阳极
材料科学
电化学
碳纤维
阴极
化学工程
钠
兴奋剂
电流密度
纳米技术
电极
复合数
复合材料
光电子学
冶金
物理化学
化学
量子力学
物理
工程类
作者
Z. Zhang,Bin Huang,Tingmin Lai,Ao Sheng,Shengkui Zhong,Jianwen Yang,Yanwei Li
出处
期刊:Nanotechnology
[IOP Publishing]
日期:2023-12-11
卷期号:35 (11): 115601-115601
被引量:3
标识
DOI:10.1088/1361-6528/ad1441
摘要
Hard carbon is a promising anode material for sodium-ion batteries (SIBs) due to its abundance. However, it exhibits low reversible capacity and slow kinetics if inappropriate microstructural features are developed during synthesis. Herein, N/S co-doped phenolic resin-based hard carbon microspheres are prepared by a scalable strategy, and the electrochemical performance is assessed both in half cells and full cells. We demonstrate that the expanded interlayer spacing, the increased active sites, and the enhanced capacitive behavior result in the enhanced reversible capacity and promoted kinetics for Na+storage. The sample with appropriate doping amount exhibits an initial charge capacity of 536.8 mAh g-1at 50 mA g-1and maintains 445.9 mAh g-1after 1000 cycles at a current density of 1 A g-1in a Na-metal half cell. Coupled with a carbon-coated Na4Fe3(PO4)2P2O7(NFPP) cathode, the full cell exhibits a capacity of 92.5 mAh g-1after 90 cycles, with a capacity retention of 91.6%. This work provides a facile and scalable method for synthesizing high-performance hard carbon anode materials for SIBs.
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