Aqueous
zinc ion batteries (ZIBs) are highly desired as potential
alternatives for rechargeable batteries owning to their low cost,
safety, and environmentally friendly features. However, cathode materials
in ZIBs deliver poor electrochemical performance in power density,
rate capability, and cycling stability, being major limitations for
the grid-scale applications. Herein, vanadium dioxides with polyaniline
(PANI) intercalation were fabricated for the first time. Layered PANI-intercalated
VO2(L-PANI-VO2) cathode with an enlarged layer
spacing of 10.2 Å delivered a specific capacity of 415 mA h g–1 and maintained 280 mA h g–1 after
50 cycles at a current density of 0.1 Ag–1. The
L-PANI-VO2 cathode exhibited good rate capability and gained
a remaining capacity of 173 mA h g–1 after 1000
cycles at a current density of 2.0 Ag–1. The dynamics
of Zn2+ ions and phase structure evolution during the charge
and discharge process were investigated by X-ray diffraction and X-ray
photoelectron spectroscopy, respectively. Our study revealed that
the intercalated PANI could provide strong charge screening effect
to Zn2+ ion insertion/extraction and enhance the electrochemical
performance of the L-PANI-VO2 cathode. In addition, the
unexpected Zn3(OH)2V2O7(H2O)2 precipitates formed both in charge and
discharge processes are found to induce the decay of the as-prepared
ZIBs.