Intrinsically Nitrogen-Enriched Biomass-Derived Hard Carbon with Enhanced Performance as a Sodium-Ion Battery Anode

阳极 碳纤维 氮气 电池(电) 生物量(生态学) 钠离子电池 离子 材料科学 环境科学 化学工程 化学 电极 功率(物理) 工程类 冶金 复合材料 物理 热力学 法拉第效率 农学 有机化学 物理化学 生物 复合数
作者
Ganesh Kumar Veerasubramani,Myung‐Soo Park,Umesh T. Nakate,Georgios N. Karanikolos,Goli Nagaraju,Ali A. AlHammadi,Dong‐Won Kim
出处
期刊:Energy & Fuels [American Chemical Society]
卷期号:38 (8): 7368-7378 被引量:8
标识
DOI:10.1021/acs.energyfuels.4c00069
摘要

Hard carbons are particularly suitable as negative electrodes for sodium-ion batteries (SIBs). To produce hard carbon particles with better sodium storage performance, such as specific capacity, Coulombic efficiency, and cycling stability, a suitable precursor and preparation strategy must be developed. In this paper, we present a new hard carbon that is created by carbonizing jackfruit seed wastes. Under various high-temperature treatment and pretreatment settings, jackfruit seed wastes have been processed. As the carbonization temperature increased, hard carbon became more graphitized. At the same time, the carbonization temperature had a great effect on how much sodium could be stored reversibly. Structural characterization of the hard carbons produced at various carbonization temperatures revealed variance in their architectures, illuminating the relationship between the capacity increase and the size of the sodium storage-available microspores. The hard carbon (HC) produced at the optimized condition (1200 °C) delivered an improved capacity of more than 221 mA h g–1 with an exceptional cycling stability of 98.8% over 100 cycles and improved rate performance relying on reversible sodium insertion. The existence of naturally occurring nitrogen atoms, the textural characteristics, and Na+ adsorption-insertion into the disordered carbon layers can explain how better Na+-ion storage occurs in developed HCs. Our study offers an environmentally friendly method of turning seed waste into a potential low-cost yet highly efficient anode material for SIBs.
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