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Published on: February 1, 2022
Decoding ultrafast water transport in graphene oxide.
Vikas Yadav1, Sangram Kishor Behera1, Anjan Das1
1Department of Physics, Indian Institute of Technology Madras, Chennai 600036, India. manu.jaiswal@iitm.ac.in.
Faraday Discussions
|May 14, 2026
Summary
Ultrafast water transport in graphene oxide (GO) membranes is driven by pinholes on GO flakes, not just interlayer spacing. This study reveals molecular mobility is lower than bulk water, but high sorption capacity ensures rapid permeation.
Area of Science:
- Materials Science
- Nanotechnology
- Physical Chemistry
Background:
- Graphene oxide (GO) membranes exhibit rapid water transport, but the underlying mechanisms remain debated.
- Understanding water diffusion is crucial for applications in separation and filtration.
Purpose of the Study:
- To comprehensively investigate water transport mechanisms in GO membranes.
- To elucidate the role of nano-confinement, surface interactions, and membrane geometry on water diffusion.
Main Methods:
- Sorption and permeation experiments across a full relative humidity (RH) range.
- Varied membrane thicknesses and flake sizes to probe diffusion pathways.
- Thermodynamic correction to Fickian diffusion coefficients to determine Maxwell-Stefan diffusion coefficients (DMS).
Main Results:
- In-plane water diffusion is significantly faster than out-of-plane diffusion (D2D/Dout ~ 10^2), attributed to pinholes on GO basal planes.
- Maxwell-Stefan diffusion coefficient (DMS) increases with interlayer spacing, indicating reduced wall friction.
- DMS is lower than bulk water self-diffusion, characteristic of hydrophilic nanoporous systems.
Conclusions:
- High water permeation rates in GO membranes result from substantial sorption capacity, despite modest molecular mobility (DMS).
- Pinholes on GO flakes play a critical role in facilitating rapid in-plane water transport.
- Findings reconcile the observed high flux with fundamental transport parameters in confined systems.

