Study on Boiling Heat Transfer Characteristics of Composite Porous Structure Fabricated by Selective Laser Melting.

Surface porosity is an important means of enhancing boiling heat transfer. In this paper, two kinds of composite porous structures of surface micropore + square channel and framework micropore + square channel were prepared by selective laser melting technology using AlSi10Mg as the powder material. The effect of composites with different pore forms on boiling heat transfer was investigated in pool boiling experiments. It was found that controlling the thickness of the powder layer manufactured by selective laser melting can change the surface roughness of the sample, and the sandblasting treatment reduced the surface roughness of the samples. The average heat transfer coefficient of the rough surface composite porous structure sample was increased by 40% compared to the sandblasted sample. The micropores on the surface of the sample and inside the framework significantly enhanced the heat transfer coefficient of the composite porous structure. The presence of surface micropores increased the heat transfer area and the vaporization core density of the composite porous structure and exhibited excellent heat transfer coefficient improvement in the low heat flux region. The framework microporous composite porous structure can form effective gas-liquid diversion at high heat flux and obtain higher heat transfer performance. The large channel in the composite porous structure is the key control factor of the critical heat flux.

Surface Defect Engineering of a Bimetallic Oxide Precatalyst Enables Kinetics-Enhanced Lithium-Sulfur Batteries.

Developing efficient electrocatalysts to accelerate the sluggish conversion of lithium polysulfides (LiPSs) is of paramount importance for improving the performances of lithium-sulfur (Li-S) batteries. However, a consensus has not yet been reached on the in situ evolution of the electrocatalysts as well as the real catalytic active sites. Herein, defective MnV2O6 (D-MVO) is designed as a precatalyst toward LiPSs' adsorption and conversion. We reveal that the introduction of surface V defects can effectively accelerate the in situ sulfurization of D-MVO during the electrochemical cycling process, which acts as the real electrocatalyst for LiPSs' retention and catalysis. The in situ-sulfurized D-MVO demonstrates much higher electrocatalytic activity than the defect-free MVO toward LiPSs' redox conversion. With these merits, the Li-S batteries with D-MVO separators achieve superior long-term cycling performance with a low decay rate of 0.056% per cycle after 1000 cycles at 1C. Even under an elevated sulfur loading of 5.5 mg cm-2, a high areal capacity of 4.21 mAh cm-2 is still retained after 50 cycles at 0.1C. This work deepens the cognition of the dynamic evolution of the electrocatalysts and provides a favorable strategy for designing efficient precatalysts for advanced Li-S batteries using defect engineering.