A covalent organic framework as a dual-active-center cathode for a high-performance aqueous zinc-ion battery.

Organic electrode materials have shown significant potential for aqueous Zn ion batteries (AZIBs) due to their flexible structure designability and cost advantage. However, sluggish ionic diffusion, high solubility, and low capacities limit their practical application. Here, we designed a covalent organic framework (TA-PTO-COF) generated by covalently bonding tris(4-formylbiphenyl)amine (TA) and 2,7-diaminopyrene-4,5,9,10-tetraone (PTO-NH).

Elastic MXene conductive layers and electrolyte engineering enable robust potassium storage.

The precisely engineered structures of materials greatly influence the manifestation of their properties. For example, in the process of alkali metal ion storage, a carefully designed structure capable of accommodating inserted and extracted ions will improve the stability of material cycling. The present study explores the uniform distribution of self-grown carbon nanotubes to provide structural support for the conductive and elastic MXene layers of TiCT-Co@NCNTs.

Enhanced cycling stability and rate capability of a graphene-supported commercialized Vat Blue 4 anode for advanced Li-ion batteries.

Commercialized Vat Blue 4 (VB4) has attracted more attention as a promising anode for large-scale applications in Li-ion batteries (LIBs) due to its high electrochemical activity, low price, and large-scale production. However, its moderate solubility results in severe capacity decay and low utilization of active components. Herein, we present a graphene-supported VB4 composite (VB4/rGO) prepared by a facile sonication and hydrothermal process for long cycling stability and high-rate capability.