TY - JOUR
T1 - Enhanced film-wise water evaporation through graphene nanostructures
T2 - A molecular dynamics insight
AU - Kueh, Tze Cheng
AU - Hung, Yew Mun
N1 - Publisher Copyright:
© 2024 The Author(s)
PY - 2024/11/15
Y1 - 2024/11/15
N2 - 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.
AB - 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.
KW - Graphene nanostructures
KW - Hydrogen bonds
KW - Hydrophilic functional groups
KW - Molecular dynamics simulations
KW - Water evaporation
UR - http://www.scopus.com/inward/record.url?scp=85199776696&partnerID=8YFLogxK
U2 - 10.1016/j.ijheatmasstransfer.2024.126010
DO - 10.1016/j.ijheatmasstransfer.2024.126010
M3 - Article
AN - SCOPUS:85199776696
SN - 0017-9310
VL - 233
JO - International Journal of Heat and Mass Transfer
JF - International Journal of Heat and Mass Transfer
M1 - 126010
ER -