0000000000217931

AUTHOR

Patrick R. Unwin

showing 3 related works from this author

Adiabatic versus non-adiabatic electron transfer at 2D electrode materials

2021

2D electrode materials are often deployed on conductive supports for electrochemistry and there is a great need to understand fundamental electrochemical processes in this electrode configuration. Here, an integrated experimental-theoretical approach is used to resolve the key electronic interactions in outer-sphere electron transfer (OS-ET), a cornerstone elementary electrochemical reaction, at graphene as-grown on a copper electrode. Using scanning electrochemical cell microscopy, and co-located structural microscopy, the classical hexaamineruthenium (III/II) couple shows the ET kinetics trend: monolayer > bilayer > multilayer graphene. This trend is rationalized quantitatively through th…

Computational chemistryMultidisciplinaryTKScienceQelektrodittiheysfunktionaaliteoriaGeneral Physics and Astronomy02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesGeneral Biochemistry Genetics and Molecular BiologyArticlesähkökemia0104 chemical sciencesCondensed Matter::Materials ScienceDensity functional theorygrafeeniQD0210 nano-technologyElectrocatalysisQC
researchProduct

Adiabatic versus Non-Adiabatic Electron Transfer at 2D Electrode Materials

2021

<div><div><div><p>Outer-sphere electron transfer (OS-ET) is a cornerstone elementary electrochemical reaction, yet microscopic understanding is largely based on idealized theories, developed in isolation from experiments that themselves are often close to the kinetic (diffusion) limit. Focusing on graphene as-grown on a copper substrate as a model 2D material/metal-supported electrode system, this study resolves the key electronic interactions in OS-ET, and identifies the role of graphene in modulating the electronic properties of the electrode/electrolyte interface. An integrated experimental-theoretical approach combining co-located multi-microscopy, centered on sc…

Electron transferMaterials scienceGraphenelawChemical physicsBilayerMonolayerOuter sphere electron transferDensity functional theoryBilayer graphenelaw.inventionElectrochemical cell
researchProduct

Scanning electrochemical microscopy as a probe of Ag+ binding kinetics at Langmuir phospholipid monolayers

2005

A new method has been developed for measuring local adsorption rates of metal ions at interfaces based on scanning electrochemical microscopy (SECM). The technique is illustrated with the example of Ag+ binding at Langmuir phospholipid monolayers formed at the water/air interface. Specifically, an inverted 25 microm diameter silver disc ultramicroelectrode (UME) was positioned in the subphase of a Langmuir trough, close to a dipalmitoyl phosphatidic acid (DPPA) monolayer, and used to generate Ag+ via Ag electro-oxidation. The method involved measuring the transient current-time response at the UME when the electrode was switched to a potential to electrogenerate Ag+. Since the Ag+/Ag couple…

LangmuirBinding SitesSilverTime FactorsSurface PropertiesChemistryMetal ions in aqueous solutionAnalytical chemistryPhosphatidic AcidsGeneral Physics and AstronomyUltramicroelectrodeMicroscopy Scanning ProbeSurface pressureKineticsScanning electrochemical microscopyAdsorptionCationsElectrodeMonolayerElectrochemistrylipids (amino acids peptides and proteins)AdsorptionPhysical and Theoretical ChemistryPhospholipidsPhysical Chemistry Chemical Physics
researchProduct