Soh Eugene Jia Hao, Astier Hippolyte P A G, Daniel Dan, Isaiah Chua Jia Qing, Miserez Ali, Jia Zian, Li Ling, O'Shea Sean J, Bhaskaran Harish, Tomczak Nikodem, Nijhuis Christian A
Department of Materials, University of Oxford, Oxford OX1 3PH, United Kingdom.
Institute of Materials Research and Engineering, Agency for Science, Technology and Research (A*STAR), Singapore 138634.
ACS Nano. 2022 Sep 27;16(9):14370-14378. doi: 10.1021/acsnano.2c04667. Epub 2022 Sep 6.
Liquid metal droplets, such as eutectic gallium-indium (EGaIn), are important in many research areas, such as soft electronics, catalysis, and energy storage. Droplet contact on solid surfaces is typically achieved without control over the applied force and without optimizing the wetting properties in different environments (e.g., in air or liquid), resulting in poorly defined contact areas. In this work, we demonstrate the direct manipulation of EGaIn microdroplets using an atomic force microscope (AFM) to generate repeated, on-demand making and breaking of contact on self-assembled monolayers (SAMs) of alkanethiols. The nanoscale positional control and feedback loop in an AFM allow us to control the contact force at the nanonewton level and, consequently, tune the droplet contact areas at the micrometer length scale in both air and ethanol. When submerged in ethanol, the droplets are highly nonwetting, resulting in hysteresis-free contact forces and minimal adhesion; as a result, we are able to create reproducible geometric contact areas of 0.8-4.5 μm with the alkanethiolate SAMs in ethanol. In contrast, there is a larger hysteresis in the contact forces and larger adhesion for the same EGaIn droplet in air, which reduced the control over the contact area (4-12 μm). We demonstrate the usefulness of the technique and of the gained insights in EGaIn contact mechanics by making well-defined molecular tunneling junctions based on alkanethiolate SAMs with small geometric contact areas of between 4 and 12 μm in air, 1 to 2 orders of magnitude smaller than previously achieved.
液态金属微滴,如共晶镓铟(EGaIn),在许多研究领域都很重要,比如软电子学、催化和能量存储。在固体表面上实现微滴接触时,通常无法控制施加的力,也无法优化在不同环境(如空气或液体中)的润湿性,导致接触面积定义不明确。在这项工作中,我们展示了使用原子力显微镜(AFM)直接操纵EGaIn微滴,以在链烷硫醇自组装单分子层(SAMs)上按需重复形成和破坏接触。AFM中的纳米级位置控制和反馈回路使我们能够在纳牛顿水平控制接触力,从而在空气和乙醇中,在微米长度尺度上调整微滴接触面积。当浸没在乙醇中时,微滴具有高度的非润湿性,导致接触力无滞后且粘附力最小;因此,我们能够在乙醇中与链烷硫醇盐SAMs创建0.8 - 4.5μm的可重复几何接触面积。相比之下,对于空气中相同的EGaIn微滴,接触力存在较大滞后且粘附力更大,这降低了对接触面积(4 - 12μm)的控制。我们通过在空气中制作基于链烷硫醇盐SAMs、几何接触面积小至4至12μm(比之前实现的小1至2个数量级)的明确定义的分子隧道结,证明了该技术的实用性以及对EGaIn接触力学所获得见解的有用性。