Vanadium-based
materials have been extensively studied as promising
cathode materials for zinc-ion batteries because of their multiple
valences and adjustable ion-diffusion channels. However, the sluggish
kinetics of Zn-ion intercalation and less stable layered structure
remain bottlenecks that limit their further development. The present
work introduces potassium ions to partially substitute ammonium ions
in ammonium vanadate, leading to a subtle shrinkage of lattice distance
and the increased oxygen vacancies. The resulting potassium ammonium
vanadate exhibits a high discharge capacity (464 mAh g–1 at 0.1 A g–1) and excellent cycling stability
(90% retention over 3000 cycles at 5 A g–1). The
excellent electrochemical properties and battery performances are
attributed to the rich oxygen vacancies. The introduction of K+ to partially replace NH4
+ appears to alleviate the irreversible deammoniation
to prevent structural collapse during ion insertion/extraction. Density
functional theory calculations show that potassium ammonium vanadate
has a modulated electron structure and a better zinc-ion diffusion
path with a lower migration barrier.