有孔小珠
材料科学
粒子(生态学)
钠
碳纳米纤维
化学工程
离子
超短脉冲
碳纤维
纳米纤维
纳米技术
化学
复合材料
工程类
冶金
碳纳米管
有机化学
光学
物理
地质学
激光器
海洋学
复合数
作者
Xin Luo,Xueyan Wu,Yanchun Pei,Yan Lv,Rui Xue,Chunmei Ma,Chan Liu,Jixi Guo
标识
DOI:10.1021/acsanm.4c06192
摘要
Antimony (Sb) exhibits excellent conductivity and reactivity with sodium ions, which can be attributed to its distinctive puckered layer structure. Additionally, it has the potential to achieve a high theoretical capacity of 660 mAh g–1 through the formation of Na3Sb. However, the significant volume expansion (approximately 390%) that occurs during the charging process restricts its practical applications. To tackle these challenges, we developed a fast Joule heating technique to successfully ultrafast construct Sb nanoparticles into the bead-like structure of N,S-codoped asphalt-based carbon fibers (N/S-CNF). This unique bead-like structure effectively inhibits the volume expansion of the metal during the charging and discharging process. In addition, the 1D carbon nanofibers contribute to the formation of a robust electrode framework and enable fast electron transfer during cycling to facilitate the kinetics. These advantages together contribute to the excellent cycling stability and rate performance of self-supported Sb@N/S-CNF nanocomposites used as anode materials for sodium-ion batteries (SIBs). The specific capacity was still as high as 263.46 mAh g–1 at 0.1 A g–1after 150 cycles and 221.1 mAh g–1 at 0.5 A g–1 after 750 cycles with a capacity retention rate of 83.9%. These findings provide ideas for the ultrafast preparation of binder-free Na+ storage nanomaterials.
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