3D MoS2 foam integrated with carbon paper as binder-free anode for high performance sodium-ion batteries

被引:54
作者
Zheng, Fangying [1 ,2 ]
Wei, Zeyu [2 ]
Xia, Huicong [2 ,3 ]
Tu, Yunchuan [2 ]
Meng, Xiangyu [2 ]
Zhu, Kaixin [2 ,4 ]
Zhao, Jiao [1 ]
Zhu, Yimin [1 ]
Zhang, Jianan [2 ,3 ]
Yang, Yan [1 ]
Deng, Dehui [2 ,4 ]
机构
[1] Dalian Maritime Univ, Inst Environm Remediat, Dalian 116026, Liaoning, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Liaoning, Peoples R China
[3] Zhengzhou Univ, Coll Mat Sci & Engn, Zhengzhou 450001, Henan, Peoples R China
[4] Dalian Univ Technol, Zhang Dayu Sch Chem, Dalian 116024, Liaoning, Peoples R China
来源
JOURNAL OF ENERGY CHEMISTRY | 2022年 / 65卷
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
3D MoS2 foam; Carbon paper; Binder-free electrode; High performance; Sodium-ion batteries; ENERGY-STORAGE; LITHIUM; NANOSHEETS; ELECTRODE;
D O I
10.1016/j.jechem.2021.05.021
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Molybdenum sulfide (MoS2) with well-designed porous structure has the potential to be great electrode materials in sodium-ion batteries due to its high theoretical capacity and abundant resource, however, hindered by its intrinsic low conductivity and stability. Herein, MoS2 with 3D macroporous foam struc-ture and high conductivity was obtained through SiO2 templates and integrated with carbon paper (3D F-MoS2/CP). It has showed superior specific capacity (225 mA h g(-1), 0.4-3 V) and cycling stability (1000 cycles) at high rate (2000 mA g(-1)), with a low decay rate (0.033% per cycle) in sodium-ion batteries. The excellent electrochemical performance may originate from its unique integrated structure: 3D MoS2 macropores providing high surface area and abundant transfer channels while carbon paper enhancing the conductivity of MoS2 and avoiding unnecessary side reactions brought by binder addition. (c) 2021 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.
引用
收藏
页码:26 / 33
页数:8
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