4.6 Article

In situ tailoring bimetallic-organic framework-derived yolk-shell NiS2/CuS hollow microspheres: an extraordinary kinetically pseudocapacitive nanoreactor for an effective sodium-ion storage anode

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 9, Issue 28, Pages 15807-15819

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ta04386b

Keywords

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Funding

  1. Natural Science Foundation of Chongqing [cstc2018jcyjAX0376, cstc2019jcyj-msxmX0550]
  2. China Postdoctoral Science Foundation [2021M690534, 2020M673650]
  3. Innovation Research Team at Institutions of Higher Education in Chongqing [CXQT20027]

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The yolk-shell NiS2/CuS hollow microspherical architecture successfully constructed in this study exhibits superb kinetically pseudocapacitive features, enabling fast charge transfer, Na+ immigration, and extraordinary Na+-storage capability.
Pseudocapacitive electrochemical Na+-storage has been highlighted as one of the exploitable strategies for overcoming the sluggish diffusion-limited redox kinetics due to the effective structural preservation and fast ion-adsorption/desorption at the surface or quasi-surface of electrode materials. However, exploiting pseudocapacitive hosts with a micro-nano hierarchitecture and further achieving competitive pseudocapacitive contributions are still in their infancy so far. Herein, a yolk-shell NiS2/CuS hollow microspherical architecture with superb kinetically pseudocapacitive features was successfully constructed through an in situ hydrothermal sulfidation and subsequent ion-exchange route using Ni-based bimetallic (NiZn) organic frameworks (NiZn-MOFs) as a template precursor. As expected, the strongly synergistic coupling effect and hollow structural characteristic of the NiS2/CuS heterostructure enabled fast charge transfer and Na+ immigration, as well as the release of the mechanical stress/strain induced by the conversion reaction, and not unexpectedly, the NiS2/CuS electrode afforded extraordinary Na+-storage capability, including a remarkable specific capacity of 410.9 mA h g(-1) after 750 cycles at 2.0 A g(-1), excellent rate capability, and prolonged cyclability in terms of a remarkable 283.4 mA h g(-1) even after 4200 cycles at 20.0 A g(-1). More significantly, the kinetic analysis demonstrated that the electrochemical charge storage of the NiS2/CuS electrode manifested considerable pseudocapacitive contributions at all rates (90.0% to 96.9%), distinctly outperforming the previously reported NiS2-/CuS-based anodes. Furthermore, the density functional theoretical calculations suggested a fast Na+-transport kinetics and enhanced antibonding state energy level and Na2S adsorption energy due to the electronic redistribution and lattice distortion in the NiS2/CuS heterointerfaces.

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