{"title":"缺陷和氧官能团调制软碳具有丰富的闭孔和坚固的界面高性能钠离子电池","authors":"Fenglian Gong, Ying Xiao, Hongyang Wang, Shunshun Zhao, Shilin Hu, Jun Chen, Shimou Chen","doi":"10.1002/adfm.202506205","DOIUrl":null,"url":null,"abstract":"Soft carbons with inherently high graphitization degree typically suffer from limited specific capacity and low initial Coulombic efficiency (ICE) for Na<sup>+</sup>-ion batteries (NIBs), hindering their development and practical application. Herein, defect and oxygen functional group engineering strategy by incorporating resin-derived hard carbon and cost-effective iron-based substances is proposed enables the design of a unique layered soft carbon with enhanced efficiency and stable interfaces with the electrolytes. The increased C═O functional groups and Fe─O─C bond contributed by Fe-based species significantly improve reversible Na<sup>+</sup>- adsorption in the inclined region and enhance the structural stability of the electrode. Additionally, phenolic resin-derived carbon increases the micropores and thus reduces the graphitization degree. The increased closed pores induced by the reconstruction of the carbon structure at high temperature enhance the Na<sup>+</sup>-storage ability. Consequently, the material achieves a high Na<sup>+</sup>-storage capacity of 311.0 mAh g<sup>−1</sup> with an improved ICE of 93.89% at 0.1 A g<sup>−1</sup>. Even cycled at 1 A g<sup>−1</sup>, it can deliver a high capacity of 269.3 mAh g<sup>−1</sup> with excellent stability over 800 cycles, outperforming previously reported soft carbon anodes. This innovative strategy provides a practical and cost-effective pathway for designing advanced carbon anodes for NIBs.","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"57 1","pages":""},"PeriodicalIF":19.0000,"publicationDate":"2025-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Defects and Oxygen Functional Groups Modulated Soft Carbon with Abundant Closed Pores and Robust Interface for High-Performance Na+-Ion Batteries\",\"authors\":\"Fenglian Gong, Ying Xiao, Hongyang Wang, Shunshun Zhao, Shilin Hu, Jun Chen, Shimou Chen\",\"doi\":\"10.1002/adfm.202506205\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Soft carbons with inherently high graphitization degree typically suffer from limited specific capacity and low initial Coulombic efficiency (ICE) for Na<sup>+</sup>-ion batteries (NIBs), hindering their development and practical application. Herein, defect and oxygen functional group engineering strategy by incorporating resin-derived hard carbon and cost-effective iron-based substances is proposed enables the design of a unique layered soft carbon with enhanced efficiency and stable interfaces with the electrolytes. The increased C═O functional groups and Fe─O─C bond contributed by Fe-based species significantly improve reversible Na<sup>+</sup>- adsorption in the inclined region and enhance the structural stability of the electrode. Additionally, phenolic resin-derived carbon increases the micropores and thus reduces the graphitization degree. The increased closed pores induced by the reconstruction of the carbon structure at high temperature enhance the Na<sup>+</sup>-storage ability. Consequently, the material achieves a high Na<sup>+</sup>-storage capacity of 311.0 mAh g<sup>−1</sup> with an improved ICE of 93.89% at 0.1 A g<sup>−1</sup>. Even cycled at 1 A g<sup>−1</sup>, it can deliver a high capacity of 269.3 mAh g<sup>−1</sup> with excellent stability over 800 cycles, outperforming previously reported soft carbon anodes. This innovative strategy provides a practical and cost-effective pathway for designing advanced carbon anodes for NIBs.\",\"PeriodicalId\":112,\"journal\":{\"name\":\"Advanced Functional Materials\",\"volume\":\"57 1\",\"pages\":\"\"},\"PeriodicalIF\":19.0000,\"publicationDate\":\"2025-05-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Functional Materials\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1002/adfm.202506205\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adfm.202506205","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
软碳本身石墨化程度高,但用于钠离子电池的比容量有限,初始库仑效率低,阻碍了软碳的发展和实际应用。本文提出了将树脂衍生的硬碳和具有成本效益的铁基物质结合的缺陷和氧官能团工程策略,可以设计出具有提高效率和与电解质稳定界面的独特层状软碳。铁基物质增加的C = O官能团和Fe─O─C键显著改善了电极在倾斜区对Na+的可逆吸附,提高了电极的结构稳定性。此外,酚醛树脂衍生的碳增加了微孔,从而降低了石墨化程度。高温下碳结构重构导致的封闭孔增加,增强了Na+的储存能力。因此,该材料获得了311.0 mAh g−1的高Na+存储容量,并在0.1 ag−1下提高了93.89%的ICE。即使在1a g−1下循环,它也可以提供269.3 mAh g−1的高容量,并且在800次循环中具有出色的稳定性,优于先前报道的软碳阳极。这一创新策略为nib先进碳阳极的设计提供了一条实用且经济的途径。
Defects and Oxygen Functional Groups Modulated Soft Carbon with Abundant Closed Pores and Robust Interface for High-Performance Na+-Ion Batteries
Soft carbons with inherently high graphitization degree typically suffer from limited specific capacity and low initial Coulombic efficiency (ICE) for Na+-ion batteries (NIBs), hindering their development and practical application. Herein, defect and oxygen functional group engineering strategy by incorporating resin-derived hard carbon and cost-effective iron-based substances is proposed enables the design of a unique layered soft carbon with enhanced efficiency and stable interfaces with the electrolytes. The increased C═O functional groups and Fe─O─C bond contributed by Fe-based species significantly improve reversible Na+- adsorption in the inclined region and enhance the structural stability of the electrode. Additionally, phenolic resin-derived carbon increases the micropores and thus reduces the graphitization degree. The increased closed pores induced by the reconstruction of the carbon structure at high temperature enhance the Na+-storage ability. Consequently, the material achieves a high Na+-storage capacity of 311.0 mAh g−1 with an improved ICE of 93.89% at 0.1 A g−1. Even cycled at 1 A g−1, it can deliver a high capacity of 269.3 mAh g−1 with excellent stability over 800 cycles, outperforming previously reported soft carbon anodes. This innovative strategy provides a practical and cost-effective pathway for designing advanced carbon anodes for NIBs.
期刊介绍:
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