材料科学
成核
沉积(地质)
电极
电解质
相(物质)
基质(水族馆)
聚合物
吸附
聚合物基片
锌
电化学
纳米技术
化学工程
冶金
复合材料
物理化学
有机化学
地质学
工程类
海洋学
古生物学
化学
生物
沉积物
作者
Ying Xia,Duo Song,Mingyi Zhang,Zhe-Ming Wang,Chenyang Shi,Jingshan S. Du,Sun Hae Ra Shin,Mark Engelhard,Praveen K. Thallapally,Christine A. Orme,Jinhui Tao,Maria L. Sushko,James J. De Yoreo,Jun Liu
标识
DOI:10.1002/adma.202503218
摘要
Abstract Polymer additives [like polyethylene oxide (PEO)] are widely used for smooth electrode deposition in aqueous zinc and many other battery systems. However, the precise mechanism by which they regulate morphology and suppress dendrite formation remains unclear. In this study, the knowledge gap is addressed by using in situ electrochemical atomic force microscopy to directly observe the interfacial evolution during Zn electrodeposition and polymer adsorption on Cu substrates in the presence of varying concentrations of ZnSO 4 and PEO. Contrary to previous literature assumptions, which emphasize the binding to the growing Zn crystal surfaces or Zn 2+ ions, the results demonstrate that PEO smooths Zn films by promoting nucleation of (002)‐oriented Zn platelets through interactions with the Cu substrate. Density functional theory simulations support this finding by showing that PEO adsorption on Cu modifies the interfacial energy of Zn/Cu/electrolyte interfaces, favoring the stabilization of Zn (002) on the Cu substrate, as well as confines Zn electrodeposition to a narrow near‐surface region. These findings elucidate a novel design principle for electrode smoothing, emphasizing the importance of substrate selection paired with polymer additives that exhibit an attractive interaction with the substrate but minimal interaction with growing crystals, offering a mechanistic perspective for improved battery performance.
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