Na 3 V 2 (PO 4 ) 3 (denoted as NVP) has been considered as a promising cathode material for room temperature sodium ion batteries. Nevertheless, NVP suffers from poor rate capability resulting from the low electronic conductivity. Here, the feasibility to approach high rate capability by designing carbon-coated NVP nanoparticles confi ned into highly ordered mesoporous carbon CMK-3 matrix (NVP@C@CMK-3) is reported. The NVP@C@CMK-3 is prepared by a simple nanocasting technique. The electrode exhibits superior rate capability and ultralong cyclability (78 mA h g −1 at 5 C after 2000 cycles) compared to carbon-coated NVP and pure NVP cathode. The improved electrochemical performance is attributed to double carbon coating design that combines a variety of advantages: very short diffusion length of Na + /e − in NVP, easy access of electrolyte, and short transport path of Na + through carbon toward the NVP nanoparticle, high conductivity transport of electrons through the 3D interconnected channels of carbon host. The optimum design of the core-shell nanostructures with double carbon coating permits fast kinetics for both transported Na + ions and electrons, enabling high-power performance.

We show that simply converting the hydrophobic moiety of an antimicrobial peptide (AMP) or synthetic mimic of AMPs (SMAMP) into a hydrophilic one could be a different pathway toward membrane-active antimicrobials preferentially acting against bacteria over host cells. Our biostatistical analysis on natural AMPs indicated that shorter AMPs tend to be more hydrophobic, and the hydrophilic-and-cationic mutants of a long AMP experimentally demonstrated certain membrane activity against bacteria. To isolate the effects of antimicrobials' hydrophobicity and systematically examine whether hydrophilic-and-cationic mutants could inherit the membrane activity of their parent AMPs/SMAMPs, we constructed a minimal prototypical system based on methacrylate-based polymer SMAMPs and compared the antibacterial membrane activity and hemolytic toxicity of analogues with and without the hydrophobic moiety. Antibacterial assays showed that the hydrophobic moiety of polymer SMAMPs consistently promoted the antibacterial activity but diminished in effectiveness for long polymers, and the resultant long hydrophilic-and-cationic polymers were also membrane active against bacteria. What distinguished these long mutants from their parent SMAMPs were their drastically reduced hemolytic toxicities and, as a result, strikingly enhanced selectivity. Similar toxicity reduction was observed with the hydrophilic-and-cationic mutants of long AMPs. Taken together, our results suggest that long hydrophilic-and-cationic polymers could offer preferential membrane activity against bacteria over host cells, which may have implications in future antimicrobial development.

Due to the volatility of P2S5, the ambient pressure synthesis of Li2S + P2S5 (LPS) has been limited to planetary ball-milling (PBM). To utilize PBM of LPS to generate a solid electrolyte (SE), the as-synthesized powder sample must be pressed into pellets, and as such the presence of as-pressed grain boundaries in the SE cannot be avoided. To eliminate the grain boundaries, LPS doped with SiS2 has been studied because SiS2 lowers the vapor pressure of the melt and promotes strong glass formation, which in combination allows for greater ease in synthesis. In this work, we have examined the structures and electrochemical properties of lithium thiosilicophosphate 0.6Li2S + 0.4­[xSiS2 + 1.5­(1 – x)­PS5/2], 0 ≤ x ≤ 1, glassy solid electrolytes (GSEs) prepared by both PBM and melt-quenching (MQ). It is shown that the critical current density improved after incorporating SiS2, reaching 1.5 mA/cm2 for the x = 0.8 composition. However, the interfacial reaction of MQ GSE with lithium metal introduced microcracks, which shows that further research is needed to explore and develop more stable GSE compositions. These fundamental results can help to understand the interface reaction and formation and as such can provide a guide to design improved homogeneous GSEs with SiS2 as a glass former, which have no grain boundaries and thereby may help suppress lithium dendrite formation.

While much of the current research on glassy solid electrolytes (GSEs) has focused on the binary Li 2 S + P 2 S 5 system, compositions with Si are of interest because Si promotes stronger glass formation and allows low-cost melt-quenching (MQ) synthesis under ambient pressure. Another advantage is that they can be formed in homogeneous and continuous glass forms, as a result they are free of grain boundaries. In this work, we have examined the structures and electrochemical properties of bulk glass pieces of sulfide and oxy-sulfide GSE compositions and have also expanded the study by using LiPON glass as a dopant to produce an entirely new class of nitrogen doped mixed oxy-sulfide nitride (MOSN) GSEs. Upon doping with oxygen and nitrogen, the solid electrolyte interface (SEI) is stabilized and the doped MOSN GSE exhibits a critical current density (CCD) of 1.8 mA cm À 2 at 100 °C. We also report on improving the glass quality, the SEI engineering and its limitations, and future plans of improving the electrochemical performance of these homogeneous MQ MOSN GSEs. These fundamental results can help to understand the structures and doping effects of the bulk GSEs, and as such can provide a guide to design improved homogeneous grain-boundary-free GSEs.