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Precise and Ultrafast Molecular Sieving Through Graphene Oxide Membranes

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TLDR
This work investigates permeation through micrometer-thick laminates prepared by means of vacuum filtration of graphene oxide suspensions, which reveal that the GO membrane can attract a high concentration of small ions into the membrane, which may explain the fast ion transport.
Abstract
Graphene-based materials can have well-defined nanometer pores and can exhibit low frictional water flow inside them, making their properties of interest for filtration and separation. We investigate permeation through micrometer-thick laminates prepared by means of vacuum filtration of graphene oxide suspensions. The laminates are vacuum-tight in the dry state but, if immersed in water, act as molecular sieves, blocking all solutes with hydrated radii larger than 4.5 angstroms. Smaller ions permeate through the membranes at rates thousands of times faster than what is expected for simple diffusion. We believe that this behavior is caused by a network of nanocapillaries that open up in the hydrated state and accept only species that fit in. The anomalously fast permeation is attributed to a capillary-like high pressure acting on ions inside graphene capillaries.

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Journal ArticleDOI

Synthetic Two‐Dimensional Materials: A New Paradigm of Membranes for Ultimate Separation

TL;DR: Groundbreaking advances in the design, synthesis, processing, and application of 2DMs for gas and ion separations, as well as water desalination are presented.
Journal ArticleDOI

Low-voltage electrostatic modulation of ion diffusion through layered graphene-based nanoporous membranes.

TL;DR: The tunable nanoconfinement in layered graphene-based nanoporous membranes is exploited to show that sub-2 nm confined ion diffusion can be strongly modulated by the surface potential-induced EDL, which suggests an anomalously enhanced diffusion that cannot be explained by conventional theoretical predictions.
Journal ArticleDOI

Metal-organic framework-graphene oxide composites: A facile method to highly improve the CO2 separation performance of mixed matrix membranes

TL;DR: In this article, mixed matrix membranes (MMMs) were fabricated by incorporating ZIF-8@GO into Pebax matrix to improve CO 2 separation performance, which increased the length of the tortuous path of gas diffusion and restricted the diffusion of larger molecules.
Journal ArticleDOI

Highly Selective Ionic Transport through Subnanometer Pores in Polymer Films

TL;DR: In this article, 12 μm long, parallel oriented polymer nanopores are fabricated in polyethylene terephthalate (PET) films by irradiation with GeV heavy ions and subsequent 3 h exposure to UV radiation.
Journal ArticleDOI

Self-Assembly of Thiourea-Crosslinked Graphene Oxide Framework Membranes toward Separation of Small Molecules.

TL;DR: Thiourea covalent-linked graphene oxide framework (TU-GOF) membranes on porous ceramics are developed through a facile hydrothermal self-assembly synthesis and feature excellent sieving capabilities for small species, leading to high hydrogen permselectivities and nearly complete rejections for methanol and small ions in gas, solvent, and saline water separations.
References
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Journal ArticleDOI

Fast parallel algorithms for short-range molecular dynamics

TL;DR: In this article, three parallel algorithms for classical molecular dynamics are presented, which can be implemented on any distributed-memory parallel machine which allows for message-passing of data between independently executing processors.

Fast parallel algorithms for short-range molecular dynamics

TL;DR: Comparing the results to the fastest reported vectorized Cray Y-MP and C90 algorithm shows that the current generation of parallel machines is competitive with conventional vector supercomputers even for small problems.
Journal ArticleDOI

Molecular dynamics with coupling to an external bath.

TL;DR: In this paper, a method is described to realize coupling to an external bath with constant temperature or pressure with adjustable time constants for the coupling, which can be easily extendable to other variables and to gradients, and can be applied also to polyatomic molecules involving internal constraints.
Journal ArticleDOI

A smooth particle mesh Ewald method

TL;DR: It is demonstrated that arbitrary accuracy can be achieved, independent of system size N, at a cost that scales as N log(N), which is comparable to that of a simple truncation method of 10 A or less.
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