Mechanistic investigation of silver vanadate as superior cathode for high rate and durable zinc-ion batteries

Rechargeable aqueous Zn-ion batteries have shown considerable potential for stationary grid-scale energy storage systems owing to their characteristics of low cost and non-pollution. Nevertheless, the development of high-performance cathode materials is still a formidable challenge. In this work, for the first time, we report a superior silver vanadate (beta-AgVO3) cathode for Zn-ion batteries, and demonstrate the fundamental Zn2+ storage mechanism in detail. In sharp contrast to the previously-reported layered vandium-based materials, the beta-AgVO3 cathode experiences an initial phase transition to form a layered Zn3V2O7(OH)(2)center dot 2H(2)O through a displacement/reduction reaction of Zn2+/Ag+ in the first discharge process. The in situ generated Ag-0 along with the residual Ag+ and structural water within the framework afford high electronic/ionic conductivity, thus enabling enhanced Zn2+ intercalation/deintercalation kinetics in the layered phase. As a consequence, the cathode can deliver remarkable rate performance (103 mAh g(-1) at 5000 mA g(-1)) and long-term cycling stability (95 mAh g(-1) after 1000 cycles at 2000 mA g(-1) ). The present study offers a totally new insight into the exploration of non-layered-structured vandium-based cathodes for high performance Zn-ion batteries. (C) 2019 Elsevier Inc. All rights reserved.