Freestanding 1T MoS2@MXene hybrid film with strong interfacial interaction for highly reversible zinc ions storage

材料科学 阴极 电极 电导率 离子 电化学 储能 纳米技术 密度泛函理论 化学工程 水溶液 扩散 物理化学 有机化学 化学 工程类 功率(物理) 物理 计算化学 量子力学 热力学
作者
Haonan Zhai,Huibin Liu,Yufen Zhang,Jinjin Wen,Wenyue Yang,Huiting Xu,Xiaoteng Yan,Wenchao Peng,Jiapeng Liu
出处
期刊:Journal of Materials Science & Technology [Elsevier]
卷期号:188: 183-190 被引量:66
标识
DOI:10.1016/j.jmst.2023.12.015
摘要

Aqueous zinc ion batteries (AZIBs) are now gaining widespread attention because of their cost-effectiveness, intrinsic safety, and high theoretical capacity. Nevertheless, it is still crucial to exploit high-performance electrode materials. Herein, the freestanding 1T MoS2@Mxene hybrid films (MMHF) were synthesized and directly served as the cathode of AZIBs. The freestanding MMHF exhibited the hierarchical layer structure with excellent conductivity and strong interfacial interaction, which promoted the exposure of more active sites and the transfer of electrons/ions. Consequently, the MMHF displayed a high specific capacity of 270 mAh g–1 (at 0.1 A g–1) and good rate performance. Impressively, even after 2500 cycles under 10 A g–1, the freestanding MMHF cathode contributed a superior specific capacity of 108 mAh g–1 with an outstanding capacity retention rate of 94.7%. Meanwhile, the energy storage mechanism of the MMHF electrode was also elucidated through ex-situ characterizations. Furthermore, the density functional theory (DFT) computations revealed the strong interfacial interactions between 1T MoS2 and MXene, high conductivity, and low Zn2+ diffusion barrier. This work provides a new viewpoint for designing freestanding transition metal disulfides (TMDs) -MXene hybrid film electrodes for AZIBs.
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