Wettability and morphology of liquid gallium on graphene surface

材料科学 润湿 表面张力 液态金属 石墨烯 接触角 化学工程 润湿转变 曲面(拓扑) 化学物理 复合材料 形态学(生物学) 纳米技术 表面能 热力学 化学 冶金 物理
作者
Junjun Wang,Li Tao,Xiongying Li,Hui Li
出处
期刊:Chinese Physics [Acta Physica Sinica, Chinese Physical Society and Institute of Physics, Chinese Academy of Sciences]
卷期号:67 (14): 149601-149601 被引量:2
标识
DOI:10.7498/aps.67.20172717
摘要

Liquid gallium and its alloy with low melting point, low toxic and high electrical conductivity are used extensively in burgeoning microfluidic and flexible electronic devices. The key to producing these devices is to effectively control the wettability and morphology of liquid metal on the solid interface in different manufacturing processes. Based on the Lennard-Jones (L-J) potential describing the solid-liquid interaction, the wettabilities of liquid gallium film on the smooth and rough graphene surfaces are effectively investigated by molecular dynamics simulation which is an available and powerful option in this field. Different regimes of wetting are discovered by changing the depth of the L-J potential, and the stable contact angle increases with Ga-C potential depth decreases. The results show that the equilibrium contact angle and the retraction velocity increase with the decrease of the L-J potential between the gallium and graphene, showing that some properties change from complete wetting to hydrophilic and to hydrophobic. The L-J potential depth obtained from the simulation results can be effectively employed to describe the interaction between the liquid gallium and the substrate because the resulting wetting angle is extremely close to the experimental value. When employing the most appropriate L-J potential, it is found that although the initial retraction velocity increases with the proportional decrease of the thickness of the liquid Ga film, there are a few of differences in equilibrium contact angle and final retraction velocity in virtue of the competition between the surface tension of the Ga film and Ga-C interaction. It means that for the wetting state the film thickness is not the crux for changing the equilibrium contact angle and retraction velocity based on a similar conversion of potential energy into kinetic energy. Finally, we investigate the effects of the L-J potential on three rough surfaces which are patterned into three types of nanopillars with different top morphologies respectively. Specifically, it is shown that in spite of similar surface roughness, the wetting morphologies of liquid gallium deposited on various nano-textured graphene surfaces range from hydrophobic to dewetting state, suggesting that not only the roughness but also the morphology of surface can exert an available influence on the wettability of liquid. The wetting transition between the wetting and dewetting state can be achieved dynamically by adjusting the morphologies of nanopillars involved although we still need to go into more detail on the configurable way to fulfill the changing requirements.
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