Core-shell meso/microporous carbon host for sulfur loading toward applications in lithium-sulfur batteries

Lithium-sulfur（Li-S） batteries belong to one of the promising technologies for high-energy-density rechargeable batteries.However,sulfur cathodes suffer from inherent problems of its poor electronic conductivity and the shuttling of highly dissoluble lithium polysulfides generated during the cycles.Loading sulfur into porous carbons has been proved to be an effective approach to alleviate these issues.Mesoporous and microporous carbons have been widely used for sulfur accommodation,but mesoporous carbons have poor sulfur confinement,whereas microporous carbons are impeded by low sulfur loading rates.Here,a core-shell carbon,combining both the merits of mesoporous carbon with large pore volume and microporous carbon with effective sulfur confinement,was prepared by coating the mesoporous CMK-3 with a microporous carbon（MPC） shell and served as the carbon host（CMK-3 @MPC） to accommodate sulfur.After sulfur infusion,the as-obtained S/（CMK-3@MPC） cathode delivered a high initial capacity of up to 1422 mAh·g-1 and sustained 654 mAh·g-1 reversible specific capacity after 36 cycles at 0.1 C.The good performance is ascribed to the unique core-shell structure of the CMK-3@MPC matrix,in which sulfur can be effectively confined within the meso/microporous carbon host,thus achieving simultaneously high electrochemical utilization.

Plasma Modified Polypropylene Membranes as the Lithium-Ion Battery Separators

To reduce the thermal shrinkage of the polymeric separators and improve the safety of the Li-ion batteries,plasma treatment and plasma enhanced vapor chemical deposition（PECVD）of SiO_x-like are carried out on polypropylene（PP）separators,respectively.Critical parameters for separator properties,such as the thermal shrinkage rate,porosity,wettability,and mechanical strength,are evaluated on the plasma treated PP membranes.O_2 plasma treatment is found to remarkably improve the wettability,porosity and electrolyte uptake.PECVD SiO_x-like coatings are found to be able to effectively reduce the thermal shrinkage rate of the membranes and increase the ionic conductivity.The electrolyte-philicity of the Si Ox-like coating surface can be tuned by the varying O_2 content in the gas mixture during the deposition.Though still acceptable,the mechanical strength is reduced after PECVD,which is due to the plasma etching.

Tubes with coated and sintered porous surface for highly efficient heat exchangers

Surface modification is a direct and effective way to enhance the efficiency of heat exchangers. Surface modification by forming a microporous coated layer can greatly enhance the boiling heat transfer and thus achieve a high performance. In this paper, we systematically investigate the boiling behavior on a plain surface with/ without sintered microporous coatings of copper powder. The results demonstrated that the sintered surface has a better performance in nucleate boiling due to the increased nucleation sites. The superheat degree is lower and the bubble departure diameter is larger for the sintered surface than for the plain surface, so the heat can be carried away more efficiently on the sintered surface. In addition, the heat transfer capacity on the sintered surface depends on both the powder size and the coating thickness for a high flux tube. The optimum heat transfer capacity can be obtained when the thickness of the microporous coating layer is 3-5 times of the sintered powder diameter. As a result, the heat transfer coefficient tube can be up to 3 times higher for the tube with a sintered surface than that with a plain surface, showing a pronounced enhancement in heat transfer and a high potential in chemical engineering industry application.