Nie Pengcheng, Jiang Xikai, Zheng Xu, Guan Dongshi
State Key Laboratory of Nonlinear Mechanics, Institute of Mechanics, Chinese Academy of Sciences, Beijing 100190, China.
School of Engineering Science, University of Chinese Academy of Sciences, Beijing 100049, China.
Phys Rev Lett. 2024 Jan 26;132(4):044002. doi: 10.1103/PhysRevLett.132.044002.
Room-temperature ionic liquids (RTILs) are intriguing fluids that have drawn much attention in applications ranging from tribology and catalysis to energy storage. With strong electrostatic interaction between ions, their interfacial behaviors can be modulated by controlling energetics of the electrified interface. In this work, we report atomic-force-microscope measurements of contact angle hysteresis (CAH) of a circular contact line formed on a micron-sized fiber, which is coated with a thin layer of conductive film and intersects an RTIL-air interface. The measured CAH shows a distinct change by increasing the voltage U applied on the fiber surface. Molecular dynamics simulations were performed to illustrate variations of the solidlike layer in the RTIL adsorbed at the electrified interface. The integrated experiments and computations demonstrate a new mechanism to manipulate the CAH by rearrangement of interfacial layers of RTILs induced by the surface energetics.
室温离子液体(RTILs)是一种引人关注的流体,在从摩擦学、催化到能量存储等广泛的应用领域中备受瞩目。由于离子之间存在强烈的静电相互作用,其界面行为可通过控制带电界面的能量来调节。在这项工作中,我们报告了在涂有导电薄膜的微米级纤维上形成的圆形接触线的接触角滞后(CAH)的原子力显微镜测量结果,该纤维与RTIL-空气界面相交。测量得到的CAH随着施加在纤维表面的电压U的增加而发生明显变化。进行了分子动力学模拟以说明在带电界面吸附的RTIL中固体状层的变化。综合实验和计算证明了一种通过表面能诱导的RTIL界面层重排来操纵CAH的新机制。