Porous ZnP matrix for long‐lifespan and dendrite‐free Zn metal anodes

Author:

Lei Xinyue1,Ma Zhipeng12,Bai Lei1,Wang Lei1,Ding Yali1,Song Shenglu1,Song Ailing12,Dong Haifeng1,Tian Hao3,Tian Huajun4,Meng Xiangtong5,Liu Hao3,Sun Bing3ORCID,Shao Guangjie12,Wang Guoxiu3

Affiliation:

1. Hebei Key Laboratory of Applied Chemistry, College of Environmental and Chemical Engineering Yanshan University Qinhuangdao China

2. State Key Laboratory of Metastable Materials Science and Technology Yanshan University Qinhuangdao China

3. Centre for Clean Energy Technology, School of Mathematical and Physical Sciences, Faculty of Science University of Technology Sydney Ultimo New South Wales Australia

4. Key Laboratory of Power Station Energy Transfer Conversion and System of Ministry of Education, School of Energy Power and Mechanical Engineering North China Electric Power University Beijing China

5. State Key Laboratory of Organic‐Inorganic Composites College of Chemical Engineering, Beijing University of Chemical Technology Beijing China

Abstract

AbstractThe reversibility of Zn plating/stripping during cycling is adversely affected by dendritic growth, electrochemical corrosion, surface passivation, and hydrogen generation on the Zn anodes for rechargeable aqueous zinc ion batteries (ZIBs). Herein, through an ordinary anodic etching process, a uniform porous ZnP matrix protective layer was created on the Zn foil (Zn@ZnP). The large and accessible specific surface area of the prepared Zn@ZnP can facilitate contact with the electrolyte, accelerating the migration and enhancing the desolvation of Zn2+, effectively enhancing the Zn deposition kinetics. According to studies from scanning electron microscopy (SEM) and multiscale optical microscopy, the Zn@ZnP electrode effectively inhibits the growth of dendrites with excellent Zn plating/stripping reversibility. In consequence, the symmetric cell with the Zn@ZnP electrodes displays a long‐term cycle life of over 1260 h at 10  mA  cm−2. The full cell, consisting of Zn@ZnP anodes and MnO2‐based cathode, demonstrated a high discharge capacity of 145 mAh g−1 after cycling 500 times at the current density of 1000 mA  g−1. A scalable method for designing a homogeneous anode protection layer enables dendrite‐free zinc metal anodes, paving the way for interface modification of other metal anodes.

Funder

Natural Science Foundation of Hebei Province

National Natural Science Foundation of China

Publisher

Wiley

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