Horizontally Arranged Zn Platelet Deposition Regulated by Bi2O3/Bi toward High‐Rate and Dendrite‐Free 3D Zn Composite Anode

Author:

Wang Xianzhen1,Xu Ziming1,Zhang Wenyuan12,Ding Gang1,Zhang Lingsheng1,Feng Yongbao1,Yong Zhenzhong3,Gong Wenbin2,Xue Pan4,Yu Lei5,Xu Peng146,Li Qiulong1ORCID

Affiliation:

1. College of Materials Science and Engineering Nanjing Tech University Nanjing 211816 China

2. School of Physics and Energy Xuzhou University of Technology Xuzhou 221018 China

3. Key Laboratory of Multifunctional Nanomaterials and Smart Systems Advanced Materials Division Suzhou Institute of Nano‐Tech and Nano‐Bionics Chinese Academy of Sciences Suzhou 215123 China

4. School of Chemistry and Chemical Engineering Yangzhou University Yangzhou 225002 China

5. School of Materials Engineering Changshu Institute of Technology Changshu 215500 China

6. Tianjin Shocktech Technology Co., Ltd Tianjin 301700 China

Abstract

AbstractAqueous Zn‐metal battery is considered as a promising energy‐storage system. However, uncontrolled zinc dendrite growth is the main cause of short‐circuit failure in aqueous Zn‐based batteries. One of the most efficient and convenient strategies to alleviate this issue is to introduce appropriate zincophilic nucleation sites to guide zinc metal deposition and regulate crystal growth. Herein, this work proposes Bi2O3/Bi nanosheets anchored on the cell wall surface of the 3D porous conductive host as the Zn deposition sites to modulate Zn deposition behavior and hence inhibit the zinc dendrite growth. Density functional theory and experimental results demonstrate that Bi2O3 has a super zinc binding energy and strong adsorption energy with zinc (002) plane, as a super‐zincophilic nucleation site, which results in the deposition of zinc preferentially along the horizontal direction of (002) crystal plane, fundamentally avoids the formation of Zn dendrites. Benefiting from the synergistic effect Bi2O3/Bi zincophilic sites and 3D porous structure in the B‐BOGC host, the electrochemical performance of the constructed Zn‐based battery is significantly improved. As a result, the Zn anode cycles for 1500 cycles at 50 mA cm−2 and 1.0 mAh cm−2. Meanwhile, the Zn@B‐BOGC//MnO2 full cell can operate stably for 2000 cycles at 2.0 A g−1.

Funder

National Natural Science Foundation of China

National Key Research and Development Program of China

Natural Science Foundation of Jiangsu Province

Priority Academic Program Development of Jiangsu Higher Education Institutions

Publisher

Wiley

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