阳极
材料科学
碳纤维
X射线光电子能谱
双金属片
纳米技术
上部结构
化学工程
电极
钠离子电池
化学
复合材料
法拉第效率
冶金
金属
物理化学
工程类
地质学
海洋学
复合数
作者
Binyang Qin,Mengqi Wang,Shimei Wu,Yining Li,C. Liu,Yufei Zhang,Haosen Fan
标识
DOI:10.1016/j.cclet.2023.108921
摘要
Na+ batteries (SIBs) have been emerging as the most promising candidate for the next generation of secondary batteries. However, the development of high-performance and cost-effective anode materials is urgently needed for the large-scale applications of SIBs. In this study, carbon dots confined bimetallic sulfide (NiCo2S4) architecture (NiCo2S4@CDs) was proposed and synthesized from assembling nanosheets into cross-stacked superstructure and the subsequent confinement of carbon dots. This novel decussated structure assembly from nanosheets is greatly beneficial to the structure stability of electrode material during the successive charge/discharge processes. Besides, the CDs based carbon conductive network can enhance the electrical conductivity for facilitating the easy transport of electron/Na+. Benefitting from these advantages, NiCo2S4@CDs exhibits high-rate performance and an ultralong cycling life in SIBs. Specifically, the specific capacity of NiCo2S4@CDs can reach the discharge specific capacity as high as 568.9 mAh/g at 0.5 A/g, which can also maintain 302.7 mAh/g after 750 cycles at t 5.0 A/g. Additionally, ex-situ characterization techniques such as ex-situ XRD and ex-situ XPS were employed to further explore the sodium storage mechanism of the NiCo2S4@CDs anode.
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