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Widths natural width

In equations (Cl. 4.4) and (Cl. 4.5) Acoj = cu - coj is the detuning of the optical field from the atomic transition frequency Q is the natural width of the atomic transition and m is tenned the Rabi frequency and reflects the... [Pg.2458]

Natural width of D lines 10 MHz Peak D2 cross section for Doppler linewidth 8.8 10 m2... [Pg.213]

The emission line is centered at the mean energy Eq of the transition (Fig. 2.2). One can immediately see that I E) = 1/2 I Eq) for E = Eq E/2, which renders r the full width of the spectral line at half maximum. F is called the natural width of the nuclear excited state. The emission line is normalized so that the integral is one f l(E)dE = 1. The probability distribution for the corresponding absorption process, the absorption line, has the same shape as the emission line for reasons of time-reversal invariance. [Pg.10]

Weisskopf and Wigner [2] have shown that the natural width of the emission and the absorption line is readily determined by the mean lifetime x of the excited state because of the relation (note the equal sign) ... [Pg.10]

In the following, we consider the shape and the width of the Mdssbauer velocity spectrum in more detail. We assume that the source is moving with velocity u, and the emission line is an unsplit Lorentzian according to (2.2) with natural width E. If we denote the total number of y-quanta emitted by the source per time unit toward the detector by Nq, the number N E)AE of recoU-free emitted y-rays with energy y in the range to -f dE is given by ([1] in Chap. 1)... [Pg.18]

Using the value t = 0.2 for the effective thickness, the amount of resonance nuclei ( Fe) for a good thin absorber can be easily estimated according to the relation = tl(fA-(to)- For a quadrupole doublet with two equal absorption peaks of natural width and a recoil-free fraction of the sample/a = 0.7 one obtains... [Pg.47]

It is difficult to give an exact limit because the impact of thickness broadening depends on the intrinsic width of experimental lines [31], which often exceeds the natural width 2r at by 0.05—0.1 mm s for Fe as studied in inorganic chemistry. This inhomogeneous broadening, which is due to heterogeneity and strain in the sample, causes a reduction of the effective thickness. Rancourt et ai. have treated this feature in detail for iron minerals [32]. [Pg.47]

The small natural width of 2E = 0.0065 mm s implies an extremely narrow relative line width of r/ y = 1.1 lO, which is about 30 times narrower than that for the 14.4 keV state of Fe. [Pg.289]

Typical absorbers contain 50-700 mg cm of natural platinum. The observed experimental line widths in Pt (99 keV) spectra range from values close to the natural width (2F at (99 keV) = 16.28 mm s ) to 25 mm s. With respect to the line width, the 130 keV transition with a natural width of (130 keV) = 3.40 mm s seems to be more favorable for the study of hyperfine interaction in platinum compounds in practice, experimental line widths of 3.4 0.4 [328] and 3.5 0.7 mm s [329] have been measured. The considerably higher energy resulting in a much smaller recoiUess fraction and the lower probability for the population... [Pg.340]

Dr. Flinn The six lines aren t fully resolved unfortunately (but probably would be with a natural width source). [Pg.162]

Electron nuclear double resonance (ENDOR) and electron spin-echo envelope modulation (ESEEM) are two of a variety of pulsed EPR techniques that are used to study paramagnetic metal centers in metalloenzymes. The techniques are discussed in Chapter 4 of reference la and will not be discussed in any detail here. The techniques can define electron-nuclear hyperfine interactions too small to be resolved within the natural width of the EPR line. For instance, as a paramagnetic transition metal center in a metalloprotein interacts with magnetic nuclei such as H, H, P, or these... [Pg.129]

Natural broadening occurs because of the finite lifetime (x) of the atom in the excited state. Heisenberg s uncertainty principle states that if we know the state of the atom, we must have uncertainty in the energy level. We assume that x for the ground state is infinity and therefore for a resonance line the natural width Av = IAtxx. [Pg.75]

Accuracy of the radiofrequency measurements of the classic 2S — 2P Lamb shift [15, 16, 23, 24, 25] is limited by the large (about 100 MHz) natural width of the 2P state, and cannot be significantly improved. New perspectives in reducing the experimental error bars of the classic 2S — 2P Lamb shift were opened with the development of the Doppler-free two-photon laser spectroscopy for measurements of the transitions between the energy levels with different principal quantum numbers. Narrow linewidth of such transi-... [Pg.237]

The second factor involves the theory that defines the natural width of the lines. Radiations emitted by atoms are not totally monochromatic. With plasmas in particular, where the collision frequency is high (this greatly reduces the lifetime of the excited states), Heisenberg s uncertainty principle is fully operational (see Fig. 15.4). Moreover, elevated temperatures increase the speed of the atoms, enlarging line widths by the Doppler effect. The natural width of spectral lines at 6000 K is in the order of several picometres. [Pg.278]

Several parameters, for example focal length, determine linear dispersion, which is expressed in millimetres per nanometre (or its inverse, which is called reciprocal dispersion). Linear dispersion represents the spread, in the focal plane, of two wavelengths differing by l nm. Bandwidth, which must not be confused with the width of the slit, is the interval of the spectrum that corresponds to the width in picometres exiting the slit. This width is generally greater than the natural width of the line being transmitted. [Pg.282]

From this equation calculate the natural width of the 589 nm emission line for sodium if At = 1 ns. [Pg.284]

Natural bandwidth, 256 Natural width, 278 Nephelometry, 208 Nemst coefficient, 4 Nernst source, 175 Nessler tube, 207 Neutral marker, 116 Nier-Johnson, 296 NPD, 36... [Pg.444]

Besides the uncertainty broadening just discussed, there are other causes of line broadening which make line widths generally considerably greater than the natural width (3.88). The Doppler effect causes an apparent change in radiation frequency for molecules with a component of velocity cobs in the direction of observation of the radiation. Different molecules have different values of cobs and we get a Doppler broadened line. [Pg.72]

Example Problem Calculate the natural line width of the state at 14.4 keV in 57Fe given that t1/2 = 98 ns. Then calculate the velocity of the source lattice that would correspond to twice the natural width and would lie outside the Mossbauer resonance effect ... [Pg.246]

Expressions for a number of main moments of the spectrum may be utilized to develop a new version of the semi-empirical method. Evaluation of the statistical characteristics of spectra with the help of their moments is also useful for studying various statistical peculiarities of the distribution of atomic levels, deviations from normal distribution law, etc. Such a statistical approach is also efficient when considering separate groups of levels in a spectrum (e.g. averaging the energy levels with respect to all quantum numbers but spin), when studying natural widths or lifetimes of excited levels, etc. [Pg.389]

Having explicit formulas for a number of first moments we can approximately restore the envelope line of the radiation spectrum without its detailed calculations. If lines in the spectrum have one symmetric maximum, then its envelope line is approximated by a normal function whose reconstruction requires only the mean energy and variance of the spectrum. Such an approach is useful for the case of complex spectra consisting of many lines, which, due to low resolutions as well as Doppler and collisional broadening or large natural width, form continuous or quasi-continuous bands. Studies of variation of these statistical characteristics along isoelectronic sequences give a wealth of information on intra-atomic interactions. [Pg.390]

Generally, when studying autoionizing levels, we have to take into consideration both (radiative and radiationless) channels of their decay. The total natural width of the autoionizing level will be the sum of its autoionizing and radiative widths. [Pg.393]

The lifetime of a separate atom in its ground state is infinite, therefore the natural width of the ground level equals zero. Typical lifetimes of excited states with an inner vacancy are of the order 10-14 — 10 16 s, giving a natural width 0.1 — 10 eV. The closer the vacancy is to the nucleus, the more possibilities there are to occupy this vacancy and then the broader the level becomes. That is why T > Tl > Tm- Generally, the total linewidth T is the sum of radiative (Tr) and Auger (T ) widths, i.e. [Pg.402]


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See also in sourсe #XX -- [ Pg.37 ]




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