Accelerating Sulfur Redox Chemistry by Atomically Dispersed Zn-N4 Sites Coupled with Pyridine-N Defects on Porous Carbon Sheets.

Single-atom catalysts (SACs) with specific N-coordinated configurations immobilized on the carbon substrates have recently been verified to effectively alleviate the shuttle effect of lithium polysulfides (LiPSs) in lithium-sulfur (Li─S) batteries. Herein, a versatile molten salt (KCl/ZnCl2 )-mediated pyrolysis strategy is demonstrated to fabricate Zn SACs composed of well-defined Zn-N4 sites embedded into porous carbon sheets with rich pyridine-N defects (Zn─N/CS). The electrochemical kinetic analysis and theoretical calculations reveal the critical roles of Zn-N4 active sites and surrounding pyridine-N defects in enhancing adsorption toward LiPS intermediates and catalyzing their liquid-solid conversion. It is confirmed by reducing the overpotential of the rate-determining step of Li2 S2 to Li2 S and the energy barrier for Li2 S decomposition, thus the Zn─N/CS guarantees fast redox kinetics between LiPSs and Li2 S products. As a proof of concept demonstration, the assembled Li─S batteries with the Zn─N/CS-based sulfur cathode deliver a high specific capacity of 1132 mAh g-1 at 0.1 C and remarkable capacity retention of 72.2% over 800 cycles at 2 C. Furthermore, a considerable areal capacity of 6.14 mAh cm-2 at 0.2 C can still be released with a high sulfur loading of 7.0 mg cm-2 , highlighting the practical applications of the as-obtained Zn─N/CS cathode in Li─S batteries.

One-step synthesis of core shell cellulose-silica/n-octadecane microcapsules and their application in waterborne self-healing multiple protective fabric coatings.

Exploiting water-based fabric coatings outfitted with multiple protections (e.g., waterproofness, ultraviolet (UV) resistance and thermal insulation) are urgently demanded. Nevertheless, achieving the multifunction and durability poses the major challenge. In the present study, novel multifunctional cellulose/silica hybrid microcapsules were developed by one-step emulsion-solvent diffusion; these microcapsules were well dispersed into waterborne silicone resins to form waterborne multiple protective fabric coatings. Since the encapsulated phase change materials were in the core of capsules, and the hydrophobic coupling reagent and UV absorber were grafted onto the silicas in the shell of capsules, these fabric coatings exhibited high superhydrophobicity, UV protection and thermal insulation. Moreover, because hydrophobic coupling reagent and UV absorber in the shell-cellulose of capsules exhibited easy mobility, the fabric coatings displayed self-repairability of superhydrophobicity and UV protection even after being damaged chemically or mechanically. The fabric coating presented in this study could have a range of applications, covering special protective fabric, high-altitude garments as well as self-cleaning materials.