Electron orbital

In quantum chemistry, an electron orbital (or more often just orbital) is a synonym for a one-electron function. Here "orbital" is used as a noun. In quantum mechanics, the adjective orbital is often used as a synonym of "spatial" (as in orbital angular momentum), in contrast to spin (as in spin angular momentum).

The majority of quantum chemical methods expect that an orbital has a finite norm, i.e., that the orbital is normalizable (quadratically integrable), and hence this requirement is often added to the definition.

Outside of quantum chemistry an orbital is often seen as a wave function. This point of view is a narrowing of the quantum chemical definition, but not contradictory to it, provided a wave function is seen in this context as a solution of an (effective) one-electron Schrödinger equation. Indeed, in the past quantum chemists, too, distinguished one-electron functions from orbitals, the former being fairly arbitrary and the latter being solutions of certain one-electron Schrödinger equations. This distinction faded away from quantum chemistry, leading to the present definition as "normalizable one-electron function."

Usually on distinguishes two kinds of orbitals: atomic orbitals and molecular orbitals. Atomic orbitals are expressed with respect to one Cartesian system of axes centered on a single atom. Molecular orbitals (MOs) are "spread out" over a molecule. Usually this is a consequence of an MO being a linear combination (weighted sum) of atomic orbitals centered on different atoms.

Definitions of orbitals

Several kinds of orbitals can be distinguished.

Atomic orbital

See the article atomic orbital

Molecular orbital

The second kind of orbital is the molecular orbital (MO). Such a one-electron function depends on several vectors: r_A1, r_B1, r_C1, ... where A, B, C, ... are different points in space (usually nuclear positions). The oldest example of an MO (without use of the name MO yet) is in the work of Burrau (1927) on the single-electron ion H₂⁺. Burrau applied spheroidal coordinates (a bipolar coordinate system) to describe the wave functions of the electron of H₂⁺.

Lennard-Jones introduced the following linear combination of atomic orbitals (LCAO) way of writing an MO φ:

$\phi (\mathbf {r} _{1})=\sum _{A=1}^{N_{\mathrm {nuc} }}\sum _{i=1}^{n_{A}}c_{Ai}\chi _{i}(\mathbf {r} _{A1}),\qquad c_{Ai}\in \mathbb {C} ,$

where A runs over N_nuc different points in space (usually A runs over all the nuclei of a molecule, hence the name molecular orbital), and i runs over the n_A different AOs centered at A. The complex coefficients c _Ai can be calculated by any of the existing effective-one-electron quantum chemical methods. Examples of such methods are the Hückel method and the Hartree-Fock method.

Spinorbitals

The AOs and MOs defined so far depend only on the spatial coordinate vector r_A1 of electron 1. In addition, an electron has a spin coordinate μ, which can have two values: spin-up or spin-down. A complete set of functions of μ consists of two functions only, traditionally these are denoted by α(μ) and β(μ). These functions are eigenfunctions of the z-component s_z of the spin angular momentum operator with eigenvalues ±½.

Spin atomic orbital

The most general spin atomic orbital of electron 1 is of the form

$\chi _{i}^{+}(\mathbf {r} _{A1})\alpha (\mu _{1})+\chi _{i}^{-}(\mathbf {r} _{A1})\beta (\mu _{1})$

which in general is not an eigenfunction of s_z. More common is the use of either

$\chi _{i}(\mathbf {r} _{A1})\alpha (\mu _{1})\quad {\hbox{or}}\quad \chi _{i}(\mathbf {r} _{A1})\beta (\mu _{1}),$

which are eigenfunctions of s_z. Since it is rare that different AOs are used for spin-up and spin-down electrons, we dropped the superscripts + and −.

Spin molecular orbital

A spin molecular orbital is usually either

$\phi ^{+}(\mathbf {r} _{1})\alpha (\mu _{1})\quad {\hbox{or}}\quad \phi ^{-}(\mathbf {r} _{1})\beta (\mu _{1}).$

Here the superscripts + and − might be necessary, because some quantum chemical methods distinguish the spatial wave functions of electrons with different spins. These are the so-called different orbitals for different spins (DODS) (or spin-unrestricted) methods. However, many quantum chemical methods apply the spin-restriction:

$\phi ^{+}(\mathbf {r} _{1})=\phi ^{-}(\mathbf {r} _{1})=\phi (\mathbf {r} _{1}).$

Chemists express this spin-restriction by stating that two electrons [electron 1 with spin up (α), and electron 2 with spin down (β)] are placed in the same spatial orbital φ. This means that the total N-electron wave function contains a factor of the type φ(r₁)α(μ₁)φ(r₂)β(μ₂).

History of term

Orbit is an old noun introduced by Johannes Kepler in 1609 to describe the paths of the earth and the planets. The adjective "orbital" had (and still has) the meaning "relating to an orbit". When Ernest Rutherford in 1911 postulated his planetary model of the atom (the nucleus as the Sun, and the electrons as the planets) it was natural to call the paths of the electrons "orbits". Bohr, although he was the first to recognize (1913) orbits as stationary states of the hydrogen atom, used the word as well. However, after Schrödinger (1926) had solved his wave equation for the hydrogen atom (see this article for details), it became clear that the electronic "orbits" did not resemble planetary orbits at all. The wave functions of the hydrogen electron are time-independent and smeared out. They are more like unmoving clouds than like planetary orbits. As a matter of fact, the angular parts of the hydrogen wave functions are spherical harmonics and hence they have the same appearance as spherical harmonics. (See spherical harmonics for a few graphical illustrations).

In the 1920s electron spin was discovered, whereupon the adjective "orbital" started to be used in the meaning of "non-spin", that is, as a synonym of "spatial". In scientific papers of around 1930 one finds discussions about "orbital degeneracy", meaning that the spatial (non-spin) parts of several one-electron wave functions have the same energy. Also the terms orbital- and spin-angular momentum date form these days.

In 1932 Robert S. Mulliken coined the noun "orbital". He wrote: From here on, one-electron orbital wave functions will be referred to for brevity as orbitals. Then he went on to distinguish atomic and molecular orbitals.

Later the somewhat unfortunate term "spinorbital" was introduced for the product functions φ(r₁)α(μ₁) and φ(r₁)β(μ₁) in which φ(r₁) has the tautological name "spatial orbital" and α(μ₁) and β(μ₁) are called "one-electron spin functions". The term "spinorbital" is unfortunate because it merges in one word the concepts of spin and orbital, which were distinguished carefully by early writers on quantum mechanics. For instance, one of the pioneers of theoretical chemistry, Walter Heitler, juxtaposes two-electron spin functions and two-electron orbital functions. In the phrase "two-electron orbital function", Heitler uses orbital as an adjective synonymous with spatial (non-spin). Note, parenthetically, that Heitler does not refer to a "two-electron orbital", (there is no such thing as a two-electron orbital!). However, an inexperienced reader may easily and erroneously interpret the term "two-electron orbital function" as "two-electron orbital".

Applications

Before the advent of electronic computers, orbitals (molecular as well as atomic) were used extensively in qualitative arguments explaining several properties of atoms and molecules. Orbitals still play this role in introductory texts and also in organic chemistry, where orbitals serve in the explanation of some reaction mechanisms, for instance in the Woodward-Hoffmann rules. In modern computational quantum chemistry the role of atomic orbitals is different; they serve as a convenient expansion basis, comparable to powers of x in a Taylor expansion of a function f(x), or sines and cosines in a Fourier series. Below, the role of molecular orbitals in qualitative theories will be discussed.

Atomic orbitals

Originally AOs were defined as approximate solutions of atomic Schrödinger equations, see the section solution of the atomic Schrödinger equation in atomic orbital for more on this.

Recently, AOs are simply seen as convenient basis functions for quantum chemical computations. See the section AO basis sets in the article atomic orbital for more on the use of atomic orbitals in quantum chemistry. See Slater orbital for the explicit analytic form of orbitals and see Gauss type orbitals for a discussion of the type of AOs that are most frequently used in computations.

Computation of molecular orbitals

To date the most widely applied method for computing molecular orbitals is a Hartree-Fock method in which the MO is expanded in atomic orbitals. Since the term "Hartree-Fock" (HF) is in quantum chemistry almost synonymous with the term "self-consistent field" (SCF), such an MO is often referred to as an SCF-LCAO-MO.

See the section computation of molecular orbitals in molecular orbital for a simple example of a case where an MO is almost completely determined by symmetry. In more complicated cases it is necessary to solve the Hartree-Fock-Roothaan equations, which have the form of a generalized eigenvalue problem. The dimension of this problem is equal to the number of atomic orbitals included in the AO basis (see AO basis sets in atomic orbital for more details).