A Universal Compensation Strategy to Anchor Polar Organic Molecules in Bilayered Hydrated Vanadates for Promoting Aqueous Zinc-Ion Storage.

Abstract

The electrochemical performance of layered vanadium oxides is often improved by introducing guest species into their interlayer. Guest species with high stability in the interlayer and weak interaction with Zn2+ during charge/discharge process are desired to promoting reversible Zn2+ transfer. Herein, a universal compensation strategy was\xa0developed to introduce various polar organic molecules into the interlayer of Alx V2 O5 ·nH2 O by replacing partial crystal water. The high-polar groups in the organic molecules have a strong electrostatic attraction with pre-intercalated Al3+ , which ensures that organic molecules can be anchored in the interlayer of hydrated vanadates. Simultaneously, the low-polar groups endow organic molecules with a weak interaction with Zn2+ during cycling, thus liberalizing reversible Zn2+ transfer. As a result, Alx V2 O5 with polar organic molecules displays enhanced electrochemical performance. Furthermore, based on above cathode material, a pouch cell was\xa0assembled by further integrating a dendrite-free N-doped carbon nanofiber@Zn anode, displaying an energy density of 50\xa0Wh kg-1 . This work provides a path for designing stable guest species with a weak interaction with Zn2+ in the interlayer of layered vanadium oxide towards high-performance cathode materials of aqueous Zn batteries.