摘要
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.
危险品化学品经营许可证（带存储）