Enhanced film-wise water evaporation through graphene nanostructures: A molecular dynamics insight

Tze Cheng Kueh, Yew Mun Hung

Research output: Contribution to journalArticleResearchpeer-review

3 Citations (Scopus)

Abstract

The functionalization of graphene nanoplatelets (GNPs) with hydrophilic hydroxyl groups through thermal curing imparts hydrophilicity and water-permeability to the GNPs, opening doors to promising applications in phase-change cooling and pervaporation water filtration. This investigation employs molecular dynamics simulations to uncover the mechanisms by which the hydroxyl functional groups enhance the film-wise water evaporation on GNPs. The introduction of hydroxyl groups disrupts the hydrogen bond network among water molecules, creating a conducive environment for enhanced evaporation. Hydroxyl-functionalized GNPs act as hub-like platforms at their edges, expediting the transport and evaporation of water. The increased hydrophilicity fosters a more efficient liquid-gas interface for water clusters. Furthermore, the substantial presence of hydroxyl groups reduces the Kapitza resistance between GNPs and water, accelerating water heating. This study also examines the impact of the attachment location of hydroxyl groups, highlighting that edge attachment, as opposed to across the graphene basal plane, offers a more promising approach for augmenting water evaporation efficiency. This study enhances the comprehension of the role of hydroxyl functionalization in promoting water evaporation on GNPs and provides valuable insights for optimizing graphene-based materials in applications requiring efficient water evaporation and transport.

Original languageEnglish
Article number126010
Number of pages11
JournalInternational Journal of Heat and Mass Transfer
Volume233
DOIs
Publication statusPublished - 15 Nov 2024

Keywords

  • Graphene nanostructures
  • Hydrogen bonds
  • Hydrophilic functional groups
  • Molecular dynamics simulations
  • Water evaporation

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