Abstract

Experimental investigations of hydrophobic/water interfaces often return controversial results, possibly due to the unknown role of gas accumulation at the interfaces. Here, during advanced atomic force microscopy of the initial evolution of gas-containing structures at a highly ordered pyrolytic graphite/water interface, a fluid phase first appeared as a circular wetting layer ~0.3 nm in thickness and was later transformed into a cap-shaped nanostructure (an interfacial nanobubble). Two-dimensional ordered domains were nucleated and grew over time outside or at the perimeter of the fluid regions, eventually confining growth of the fluid regions to the vertical direction. We determined that interfacial nanobubbles and fluid layers have very similar mechanical properties, suggesting low interfacial tension with water and a liquid-like nature, explaining their high stability and their roles in boundary slip and bubble nucleation. These ordered domains may be the interfacial hydrophilic gas hydrates and/or the long-sought chemical surface heterogeneities responsible for contact line pinning and contact angle hysteresis. The gradual nucleation and growth of hydrophilic ordered domains renders the original homogeneous hydrophobic/water interface more heterogeneous over time, which would have great consequence for interfacial properties that affect diverse phenomena, including interactions in water, chemical reactions, and the self-assembly and function of biological molecules.

Highlights

  • Gases dissolved in water tend to accumulate at the interfaces between hydrophobic solids and water to form cap-shaped structures that are nanometers in height; these structures are known as interfacial nanobubbles (INBs) or surface nanobubbles[1,2,3,4,5,6,7,8,9,10]

  • Higher-resolution images showed that the speckles were small domains with an ordered row-like structure (Fig. 1b,c) that increased in coverage of the interface over time (Fig. 1d–h). This structure and its nucleation and growth behaviours resemble the ordered pattern reported in our earlier studies of the highly ordered pyrolytic graphite (HOPG)/water interface using pre-degassed water under air or nitrogen[25,26,27,28]

  • This work underlies the importance of microscopic observations of the formation processes of various gas-containing structures at solid/water interfaces using highly sensitive atomic force microscopy (AFM)

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Summary

Introduction

Gases dissolved in water tend to accumulate at the interfaces between hydrophobic solids and water to form cap-shaped structures that are nanometers in height; these structures are known as interfacial nanobubbles (INBs) or surface nanobubbles[1,2,3,4,5,6,7,8,9,10]. Our observations, which were conducted in the frequency-modulation (FM) and PeakForce (PF) modes, provide important insights into the behaviours of dissolved gases in water and at hydrophobic/water interfaces, including formation of INBs, their nature, their high stability, the pinning of the three-phase contact lines, boundary slip, and bubble nucleation. This new understanding highlights new directions for further quantitative investigation of these behaviours under various conditions and at various interfaces, which will allow www.nature.com/scientificreports/. These advances will strongly impact research and technology in diverse fields, such as physics, chemistry, biology, and medicine

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