RESUMO
Deleterious volumetric expansion and poor electrical conductivity seriously hinder the application of Si-based anode materials in lithium-ion batteries (LIBs). Herein, boron-doped three-dimensional (3D) porous carbon framework/carbon shell encapsulated silicon (B-3DCF/Si@C) hybrid composites are successfully prepared by two coating and thermal treatment processes. The presence of 3D porous carbon skeleton and carbon shell effectively improves the mechanical properties of the B-3DCF/Si@C electrode during the cycling process, ensures the stability of the electrical contacts of the silicon particles and stabilizes the solid electrolyte interface (SEI) layer, thus enhancing the electronic conductivity and ion migration efficiency of the anode. The developed B-3DCF/Si@C anode has a high reversible capacity, excellent cycling stability and outstanding rate performance. A reversible capacity of 1288.5 mAh/g is maintained after 600 cycles at a current density of 400 mA g-1. The improved electrochemical performance is demonstrated in a full cell using a LiFePO4-based cathode. This study presents a novel approach that not only mitigates the large volume expansion effects in LIB anode materials, but also provides a reference model for the preparation of porous composites with various functionalities.
RESUMO
The safety issues caused by sodium dendrites limit the widespread application of sodium metal batteries. Herein, a self-healing polymer electrolyte (SPE) is prepared by immersing the self-healing polymer in a liquid electrolyte. Benefiting from the self-healing properties, elastic interface, and dense nonporous structure of the SPE, the fabricated NaK|MC SPE|NaK symmetric battery presents a long battery life (â¼590 h) and low polarization voltage (192 mV). Moreover, the PTCDA|MC SPE|NaK full cell also delivers stable long cycles and outstanding rate performance.
