N, S co-doped coal-based hard carbon prepared by two-step carbonization and a molten salt template method for sodium storage

碳化 材料科学 熔盐 碳纤维 兴奋剂 盐(化学) 化学工程 冶金 废物管理 有机化学 复合材料 化学 复合数 扫描电子显微镜 光电子学 工程类
作者
Huizhu Niu,Haihua Wang,Liyu Sun,Chen-rong Yang,Yu Wang,Rui Cao,Cun-guo Yang,Jie Wang,Kewei Shu
出处
期刊:New Carbon Materials [Elsevier BV]
卷期号:39 (2): 297-307 被引量:29
标识
DOI:10.1016/s1872-5805(24)60842-5
摘要

Hard carbon, known for its abundant resources, stable structure and high safety, has emerged as the most popular anode material for sodium-ion batteries (SIBs). Among various sources, coal-derived hard carbon has attracted extensive attention. In this work, N and S co-doped coal-based carbon material (NSPC1200) was synthesized through a combination of two-step carbonization process and heteroatom doping using long-flame coal as a carbon source, thiourea as a nitrogen and sulfur source, and NaCl as a template. The two-step carbonization process played a crucial role in adjusting the structure of carbon microcrystals and expanding the interlayer spacing. The N and S co-doping regulated the electronic structure of carbon materials, endowing more active sites. Additionally, the introduction of NaCl as a template contributed to the construction of pore structure, which facilitates better contact between electrodes and electrolytes, enabling more efficient transport of Na+ and electrons. Under the synergistic effect, NSPC1200 exhibited exceptional sodium storage capacity, reaching 314.2 mAh g-1 at 20 mA g-1. Furthermore, NSPC1200 demonstrated commendable cycling stability, maintaining a capacity of 224.4 mAh g-1 even after 200 cycles. This work successfully achieves the strategic tuning of the microstructure of coal-based carbon materials, ultimately obtaining hard carbon anode with excellent electrochemical performance.
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