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Brownian Diffusion of Hexagonal Boron Nitride Nanosheets and Graphene in Two Dimensions.
Umezaki, Utana; Smith McWillams, Ashleigh D; Tang, Zhao; He, Zhi Mei Sonia; Siqueira, Ivan R; Corr, Stuart J; Ryu, Hijun; Kolomeisky, Anatoly B; Pasquali, Matteo; Martí, Angel A.
Afiliación
  • Umezaki U; Department of Chemistry, Rice University, Houston, Texas 77005, United States.
  • Smith McWillams AD; Department of Chemistry, Rice University, Houston, Texas 77005, United States.
  • Tang Z; Department of Chemical and Biomolecular Engineering, Rice University, Houston, Texas 77005, United States.
  • He ZMS; Department of Chemistry, Rice University, Houston, Texas 77005, United States.
  • Siqueira IR; Department of Chemical and Biomolecular Engineering, Rice University, Houston, Texas 77005, United States.
  • Corr SJ; Department of Cardiovascular Surgery, Houston Methodist Hospital, Houston, Texas 77030, United States.
  • Ryu H; Department of Bioengineering, Rice University, Houston, Texas 77005, United States.
  • Kolomeisky AB; Department of Chemistry, Rice University, Houston, Texas 77005, United States.
  • Pasquali M; Department of Chemistry, Rice University, Houston, Texas 77005, United States.
  • Martí AA; Department of Chemistry, Rice University, Houston, Texas 77005, United States.
ACS Nano ; 18(3): 2446-2454, 2024 Jan 23.
Article en En | MEDLINE | ID: mdl-38207242
ABSTRACT
Two-dimensional (2D) nanomaterials have numerous interesting chemical and physical properties that make them desirable building blocks for the manufacture of macroscopic materials. Liquid-phase processing is a common method for forming macroscopic materials from these building blocks including wet-spinning and vacuum filtration. As such, assembling 2D nanomaterials into ordered functional materials requires an understanding of their solution dynamics. Yet, there are few experimental studies investigating the hydrodynamics of disk-like materials. Herein, we report the lateral diffusion of hexagonal boron nitride nanosheets (h-BN and graphene) in aqueous solution when confined in 2-dimensions. This was done by imaging fluorescent surfactant-tagged nanosheets and visualizing them by using fluorescence microscopy. Spectroscopic studies were conducted to characterize the interactions between h-BN and the fluorescent surfactant, and atomic force microscopy (AFM) was conducted to characterize the quality of the dispersion. The diffusion data under different gap sizes and viscosities displayed a good correlation with Kramers' theory. We propose that the yielded activation energies by Kramers' equation express the magnitude of the interaction between fluorescent surfactant tagged h-BN and glass because the energies remain constant with changing viscosity and decrease with increasing confinement size. The diffusion of graphene presented a similar trend with similar activation energy as the h-BN. This relationship suggests that Kramers' theory can also be applied to simulate the diffusion of other 2D nanomaterials.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: ACS Nano Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: ACS Nano Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos