Delving into the dissimilarities in electrochemical performance and underlying mechanisms for sodium and potassium ion storage in N-doped carbon-encapsulated metallic Cu2Se nanocubes

被引:0
|
作者
Xinyu Wang [1 ,2 ]
Yanan Xu [1 ,2 ]
Xiaofeng Liu [1 ,2 ]
Lei Tan [3 ]
Huaiqiang Gu [4 ]
Xin Du [1 ,2 ]
Dan Li [1 ,2 ,5 ,6 ]
机构
[1] College of Chemistry, Zhengzhou University
[2] Green Catalysis Center, College of Chemistry, Zhengzhou University
[3] Institute of Theoretical Physics, Lanzhou University
[4] School of Nuclear Science and Technology, Lanzhou University
[5] Key Laboratory of Advanced Energy Materials Chemistry(Ministry of Education), College of Chemistry, Nankai University
[6] State Key Laboratory of Chemistry and Utilization of Carbon Based Energy Resources, College of Chemistry, Xinjiang University
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中图分类号
TM912 [蓄电池];
学科分类号
0808 ;
摘要
The large volumetric variations experienced by metal selenides within conversion reaction result in inferior rate capability and cycling stability,ultimately hindering the achievement of superior electrochemical performance.Herein,metallic Cu2Se encapsulated with N-doped carbon(Cu2Se@NC) was prepared using Cu2O nanocubes as templates through a combination of dopamine polymerization and hightemperature selenization.The unique nanocubic structure and uniform N-doped carbon coating could shorten the ion transport distance,accelerate electron/charge diffusion,and suppress volume variation,ultimately ensuring Cu2Se@NC with excellent electrochemical performance in sodium ion batteries(SIBs) and potassium ion batteries(PIBs).The composite exhibited excellent rate performance(187.7 mA h g-1at 50 A g-1in SIBs and 179.4 mA h g-1at 5 A g-1in PIBs) and cyclic stability(246,8 mA h g-1at 10 A g-1in SIBs over 2500 cycles).The reaction mechanism of intercalation combined with conversion in both SIBs and PIBs was disclosed by in situ X-ray diffraction(XRD) and ex situ transmission electron microscope(TEM).In particular,the final products in PIBs of K2Se and K2Se3species were determined after discharging,which is different from that in SIBs with the final species of Na2Se.The density functional theory calculation showed that carbon induces strong coupling and charge interactions with Cu2Se,leading to the introduction of built-in electric field on heterojunction to improve electron mobility.Significantly,the theoretical calculations discovered that the underlying cause for the relatively superior rate capability in SIBs to that in PIBs is the agile Na+diffusion with low energy barrier and moderate adsorption energy.These findings offer theoretical support for in-depth understanding of the performance differences of Cu-based materials in different ion storage systems.
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页码:336 / 347
页数:12
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