阳极
锌
剥离(纤维)
电解质
电镀(地质)
材料科学
金属
电池(电)
平面的
电极
阴极
冶金
双层
化学工程
膜
计算机科学
化学
复合材料
地质学
工程类
物理化学
量子力学
生物化学
物理
功率(物理)
地球物理学
计算机图形学(图像)
作者
S. H. Chen,Yufan Xia,Ruosheng Zeng,Zhen Luo,Xingxing Wu,Xuzhi Hu,Jian R. Lu,Ehud Gazit,Hongge Pan,Zijian Hong,Mi Yan,Kai Tao,Yinzhu Jiang
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2024-03-08
卷期号:10 (10)
标识
DOI:10.1126/sciadv.adn2265
摘要
Metal anodes are emerging as culminating solutions for the development of energy-dense batteries in either aprotic, aqueous, or solid battery configurations. However, unlike traditional intercalation electrodes, the low utilization of "hostless" metal anodes due to the intrinsically disordered plating/stripping impedes their practical applications. Herein, we report ordered planar plating/stripping in a bulk zinc (Zn) anode to achieve an extremely high depth of discharge exceeding 90% with negligible thickness fluctuation and long-term stable cycling. The Zn can be plated/stripped with (0001)Zn preferential orientation throughout the consecutive charge/discharge process, assisted by a self-assembled supramolecular bilayer at the Zn anode-electrolyte interface. Through real-time tracking of the Zn atoms migration, we reveal that the ordered planar plating/stripping is driven by the construction of in-plane Zn─N bindings and the gradient energy landscape at the reaction fronts. The breakthrough results provide alternative insights into the ordered plating/stripping of metal anodes toward rechargeable energy-dense batteries.
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