Amplitude functions, definitions

Next, having these examples in hand, one tries to check them by deriving by an appropriate generating functional (3.56) working with the connected function definition (3.58). At this moment one uses the previously reasoned dual nature of fluctuation paths, as free-harmonic motion — see Eq. (3.55), to reconsider the free imaginary time amplitude (3.51) for free + harmonic fluctuation contribution (Putz, 2009b)... 

The size-dependence of the intensity of single shake-up lines is dictated by the squares of the coupling amplitudes between the Ih and 2h-lp manifolds, which by definition (22) scale like bielectron integrals. Upon a development based on Bloch functions ((t>n(k)), a LCAO expansion over atomic primitives (y) and lattice summations over cell indices (p), these, in the limit of a stereoregular polymer chain consisting of a large number (Nq) of cells of length ao, take the form (31) ... 

I function which carries maximum information about that system. Definition of the -function itself, depends on a probability aggregate or quantum-mechanical ensemble. The mechanical state of the systems of this ensemble cannot be defined more precisely than by stating the -function. It follows that the same -function and hence the same mechanical state must be assumed for all systems of the quantum-mechanical ensemble. A second major difference between classical and quantum states is that the -function that describes the quantum-mechanical ensemble is not a probability density, but a probability amplitude. By comparison the probability density for coordinates q is... 

Here Q2 is the average value of the square of the oscillation amplitude, K(r) is the correlation function of the random process, and Vf are definite functions of the 4/electron coordinates (40). 

The amplitude of electron tunneling transfer with simultaneous change of the vibrations in the case of the non-adiabatic asymptotics (56) may be found, if to substitute the expression (56) instead of F ) to the definition (9) and the acceptor wave function in the matrix element (9) should be its total expression... 

The expressions eqs. (1.197), (1.199), (1.200), (1.201) are completely general. From them it is clear that the reduced density matrices are much more economical tools for representing the electronic structure than the wave functions. The two-electron density (more demanding quantity of the two) depends only on two pairs of electronic variables (either continuous or discrete) instead of N electronic variables required by the wave function representation. The one-electron density is even simpler since it depends only on one pair of such coordinates. That means that in the density matrix representation only about (2M)4 numbers are necessary to describe the system (in fact - less due to antisymmetry), whereas the description in terms of the wave function requires, as we know n 2m-n) numbers (FCI expansion amplitudes). However, the density matrices are rarely used directly in quantum chemistry procedures. The reason is the serious problem which appears when one is trying to construct the adequate representation for the left hand sides of the above definitions without addressing any wave functions in the right hand sides. This is known as the (V-representability problem, unsolved until now [51] for the two-electron density matrices. The second is that the symmetry conditions for the electronic states are much easier formulated and controlled in terms of the wave functions (Density matrices are the entities of the second power with respect to the wave functions so their symmetries are described by the second tensor powers of those of the wave functions). 

The electron density in a crystal precisely fits the definition of a periodic function in which an exact repeat occurs at regularly fixed intervals in any direction (the crystal lattice translations). Therefore the electron density in a crystal with a periodicity d can be described by a Fourier synthesis in which each component cosine wave (which we will call an electron-density wave) has a periodicity (i.e., wavelength) d/n, and the amplitude of the rath-order Bragg reflection. 

Fourier synthesis The summation of sine and cosine waves to give a periodic function an example is the computation of an electron density map from waves of known phase, frequency, and amplitude F (. See also the definition in Chapter 1. 

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