材料科学
异质结
阳极
钼
电化学
堆积
钾
二硫化钼
纳米技术
碳纤维
电极
化学工程
光电子学
复合材料
化学
物理化学
冶金
复合数
工程类
有机化学
作者
Mingze Ma,Shipeng Zhang,Yu Yao,Haiyun Wang,Huijuan Huang,Rui Xu,Jiawei Wang,Xuefeng Zhou,Wen Yang,Zhangquan Peng,Xiaojun Wu,Yanglong Hou,Yan Yu
标识
DOI:10.1002/adma.202000958
摘要
Abstract Constructing 2D heterostructure materials by stacking different 2D materials can combine the merits of the individual building blocks while eliminating their shortcomings. Dichalcogenides are attractive anodes for potassium‐ion batteries (KIBs) due to their high theoretical capacity. However, the practical application of dichalcogenide is greatly hampered by the poor electrochemical performance due to sluggish kinetics of K + insertion and the electrode structure collapse resulting from the large K + insertion. Herein, heterostructures of 2D molybdenum dichalcogenide on 2D nitrogen‐doped carbon (MoS 2 , MoSe 2 ‐on‐NC) are prepared to boost their potassium storage performance. The unique 2D heterostructures possess built‐in heterointerfaces, facilitating K + diffusion. The robust chemical bonds (CS, CSe, CMo bonds) enhance the mechanical strength of electrodes, thus suppressing the volume expansion. The 2D N‐doped carbon nanosheets interconnected as a 3D structure offer a fast diffusion path for electrons. Benefitting from these merits, both the MoS 2 ‐on‐NC and the MoSe 2 ‐on‐NC exhibit unprecedented cycle life. Moreover, the electrochemical reaction mechanism of MoSe 2 is revealed during the process of potassiation and depotassiation.
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