Direct visualization of fluid dynamics in sub-10 nm nanochannels

Abstract

Optical microscopy is the most direct method to probe fluid dynamics at small scales. However, contrast between fluid phases vanishes at ∼10 nm lengthscales, limiting direct optical interrogation to larger systems. Here, we present a method for direct, high-contrast and label-free visualization of fluid dynamics in sub-10 nm channels, and apply this method to study capillary filling dynamics at this scale. The direct visualization of confined fluid dynamics in 8-nm high channels is achieved with a conventional bright-field optical microscope by inserting a layer of a high-refractive-index material, silicon nitride (Si₃N₄), between the substrate and the nanochannel, and the height of which is accurately controlled down to a few nanometers by a SiO₂ spacer layer. The Si₃N₄ layer exhibits a strong Fabry–Perot resonance in reflection, providing a sharp contrast between ultrathin liquid and gas phases. In addition, the Si₃N₄ layer enables robust anodic bonding without nanochannel collapse. With this method, we demonstrate the validity of the classical Lucas–Washburn equation for capillary filling in the sub-10 nm regime, in contrast to the previous studies, for both polar and nonpolar liquids, and for aqueous salt solutions.