{"title":"Facile synthesis of carbon-coated silicon nanocomposite with tremella-like porous structure for superior lithium-ion storage.","authors":"Lihua Ma, Jibin Tian, Xiaozhong Zhou","doi":"10.1063/5.0265543","DOIUrl":null,"url":null,"abstract":"<p><p>Silicon/carbon (Si/C) composites have been envisaged as one of the most promising anode materials for the next-generation lithium-ion batteries (LIBs) with high energy density, and constructing reasonable and cross-scale structures is crucial adjective for high-performance Si/C electrodes. Herein, a facile synthesis strategy was developed by combining gel coating, carbonization, and molten salt-assisted magnesiothermic reduction (MSA-MR), and a unique tremella-like Si/C composite with internal void structure (IV-Si/C) was successfully prepared. The working mechanisms of both sodium alginate (SA) and molten salt (NaCl) on the successful preparation of the target IV-Si/C nanocomposite were also investigated in detail. It was demonstrated that, α-L-guluronic (G) blocks in SA can be cross-linked with cations to promote the interactions with silicon dioxide (SiO2) particles, boosting uniform distribution of nanosized Si particles in the SA-derived carbon matrix. Meanwhile, NaCl generated from SA not only effectively boosted the crystallization of SiO2 during the high-temperature carbonization process but also can effectively inhibit the formation of inert SiC and strengthen reduction of carbon during the MSA-MR treatment, resulting in successful preparation of the tremella-like Si/C composite with abundant internal voids. Benefitting from its unique structure, when used as an alternative anode material for electrochemical lithium storage, the as-obtained IV-Si/C nanocomposite delivered a high reversible specific capacity of 1899.6 mAh g-1 with an initial Coulomb efficiency of 75.96% and superior rate capability and long-term cycling stability. This facile and low-cost synthesis strategy may shed light on the controllable preparation of functional nanomaterials with unique structures, especially high-performance Si/C anode materials for their large-scale application in LIBs.</p>","PeriodicalId":15313,"journal":{"name":"Journal of Chemical Physics","volume":"162 18","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2025-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Physics","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1063/5.0265543","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Silicon/carbon (Si/C) composites have been envisaged as one of the most promising anode materials for the next-generation lithium-ion batteries (LIBs) with high energy density, and constructing reasonable and cross-scale structures is crucial adjective for high-performance Si/C electrodes. Herein, a facile synthesis strategy was developed by combining gel coating, carbonization, and molten salt-assisted magnesiothermic reduction (MSA-MR), and a unique tremella-like Si/C composite with internal void structure (IV-Si/C) was successfully prepared. The working mechanisms of both sodium alginate (SA) and molten salt (NaCl) on the successful preparation of the target IV-Si/C nanocomposite were also investigated in detail. It was demonstrated that, α-L-guluronic (G) blocks in SA can be cross-linked with cations to promote the interactions with silicon dioxide (SiO2) particles, boosting uniform distribution of nanosized Si particles in the SA-derived carbon matrix. Meanwhile, NaCl generated from SA not only effectively boosted the crystallization of SiO2 during the high-temperature carbonization process but also can effectively inhibit the formation of inert SiC and strengthen reduction of carbon during the MSA-MR treatment, resulting in successful preparation of the tremella-like Si/C composite with abundant internal voids. Benefitting from its unique structure, when used as an alternative anode material for electrochemical lithium storage, the as-obtained IV-Si/C nanocomposite delivered a high reversible specific capacity of 1899.6 mAh g-1 with an initial Coulomb efficiency of 75.96% and superior rate capability and long-term cycling stability. This facile and low-cost synthesis strategy may shed light on the controllable preparation of functional nanomaterials with unique structures, especially high-performance Si/C anode materials for their large-scale application in LIBs.
硅/碳(Si/C)复合材料被认为是下一代高能量密度锂离子电池(LIBs)最有前途的负极材料之一,而构建合理的跨尺度结构是高性能Si/C电极的关键。本文采用凝胶包覆、碳化和熔盐辅助镁热还原(MSA-MR)相结合的简易合成策略,成功制备了一种独特的具有内部空洞结构的银耳状Si/C复合材料(IV-Si/C)。研究了海藻酸钠(SA)和熔融盐(NaCl)在成功制备ⅳ- si /C纳米复合材料中的作用机理。结果表明,SA中的α- l -古鲁醛酸(G)嵌段可以与阳离子交联,促进与二氧化硅(SiO2)颗粒的相互作用,促进纳米Si颗粒在SA衍生的碳基体中的均匀分布。同时,SA生成的NaCl不仅在高温碳化过程中有效促进了SiO2的结晶,而且在MSA-MR处理过程中有效抑制了惰性SiC的形成,加强了碳的还原,成功制备了内部空隙丰富的银耳状Si/C复合材料。得益于其独特的结构,当用作电化学锂存储的替代阳极材料时,所获得的IV-Si/C纳米复合材料具有1899.6 mAh g-1的高可逆比容量,初始库仑效率为75.96%,具有优越的倍率容量和长期循环稳定性。这种简单、低成本的合成策略可能为具有独特结构的功能纳米材料的可控制备,特别是高性能Si/C负极材料在lib中的大规模应用提供了思路。
期刊介绍:
The Journal of Chemical Physics publishes quantitative and rigorous science of long-lasting value in methods and applications of chemical physics. The Journal also publishes brief Communications of significant new findings, Perspectives on the latest advances in the field, and Special Topic issues. The Journal focuses on innovative research in experimental and theoretical areas of chemical physics, including spectroscopy, dynamics, kinetics, statistical mechanics, and quantum mechanics. In addition, topical areas such as polymers, soft matter, materials, surfaces/interfaces, and systems of biological relevance are of increasing importance.
Topical coverage includes:
Theoretical Methods and Algorithms
Advanced Experimental Techniques
Atoms, Molecules, and Clusters
Liquids, Glasses, and Crystals
Surfaces, Interfaces, and Materials
Polymers and Soft Matter
Biological Molecules and Networks.