Simultaneously Tailoring Zinc Deposition and Solvation Structure by Electrolyte Additive

Aqueous zinc ion batteries (AZIBs) have attracted intense attention due to their high safety and low cost. Unfortunately, the serious dendrite growth and side reactions of the Zn metal anode in an aqueous electrolyte result in rapid battery failure, hindering the practical application of AZIBs. Herein, sodium gluconate as a dual-functional electrolyte additive has been employed to enhance the electrochemical performance of AZIBs. Gluconate anions preferentially adsorb on the surface of the Zn anode, which effectively prevents H 2 evolution and induces uniform Zn deposition to suppress dendrite growth. Moreover, the gluconate anions can highly coordinate with Zn 2+, promoting the dissolution of [Zn(H 2 O) 6 ] 2+ to inhibit side reactions and the water-induced corrosion reaction. As a result, the Zn||Zn symmetric battery exhibits a long-term cycling stability of over 3000 h at 1 mA cm –2 /1 mA h cm –2 and 600 h at 10 mA cm –2 /10 mA h cm –2 . Furthermore, the NH 4 V 4 O 10 ||Zn full battery also displays excellent cycling stability and a high reversible capacity of 193 mA h g –1 at 2 A g –1 after 1000 cycles. Given the low-cost advantage of SG, the proposed interface chemistry modulation strategy holds considerable potential for promoting the commercialization of AZIBs.