Search results for "PHOTOELECTRON"
showing 10 items of 458 documents
Polystyrene as Graphene Film and 3D Graphene Sponge Precursor
2019
[EN] Polystyrene as a thin film on arbitrary substrates or pellets form defective graphene/graphitic films or powders that can be dispersed in water and organic solvents. The materials were characterized by visible absorption, Raman and X-ray photoelectron spectroscopy, electron and atomic force microscopy, and electrochemistry. Raman spectra of these materials showed the presence of the expected 2D, G, and D peaks at 2750, 1590, and 1350 cm(-1), respectively. The relative intensity of the G versus the D peak was taken as a quantitative indicator of the density of defects in the G layer.
Layer-by-Layer Graphene Growth on β-SiC/Si(001)
2019
ACS nano 13(1), 526 - 535 (2019). doi:10.1021/acsnano.8b07237
Photoelectron emission induced by low temperature hydrogen plasmas
2018
Experimental results of low temperature hydrogen plasma induced photoelectron emission measurements comparing two different plasma heating methods are summarized. By exposing the samples to the vacuum ultraviolet radiation of a filament-driven multi-cusp arc discharge ion source and a 2.45 GHz microwave-driven ion source, it has been measured that the total photoelectron emission from various metal surfaces is on the order of 1 A per kW of plasma heating power, which can be increased by a factor of 2–3.5 with a thin layer of alkali metal. The possible effects of the photoelectrons on the plasma sheath structure are studied with a 1D collisionless model extended to include the contribution o…
The co-reactant role during plasma enhanced atomic layer deposition of palladium
2020
Atomic layer deposition (ALD) of noble metals is an attractive technology potentially applied in nanoelectronics and catalysis. Unlike the combustion-like mechanism shown by other noble metal ALD processes, the main palladium (Pd) ALD process using palladium(ii)hexafluoroacetylacetonate [Pd(hfac)2] as precursor is based on true reducing surface chemistry. In this work, a thorough investigation of plasma-enhanced Pd ALD is carried out by employing this precursor with different plasmas (H2*, NH3*, O2*) and plasma sequences (H2* + O2*, O2* + H2*) as co-reactants at varying temperatures, providing insights in the co-reactant and temperature dependence of the Pd growth per cycle (GPC). At all te…
Electronic Structure Changes across the Metamagnetic Transition in FeRh via Hard X-Ray Photoemission
2012
International audience; Stoichiometric FeRh undergoes a temperature-induced antiferromagnetic (AFM) to ferromagnetic (FM) transition at similar to 350 K. In this Letter, changes in the electronic structure accompanying this transition are investigated in epitaxial FeRh thin films via bulk-sensitive valence-band and core-level hard x-ray photoelectron spectroscopy with a photon energy of 5.95 keV. Clear differences between the AFM and FM states are observed across the entire valence-band spectrum and these are well reproduced using density-functional theory. Changes in the 2p core levels of Fe are also observed and interpreted using Anderson impurity model calculations. These results indicat…
Spatially resolved nanostructural transformation in graphite under femtosecond laser irradiation
2015
Abstract A polycrystalline graphite target was irradiated using infrared (800 nm) femtosecond (120 fs) laser pulses of different energies. Increase of sp 3 bonds percentage and possible diamond crystal formation were investigated ‘in-depth’ and on the irradiated surfaces. Synchrotron X-ray diffraction pattern have shown the presence of a diamond peak in one of the irradiated zones while X-ray photoelectron spectroscopy investigations have shown an increasing tendency of the sp 3 percent in the low power irradiated areas and similarly ‘in the depth’ of the higher power irradiated zones. Multiple wavelength Micro-Raman investigations have confirmed this trend along with an ‘in-depth’ (but not…
XPS study of pumice-supported palladium and platinum catalysts
1992
An XPS study has been performed on samples of monometallic of palladium and platinum and on bimetallic Pd-Pt catalysts supported on pumice. A negative shift of about 0.5 eV in the Pd 3d and Pt 4f binding energies of the catalysis relative to the energies of the same levels in the pure metals suggested an increase in the electron density in both metals. A quantitative XPS analysis indicated that the supported metals did not modify the surface atomic composition of pumice
H2-TPR, XPS and TEM Study of the Reduction of Ru and Re promoted Co/γ-Al2O3, Co/TiO2 and Co/SiC Catalysts
2016
<p class="1Body">Effects of Ru and Re promoters on Co-CoO<sub>x </sub>catalysts supported on γ-Al<sub>2</sub>O<sub>3</sub>, TiO<sub>2</sub> and SiC were investigated to improve the understanding of the role of promoters of the active phase of Co-CoO<sub>x</sub>-Ru and Co-CoO<sub>x</sub>-Re. The influence of promoter addition on the composition and activity of the catalysts was characterized by several methods, such as H<sub>2</sub>-TPR, XPS, chemisorption and TEM. Furthermore, the role of support and metal-support interaction was especially studied and different support materials were compared.</p&g…
Support effect on the structure and CO oxidation activity of Cu-Cr mixed oxides over Al2O3 and SiO2
2009
Abstract Cu-Cr based catalysts supported on silica and alumina with 5 wt% total loading of (CuO + Cr2O3), in different molar ratios, were prepared by wet impregnation. The samples were studied by nitrogen adsorption isotherms (BET), temperature-programmed reduction (TPR), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). Their catalytic activity was tested in the CO oxidation reaction. Different structures were obtained in dependence of the support, the atomic ratio and the calcination temperature. In particular, whereas on Al2O3 there was no experimental evidence for interaction between Cu and Cr, over the silica supported systems formation of new phases CuCr2O4 and CuCrO…
A photoemission study of molybdenum hexacarbonyl adsorption and decomposition on TiO2(110) surface.
2007
International audience; The adsorption and decomposition of molybdenum hexacarbonyl on (110) TiO2 surfaces were studied using both core levels and valence band photoemission spectroscopies. It was found that after an adsorption at 140 K, when going back to room temperature, only a small part of molybdenum compounds, previously present at low temperature, remained on the TiO2 surface. This indicates that the desorption temperature on such a surface is lower than the decomposition one. The use of photon irradiation to decompose the hexacarbonyl molecule was also studied. It was shown that during such a decomposition molecular fragments were chemisorbed on the surface allowing a higher amount …