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Bimetallic Sulfide Sb2S3@FeS2 Hollow Nanorods as High-Performance Anode Materials for Sodium-Ion Batteries

机译:双金属硫化物SB2S3 @ FES2中空纳米棒作为钠离子电池的高性能阳极材料

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摘要

Constructing a heterojunction and introducing an interfacial interaction by designing ideal structures have the inherent advantages of optimizing electronic structures and macroscopic mechanical properties. An exquisite hierarchical heterogeneous structure of bimetal sulfide Sb2S3@FeS2 hollow nanorods embedded into a nitrogen-doped carbon matrix is fabricated by a concise two-step solvothermal method. The FeS2 interlayer expands in situ grow on the interface of hollow Sb2S3 nanorods within the nitrogen-doped graphene matrix, forming a delicate heterostructure. Such a well-designed architecture affords rapid Na+ diffusion and improves charge transfer at the heterointerfaces. Meanwhile, the strongly synergistic coupling interaction among the interior Sb2S3, interlayer FeS2, and external nitrogen-doped carbon matrix creates a stable nanostructure, which extremely accelerates the electronic/ion transport and effectively alleviates the volume expansion upon long cyclic performance. As a result, the composite, as an anode material for sodium-ion batteries, exhibits a superior rate capability of 537.9 mAh g(-1) at 10 A g(-1) and excellent cyclic stability with 85.7% capacity retention after 1000 cycles at 5 A g(-1). Based on the DFT calculation, the existing constructing heterojunction in this composite can not only optimize the electronic structure to enhance the conductivity but also favor the Na2S adsorption energy to accelerate the reaction kinetics. The outstanding electrochemical performance sheds light on the strategy by the rational design of hierarchical heterogeneous nanostructures for energy storage applications.
机译:通过设计理想结构构造异质结并引入界面相互作用具有优化电子结构和宏观机械性能的固有优点。通过简洁的两步溶液法制造嵌入氮掺杂碳基质中的二金属硫化物SB2S3 @ FES2中空纳米棒的精致分层异质结构。 FES2中间层在氮掺杂石墨烯基质内的中空SB2S3纳米棒的界面上膨胀,形成精细异质结构。这种精心设计的架构提供了快速的Na +扩散,并在异待饲料上提高电荷转移。同时,内部SB2S3,中间层FES2和外氮掺杂碳基质之间的强烈协同耦合相互作用产生稳定的纳米结构,其极大地加速了电子/离子运输,并有效地减轻了长循环性能时的体积扩展。结果,作为钠离子电池的阳极材料的复合材料,其优异的速率能力为537.9mahg(-1),10 a g(-1),优异的循环稳定性,1000次循环后的容量保持85.7%在5 a g(-1)。基于DFT计算,该复合材料中现有的构建异质结不能优化电子结构以增强电导率,也有利于Na2S吸附能量,以加速反应动力学。优异的电化学性能通过储能应用的分层异质纳米结构的合理设计阐明了策略。

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