<p>The interaction between graphene and water is fundamental to applications ranging from filtration to nano-electronics, yet the intrinsic wettability of graphene remains a subject of longstanding debate. In particular, it is disputed whether graphene is wetting transparent—transmitting the wettability of an underlying substrate to the surface. Here, we show using machine-learning enhanced molecular dynamics simulations that pristine graphene is intrinsically hydrophobic and microscopically not wetting transparent. By simulating vibrational sum-frequency generation spectra, we demonstrate that the apparent hydrophilic signatures often observed for monolayer graphene on hydrophilic substrates originate not from wetting transparency, but from signal cancellation caused by water molecules intercalated between the graphene and the substrate. Furthermore, we find that while water intercalation is thermodynamically favorable for monolayers, it becomes unfavorable for multilayer graphene, explaining experimentally observed thickness-dependent wetting behaviors. These findings provide a unified microscopic framework for understanding graphene-water interactions and clarify the crucial role of confined water in two-dimensional material interfaces.</p>

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Machine-learning enhanced simulations predict graphene is microscopically hydrophobic and not wetting transparent

  • Dianwei Hou,
  • Yevhen Horbatenko,
  • Stefan Ringe,
  • Minhaeng Cho

摘要

The interaction between graphene and water is fundamental to applications ranging from filtration to nano-electronics, yet the intrinsic wettability of graphene remains a subject of longstanding debate. In particular, it is disputed whether graphene is wetting transparent—transmitting the wettability of an underlying substrate to the surface. Here, we show using machine-learning enhanced molecular dynamics simulations that pristine graphene is intrinsically hydrophobic and microscopically not wetting transparent. By simulating vibrational sum-frequency generation spectra, we demonstrate that the apparent hydrophilic signatures often observed for monolayer graphene on hydrophilic substrates originate not from wetting transparency, but from signal cancellation caused by water molecules intercalated between the graphene and the substrate. Furthermore, we find that while water intercalation is thermodynamically favorable for monolayers, it becomes unfavorable for multilayer graphene, explaining experimentally observed thickness-dependent wetting behaviors. These findings provide a unified microscopic framework for understanding graphene-water interactions and clarify the crucial role of confined water in two-dimensional material interfaces.