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Humidity-induced significant microstructural reordering in partially reduced graphene oxide: Insights on water permeation mechanism

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TLDR
In this paper, the authors study the evolution of the structure of GO in a partially reduced form, before and after being hydrated in high humidity conditions, and they reconcile the gravimetry outcomes by suggesting the possibilities of both super-permeating channels and void assisted permeation.
Abstract
Interaction of water and water-based solvents with graphene oxide (GO) has attracted much attention, due to the ability of GO to serve as a highly effective water filtration membrane. In this work, we study the evolution of the structure of GO in a partially reduced form, before and after being hydrated in high humidity conditions. X-ray diffraction (XRD) studies reveal that progressive thermal reduction leads to the increase in the microstructural disorder in the stacking of GO flakes. However, upon hydration of partially reduced GO, microstructural ordering is revealed. This ordered state is characterized by two XRD peaks with substantially smaller full-width-at-half-maximum (FWHM), when compared to the pre-hydration state. The peak corresponding to the sp3 regions has larger d-spacing of ∼9.7 A and an FWHM ∼6 times smaller compared to pre-hydration state, while the other peak corresponds to the ordered sp2 regions with a d-spacing of ∼3.3 A, observed at the characteristic graphitic peak position. Gravimetry studies on suspended films reveal both accelerated and diminished water permeation rates upon annealing when compared to unreduced GO films, which can be attributed to void-assisted permeation in the microstructurally disordered films. The hydrated films in a similar way show a permeation behavior that involves either the increase or decrease in water permeation rates in comparison with pre-hydrated samples. We reconcile to the gravimetry outcomes by suggesting the possibilities of both super-permeating channels and void assisted permeation, and the contribution of each of the mechanisms to the permeation flux.Interaction of water and water-based solvents with graphene oxide (GO) has attracted much attention, due to the ability of GO to serve as a highly effective water filtration membrane. In this work, we study the evolution of the structure of GO in a partially reduced form, before and after being hydrated in high humidity conditions. X-ray diffraction (XRD) studies reveal that progressive thermal reduction leads to the increase in the microstructural disorder in the stacking of GO flakes. However, upon hydration of partially reduced GO, microstructural ordering is revealed. This ordered state is characterized by two XRD peaks with substantially smaller full-width-at-half-maximum (FWHM), when compared to the pre-hydration state. The peak corresponding to the sp3 regions has larger d-spacing of ∼9.7 A and an FWHM ∼6 times smaller compared to pre-hydration state, while the other peak corresponds to the ordered sp2 regions with a d-spacing of ∼3.3 A, observed at the characteristic graphitic peak position. Gravi...

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Journal ArticleDOI

Ion percolation through annealed, supported graphene oxide films: Role of nanochannels and voids

TL;DR: In this article, the relative contributions of nanochannels and voids, gaps between the lamellae, using electro-impedance spectroscopy, were analyzed with support of supported GO films annealed at different temperatures and the results were fitted to equivalent circuits.
Journal ArticleDOI

Dielectric response and proton transport in water confined in graphene oxide.

TL;DR: In this paper , the authors systematically studied various properties of Graphene oxide (GO) membranes exposed to controlled humidity levels ranging from 0% to 90% RH and found that most water gets absorbed in interlayer spaces at low humidity (<25% RH), the fraction of water in the void spaces increases with RH, and the lower bound for the dielectric constant of confined water is estimated to be εwater > 17.
Journal ArticleDOI

Intercalated water mediated electromechanical response of graphene oxide films on flexible substrates.

TL;DR: In this article, the authors examined the influence of confined water on the mechanical and electromechanical response of graphene oxide films, prepared with variable oxidative states, casted on polydimethylsiloxane (PDMS) substrates.
References
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Journal ArticleDOI

Dynamic microstructure of graphene oxide membranes and the permeation flux

TL;DR: In this article, the dynamic microstructure of GO membranes was revealed, which affected the membrane performance significantly, and showed that all GO membranes prepared by varied methods and on different substrates presented a severe reduction in water permeability during filtration, due to the compaction of their original loose micro-structure.
Journal ArticleDOI

Role of Adsorbed Water on Charge Carrier Dynamics in Photoexcited TiO2

TL;DR: Adsorbed associated water can efficiently stabilize photogenerated charge carriers in nanocrystalline TiO2 and suppress their recombination at the time scale up to minutes, demonstrating that hole mobility should be higher in the hydrated material than in the dehydrated system.
Journal ArticleDOI

Role of Oxygen Functionalities in Graphene Oxide Architectural Laminate Subnanometer Spacing and Water Transport

TL;DR: Investigating how individual GO properties can impact GO membrane characteristics and water permeability helps create a clearer picture of water transport in GOAL and can be used to rationally design more effective and efficient GO membranes.
Journal ArticleDOI

Invariance of Water Permeance through Size-Differentiated Graphene Oxide Laminates

TL;DR: This study synthesized chemically identical graphene oxide nanosheets with 2 orders of magnitude difference in lateral sizes and measured water permeance through laminates of different thicknesses fabricated by pressure-assisted deposition of these nanoshets to provide further insight toward understanding water transport through graphene oxide laminate.
Journal ArticleDOI

Molecular mechanism of water permeation in a helium impermeable graphene and graphene oxide membrane.

TL;DR: Based on the entropy calculations for water trapped between graphene sheets and oxidized graphene sheets at different inter-sheet spacings, the thermodynamics of filling is shown and the increased electrostatic interaction between water with the oxidized part of the sheet helps the sheet open up and pushes water inside.
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