法拉第效率
微观结构
阳极
材料科学
碳化
电解质
碳纤维
化学工程
高原(数学)
电化学
吸附
复合材料
纳米技术
电池(电)
储能
密度泛函理论
堆积密度
作者
Abdul Mateen,Tongde Wang,Zidong Zhou,Abdul Jabbar Khan,Shengyuan Deng,Zhihao Bao
摘要
ABSTRACT Hard carbon (HC) is recognized as a viable anode candidate for sodium‐ion batteries (SIBs), its widespread adoption is frequently restricted by low reversible capacity, poor initial Coulombic efficiency (ICE) and inferior rate performance. Herein, a mechanical pretreatment technique, followed by carbonization, is presented to modify the microstructure of basswood‐derived HC for excellent Na + storage performance. The mechanical processing followed by carbonization of basswood transforms its biopolymer structure into a HC with smaller pseudo‐graphitic domains, increased closed porosity, and wider interlayer spacing compared to the untreated samples. This distinctive microstructure enhances low‐voltage plateau Na + storage and accelerates reaction kinetics. This microstructure design delivers three benefits; high‐rate Na + transport, consistent (de)intercalation, and minimized undesirable electrolyte decomposition. The optimized HC sample demonstrates a substantial reversible capacity of 324 mAh g −1 at 0.1 C, an exceptional ICE of 94.1%, impressive rate performance of 238.8 mAh g −1 at 10 C, and remarkable capacity retention of 84.24% after 500 cycles. Density functional theory simulations demonstrate improved Na+ adsorption energies and charge distribution in the modified carbon framework, supporting rapid ion movement and higher electrochemical stability.
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