材料科学
碳化
化学工程
阳极
水热碳化
热液循环
碳纤维
间苯二酚
产量(工程)
钠
微观结构
复合材料
有机化学
扫描电子显微镜
化学
复合数
电极
工程类
冶金
物理化学
作者
Liewen Guo,Chuang Qiu,Renlu Yuan,Xiaotian Li,Xin Li,K Li,Wanxiong Zhu,Xue‐Wei Liu,Ang Li,Haiyan Liu,Xiaohong Chen,Huaihe Song
标识
DOI:10.1021/acsami.4c04101
摘要
Phenolic resin (PF) is considered a promising precursor of hard carbon (HC) for advanced-performance anodes in sodium-ion batteries (SIBs) because of its facile designability and high residual carbon yield. However, understanding how the structure of PF precursors influences sodium storage in their derived HC remains a significant challenge. Herein, the microstructure of HC is controlled by the degree of cross-linking of resorcinol-benzaldehyde (RB) resin. We reveal that robust molecular cross-linking in RB resin induced by hydrothermal treatment promotes closed-pore formation in the derived HC. The mechanism is devised for the decomposition of a highly cross-linked RB three-dimensional network into randomly stacked short-range graphitic microcrystals during high-temperature carbonization, contributing to the abundant closed pores in the derived HC. In addition, the high cross-linking degree of RB resin endows its derived HC with a small-sized spherical morphology and large interlayer spacing, which improves the rate performance of HC. Consequently, the optimized hydrothermal treatment HC anode shows a higher specific capacity of 372.7 mAh g
科研通智能强力驱动
Strongly Powered by AbleSci AI