The
anode electrochemical performance of lithium-ion batteries
(LIBs) depends mainly on the structural stability of the electrode
material and its conductivity, and its energy storage mechanism is
mainly derived from the Faraday charge transfer that occurs around
the electrode surface and the Faraday pseudocapacitance. Due to the
high theoretical specific capacity of transition metal sulfides (TMS)
and the mechanical stability and high conductivity of carbon cloth
(CC), the strategy of growing TMS in situ in CC can simultaneously
improve reversibility, structural stability, and conductivity. In
this work, hierarchical 3D-Zn-ZIF-on-2D-Co-ZIF precursors are grown
in situ on CC by a strategy called MOF-on-MOF, and the ZnS/CoS2/CC stable framework is obtained by sulfuration. The interfacial
electron transfer mechanism was explored by ultraviolet photoelectron
spectroscopy, and the synergistic interaction between ZnS and CoS2 in ZnS/CoS2/CC was further elaborated. Specifically,
the work functions of ZnS and CoS2 are 15.9 and 16.6 eV,
respectively, and the corresponding Fermi energy levels are 5.32 eV
for ZnS and 4.62 eV for CoS2. Therefore, after doping with
ZnS, electrons will be transferred and enriched from the ZnS surface
to the CoS2 surface to accelerate the reduction process
of CoS2, and this plays such a decisive part during the
electrochemical reaction. Thereby, the charge enrichment and rapid
transfer at the ZnS/CoS2/CC interface facilitates the Faraday
reaction. As a result, ZnS/CoS2/CC exhibits an outstanding
electrochemical performance as an anode material for LIBs, with a
capacity of up to 1644.7 mA h g–1 after 160 cycles
at a high current density of 1 A g–1.