The commercialization of aqueous zinc ion batteries (ZIBs)
is seriously
hindered by the inferior stability of the Zn anode, which principally
originates from water-induced side reactions and dendrite issues.
Interfacial engineering has been considered as a cost-effective way
to tackle these bottlenecks. However, most artificial solid electrolyte
interphase (SEI) suffers from sluggish Zn2+ migration and
thus compromises the kinetic merits of aqueous ZIBs especially at
ultrahigh rates. Herein, we present a unique H2O molecules-rich
zinc phytate (PAZn) interphase for the optimization of Zn anodes.
The critical role of crystal water on the Zn2+ transport
process is demonstrated. Benefiting from the shielding effect, the
Zn2+ diffusion coefficient increases by orders of magnitude
in the presence of crystal water. Accordingly, the Zn anode modified
by PAZn interphase delivers an impressive lifespan of 1200 h and dramatically
reduced voltage hysteresis even under an ultrahigh current density
of 10 mA cm–2, and it remains stable even at a higher
Zn utilization exceeding 50%. Moreover, the V2O5//PAZn@Zn full cell exhibits remarkable performance with a high capacity
retention of 89.3% after 600 cycles. This work provides an effective
strategy for rationally designing highly Zn2+-conductive
artificial SEI for durable Zn anodes and high-performance commercially
available ZIBs.