Spin quantum number

The phrase spin quantum number refers to quantized spin angular momentum. The symbol s is used for the spin quantum number, and m_s is described as the spin magnetic quantum number[3] or as the z-component of spin s_z.[4]

Both the total spin and the z-component of spin are quantized, leading to two quantum numbers spin and spin magnet quantum numbers.[5] The (total) spin quantum number has only one value for every elementary particle. Some introductory chemistry textbooks describe m_s as the spin quantum number,[6][7] and s is not mentioned since its value 1/2 is a fixed property of the electron; some even use the variable s in place of m_s.[5]

The two spin quantum numbers ${\displaystyle s}$ and ${\displaystyle m_{s}}$ are the spin angular momentum analogs of the two orbital angular momentum quantum numbers ${\displaystyle l}$ and ${\displaystyle m_{l}}$.[8]^: 152

Spin quantum numbers apply also to systems of coupled spins, such as atoms that may contain more than one electron. Capitalized symbols are used: S for the total electronic spin, and m_S or M_S for the z-axis component. A pair of electrons in a spin singlet state has S = 0, and a pair in the triplet state has S = 1, with m_S = −1, 0, or +1. Nuclear-spin quantum numbers are conventionally written I for spin, and m_I or M_I for the z-axis component.

The name "spin" comes from a geometrical spinning of the electron about an axis, as proposed by Uhlenbeck and Goudsmit. However, this simplistic picture was quickly realized to be physically unrealistic, because it would require the electrons to rotate faster than the speed of light.[9] It was therefore replaced by a more abstract quantum-mechanical description.

During the period between 1916 and 1925, much progress was being made concerning the arrangement of electrons in the periodic table. In order to explain the Zeeman effect in the Bohr atom, Sommerfeld proposed that electrons would be based on three 'quantum numbers', n, k, and m, that described the size of the orbit, the shape of the orbit, and the direction in which the orbit was pointing.[10] Irving Langmuir had explained in his 1919 paper regarding electrons in their shells, "Rydberg has pointed out that these numbers are obtained from the series ${\displaystyle N=2(1+2^{2}+2^{2}+3^{2}+3^{2}+4^{2})}$. The factor two suggests a fundamental two-fold symmetry for all stable atoms."[11] This ${\displaystyle 2n^{2}}$ configuration was adopted by Edmund Stoner, in October 1924 in his paper 'The Distribution of Electrons Among Atomic Levels' published in the Philosophical Magazine.

The qualitative success of the Sommerfeld quantum number scheme failed to explain the Zeeman effect in weak magnetic field strengths, the anomalous Zeeman effect. In December 1924, Wolfgang Pauli showed that the core electron angular momentum was not related to the effect as had previously been assumed.[12]^: 563 Rather he proposed that only the outer "light" electrons determined the angular momentum and he hypothesized that this required a fourth quantum number with a two-valuedness.[13] This fourth quantum number became the spin magnetic quantum number.

A spin- 1 /2 particle is characterized by an angular momentum quantum number for spin s =  1 /2. In solutions of the Schrödinger-Pauli equation, angular momentum is quantized according to this number, so that magnitude of the spin angular momentum is

The hydrogen spectrum fine structure is observed as a doublet corresponding to two possibilities for the z-component of the angular momentum, where for any given direction z:

whose solution has only two possible z-components for the electron. In the electron, the two different spin orientations are sometimes called "spin-up" or "spin-down".

The spin property of an electron would give rise to magnetic moment, which was a requisite for the fourth quantum number.

The magnetic moment vector of an electron spin is given by:

where ${\displaystyle -e}$ is the electron charge, ${\displaystyle m}$ is the electron mass, and ${\displaystyle g_{\text{s}}}$ is the electron spin g-factor, which is approximately 2.0023. Its z-axis projection is given by the spin magnetic quantum number ${\displaystyle m_{\text{s}}}$ according to:

where ${\displaystyle \ \mu _{\mathsf {B}}\ }$ is the Bohr magneton.

When atoms have even numbers of electrons the spin of each electron in each orbital has opposing orientation to that of its immediate neighbor(s). However, many atoms have an odd number of electrons or an arrangement of electrons in which there is an unequal number of "spin-up" and "spin-down" orientations. These atoms or electrons are said to have unpaired spins that are detected in electron spin resonance.

Atomic nuclei also have spins. The nuclear spin I is a fixed property of each nucleus and may be either an integer or a half-integer. The component m_I of nuclear spin parallel to the z–axis can have (2I + 1) values I, I–1, ..., –I. For example, a ¹⁴N nucleus has I = 1, so that there are 3 possible orientations relative to the z–axis, corresponding to states m_I = +1, 0 and −1.[14]

The spins I of different nuclei are interpreted using the nuclear shell model. Even-even nuclei with even numbers of both protons and neutrons, such as ¹²C and ¹⁶O, have spin zero. Odd mass number nuclei have half-integer spins, such as 3/ 2  for ⁷Li,  1 /2 for ¹³C and 5/ 2  for ¹⁷O, usually corresponding to the angular momentum of the last nucleon added. Odd-odd nuclei with odd numbers of both protons and neutrons have integer spins, such as 3 for ¹⁰B, and 1 for ¹⁴N.[15] Values of nuclear spin for a given isotope are found in the lists of isotopes for each element. (See isotopes of oxygen, isotopes of aluminium, etc. etc.)

When lines of the hydrogen spectrum are examined at very high resolution, they are found to be closely spaced doublets. This splitting is called fine structure, and was one of the first experimental evidences for electron spin. The direct observation of the electron's intrinsic angular momentum was achieved in the Stern–Gerlach experiment.

For a solution of either the nonrelativistic Pauli equation or the relativistic Dirac equation, the quantized angular momentum (see angular momentum quantum number) can be written as:

where

• ${\displaystyle \mathbf {s} }$ is the quantized spin vector or spinor
• ${\displaystyle \Vert \mathbf {s} \Vert }$ is the norm of the spin vector
• s is the spin quantum number associated with the spin angular momentum
• ${\displaystyle \hbar }$ is the reduced Planck constant.

Given an arbitrary direction z (usually determined by an external magnetic field) the spin z-projection is given by

${\displaystyle s_{z}=m_{s}\,\hbar }$

where m_s is the magnetic spin quantum number, ranging from −s to +s in steps of one. This generates 2 s + 1 different values of m_s.

The allowed values for s are non-negative integers or half-integers. Fermions have half-integer values, including the electron, proton and neutron which all have s = ++ 1 /2 . Bosons such as the photon and all mesons) have integer spin values.

The algebraic theory of spin is a carbon copy of the angular momentum in quantum mechanics theory.[16] First of all, spin satisfies the fundamental commutation relation:

where ${\displaystyle \ \epsilon _{ijk}\ }$ is the (antisymmetric) Levi-Civita symbol. This means that it is impossible to know two coordinates of the spin at the same time because of the restriction of the uncertainty principle.

Next, the eigenvectors of ${\displaystyle \ S^{2}\ }$ and ${\displaystyle \ S_{z}\ }$ satisfy:

where ${\displaystyle \ S_{\pm }=S_{x}\pm iS_{y}\ }$ are the ladder (or "raising" and "lowering") operators.

In 1928, Paul Dirac developed a relativistic wave equation, now termed the Dirac equation, which predicted the spin magnetic moment correctly, and at the same time treated the electron as a point-like particle. Solving the Dirac equation for the energy levels of an electron in the hydrogen atom, all four quantum numbers including s occurred naturally and agreed well with experiment.

For some atoms the spins of several unpaired electrons (s₁, s₂, ...) are coupled to form a total spin quantum number S.[17][18] This occurs especially in light atoms (or in molecules formed only of light atoms) when spin–orbit coupling is weak compared to the coupling between spins or the coupling between orbital angular momenta, a situation known as L S coupling because L and S are constants of motion. Here L is the total orbital angular momentum quantum number.[18]

For atoms with a well-defined S, the multiplicity of a state is defined as 2S + 1. This is equal to the number of different possible values of the total (orbital plus spin) angular momentum J for a given (L, S) combination, provided that S ≤ L (the typical case). For example, if S = 1, there are three states which form a triplet. The eigenvalues of S_z for these three states are +1ħ, 0, and −1ħ.[17] The term symbol of an atomic state indicates its values of L, S, and J.

As examples, the ground states of both the oxygen atom and the dioxygen molecule have two unpaired electrons and are therefore triplet states. The atomic state is described by the term symbol ³P, and the molecular state by the term symbol ³Σ⁻
_g.

• Total angular momentum quantum number
• Rotational spectroscopy
• Basic quantum mechanics

• Weiss, Michael (2001). "Full treatment of spin – including origins, evolution of spin theory, and details of the spin equations". Department of Mathematics. UC Riverside.