-based TEG of Sb2Te3 exhibit higher efficiency (∼10 %) under a near-ambient temperature gradient. Also, the 3ω-method is utilized to assess the thermal conductivity of fabricated thin films of Sb2Te3, yielding a value of 0.41 Wm⁻1K⁻1. Furthermore, these thermoelectric generators (TEGs) showcase their versatility across various applications, efficiently harnessing near-room temperature waste heat from a range of sources such as tea coasters, the human body, and gas cookstoves into useable energy near room temperature.

Defect and dopant complex mediated high power factor in transparent selenium-doped copper iodide thin films

Copper iodide (CuI) is a promising p-type transparent thermoelectric material for near-room temperature energy harvesting. We report a high-power factor for selenium (Se)-doped CuI films. Ion beam-sputtered CuI films were doped using 30 keV 80Se+ implantation with Se concentration varying between 0.50% and 6.50%. Hall effect measurements showed a ∼34% increase in electrical conductivity (σ ≈ 36.1 Ω−1cm−1) due to a ∼54% increase in carrier density (pH ≈ 5.4 × 1019 cm−3) in the p-type γ-CuI film implanted with 5.0 × 1014 Se.cm−2. A high Seebeck coefficient, α ≈ 388.9 μVK−1−1, and moderate electrical conductivity, σ ≈ 29.1 Ω−1cm−1, yield a nearly 85% increase in the power factor, α2σ ≈ 439.7 μWm−1K−2, for a 1.0 × 1015 Se.cm−2 implanted film compared to the unimplanted film (α2σ ≈ 236.4 μWm−1K−2). Monte Carlo simulation and ab initio density functional theory calculations revealed that the increased displacement per atom values and the {SeI−VCu} defect complex-induced shallow acceptor could be attributed to the observed increase in hole density. Our results highlight that native defects and defect complexes are beneficial for enhancing the power factor in transparent CuI for thermoelectric applications.

High-energy, high-peak-power diode-pumped Q-switched Tm:YAG laser at 2.02 μm with tunable repetition rate from 100 Hz to 1000 Hz

A high-energy, high-peak-power Q-switched Tm:YAG laser at 2.02 μm with a tunable repetition rate from 100 Hz to 1000 Hz and pulse duration in the hundreds of nanoseconds is demonstrated. The high energy output was achieved by employing a thermally stable linear cavity, including two compact laser diode continuous-wave side-pumped Tm:YAG laser modules. For Q-switched operation, stable Q-switched performance from 100 Hz to 1000 Hz was realized at near-room temperature. At a repetition rate of 100 Hz, the laser delivered a maximum pulse energy of 215 mJ with a pulse duration of 124.4 ns, resulting in a peak power of up to 1.73 MW. When the repetition rate was tuned to 200 Hz, 500 Hz, and 1000 Hz, pulse energies of 212 mJ, 125.6 mJ, and 68.2 mJ were obtained, with pulse durations of 133.6 ns, 176.3 ns, and 262 ns, respectively. To the best of our knowledge, these results represent the highest single pulse energies and peak powers ever accomplished for a diode-pumped Q-switched Tm-doped 2 μm laser operating at high repetition rates exceeding 100 Hz.

High cooling and power generation performance of α-MgAgSb with intrinsic low lattice thermal conductivity

α-MgAgSb is a promising near-room temperature thermoelectric material, characterized by its intrinsically low lattice thermal conductivity, a feature attributed to the significant atomic mass contrast and complex crystal structure. In this work, we achieved respective zTavg values of 0.58 in the temperature range of 150–300 K and 1.22 in the range of 300–550 K for α-MgAgSb, indicating exceptional potential for both cooling and power generation applications. Additionally, through the reduction of cross-sectional size, the stability of MgAgSb/Ag interface was enhanced under high temperature, which is crucial for the practical application of thermoelectric module. To verify the property of α-MgAgSb material, a 7-pair MgAgSb/Bi2Te3 module was fabricated, demonstrating a maximum cooling temperature difference ΔTmax of 60 K at hot-side temperature of 300 K and a power generation efficiency ηmax of 7.2 % with ΔT of 275 K. This work paves the way for the application of Mg-based thermoelectric materials.

Semiconductor fibers for textile integrated electronic systems.

The near-room temperature resistance transition in the Lu-H-N compound is repeatedly reproduced, which is clarified to originate from a metal-to-semiconductor/insulator transition rather than superconductivity.

Giant Deformation Induced Staggered-Layer Structure Promoting the Thermoelectric and Mechanical Performance in n-Type Bi2(Te, Se)3.

Bismuth telluride has long been recognized as the most promising near-room temperature thermoelectric material for commercial application; however, the thermoelectric performance for n-type Bi2(Te, Se)3-based alloys is far lagging behind that of its p-type counterpart. In this work, a giant hot deformation (GD) process is implemented in an optimized Bi2Te2.694Se0.3I0.006+3 wt%K2Bi8Se13 precursor and generates a unique staggered-layer structure. The staggered-layered structure, which is only observed in severely deformed crystals, exhibits a preferential scattering on heat-carrying phonons rather than charge-carrying electrons, thus resulting in an ultralow lattice thermal conductivity while retaining high-weight carrier mobility. Moreover, the staggered-layer structure is located adjacent to the van der Waals gap in Bi2(Te, Se)3 lattice and is able to strengthen the interaction between anion layers across the gap, leading to obviously improved compressive strength and Vickers hardness. Consequently, a high peak figure of merit ZT of ≈ 1.3 at 423 K, and an average ZT of ≈ 1.2 at 300-473 K can be achieved in GD sample. This study demonstrates that the GD process can successfully decouple the electrical and thermal transports with simultaneously enhanced mechanic performance.

Mechanical effects of Cr and V substitutions in AlFe2B2 by first-principles calculations

MAB phase AlFe2B2 has attracted a lot of attention as a ternary transition metal boride with layered structure due to its near-room temperature magneto-caloric effect (MCE), composed of earth-abundant elements and other properties. In this work the electronic structure, chemical bonding characteristics, mechanical stability, elastic properties, and elastic anisotropy of AlFe2B2-based compounds (borides) have been investigated using first-principles calculations based on density functional theory (DFT). The substitution effect of transition metals (TM) Cr and V in AlFe(2-x)TMxB2 (x = 0–1), (TM = Cr, V) compounds have been investigated. It was determined that all the elements added instead of the removed Fe element in the borides increased the mechanical properties such as hardness, brittleness, and isotropy. Moreover, it has been observed that hardness, brittleness, and isotropy increase with the increasing amount of the fourth alloying element. In AlFe(2-x)TMxB2, it has been observed that for x = 0.25 and 0.5 values, V causes an increase in stiffness more than Cr; however, for x = 1, while the increase in Cr continues to have an effect, a reverse trend is observed for V. Additionally, it has been observed that an increase in isotropy is significantly more influenced by Cr than by V. Among borides, it has been determined that AlFeCrB2 exhibits the highest elastic moduli (bulk, shear, and Young's modulus), hardness, and isotropy.

Near-Room Temperature Magnetocaloric Effect and Critical Exponent Analysis in Mn4.8Cu0.2Ge3 Compound

Near-Room Temperature Magnetocaloric Effect and Critical Exponent Analysis in Mn4.8Cu0.2Ge3 Compound

Lattice Plainification Leads to High Thermoelectric Performance of P-Type PbSe Crystals.

Thermoelectrics has applications in power generation and refrigeration. Since only commercial Bi2Te3 has a low abundance Te, PbSe gets attention. This work enhances the near-room temperature performance of p-type PbSe through enhancing carrier mobility via lattice plainification. Composition controlled and Cu-doped p-type PbSe crystals are grown through physical vapor deposition. Results exhibit an enhanced carrier mobility ≈2578cm2V-1s-1 for Pb0.996Cu0.0004Se. Microstructure characterization and density functional theory calculations verify the introduced Cu atoms filled Pb vacancies, realizing lattice plainification and enhancing the carrier mobility. The Pb0.996Cu0.0004Se sample achieves a power factor ≈42µWcm-1K-2 and a ZT ≈ 0.7 at 300K. The average ZT of it reaches ≈0.9 (300-573K), resulting in a single-leg power generation efficiency of 7.1% at temperature difference of 270K, comparable to that of p-type commercial Bi2Te3. A 7-pairs device paired the p-type Pb0.996Cu0.0004Se with the n-type commercial Bi2Te3 shows a maximum cooling temperature difference ≈42K with the hot side at 300K, ≈65% of that of the commercial Bi2Te3 device. This work highlights the potential of p-type PbSe for power generation and refrigeration near room temperature and hope to inspire researchers on replacing commercial Bi2Te3.

The Sensitizing Effect of Enhanced NO2 Gas Sensing at Near-Room Temperature Using Pd-Decorated VO2 Nanowires

The Sensitizing Effect of Enhanced NO2 Gas Sensing at Near-Room Temperature Using Pd-Decorated VO2 Nanowires

Synthesis and enhanced room-temperature thermoelectric properties of CuO-MWCNT hybrid nanostructured composites.

This work presents the synthesis of novel copper oxide-multiwalled carbon nanotube (CuO-MWCNT) hybrid nanostructured composites and a systematic study of their thermoelectric performance at near-room temperatures as a function of MWCNT wt% in the composite. The CuO-MWCNT hybrid nanostructured composites were synthesized by thermal oxidation of a thin metallic Cu layer pre-deposited on the MWCNT network. This resulted in the complete incorporation of MWCNTs in the nanostructured CuO matrix. The thermoelectric properties of the fabricated CuO-MWCNT composites were compared with the properties of CuO-MWCNT networks prepared by mechanical mixing and with the properties of previously reported thermoelectric [CuO]99.9[SWCNT]0.1 composites. CuO-MWCNT hybrid composites containing MWCNTs below 5 wt% showed an increase in the room-temperature thermoelectric power factor (PF) by ∼2 times compared with a bare CuO nanostructured reference thin film, by 5-50 times compared to mixed CuO-MWCNT networks, and by ∼10 times the PF of [CuO]99.9[SWCNT]0.1. The improvement of the PF was attributed to the changes in charge carrier concentration and mobility due to the processes occurring at the large-area CuO-MWCNT interfaces. The Seebeck coefficient and PF reached by the CuO-MWCNT hybrid nanostructured composites were 688 μV K-1 and ∼4 μW m-1 K-2, which exceeded the recently reported values for similar composites based on MWCNTs and the best near-room temperature inorganic thermoelectric materials such as bismuth and antimony chalcogenides and highlighted the potential of CuO-MWCNT hybrid nanostructured composites for applications related to low-grade waste heat harvesting and conversion to useable electricity.

Stabilization of Fast Lithium-ionic Conduction Phase of Nanaoconfined LiBH4 for Lithium Metal Solid-State Batteries

Nanoconfined LiBH4 into mesoporous Al2O3 as a fast lithium-ion conductor is presented that its high-temperature phase can be kept at near-room temperature. It exhibits an excellent electrochemical stability and Li+...

Near-room temperature ferromagnetism and a tunable anomalous Hall effect in atomically thin Fe4CoGeTe2.

Itinerant ferromagnetism at room temperature is a key factor for spin transport and manipulation. Here, we report the realization of near-room temperature itinerant ferromagnetism in Co doped Fe5GeTe2 thin flakes. The ferromagnetic transition temperature TC (∼323 K-337 K) is almost unchanged when the thickness is as low as 12 nm and is still about 284 K at 2 nm (bilayer thickness). Theoretical calculations further indicate that the ferromagnetism persists in monolayer Fe4CoGeTe2. In addition to the robust ferromagnetism down to the ultrathin limit, Fe4CoGeTe2 exhibits an unusual temperature- and thickness-dependent intrinsic anomalous Hall effect. We propose that it could be ascribed to the dependence of the band structure on thickness that changes the Berry curvature near the Fermi energy level subtly. The near-room temperature ferromagnetism and tunable anomalous Hall effect in atomically thin Fe4CoGeTe2 provide opportunities to understand the exotic transport properties of two-dimensional van der Waals magnetic materials and explore their potential applications in spintronics.