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Graham Beamson

Researcher at Daresbury Laboratory

Publications -  59
Citations -  1999

Graham Beamson is an academic researcher from Daresbury Laboratory. The author has contributed to research in topics: X-ray photoelectron spectroscopy & Auger. The author has an hindex of 25, co-authored 59 publications receiving 1857 citations.

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Quantification of oxide film thickness at the surface of aluminium using XPS

TL;DR: In this article, a surface layer of hydration is identified from the curve fitting of the O is core level, which would qualitatively account for the slight underestimate of film thickness provided by the expression for d XPS.
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Analysis of chemical vapour deposited diamond films by X-ray photoelectron spectroscopy

TL;DR: In this article, the surface reconstructions for diamond surfaces in the presence of hydrogen or following thermal annealing are reviewed, and the destructive effects of argon ion bombardment cleaning are discussed.
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Interaction of carboxylic acids with the oxyhydroxide surface of aluminium: poly(acrylic acid), acetic acid and propionic acid on pseudoboehmite

TL;DR: In this paper, high sensitivity and spectral resolution XPS, polarisation-modulation reflection FTIR and static SIMS have been used in the investigation of the interfacial chemistry between poly(acrylic acid) (PAA) and an aluminium oxyhydroxide surface.
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Performance and application of the scienta ESCA300 spectrometer

TL;DR: The Scienta ESCA300 as mentioned in this paper is a state-of-the-art x-ray photoelectron spectrometer with high intensity, and high energy and spatial resolution, made possible by the use of a high-power rotating anode xray source with monochromatization, high transmission and imaging electron optics and multichannel detector.
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Selective hydrogenation of amides using bimetallic Ru/Re and Rh/Re catalysts

TL;DR: Heterogeneous Ru/Re and Rh/Re catalysts, formed in situ from Ru 3 (CO) 12 /Re 2 (CO), 10 and Rh 6 (CO, 16 /RRe 2, 10 respectively, are effective for the liquid phase hydrogenation of cyclohexanecarboxamide (CyCONH 2 ) to CyCH 2 NH 2 in up to 95% selectivity without the requirement for ammonia to inhibit secondary and tertiary amine formation as discussed by the authors.