碳化
碳纤维
杂原子
煤
化学工程
材料科学
法拉第效率
化学
吸附
阳极
无机化学
有机化学
复合材料
戒指(化学)
电极
物理化学
复合数
工程类
作者
Limin Deng,Yakun Tang,Jingmei Liu,Yue Zhang,Wenjun Song,Yuandong Li,Lang Liu
出处
期刊:Molecules
[MDPI AG]
日期:2023-06-22
卷期号:28 (13): 4921-4921
被引量:2
标识
DOI:10.3390/molecules28134921
摘要
The use of coal as a precursor for producing hard carbon is favored due to its abundance, low cost, and high carbon yield. To further optimize the sodium storage performance of hard carbon, the introduction of heteroatoms has been shown to be an effective approach. However, the inert structure in coal limits the development of heteroatom-doped coal-based hard carbon. Herein, coal-based P-doped hard carbon was synthesized using Ca3(PO4)2 to achieve homogeneous phosphorus doping and inhibit carbon microcrystal development during high-temperature carbonization. This involved a carbon dissolution reaction where Ca3(PO4)2 reacted with SiO2 and carbon in coal to form phosphorus and CO. The resulting hierarchical porous structure allowed for rapid diffusion of Na+ and resulted in a high reversible capacity of 200 mAh g−1 when used as an anode material for Na+ storage. Compared to unpretreated coal-based hard carbon, the P-doped hard carbon displayed a larger initial coulombic efficiency (64%) and proportion of plateau capacity (47%), whereas the unpretreated carbon only exhibited an initial coulombic efficiency of 43.1% and a proportion of plateau capacity of 29.8%. This work provides a green, scalable approach for effective microcrystalline regulation of hard carbon from low-cost and highly aromatic precursors.
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