阳极
材料科学
电池(电)
阴极
离子
纤维
碳纤维
异质结
锂(药物)
化学工程
纳米技术
电极
光电子学
复合材料
化学
复合数
内分泌学
医学
功率(物理)
物理
有机化学
物理化学
量子力学
工程类
作者
Qi Zhang,Yaping Zeng,Xuemei Chen,Yingchun Ding,Hu Wang,Liu Wang,Heng Wang,Xinyu Li,Jiang Xiao,Tianran Zhang
标识
DOI:10.1016/j.electacta.2023.143363
摘要
Metal sulfides based on a conversion mechanism possess high theoretical specific capacity, making them suitable for high-energy-density sodium-ion batteries (SIBs). However, they suffer from rapid capacity decay when assembled into full batteries due to dynamic hysteresis and large volume expansion. In this paper, the architectural engineering approach to construct MoS2/Fe2O3 @ carbon fiber heterostructures is proposed to overcome the above issues. The heterojunction formed by MoS2 and Fe2O3 would promote ion/electron transfer, while the carbon nano-fibers serve as a holder to maintain structural stability and ensure the rapid transport of electrons. The full battery in which the as-prepared MoS2/Fe2O3 @ carbon fiber anode is paired with a Na3V2(PO4)3/C cathode delivers a reversible capacity of 61.1 mAh g−1 at 500 mA g−1 for 1600 cycles without attenuation. Experimental characterization and theoretical calculation results show that this structural engineering approach improves the ion diffusion efficiency, enhances the conductivity, provides a more appropriate sodium ion adsorption energy, and thus extends the cycling life of the SIB. This work demonstrates the efficiency of architectural engineering and paves the way to design ultra-long-cycling Na-ion batteries.
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