Abstract
Polyethylene glycol (PEO) is a commonly used polymer in the field of batteries for achieving flat and uniform electrodes to enhance the performance of batteries, such as lithium batteries and zinc (Zn) batteries. However, the impact of PEO on the electrochemical deposition of Zn metal on electrodes remains uncertain. In this study, we selected ZnSO4 solution as electrolyte and copper (Cu) substrates as electrodes, which are widely applied in Zn batteries. We used in situ electrochemical atomic force microscopy (EC-AFM) to observe the nucleation and growth of Zn metal plates on the Cu substrate in the presence of different concentrations of ZnSO4 and PEO additives. Our results indicate that PEO biases the crystallographic orientation of the initially deposited Zn metal nuclei, but does not have an obvious influence on subsequent growth. Based on our findings, we hypothesize that PEO primarily interacts with the Cu substrate to adjust the interfacial energy of the Cu-electrolyte interfaces. In contrast, due to the lack of apparent change in the Zn growth rate, we postulate that PEO does not affect the delivery rate of Zn2+ to the electrode surface. The consistent aspect ratio of the Zn plates combined with the lack of an effect on growth rates further suggests that PEO does not interact significantly with the surface of the newly formed Zn plates. The Zn metal will undergo surface reorganization in a mildly acidic aqueous solution as a result of oxidation of Zn, which is not affected by PEO adsorption. Our findings provide both insight into the underlying mechanism by which PEO promotes electrode flattening in Zn batteries and a standardized protocol for elucidating the impact of additives on the morphological evolution of interfaces during electrochemical deposition.Work by C.O. was performed under the auspices of the U.S. Department of Energy by Lawrence Livermore National Laboratory under Contract DE-AC52-07NA27344.
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