Surface layers on superconducting Y‐Ba‐Cu‐O films studied with x‐ray photoelectron spectroscopy

1989 ◽  
Vol 55 (16) ◽  
pp. 1680-1682 ◽  
Author(s):  
C. C. Chang ◽  
M. S. Hegde ◽  
X. D. Wu ◽  
B. Dutta ◽  
A. Inam ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Surface Layers ◽  
X Ray

X-ray photoelectron spectroscopic analysis of halloysites with different composition and particle morphology

Clay Minerals ◽  
1992 ◽  
Vol 27 (4) ◽  
pp. 413-421 ◽  
Author(s):  
M. Soma ◽  
G. J. Churchman ◽  
B. K. G. Theng
Keyword(s):  
Photoelectron Spectroscopy ◽  
Cation Exchange Capacity ◽  
Spectroscopic Analysis ◽  
Surface Composition ◽  
Particle Morphology ◽  
Exchange Capacity ◽  
Surface Layers ◽  
X Ray ◽  
Fe Content ◽  
Before And After

AbstractThe surface composition of some halloysites with different particle morphology has been investigated by X-ray photoelectron spectroscopy (XPS) before and after removal of external Fe. The Fe(III) 2p3/2 binding energy of external Fe is appreciably smaller than that of structural Fe. Particle morphology is influenced by structural Fe content. The long-tubular halloysite has very little surface Fe, and its concentration tends to increase with the proportion of non-tubular particles in the samples. The spheroidal sample contains the most structural Fe which, however, does not appear to influence particle shape directly. Study by XPS indicates that Fe substitutes for Al in octahedral positions in approximately 1 : 2 proportion. As a result, an increase in octahedral vacancies and cation exchange capacity would be predicted. Further, halloysite layers within a crystal are generally inhomogeneous in composition. Built up like “onion skins”, the surface layers would either be enriched or depleted in Fe depending on the chemical environment in which crystal growth occurs.

X-Ray Photoelectron Spectroscopic Studies of Palladium Dispersed on Carbon Surfaces Modified by Ion Beams and Plasmatic Oxidation

1995 ◽  
Vol 60 (3) ◽  
pp. 383-392 ◽  
Author(s):  
Zdeněk Bastl
Keyword(s):  
Binding Energy ◽  
Photoelectron Spectroscopy ◽  
Surface Coverage ◽  
Spectroscopic Studies ◽  
Core Level ◽  
Graphite Surface ◽  
Photoelectron Spectra ◽  
Surface Layers ◽  
X Ray ◽  
Core Level Binding Energy

The effects of ion bombardment and r.f. plasma oxidation of graphite surfaces on subsequent growth and electronic properties of vacuum deposited palladium clusters have been investigated by methods of X-ray photoelectron spectroscopy (XPS) and Auger electron spectroscopy with X-ray excitation (XAES). Due to the significantly increased density of surface defects on which the nucleation process occurs the bulk value of the Pd 3d core level binding energy is achieved at higher surface coverage by palladium on bombarded surfaces than on ordered graphite. Angle resolved photoelectron spectra of oxidized graphite surfaces reveal significant embedding of oxygen in graphite surface layers. The C 1s and O 1s photoelectron spectra are consistent with presence of two major oxygen species involving C-O and C=O type linkages which are not homogeneously distributed within the graphite surface layers. Two effects were observed on oxidized surfaces: an increase of palladium dispersion and interaction of the metal clusters with surface oxygen groups. Using the simple interpretation of the modified Auger parameter the relaxation and chemical shift contributions to the measured Pd core level shifts are estimated. In the region of low surface coverage by palladium the effect of palladium-oxygen interaction on Pd core level binding energy exceeds the effects of increased dispersity.

X-Ray photoelectron spectroscopy investigations of atomic interactions in surface layers of multilayered nanostructures (Co45Fe45Zr10/a-Si)40 and (Co45Fe45Zr10/SiO2)32

2014 ◽  
Vol 56 (11) ◽  
pp. 2294-2306 ◽  
Author(s):  
E. P. Domashevskaya ◽  
A. V. Chernyshev ◽  
S. Yu. Turishchev ◽  
Yu. E. Kalinin ◽  
A. V. Sitnikov ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Surface Layers ◽  
X Ray ◽  
Atomic Interactions ◽  
Multilayered Nanostructures

scholarly journals Poly(styrene/acrolein) and poly(styrene/α-tert-butoxy-ω- vinylbenzyl-polyglycidol) microspheres. Similarities and differences

e-Polymers ◽  
2002 ◽  
Vol 2 (1) ◽  
Author(s):  
Teresa Basinska
Keyword(s):  
Photoelectron Spectroscopy ◽  
Particle Surface ◽  
Surface Concentration ◽  
Covalent Immobilization ◽  
Maximal Surface ◽  
Polystyrene Microspheres ◽  
Surface Layers ◽  
X Ray ◽  
Surface Fraction ◽  
Model Protein

AbstractProperties of two types of polystyrene microspheres with polyacrolein and polyglycidol components in their surface layers are compared. Microspheres were prepared in batch radical emulsifier-free emulsion copolymerizations of styrene with acrolein and/or α-tert-butoxy-ω-vinylbenzyl-polyglycidol macromonomer ( Mn̅ = 2700). Polymerizations were initiated with potassium peroxodisulfate, and the ratio of initial concentrations of styrene and initiator was constant. Number average diameters of poly(styrene/acrolein) (P(S/A)) and of poly(styrene/polyglycidol) (P(S/PGL)) particles were in the range of 200 - 650 nm and decreased with increasing concentration of acrolein and/or polyglycidol in the polymerizing mixtures. The diameter polydispersity of synthesized particles ( Dw ̅ /Dn̅) was usually lower than 1.02. X-ray photoelectron spectroscopy for P(S/A) and P(S/PGL) microspheres showed that surface layers of particles were significantly enriched in polyacrolein or polyglycidol segments, surface fractions of which increased with increasing concentration of the more hydrophilic comonomer in the polymerizing mixture. In the case of P(S/A) particles, the maximal fraction of polyacrolein approached 80 mol-%, whereas for P(S/PGL) particles the maximal surface fraction of PGL was 42 mol-%. Human serum albumin was used as a model protein for studies of attachment onto P(S/A) and P(S/PGL) microspheres. It has been found that for both kinds of particles, the maximal surface concentration of attached (adsorbed and/or covalently immobilized) protein decreased with increasing fraction of hydrophilic component in the particle surface layer (polyacrolein or polyglycidol units). In the case of P(S/A) particles, adsorption always accompanied covalent immobilization of proteins. To the contrary, covalent immobilization of proteins onto the P(S/PGL) microspheres proceeded without adsorption of proteins.

scholarly journals Applying Cryo-X-ray Photoelectron Spectroscopy to Study the Surface Chemical Composition of Fungi and Viruses

2021 ◽  
Vol 9 ◽  
Author(s):  
Andrey Shchukarev ◽  
Emelie Backman ◽  
Samuel Watts ◽  
Stefan Salentinig ◽  
Constantin F. Urban ◽  
...  
Keyword(s):  
Chemical Composition ◽  
Photoelectron Spectroscopy ◽  
Biological Systems ◽  
Building Blocks ◽  
Model Organisms ◽  
Surface Chemical ◽  
Surface Layers ◽  
Xps Spectra ◽  
X Ray ◽  
Surface Chemical Composition

Interaction between microorganisms and their surroundings are generally mediated via the cell wall or cell envelope. An understanding of the overall chemical composition of these surface layers may give clues on how these interactions occur and suggest mechanisms to manipulate them. This knowledge is key, for instance, in research aiming to reduce colonization of medical devices and device-related infections from different types of microorganisms. In this context, X-ray photoelectron spectroscopy (XPS) is a powerful technique as its analysis depth below 10 nm enables studies of the outermost surface structures of microorganism. Of specific interest for the study of biological systems is cryogenic XPS (cryo-XPS). This technique allows studies of intact fast-frozen hydrated samples without the need for pre-treatment procedures that may cause the cell structure to collapse or change due to the loss of water. Previously, cryo-XPS has been applied to study bacterial and algal surfaces with respect to their composition of lipids, polysaccharides and peptide (protein and/or peptidoglycan). This contribution focuses onto two other groups of microorganisms with widely different architecture and modes of life, namely fungi and viruses. It evaluates to what extent existing models for data treatment of XPS spectra can be applied to understand the chemical composition of their very different surface layers. XPS data from model organisms as well as reference substances representing specific building blocks of their surface were collected and are presented. These results aims to guide future analysis of the surface chemical composition of biological systems.

Halogen Based Surface Chemistries for Graphene Synthesis

2010 ◽  
Vol 1259 ◽  
Author(s):  
Srikanth Raghavan ◽  
Timothy C. Nelson ◽  
Tobias Denig ◽  
C D Stinespring
Keyword(s):  
Electron Transfer ◽  
Photoelectron Spectroscopy ◽  
Surface Layers ◽  
Near Surface ◽  
X Ray ◽  
Inductively Coupled ◽  
Graphene Synthesis ◽  
P Type ◽  
Surface Chemistries ◽  
Second Peak

AbstractHalogen based (CF4 and Cl2) inductively coupled reactive ion etching (ICP-RIE) has been used to selectively etch silicon from 6H-SiC to produce a controlled number of carbon layers. After annealing at temperatures in the range of 550 °C to 1100 °C to reconstruct the near surface layers, x-ray photoelectron spectroscopy has been used to characterize the composition of the films. For the Cl2 based ICP-RIE, two carbon species are observed. One is due to carbon bound as SiC in the substrate and a second which can be attributed to graphene. In the case of CF4 based etching the situation is similar except the second peak is most closely aligned with p-type graphene. This is most likely due to electron transfer from the graphene to the trace levels of fluorine remaining on the surface after annealing.

The X-ray photoelectron spectroscopy of ancient murals in the tombs at Beni Hasan, Egypt

1987 ◽  
Vol 65 (5) ◽  
pp. 1058-1064 ◽  
Author(s):  
K. M. Wilson-Yang ◽  
George Burns
Keyword(s):  
Photoelectron Spectroscopy ◽  
Archaeological Site ◽  
Photoelectron Spectra ◽  
Surface Layers ◽  
X Ray ◽  
The Past ◽  
Mural Paintings ◽  
Adsorption Of Water ◽  
Aluminium Silicates ◽  
Trace Components

The once colourful mural paintings at the Beni Hasan tombs (ca. 2100 B.C.), an important Egyptian archaeological site, are covered with an obscuring grey deposit. Qualitative observations made over the past 150 years were assembled and correlated with each other by us. Cumulatively, they indicate that recently the development of this layer has accelerated. To study this surface degradation, X-ray photoelectron spectra of fragments from the painted walls have been collected. Empirical XPS sensitivity factors have been employed to treat the data semiquantitatively. Three types of surfaces were identified. The first surface consists of CaCO3 and SiO2 as major constituents, and was the only surface identified previously. Our XPS data indicate that it also contains Al2O3, NaCl, MgO, sulphates, and phosphates as minor and trace components. The second surface consists predominantly of aluminium silicates. The third surface consists mostly of calcium carbonate. A preliminary mechanism for opaque layer formation is proposed herein. It suggests that the principal physicochemical processes are adsorption of water in the presence of carbon dioxide, followed by dissolution of the substrate walls upon which the murals were painted. This mechanism is consistent with our finding that mural deterioration is recent; it also indicates that deterioration is progressive, continuous, and cumulative. Further experiments are designed to verify the proposed mechanism. Two mechanisms proposed earlier are found to be inconsistent with at least some of our findings. Relatively recent efforts in removing obtrusive surface layers with dilute HCl were found to be performed carefully; there was no evidence of excess chlorides on cleaned surfaces. However, this finding does not provide a guarantee that murals were undamaged by HCl below the surface. It does suggest that progressive damage due to the formation of hygroscopic CaCl2 on the surface has been avoided.

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