Unveiling The Mechanism of The Dendrite Nucleation and Growth in Aqueous Zinc Ion Batteries

Author:

Zhang Mingchang123ORCID,Xu Weidong1,Han Xuefei245,Fan Huiqing3ORCID,Chen Tao2,Yang YaXiong1,Gao Yong1,Zheng Chao1,Yang Yi2,Xiong Ting2,Zhang Yong‐Wei24,Lee Wee Siang Vincent2,Wang Weijia3,Pan Hongge1,Yu Zhi Gen23,Xue Junmin2ORCID

Affiliation:

1. Institute of Science and Technology for New Energy Xi'an Technological University Xi'an 710021 P. R. China

2. Department of Materials Science and Engineering National University of Singapore Singapore 117573 Singapore

3. State Key Laboratory of Solidification Processing School of Materials Science and Engineering Northwestern Polytechnical University Xi'an 710072 China

4. Institute of High Performance Computing (IHPC) Agency for Science Technology and Research (A*STAR) 1 Fusionopolis Way, #16‐16 Connexis Singapore 138632 Republic of Singapore

5. AVIC Xi'an Flight Automatic Control Research Institute Shaanxi 710065 China

Abstract

AbstractAqueous zinc ion batteries (ZIBs) exhibit great potential for next‐generation energy storage devices. However, significant challenges exist, including the uncontrollable formation of Zn dendrite and side reactions during zinc stripping and plating. The mechanism of Zn dendrite nucleation has yet to be fully understood. In this work, the first principles simulations are used to investigate the Zn dendrite formation process. The unintentionally adsorbed O2− and OH ions are the inducing factors for Zn dendrite nucleation and growth on the Zn (0001) plane due to significantly increased Zn diffusion barriers. A top‐down method is demonstrated to suppress the dendrite using delaminated V2CTx to capture O2− and OH ions thanks to reduced Zn diffusion barriers. The experimental results revealed significantly suppressed Zn dendrite nucleation and growth, resulting in a layer‐by‐layer deposit/stripping of Zn. Based on the electrochemical evaluations, the V2CTx‐coated Zn composite delivers a high coulombic efficiency of 99.3% at 1.0 mAh cm−2. Furthermore, the full cell achieves excellent cyclic performance of 93.6% capacity retention after 2000 cycles at 1 A g−1. This strategy has broad scalability and can be widely applied in designing metallic anodes for rechargeable batteries.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Wiley

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