Yang Chen, Yu Tang, Leiyun Han, Yingjie Hua, Xudong Zhao, Xiaoyang Liu
{"title":"原位氮掺杂双壳SiOx纳米球:提高锂离子电池性能的新方法","authors":"Yang Chen, Yu Tang, Leiyun Han, Yingjie Hua, Xudong Zhao, Xiaoyang Liu","doi":"10.1039/d5qi01215e","DOIUrl":null,"url":null,"abstract":"Effectively alleviating the volume change of silicon oxide (SiO<small><sub><em>x</em></sub></small>) anodes and improving their conductivity are crucial for enhancing the structural integrity and cycling stability of lithium-ion batteries (LIBs). In this study, ZIF-67 hollow nanospheres (ZIF-67 HNSs) were synthesized for the first time and used as templates to achieve a hollow structure, nanostructuring, and <em>in situ</em> nitrogen doping in SiO<small><sub><em>x</em></sub></small> anodes, resulting in the successful preparation of N/SiO<small><sub><em>x</em></sub></small>@N/SiO<small><sub><em>x</em></sub></small>@C double-shell layer hollow nanospheres. The material features a robust nitrogen-doped SiO<small><sub><em>x</em></sub></small> double-shell structure, which, combined with oxygen content regulation, effectively alleviates the volume expansion of high-capacity SiO<small><sub><em>x</em></sub></small> anodes. Additionally, <em>in situ</em> nitrogen doping into the SiO<small><sub><em>x</em></sub></small> matrix further optimizes the electronic conductivity and ion diffusivity. Electrochemical impedance spectroscopy and distribution of relaxation time analyses indicate that the anode exhibits excellent charge transfer kinetics and a stable solid electrolyte interfacial layer, which remains stable even after prolonged cycling. <em>In situ</em> Raman spectroscopy further confirms that the double-shell structure effectively preserves the integrity of the electrode. The anode achieves a high specific capacity of 893.1 mAh g<small><sup>−1</sup></small> after 1000 cycles at 1 A g<small><sup>−1</sup></small> and demonstrates excellent rate capability (447.4 mAh g<small><sup>−1</sup></small> at 3 A g<small><sup>−1</sup></small>). This study presents a novel approach for designing SiO<small><sub><em>x</em></sub></small> anodes with <em>in situ</em> nitrogen doping and spatially engineered double-shell structures, offering new insights into the design of high-performance LIB anodes with enhanced cycling stability and capacity retention.","PeriodicalId":79,"journal":{"name":"Inorganic Chemistry Frontiers","volume":"8 1","pages":""},"PeriodicalIF":6.4000,"publicationDate":"2025-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"In situ nitrogen-doped double-shell SiOx nanospheres: a novel approach for enhancing lithium-ion battery performance\",\"authors\":\"Yang Chen, Yu Tang, Leiyun Han, Yingjie Hua, Xudong Zhao, Xiaoyang Liu\",\"doi\":\"10.1039/d5qi01215e\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Effectively alleviating the volume change of silicon oxide (SiO<small><sub><em>x</em></sub></small>) anodes and improving their conductivity are crucial for enhancing the structural integrity and cycling stability of lithium-ion batteries (LIBs). In this study, ZIF-67 hollow nanospheres (ZIF-67 HNSs) were synthesized for the first time and used as templates to achieve a hollow structure, nanostructuring, and <em>in situ</em> nitrogen doping in SiO<small><sub><em>x</em></sub></small> anodes, resulting in the successful preparation of N/SiO<small><sub><em>x</em></sub></small>@N/SiO<small><sub><em>x</em></sub></small>@C double-shell layer hollow nanospheres. The material features a robust nitrogen-doped SiO<small><sub><em>x</em></sub></small> double-shell structure, which, combined with oxygen content regulation, effectively alleviates the volume expansion of high-capacity SiO<small><sub><em>x</em></sub></small> anodes. Additionally, <em>in situ</em> nitrogen doping into the SiO<small><sub><em>x</em></sub></small> matrix further optimizes the electronic conductivity and ion diffusivity. Electrochemical impedance spectroscopy and distribution of relaxation time analyses indicate that the anode exhibits excellent charge transfer kinetics and a stable solid electrolyte interfacial layer, which remains stable even after prolonged cycling. <em>In situ</em> Raman spectroscopy further confirms that the double-shell structure effectively preserves the integrity of the electrode. The anode achieves a high specific capacity of 893.1 mAh g<small><sup>−1</sup></small> after 1000 cycles at 1 A g<small><sup>−1</sup></small> and demonstrates excellent rate capability (447.4 mAh g<small><sup>−1</sup></small> at 3 A g<small><sup>−1</sup></small>). 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引用次数: 0
摘要
有效缓解氧化硅(SiOx)阳极的体积变化,提高其导电性是提高锂离子电池(LIBs)结构完整性和循环稳定性的关键。本研究首次合成了ZIF-67空心纳米球(ZIF-67 HNSs),并以其为模板实现了空心结构、纳米化和SiOx阳极的原位氮掺杂,成功制备了N/SiOx@N/SiOx@C双壳层空心纳米球。该材料具有坚固的氮掺杂SiOx双壳结构,结合氧含量调节,有效缓解了高容量SiOx阳极的体积膨胀。此外,原位氮掺杂到SiOx基体中进一步优化了电子导电性和离子扩散率。电化学阻抗谱和弛豫时间分布分析表明,阳极表现出良好的电荷转移动力学和稳定的固体电解质界面层,即使长时间循环也保持稳定。原位拉曼光谱进一步证实了双壳结构有效地保持了电极的完整性。在1ag - 1下循环1000次后,阳极达到893.1 mAh g - 1的高比容量,并表现出优异的倍率能力(在3ag - 1下为447.4 mAh g - 1)。本研究提出了一种采用原位氮掺杂和空间工程双壳结构设计SiOx阳极的新方法,为设计具有增强循环稳定性和容量保持性的高性能锂离子电池阳极提供了新的见解。
In situ nitrogen-doped double-shell SiOx nanospheres: a novel approach for enhancing lithium-ion battery performance
Effectively alleviating the volume change of silicon oxide (SiOx) anodes and improving their conductivity are crucial for enhancing the structural integrity and cycling stability of lithium-ion batteries (LIBs). In this study, ZIF-67 hollow nanospheres (ZIF-67 HNSs) were synthesized for the first time and used as templates to achieve a hollow structure, nanostructuring, and in situ nitrogen doping in SiOx anodes, resulting in the successful preparation of N/SiOx@N/SiOx@C double-shell layer hollow nanospheres. The material features a robust nitrogen-doped SiOx double-shell structure, which, combined with oxygen content regulation, effectively alleviates the volume expansion of high-capacity SiOx anodes. Additionally, in situ nitrogen doping into the SiOx matrix further optimizes the electronic conductivity and ion diffusivity. Electrochemical impedance spectroscopy and distribution of relaxation time analyses indicate that the anode exhibits excellent charge transfer kinetics and a stable solid electrolyte interfacial layer, which remains stable even after prolonged cycling. In situ Raman spectroscopy further confirms that the double-shell structure effectively preserves the integrity of the electrode. The anode achieves a high specific capacity of 893.1 mAh g−1 after 1000 cycles at 1 A g−1 and demonstrates excellent rate capability (447.4 mAh g−1 at 3 A g−1). This study presents a novel approach for designing SiOx anodes with in situ nitrogen doping and spatially engineered double-shell structures, offering new insights into the design of high-performance LIB anodes with enhanced cycling stability and capacity retention.