杂原子
阳极
材料科学
碳纤维
电解质
化学工程
热解
热液循环
储能
电化学
兴奋剂
多孔性
纳米技术
电导率
比表面积
超级电容器
碳纳米纤维
法拉第效率
水热合成
碳捕获和储存(时间表)
聚磷酸铵
电极
作者
Jingyi Jing,Gaohui Du,Shaochen Wei,Di Han,Yunting Wang,Huayu Li,Shixian Chen,Wenqi Zhao,Qingmei Su
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2025-12-19
卷期号:40 (1): 894-903
被引量:8
标识
DOI:10.1021/acs.energyfuels.5c05110
摘要
Sodium-ion batteries (SIBs) are emerging as a sustainable alternative to lithium-ion batteries for large-scale energy storage, but their development is hindered by the lack of cost-effective, high-performance anode materials. This study introduces an eco-friendly synthesis method for nitrogen/phosphorus (N/P) codoped hollow hard carbon microspheres derived from cornstarch, leveraging hydrothermal precarbonization with ammonium polyphosphate (APP) followed by high-temperature pyrolysis. The APP facilitates simultaneous N/P doping and gas evolution during pyrolysis to form hollow architectures. The combined effects of heteroatom doping and structural engineering significantly enhance ion transport kinetics and improve electrolyte accessibility, resulting in notably improved sodium-storage performances. The optimized hard carbon has a reversible capacity of 309.5 mAh g –1 at 0.03 Ag –1 and demonstrates excellent cycling stability with a capacity retention of 86.7% after 1000 cycles at 1 Ag –1 . The improvements can be attributed to the heteroatom doping that induces a large interlayer spacing (0.392 nm), high defect content, and a substantial hierarchical porous surface area (415.88 m 2 /g), which collectively enhance conductivity and sodium-ion kinetics. This work not only advances the design of biomass-derived hard carbon anodes but also provides a scalable strategy for sustainable energy-storage materials.
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