{"title":"离子液体辅助合成钠离子电池用N/B/F共掺杂生物质衍生硬碳","authors":"Fanming Meng, Fengning Bai, Tingting Wu, Wenxu Qi, Yichen Mou, Nianrun Li, Peng Dong, Xiaoyuan Zeng, Chengxu Zhang, Yingjie Zhang, Jue Hu","doi":"10.1007/s11581-025-06421-y","DOIUrl":null,"url":null,"abstract":"<div><p>Biomass-derived hard carbon is currently a promising anode material for commercial sodium-ion batteries. The incorporation of heteroatoms into hard carbon materials brings about remarkable improvements in their electrochemical performance. Nevertheless, the variety of biomass precursors and the constraints of traditional doping techniques present formidable hurdles for their practical application. In this study, a simple impregnation doping and two-step carbonization process was employed to prepare N/B/F co-doped hard carbon using <i>Metaplexis japonica</i> tomentum as a precursor and 1-butyl-3-methylimidazole tetrafluoroborate ionic liquid as the dopant source. The doping effect was confirmed by TEM and XPS. Furthermore, Raman spectroscopy results demonstrate that pseudo-graphitic structures, with large interlayer spacing, provide sufficient diffusion channels for Na<sup>+</sup> ion intercalation and pore-filling. When evaluated for sodium-ion batteries, the as-prepared NBF co-doped hard carbon exhibits a discharge capacity of 140.3 mAh g<sup>−1</sup> at 0.1 Ag<sup>−1</sup> and 84.6 mAh g<sup>−1</sup> at 1.5 Ag<sup>−1</sup>, which shows a better performance than commercial hard carbon products. Furthermore, EIS and DFT results demonstrate that co-doping could provide the highest electrical conductivity and synergistic effects, which can significantly alter the adsorption properties of carbon hosts. This method leverages biomass resources and ionic liquids to achieve controlled carbonization at relatively low temperatures, thereby optimizing the pore structure and graphitization degree of the material, which opens a feasible pathway for the preparation of heteroatom-doped biomass-derived hard carbon.</p><h3>Graphical abstract</h3>\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":599,"journal":{"name":"Ionics","volume":"31 7","pages":"6949 - 6961"},"PeriodicalIF":2.6000,"publicationDate":"2025-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s11581-025-06421-y.pdf","citationCount":"0","resultStr":"{\"title\":\"Ionic liquid–assisted synthesis of N/B/F co-doped biomass-derived hard carbon for sodium-ion batteries\",\"authors\":\"Fanming Meng, Fengning Bai, Tingting Wu, Wenxu Qi, Yichen Mou, Nianrun Li, Peng Dong, Xiaoyuan Zeng, Chengxu Zhang, Yingjie Zhang, Jue Hu\",\"doi\":\"10.1007/s11581-025-06421-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Biomass-derived hard carbon is currently a promising anode material for commercial sodium-ion batteries. 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When evaluated for sodium-ion batteries, the as-prepared NBF co-doped hard carbon exhibits a discharge capacity of 140.3 mAh g<sup>−1</sup> at 0.1 Ag<sup>−1</sup> and 84.6 mAh g<sup>−1</sup> at 1.5 Ag<sup>−1</sup>, which shows a better performance than commercial hard carbon products. Furthermore, EIS and DFT results demonstrate that co-doping could provide the highest electrical conductivity and synergistic effects, which can significantly alter the adsorption properties of carbon hosts. 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引用次数: 0
摘要
生物质硬碳是目前商用钠离子电池极具潜力的负极材料。杂原子掺入硬碳材料后,其电化学性能得到显著改善。然而,生物质前体的多样性和传统掺杂技术的局限性为其实际应用带来了巨大的障碍。本研究采用简单浸渍掺杂和两步炭化工艺,以刺参为前驱体,1-丁基-3-甲基咪唑四氟硼酸盐离子液体为掺杂源,制备了N/B/F共掺杂硬碳。通过TEM和XPS证实了掺杂效果。此外,拉曼光谱结果表明,具有较大层间距的伪石墨结构为Na+离子的嵌入和孔隙填充提供了充分的扩散通道。在钠离子电池中,制备的NBF共掺杂硬碳在0.1 Ag−1和1.5 Ag−1下的放电容量分别为140.3 mAh g−1和84.6 mAh g−1,表现出比商用硬碳产品更好的性能。此外,EIS和DFT结果表明,共掺杂可以提供最高的电导率和协同效应,这可以显著改变碳宿主的吸附性能。该方法利用生物质资源和离子液体在相对低温下实现可控碳化,从而优化了材料的孔隙结构和石墨化程度,为制备杂原子掺杂的生物质衍生硬碳开辟了一条可行的途径。图形抽象
Ionic liquid–assisted synthesis of N/B/F co-doped biomass-derived hard carbon for sodium-ion batteries
Biomass-derived hard carbon is currently a promising anode material for commercial sodium-ion batteries. The incorporation of heteroatoms into hard carbon materials brings about remarkable improvements in their electrochemical performance. Nevertheless, the variety of biomass precursors and the constraints of traditional doping techniques present formidable hurdles for their practical application. In this study, a simple impregnation doping and two-step carbonization process was employed to prepare N/B/F co-doped hard carbon using Metaplexis japonica tomentum as a precursor and 1-butyl-3-methylimidazole tetrafluoroborate ionic liquid as the dopant source. The doping effect was confirmed by TEM and XPS. Furthermore, Raman spectroscopy results demonstrate that pseudo-graphitic structures, with large interlayer spacing, provide sufficient diffusion channels for Na+ ion intercalation and pore-filling. When evaluated for sodium-ion batteries, the as-prepared NBF co-doped hard carbon exhibits a discharge capacity of 140.3 mAh g−1 at 0.1 Ag−1 and 84.6 mAh g−1 at 1.5 Ag−1, which shows a better performance than commercial hard carbon products. Furthermore, EIS and DFT results demonstrate that co-doping could provide the highest electrical conductivity and synergistic effects, which can significantly alter the adsorption properties of carbon hosts. This method leverages biomass resources and ionic liquids to achieve controlled carbonization at relatively low temperatures, thereby optimizing the pore structure and graphitization degree of the material, which opens a feasible pathway for the preparation of heteroatom-doped biomass-derived hard carbon.
期刊介绍:
Ionics is publishing original results in the fields of science and technology of ionic motion. This includes theoretical, experimental and practical work on electrolytes, electrode, ionic/electronic interfaces, ionic transport aspects of corrosion, galvanic cells, e.g. for thermodynamic and kinetic studies, batteries, fuel cells, sensors and electrochromics. Fast solid ionic conductors are presently providing new opportunities in view of several advantages, in addition to conventional liquid electrolytes.