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Effects elucidation of carbon nanofibers structural evolution on sodium ion storage behavior
被引:1
|作者:
Qin, Chen
[1
]
Meng, Liang
[1
]
Cao, Hailiang
[1
]
Deng, Wei
[3
]
Yang, Liangtao
[3
]
Li, Peng
[4
]
Liu, Peizhi
[1
]
Dong, Hailiang
[1
]
Zheng, Zhi
[2
]
Guo, Junjie
[1
]
机构:
[1] Taiyuan Univ Technol, Coll Mat Sci & Engn, Key Lab Interface Sci & Engn Adv Mat, Minist Educ, Taiyuan 030024, Peoples R China
[2] Univ Sydney, Sch Chem & Biomol Engn, Darlington, NSW 2006, Australia
[3] Chinese Acad Sci, Shenzhen Inst Adv Technol, Shenzhen 518055, Peoples R China
[4] RMIT Univ, Sch Sci, Melbourne, Vic 3000, Australia
基金:
澳大利亚研究理事会;
中国国家自然科学基金;
关键词:
Sodium-ion batteries;
Hard carbon;
Structural evolution;
Sodium storage mechanism;
In-situ Raman;
ANODE MATERIALS;
HARD CARBONS;
RAMAN;
ELECTRODES;
BATTERIES;
INSERTION;
D O I:
10.1016/j.est.2024.113831
中图分类号:
TE [石油、天然气工业];
TK [能源与动力工程];
学科分类号:
0807 ;
0820 ;
摘要:
Hard carbon (HC) is a promising anode material for sodium-ion batteries (SIBs) due to its large capacity, highly abundant, and low cost. However, the lack of understanding for its sodium ion storage mechanism, especially in the low potential plateau region, hinders the design and development of high-performance HC anode materials. Herein, hard carbon nanofibers (CNFs) are prepared by electrospinning and a subsequent carbonization step. The correlation between the microstructure of CNFs and their sodium ion storage behaviors is systematically investigated, demonstrating that the electrochemical performance is closely related to their microstructure. CNFs carbonized at 1300 C-degrees (CNF-1300) achieves excellent reversible capacity, rate performance and cycling stability. Furthermore, the sodium ion storage mechanism of CNF-1300 is elucidated by linking its microstructure and the electrochemical properties via galvanostatic intermittent titration technique measurements and in-situ Raman spectroscopy, demonstrating the capacity in the low potential plateau region is mainly contributed by pore filling. At last, a sodium ion storage mechanism based on adsorption-intercalation-pore filling is proposed, providing guidance for the design of high-performance HC anode materials in SIBs.
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页数:9
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