阳极
材料科学
成核
电化学
电解质
X射线光电子能谱
金属
锌
化学工程
拉曼光谱
扫描电子显微镜
电池(电)
电极
分析化学(期刊)
化学
冶金
物理化学
复合材料
光学
物理
工程类
功率(物理)
有机化学
量子力学
色谱法
作者
Ziyi Hu,Linming Zhou,Dechao Meng,Liyan Zhao,Yihua Li,Yuhui Huang,Yongjun Wu,Shikuan Yang,Linsen Li,Zijian Hong
标识
DOI:10.48550/arxiv.2206.05115
摘要
Zn metal battery has been considered a promising alternative energy storage technology in renewable energy storage and grid storage. It is well-known that the surface orientation of a Zn metal anode is vital to the reversibility of a Zn metal battery. Herein, the (101)-oriented thin Zn metal anode (down to 2 μm) is electrodeposited on a Cu surface by adding dimethyl sulfoxide (DMSO) electrolyte additive in ZnSO4 aqueous solution. Scanning electron microscope (SEM) observation indicates the formation of flat terrace-like compact (101)-oriented surfaces. Insitu optical observation confirms that the (101)-oriented surfaces can be reversibly plated and stripped. DFT calculations reveal two mechanisms for the nucleation and growth of the Zn-(101) surface: (1) formation of Zn(101)//Cu(001) could lower the interface energy as compared to Zn(002)//Cu(001); (2) large reconstruction of the Zn (101) surface with DMSO and H2O absorption. Raman, XPS, and ToF-SIMS characterizations indicate that adding DMSO in ZnCl2 could facilitate the formation of ZnO-based SEI on Zn metal surface, while OH- and S-based SEI can be obtained with DMSO in ZnSO4. The electrochemical testings are performed, which demonstrates a higher cyclability for the (101)-oriented Zn in the half cell as well as a lower charge transfer barrier with respect to the (002)-dominated surface of the same electrode thickness. Zn||V2O5 full cells are further assembled, showing better capacity retention for the (101)-Zn as compared to the (002)-Zn with the same thickness (5 μm, 3 μm, and 2 μm). We hope this study to spur further interest in the control of Zn metal surface crystallographic orientation towards ultrathin Zn metal anodes.
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