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Four-phonon processes

We first consider the vibrational relaxation that can be induced by aijQqiqj (three-phonon processes) or Qq qi (four-phonon processes). In the three-phonon processes there are two accepting modes, while in the four-phonon processes there are three accepting modes. To calculate the rate of vibrational relaxation, we use... [Pg.78]

The s are then the generalized elastic constants. The third and fourth order s are directly proportional to the matrix elements for the three- and four-phonon processes respectively. [Pg.356]

All other terms that are not related to the above terms by permutation of the Indices are zero. As noted before, < gives the optical phonon frequency y gives the amplitudes for three-phonon processes and a and 3 give the amplitudes for the bare four-phonon processes. [Pg.358]

The similarity between the A C o spectra doped with different alkali metals again indicates that the observed modes are due only to the Cfio molecule, and that there are no observable A-Cfto modes above 100 cm The mode at 270 cm has a resolution-limited FWHM for CSftCfio, is broadened in nd is a doublet in K C q. The high-frequency mode of the doublet may result from a two-phonon process involving a low cnergy-A-Cfrequency modes (1383 cm and 1478 cm ). If this is the case, it is not clear that these modes should be broadened in the same way as the... [Pg.168]

Notice that it is not always easy to distinguish between these processes on an a priori basis. For example, three- or four-phonon asymmetric up-conversion rates vary approximately as the occupation number of some (low-frequency) phonon at low temperature and as T thereafter. The pure... [Pg.341]

This work contributed in two major ways. First, the calculation shows that it is now possible for the first time to calculate from first principles phonon-phonon interaction parameters that are inaccessible from experiment. Second, since all the effective four-phonon terms (direct plus mediated processes up to are attractive for the k = 0 optical phonons in diamond, the formation of the two-phonon bound state is unlikely in this system. [Pg.361]

This mechanism concerns the relaxation of vibrationally excited molecules near surfaces. It depends strongly on the ratio between the vibrational frequency of a molecule, coq, and the Debye frequency of the substrate, cup, which determines the upper limit of the phonon spectrum. If a>o < cod, relaxation through creation of a single phonon is possible. Usually the corresponding decay rates are of the order of lO -lO s . For (n — 1)cud < o o < ncup, the relaxation is accompanied by the generation of n phonons. The probability of an n-phonon process to occur rapidly decreases with order n. Typical values for the two-, three- and four-phonon decay rates are 10 -10 10 -10 and 10 -10 s, respectively (Zhdanov and Zamaraev 1982). [Pg.40]

From Table 5.1, it follows that there are four basic processes (i) absorption of a phonon with the creation of two other phonons, (ii) absorption of two phonons with the creation of another, (iii) simultaneous disappearance... [Pg.189]

A spin-dependent recombination rate is another consequence of the electron-hole correlation. The conservation of spin selection rule is preserved in amorphous materials. The final state of the recombination process has zero spin and both radiative and phonon-assisted non-radiative transitions occur without change in spin, so that recombination can only proceed from an initial state of zero spin. A weakly interacting electron-hole pair forms four possible spin states, one singlet and one triplet. Of the four states, only the singlet and one... [Pg.287]


See other pages where Four-phonon processes is mentioned: [Pg.105]    [Pg.113]    [Pg.189]    [Pg.190]    [Pg.105]    [Pg.113]    [Pg.189]    [Pg.190]    [Pg.316]    [Pg.200]    [Pg.87]    [Pg.54]    [Pg.87]    [Pg.18]    [Pg.215]    [Pg.23]    [Pg.210]    [Pg.229]    [Pg.177]    [Pg.159]    [Pg.17]    [Pg.546]    [Pg.46]    [Pg.204]    [Pg.112]    [Pg.99]    [Pg.188]    [Pg.561]    [Pg.234]    [Pg.1029]    [Pg.160]    [Pg.7]    [Pg.524]    [Pg.113]    [Pg.341]    [Pg.257]    [Pg.38]    [Pg.246]    [Pg.496]    [Pg.175]    [Pg.160]    [Pg.415]    [Pg.305]   
See also in sourсe #XX -- [ Pg.356 ]

See also in sourсe #XX -- [ Pg.189 , Pg.220 ]




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