石墨烯
阳极
插层(化学)
材料科学
无定形固体
氧化物
化学工程
扩散阻挡层
纳米技术
无定形碳
电极
无机化学
化学
图层(电子)
结晶学
冶金
工程类
物理化学
作者
Jun Xu,Jinchi Jiang,Shoufu Cao,Suwan Li,Yuanming Ma,Junwei Chen,Y. Zhang,Xiaoqing Lü
出处
期刊:EcoMat
[Wiley]
日期:2024-07-08
卷期号:6 (8)
摘要
Abstract MoS 2 as a typical layered transition metal dichalcogenide (LTMD) has attracted considerable attention to work as sodium host materials for sodium‐ion batteries (SIBs). However, it suffers from low semiconducting behavior and high Na + diffusion barriers. Herein, intercalation of N‐doped amorphous carbon (NAC) into each interlayer of the tiny MoS 2 nanosheets embedded on rGO conductive network is achieved, resulting in formation of rGO@MoS 2 /NAC hierarchy with interoverlapped MoS 2 /NAC superlattices for high‐performance SIBs. Attributed to intercalation of NAC, the resulting MoS 2 /NAC superlattices with wide MoS 2 interlayer of 1.02 nm facilitates rapid Na + insertion/extraction and accelerates reaction kinetics. Theoretical calculations uncover that the MoS 2 /NAC superlattices are beneficial for enhanced electron transport, decreased Na + diffusion barrier and improved Na + adsorption energy. The rGO@MoS 2 /NAC anode presents significantly improved high‐rate capabilities of 228, 207, and 166 mAh g −1 at 20, 30, and 50 A g −1 , respectively, compared with two control samples of pristine MoS 2 and MoS 2 /NAC counterparts. Excellent long‐term cyclability over 10 000 cycles with extremely low capacity decay is demonstrated at high current densities of 20 and 50 A g −1 . Sodium‐ion full cells based on the rGO@MoS 2 /NAC anode are also demonstrated, yielding decent cycling stability of 200 cycles at 5C. Our work provides a novel interlayer strategy to regulate electron/Na + transport for fast‐charging SIBs. image
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