MoS2@CoS2 heterostructured tube-in-tube hollow nanofibers with enhanced reaction reversibility and kinetics for sodium-ion storage

被引:56
作者
Gao, Songwei [1 ]
He, Yixiang [3 ]
Li, Huaike [1 ]
Yue, Guichu [1 ]
Cui, Zhimin [1 ]
Li, Yijie [5 ]
Bai, Jie [4 ]
Wang, Nu [1 ]
Zhang, Qianfan [3 ]
Yu, Yan [2 ]
Zhao, Yong [1 ]
机构
[1] Beihang Univ, Sch Chem, Key Lab Bioinspired Smart Interfacial Sci & Techno, Beijing Key Lab Bioinspired Energy Mat & Devices,M, Beijing 100191, Peoples R China
[2] Univ Sci & Technol China, Hefei Natl Res Ctr Phys Sci Microscale, CAS Key Lab Mat Energy Convers, Dept Mat Sci & Engn, Hefei 230026, Anhui, Peoples R China
[3] Beihang Univ, Sch Mat Sci & Engn, Beijing 100191, Peoples R China
[4] Inner Mongolia Univ Technol, Chem Engn Coll, Hohhot 010051, Peoples R China
[5] Minist Ecol & Environm, Foreign Environm Cooperat Ctr, Beijing 100035, Peoples R China
基金
中国国家自然科学基金;
关键词
DFT calculations; MOS2-COS2; heterostructures; Hollow nanofiber; Reaction mechanism; Sodium-ion batteries; HIGH-PERFORMANCE; ENERGY-STORAGE; NANOSHEETS; STRATEGY; BATTERY; ANODES;
D O I
10.1016/j.ensm.2023.103170
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Rational synergism in spatial nanostructures and heterogeneity are effective ways to enhance reaction reversibility and kinetics of materials for sodium-ion battery electrodes. Herein, we have designed MoS2@CoS2 heterostructured tube-in-tube hollow nanofibers via simple electrospinning, pyrolysis and sulfuration processes. The unique double-walled tubular structure resulted from a stepwise crystallization accompanied by pyrolysis volume shrinkage. It has appropriate void space and abundant MoS2@CoS2 heterointerfaces that can effectively avoid the volumetric change during the reaction process and accelerate the whole infiltration of the electrolyte. The formed MoS2/CoS2 heterojunction introduces a built-in electric field, which increases the adsorption energy and reduces the migration energy barrier of sodium ions. The synergies between distinctive hollow structures and heterogeneous compositional advantages lead to enhanced electrochemical performance for sodium storage with remarkable reversible capacity (858.3 mAh g(-1) at 0.5 A g(-1)), high-rate performance (555.7 mAh g(-1) at 5 A g(-1)), and superior long-term cycling stability (399.6 mAh g(-1) after 1400 cycles at 8 A g(-1)). This rational spatial structures and heterogeneity synergetic strategy provide favorable inspiration for designing extraordinary performance electrode materials for sodium-ion batteries.
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页数:9
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