Transversal optical

Observation of absorption bands due to LO phonons in RAIR spectra of thin, silica-like films deposited onto reflecting substrates demonstrates an important difference between RAIR and transmission spectra. Berreman has shown that absorption bands related to transverse optical (TO) phonons are observed in transmission infrared spectra of thin films obtained at normal incidence [17]. However, bands related to LO phonons are observed in transmission spectra of the same films obtained at non-normal incidence and in RAIR spectra. Thus, it is possible for RAIR and transmission spectra of thin films of some materials to appear very different for reasons that are purely optical in nature. For example, when the transmission infrared spectrum of a thin, silica-like film on a KBr disc was obtained at normal incidence, bands due to TO phonons were observed near 1060,790,and450cm [18]. 

When metals have Raman active phonons, optical pump-probe techniques can be applied to study their coherent dynamics. Hase and coworkers observed a periodic oscillation in the reflectivity of Zn and Cd due to the coherent E2g phonons (Fig. 2.17) [56]. The amplitude of the coherent phonons of Zn decreased with raising temperature, in accordance with the photo-induced quasi-particle density n.p, which is proportional to the difference in the electronic temperature before and after the photoexcitation (Fig. 2.17). The result indicated the resonant nature of the ISRS generation of coherent phonons. Under intense (mJ/cm2) photoexcitation, the coherent Eg phonons of Zn exhibited a transient frequency shift similar to that of Bi (Fig. 2.9), which can be understood as the Fano interference [57], A transient frequency shift was aslo observed for the coherent transverse optical (TO) phonon in polycrystalline Zr film, in spite of much weaker photoexcitation [58],... 

Bulk silicon is a semiconductor with an indirect band structure, as schematically shown in Fig. 7.12 c. The top of the VB is located at the center of the Brillouin zone, while the CB has six minima at the equivalent (100) directions. The only allowed optical transition is a vertical transition of a photon with a subsequent electron-phonon scattering process which is needed to conserve the crystal momentum, as indicated by arrows in Fig. 7.12 c. The relevant phonon modes include transverse optical phonons (TO 56 meV), longitudinal optical phonons (LO 53.5 meV) and transverse acoustic phonons (TA 18.7 meV). At very low temperature a splitting (2.5 meV) of the main free exciton line in TO and LO replicas can be observed [Kol5]. 

At high temperatures above Tb 617 K PMN behaves Hke all other simple perovskites. The dynamics of the system is determined by the soft transverse optical (TO) phonon which exhibits a normal dispersion and is imderdamped at all wave vectors. Below Tb, in addition to the soft mode—which becomes overdamped—a new dielectric dispersion mechanism appears at lower frequencies which can be described by a correlation time distribution function /(t). 

I he notation 0e indicates that this is the dielectric function at frequencies low i ompared with electronic excitation frequencies. We have also replaced co0 with l (, the frequency of the transverse optical mode in an ionic crystal microscopic theory shows that only this type of traveling wave will be readily excited bv a photon. Note that co2 in (9.20) corresponds to 01 e2/me0 for the lattice vibrations (ionic oscillators) rather than for the electrons. The mass of an electron is some thousands of times less than that of an ion thus, the plasma liequency for lattice vibrations is correspondingly reduced compared with that lor electrons. 

For frequencies low compared with the transverse optical frequency dielectric function (9.21) approaches the limiting value 0v ... 

At infrared wavelengths extinction by the MgO particles of Fig. 11.2, including those with radius 1 jam, which can be made by grinding, is dominated by absorption. This is why the KBr pellet technique is commonly used for infrared absorption spectroscopy of powders. A small amount of the sample dispersed in KBr powder is pressed into a pellet, the transmission spectrum of which is readily obtained. Because extinction is dominated by absorption, this transmission spectrum should follow the undulations of the intrinsic absorption spectrum—but not always. Comparison of Figs. 10.1 and 11.2 reveals an interesting discrepancy calculated peak extinction occurs at 0.075 eV, whereas absorption in bulk MgO peaks at the transverse optic mode frequency, which is about 0.05 eV. This is a large discrepancy in light of the precision of modern infrared spectroscopy and could cause serious error if the extinction peak were assumed to lie at the position of a bulk absorption band. This is the first instance we have encountered where the properties of small particles deviate appreciably from those of the bulk solid. It is the result of surface mode excitation, which is such a dominant effect in small particles of some solids that we have devoted Chapter 12 to its fuller discussion. 

Comparison of measurements for particles dispersed on and in KBr is quite revealing. The extinction curve for particles on a KBr substrate shows a peak at approximately 400 cm-1, the transverse optical mode frequency for bulk MgO. This feature has been observed a number of times and it is discussed in some of the references already cited. Its explanation now appears to be the tendency of MgO cubes to link together into chains, which more closely... 

So far only one degree of freedom of the vibration has been considered, namely, in the direction of the wave vector. The removal of this restriction gives transverse optical and acoustical phonons. For these, the atoms or ions move perpendicular to the direction of wave propagation. Again, there are two possibilities. When A and B atoms vibrate in phase, there is no change of dipole moment and one speaks of a transverse acoustical phonon (TA). However, for a vibration with opposite phases in the A and B atoms, the electric dipole moment changes so that we have a transverse optical phonon (TO). 

This is the background for the Lyddane-Sachs-Teller relation to be treated below. For transverse optical vibrations the origin of an is field is less obvious, but it is also present and its reaction on the eigenfrequency of the TO phonon later gives rise to the polaritons. 

The other solution ej - 2 =0 leads to strictly transverse optical phonons. They degenerate with the ordinary phonons given by Eq. (11.29). 

To identify c-BN, the characteristic transverse optical mode (TO) at 1065 cm-1 and longitudinal optical mode (LO) at 1340 cm-1 have been described [56]. When investigating commercial c-BN, commonly only one IR-peak between 1050 and 1100 cm-1 is observed. 

From the lattice dynamics viewpoint a transition to the ferroelectric state is seen as a limiting case of a transverse optical mode, the frequency of which is temperature dependent. If, as the temperature falls, the force constant controlling a transverse optical mode decreases, a temperature may be reached when the frequency of the mode approaches zero. The transition to the ferroelectric state occurs at the temperature at which the frequency is zero. Such a vibrational mode is referred to as a soft mode . 

Hereby, the branches with E - and / -symmetry are twofold degenerated. Both A - and / d-modes are polar, and split into transverse optical (TO) and longitudinal optical (LO) phonons with different frequencies wto and wlo, respectively, because of the macroscopic electric fields associated with the LO phonons. The short-range interatomic forces cause anisotropy, and A - and / d-modcs possess, therefore, different frequencies. The electrostatic forces dominate the anisotropy in the short-range forces in ZnO, such that the TO-LO splitting is larger than the A -E splitting. For the lattice vibrations with Ai- and F -symmetry, the atoms move parallel and perpendicular to the c-axis, respectively (Fig. 3.2). 

Indium nitride has twelve phonon modes at the zone centre (symmetry group Cev), three acoustic and nine optical with the acoustic branches essentially zero at k = 0. The infrared active modes are Ei(LO), Ei(TO), Ai(LO) and Ai(TO). A transverse optical mode has been identified at 478 cm 1 (59.3 meV) by reflectance [6] and 460 cm 1 (57.1 meV) by transmission [24], In both reports the location of a longitudinal optical mode is inferred from the Brout sum rule, giving respective values of 694 cm 1 (86.1 meV) and 719 cm 1 (89.2 meV). Raman scattering of single crystalline wurtzite InN reveals Ai(LO) and E22 peaks at 596 cm 1 and at 495 cm 1 respectively [25],... 

FIGURE 4(a), the relation between device diameter and threshold current is shown. In this estimation, the structure shown in FIGURE 4(b) has been assumed. The transverse optical confinement factor for a cylindrical waveguide with GaN core and AIN cladding was taken into account in this estimation [8,17]. If we can fabricate the device with a diameter less than 10 pm, a GaN-based VCSEL with sub-milliampere threshold currents can be expected. 

The equations of motion describing the transverse optic phonon and electromagnetic modes (modeled as oscillators with charged masses, whose displacements lie along the x direction and whose wavevectors lie mainly along the y direction in the yz plane), their coupling, and their responses... 

The vibration spectruin of GaAs, calculated by using the C, and C l values of Tabic 8-4 (TO = transverse optical LO = longitudinal optical LA = longitudinal acoustical TA = transverse acoustical). Experimental points arc from Dolling and Waugh (1965). 

We could have used particular frequencies instead of the elastic constants to determine the force constants in the model that alternative is of some interest, We have used, for reasons to be discussed, the measured transverse optical frequency at /( = 0 and the transverse acoustical mode at k — Inja to obtain alternate values of C,) and C, which are listed in Table 9-1. The differences from the values given... 

Transverse acoustical mode, /< = In/a Transverse optical mode, /c = 0 0 C ... 

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