RESUMO
Zinc metal is widely considered as the primary option for constructing various aqueous batteries due to its cost-effectiveness, safety, and environmental friendliness. However, the Zn anode continues to be plagued by parasitic reactions and dendrite growth in aqueous electrolytes, limiting the practical implementation of zinc ion batteries (ZIBs) for large-scale energy storage. Herein, a foveolate ZnTe nanoarray is developed as a protective layer to enhance the chemical reversibility during Zn plating/stripping. The semi-conductive ZnTe with excellent ionic conductivity and hydrophobicity can effectually prevent the corrosion reactions, hydrogen generation and dendritic growth on the surface of the Zn anode. As a result, the Zn@ZnTe symmetrical cells achieve ultrahigh cycling stability (over 2800 h at 2 mA cm-2 and 1 mA h cm-2) and simultaneously deliver a low voltage hysteresis of 28 mV. Additionally, the durable Zn@ZnTe//V2O5 cells exhibit a remarkable capacity retention of 96.7% after 3000 cycles, surpassing that of the Zn//V2O5 cells. This work provides a straightforward and low-cost strategy to regulate the interface chemistry of the Zn anode, which may open a way for the development of practical ZIBs.
RESUMO
Cordycepin exhibits various bio-activities, including anticancer, antibacterial, antiviral and immune regulation activities, and is a significant focus of research. However, the preparation of high-purity cordycepin remains challenging. Also, the molecular target with which cordycepin interacts to cause an antibacterial effect remains unknown. In the present study, cordycepin was prepared by preparative high-performance liquid chromatography (prep-HPLC) and the purity obtained was 99.6%, indicating that this technique may be useful for the large-scale isolation of cordycepin in the future. The results of computational molecular docking analysis indicated that the interaction energy between cordycepin and NAD+-dependent DNA ligase (LigA) was lower than that between cordycepin and other common antibacterial targets. The highly pure cordycepin obtained by prep-HPLC demonstrated inhibitory activity against LigA from various bacteria in vitro. In conclusion, cordycepin may be useful as a broad-spectrum antibiotic targeting LigA in various bacteria.
RESUMO
Two new compounds, (3R)-5,6,7-trihydroxy-3-isopropyl-3-methylisochroman-1-one (1) and rhamnocitrin-3-O-ß-glucopyranosyl-4'-O-ß-galactosyl-(1 --> 3)-glucopyranoside (2), were isolated from the whole plants of Selaginella moellendorffii Hieron. Their structures were determined by spectroscopic methods Additionally, compound 1 could inhibit the proliferation of HT29 cells through inducing cell apoptosis.