Local Electric Field Promoted Kinetics and Interfacial Stability of a Phosphorus Anode with Ionic Covalent Organic Frameworks

A phosphorus anode is a promising option for energy-storage applications because of its high theoretical specific capacity and safe lithiation potential. However, the multiphase phosphorus lithiation/delithiation reactions and soluble reaction intermediates cause sluggish reaction kinetics and loss of active materials. Herein, a novel local electric field (LEF) strategy is proposed to inhibit the intermediates dissolution and promote the reaction kinetics by optimizing ionic covalent organic frameworks (iCOFs). Among them, the LEF induced by the cationic covalent organic framework effectively enhances the electrochemical performance of the phosphorus anode. The strong electrostatic interaction between the polyphosphides and cationic covalent organic framework confines the dissolution of active materials and tailors the electronic structure of polyphosphides to accelerate the reaction kinetics. The cationic covalent-organic-framework-assisted phosphorus anode provides a high capacity of 1227.8 mAh g(-1) at 10.4 A g(-1) (8.6 C) and a high-capacity retention of 87% after 500 cycles at 1.3 A g(-1). This work not only broadens the application of iCOFs for phosphorus anode but also inspires the great potential of the local electric field in battery technology.

Automated summary

This study proposes a novel local electric field strategy to improve the reaction kinetics and minimize the loss of active materials in phosphorus anode. By optimizing ionic covalent organic frameworks, the introduction of local electric field restricts the dissolution of active materials and accelerates the reaction kinetics. The experimental results show that this strategy significantly enhances the electrochemical performance and capacity retention of the phosphorus anode.