Atomic systems Schrodinger equation

Other atoms with only a single electron (He+, Li2+, etc.) are known as hydrogen-like atoms. The Schrodinger equation for such a system is the same as that for the hydrogen atom... 

The atomic units system (au system) is a system of units meant to simplify the equations of molecular and atomic quantum mechanics. The units of the au system are combinations of the fundamental units of mass (mass of the electron), charge (charge of the electron), and of Planck s constant. By setting these three quantities to unity one gets simpler equations. Si in the usual SI system, Schrodinger equation takes the form ... 

The ab initio method begins by solving the Schrodinger equation for the orbitals of electrons around a molecule, using as little simplification and approximation as is practical. This exact method is available only for small molecules with few atoms. The Schrodinger equation for a system with only one nucleus and a single electron... 

A rigorous derivation of the form of the hybrid potentials treated in this chapter requires the construction an effective Hamiltonian, Her, for the system. This Hamiltonian can then be used as the Hamiltonian for the solution of the time-independent Schrodinger equation for the wavefunc-tion of the electrons on the QM atoms, P, and for the potential energy of the system, qm/mm- If R are the coordinates of the MM atoms, the Schrodinger equation (equation 1) becomes ... 

For systems containing heavy atoms, the Schrodinger equation becomes inadequate and the calculations must instead be based directly or indirectly on Dirac s relativistic equation [9], although in many cases, the relativistic corrections may be sufficiently well accounted for by effective potentials [10] or by low-order perturbation theory [11]. 

In the q-coordinate system, the vibrational normal coordinates, the SA atom-dimensional Schrodinger equation can be separated into SA atom one-dimensional Schrodinger equations, which are just in the form of a standard harmonic oscillator, with the solutions being Hermite polynomials in the q-coordinates. The eigenvectors of the F G matrix are the (mass-weighted) vibrational normal coordinates, and the eigenvalues ( are related to the vibrational frequencies as shown in eq. (16.42) (analogous to eq. (13.31)). 

Equation (3.85) T is a translation vector that maps each position into an equivalent ition in a neighbouring cell, r is a general positional vector and k is the wavevector ich characterises the wavefunction. k has components k, and ky in two dimensions and quivalent to the parameter k in the one-dimensional system. For the two-dimensional lare lattice the Schrodinger equation can be expressed in terms of separate wavefunctions ng the X- and y-directions. This results in various combinations of the atomic Is orbitals, ne of which are shown in Figure 3.13. These combinations have different energies. The /est-energy solution corresponds to (k =0, ky = 0) and is a straightforward linear... 

The Schrodinger equation is a nonreiativistic description of atoms and molecules. Strictly speaking, relativistic effects must be included in order to obtain completely accurate results for any ah initio calculation. In practice, relativistic effects are negligible for many systems, particularly those with light elements. It is necessary to include relativistic effects to correctly describe the behavior of very heavy elements. With increases in computer capability and algorithm efficiency, it will become easier to perform heavy atom calculations and thus an understanding of relativistic corrections is necessary. 

Some coordinate transformations are non-linear, like transforming Cartesian to polar coordinates, where the polar coordinates are given in terms of square root and trigonometric functions of the Cartesian coordinates. This for example allows the Schrodinger equation for the hydrogen atom to be solved. Other transformations are linear, i.e. the new coordinate axes are linear combinations of the old coordinates. Such transfonnations can be used for reducing a matrix representation of an operator to a diagonal form. In the new coordinate system, the many-dimensional operator can be written as a sum of one-dimensional operators. 

In the previous chapter we considered a rather simple solvent model, treating each solvent molecule as a Langevin-type dipole. Although this model represents the key solvent effects, it is important to examine more realistic models that include explicitly all the solvent atoms. In principle, we should adopt a model where both the solvent and the solute atoms are treated quantum mechanically. Such a model, however, is entirely impractical for studying large molecules in solution. Furthermore, we are interested here in the effect of the solvent on the solute potential surface and not in quantum mechanical effects of the pure solvent. Fortunately, the contributions to the Born-Oppenheimer potential surface that describe the solvent-solvent and solute-solvent interactions can be approximated by some type of analytical potential functions (rather than by the actual solution of the Schrodinger equation for the entire solute-solvent system). For example, the simplest way to describe the potential surface of a collection of water molecules is to represent it as a sum of two-body interactions (the interac-... 

Unfortunately, the Schrodinger equation can be solved exactly only for one-electron systems such as the hydrogen atom. If it could be solved exactly for... 

Quantum mechanical effects—tunneling and interference, resonances, and electronic nonadiabaticity— play important roles in many chemical reactions. Rigorous quantum dynamics studies, that is, numerically accurate solutions of either the time-independent or time-dependent Schrodinger equations, provide the most correct and detailed description of a chemical reaction. While hmited to relatively small numbers of atoms by the standards of ordinary chemistry, numerically accurate quantum dynamics provides not only detailed insight into the nature of specific reactions, but benchmark results on which to base more approximate approaches, such as transition state theory and quasiclassical trajectories, which can be applied to larger systems. 

In order to apply quantum-mechanical theory to the hydrogen atom, we first need to find the appropriate Hamiltonian operator and Schrodinger equation. As preparation for establishing the Hamiltonian operator, we consider a classical system of two interacting point particles with masses mi and m2 and instantaneous positions ri and V2 as shown in Figure 6.1. In terms of their cartesian components, these position vectors are... 

In Chapters 4, 5, and 6 the Schrodinger equation is applied to three systems the harmonie oseillator, the orbital angular momentum, and the hydrogen atom, respectively. The ladder operator technique is used in each case to solve the resulting differential equation. We present here the solutions of these differential equations using the Frobenius method. 

This, at first glance innocuous-looking functional FHK[p] is the holy grail of density functional theory. If it were known exactly we would have solved the Schrodinger equation, not approximately, but exactly. And, since it is a universal functional completely independent of the system at hand, it applies equally well to the hydrogen atom as to gigantic molecules such as, say, DNA FHK[p] contains the functional for the kinetic energy T[p] and that for the electron-electron interaction, Eee[p], The explicit form of both these functionals lies unfortunately completely in the dark. However, from the latter we can extract at least the classical Coulomb part J[p], since that is already well known (recall Section 2.3),... 

Most semi-empirical models are based on the fundamental equations of Hartree-Fock theory. In the following section, we develop these equations for a molecular system composed of A nuclei and N electrons in the stationary state. Assuming that the atomic nuclei are fixed in space (the Born-Oppenheimer approximation), the electronic wavefunction obeys the time-independent Schrodinger equation ... 

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