P-doped spherical hard carbon with high initial coulombic efficiency and enhanced capacity for sodium ion batteries

法拉第效率 兴奋剂 离子 碳纤维 材料科学 纳米技术 化学工程 化学 光电子学 有机化学 工程类 复合材料 物理化学 电解质 电极 复合数
作者
Zhengguang Liu,Jiahua Zhao,Hao Yao,Xiang‐Xi He,Hang Zhang,Yun Qiao,Xingqiao Wu,Li Li,Shulei Chou
出处
期刊:Chemical Science [Royal Society of Chemistry]
卷期号:15 (22): 8478-8487 被引量:18
标识
DOI:10.1039/d4sc01395f
摘要

Hard carbon (HC) is one of the most promising anode materials for sodium-ion batteries (SIBs) due to its cost-effectiveness and low-voltage plateau capacity. Heteroatom doping is considered as an effective strategy to improve the sodium storage capacity of HC. However, most of the previous heteroatom doping strategies are performed at a relatively low temperature, which could not be utilized to raise the low-voltage plateau capacity. Moreover, extra doping of heteroatoms could create new defects, leading to a low initial coulombic efficiency (ICE). Herein, we propose a repair strategy based on doping a trace amount of P to achieve a high capacity along with a high ICE. By employing the cross-linked interaction between glucose and phytic acid to achieve the in situ P doped spherical hard carbon, the obtained PHC-0.2 possesses a large interlayer space that facilitates Na+ storage and transportation. In addition, doping a suitable amount of P could repair some defects in carbon layers. When used as an anode material for SIBs, the PHC-0.2 exhibits an enhanced reversible capacity of 343 mA h g-1 at 20 mA g-1 with a high ICE of 92%. Full cells consisting of a PHC-0.2 anode and a Na2Fe0.5Mn0.5[Fe(CN)6] cathode exhibited an average potential of 3.1 V with an initial discharge capacity of 255 mA h g-1 and an ICE of 85%. The full cell displays excellent cycling stability with a capacity retention of 80.3% after 170 cycles. This method is simple and low-cost, which can be extended to other energy storage materials.
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