Detuning

Figure Al.6.4. FVH diagram, showing the eoneept of adiabatie following. The Bloeh veetor, f, preeesses m a narrow eone about the rotating frame torque veetor, i2. As the detuning. A, ehanges from negative to positive, the field veetor, J , beeomes inverted. If the ehange m j is adiabatie the Bloeh veetor follows the...

We will explore the effect of three parameters 2 -and < )> that is, the time delay between the pulses, the tuning or detuning of the carrier frequency from resonance with an excited-state vibrational transition and the relative phase of the two pulses. We follow closely the development of [22]. Using equation (Al.6.73). 

One of the most interesting features of the Raman spectmm is its dependence on tire incident light frequency, coj. When Wj is on resonance with the excited electronic state, the scattering process closely resembles a process of absorption followed by emission. However, as Uj is detuned from resonance there are no longer... 

Figure Al.6.15. Schematic diagram, showing the time-energy uncertainty principle operative in resonance Raman scattering. If the incident light is detuned from resonance by an amount Aco, the effective lifetime on the excited-state is i 1/Aco (adapted from [15]).

Equation (A 1.6.94) is called the KHD expression for the polarizability, a. Inspection of the denominators indicates that the first temi is the resonant temi and the second temi is tire non-resonant temi. Note the product of Franck-Condon factors in the numerator one corresponding to the amplitude for excitation and the other to the amplitude for emission. The KHD fonnula is sometimes called the siim-over-states fonnula, since fonnally it requires a sum over all intennediate states j, each intennediate state participating according to how far it is from resonance and the size of the matrix elements that coimect it to the states i. and The KHD fonnula is fiilly equivalent to the time domain fonnula, equation (Al.6.92). and can be derived from the latter in a straightforward way. However, the time domain fonnula can be much more convenient, particularly as one detunes from resonance, since one can exploit the fact that the effective dynamic becomes shorter and shorter as the detuning is increased. 

As already mentioned, electronically resonant, two-pulse impulsive Raman scattering (RISRS) has recently been perfonned on a number of dyes [124]. The main difference between resonant and nom-esonant ISRS is that the beats occur in the absorption of tlie probe rather than the spectral redistribution of the probe pulse energy [124]. These beats are out of phase with respect to the beats that occur in nonresonant ISRS (cosinelike rather tlian sinelike). RISRS has also been shown to have the phase of oscillation depend on the detuning from electronic resonance and it has been shown to be sensitive to the vibrational dynamics in both the ground and excited electronic states [122. 124]. 

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... 

Note that negative Acoj (red detuning) produces a force attracting the atom to the intensity maximum while positive (blue detuning) repels the atom away from the intensity maximum. The spontaneous force or cooling force can also be written in tenns of the saturation parameter and the spontaneous emission rate. 

Now if we consider die atom moving in die +z direction widi velocity and counteriiropagating to die light wave detuned from resonance by Acuj, die net detuning will be... 

This expression shows diat if die detuning Acuj is negative (i.e. red detuned from resonance), dieii die cooling force will oppose die motion and be proportional to die atomic velocity. The one-diniensional motion of die atom, subject to an opposing force proportional to its velocity, is described by a damped haniionic oscillator. The Doppler damping or friction coefficient is die proportionality factor. 

This expression shows tiiat T is a fimction of tire iaser detuning, and tire minimum temperature is obtained when 2 At tills detuning. 

We assume that tlie light field is detuned to tlie red of tire J —> J atomic resonance frequency. 

A. Since tire applied field is red detuned, all A have negative values. Now in order for tire cooling mechanism to be effective tire optical pumping time tp should be comparable to tire time required for tire atom with velocity v to travel from tire bottom to tire top of a potential hill,... 

Note that since A < 0, a p is a positive quantity. Note also tliat at far detunings equation (Cl.4.11) shows... 

Equation (Cl.4.35) yields two remarkable predictions first, tliat tire sub-Doppler friction coefficient can be a big number compared to since at far detuning Aj /T is a big number and second, tliat a p is independent of tire applied field intensity. This last result contrasts sharjDly witli tire Doppler friction coefficient which is proportional to field intensity up to saturation (see equation (C1.4.24). However, even tliough a p looks impressive, tire range of atomic velocities over which is can operate are restricted by tire condition tliat T lcv. The ratio of tire capture velocities for Doppler versus sub-Doppler cooling is tlierefore only uipi/uj 2 Figure Cl. 4.6 illustrates... 

The atom will therefore experience a net restoring force pushing it back to the origin. If the light beams are red detuned F, then the Doppler shift of the atomic motion will introduce a velocity-dependent tenn to the restoring force such that, for small displacements and velocities, the total restoring force can be expressed as the sum of a tenn linear in velocity and a tenn linear in displacement. 

Two colliding atoms approach on tire molecular ground-state potential. During tire molasses cycle witli tire optical fields detuned only about one line widtli to tire red of atomic resonance, tire initial excitation occurs at very long range, around a Condon point at 1800 a. A second Condon point at 1000 takes tire population to a 1 doubly excited potential tliat, at shorter intemuclear distance, joins adiabatically to a 3 potential, drought to be die... 

Figure Cl.5.2. Fluorescence excitation spectra (cps = counts per second) of pentacene in /i-teriDhenyl at 1.5 K. (A) Broad scan of the inhomogeneously broadened electronic origin. The spikes are repeatable features each due to a different single molecule. The laser detuning is relative to the line centre at 592.321 nm. (B) Expansion of a 2 GHz region of this scan showing several single molecules. (C) Low-power scan of a single molecule at 592.407 nm showing the lifetime-limited width of 7.8 MHz and a Lorentzian fit. Reprinted with pennission from Moemer [198]. Copyright 1994 American Association for the Advancement of Science.

Detuning a controller (e.g., using a smaller controller gain or a larger reset time) tends to reduce control loop interactions by sacrificing the performance for the detuned loops. This approach may be acceptable if some of the controlled variables are faster or less important than others. 

The use of a reactor in series with the ctipacitors w ill reduce the harmonic effects in a power network, as well as their effect on other circuits in the vicinity, such as a telecommunication network (see also Section 23.1 1 and Example 23.4). The choice of reactance should be such that it W ill provide the required detuning by resonating below the required harmonic, to provide a least impedance path for that harmonic and filter it out from the circuit. The basic idea of a filter circuit is to make it respond to the current of one frequency and reject all other frequency components. At power frequency, the circuit should act as a capacitive load and improve the p.f. of the system. For the fifth harmonic, for instance, it should resonate below X 50 Hz for a 50 Hz system, say at around 200-220 Hz, to avoid excessive charging voltages w hich may lead to... 

Unlike in the case of the gas-phase measurements, no tunneling has been detected in the IR spectra of the malonaldehyde molecule in the noble matrices at 15-30K [Firth et al. 1989], The lack of tunneling is caused by detuning of the potential as a result of weak antisymmetric coupling to the environment. 

Fig. 40. Flole-burning spectra of thioindigo in benzoic acid crystal at 1.35 K. The scanning laser frequency cu is measured with respect to the burning laser frequency cUb is detuning of the burning laser frequency relative to the center of absorption line.

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