材料科学
锌
成核
阳极
法拉第效率
沉积(地质)
化学工程
水溶液
图层(电子)
吸附
纳米技术
电极
冶金
化学
有机化学
沉积物
古生物学
物理化学
工程类
生物
作者
Yuying Han,Fangzheng Wang,Bin Zhang,Lijin Yan,Jiangyu Hao,Chong Zhu,Xuefeng Zou,Yang Zhou,Bin Xiang
标识
DOI:10.1016/j.ensm.2023.102928
摘要
The practical application of zinc anodes for rechargeable aqueous zinc-ion batteries is hindered to uncontrollable dendritic zinc deposition and side reactions. And the deposition of zinc is like building blocks layer by layer, typically considered as nucleation, growth and evolution driven by electric field. Yet the important role of the bottommost deposits is generally ignored. Here, we developed a highly self-adaptable polydimethylsiloxane (PDMS)/montmorillonite (MMT) film to regulate the process of zinc deposition sustainably. In the nucleation and growth stages of zinc, the two-step regulation of the building block effect benefits from the adsorption of oxygen-containing sites on PDMS and fast zinc ion nanochannels in the negatively charged interlayer of MMT to achieve targeted-capture of zinc ions and ordered-deposition, thus inducing horizontally oriented Zn(002) deposition in the initial nucleation layer and providing a flat deposition site for the subsequently deposited metal. In the evolutionary stage of Zn, the PDMS/MMT (PMZn) interfacial layer can achieve a conformal contact with the anode due to the high dynamic adaptability and self-healing of the micro-crosslinking of Si-O-Si and B-O bonds. Consequently, PMZn@Cu||Zn offers higher coulombic efficiency(CE) (99.77%) and the PMZn@Zn anodes exhibit an ultra-long cycle life of 2000 h, more than 10 times that of bare zinc anodes. The stability of the high capacity of PMZn@Zn||MnO2 full cells far exceeds that of Zn||MnO2. This strategy provides an effective approach to develop a stable Zn metal anode for aqueous rechargeable Zn batteries.
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