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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Flavell, Wendy R.
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (16/16 displayed)
- 2024Toward Water-Resistant, Tunable Perovskite Absorbers Using Peptide Hydrogel Additives
- 2023Elucidating the mechanism of self healing in hydro gel lead halide perovskite composites for use in photovoltaic devices
- 2022Surface stability of ionic-liquid-passivated mixed-cation perovskite probed with in-situ photoelectron spectroscopycitations
- 2021Inelastic background modelling applied to Hard X-ray Photoelectron Spectroscopy of deeply buried layers: a comparison of synchrotron and lab-based (9.25 keV) measurementscitations
- 2020Spatially and temporally resolved degradation in antisolvent treated perovskite films
- 2020Spatially and temporally resolved degradation in antisolvent treated perovskite films
- 2019Air-Stable Methylammonium Lead Iodide Perovskite Thin Films Fabricated via Aerosol-Assisted Chemical Vapor Deposition from a Pseudohalide Pb(SCN)2 Precursorcitations
- 2018Ambient-Air-Stable Inorganic Cs2SnI6 Double Perovskite Thin Films via Aerosol-Assisted Chemical Vapour Depositioncitations
- 2012Growth and characterization of strained and alloyed type-II ZnTe/ZnSe core-shell nanocrystalscitations
- 2011Controlled synthesis of tuned bandgap nanodimensional alloys of PbS xSe1-xcitations
- 2007Electronic properties of the interface between p-CuI and anatase-phase n-Ti O2 single crystal and nanoparticulate surfaces: A photoemission studycitations
- 2005Resonant photoemission of transition metal perovskitescitations
- 2003Local investigation of electronic structure modulation in BaPbxBi1-xO3 via highly spatially resolved low-loss electron energy loss spectroscopy.
- 2003Investigations of chemical and electronic inhomogeneities in BaPb 1-xBixO3 via highly spatially resolved electron energy loss spectroscopycitations
- 2002Electronic structure and reactivity of TM-doped La1-xSrxCoO3 (TM = Ni, Fe) catalystscitations
- 2001X-ray powder diffraction and EXAFS studies on SnAPO-5 and Cu:SnAPO-5citations
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article
Inelastic background modelling applied to Hard X-ray Photoelectron Spectroscopy of deeply buried layers: a comparison of synchrotron and lab-based (9.25 keV) measurements
Abstract
<p>Hard X-ray Photoelectron Spectroscopy (HAXPES) provides minimally destructive depth profiling into the bulk, extending the photoelectron sampling depth. Detection of deeply buried layers beyond the elastic limit is enabled through inelastic background analysis. To test the robustness of this technique, we present results on a thin (18 nm) layer of metal–organic complex buried up to 200 nm beneath organic material. Overlayers with thicknesses 25–140 nm were measured using photon energies ranging 6–10 keV at the I09 end station at Diamond Light Source, and a new fixed energy Ga Kα (9.25 keV) laboratory-based HAXPES spectrometer was also used to measure samples with overlayers up to 200 nm thick. The sampling depth was varied: at Diamond Light Source by changing the photon energy, and in the lab system by performing angle-resolved measurements. For all the different overlayers and sampling depths, inelastic background modelling consistently provided thicknesses which agreed, within reasonable error, with the ellipsometric thickness. Relative sensitivity factors were calculated, and these factors consistently provided reasonable agreement with the expected nominal stoichiometry, suggesting the calculation method can be extended to any element. These results demonstrate the potential for the characterisation of deeply buried layers using synchrotron and laboratory-based HAXPES.</p>