Lu Huang, Yuan Qin, Kebiao Zhang, Zihao Ou, Xinwen Rao, YuYing Wang, Bin Xiang, Xuefeng Zou, Yang Zhou, Hujun Shen
{"title":"双活性CoFe@N-CNTs纳米杂化:高容量独立锂离子阳极的富氮前驱体协同封装","authors":"Lu Huang, Yuan Qin, Kebiao Zhang, Zihao Ou, Xinwen Rao, YuYing Wang, Bin Xiang, Xuefeng Zou, Yang Zhou, Hujun Shen","doi":"10.1039/d5qi01051a","DOIUrl":null,"url":null,"abstract":"Addressing the capacity degradation challenge in carbon nanotube-based anode materials, this study novel proposes a synergistic strategy integrating 3D conductive network construction with robust metal-carbon coupling interfaces. By selecting dicyandiamide (DCDA) as an optimal carbon/nitrogen precursor and combining solvothermal synthesis with chemical vapor deposition (CVD), we achieved in-situ growth of nitrogen-doped carbon nanotubes and uniform anchoring of Co-Fe nanoparticles. Pyrolysis characterization reveals that the DCDA system exhibits superior thermal stability and nitrogen-rich capability compared to cyanamide (CA) and melamine (MA) counterparts. Benefiting from the synergistic effects between the 3D conductive network and metal active sites, the CoFe@NCNTs/CC(DCDA) anode demonstrates exceptional lithium storage performance: delivering a high specific capacity of 1717.6 mAh·g⁻¹ at 1 A·g⁻¹ with 93.6% capacity retention after 250 cycles, while maintaining 1413.1 mAh·g⁻¹ at an elevated current density of 2 A·g⁻¹. When paired with NCM811 cathodes in full-cell configuration, the system achieves 84.8% capacity retention over 550 cycles at 1C rate, demonstrating its potential for practical applications. This work provides novel insights into interface engineering for designing highly stable metal-carbon composite electrodes.","PeriodicalId":79,"journal":{"name":"Inorganic Chemistry Frontiers","volume":"49 1","pages":""},"PeriodicalIF":6.4000,"publicationDate":"2025-06-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dual-Active CoFe@N-CNTs Nanohybrids: Synergistic Encapsulation via Nitrogen-Rich Precursors for High-Capacity Freestanding Lithium-Ion Anodes\",\"authors\":\"Lu Huang, Yuan Qin, Kebiao Zhang, Zihao Ou, Xinwen Rao, YuYing Wang, Bin Xiang, Xuefeng Zou, Yang Zhou, Hujun Shen\",\"doi\":\"10.1039/d5qi01051a\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Addressing the capacity degradation challenge in carbon nanotube-based anode materials, this study novel proposes a synergistic strategy integrating 3D conductive network construction with robust metal-carbon coupling interfaces. By selecting dicyandiamide (DCDA) as an optimal carbon/nitrogen precursor and combining solvothermal synthesis with chemical vapor deposition (CVD), we achieved in-situ growth of nitrogen-doped carbon nanotubes and uniform anchoring of Co-Fe nanoparticles. Pyrolysis characterization reveals that the DCDA system exhibits superior thermal stability and nitrogen-rich capability compared to cyanamide (CA) and melamine (MA) counterparts. Benefiting from the synergistic effects between the 3D conductive network and metal active sites, the CoFe@NCNTs/CC(DCDA) anode demonstrates exceptional lithium storage performance: delivering a high specific capacity of 1717.6 mAh·g⁻¹ at 1 A·g⁻¹ with 93.6% capacity retention after 250 cycles, while maintaining 1413.1 mAh·g⁻¹ at an elevated current density of 2 A·g⁻¹. When paired with NCM811 cathodes in full-cell configuration, the system achieves 84.8% capacity retention over 550 cycles at 1C rate, demonstrating its potential for practical applications. This work provides novel insights into interface engineering for designing highly stable metal-carbon composite electrodes.\",\"PeriodicalId\":79,\"journal\":{\"name\":\"Inorganic Chemistry Frontiers\",\"volume\":\"49 1\",\"pages\":\"\"},\"PeriodicalIF\":6.4000,\"publicationDate\":\"2025-06-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Inorganic Chemistry Frontiers\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5qi01051a\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5qi01051a","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Dual-Active CoFe@N-CNTs Nanohybrids: Synergistic Encapsulation via Nitrogen-Rich Precursors for High-Capacity Freestanding Lithium-Ion Anodes
Addressing the capacity degradation challenge in carbon nanotube-based anode materials, this study novel proposes a synergistic strategy integrating 3D conductive network construction with robust metal-carbon coupling interfaces. By selecting dicyandiamide (DCDA) as an optimal carbon/nitrogen precursor and combining solvothermal synthesis with chemical vapor deposition (CVD), we achieved in-situ growth of nitrogen-doped carbon nanotubes and uniform anchoring of Co-Fe nanoparticles. Pyrolysis characterization reveals that the DCDA system exhibits superior thermal stability and nitrogen-rich capability compared to cyanamide (CA) and melamine (MA) counterparts. Benefiting from the synergistic effects between the 3D conductive network and metal active sites, the CoFe@NCNTs/CC(DCDA) anode demonstrates exceptional lithium storage performance: delivering a high specific capacity of 1717.6 mAh·g⁻¹ at 1 A·g⁻¹ with 93.6% capacity retention after 250 cycles, while maintaining 1413.1 mAh·g⁻¹ at an elevated current density of 2 A·g⁻¹. When paired with NCM811 cathodes in full-cell configuration, the system achieves 84.8% capacity retention over 550 cycles at 1C rate, demonstrating its potential for practical applications. This work provides novel insights into interface engineering for designing highly stable metal-carbon composite electrodes.