MoS2 Hollow Multishelled Nanospheres Doped Fe Single Atoms Capable of Fast Phase Transformation for Fast‐charging Na‐ion Batteries

Author:

Zhang Hui1,Zhang Shaocheng2,Guo Baiyu3,Yu Li‐juan4,Ma Linlin1,Hou Baoxiu1,Liu Haiyan1,Zhang Shuaihua1,Wang Jiangyan5,Song Jianjun6,Tang Yongfu3,Zhao Xiaoxian1ORCID

Affiliation:

1. Department of Chemistry College of science Hebei Agriculture University Baoding 071001 P.R. China

2. College of Chemical Engineering and Technology Taiyuan University of Technology Taiyuan 030024 China

3. Clean Nano Energy Center State Key Laboratory of Metastable Materials Science and Technology Yanshan University Qinhuangdao 066004 China

4. ARC Centre of Excellence for Electromaterials Science Research School of Chemistry Australian National University Canberra Australian Capital Territory 2601 Australia

5. State Key Laboratory of Biochemical Engineering Institute of Process Engineering Chinese Academy of Sciences No. 1, Beierjie, Zhongguancun Beijing 100190 P. R. China

6. College of Physics Qingdao University Qingdao 266071 China

Abstract

AbstractLow Na+ and electron diffusion kinetics severely restrain the rate capability of MoS2 as anode for sodium‐ion batteries (SIBs). Slow phase transitions between 2H and 1T, and from NaxMoS2 to Mo and Na2S as well as the volume change during cycling, induce a poor cycling stability. Herein, an original Fe single atom doped MoS2 hollow multishelled structure (HoMS) is designed for the first time to address the above challenges. The Fe single atom in MoS2 promotes the electron transfer, companying with shortened charge diffusion path from unique HoMS, thereby achieving excellent rate capability. The strong adsorption with Na+ and self‐catalysis of Fe single atom facilitates the reversible conversion between 2H and 1T, and from NaxMoS2 to Mo and Na2S. Moreover, the buffering effect of HoMS on volume change during cycling improves the cyclic stability. Consequently, the Fe single atom doped MoS2 quadruple‐shelled sphere exhibits a high specific capacity of 213.3 mAh g−1 at an ultrahigh current density of 30 A g−1, which is superior to previously‐reported results. Even at 5 A g−1, 259.4 mAh g−1 (83.68 %) was reserved after 500 cycles. Such elaborate catalytic site decorated HoMS is also promising to realize other “fast‐charging” high‐energy‐density rechargeable batteries.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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