{"title":"Si/C阳极双模碳结构的可控工程设计","authors":"Jiapeng Zhang, Renlu Yuan, Dengke Wang, Jiangchuan Li, Xue Yao, Lixin Chen, Xiaotian Li, Zhijie Jiang, Haiyan Liu, Yu Hou, Ang Li, Xiaohong Chen, Zhiwen Chen, Chandra Veer Singh, Huaihe Song","doi":"10.1002/adfm.202423700","DOIUrl":null,"url":null,"abstract":"Silicon-carbon composites (Si/C) with multistage structures enable structural integrity during cycling. However, the lack of controllable structure preparation on a large scale hinders the stability improvement in practical applications. Herein, a new strategy is proposed to synthesize kilogram-scale Si/C (PySi/C) featuring a dual-model carbon structure in one step. The controllable combination of an onion-like carbon coating on the Si surface with independent pyrolytic carbon is accomplished through the precise adjustment of the pyrolysis temperature. The dual-model carbon formation mechanism is unraveled, detailing the cooperative coupling of the nucleation laws of carbon compositions as well as the changes trends in morphology and crystallinity. This density functional theory and finite element analysis highlight the dual-model structure's essential contribution to the electrochemical behavior and structural stability. As expected, PySi/Cs anodes deliver stable cycling performance with retention of 91.5% after 800 cycles at 2 A g<sup>−1</sup>. Its comprehensive electrochemical performance surpasses that of the state-of-the-art kilogram-scale Si-based anode reported. Moreover, the assembled pouch cell exhibits actual competitiveness, showing a capacity of 1.97 Ah and a retention of 88.9% after 300 cycles at 1 C. This work provides valuable design concepts to further advance the development of Si/C anodes.","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"29 1","pages":""},"PeriodicalIF":18.5000,"publicationDate":"2025-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Orchestrating a Controllable Engineering of Dual-Model Carbon Structure in Si/C Anodes\",\"authors\":\"Jiapeng Zhang, Renlu Yuan, Dengke Wang, Jiangchuan Li, Xue Yao, Lixin Chen, Xiaotian Li, Zhijie Jiang, Haiyan Liu, Yu Hou, Ang Li, Xiaohong Chen, Zhiwen Chen, Chandra Veer Singh, Huaihe Song\",\"doi\":\"10.1002/adfm.202423700\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Silicon-carbon composites (Si/C) with multistage structures enable structural integrity during cycling. However, the lack of controllable structure preparation on a large scale hinders the stability improvement in practical applications. Herein, a new strategy is proposed to synthesize kilogram-scale Si/C (PySi/C) featuring a dual-model carbon structure in one step. The controllable combination of an onion-like carbon coating on the Si surface with independent pyrolytic carbon is accomplished through the precise adjustment of the pyrolysis temperature. The dual-model carbon formation mechanism is unraveled, detailing the cooperative coupling of the nucleation laws of carbon compositions as well as the changes trends in morphology and crystallinity. This density functional theory and finite element analysis highlight the dual-model structure's essential contribution to the electrochemical behavior and structural stability. As expected, PySi/Cs anodes deliver stable cycling performance with retention of 91.5% after 800 cycles at 2 A g<sup>−1</sup>. Its comprehensive electrochemical performance surpasses that of the state-of-the-art kilogram-scale Si-based anode reported. Moreover, the assembled pouch cell exhibits actual competitiveness, showing a capacity of 1.97 Ah and a retention of 88.9% after 300 cycles at 1 C. This work provides valuable design concepts to further advance the development of Si/C anodes.\",\"PeriodicalId\":112,\"journal\":{\"name\":\"Advanced Functional Materials\",\"volume\":\"29 1\",\"pages\":\"\"},\"PeriodicalIF\":18.5000,\"publicationDate\":\"2025-01-12\",\"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.202423700\",\"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.202423700","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
具有多级结构的硅碳复合材料(Si/C)可以在循环过程中保持结构完整性。然而,缺乏大规模的可控结构制备,阻碍了实际应用中稳定性的提高。本文提出了一种一步合成具有双模式碳结构的公斤级Si/C (PySi/C)的新策略。通过对热解温度的精确调节,实现了硅表面洋葱状碳涂层与独立热解碳的可控结合。揭示了双模式碳的形成机制,详细阐述了碳组分成核的协同耦合规律以及形貌和结晶度的变化趋势。这种密度泛函理论和有限元分析强调了双模型结构对电化学行为和结构稳定性的重要贡献。正如预期的那样,PySi/Cs阳极具有稳定的循环性能,在2 A g−1下循环800次后保持率为91.5%。其综合电化学性能超过了目前报道的最先进的公斤级硅基阳极。此外,组装的袋状电池具有实际的竞争力,在1c下循环300次后,其容量为1.97 Ah,保留率为88.9%。这项工作为进一步推进Si/C阳极的发展提供了有价值的设计理念。
Orchestrating a Controllable Engineering of Dual-Model Carbon Structure in Si/C Anodes
Silicon-carbon composites (Si/C) with multistage structures enable structural integrity during cycling. However, the lack of controllable structure preparation on a large scale hinders the stability improvement in practical applications. Herein, a new strategy is proposed to synthesize kilogram-scale Si/C (PySi/C) featuring a dual-model carbon structure in one step. The controllable combination of an onion-like carbon coating on the Si surface with independent pyrolytic carbon is accomplished through the precise adjustment of the pyrolysis temperature. The dual-model carbon formation mechanism is unraveled, detailing the cooperative coupling of the nucleation laws of carbon compositions as well as the changes trends in morphology and crystallinity. This density functional theory and finite element analysis highlight the dual-model structure's essential contribution to the electrochemical behavior and structural stability. As expected, PySi/Cs anodes deliver stable cycling performance with retention of 91.5% after 800 cycles at 2 A g−1. Its comprehensive electrochemical performance surpasses that of the state-of-the-art kilogram-scale Si-based anode reported. Moreover, the assembled pouch cell exhibits actual competitiveness, showing a capacity of 1.97 Ah and a retention of 88.9% after 300 cycles at 1 C. This work provides valuable design concepts to further advance the development of Si/C anodes.
期刊介绍:
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