Enhancing Zn<sup>2+</sup> Storage Performance by Constructing the Interfaces Between VO<sub>2</sub> and Co–N–C Layers
Guoqiang Yuan, Xing Wei, Yichun Su, Tianyu Zhou, Jin‐Liang Hu, Yang An, Songlin Zhou, Wen‐Qiang Zhao, Jun Xia, Yang‐Yi Liu
Abstract
Abstract Vanadium oxides have aroused attention as cathode materials in aqueous zinc‐ion batteries (AZIBs) due to their low cost and high safety. However, low ion diffusion and vanadium dissolution often lead to capacity decay and deteriorating stability during cycling. Herein, vanadium dioxides (VO 2 ) nanobelts are coated with a single‐atom cobalt dispersed N‐doped carbon (Co–N–C) layer via a facile calcination strategy to form Co–N–C layer coated VO 2 nanobelts (VO 2 @Co–N–C NBs) for cathodes in AZIBs. Various in‐ / ex situ characterizations demonstrate the interfaces between VO 2 layers and Co–N–C layers can protect the VO 2 NBs from collapsing, increase ion diffusion, and enhance the Zn 2+ storage performance. Additional density functional theory (DFT) simulations demonstrate that Co─O─V bonds between VO 2 and Co–N–C layers can enhance interfacial Zn 2+ storage. Moreover, the VO 2 @Co–N–C NBs provided an ultrahigh capacity (418.7 mAh g −1 at 1 A g −1 ), outstanding long‐term stability (over 8000 cycles at 20 A g −1 ), and superior rate performance.