State Key Laboratory of Chemistry and Utilization of Carbon Based Energy Resources, College of Chemistry, Xinjiang University, Urumqi 830017, China.
Molecules. 2023 Jun 22;28(13):4921. doi: 10.3390/molecules28134921.
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 Ca(PO) to achieve homogeneous phosphorus doping and inhibit carbon microcrystal development during high-temperature carbonization. This involved a carbon dissolution reaction where Ca(PO) reacted with SiO 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 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.
由于煤炭储量丰富、成本低廉且产碳率高,因此将其作为前驱体制备硬碳受到青睐。为了进一步优化硬碳的储钠性能,引入杂原子被证明是一种有效的方法。然而,煤炭中的惰性结构限制了杂原子掺杂煤基硬碳的发展。在此,通过 Ca(PO) 来实现均匀的磷掺杂,并抑制高温碳化过程中碳微晶的生长,合成了基于煤的 P 掺杂硬碳。这涉及一个碳溶解反应,其中 Ca(PO) 与煤中的 SiO 和碳反应,形成磷和 CO。所得的分级多孔结构允许 Na 快速扩散,用作 Na 存储的阳极材料时可实现 200 mAh g 的高可逆容量。与未经预处理的煤基硬碳相比,P 掺杂硬碳的初始库仑效率(64%)和平台容量比例(47%)更大,而未经预处理的碳仅表现出 43.1%的初始库仑效率和 29.8%的平台容量比例。这项工作为从低成本、高芳构化前驱体制备有效微晶调控的硬碳提供了一种绿色、可扩展的方法。