Realization of Fine-Tuning the Lattice Thermal Conductivity and Anharmonicity in Layered Semiconductors via Entropy Engineering.

Entropy engineering is widely proven to be effective in achieving ultra-low thermal conductivity for well-performed thermoelectric and heat management applications. However, no strong correlation between entropy and lattice thermal conductivity is found until now, and the fine-tuning of thermal conductivity continuously via entropy-engineering in a wide entropy range is still lacking. Here, a series of high-entropy layered semiconductors, Ni1- x(Fe0.25Co0.25Mn0.25Zn0.25)xPS3, where 0 ≤ x < 1, with low mass/size disorder is designed. High-purity samples with mixing configuration entropy of metal atomic site in a wide range of 0-1.61R are achieved. Umklapp phonon-phonon scattering is found to be the dominating phonon scattering mechanism, as revealed by the linear T-1 dependence of thermal conductivity. Meanwhile, fine tuning of the lattice thermal conductivity via continuous entropy engineering at metal atomic sites is achieved, in an almost linear dependence in middle-/high- entropy range. Moreover, the slope of the κ - T-1 curve reduces with the increase in entropy, and a linear response of the reduced Grüneisen parameter is revealed. This work provides an entropy engineering strategy by choosing multiple metal elements with low mass/size disorder to achieve the fine tuning of the lattice thermal conductivity and the anharmonic effect.

Effects of ß-Si3N4 Seeds on Microstructure and Performance of Si3N4 Ceramics in Semiconductor Package.

Among the various ceramic substrate materials, Si3N4 ceramics have demonstrated high thermal conductivity, good thermal shock resistance, and excellent corrosion resistance. As a result, they are well-suited for semiconductor substrates in high-power and harsh conditions encountered in automobiles, high-speed rail, aerospace, and wind power. In this work, Si3N4 ceramics with various ratios of α-Si3N4 and ß-Si3N4 in raw powder form were prepared by spark plasma sintering (SPS) at 1650 °C for 30 min under 30 MPa. When the content of ß-Si3N4 was lower than 20%, with the increase in ß-Si3N4 content, the ceramic grain size changed gradually from 1.5 µm to 1 µm and finally resulted in 2 µm mixed grains. However, As the content of ß-Si3N4 seed crystal increased from 20% to 50%, with the increase in ß-Si3N4 content, the ceramic grain size changed gradually from 1 µm and 2 µm to 1.5 µm. Therefore, when the content of ß-Si3N4 in the raw powder is 20%, the sintered ceramics exhibited a double-peak structure distribution and the best overall performance with a density of 97.5%, fracture toughness of 12.1 MPa·m1/2, and a Vickers hardness of 14.5 GPa. The results of this study are expected to provide a new way of studying the fracture toughness of silicon nitride ceramic substrates.

Design and Preparation of CNTs/Mg Layered Composites.

In order to effectively solve the problem of strength and ductility mismatch of magnesium (Mg) matrix composites, carbon nanotubes (CNTs) are added as reinforcement. However, it is difficult to uniformly disperse CNTs in a metal matrix to form composites. In this paper, electrophoretic deposition (EPD) was used to obtain layered units, and then the CNTs/Mg layered units were sintered by spark plasma sintering to synthesize layered CNTs/Mg composites. The deposition morphology of the layered units obtained by EPD and the microstructure, damping properties, and mechanical properties of the composite material were analyzed. The results show that the strength and ductility of the composite sample sintered at 590 °C were improved compared with the layered pure Mg and the composite sample sintered at 600 °C. Compared with pure Mg, the composites rolled by 40% had a much higher strength but no significant decrease in ductility. The damping properties of the CNTs/Mg composites were tested. The damping-test-temperature curve (tanδ~T) rose gradually with increasing temperature in the range of room temperature to 350 °C, and two internal friction peaks appeared. The damping properties of the tested composites at room temperature decreased with increasing frequency. The layered structure of the CNTs/Mg had ultra-high strengthening efficiency and maintained its ductility. The layered units prepared by EPD can uniformly disperse the CNTs in the composites.

Effect of Al Addition on Microstructure and Properties of CoCrNi Medium-Entropy Alloy Prepared by Powder Metallurgy.

Powder metallurgy possesses the advantages of low energy consumption, less material consumption, uniform composition, and near-final forming. In order to improve the mechanical properties and high-temperature oxidation resistance of CoCrNi medium-entropy alloy (MEA), CoCrNiAlX (X = 0, 0.1, 0.3, 0.5, 0.7) MEAs were prepared using mechanical alloying (MA) and spark-plasma sintering (SPS). The effect of aluminum content on the microstructure and properties of the MEAs was investigated. The results show that the CoCrNi MEA is composed of face center cubic (fcc) phase and some carbides (Cr23C6). With the increase in Al content, there exists Al2O3 precipitation. When the Al content is increased to Al0.5 and Al0.7, the body center cubic (bcc) phase begins to precipitate. The addition of aluminum significantly enhances the properties of the alloys, especially those containing fcc+bcc dual-phase solid solutions. The yield strength, compressive strength, and hardness of CoCrNiAl0.7 alloy are as high as 2083 MPa, 2498 MPa, and 646 HV, respectively. The high-temperature resistance also reaches the oxidation resistance level. Different oxides include Cr2O3, Al2O3, and (Co, Ni) Cr2O4 and NiCrO3 spinel oxides formed on the surface of alloys. The formation of an Al2O3 oxidation film prevents the further erosion of the matrix by oxygen elements.

Cost-Effective, High-Yield Production of Biotemplated Catalytic Tubular Micromotors as Self-Propelled Microcleaners for Water Treatment.

Micro/nano-motors (MNMs) that combine attributes of miniaturization and self-propelled swimming mobility have been explored for efficient environmental remediation in the past decades. However, their progresses in practical applications are now subject to several critical issues including a complicated fabrication process, low production yield, and high material cost. Herein, we propose a biotemplated catalytic tubular micromotor consisting of a kapok fiber (KF, abundant in nature) matrix and manganese dioxide nanoparticles (MnO2 NPs) deposited on the outer and inner walls of the KF and demonstrate its applications for rapid removal of methylene blue (MB) in real-world wastewater. The fabrication is straightforward via dipping the KF into a potassium permanganate (KMnO4) solution, featured with high yield and low cost. The distribution and amount of MnO2 can be easily controlled by varying the dipping time. The obtained motors are actuated and propelled by oxygen (O2) bubbles generated from MnO2-triggered catalytic decomposition of hydrogen peroxide (H2O2), with the highest speed at 615 µm/s (i.e., 6 body length per second). To enhance decontamination efficacy and also enable magnetic navigation/recycling, magnetite nanoparticles (Fe3O4 NPs) are adsorbed onto such motors via an electrostatic effect. Both the Fe3O4-induced Fenton reaction and hydroxyl radicals from MnO2-catalyzed H2O2 decomposition can account for the MB removal (or degradation). Results of this study, taken together, provide a cost-effective approach to achieve high-yield production of the MNMs, suggesting an automatous microcleaner able to perform practical wastewater treatment.

On the Microstructure and Mechanical Properties of CrNx/Ag Multilayer Films Prepared by Magnetron Sputtering.

CrNx/Ag multilayer coatings and a comparative CrNx single layer were deposited via reactive magnetron sputtering. In multilayer coatings, the thickness of each CrNx layer was constant at 60 nm, while that of the Ag layer was adjusted from 3 to 10 nm. Microstructure of the films was characterized by X-ray diffraction and transmission electron spectroscopy. The results suggest that the film containing 3 nm of Ag layer presents a nanocomposite structure comprising fine nano-grains and quasi-amorphous clusters. With Ag layer thickness reaching 4.5 nm and above, Ag grains coalesce to produce continuous an Ag layer and exhibit (111) preferential crystallization. Hardness of the films was detected by nanoindentation and it reveals that with increasing the Ag layer thickness, the hardness continuously decreases from 30.2 to 11.6 GPa. Wear performance of the films was examined by the ball-on-disk test at 500 °C. The result suggests that the out-diffusion of Ag towards film surface contributes to the friction reduction, while the wear performance of films depends on the thickness of the Ag layer.