Three-dimensional atomic force microscopy reveals interfacial layer structures in various pH conditions, indicating hydrocarbon layers are crucial.
The structure of interfacial water governs the reactivity and surface properties of solid surfaces. Yet a molecular-scale understanding of how the concentration of H⁺ or OH⁻ species affects the interfacial hydration structure remains elusive. Here, we use three-dimensional atomic force microscopy (3D-AFM) to map with angstrom-scale resolution the interfacial liquid layer structure on mildly hydrophobic van der Waals (vdW) materials as a function of the pH. The liquid layer structure of MoS₂ and graphite surfaces revealed the presence of 2-3 hydrocarbon layers separated by ∼0.45 nm. The pH value neither prevented the presence of hydrocarbon layers nor facilitated the removal of hydrocarbon layers from graphite or MoS₂ surfaces. In contrast, the interfacial layer structure on a hydrophilic surface (mica) revealed the formation of 2-3 hydration layers separated by ∼0.28 nm for both acidic and basic conditions. A theoretical model predicted the formation of hydrocarbon layers on van der Waals materials in the presence of trace amounts of hydrocarbons (∼15 μg/m³). We propose that hydrocarbon layers are indispensable to explain the properties of van der Waals material-water interfaces.
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Tang et al. (2026) studied this question.
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