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通过构建VO与Co-N-C层之间的界面来提高锌存储性能。

Enhancing Zn Storage Performance by Constructing the Interfaces Between VO and Co-N-C Layers.

作者信息

Yuan Guo-Qiang, Wei Xing, Su Yi-Chun, Zhou Tian-Yu, Hu Jin-Liang, An Yang, Zhou Song-Lin, Zhao Wen-Qiang, Xia Jun, Liu Yang-Yi

机构信息

School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou, Jiangsu, 225009, P. R. China.

School of Electrical Engineering, Engineering Technology Research Center of Optoelectronic Technology Appliance, Tongling University, Tongling, Anhui, 244061, P. R. China.

出版信息

Small. 2024 May;20(22):e2308851. doi: 10.1002/smll.202308851. Epub 2023 Dec 19.

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) 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 nanobelts (VO@Co-N-C NBs) for cathodes in AZIBs. Various in-/ex situ characterizations demonstrate the interfaces between VO layers and Co-N-C layers can protect the VO NBs from collapsing, increase ion diffusion, and enhance the Zn storage performance. Additional density functional theory (DFT) simulations demonstrate that Co─O─V bonds between VO and Co-N-C layers can enhance interfacial Zn storage. Moreover, the VO@Co-N-C NBs provided an ultrahigh capacity (418.7 mAh g at 1 A g), outstanding long-term stability (over 8000 cycles at 20 A g), and superior rate performance.

摘要

由于成本低且安全性高,钒氧化物作为水系锌离子电池(AZIBs)的阴极材料引起了关注。然而,低离子扩散和钒溶解常常导致循环过程中的容量衰减和稳定性恶化。在此,通过简便的煅烧策略,在二氧化钒(VO)纳米带上包覆单原子钴分散的氮掺杂碳(Co-N-C)层,以形成用于AZIBs阴极的Co-N-C层包覆VO纳米带(VO@Co-N-C NBs)。各种原位/非原位表征表明,VO层与Co-N-C层之间的界面可以保护VO纳米带不坍塌,增加离子扩散,并提高锌存储性能。额外的密度泛函理论(DFT)模拟表明,VO与Co-N-C层之间的Co─O─V键可以增强界面锌存储。此外,VO@Co-N-C NBs具有超高容量(1 A g下为418.7 mAh g)、出色的长期稳定性(20 A g下超过8000次循环)和优异的倍率性能。

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