材料科学
法拉第效率
阳极
堆积
微观结构
碳纤维
电解质
化学工程
吸收(声学)
透射电子显微镜
纳米技术
合理设计
工作(物理)
扫描透射电子显微镜
反应性(心理学)
氧气
乙醚
氧化还原
中子衍射
高原(数学)
析氧
曲率
扩展X射线吸收精细结构
钠
密度泛函理论
化学物理
作者
Yufei He,Da Liu,Zeyu Zhu,Qinyu Li,Shengnan He,Yuanguang Xia,Wen Yin,Zhijun Wu,Xusheng Zheng,Hongge Pan,Renbing Wu
标识
DOI:10.1002/adfm.202529699
摘要
ABSTRACT Hard carbon (HC) is a promising anode material for sodium‐ion batteries (SIBs), yet the role of oxygen‐containing functional groups (OFGs) in shaping its structure and performance remains unclear. In this study, we systematically investigate the influence of OFGs on the microstructure and sodium storage behavior of HC. The combined X‐ray absorption near‐edge structure (XANES), neutron total scattering, and high‐resolution transmission electron microscopy (HRTEM) investigations reveal that carbonyl (C═O) and carboxyl (COOH) groups contribute to the curvature and dense stacking of graphitic‐like layers, promoting closed‐pore formation and enhancing plateau capacity. Meanwhile, the ether bond (C─O─C) is positively correlated with the lateral growth of graphitic domains ( L a ). Accordingly, an optimal OFG configuration consisting of low C─O─C content, moderate levels of C═O, and high COOH concentration enables a favorable balance between reversible capacity and initial Coulombic efficiency (ICE). This work provides new insights into the role of oxygen in HC and establishes a compositional and structural framework for the rational design of high‐performance HC anodes for next‐generation SIBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI