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Synchrotron spectrum

EXAES Extended X-Ray Absorplion Eine SIruclure Films, toils High inlensily X-rays (synchrotron) Spectrum near absorption edge nm-pm Locai atomic SIruclure order/ disorder in vicinity ol absorbing atom 27... [Pg.1968]

In contrast, an optically thick thermal spectrum varies as oP at low frequencies. The emission is polarized, since the electron radiates orthogonally to the local field direction circular polarization results from viewing the source longitudinally. The synchrotron spectrum thus reflects the exponent of N E), so the identification of this radiation is... [Pg.166]

Relativistic electrons radiate not only at the gyrofrequency, but also at the harmonics. The relativistic mass increase with energy causes the harmonic spacing to decrease with increasing energy until the synchrotron spectrum is essentially smeared into a continuum. The radiation from a relativistic electron is highly nonisotropic. The emitted radiation is concentrated within a narrow cone about the instantaneous direction of the velocity vector with an approximate half-cone-width given by... [Pg.255]

Figure 2 Molybdenum K-edge X-ray absorption spectrum, ln(i /i ) versus X-ray energy (eV), for molybdenum metal foil (25- jjn thick), obtained by transmission at 77 K with synchrotron radiation. The energy-dependent constructive and destructive interference of outgoing and backscattered photoelectrons at molybdenum produces the EXAFS peaks and valleys, respectively. The preedge and edge structures marked here are known together as X-ray absorption near edge structure, XANES and EXAFS are provided in a new compilation of literature entitled X-rsy Absorption Fine Structure (S.S. Hasain, ed.) Ellis Norwood, New York, 1991. Figure 2 Molybdenum K-edge X-ray absorption spectrum, ln(i /i ) versus X-ray energy (eV), for molybdenum metal foil (25- jjn thick), obtained by transmission at 77 K with synchrotron radiation. The energy-dependent constructive and destructive interference of outgoing and backscattered photoelectrons at molybdenum produces the EXAFS peaks and valleys, respectively. The preedge and edge structures marked here are known together as X-ray absorption near edge structure, XANES and EXAFS are provided in a new compilation of literature entitled X-rsy Absorption Fine Structure (S.S. Hasain, ed.) Ellis Norwood, New York, 1991.
In a synchrotron, electrons are accelerated to near relativistic velocities and constrained magnetically into circular paths. When a charged particle is accelerated, it emits radiation, and when the near-relativistic electrons are forced into curved paths they emit photons over a continuous spectrum. The general shape of the spectrum is shown in Fig. 2.4. For a synchrotron with an energy of several gigaelectronvolts and a radius of some tens of meters, the energy of the emitted photons near the maximum is of the order of 1 keV (i.e., ideal for XPS). As can be seen from the universal curve, plenty of usable intensity exists down into the UV region. With suitable mono-... [Pg.12]

Other techniques utilize various types of radiation for the investigation of polymer surfaces (Fig. 2). X-ray photoelectron spectroscopy (XPS) has been known in surface analysis for approximately 23 years and is widely applied for the analysis of the chemical composition of polymer surfaces. It is more commonly referred to as electron spectroscopy for chemical analysis (ESCA) [22]. It is a very widespread technique for surface analysis since a wide range of information can be obtained. The surface is exposed to monochromatic X-rays from e.g. a rotating anode generator or a synchrotron source and the energy spectrum of electrons emitted... [Pg.365]

Bowmaker et al. (1998) have also used IR from a synchrotron source in the SNIFTIRS mode to smdy cyanate adsorption on silver. The spectra are shown in Fig. 27.38. The far-IR spectrum shows a broad band at about 360 cm at electrode... [Pg.505]

Single-line sources are now available which cut down the number of resonance lines in a spectrum and thereby reduce the resolution problems considerably. Since many laboratories have access to electron and ion accelerators to produce the parent nuclides Co and Cu, the major experimental obstacles to Ni spectroscopy have been overcome and a good deal of successful work has been performed in recent years. Moreover, the development of synchrotron radiation instead of conventional Mossbauer sources is of additional advantage for future Mossbauer applications (see below). [Pg.237]

Nuclear absorption of incident X-rays (from the synchrotron beam) occurs elastically, provided their energy, y, coincides precisely with the energy of the nuclear transition, Eq, of the Mossbauer isotope (elastic or zero-phonon peak at = E m Fig. 9.34). Nuclear absorption may also proceed inelasticaUy, by creation or annihilation of a phonon. This process causes inelastic sidebands in the energy spectrum around the central elastic peak (Fig. 9.34) and is termed nuclear inelastic scattering (NIS). [Pg.516]

In the case of the LiMg momentum density and occupation number density reconstruction of Stutz et al, who collected 6 x 105 6 counts for Li and 6 x 107 counts for LiMg, this would mean that 6 x 10s—6 x 10 counts per spectrum were required, which hardly can be accomplished in a reasonable amount of time even at modem synchrotron radiation sources. [Pg.318]

To test the feasibility of obtaining submicron size patterns in the resist films, an exposure source was used which consisted of the X-ray continuous spectrum produced by synchrotron radiation from the 5 0 MeV storage ring of the University of Orsay (ACO) since synchrotron radiation had been shown previously (2.,8.) to be a suitable source for providing very high resolution due to the small divergence of the beam. The maximum output flux of ACO... [Pg.279]

An interesting feature of polarized IR spectroscopy is that rapid measurements can be performed while preserving molecular information (in contrast with birefringence) and without the need for a synchrotron source (X-ray diffraction). Time-resolved IRLD studies are almost exclusively realized in transmission because of its compatibility with various types of tensile testing devices. In the simplest implementation, p- and s-polarized spectra are sequentially acquired while the sample is deformed and/or relaxing. The time resolution is generally limited to several seconds per spectrum by the acquisition time of two spectra and by the speed at which the polarizer can be rotated. Siesler et al. have used such a rheo-optical technique to study the dynamics of multiple polymers and copolymers [40]. [Pg.312]


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