Aqueous zinc-ion batteries are highly desirable for large-scale energy storage because of their low cost and high-level safety. However, achieving high energy and high power densities simultaneously is challenging. Herein, a VOx sub-nanometer cluster/reduced graphene oxide (rGO) cathode material composed of interfacial VOC bonds is artificially constructed. Therein, a new mechanism is revealed, where Zn2+ ions are predominantly stored at the interface between VOx and rGO, which causes anomalous valence changes compared to conventional mechanisms and exploits the storage ability of non-energy-storing active yet highly conductive rGO. Further, this interface-dominated storage triggers decoupled transport of electrons/Zn2+ ions, and the reversible destruction/reconstruction allows the interface to store more ions than the bulk. Finally, an ultrahigh rate capability (174.4 mAh g-1 at 100 A g-1 , i.e., capacity retention of 39.4% for a 1000-fold increase in current density) and a high capacity (443 mAh g-1 at 100 mA g-1 , exceeding the theoretical capacities of each interfacial component) are achieved. Such interface-dominated storage is an exciting way to build high-energy- and high-power-density devices.
Keywords: aqueous zinc-ion batteries; decoupled electron/ion transport; heterostructures; interface pseudocapacitance; interface-dominated storage.
© 2021 Wiley-VCH GmbH.