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Atoms excited state

If we expand Eq. (10-7) and simplify aeeording to the symmetry of the problem, (Richards and Cooper, 1983) the integral breaks up in the way it did for the helium atom excited state... [Pg.305]

Multiple-Bubble Sonoluminescence. The sonoluminescence of aqueous solutions has been often examined over the past thirty years. The spectmm of MBSL in water consists of a peak at 310 nm and a broad continuum throughout the visible region. An intensive study of aqueous MBSL was conducted by VerraH and Sehgal (35). The emission at 310 nm is from excited-state OH, but the continuum is difficult to interpret. MBSL from aqueous and alcohol solutions of many metal salts have been reported and are characterized by emission from metal atom excited states (36). [Pg.259]

In spite of the fact that in alkali vapors, which contain about 1 % diatomic alkali-molecules at a total vapor-pressure of 10 torr, the atoms cannot absorb laser lines (because there is no proper resonance transition), atomic fluorescence lines have been observed 04) upon irradiating the vapor cell with laser light. The atomic excited states can be produced either by collision-induced dissociation of excited molecules or by photodissociation from excited molecular states by a second photon. The latter process is not improbable, because of the large light intensities in the exciting laser beam. These questions will hopefully be solved by the investigations currently being performed in our laboratory. [Pg.32]

Wavelength difference of states (nm) Energy difference of states (J/atom) Excited-state fraction (N IN, 2 500 K 6 000 K ... [Pg.462]

Rebane, V.N. and Rebane, T.K. (1992). Effect of the optical cell wall on atomic-excited-state relaxation, Optika i Spektroskopiya, 72, 271-275. [Opt. Spectrosc. (USSR), 72, 148-150]. [Pg.288]

The spectra may also be described in the language of solid state theory. The atomic excited states are the same as the excitons that were described, for semiconductors, at the close of Chapter 6. They are electrons in the conduction band that are bound to the valence-band hole thus they form an excitation that cannot carry current. The difference between atomic excited states and excitons is merely that of different extremes the weakly bound exciton found in the semiconductor is frequently called a Mott-Wannier exciton-, the tightly bound cxciton found in the inert-gas solid is called a Frenkel exciton. The important point is that thecxcitonic absorption that is so prominent in the spectra for inert-gas solids does not produce free carriers and therefore it docs not give a measure of the band gap but of a smaller energy. Values for the exciton energy are given in Table 12-4. [Pg.296]

Enzymatically active NADH has been selectively produced by visible light photoreduction of NAD using [Ru(bipy)3]S04 and [Ru(bipy)3]2(S04)3 as sensitizers and triethanolamine as electron donor (Wienkamp and Steckhan). There is continuing interest in the photogeneration of co-ordinatedly unsaturated species from metal carbonyls etc. which can act as or give rise to catalysts, e.g., for cis-trans isomerization and hydrogenation of alkenes. Ger-rity et al. have used chromium hexacarbonyl to make the first quantitative measurements of the distribution of atomic excited states produced by multiphoton dissociation of a metal carbonyl. The distribution of states turns out to be statistical rather than spin- or polarity-difierentiated. The use of perfluoromethylcyclohexane as solvent has enabled Simon and Peters to observe naked Cr(CO)s as a transient from Cr(CO)6. [Pg.620]

In its simplest form, LEI is a two-step process (see Fig. 3). It involves three quantum states the atomic ground state, an atomic excited state, and an ionic ground state. For excited levels very near the ionization potential, ionization rates approach collision rates, giving ion yields near unity. The essential steps for LEI, photoexcitation and thermal ionization, are not the only processes occurring in an atmospheric pressure flame. An excited atom can also be collisionally deactivated or fluoresce. A detailed description of signal production requires a complex expression involving several competing rate constants 25). [Pg.7]

A second spectroscopic thermometer comes from the relative intensities of atomic emission lines in the sonoluminescence spectra of excited-state metal atoms produced by sonolysis of volatile Fe, Cr, and Mo carbonyls. Sufficient spectral information about emissivities of many metal atom excited states are available to readily calculate emission spectra as a function of temperature. Because of this, the emission spectra of metal atoms are extensively used by astronomers to monitor the surface temperature of stars. From comparison of calculated spectra and the observed MBSL spectra from metal carbonyls, another measurement of the cavitation temperature was obtained.6 The effective emission temperature from metal atom emission during cavitation under argon at 20 kHz is 4,900 250 K. [Pg.735]

We also can see that, if /3 is very small, the gap would be constant, independently of k. But it is a dependence of e on that produces the band width, or dispersion. Compounds which are highly ionic will have narrow bands. The ground state will have the electrons concentrated on B, the non-metallic atom. Excited states result from the transfer of an electron from B to A+, forming A,B. [Pg.142]

An alternative way of viewing the process of the reduction of the dressed trapping state to the state a) in a very strong field is to analyze the equations of motion for the density matrix elements in terms of the symmetric and antisymmetric superpositions of the atomic excited states... [Pg.114]

There are two other collective states of the two-atom system the double atomic ground state g) = gi) g2) and the double atomic excited state e) = ei) e2), which are also product states of the individual atomic states. These states are not affected by the dipole-dipole interaction Q.n, the detuning A and the spontaneous emission rates. [Pg.248]

The London theory uses second-order perturbation theory in its usual (R.S.) form an infinite sum over a complete basis set. The set taken for the composite system of two interacting molecules a and b consists of all products of the complete set of eigenfunctions of a and b separately. Thus, the London theory not only assumes that there is no overlap between the ground-state atoms but also that there is no overlap between any of the virtual atomic excited states. ... [Pg.398]

An alternative approach to trace analyte detection results from the measurement of chemiluminescence in a laser-generated plume of plasma, formed when the laser beam evaporates a small amount of sample (43). In these experiments, a pulsed excimer laser-induced-plasma, formed by laser vaporization and ionization, is probed direcdy to measure ion intensity. Ground state sodium atoms, excited state copper atoms, and sodium dimer molecules have all been monitored using this technique. This laser enhanced ionization may well be one of a very few techniques which can be used to probe extremely dense plasmas with good spatial and temporal resolution. [Pg.395]

N(a D or b P) + SiH (X At ). If we now consider excited states of N as reagents, the exothermicity requirement is fulfilled for almost aU products in the previous list, which can be produced in either singlet or triplet stales. However, the abundance of atomic excited states of nitrogen is certainly very low in the interstellar medium, at least in dark clouds. This makes these reactions rather inefficient. [Pg.292]

In practice, the actual energy-level diagram for an atom is derived from the emission spectrum of the excited atom. Figure 2.6 shows an energy-level diagram for mercury atoms. Notice that there are no rotational or vibrational sublevels in atoms A free gas phase atom has no rotational or vibrational energy associated with it. When an electron is promoted to a higher atomic excited state, the... [Pg.69]

There are a number of methods to overcome this loss of atoms by optical pumping. For example, there could be two laser beams tuned for excitation out of each hfs state, the laser spectrum could be sufficiently broad to excite both hfs states, there could be an rf or microwave field that would induce hfs transitions to return atoms to the appropriate hfs state, or optical pumping could be inhibited by careful choice of experimental conditions. For a variety of carefully considered technical reasons, we employ the last of these alternatives. We use circularly polarized light and the axis provided by the magnetic tuning field to allow only excitations to a particular sublevel of the atomic excited state. The only strongly allowed decay process returns the atom to the original state. [Pg.36]

We have shown [56] in the past that in atomic excited states, the density in asymptotic regions (r °o) far from the nucleus varies as exp(-2. -2e r), where e ax is... [Pg.115]

When a beam of electromagnetic radiation with a continuous frequency distribution is made to pass through a gaseous element or metallic vapor, certain frequencies will get absorbed. These frequencies correspond to the allowed excited states. Similarly the atomic nuclei will absorb the y-rays as the atomic excited states fall in the y-region. The important aspect of such absorption is that it is very sensitive to the y-ray energy in the sense that if the y-ray has frequency different from resonance by one part in 10, it will not be absorbed. Such sensitivity will not be realized unless the natural frequency spread (line width for atomic systems) of the y-ray is small which will happen if the life time of the excited state emitting the y-ray is long (>10 s). [Pg.177]

K crystal field parameter e) two-level atom excited state wave... [Pg.508]


See other pages where Atoms excited state is mentioned: [Pg.2475]    [Pg.2478]    [Pg.395]    [Pg.628]    [Pg.303]    [Pg.162]    [Pg.306]    [Pg.308]    [Pg.15]    [Pg.89]    [Pg.5]    [Pg.7]    [Pg.448]    [Pg.207]    [Pg.48]    [Pg.448]    [Pg.2475]    [Pg.484]    [Pg.5]    [Pg.73]    [Pg.33]    [Pg.110]    [Pg.292]    [Pg.18]   
See also in sourсe #XX -- [ Pg.470 ]




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Atoms excitation

States, atomic

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