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

• Published in: Advanced materials (Weinheim) 2021-09, Vol.33 (36), p.e2102701-n/a
• Main Authors: Wan, Fang, Hao, Zhimeng, Wang, Shuai, Ni, Youxuan, Zhu, Jiacai, Tie, Zhiwei, Bi, Songshan, Niu, Zhiqiang, Chen, Jun
• Format: Article
• Language: English
• Subjects: aqueous batteries; Carbon fibers; Cathodes; Compensation; dendrite‐free Zn anodes; Dendritic structure; Electrochemical analysis; Electrode materials; Flux density; Interlayers; Ion storage; layered vanadium oxides; Materials science; Nanofibers; Organic chemistry; polar organic molecules; pouch full cells; Vanadates; Vanadium oxides; Zinc
• ISSN: 0935-9648; 1521-4095
• DOI: 10.1002/adma.202102701

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 developed to introduce various polar organic molecules into the interlayer of AlxV2O5·nH2O 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, AlxV2O5 with polar organic molecules displays enhanced electrochemical performance. Furthermore, based on above cathode material, a pouch cell was assembled by further integrating a dendrite‐free N‐doped carbon nanofiber@Zn anode, displaying an energy density of 50 Wh 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. A universal compensation strategy is reported to introduce polar organic molecules into the interlayer of AlxV2O5·nH2O by replacing partial crystal water. Owing to the high‐polar carbonyl/sulfenyl and low‐polar alkyl, the organic molecules display a strong interaction with pre‐intercalated Al3+ and a weak interaction with Zn2+. Consequently, the cathode displays superior structural stability and ion transfer kinetics, leading to excellent performance.