RESUMO
The use of porous hard carbons (PHCs) as electrode materials in sodium-ion batteries has great potential; however, the exposure of large surface areas to electrolyte flow results in irregular and irreversible solid electrolyte interfaces (SEIs), leading to deteriorated ionic and electronic mobility and inferior initial Coulombic efficiency (ICE). These issues can be addressed through suitable structural modifications of PHC materials. Herein, the integration of high-surface-area PHCs with carbon nanofibers (CNFs) was accomplished by a simple electrospinning technique, which resulted in a uniform and reversible SEI layer. In the meantime, the CNFs' mesh provided connectivity and conductivity in the as-integrated electrodes, whereas PHCs offered fast diffusion kinetics and high Na+ ion storage capacity. Additionally, PHC integration with CNFs demonstrated an excellent ICE of 77% and a specific capacity of 505 mAh/g at 25 mA/g. Furthermore, the conjugated microstructure also provided flexibility and stability to the electrode (260 mAh/g after 500 cycles). This remarkable synergy may promote the development of free-standing, flexible, and highly porous properties in a single material for advanced energy storage applications.
RESUMO
A facile one-step sonochemical activation method is utilized to fabricate biomass-derived 3D porous hard carbon (PHC-1) with tuned-surface and is compared with the conventional two-step activation method. As raw biomass offers good KOH impregnation, ultrasonication power diffuses both K+ and OH- ions deep into its interior, creating various nanopores and attaching copious functional groups. In contrast, conventional activation lacks these features under the same carbonization/activation parameters. The high porosity (1599 m2/g), rich functional groups (O = 8.10%, N = 0.95%), and well-connected nanoporous network resulting from sonochemical activation, remarkably increased specific capacity, surface wettability, and electrode stability, consequently improved electrochemical performance. Benefiting from its suitable microstructure, PHC-1 possesses superior specific capacity (330 mAh/g at 20 mA/g), good capacity retention (89.5%), and excellent structural stability over 500 sodiation/desodiation cycles at high current density (1000 mA/g). Apart from modus operandi comparison, the two activation methods also provide mechanistic insights as the low-voltage plateau region and graphitic layers decrease simultaneously. This work suggests a scalable and economical approach for synthesizing large-scale activated porous carbons that are used in various applications, be it energy storage, water purification, or gas storage, to name a few.
