Affiliation:
1. Collaborative Innovation Center of Steel Technology University of Science and Technology Beijing Beijing 100083 P. R. China
2. State Key Laboratory of Advanced Metallurgy University of Science and Technology Beijing Beijing 100083 P. R. China
Abstract
AbstractIron group metals chalcogenides, especially NiS, are promising candidates for K‐ion battery anodes due to their high theoretical specific capacity and abundant reserves. However, the practical application of NiS‐based anodes is hindered by slow electrochemical kinetics and unstable structure. Herein, a novel structure of Ni3S2–Ni hybrid nanosphere with intra‐core voids encapsulated by N‐doped carbon shells (Ni3S2‐Ni@NC‐AE) is constructed, based on the first electrodeposited NiS nanosphere particles, dopamine coating outer layer, oxygen‐free annealing treatment to form Ni3S2‐Ni core and N‐doped carbon shell, and selective etching of the Ni phase to form intra‐core void. The electron/K+ transport and K+ storage reaction kinetics are enhanced due to shortened diffusion pathways, increased active sites, generation of built‐in electric field, high K+ adsorption energies, and large electronic density of states at Fermi energy level, resulting from the multi‐structures synergistic effect of Ni3S2‐Ni@NC‐AE. Simultaneously, the volume expansion is alleviated due to the sufficient buffer space and strong chemical bonding provided by intra‐core void and yolk–shell structure. Consequently, the Ni3S2‐Ni@NC‐AE exhibits excellent specific capacity (438 mAh g−1 at 0.1 A g−1 up to 150 cycles), outstanding rate performances, and ultra‐stable long‐cycle performance (176.4 mAh g−1 at 1 A g−1 up to 5000 cycles) for K‐ion storage.
Funder
National Natural Science Foundation of China
Fundamental Research Funds for the Central Universities
Subject
General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)
Cited by
18 articles.
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