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Robert A. W. Dryfe

Researcher at University of Manchester

Publications -  266
Citations -  10778

Robert A. W. Dryfe is an academic researcher from University of Manchester. The author has contributed to research in topics: Graphene & Electrolyte. The author has an hindex of 47, co-authored 251 publications receiving 8390 citations. Previous affiliations of Robert A. W. Dryfe include University of Oxford.

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Proton transport through one-atom-thick crystals

TL;DR: Transport and mass spectroscopy measurements are reported which establish that monolayers of graphene and hexagonal boron nitride are highly permeable to thermal protons under ambient conditions, whereas no proton transport is detected for thicker crystals such as monolayer molybdenum disulphide, bilayer graphene or multilayer hBN.
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Oxygen Reduction Reaction in a Droplet on Graphite: Direct Evidence that the Edge Is More Active than the Basal Plane†

TL;DR: DFT calculations elucidated the mechanism by which the charged edge carbon atoms result in the higher ORR activity and provided a direct way to identify the active sites of carbon materials for the ORR.
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Characterization of MoS2–Graphene Composites for High-Performance Coin Cell Supercapacitors

TL;DR: The performance of solution exfoliated MoS2 thin flexible membranes as supercapacitor electrodes in a symmetrical coin cell arrangement using an aqueous electrolyte (Na2SO4) demonstrates a simple and scalable application of layered 2D materials toward electrochemical energy storage.
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How to get between the sheets: a review of recent works on the electrochemical exfoliation of graphene materials from bulk graphite

TL;DR: This work reviews various works on the electrochemical fabrication of graphene materials specifically through the use of electrochemical intercalation and exfoliation of a graphite source electrode, focusing on the quality and purity of products formed.
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Visible Light-Mediated Generation of Nitrogen-Centered Radicals: Metal-Free Hydroimination- and Iminohydroxylation-Cyclization Reactions

TL;DR: Reaction conditions for a unique iminohydroxylation were identified; visible-light-mediated electron transfer from novel electron donor–acceptor complexes of the oximes and Et3N was proposed as a key step of this process.