4.7 Article

An integrated electrode strengthened by dense layer for aqueous zinc ion batteries with long lifespan

期刊

JOURNAL OF ALLOYS AND COMPOUNDS
卷 896, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2021.162948

关键词

Aqueous zinc ion batteries; Layered double hydroxides; Zn dendrites; Anode protection

资金

  1. LiaoNing Revitalization Talents Program [XLYC2007155]
  2. Fundamental Research Funds for the Central Universities [N2025018, N2025009]
  3. National Key Research and Development Project [2019YFC1905200, 2017YFB0304001]
  4. National Natural Science Foundation of China [51904073]
  5. Fundamental Research Funds for the central Universities [N182508027]

向作者/读者索取更多资源

The strategy of using Zn-Al-layered double hydroxides hexagonal nanoplates to modify the zinc metal anode has successfully improved the rechargeability and stability of rechargeable aqueous zinc ion batteries. The integrated electrode shows long-term stability and effectively suppresses zinc deposition and dendrite growth, offering a new pathway for Zn metal anode protection and accelerating the practical application of these batteries.
Rechargeable aqueous zinc ion batteries have attracted increasing attention for large-scale energy storage system. Restricted by the zinc deposition and dendrite growth, the practical application was hindered seriously by the poor rechargeability and instability. The strategy of utilizing Zn-Al-layered double hy-droxides hexagonal nanoplates modifying zinc metal anode was employed by a scalable method of spinning coating. This integrated electrode can not only realize ions well-distributed reaction on the electrode surface due to the dense protection layer weak adsorption behavior and low surface area, but also can efficiently avoid excessive zinc deposition and growth of zinc dendrites. The nucleation and dissolution energy barriers in the phase transition between zinc ions and the integrated electrode are decreased as well. The integrated electrode harvests a long-term stability of 1000 h at 1.0 mA h cm(-2) and effectively suppresses side reactions in the Zn//Zn symmetric cells. In addition, coupled with MnO2 as full cell, the capacity remains 195 mA h g(-1) with the retention of 81.2% after 200 cycles. It is promising that the employed scalable strategy will provide new pathway into Zn metal anode protection and accelerate the practical application of aqueous zinc ion batteries. (C) 2021 Elsevier B.V. All rights reserved.

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