NiCo LDH nanozymes with selective antibacterial activity against Gram-negative bacteria for wound healing.

Bacterial infections have been a major threat to human health. Especially, Gram-negative (G-) bacterial infections have been an increasing problem worldwide. The overuse of antibiotics leads to an emergence of drug resistance, and thus the development of novel antimicrobial agents is important, particularly against G- bacteria. Nanozymes use reactive oxygen species (ROS) to kill bacteria, reducing the risk of bacterial resistance and providing new opportunities to meet the challenges of strain selectivity. Here, we synthesized NiCo layered double hydroxide (LDH) nanozymes, which exhibit selective antibacterial activity based on their peroxide-like (POD-like) activity. To obtain the highest antibacterial activity, the POD-like activity of NiCo LDH nanozyme was further optimized by tuning the ratio of nickel and cobalt, and Ni4Co6 LDHs showed the highest POD activity and antibacterial activity. More importantly, Ni4Co6 LDHs can achieve selective sterilization of G- bacteria due to their electrostatic adsorption and hydrophilic interactions with the bacterial cell wall. Animal experiments further indicated that the healing of G- bacteria-infected wounds was effectively promoted without damaging their normal biological tissues. In conclusion, we provide a selective antibacterial agent through a simple strategy, which provides a new direction for the application of nanozymes.

Nylon-Based Composite Gel Membrane Fabricated via Sequential Layer-by-Layer Electrospinning for Rechargeable Lithium Batteries with High Performance.

With the raw materials of poly(vinylidene-co-hexafluoropropylene) (P(VDF-HFP)) and polyamide 6 (PA6, nylon 6), a sandwich-structured composite membrane, PA6/P(VDF-HFP)/PA6, is fabricated via sequential layer-by-layer electrospinning. The nylon-based composite exhibits high absorption to organic liquid electrolyte (270 wt%) owing to its high porosity (90.35%), good mechanical property (17.11 MPa), and outstanding shut-down behavior from approximately 145 to 230 °C. Moreover, the dimensional shrink of a wet PA6 porous membrane immersed into liquid electrolyte is cured due to the existence of the P(VDF-HFP) middle layer. After swelling by the LiPF6-based organic liquid electrolyte, the obtained PA6/P(VDF-HFP)/PA6-based gel polymer electrolytes (GPE) shows high ionic conductivity at room temperature (4.2 mS cm-1), a wide electrochemical stable window (4.8 V), and low activation energy for Li+ ion conduction (4.68 kJ mol-1). Benefiting from the precise porosity structure made of the interlaced electrospinning nanofibers and the superior physicochemical properties of the nylon-based composite GPE, the reversible Li+ ion dissolution/deposition behaviors between the GPE and Li anode are successfully realized with the Li/Li symmetrical cells (current density: 1.0 mA cm-2; areal capacity: 1.0 mAh cm-2) proceeding over 400 h at a polarization voltage of no more than 70 mV. Furthermore, the nylon-based composite GPE in assembled Li/LiFePO4 cells displays good electrochemical stability, high discharge capacity, good cycle durability, and high rate capability. This research provides a new strategy to fabricate gel polymer electrolytes via the electrospinning technique for rechargeable lithium batteries with good electrochemical performance, high security, and low cost.