The Use of X-Ray Photoelectron Spectroscopy in Materials Science

1991 ◽  
Vol 35 (B) ◽  
pp. 869-882 ◽  
Author(s):  
James Castle

AbstractThis review will attempt to show how XPS now makes an important contribution to Materials Science and to highlight the developments which have brought it to this position. XPS is now a mature technique for surface analysis but it has in addition a major role as a specialised tool, being essential to studies in which derivitization methods are used to tag surface groups.The requirements of users in this field have led to the development of X-ray sources which were not envisaged in the early development of the spectroscopy. The usual sources of aluminium Kα and magnesium Kα have limitations for those elements beyond magnesium in the periodic table which would have the Is lino as the principal peak - aluminium, silicon, oulphur and phosphorus for example. Higher energy sources such as silicon Kα or zirconium and silver Lα have made it possible to utilise the Is lines up to chlorine and have the additional advantage that a strong and well resolved series of Auger lines also becomes available. The higher energy radiations are thus particularly suited to the determination of relaxation energies in materials by use of relative shifts between the photo- and Auger lines of the spectrum. Such has been the utility of such relaxation energies that use is often made of Auger lines derived from the Bremmstrahlung component of the normal x-ray sources to make a similar measurement. This measurement is used in the study of insulating ceramics in which electrostatic charging makes measurement of binding energies uncertain.Modern materials technology is particularly concerned with the manufacture of composites; particulate, fibre and laminate composites are all well known and the key to their success often lies within the interface between the phases. Transfer of load across the interface places particular requirements on adhesion at the phase boundary and an understanding of the locus of failure during destructive testing is crucial to the development of satisfactory bonding processes. In coated and laminated products there is no problem in the use of XPS, with its excellent chemical sensitivity but there is a problem of increasing magnitude in fibre and particulate composites as the substructures become finer. This stems, of course, from the difficulty of providing a focused source of X-rays of sufficient magnitude. Imaging XPS is slowly becoming a reality with several systems having a capability of 10μm now available, and one of the markets for such instruments is that of composite materials.There are important areas of Materials Science in which XPS has been displaced by other techniques such as SIMS. One such area is that of polymer surface analysis. The selectivity of XPS for substituent groups in the surface region is not good. Derivitization methods have made an impact, enabling acidic or basic groups to be determined, but SIMS, which has the ability to detach molecular clusters, has obvious advantages which will become increasingly exploited aa the problems of charging become solved. Until then however XPS will continue to find a role in polymer research and development.

1986 ◽  
Vol 40 (2) ◽  
pp. 224-232 ◽  
Author(s):  
Joseph A. Gardella ◽  
Susan A. Ferguson ◽  
Roland L. Chin

The applications of ESCA to polymer surface analysis include the use of the secondary final-state effects which lead to satellite structure near the core-level photoemission (PE) lines. Specifically, unsaturated and aromatic functionalities in organic compounds and polymers lead to π* ← π shakeup peaks of less than 10 eV lower kinetic energy (higher binding energy). In the surface analysis of polymers, these features can be utilized for qualitative analysis, identification of the presence and structure of aromatic bonding, and quantitative analysis in determining the amount of a particular block or the aromatic containing function in the near-surface region. Carbon Is shakeups are most often used, but the present study includes detailed qualitative and quantitative analysis of shakeup structures from PE lines from each type of atom in hydrocarbon-, siloxane-, and sulfur-containing polymers. These results show the importance of including the shakeup intensity in quantitative peak area calculations and in peak fitting of complex PE envelopes. These studies prove in a variety of systems that the effects of third-row atoms on the final state lead to the presence of shakeup features in atoms with orbitals which do not participate in the aromatic orbital initial state, thus complicating interpretation of structure from the presence of these features. Results from the siloxane and sulfone polymers indicate that previously held assumptions about the nature of the initial-state molecular orbital may overlook the contribution of empty 3d orbitals or increased charge density on the Si or S atom which would spread the pi orbitals to the oxygen in the aromatic siloxane or sulfone systems. Finally, analysis of these features can provide quantitative analysis of polymeric surface structure by monitoring the relative intensity of the feature to the main PE line.


2010 ◽  
Vol 34-35 ◽  
pp. 172-176
Author(s):  
Ying Wu ◽  
Wei Gao ◽  
Man Di ◽  
Chang Zhang Zhao

At most fire scenes, electric short circuit (ESC) arc beads that may be provide useful information on the cause and development of the fire are found. Various physical or chemical methods have been proposed for identifying these electric short circuit beads to be either the cause of a fire (primary arc beads) or one caused by the flames of the fire (secondary arc beads). Little was studied, however, on their identification using the cupreous oxides formed in the molten marks. In this study, the concentration of metallic Cu and Cu2O in the surface region and subsurface was quantified by X-ray photoelectron spectroscopy (XPS). As a result, it can be examined to distinguish the primary and secondary arc beads by comparing the distribution of the substances of Cu and Cu2O.


Nano Research ◽  
2021 ◽  
Author(s):  
Alevtina Smekhova ◽  
Alexei Kuzmin ◽  
Konrad Siemensmeyer ◽  
Chen Luo ◽  
Kai Chen ◽  
...  

AbstractModern design of superior multi-functional alloys composed of several principal components requires in-depth studies of their local structure for developing desired macroscopic properties. Herein, peculiarities of atomic arrangements on the local scale and electronic states of constituent elements in the single-phase face-centered cubic (fcc)- and body-centered cubic (bcc)-structured high-entropy Alx-CrFeCoNi alloys (x = 0.3 and 3, respectively) are explored by element-specific X-ray absorption spectroscopy in hard and soft X-ray energy ranges. Simulations based on the reverse Monte Carlo approach allow to perform a simultaneous fit of extended X-ray absorption fine structure spectra recorded at K absorption edges of each 3d constituent and to reconstruct the local environment within the first coordination shells of absorbers with high precision. The revealed unimodal and bimodal distributions of all five elements are in agreement with structure-dependent magnetic properties of studied alloys probed by magnetometry. A degree of surface atoms oxidation uncovered by soft X-rays suggests different kinetics of oxide formation for each type of constituents and has to be taken into account. X-ray magnetic circular dichroism technique employed at L2.3 absorption edges of transition metals demonstrates reduced magnetic moments of 3d metal constituents in the sub-surface region of in situ cleaned fcc-structured Al0.3-CrFeCoNi compared to their bulk values. Extended to nanostructured versions of multicomponent alloys, such studies would bring new insights related to effects of high entropy mixing on low dimensions.


1998 ◽  
Vol 4 (S2) ◽  
pp. 378-379
Author(s):  
Z. W. Chen ◽  
D. B. Wittry

A monochromatic x-ray microprobe based on a laboratory source has recently been developed in our laboratory and used for fluorescence excitation. This technique provides high sensitivity (ppm to ppb), nondestructive, quantitative microanalysis with minimum sample preparation and does not require a high vacuum specimen chamber. It is expected that this technique (MMXRF) will have important applications in materials science, geological sciences and biological science.Three-dimensional focusing of x-rays can be obtained by using diffraction from doubly curved crystals. In our MMXRF setup, a small x-ray source was produced by the bombardment of a selected target with a focused electron beam and a toroidal mica diffractor with Johann pointfocusing geometry was used to focus characteristic x-rays from the source. In the previous work ∼ 108 photons/s were obtained in a Cu Kα probe of 75 μm × 43 μm in the specimen plane using the fifth order reflection of the (002) planes of mica.


2001 ◽  
Vol 702 ◽  
Author(s):  
Giovanni F Crosta ◽  
Art J Nelson ◽  
Marina C Camatini

ABSTRACTThree types of debris particles, denoted by L2, H2 and K3 respectively, originated from the abrasion of silica-filled, vulcanized rubber under different test conditions (severity) were analyzed and compared. The structural fractal dimension, DFS, of the particle perimeter was chosen as a morphological descriptor (but not necessarily as an intrinsic property of the fractured material !). Said dimension was estimated by processing light microscopy images. A value of the morphological threshold, TST, which separates the textural from the structural domain in the RICHARDSON plot was determined in order to maximize discrimination between the three particle types and rank them by increasing values of DFS. Particles from the highest severity test (K3) exhibited the highest value of DFS. X ray photoelectron spectroscopy (XPS) provided elemental composition, core level binding energies and the speciation of C, N, O, Si and S. As a result, L2 debris was found to originate from two processes: fracture of rubber and segregation of extender oil. Evidence has come both from morphology and XPS. Particles of H2 and K3 were ascribed to fracture alone. Comparison between K3 and the reference material, rasped rubber (RAS), shows the following: a) increase of the [S]/[C] surface atomic concentration ratio from RAS to K3; b) existence of multiple bonding states of S in K3 with energy peaking at 162.9 ± 0.3 eV ([-S-S-]n); c) weak contribution of R-S-O-R oxidized S species in K3 at 165 eV, not seen in RAS; d) no evidence of either SO3 or SO4 groups in any material. Although preliminary, these results prove the ability of morphological analysis and XPS to characterize the surface properties of debris particles non destructively.


2007 ◽  
Vol 111 (40) ◽  
pp. 11850-11857 ◽  
Author(s):  
Sabrina S. Jedlicka ◽  
Jenna L. Rickus ◽  
Dmitry Y. Zemlyanov

2017 ◽  
Vol 3 (6) ◽  
pp. 882-889 ◽  
Author(s):  
Efrat Korin ◽  
Natalya Froumin ◽  
Smadar Cohen

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