材料科学
表面张力
镓
铟
共晶体系
氧化物
电解质
磁滞
化学物理
纳米技术
化学工程
复合材料
热力学
电极
冶金
凝聚态物理
物理化学
微观结构
化学
工程类
物理
作者
Keith D. Hillaire,Praneshnandan Nithyanandam,Minyung Song,Sahar Rashid‐Nadimi,Abolfazl Kiani,Michael D. Dickey,Karen E. Daniels
标识
DOI:10.1002/adfm.202311501
摘要
Abstract When in a pristine state, gallium and its alloys have the largest interfacial tensions of any liquid at room temperature. Nonetheless, applying as little as 0.8 V of electric potential across eutectic gallium indium (EGaIn) placed within aqueous sodium hydroxide (NaOH, or other electrolyte) solution will cause the metal to behave as if its interfacial tension is near zero. The mechanism behind this phenomenon has remained poorly understood because NaOH dissolves the oxide species, making it difficult to directly measure the concentration, thickness, or chemical composition of the film that forms at the interface. In addition, the oxide layers formed are atomically‐thin. Here, it presents a suite of techniques that allow to simultaneously measure both electrical and interfacial properties as a function of applied electric potential, allowing for new insights into the mechanisms, which cause the dramatic decrease in interfacial tension. A key discovery from this work is that the interfacial tension displays hysteresis while lowering the applied potential. It combines these observations with electrochemical impedance spectroscopy to evaluate how these changes in interfacial tension arise from chemical, electrical, and mechanical changes on the interface, and close with ideas for how to build a free energy model to predict these changes from first principles.
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