Displaced potential surface model

Taking the explicit expression (3.75) for the single-promoting mode generating function, the expression for the nonradiative decay rate in the simple displaced potential surface model can be written as... 

Apart from the heat bath mode, the harmonic potential surface model has been used for the molecular vibrations. It is possible to include the generalized harmonic potential surfaces, i.e., displaced-distorted-rotated surfaces. In this case, the mode coupling can be treated within this model. Beyond the generalized harmonic potential surface model, there is no systematic approach in constructing the generalized (multi-mode coupled) master equation that can be numerically solved. The first step to attack this problem would start with anharmonicity corrections to the harmonic potential surface model. Since anharmonicity has been recognized as an important mechanism in the vibrational dynamics in the electronically excited states, urgent realization of this work is needed. 

Because we are concerned only with the analysis of the absorption spectra of P band and B band, we consider the excitonic interactions among P, BL, and BM shown in Fig. 8. Here (oti, ot2,0C3,014) represent the diagonal matrix elements, while (p, (314, P23, P34) represent the off-diagonal matrix elements [67]. As shown in Introduction, a main feature of the P band is that its absorption maximum shows a pronounced temperature shift [42,52], According to the displaced oscillator model, the absorption maximum is independent of T. Although the distortion effect of potential surfaces will introduce some temperature shift, the effect cannot be as large as that shown in Fig. 2. 

The model triple-well potential surface is defined by the sum of a sixth-order polynomial in the displacement of y-coordinate, a Morse potential in the orthogonal x-coordinate, and a potential describing the coupling between x and y ... 

Such a potential energy function gives rise to the famihar parabolic curve (Figure 22) where the curvature of the function is related to the force constant. The success of this simple harmonic model in treating surface atom vibrations lies in the relatively small displacement of surface atoms during a period of vibration. For some crystal properties, such as thermal expansion at elevated temperature, anharmoitic contributions to the potential must be included for an accurate description. 

In the second part of this work, we addressed the problem of how to use the above described effects of a space-dependent interaction to steer molecular transition. We proposed a model that allows us to induce a space-dependent coupling between two molecular potentials via a steady-state coupling to a third potential surface. By changing the frequency and intensity of the steady state laser, we can shape the space-dependence of the coupling. We illustrated the method with an example of three coupled harmonic oscillators and showed how displacement and width of the excited wave packet can be controlled. 

The sessile drop method has several drawbacks. Several days elapse between each displacement, and total test times exceeding one month are not uncommon. It can be difficult to determine that the interface has actually advanced across the face of the crystal. Displacement frequency and distance are variable and dependent upon the operator. Tests are conducted on pure mineral surfaces, usually quartz, which does not adequately model the heterogeneous rock surfaces in reservoirs. There is a need for a simple technique that gives reproducible data and can be used to characterize various mineral surfaces. The dynamic Wilhelmy plate technique has such a potential. This paper discusses the dynamic Wilhelmy plate apparatus used to study wetting properties of liquid/liquid/solid systems important to the oil industry. 

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