Comprehensive study on improving the sodium storage performance of low-defect biomass-derived carbon through S or N doping

被引:5
|
作者
Li, Xiangji [1 ,2 ]
Yang, Chao [1 ,2 ]
Wang, Shaoqiang [3 ]
Mao, Xinyu [1 ,2 ]
Yu, Kaifeng [1 ,2 ]
机构
[1] Jilin Univ, Key Lab Automobile Mat, Minist Educ, Changchun 130025, Peoples R China
[2] Jilin Univ, Coll Mat Sci & Engn, Changchun 130025, Peoples R China
[3] Changchun Univ, Sch Comp Sci & Technol, Changchun 130022, Peoples R China
关键词
Biomass carbon; Sulfur doping; Nitrogen doping; Temperature; Electrolyte; ION BATTERIES; HARD CARBON; ANODE MATERIALS; DOPED CARBON; GRAPHENE; SULFUR; MECHANISM; CAPACITY; INSIGHTS;
D O I
10.1016/j.diamond.2022.109382
中图分类号
T [工业技术];
学科分类号
08 ;
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.
引用
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页数:12
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