过电位
成核
材料科学
水溶液
动力学
纳米技术
化学工程
碳纤维
化学物理
电化学
化学
电极
物理
物理化学
工程类
复合材料
复合数
有机化学
量子力学
作者
Hongpeng Li,Can Guo,Tengsheng Zhang,Pan Xue,Ruizheng Zhao,Wanhai Zhou,Wei Li,Ahmed A. Elzatahry,Dongyuan Zhao,Dongliang Chao
出处
期刊:Nano Letters
[American Chemical Society]
日期:2022-05-04
卷期号:22 (10): 4223-4231
被引量:138
标识
DOI:10.1021/acs.nanolett.2c01235
摘要
Zn-based aqueous batteries (ZABs) have been regarded as promising candidates for safe and large-scale energy storage in the "post-Li" era. However, kinetics and stability problems of Zn capture cannot be concomitantly regulated, especially at high rates and loadings. Herein, a hierarchical confinement strategy is proposed to design zincophilic and spatial traps through a host of porous Co-embedded carbon cages (denoted as CoCC). The zincophilic Co sites act as preferred nucleation sites with low nucleation barriers (within 0.5 mA h cm-2), and the carbon cage can further spatially confine Zn deposition (within 5.0 mA h cm-2). Theoretical simulations and in situ/ex situ structural observations reveal the hierarchical spatial confinement by the elaborated all-in-one network (within 12 mA h cm-2). Consequently, the elaborate strategy enables a dendrite-free behavior with excellent kinetics (low overpotential of ca. 65 mV at a high rate of 20 mA cm-2) and stable cycle life (over 800 cycles), pushing forward the next-generation high-performance ZABs.
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