Zn
metal with high specific capacity and low redox potential is
deemed to be an ideal anode material for aqueous zinc-ion batteries
(ZIBs). However, the serious dendrite problems induced by the uneven
deposition of zinc shorten the service life and hinder the development
of ZIBs. According to the nucleation and growth mechanism, the charge
distribution at the anode interface is the critical factor affecting
the deposition morphology. Herein, CF4 plasma technology
is applied for the first time to in situ modification of the Zn anode,
and then, the uniform nanoscale ZnF2 particles are formed.
Due to the excellent ionic conductivity and poor electronic conductivity
of ZnF2, the ion and electron distribution at the anode
interface is orderly regulated, thus guiding uniform and reversible
deposition behavior and restraining the dendrite growth. As a result,
the Zn@ZnF2-5 anode exhibits low nucleation overpotential
(16 mV), long cycle life (2500 h at 1 mA cm–2 and
1 mA h cm–2), and excellent resistance to high current
density (20 mA cm–2) and high discharge depth (16%).
Meanwhile, the Zn@ZnF2-5|I2@AC full battery
shows remarkable cycle stability (1000 cycles) with ∼10% discharge
depth of the anode. The novel and practical CF4 plasma
in situ modification strategy provides a new idea for the interface
modification of zinc anode.