ABSTRACT
Hydrogen prepared by electrocatalytic decomposition of water ("green hydrogen") has the advantages of high energy density and being clean and pollution-free, which is an important energy carrier to face the problems of the energy crisis and environmental pollution. However, the most used commercial electrocatalysts are based on expensive and scarce precious metals and their alloy materials, which seriously restricts the large-scale industrial application of hydrogen energy. The development of efficient non-precious metal electrocatalysts is the key to achieving the sustainable development of the hydrogen energy industry. Transition metal sulfides (TMS) have become popular non-precious metal electrocatalysts with great application potential due to their large specific surface area, unique electronic structure, and rich regulatory strategies. To further improve their catalytic activities for practical application, many methods have been tried in recent years, including control of morphology and crystal plane, metal/nonmetal doping, vacancy engineering, building of self-supporting electrocatalysts, interface engineering, etc. In this review, we introduce firstly the common types of TMS and their preparation. Additionally, we summarize the recent developments of the many different strategies mentioned above for efficient water electrolysis applications. Furthermore, the rationales behind their enhanced electrochemical performances are discussed. Lastly, the challenges and future perspectives are briefly discussed for TMS-based water dissociation catalysts.
ABSTRACT
Hot deformation at elevated temperature is essential to densify particle-reinforced aluminum matrix composites (AMCs) and improve their performance. However, hot deformation behavior of the AMCs is sensitive to the variation of hot-processing parameters. In this paper, optimal processing parameters of dual-scale SiCp/A356 composites were determined to explore the control strategy of the microstructure. Hot-compression tests were conducted at temperatures ranging from 460 to 520 °C under strain rates from 0.01 to 5 s-1. Constitutive equation and processing maps were presented to determine the hot-processing parameters. Microstructure evolution of the dual-scale SiCp/A356 composites was analyzed. The strain rate of 0.62-5 s-1 and deformation temperature of 495-518 °C is suitable for the hot processing. The number of dynamic recrystallization (DRX) grains in the "safe" domains is larger and the dislocation density is lower compared to those of instability domains. DRX grains mainly occurred around SiC particles. The presence of SiC particles can promote effectively the DRX nucleation, which results in the dynamic softening mechanism of the dual-scale SiCp/A356 composites being dominated by DRX.
ABSTRACT
In this paper, molybdenum (Mo) thin films are deposited on soda-lime glass (SLG) substrates by direct current magnetron sputtering and heated in three different modes at different temperatures, including substrate heating, annealing treatment, and both substrate heating and annealing treatment. The effects of heating temperature and heating mode on the structures, morphology, optical and electrical properties of Mo thin films were systematically investigated by X-ray diffraction (XRD), Scanning electron microscopy (SEM), atomic force microscope (AFM) and UV-visible spectrophotometer (UV-vis spectra). It is shown that as the substrate and annealing temperature increase, the crystallinity of Mo thin films is improved, and the grain sizes become bigger. Especially in the mode of both substrate heating and annealing treatment at higher temperature, the obtained Mo thin films show higher crystallinity and conductivity. Moreover, with the increase of substrate and annealing temperature in different heating modes, both the surface compactness of Mo films and the optical reflectance increase correspondingly. Furthermore, the Mo film, prepared at the substrate heating temperature of 400 °C and annealed at 400 °C, showed excellent comprehensive performance, and the resistivity is as low as 1.36 × 10-5 Ω·cm. Using this optimized Mo thin film as an electrode, copper indium gallium selenium (CIGS) solar cells have a maximum photo-conversion efficiency of 12.8%.
