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Journal ArticleDOI

Effect of airborne contaminants on the wettability of supported graphene and graphite

TLDR
It is demonstrated that airborne hydrocarbons adsorb on graphitic surfaces, and that a concurrent decrease in the water contact angle occurs when these contaminants are partially removed by both thermal annealing and controlled ultraviolet-O3 treatment.
Abstract
It is generally accepted that supported graphene is hydrophobic and that its water contact angle is similar to that of graphite Here, we show that the water contact angles of freshly prepared supported graphene and graphite surfaces increase when they are exposed to ambient air By using infrared spectroscopy and X-ray photoelectron spectroscopy we demonstrate that airborne hydrocarbons adsorb on graphitic surfaces, and that a concurrent decrease in the water contact angle occurs when these contaminants are partially removed by both thermal annealing and controlled ultraviolet-O3 treatment Our findings indicate that graphitic surfaces are more hydrophilic than previously believed, and suggest that previously reported data on the wettability of graphitic surfaces may have been affected by unintentional hydrocarbon contamination from ambient air

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Citations
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Dissertation

Understanding the mechanism of permeation through graphene-based membranes using molecular dynamics simulations

James Dix
TL;DR: In this paper, it was shown that charged species are attracted to graphene surfaces due to polarisation of the pi-electron system, resulting in limited ion permeation of abundant cations in seawater, like Na+ and K+.
Journal ArticleDOI

Wetting at the Nanoscale: Molecular Mobility Induced by Contact Line Forces.

TL;DR: In this article , a nanoneedle attached at the extremity of a cantilever is dipped in a liquid droplet and a specific atomic force microscopy (AFM) experiment is conducted to study the interaction of a contact line with molecules physically adsorbed on a surface.
Journal ArticleDOI

Effect of Layer Orientation and Pore Morphology on Water Transport in Multilayered Porous Graphene

ckstMaNA
- 20 Oct 2022 - 
TL;DR: In this paper , the effects on water transport due to the orientation of the layer in the multilayered porous graphene and the different patterns formed when the layer is oriented to some degrees are studied for both circular and non-circular pore configurations.
Journal ArticleDOI

Registry-Dependent Potential for Interfaces of Water with Graphene

TL;DR: In this paper , an anisotropic interlayer potential that can accurately describe the van der Waals interaction of the water-graphene interface is presented, and the force field is benchmarked against the many-body dispersion-corrected density functional theory.
Posted Content

Water affinity to epitaxial graphene: the impact of layer thickness

TL;DR: In this article, the sensitivity to water vapour of one-, two-, and three-layer epitaxial graphene (1, 2, and 3LG) is examined, as measured by changes in work function and carrier density, with 1LG being the most sensitive to water adsorption and environmental concentration changes.
References
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Book

Physical chemistry of surfaces

TL;DR: In this paper, the authors discuss the nature and properties of liquid interfaces, including the formation of a new phase, nucleation and crystal growth, and the contact angle of surfaces of solids.
Journal ArticleDOI

Large-Area Synthesis of High-Quality and Uniform Graphene Films on Copper Foils

TL;DR: It is shown that graphene grows in a self-limiting way on copper films as large-area sheets (one square centimeter) from methane through a chemical vapor deposition process, and graphene film transfer processes to arbitrary substrates showed electron mobilities as high as 4050 square centimeters per volt per second at room temperature.
Journal ArticleDOI

Carbon-based Supercapacitors Produced by Activation of Graphene

TL;DR: This work synthesized a porous carbon with a Brunauer-Emmett-Teller surface area, a high electrical conductivity, and a low oxygen and hydrogen content that has high values of gravimetric capacitance and energy density with organic and ionic liquid electrolytes.
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