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用于高性能钠/钾离子半电池/全电池的氮/硫共掺杂中空碳纳米球封装双金属硒化物的构建

Construction of Bimetallic Selenides Encapsulated in Nitrogen/Sulfur Co-Doped Hollow Carbon Nanospheres for High-Performance Sodium/Potassium-Ion Half/Full Batteries.

作者信息

Sun Zhonghui, Wu Xing-Long, Xu Jianan, Qu Dongyang, Zhao Bolin, Gu Zhenyi, Li Wenhao, Liang Haojie, Gao Lifang, Fan Yingying, Zhou Kai, Han Dongxue, Gan Shiyu, Zhang Yuwei, Niu Li

机构信息

Center for Advanced Analytical Science, School of Chemistry and Chemical Engineering c/o School of Civil Engineering, Guangzhou University, Guangzhou, Guangdong, 510006, China.

National and Local United Engineering Laboratory for Power Batteries, Northeast Normal University, Changchun, Jilin, 130024, China.

出版信息

Small. 2020 May;16(19):e1907670. doi: 10.1002/smll.201907670. Epub 2020 Apr 20.

Abstract

Metallic selenides have been widely investigated as promising electrode materials for metal-ion batteries based on their relatively high theoretical capacity. However, rapid capacity decay and structural collapse resulting from the larger-sized Na /K greatly hamper their application. Herein, a bimetallic selenide (MoSe /CoSe ) encapsulated in nitrogen, sulfur-codoped hollow carbon nanospheres interconnected reduced graphene oxide nanosheets (rGO@MCSe) are successfully designed as advanced anode materials for Na/K-ion batteries. As expected, the significant pseudocapacitive charge storage behavior substantially contributes to superior rate capability. Specifically, it achieves a high reversible specific capacity of 311 mAh g at 10 A g in NIBs and 310 mAh g at 5 A g in KIBs. A combination of ex situ X-ray diffraction, Raman spectroscopy, and transmission electron microscopy tests reveals the phase transition of rGO@MCSe in NIBs/KIBs. Unexpectedly, they show quite different Na /K insertion/extraction reaction mechanisms for both cells, maybe due to more sluggish K diffusion kinetics than that of Na . More significantly, it shows excellent energy storage properties in Na/K-ion full cells when coupled with Na V (PO ) O F and PTCDA@450 °C cathodes. This work offers an advanced electrode construction guidance for the development of high-performance energy storage devices.

摘要

金属硒化物因其相对较高的理论容量,作为金属离子电池有前景的电极材料已被广泛研究。然而,较大尺寸的Na/K导致的快速容量衰减和结构坍塌极大地阻碍了它们的应用。在此,一种封装在氮、硫共掺杂空心碳纳米球中的双金属硒化物(MoSe₂/CoSe₂)与还原氧化石墨烯纳米片相互连接(rGO@MCSe),被成功设计为用于Na/K离子电池的先进负极材料。正如预期的那样,显著的赝电容电荷存储行为对优异的倍率性能有很大贡献。具体而言,它在Na离子电池中10 A g⁻¹ 时实现了311 mAh g⁻¹ 的高可逆比容量,在K离子电池中5 A g⁻¹ 时实现了310 mAh g⁻¹ 的高可逆比容量。非原位X射线衍射、拉曼光谱和透射电子显微镜测试相结合揭示了rGO@MCSe在Na离子电池/K离子电池中的相变。出乎意料的是,它们在两个电池中显示出截然不同的Na/K嵌入/脱出反应机制,这可能是由于K的扩散动力学比Na更缓慢。更重要的是,当与Na₃V₂(PO₄)₃O₂F和PTCDA@450 °C正极耦合时,它在Na/K离子全电池中表现出优异的储能性能。这项工作为高性能储能装置的开发提供了先进的电极构建指导。

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