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Overlap integral time-dependent

Detection limits for a particular sample depend on a number of parameters, including observation height in the plasma, applied power, gas flow rates, spectrometer resolution, integration time, the sample introduction system, and sample-induced background or spectral overlaps. ... [Pg.638]

Figure 12 Temperature dependence of the spectral overlap of DPH-loaded zeolite L. Note that the values are 10 times smaller compared with the overlap integrals in Fig. 10. Figure 12 Temperature dependence of the spectral overlap of DPH-loaded zeolite L. Note that the values are 10 times smaller compared with the overlap integrals in Fig. 10.
Bardeen considers two separate subsystems first. The electronic states of the separated subsystems are obtained by solving the stationary Schrodinger equations. For many practical systems, those solutions are known. The rate of transferring an electron from one electrode to another is calculated using time-dependent perturbation theory. As a result, Bardeen showed that the amplitude of electron transfer, or the tunneling matrix element M, is determined by the overlap of the surface wavefunctions of the two subsystems at a separation surface (the choice of the separation surface does not affect the results appreciably). In other words, Bardeen showed that the tunneling matrix element M is determined by a surface integral on a separation surface between the two electrodes, z = zo. [Pg.22]

Use of the Condon approximation for the active and inactive modes causes the matrix element (2.59) to break up into a product of overlap integrals (for the inactive modes) and a constant factor V responsible for interaction of the potential energy terms (for the active modes). In this approximation the time dependence of the survival probability of A1 is given by... [Pg.38]

The Z)< V) elements may thus be computed once and for all and kept on a file. The elements of > are formed from this by multiplying each entry in the list of D(x > elements by the appropriate overlap integral K/P > >, the D N 2. . . Dl3), D,2 and D0) elements being formed in succession in a similar way. Once the elements of DIX) have been formed, this is an extremely fast process and, moreover, is independent of the size of the basis set in which the orbitals are expanded. A particularly convenient feature of this method is that the 3- and 4-electron density matrices, D<3) and are formed simultaneously, and these are necessary in constructing the equations from which the are determined,65 or in minimizing the energy directly. The Nl problem is of course still present, but this mainly occurs in the calculation of 2)<-v> which may well take a considerable time. However, this has to be carried out once only, and in this way the purely group theoretical aspects of the problem are separated from those quantities which depend upon the physical details of the situation. [Pg.96]

Positroniums (Ps) have two spin states ortho (o-Ps) (triplet) and para (p-Ps) (singlet). In condensed matter 75% of the Ps formed will be o-Ps and 25% p-Ps and their existence will depend on the existence of regions with low electron density [4]. The lifetime of positrons depends on the overlap integral of the wave functions of the positron and local electrons and, thus, it is related with the electronic structure of the material [5]. Since the positrons thermalize after a few ps, and the subsequent lifetime is roughly two orders of magnitude higher than the thermalization time, the lifetime of positrons within the matter will effectively depend upon the local electron density [5]. Thus, PALS implies the measurement of the lifetime, t, which is the inverse of the annihilation rate, X, defined by [ 1 ] C p r)p r)dr (1)... [Pg.523]

A quantitative theoretical treatment was developed by Forster [39], who applied time-dependent perturbation theory to dipole-dipole interactions. The following is a simplified account. The probability of resonance energy-transfer from D to A at a distance R may be represented by a first-order rate parameter et (often, but inaccurately, called a rate constant), which is proportional to R and to the integral J representing the spectral overlap between the emission spectrum of the donor and the absorption spectrum of the acceptor. Forster s expression is ... [Pg.177]


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See also in sourсe #XX -- [ Pg.502 , Pg.503 ]




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