Influences of Ultrafine Ti(C, N) on the Sintering Process and Mechanical Properties of Micron Ti(C, N)-Based Cermets.

For investigating the influence mechanism underlying ultrafine Ti(C, N) within micron Ti(C, N)-based cermets, three cermets including diverse ultrafine Ti(C, N) contents were employed. In addition, for the prepared cermets, their sintering process, microstructure, and mechanical properties were systematically studied. According to our findings, adding ultrafine Ti(C, N) primarily affects the densification and shrinkage behavior in the solid-state sintering stage. Additionally, material-phase and microstructure evolution were investigated under the solid-state stage from 800 to 1300 °C. Adding ultrafine Ti(C, N) enhanced the diffusion and dissolution behavior of the secondary carbide (Mo2C, WC, and (Ta, Nb)C) under a lower sintering temperature of 1200 °C. Further, as sintering temperature increased, adding ultrafine Ti(C, N) enhanced heavy element transformation behaviors in the binder phase and accelerated solid-solution (Ti, Me) (C, N) phase formation. When the addition of ultrafine Ti(C, N) reached 40 wt%, the binder phase had increased its liquefying speed. Moreover, the cermet containing 40 wt% ultrafine Ti(C, N) displayed superb mechanical performances.

Microstructure and Tribo-Behavior of WC-Cr3C2-Ni Coatings by Laser Cladding and HVAF Sprayed: A Comparative Assessment.

SK5 steel is the base material used for the preparation of the wrinkle scraper, whose service life strongly affects the working efficiency and economic benefits. In this work, WC-Cr3C2-Ni coating was deposited on the SK5 steel substrate by using High-velocity air fuel spray (HVAF) and Laser cladding (LC) processes respectively, named HVAF-WC coating and LC-WC coating. The microstructure and wear resistance of both coatings were analyzed, and were compared with the substrate sample. Results showed that the coatings were adhesive well onto the substrate. More WC with fine crystals is retained in HVAF-WC coating due to low flame flow temperature, while WC of LC-WC coating is characterized by columnar crystals. The wear rate of HVAF-WC and LC-WC coating was 4.00 × 10-7 mm3/(N•m) and 3.47 × 10-6 mm3/(N•m), respectively, which was two and one orders of magnitude lower than SK5 steel with 3.54 × 10-5 mm3/Nm. HVAF-WC coating exhibited the best wear resistance because of significant fine grain strengthening, which wear mechanism is mainly dominated by abrasive wear. Thus, it was thought that HVAF-WC coating is more effective ways to improve the wear resistance of SK5 steel, comparing with LC-WC coating.

Cube-like anatase TiO2 mesocrystals as effective electron-transporting materials toward high-performance perovskite solar cells.

Electron-transporting materials (ETMs) with higher carrier mobility and a suitable band gap structure play a significant role in determining the photovoltaic performance of perovskite solar cells (PSCs). Herein, cube-like mesoporous single-crystal anatase TiO2 (Meso-TiO2) nanoparticles synthesized by using a facile hydrothermal method were utilized as an efficient ETM for PSCs. The superior semiconducting properties of the Meso-TiO2 based ETM enabled the best power conversion efficiency (PCE) of 20.05% for a PSC. Moreover, the device retained 80% of its initial PCE after being stored in ambient conditions for 20 days under 25 ± 5% relative humidity. In contrast to the commercial TiO2 ETM, the Meso-TiO2 ETM based PSC showed a distinguished interface with better interfacial conditions and improved carrier extraction originating from the cube-like mesoporous single-crystal anatase TiO2 ETM.

Fabrication of La2O3 Uniformly Doped Mo Nanopowders by Solution Combustion Synthesis Followed by Reduction under Hydrogen.

This work reports the preparation of La2O3 uniformly doped Mo nanopowders with the particle sizes of 40⁻70 nm by solution combustion synthesis and subsequent hydrogen reduction (SCSHR). To reach this aim, the foam-like MoO2 precursors (20⁻40 nm in size) with different amounts of La2O3 were first synthesized by a solution combustion synthesis method. Next, these precursors were used to prepare La2O3 doped Mo nanopowders through hydrogen reduction. Thus, the content of La2O3 used for doping can be accurately controlled via the SCSHR route to obtain the desired loading degree. The successful doping of La2O3 into Mo nanopowders with uniform distribution were proved by X-ray photon spectroscopy and transmission electron microscopy. The preservation of the original morphology and size of the MoO2 precursor by the La2O3 doped Mo nanopowders was attributed to the pseudomorphic transport mechanism occurring at 600 °C. As shown by X-ray diffraction, the formation of Mo2C impurity, which usually occurs in the direct H2 reduction process, can be avoided by using the Ar calcination-H2 reduction process, when residual carbon is removed by the carbothermal reaction during Ar calcination at 500 °C.

Microwave Deposition of Palladium Catalysts on Graphite Spheres and Reduced Graphene Oxide Sheets for Electrochemical Glucose Sensing.

This work outlines a synthetic strategy inducing the microwave-assisted synthesis of palladium (Pd) nanocrystals on a graphite sphere (GS) and reduced graphene oxide (rGO) supports, forming the Pd catalysts for non-enzymatic glucose oxidation reaction (GOR). The pulse microwave approach takes a short period (i.e., 10 min) to fast synthesize Pd nanocrystals onto a carbon support at 150 °C. The selection of carbon support plays a crucial role in affecting Pd particle size and dispersion uniformity. The robust design of Pd-rGO catalyst electrode displays an enhanced electrocatalytic activity and sensitivity toward GOR. The enhanced performance is mainly attributed to the synergetic effect that combines small crystalline size and two-dimensional conductive support, imparting high accessibility to non-enzymatic GOR. The rGO sheets serve as a conductive scaffold, capable of fast conducting electron. The linear plot of current response versus glucose concentration exhibits good correlations within the range of 1-12 mM. The sensitivity of the Pd-rGO catalyst is significantly enhanced by 3.7 times, as compared to the Pd-GS catalyst. Accordingly, the Pd-rGO catalyst electrode can be considered as a potential candidate for non-enzymatic glucose biosensor.