High-efficiently doping nitrogen in kapok fiber-derived hard carbon used as anode materials for boosting rate performance of sodium-ion batteries

Boosting(机器学习) 阳极 兴奋剂 离子 材料科学 氮气 化学工程 纤维 化学 复合材料 光电子学 冶金 计算机科学 有机化学 电极 工程类 物理化学 机器学习
作者
Tianyun Zhang,Tian Zhang,Tian Zhang,Tian Zhang,Fujuan Wang,Fen Ran
出处
期刊:Journal of Energy Chemistry [Elsevier BV]
卷期号:96: 472-482 被引量:108
标识
DOI:10.1016/j.jechem.2024.05.005
摘要

A high content N-doped hard carbon is prepared through the effects of 2,6-pyridine dicarboxylic acid and zinc chloride , exhibiting an excellent rate performance due to abundant pyridine N and C=O. The engineering of plant-based precursor for nitrogen doping has become one of the most promising strategies to enhance rate capability of hard carbon materials for sodium-ion batteries; however, the poor rate performance is mainly caused by lack of pyridine nitrogen, which often tends to escape because of high temperature in preparation process of hard carbon. In this paper, a high-rate kapok fiber-derived hard carbon is fabricated by cross-linking carboxyl group in 2,6-pyridinedicarboxylic acid with the exposed hydroxyl group on alkalized kapok with assistance of zinc chloride . Specially, a high nitrogen doping content of 4.24% is achieved, most of which are pyridine nitrogen; this is crucial for improving the defect sites and electronic conductivity of hard carbon. The optimized carbon with feature of high nitrogen content, abundant functional groups, degree of disorder, and large layer spacing exhibits high capacity of 401.7 mAh g −1 at a current density of 0.05 A g −1 , and more importantly, good rate performance, for example, even at the current density of 2 A g −1 , a specific capacity of 159.5 mAh g −1 can be obtained. These findings make plant-based hard carbon a promising candidate for commercial application of sodium-ion batteries, achieving high-rate performance with the enhanced pre-cross-linking interaction between plant precursors and dopants to optimize aromatization process by auxiliary pyrolysis.
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