杂原子
法拉第效率
材料科学
碳化
碳纤维
兴奋剂
化学工程
电解质
电化学
石墨
纳米技术
化学
复合材料
电极
有机化学
复合数
光电子学
工程类
物理化学
扫描电子显微镜
戒指(化学)
作者
Xiangji Li,Chao Yang,Shaoqiang Wang,Xinyu Mao,Kaifeng Yu
标识
DOI:10.1016/j.diamond.2022.109382
摘要
As a promising alternative to graphite, biomass hard carbon has attracted widespread attention in sodium-ion batteries (SIBs). Heteroatom doping can overcome the inherent shortcomings of hard carbon materials, such as low reversible capacity and poor rate performance. Herein, in this paper, a simple and efficient one-step synthesis method is adopted to pyrolyze the mixture of jute fiber carbon with urea (JFCN) or sulfur powder (JFCS) from high to low carbonization temperatures, and determines that high-performance doping is only suitable for relatively low temperatures. Benefiting from the low-defect and ordered structure doped by proper S or N under these temperatures, initial Coulombic efficiency and electrochemical stability of hard carbon materials have been significantly improved. Meanwhile, S doping is a more effective way than N doping, the former shows an ultrahigh reversible capacity exceeding 410 mAh g−1 after 100 cycles at 0.1 A g−1 and a remarkable rate performance of 234.3 mAh g−1 at 2.0 A g−1. Impressively, JFCN exhibits greater rate performance in ether electrolytes, while JFCS shows better stability in ester electrolytes. This work provides a broad application prospect for hard carbon materials to achieve low cost and high capacity as practical SIBs.
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