Wave function

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Comparison of classical and quantum harmonic oscillator conceptions for a single spinless particle. The two processes differ greatly. The classical process (A–B) is represented as the motion of a particle along a trajectory. The quantum process (C–H) has no such trajectory. Rather, it is represented as a wave; here, the vertical axis shows the real part (blue) and imaginary part (red) of the wave function. Panels (C–F) show four different standing-wave solutions of the Schrödinger equation. Panels (G–H) further show two different wave functions that are solutions of the Schrödinger equation but not standing waves.

In quantum physics, a wave function is a mathematical description of the quantum state of an isolated quantum system. The wave function is a complex-valued probability amplitude, and the probabilities for the possible results of measurements made on the system can be derived from it. The most common symbols for a wave function are the Greek letters ψ and Ψ (lower-case and capital psi, respectively).

The wave function is a function of the degrees of freedom corresponding to some maximal set of commuting observables. Once such a representation is chosen, the wave function can be derived from the quantum state.

For a given system, the choice of which commuting degrees of freedom to use is not unique, and correspondingly the domain of the wave function is also not unique. For instance, it may be taken to be a function of all the position coordinates of the particles over position space, or the momenta of all the particles over momentum space; the two are related by a Fourier transform. Some particles, like electrons and photons, have nonzero spin, and the wave function for such particles includes spin as an intrinsic, discrete degree of freedom; other discrete variables can also be included, such as isospin. When a system has internal degrees of freedom, the wave function at each point in the continuous degrees of freedom (e.g., a point in space) assigns a complex number for each possible value of the discrete degrees of freedom (e.g., z-component of spin) – these values are often displayed in a column matrix (e.g., a 2 × 1 column vector for a non-relativistic electron with spin 1⁄2).

According to the superposition principle of quantum mechanics, wave functions can be added together and multiplied by complex numbers to form new wave functions and form a Hilbert space. The inner product between two wave functions is a measure of the overlap between the corresponding physical states and is used in the foundational probabilistic interpretation of quantum mechanics, the Born rule, relating transition probabilities to inner products. The Schrödinger equation determines how wave functions evolve over time, and a wave function behaves qualitatively like other waves, such as water waves or waves on a string, because the Schrödinger equation is mathematically a type of wave equation. This explains the name "wave function", and gives rise to wave–particle duality. However, the wave function in quantum mechanics describes a kind of physical phenomenon, still open to different interpretations, which fundamentally differs from that of classic mechanical waves.

In Born's statistical interpretation in non-relativistic quantum mechanics, the squared modulus of the wave function, |ψ|², is a real number interpreted as the probability density of measuring a particle as being at a given place – or having a given momentum – at a given time, and possibly having definite values for discrete degrees of freedom. The integral of this quantity, over all the system's degrees of freedom, must be 1 in accordance with the probability interpretation. This general requirement that a wave function must satisfy is called the normalization condition. Since the wave function is complex-valued, only its relative phase and relative magnitude can be measured—its value does not, in isolation, tell anything about the magnitudes or directions of measurable observables; one has to apply quantum operators, whose eigenvalues correspond to sets of possible results of measurements, to the wave function ψ and calculate the statistical distributions for measurable quantities.

Historical background

In 1900, Max Planck postulated the proportionality between the frequency ${\displaystyle f}$ of a photon and its energy ${\displaystyle E}$, ${\displaystyle E=hf}$, and in 1916 the corresponding relation between a photon's momentum ${\displaystyle p}$ and wavelength ${\displaystyle \lambda }$, ${\displaystyle \lambda =\frac{h}{p}}$, where ${\displaystyle h}$ is the Planck constant. In 1923, De Broglie was the first to suggest that the relation ${\displaystyle \lambda =\frac{h}{p}}$, now called the De Broglie relation, holds for massive particles, the chief clue being Lorentz invariance, and this can be viewed as the starting point for the modern development of quantum mechanics. The equations represent wave–particle duality for both massless and massive particles.

In the 1920s and 1930s, quantum mechanics was developed using calculus and linear algebra. Those who used the techniques of calculus included Louis de Broglie, Erwin Schrödinger, and others, developing "wave mechanics". Those who applied the methods of linear algebra included Werner Heisenberg, Max Born, and others, developing "matrix mechanics". Schrödinger subsequently showed that the two approaches were equivalent.

In 1926, Schrödinger published the famous wave equation now named after him, the Schrödinger equation. This equation was based on classical conservation of energy using quantum operators and the de Broglie relations and the solutions of the equation are the wave functions for the quantum system. However, no one was clear on how to interpret it. At first, Schrödinger and others thought that wave functions represent particles that are spread out with most of the particle being where the wave function is large. This was shown to be incompatible with the elastic scattering of a wave packet (representing a particle) off a target; it spreads out in all directions. While a scattered particle may scatter in any direction, it does not break up and take off in all directions. In 1926, Born provided the perspective of probability amplitude. This relates calculations of quantum mechanics directly to probabilistic experimental observations. It is accepted as part of the Copenhagen interpretation of quantum mechanics. There are many other interpretations of quantum mechanics. In 1927, Hartree and Fock made the first step in an attempt to solve the N-body wave function, and developed the self-consistency cycle: an iterative algorithm to approximate the solution. Now it is also known as the Hartree–Fock method. The Slater determinant and permanent (of a matrix) was part of the method, provided by John C. Slater.

Schrödinger did encounter an equation for the wave function that satisfied relativistic energy conservation before he published the non-relativistic one, but discarded it as it predicted negative probabilities and negative energies. In 1927, Klein, Gordon and Fock also found it, but incorporated the electromagnetic interaction and proved that it was Lorentz invariant. De Broglie also arrived at the same equation in 1928. This relativistic wave equation is now most commonly known as the Klein–Gordon equation.

In 1927, Pauli phenomenologically found a non-relativistic equation to describe spin-1/2 particles in electromagnetic fields, now called the Pauli equation. Pauli found the wave function was not described by a single complex function of space and time, but needed two complex numbers, which respectively correspond to the spin +1/2 and −1/2 states of the fermion. Soon after in 1928, Dirac found an equation from the first successful unification of special relativity and quantum mechanics applied to the electron, now called the Dirac equation. In this, the wave function is a spinor represented by four complex-valued components: two for the electron and two for the electron's antiparticle, the positron. In the non-relativistic limit, the Dirac wave function resembles the Pauli wave function for the electron. Later, other relativistic wave equations were found.

Wave functions and wave equations in modern theories

All these wave equations are of enduring importance. The Schrödinger equation and the Pauli equation are under many circumstances excellent approximations of the relativistic variants. They are considerably easier to solve in practical problems than the relativistic counterparts.

The Klein–Gordon equation and the Dirac equation, while being relativistic, do not represent full reconciliation of quantum mechanics and special relativity. The branch of quantum mechanics where these equations are studied the same way as the Schrödinger equation, often called relativistic quantum mechanics, while very successful, has its limitations (see e.g. Lamb shift) and conceptual problems (see e.g. Dirac sea).

Relativity makes it inevitable that the number of particles in a system is not constant. For full reconciliation, quantum field theory is needed. In this theory, the wave equations and the wave functions have their place, but in a somewhat different guise. The main objects of interest are not the wave functions, but rather operators, so called field operators (or just fields where "operator" is understood) on the Hilbert space of states (to be described next section). It turns out that the original relativistic wave equations and their solutions are still needed to build the Hilbert space. Moreover, the free fields operators, i.e. when interactions are assumed not to exist, turn out to (formally) satisfy the same equation as do the fields (wave functions) in many cases.

Thus the Klein–Gordon equation (spin 0) and the Dirac equation (spin 1⁄2) in this guise remain in the theory. Higher spin analogues include the Proca equation (spin 1), Rarita–Schwinger equation (spin 3⁄2), and, more generally, the Bargmann–Wigner equations. For massless free fields two examples are the free field Maxwell equation (spin 1) and the free field Einstein equation (spin 2) for the field operators. All of them are essentially a direct consequence of the requirement of Lorentz invariance. Their solutions must transform under Lorentz transformation in a prescribed way, i.e. under a particular representation of the Lorentz group and that together with few other reasonable demands, e.g. the cluster decomposition property, with implications for causality is enough to fix the equations.

This applies to free field equations; interactions are not included. If a Lagrangian density (including interactions) is available, then the Lagrangian formalism will yield an equation of motion at the classical level. This equation may be very complex and not amenable to solution. Any solution would refer to a fixed number of particles and would not account for the term "interaction" as referred to in these theories, which involves the creation and annihilation of particles and not external potentials as in ordinary "first quantized" quantum theory.

In string theory, the situation remains analogous. For instance, a wave function in momentum space has the role of Fourier expansion coefficient in a general state of a particle (string) with momentum that is not sharply defined.

Definition (one spinless particle in one dimension)

Standing waves for a particle in a box, examples of stationary states.

 

Travelling waves of a free particle.

 

The real parts of position wave function Ψ(x) and momentum wave function Φ(p), and corresponding probability densities |Ψ(x)|² and |Φ(p)|², for one spin-0 particle in one x or p dimension. The colour opacity of the particles corresponds to the probability density (not the wave function) of finding the particle at position x or momentum p.

For now, consider the simple case of a non-relativistic single particle, without spin, in one spatial dimension. More general cases are discussed below.

Position-space wave functions

The state of such a particle is completely described by its wave function,

$${\displaystyle \mathrm{\Psi }(x,t),}$$

where x is position and t is time. This is a complex-valued function of two real variables x and t.

For one spinless particle in one dimension, if the wave function is interpreted as a probability amplitude, the square modulus of the wave function, the positive real number

$${\displaystyle {\left|\mathrm{\Psi }(x,t)\right|}^2={\mathrm{\Psi }}^{\ast }(x,t)\mathrm{\Psi }(x,t)=p(x,t),}$$

is interpreted as the probability density that the particle is at x. The asterisk indicates the complex conjugate. If the particle's position is measured, its location cannot be determined from the wave function, but is described by a probability distribution.

Normalization condition

The probability that its position x will be in the interval a ≤ x ≤ b is the integral of the density over this interval:

$${\displaystyle P_{a\le x\le b}(t)={\int }_a^b|\mathrm{\Psi }(x,t){|}^{2}dx}$$

where t is the time at which the particle was measured. This leads to the normalization condition:

$${\displaystyle {\int }_{-\mathrm{\infty }}^{\mathrm{\infty }}|\mathrm{\Psi }(x,t){|}^{2}dx=1,}$$

because if the particle is measured, there is 100% probability that it will be somewhere.

For a given system, the set of all possible normalizable wave functions (at any given time) forms an abstract mathematical vector space, meaning that it is possible to add together different wave functions, and multiply wave functions by complex numbers (see vector space for details). Technically, because of the normalization condition, wave functions form a projective space rather than an ordinary vector space. This vector space is infinite-dimensional, because there is no finite set of functions which can be added together in various combinations to create every possible function. Also, it is a Hilbert space, because the inner product of two wave functions Ψ₁ and Ψ₂ can be defined as the complex number (at time t)

$${\displaystyle ({\mathrm{\Psi }}_1,{\mathrm{\Psi }}_2)={\int }_{-\mathrm{\infty }}^{\mathrm{\infty }}{\mathrm{\Psi }}_1^{\ast }(x,t){\mathrm{\Psi }}_2(x,t)dx.}$$

More details are given below. Although the inner product of two wave functions is a complex number, the inner product of a wave function Ψ with itself,

$${\displaystyle (\mathrm{\Psi },\mathrm{\Psi })=\Vert \mathrm{\Psi }{\Vert }^2,}$$

is always a positive real number. The number ‖Ψ‖ (not ‖Ψ‖²) is called the norm of the wave function Ψ.

If (Ψ, Ψ) = 1, then Ψ is normalized. If Ψ is not normalized, then dividing by its norm gives the normalized function Ψ/‖Ψ‖. Two wave functions Ψ₁ and Ψ₂ are orthogonal if (Ψ₁, Ψ₂) = 0. If they are normalized and orthogonal, they are orthonormal. Orthogonality (hence also orthonormality) of wave functions is not a necessary condition wave functions must satisfy, but is instructive to consider since this guarantees linear independence of the functions. In a linear combination of orthogonal wave functions Ψ_n we have,

$${\displaystyle \mathrm{\Psi }=\sum _n{a}_n{\mathrm{\Psi }}_n,a_n=\frac{({\mathrm{\Psi }}_n,\mathrm{\Psi })}{({\mathrm{\Psi }}_n,{\mathrm{\Psi }}_n)}}$$

If the wave functions Ψ_n were nonorthogonal, the coefficients would be less simple to obtain.

Quantum states as vectors

In the Copenhagen interpretation, the modulus squared of the inner product (a complex number) gives a real number

$${\displaystyle {\left|({\mathrm{\Psi }}_1,{\mathrm{\Psi }}_2)\right|}^2=P\left({\mathrm{\Psi }}_2\to {\mathrm{\Psi }}_1\right),}$$

which, assuming both wave functions are normalized, is interpreted as the probability of the wave function Ψ₂ "collapsing" to the new wave function Ψ₁ upon measurement of an observable, whose eigenvalues are the possible results of the measurement, with Ψ₁ being an eigenvector of the resulting eigenvalue. This is the Born rule, and is one of the fundamental postulates of quantum mechanics.

At a particular instant of time, all values of the wave function Ψ(x, t) are components of a vector. There are uncountably infinitely many of them and integration is used in place of summation. In Bra–ket notation, this vector is written

$${\displaystyle |\mathrm{\Psi }(t)⟩=\int \mathrm{\Psi }(x,t)|x⟩dx}$$

and is referred to as a "quantum state vector", or simply "quantum state". There are several advantages to understanding wave functions as representing elements of an abstract vector space:

• All the powerful tools of linear algebra can be used to manipulate and understand wave functions. For example:
  • Linear algebra explains how a vector space can be given a basis, and then any vector in the vector space can be expressed in this basis. This explains the relationship between a wave function in position space and a wave function in momentum space and suggests that there are other possibilities too.
  • Bra–ket notation can be used to manipulate wave functions.
• The idea that quantum states are vectors in an abstract vector space is completely general in all aspects of quantum mechanics and quantum field theory, whereas the idea that quantum states are complex-valued "wave" functions of space is only true in certain situations.

The time parameter is often suppressed, and will be in the following. The x coordinate is a continuous index. The |x⟩ are the basis vectors, which are orthonormal so their inner product is a delta function;

$${\displaystyle ⟨x^{\prime }|x⟩=\delta (x^{\prime }-x)}$$

thus

$${\displaystyle ⟨x^{\prime }|\mathrm{\Psi }⟩=\int \mathrm{\Psi }(x)⟨x^{\prime }|x⟩dx=\mathrm{\Psi }(x^{\prime })}$$

and

$${\displaystyle |\mathrm{\Psi }⟩=\int |x⟩⟨x|\mathrm{\Psi }⟩dx=\left(\int |x⟩⟨x|dx\right)|\mathrm{\Psi }⟩}$$

which illuminates the identity operator

$${\displaystyle I=\int |x⟩⟨x|dx.}$$

Finding the identity operator in a basis allows the abstract state to be expressed explicitly in a basis, and more (the inner product between two state vectors, and other operators for observables, can be expressed in the basis).

Momentum-space wave functions

The particle also has a wave function in momentum space:

$${\displaystyle \mathrm{\Phi }(p,t)}$$

where p is the momentum in one dimension, which can be any value from −∞ to +∞, and t is time.

Analogous to the position case, the inner product of two wave functions Φ₁(p, t) and Φ₂(p, t) can be defined as:

$${\displaystyle ({\mathrm{\Phi }}_1,{\mathrm{\Phi }}_2)={\int }_{-\mathrm{\infty }}^{\mathrm{\infty }}{\mathrm{\Phi }}_1^{\ast }(p,t){\mathrm{\Phi }}_2(p,t)dp.}$$

One particular solution to the time-independent Schrödinger equation is

$${\displaystyle {\mathrm{\Psi }}_p(x)=e^{ipx/\hslash },}$$

a plane wave, which can be used in the description of a particle with momentum exactly p, since it is an eigenfunction of the momentum operator. These functions are not normalizable to unity (they aren't square-integrable), so they are not really elements of physical Hilbert space. The set

$${\displaystyle \{{\mathrm{\Psi }}_p(x,t),-\mathrm{\infty }\le p\le \mathrm{\infty }\}}$$

forms what is called the momentum basis. This "basis" is not a basis in the usual mathematical sense. For one thing, since the functions aren't normalizable, they are instead normalized to a delta function,^{[nb 2]}

$${\displaystyle ({\mathrm{\Psi }}_p,{\mathrm{\Psi }}_{p^{\prime }})=\delta (p-p^{\prime }).}$$

For another thing, though they are linearly independent, there are too many of them (they form an uncountable set) for a basis for physical Hilbert space. They can still be used to express all functions in it using Fourier transforms as described next.

Relations between position and momentum representations

The x and p representations are

$${\displaystyle \begin{array}{rl}|\mathrm{\Psi }⟩=I|\mathrm{\Psi }⟩& =\int |x⟩⟨x|\mathrm{\Psi }⟩dx=\int \mathrm{\Psi }(x)|x⟩dx,\\ |\mathrm{\Psi }⟩=I|\mathrm{\Psi }⟩& =\int |p⟩⟨p|\mathrm{\Psi }⟩dp=\int \mathrm{\Phi }(p)|p⟩dp.\end{array}}$$

Now take the projection of the state Ψ onto eigenfunctions of momentum using the last expression in the two equations,

$${\displaystyle \int \mathrm{\Psi }(x)⟨p|x⟩dx=\int \mathrm{\Phi }(p^{\prime })⟨p|p^{\prime }⟩d{p}^{\prime }=\int \mathrm{\Phi }(p^{\prime })\delta (p-p^{\prime })d{p}^{\prime }=\mathrm{\Phi }(p).}$$

Then utilizing the known expression for suitably normalized eigenstates of momentum in the position representation solutions of the free Schrödinger equation

$${\displaystyle ⟨x|p⟩=p(x)=\frac{1}{\sqrt{2\pi \hslash }}{e}^{\frac{i}{\hslash }px}\Rightarrow ⟨p|x⟩=\frac{1}{\sqrt{2\pi \hslash }}{e}^{-\frac{i}{\hslash }px},}$$

one obtains

$${\displaystyle \mathrm{\Phi }(p)=\frac{1}{\sqrt{2\pi \hslash }}\int \mathrm{\Psi }(x)e^{-\frac{i}{\hslash }px}dx.}$$

Likewise, using eigenfunctions of position,

$${\displaystyle \mathrm{\Psi }(x)=\frac{1}{\sqrt{2\pi \hslash }}\int \mathrm{\Phi }(p)e^{\frac{i}{\hslash }px}dp.}$$

The position-space and momentum-space wave functions are thus found to be Fourier transforms of each other. The two wave functions contain the same information, and either one alone is sufficient to calculate any property of the particle. As representatives of elements of abstract physical Hilbert space, whose elements are the possible states of the system under consideration, they represent the same state vector, hence identical physical states, but they are not generally equal when viewed as square-integrable functions.

In practice, the position-space wave function is used much more often than the momentum-space wave function. The potential entering the relevant equation (Schrödinger, Dirac, etc.) determines in which basis the description is easiest. For the harmonic oscillator, x and p enter symmetrically, so there it does not matter which description one uses. The same equation (modulo constants) results. From this, with a little bit of afterthought, it follows that solutions to the wave equation of the harmonic oscillator are eigenfunctions of the Fourier transform in L².

Definitions (other cases)

Following are the general forms of the wave function for systems in higher dimensions and more particles, as well as including other degrees of freedom than position coordinates or momentum components.

One-particle states in 3d position space

The position-space wave function of a single particle without spin in three spatial dimensions is similar to the case of one spatial dimension above:

$${\displaystyle \mathrm{\Psi }(\mathbf{r},t)}$$

where r is the position vector in three-dimensional space, and t is time. As always Ψ(r, t) is a complex-valued function of real variables. As a single vector in Dirac notation

$${\displaystyle |\mathrm{\Psi }(t)⟩=\int d^3\mathbf{r}\mathrm{\Psi }(\mathbf{r},t)|\mathbf{r}⟩}$$

All the previous remarks on inner products, momentum space wave functions, Fourier transforms, and so on extend to higher dimensions.

For a particle with spin, ignoring the position degrees of freedom, the wave function is a function of spin only (time is a parameter);

$${\displaystyle \xi (s_z,t)}$$

where s_z is the spin projection quantum number along the z axis. (The z axis is an arbitrary choice; other axes can be used instead if the wave function is transformed appropriately, see below.) The s_z parameter, unlike r and t, is a discrete variable. For example, for a spin-1/2 particle, s_z can only be +1/2 or −1/2, and not any other value. (In general, for spin s, s_z can be s, s − 1, ..., −s + 1, −s). Inserting each quantum number gives a complex valued function of space and time, there are 2s + 1 of them. These can be arranged into a column vector

$${\displaystyle \xi =\left[\begin{array}{c}\xi (s,t)\\ \xi (s-1,t)\\ ⋮\\ \xi (-(s-1),t)\\ \xi (-s,t)\end{array}\right]=\xi (s,t)\left[\begin{array}{c}1\\ 0\\ ⋮\\ 0\\ 0\end{array}\right]+\xi (s-1,t)\left[\begin{array}{c}0\\ 1\\ ⋮\\ 0\\ 0\end{array}\right]+\cdots +\xi (-(s-1),t)\left[\begin{array}{c}0\\ 0\\ ⋮\\ 1\\ 0\end{array}\right]+\xi (-s,t)\left[\begin{array}{c}0\\ 0\\ ⋮\\ 0\\ 1\end{array}\right]}$$

In bra–ket notation, these easily arrange into the components of a vector

$${\displaystyle |\xi (t)⟩=\sum _{s_z=-s}^s\xi (s_z,t)|s_z⟩}$$

The entire vector ξ is a solution of the Schrödinger equation (with a suitable Hamiltonian), which unfolds to a coupled system of 2s + 1 ordinary differential equations with solutions ξ(s, t), ξ(s − 1, t), ..., ξ(−s, t). The term "spin function" instead of "wave function" is used by some authors. This contrasts the solutions to position space wave functions, the position coordinates being continuous degrees of freedom, because then the Schrödinger equation does take the form of a wave equation.

More generally, for a particle in 3d with any spin, the wave function can be written in "position–spin space" as:

$${\displaystyle \mathrm{\Psi }(\mathbf{r},s_z,t)}$$

and these can also be arranged into a column vector

$${\displaystyle \mathrm{\Psi }(\mathbf{r},t)=\left[\begin{array}{c}\mathrm{\Psi }(\mathbf{r},s,t)\\ \mathrm{\Psi }(\mathbf{r},s-1,t)\\ ⋮\\ \mathrm{\Psi }(\mathbf{r},-(s-1),t)\\ \mathrm{\Psi }(\mathbf{r},-s,t)\end{array}\right]}$$

in which the spin dependence is placed in indexing the entries, and the wave function is a complex vector-valued function of space and time only.

All values of the wave function, not only for discrete but continuous variables also, collect into a single vector

$${\displaystyle |\mathrm{\Psi }(t)⟩=\sum _{s_z}\int d^3\mathbf{r}\mathrm{\Psi }(\mathbf{r},s_z,t)|\mathbf{r},s_z⟩}$$

For a single particle, the tensor product ⊗ of its position state vector |ψ⟩ and spin state vector |ξ⟩ gives the composite position-spin state vector

$${\displaystyle |\psi (t)⟩\otimes |\xi (t)⟩=\sum _{s_z}\int d^3\mathbf{r}\psi (\mathbf{r},t)\xi (s_z,t)|\mathbf{r}⟩\otimes |s_z⟩}$$

with the identifications

$${\displaystyle |\mathrm{\Psi }(t)⟩=|\psi (t)⟩\otimes |\xi (t)⟩}$$

$${\displaystyle \mathrm{\Psi }(\mathbf{r},s_z,t)=\psi (\mathbf{r},t)\xi (s_z,t)}$$

$${\displaystyle |\mathbf{r},s_z⟩=|\mathbf{r}⟩\otimes |s_z⟩}$$

The tensor product factorization is only possible if the orbital and spin angular momenta of the particle are separable in the Hamiltonian operator underlying the system's dynamics (in other words, the Hamiltonian can be split into the sum of orbital and spin terms). The time dependence can be placed in either factor, and time evolution of each can be studied separately. The factorization is not possible for those interactions where an external field or any space-dependent quantity couples to the spin; examples include a particle in a magnetic field, and spin–orbit coupling.

The preceding discussion is not limited to spin as a discrete variable, the total angular momentum J may also be used. Other discrete degrees of freedom, like isospin, can expressed similarly to the case of spin above.

Many-particle states in 3d position space

Traveling waves of two free particles, with two of three dimensions suppressed. Top is position-space wave function, bottom is momentum-space wave function, with corresponding probability densities.

If there are many particles, in general there is only one wave function, not a separate wave function for each particle. The fact that one wave function describes many particles is what makes quantum entanglement and the EPR paradox possible. The position-space wave function for N particles is written:

$${\displaystyle \mathrm{\Psi }({\mathbf{r}}_1,{\mathbf{r}}_2\cdots {\mathbf{r}}_N,t)}$$

where r_i is the position of the i-th particle in three-dimensional space, and t is time. Altogether, this is a complex-valued function of 3N + 1 real variables.

In quantum mechanics there is a fundamental distinction between identical particles and distinguishable particles. For example, any two electrons are identical and fundamentally indistinguishable from each other; the laws of physics make it impossible to "stamp an identification number" on a certain electron to keep track of it. This translates to a requirement on the wave function for a system of identical particles:

$${\displaystyle \mathrm{\Psi }\left(\dots {\mathbf{r}}_a,\dots ,{\mathbf{r}}_b,\dots \right)=\pm \mathrm{\Psi }\left(\dots {\mathbf{r}}_b,\dots ,{\mathbf{r}}_a,\dots \right)}$$

where the + sign occurs if the particles are all bosons and − sign if they are all fermions. In other words, the wave function is either totally symmetric in the positions of bosons, or totally antisymmetric in the positions of fermions. The physical interchange of particles corresponds to mathematically switching arguments in the wave function. The antisymmetry feature of fermionic wave functions leads to the Pauli principle. Generally, bosonic and fermionic symmetry requirements are the manifestation of particle statistics and are present in other quantum state formalisms.

For N distinguishable particles (no two being identical, i.e. no two having the same set of quantum numbers), there is no requirement for the wave function to be either symmetric or antisymmetric.

For a collection of particles, some identical with coordinates r₁, r₂, ... and others distinguishable x₁, x₂, ... (not identical with each other, and not identical to the aforementioned identical particles), the wave function is symmetric or antisymmetric in the identical particle coordinates r_i only:

$${\displaystyle \mathrm{\Psi }\left(\dots {\mathbf{r}}_a,\dots ,{\mathbf{r}}_b,\dots ,{\mathbf{x}}_1,{\mathbf{x}}_2,\dots \right)=\pm \mathrm{\Psi }\left(\dots {\mathbf{r}}_b,\dots ,{\mathbf{r}}_a,\dots ,{\mathbf{x}}_1,{\mathbf{x}}_2,\dots \right)}$$

Again, there is no symmetry requirement for the distinguishable particle coordinates x_i.

The wave function for N particles each with spin is the complex-valued function

$${\displaystyle \mathrm{\Psi }({\mathbf{r}}_1,{\mathbf{r}}_2\cdots {\mathbf{r}}_N,s_{z1},s_{z2}\cdots s_{zN},t)}$$

Accumulating all these components into a single vector,

$${\displaystyle |\mathrm{\Psi }⟩=\stackrel{\text{discrete labels}}{\overbrace{\sum _{s_{z1},\dots ,s_{zN}}}}\stackrel{\text{continuous labels}}{\overbrace{{\int }_{R_N}{d}^3{\mathbf{r}}_N\cdots {\int }_{R_1}{d}^3{\mathbf{r}}_1}}\underset{\begin{array}{c}\text{wave function (component of }\\ \text{ state vector along basis state)}\end{array}}{\underbrace{\mathrm{\Psi }({\mathbf{r}}_1,\dots ,{\mathbf{r}}_N,s_{z1},\dots ,s_{zN})}}\underset{\text{basis state (basis ket)}}{\underbrace{|{\mathbf{r}}_1,\dots ,{\mathbf{r}}_N,s_{z1},\dots ,s_{zN}⟩}}.}$$

For identical particles, symmetry requirements apply to both position and spin arguments of the wave function so it has the overall correct symmetry.

The formulae for the inner products are integrals over all coordinates or momenta and sums over all spin quantum numbers. For the general case of N particles with spin in 3-d,

$${\displaystyle ({\mathrm{\Psi }}_1,{\mathrm{\Psi }}_2)=\sum _{s_{zN}}\cdots \sum _{s_{z2}}\sum _{s_{z1}}\underset{\mathrm{a}\mathrm{l}\mathrm{l}\mathrm{s}\mathrm{p}\mathrm{a}\mathrm{c}\mathrm{e}}{\int }{d}^3{\mathbf{r}}_1\underset{\mathrm{a}\mathrm{l}\mathrm{l}\mathrm{s}\mathrm{p}\mathrm{a}\mathrm{c}\mathrm{e}}{\int }{d}^3{\mathbf{r}}_2\cdots \underset{\mathrm{a}\mathrm{l}\mathrm{l}\mathrm{s}\mathrm{p}\mathrm{a}\mathrm{c}\mathrm{e}}{\int }{d}^3{\mathbf{r}}_N{\mathrm{\Psi }}_1^{\ast }\left({\mathbf{r}}_1\cdots {\mathbf{r}}_N,s_{z1}\cdots s_{zN},t\right){\mathrm{\Psi }}_2\left({\mathbf{r}}_1\cdots {\mathbf{r}}_N,s_{z1}\cdots s_{zN},t\right)}$$

this is altogether N three-dimensional volume integrals and N sums over the spins. The differential volume elements d³r_i are also written "dV_i" or "dx_i dy_i dz_i".

The multidimensional Fourier transforms of the position or position–spin space wave functions yields momentum or momentum–spin space wave functions.

Probability interpretation

For the general case of N particles with spin in 3d, if Ψ is interpreted as a probability amplitude, the probability density is

$${\displaystyle \rho \left({\mathbf{r}}_1\cdots {\mathbf{r}}_N,s_{z1}\cdots s_{zN},t\right)={\left|\mathrm{\Psi }\left({\mathbf{r}}_1\cdots {\mathbf{r}}_N,s_{z1}\cdots s_{zN},t\right)\right|}^2}$$

and the probability that particle 1 is in region R₁ with spin s_z1 = m₁ and particle 2 is in region R₂ with spin s_z2 = m₂ etc. at time t is the integral of the probability density over these regions and evaluated at these spin numbers:

$${\displaystyle P_{{\mathbf{r}}_1\in R_1,s_{z1}=m_1,\dots ,{\mathbf{r}}_N\in R_N,s_{zN}=m_N}(t)={\int }_{R_1}{d}^3{\mathbf{r}}_1{\int }_{R_2}{d}^3{\mathbf{r}}_2\cdots {\int }_{R_N}{d}^3{\mathbf{r}}_N{\left|\mathrm{\Psi }\left({\mathbf{r}}_1\cdots {\mathbf{r}}_N,m_1\cdots m_N,t\right)\right|}^2}$$

Time dependence

Main article: Dynamical pictures

For systems in time-independent potentials, the wave function can always be written as a function of the degrees of freedom multiplied by a time-dependent phase factor, the form of which is given by the Schrödinger equation. For N particles, considering their positions only and suppressing other degrees of freedom,

$${\displaystyle \mathrm{\Psi }({\mathbf{r}}_1,{\mathbf{r}}_2,\dots ,{\mathbf{r}}_N,t)=e^{-iEt/\hslash }\psi ({\mathbf{r}}_1,{\mathbf{r}}_2,\dots ,{\mathbf{r}}_N),}$$

where E is the energy eigenvalue of the system corresponding to the eigenstate Ψ. Wave functions of this form are called stationary states.

The time dependence of the quantum state and the operators can be placed according to unitary transformations on the operators and states. For any quantum state |Ψ⟩ and operator O, in the Schrödinger picture |Ψ(t)⟩ changes with time according to the Schrödinger equation while O is constant. In the Heisenberg picture it is the other way round, |Ψ⟩ is constant while O(t) evolves with time according to the Heisenberg equation of motion. The Dirac (or interaction) picture is intermediate, time dependence is places in both operators and states which evolve according to equations of motion. It is useful primarily in computing S-matrix elements.

Non-relativistic examples

The following are solutions to the Schrödinger equation for one non-relativistic spinless particle.

Finite potential barrier

Scattering at a finite potential barrier of height V₀. The amplitudes and direction of left and right moving waves are indicated. In red, those waves used for the derivation of the reflection and transmission amplitude. E > V₀ for this illustration.

One of the most prominent features of wave mechanics is the possibility for a particle to reach a location with a prohibitive (in classical mechanics) force potential. A common model is the "potential barrier", the one-dimensional case has the potential

$${\displaystyle V(x)=\{\begin{array}{ll}{V}_0& |x|<a\\ 0& |x|\ge a\end{array}}$$

and the steady-state solutions to the wave equation have the form (for some constants k, κ)

$${\displaystyle \mathrm{\Psi }(x)=\{\begin{array}{ll}{A}_{\mathrm{r}}{e}^{ikx}+A_{\mathrm{l}}{e}^{-ikx}& x<-a,\\ B_{\mathrm{r}}{e}^{\kappa x}+B_{\mathrm{l}}{e}^{-\kappa x}& |x|\le a,\\ C_{\mathrm{r}}{e}^{ikx}+C_{\mathrm{l}}{e}^{-ikx}& x>a.\end{array}}$$

Note that these wave functions are not normalized; see scattering theory for discussion.

The standard interpretation of this is as a stream of particles being fired at the step from the left (the direction of negative x): setting A_r = 1 corresponds to firing particles singly; the terms containing A_r and C_r signify motion to the right, while A_l and C_l – to the left. Under this beam interpretation, put C_l = 0 since no particles are coming from the right. By applying the continuity of wave functions and their derivatives at the boundaries, it is hence possible to determine the constants above.

3D confined electron wave functions in a quantum dot. Here, rectangular and triangular-shaped quantum dots are shown. Energy states in rectangular dots are more s-type and p-type. However, in a triangular dot the wave functions are mixed due to confinement symmetry. (Click for animation)

In a semiconductor crystallite whose radius is smaller than the size of its exciton Bohr radius, the excitons are squeezed, leading to quantum confinement. The energy levels can then be modeled using the particle in a box model in which the energy of different states is dependent on the length of the box.

Quantum harmonic oscillator

The wave functions for the quantum harmonic oscillator can be expressed in terms of Hermite polynomials H_n, they are

$${\displaystyle {\mathrm{\Psi }}_n(x)=\sqrt{\frac{1}{2^{n}n!}}\cdot {\left(\frac{m\omega }{\pi \hslash }\right)}^{1/4}\cdot e^{-\frac{m\omega x^2}{2\hslash }}\cdot H_n\left(\sqrt{\frac{m\omega }{\hslash }}x\right)}$$

where n = 0, 1, 2, ....

The electron probability density for the first few hydrogen atom electron orbitals shown as cross-sections. These orbitals form an orthonormal basis for the wave function of the electron. Different orbitals are depicted with different scale.

Hydrogen atom

The wave functions of an electron in a Hydrogen atom are expressed in terms of spherical harmonics and generalized Laguerre polynomials (these are defined differently by different authors—see main article on them and the hydrogen atom).

It is convenient to use spherical coordinates, and the wave function can be separated into functions of each coordinate,

$${\displaystyle {\mathrm{\Psi }}_{n\ell m}(r,\theta ,\varphi )=R(r)Y_{\ell }^m(\theta ,\varphi )}$$

where R are radial functions and Y^m
_ℓ(θ, φ) are spherical harmonics of degree ℓ and order m. This is the only atom for which the Schrödinger equation has been solved exactly. Multi-electron atoms require approximative methods. The family of solutions is:

$${\displaystyle {\mathrm{\Psi }}_{n\ell m}(r,\theta ,\varphi )=\sqrt{{\left(\frac{2}{n{a}_0}\right)}^3\frac{(n-\ell -1)!}{2n[(n+\ell )!]}}{e}^{-r/n{a}_0}{\left(\frac{2r}{n{a}_0}\right)}^{\ell }{L}_{n-\ell -1}^{2\ell +1}\left(\frac{2r}{n{a}_0}\right)\cdot Y_{\ell }^m(\theta ,\varphi )}$$

where a₀ = 4πε₀ħ²/m_ee² is the Bohr radius, L^{2ℓ + 1}
_{n − ℓ − 1} are the generalized Laguerre polynomials of degree n − ℓ − 1, n = 1, 2, ... is the principal quantum number, ℓ = 0, 1, ..., n − 1 the azimuthal quantum number, m = −ℓ, −ℓ + 1, ..., ℓ − 1, ℓ the magnetic quantum number. Hydrogen-like atoms have very similar solutions.

This solution does not take into account the spin of the electron.

In the figure of the hydrogen orbitals, the 19 sub-images are images of wave functions in position space (their norm squared). The wave functions represent the abstract state characterized by the triple of quantum numbers (n, ℓ, m), in the lower right of each image. These are the principal quantum number, the orbital angular momentum quantum number, and the magnetic quantum number. Together with one spin-projection quantum number of the electron, this is a complete set of observables.

The figure can serve to illustrate some further properties of the function spaces of wave functions.

• In this case, the wave functions are square integrable. One can initially take the function space as the space of square integrable functions, usually denoted L².
• The displayed functions are solutions to the Schrödinger equation. Obviously, not every function in L² satisfies the Schrödinger equation for the hydrogen atom. The function space is thus a subspace of L².
• The displayed functions form part of a basis for the function space. To each triple (n, ℓ, m), there corresponds a basis wave function. If spin is taken into account, there are two basis functions for each triple. The function space thus has a countable basis.
• The basis functions are mutually orthonormal.

Wave functions and function spaces

The concept of function spaces enters naturally in the discussion about wave functions. A function space is a set of functions, usually with some defining requirements on the functions (in the present case that they are square integrable), sometimes with an algebraic structure on the set (in the present case a vector space structure with an inner product), together with a topology on the set. The latter will sparsely be used here, it is only needed to obtain a precise definition of what it means for a subset of a function space to be closed. It will be concluded below that the function space of wave functions is a Hilbert space. This observation is the foundation of the predominant mathematical formulation of quantum mechanics.

Vector space structure

A wave function is an element of a function space partly characterized by the following concrete and abstract descriptions.

• The Schrödinger equation is linear. This means that the solutions to it, wave functions, can be added and multiplied by scalars to form a new solution. The set of solutions to the Schrödinger equation is a vector space.
• The superposition principle of quantum mechanics. If Ψ and Φ are two states in the abstract space of states of a quantum mechanical system, and a and b are any two complex numbers, then aΨ + bΦ is a valid state as well. (Whether the null vector counts as a valid state ("no system present") is a matter of definition. The null vector does not at any rate describe the vacuum state in quantum field theory.) The set of allowable states is a vector space.

This similarity is of course not accidental. There are also a distinctions between the spaces to keep in mind.

Representations

Basic states are characterized by a set of quantum numbers. This is a set of eigenvalues of a maximal set of commuting observables. Physical observables are represented by linear operators, also called observables, on the vectors space. Maximality means that there can be added to the set no further algebraically independent observables that commute with the ones already present. A choice of such a set may be called a choice of representation.

• It is a postulate of quantum mechanics that a physically observable quantity of a system, such as position, momentum, or spin, is represented by a linear Hermitian operator on the state space. The possible outcomes of measurement of the quantity are the eigenvalues of the operator. At a deeper level, most observables, perhaps all, arise as generators of symmetries.
• The physical interpretation is that such a set represents what can – in theory – simultaneously be measured with arbitrary precision. The Heisenberg uncertainty relation prohibits simultaneous exact measurements of two non-commuting observables.
• The set is non-unique. It may for a one-particle system, for example, be position and spin z-projection, (x, S_z), or it may be momentum and spin y-projection, (p, S_y). In this case, the operator corresponding to position (a multiplication operator in the position representation) and the operator corresponding to momentum (a differential operator in the position representation) do not commute.
• Once a representation is chosen, there is still arbitrariness. It remains to choose a coordinate system. This may, for example, correspond to a choice of x, y- and z-axis, or a choice of curvilinear coordinates as exemplified by the spherical coordinates used for the Hydrogen atomic wave functions. This final choice also fixes a basis in abstract Hilbert space. The basic states are labeled by the quantum numbers corresponding to the maximal set of commuting observables and an appropriate coordinate system.

The abstract states are "abstract" only in that an arbitrary choice necessary for a particular explicit description of it is not given. This is the same as saying that no choice of maximal set of commuting observables has been given. This is analogous to a vector space without a specified basis. Wave functions corresponding to a state are accordingly not unique. This non-uniqueness reflects the non-uniqueness in the choice of a maximal set of commuting observables. For one spin particle in one dimension, to a particular state there corresponds two wave functions, Ψ(x, S_z) and Ψ(p, S_y), both describing the same state.

• For each choice of maximal commuting sets of observables for the abstract state space, there is a corresponding representation that is associated to a function space of wave functions.
• Between all these different function spaces and the abstract state space, there are one-to-one correspondences (here disregarding normalization and unobservable phase factors), the common denominator here being a particular abstract state. The relationship between the momentum and position space wave functions, for instance, describing the same state is the Fourier transform.

Each choice of representation should be thought of as specifying a unique function space in which wave functions corresponding to that choice of representation lives. This distinction is best kept, even if one could argue that two such function spaces are mathematically equal, e.g. being the set of square integrable functions. One can then think of the function spaces as two distinct copies of that set.

Inner product

There is an additional algebraic structure on the vector spaces of wave functions and the abstract state space.

• Physically, different wave functions are interpreted to overlap to some degree. A system in a state Ψ that does not overlap with a state Φ cannot be found to be in the state Φ upon measurement. But if Φ₁, Φ₂, … overlap Ψ to some degree, there is a chance that measurement of a system described by Ψ will be found in states Φ₁, Φ₂, …. Also selection rules are observed apply. These are usually formulated in the preservation of some quantum numbers. This means that certain processes allowable from some perspectives (e.g. energy and momentum conservation) do not occur because the initial and final total wave functions do not overlap.
• Mathematically, it turns out that solutions to the Schrödinger equation for particular potentials are orthogonal in some manner, this is usually described by an integral
  $${\displaystyle \int {\mathrm{\Psi }}_m^{\ast }{\mathrm{\Psi }}_{n}wdV={\delta }_{nm},}$$

  
  where m, n are (sets of) indices (quantum numbers) labeling different solutions, the strictly positive function w is called a weight function, and δ_mn is the Kronecker delta. The integration is taken over all of the relevant space.

This motivates the introduction of an inner product on the vector space of abstract quantum states, compatible with the mathematical observations above when passing to a representation. It is denoted (Ψ, Φ), or in the Bra–ket notation ⟨Ψ|Φ⟩. It yields a complex number. With the inner product, the function space is an inner product space. The explicit appearance of the inner product (usually an integral or a sum of integrals) depends on the choice of representation, but the complex number (Ψ, Φ) does not. Much of the physical interpretation of quantum mechanics stems from the Born rule. It states that the probability p of finding upon measurement the state Φ given the system is in the state Ψ is

$${\displaystyle p=|(\mathrm{\Phi },\mathrm{\Psi }){|}^2,}$$

where Φ and Ψ are assumed normalized. Consider a scattering experiment. In quantum field theory, if Φ_out describes a state in the "distant future" (an "out state") after interactions between scattering particles have ceased, and Ψ_in an "in state" in the "distant past", then the quantities (Φ_out, Ψ_in), with Φ_out and Ψ_in varying over a complete set of in states and out states respectively, is called the S-matrix or scattering matrix. Knowledge of it is, effectively, having solved the theory at hand, at least as far as predictions go. Measurable quantities such as decay rates and scattering cross sections are calculable from the S-matrix.

Hilbert space

The above observations encapsulate the essence of the function spaces of which wave functions are elements. However, the description is not yet complete. There is a further technical requirement on the function space, that of completeness, that allows one to take limits of sequences in the function space, and be ensured that, if the limit exists, it is an element of the function space. A complete inner product space is called a Hilbert space. The property of completeness is crucial in advanced treatments and applications of quantum mechanics. For instance, the existence of projection operators or orthogonal projections relies on the completeness of the space. These projection operators, in turn, are essential for the statement and proof of many useful theorems, e.g. the spectral theorem. It is not very important in introductory quantum mechanics, and technical details and links may be found in footnotes like the one that follows. The space L² is a Hilbert space, with inner product presented later. The function space of the example of the figure is a subspace of L². A subspace of a Hilbert space is a Hilbert space if it is closed.

In summary, the set of all possible normalizable wave functions for a system with a particular choice of basis, together with the null vector, constitute a Hilbert space.

Not all functions of interest are elements of some Hilbert space, say L². The most glaring example is the set of functions e^{2πip · x⁄h}. These are plane wave solutions of the Schrödinger equation for a free particle, but are not normalizable, hence not in L². But they are nonetheless fundamental for the description. One can, using them, express functions that are normalizable using wave packets. They are, in a sense, a basis (but not a Hilbert space basis, nor a Hamel basis) in which wave functions of interest can be expressed. There is also the artifact "normalization to a delta function" that is frequently employed for notational convenience, see further down. The delta functions themselves aren't square integrable either.

The above description of the function space containing the wave functions is mostly mathematically motivated. The function spaces are, due to completeness, very large in a certain sense. Not all functions are realistic descriptions of any physical system. For instance, in the function space L² one can find the function that takes on the value 0 for all rational numbers and -i for the irrationals in the interval [0, 1]. This is square integrable, but can hardly represent a physical state.

Common Hilbert spaces

While the space of solutions as a whole is a Hilbert space there are many other Hilbert spaces that commonly occur as ingredients.

• Square integrable complex valued functions on the interval [0, 2π]. The set {e^int/2π, n ∈ ℤ} is a Hilbert space basis, i.e. a maximal orthonormal set.
• The Fourier transform takes functions in the above space to elements of l²(ℤ), the space of square summable functions ℤ → ℂ. The latter space is a Hilbert space and the Fourier transform is an isomorphism of Hilbert spaces. Its basis is {e_i, i ∈ ℤ} with e_i(j) = δ_ij, i, j ∈ ℤ.
• The most basic example of spanning polynomials is in the space of square integrable functions on the interval [–1, 1] for which the Legendre polynomials is a Hilbert space basis (complete orthonormal set).
• The square integrable functions on the unit sphere S² is a Hilbert space. The basis functions in this case are the spherical harmonics. The Legendre polynomials are ingredients in the spherical harmonics. Most problems with rotational symmetry will have "the same" (known) solution with respect to that symmetry, so the original problem is reduced to a problem of lower dimensionality.
• The associated Laguerre polynomials appear in the hydrogenic wave function problem after factoring out the spherical harmonics. These span the Hilbert space of square integrable functions on the semi-infinite interval [0, ∞).

More generally, one may consider a unified treatment of all second order polynomial solutions to the Sturm–Liouville equations in the setting of Hilbert space. These include the Legendre and Laguerre polynomials as well as Chebyshev polynomials, Jacobi polynomials and Hermite polynomials. All of these actually appear in physical problems, the latter ones in the harmonic oscillator, and what is otherwise a bewildering maze of properties of special functions becomes an organized body of facts. For this, see Byron & Fuller (1992, Chapter 5).

There occurs also finite-dimensional Hilbert spaces. The space ℂⁿ is a Hilbert space of dimension n. The inner product is the standard inner product on these spaces. In it, the "spin part" of a single particle wave function resides.

• In the non-relativistic description of an electron one has n = 2 and the total wave function is a solution of the Pauli equation.
• In the corresponding relativistic treatment, n = 4 and the wave function solves the Dirac equation.

With more particles, the situations is more complicated. One has to employ tensor products and use representation theory of the symmetry groups involved (the rotation group and the Lorentz group respectively) to extract from the tensor product the spaces in which the (total) spin wave functions reside. (Further problems arise in the relativistic case unless the particles are free. See the Bethe–Salpeter equation.) Corresponding remarks apply to the concept of isospin, for which the symmetry group is SU(2). The models of the nuclear forces of the sixties (still useful today, see nuclear force) used the symmetry group SU(3). In this case, as well, the part of the wave functions corresponding to the inner symmetries reside in some ℂⁿ or subspaces of tensor products of such spaces.

• In quantum field theory the underlying Hilbert space is Fock space. It is built from free single-particle states, i.e. wave functions when a representation is chosen, and can accommodate any finite, not necessarily constant in time, number of particles. The interesting (or rather the tractable) dynamics lies not in the wave functions but in the field operators that are operators acting on Fock space. Thus the Heisenberg picture is the most common choice (constant states, time varying operators).

Due to the infinite-dimensional nature of the system, the appropriate mathematical tools are objects of study in functional analysis.

Simplified description

Continuity of the wave function and its first spatial derivative (in the x direction, y and z coordinates not shown), at some time t.

Not all introductory textbooks take the long route and introduce the full Hilbert space machinery, but the focus is on the non-relativistic Schrödinger equation in position representation for certain standard potentials. The following constraints on the wave function are sometimes explicitly formulated for the calculations and physical interpretation to make sense:

• The wave function must be square integrable. This is motivated by the Copenhagen interpretation of the wave function as a probability amplitude.
• It must be everywhere continuous and everywhere continuously differentiable. This is motivated by the appearance of the Schrödinger equation for most physically reasonable potentials.

It is possible to relax these conditions somewhat for special purposes. If these requirements are not met, it is not possible to interpret the wave function as a probability amplitude.

This does not alter the structure of the Hilbert space that these particular wave functions inhabit, but the subspace of the square-integrable functions L², which is a Hilbert space, satisfying the second requirement is not closed in L², hence not a Hilbert space in itself. The functions that does not meet the requirements are still needed for both technical and practical reasons.

More on wave functions and abstract state space

Main article: Quantum state

As has been demonstrated, the set of all possible wave functions in some representation for a system constitute an in general infinite-dimensional Hilbert space. Due to the multiple possible choices of representation basis, these Hilbert spaces are not unique. One therefore talks about an abstract Hilbert space, state space, where the choice of representation and basis is left undetermined. Specifically, each state is represented as an abstract vector in state space. A quantum state |Ψ⟩ in any representation is generally expressed as a vector

$${\displaystyle |\mathrm{\Psi }⟩=\sum _{\mathit{\alpha }}\int d^m\mathit{\omega }\mathrm{\Psi }(\mathit{\alpha },\mathit{\omega },t)|\mathit{\alpha },\mathit{\omega }⟩}$$

where

• |α, ω⟩ the basis vectors of the chosen representation
• d^mω = dω₁dω₂...dω_m a "differential volume element" in the continuous degrees of freedom
• Ψ(α, ω, t) a component of the vector |Ψ⟩, called the wave function of the system
• α = (α₁, α₂, ..., α_n) dimensionless discrete quantum numbers
• ω = (ω₁, ω₂, ..., ω_m) continuous variables (not necessarily dimensionless)

These quantum numbers index the components of the state vector. More, all α are in an n-dimensional set A = A₁ × A₂ × ... × A_n where each A_i is the set of allowed values for α_i; all ω are in an m-dimensional "volume" Ω ⊆ ℝ^m where Ω = Ω₁ × Ω₂ × ... × Ω_m and each Ω_i ⊆ R is the set of allowed values for ω_i, a subset of the real numbers R. For generality n and m are not necessarily equal.

Example:

1. For a single particle in 3d with spin s, neglecting other degrees of freedom, using Cartesian coordinates, we could take α = (s_z) for the spin quantum number of the particle along the z direction, and ω = (x, y, z) for the particle's position coordinates. Here A = {−s, −s + 1, ..., s − 1, s} is the set of allowed spin quantum numbers and Ω = R³ is the set of all possible particle positions throughout 3d position space.
2. An alternative choice is α = (s_y) for the spin quantum number along the y direction and ω = (p_x, p_y, p_z) for the particle's momentum components. In this case A and Ω are the same as before.

The probability density of finding the system at time ${\displaystyle t}$at state |α, ω⟩ is

$${\displaystyle {\rho }_{\alpha ,\omega }(t)=|\mathrm{\Psi }(\mathit{\alpha },\mathit{\omega },t){|}^2}$$

The probability of finding system with α in some or all possible discrete-variable configurations, D ⊆ A, and ω in some or all possible continuous-variable configurations, C ⊆ Ω, is the sum and integral over the density,

$${\displaystyle P(t)=\sum _{\mathit{\alpha }\in D}{\int }_C{\rho }_{\alpha ,\omega }(t)d^m\mathit{\omega }}$$

Since the sum of all probabilities must be 1, the normalization condition

$${\displaystyle 1=\sum _{\mathit{\alpha }\in A}{\int }_{\mathrm{\Omega }}{\rho }_{\alpha ,\omega }(t)d^m\mathit{\omega }}$$

must hold at all times during the evolution of the system.

The normalization condition requires ρ d^mω to be dimensionless, by dimensional analysis Ψ must have the same units as (ω₁ω₂...ω_m)^−1/2.

Ontology

Main article: Interpretations of quantum mechanics

Whether the wave function really exists, and what it represents, are major questions in the interpretation of quantum mechanics. Many famous physicists of a previous generation puzzled over this problem, such as Schrödinger, Einstein and Bohr. Some advocate formulations or variants of the Copenhagen interpretation (e.g. Bohr, Wigner and von Neumann) while others, such as Wheeler or Jaynes, take the more classical approach and regard the wave function as representing information in the mind of the observer, i.e. a measure of our knowledge of reality. Some, including Schrödinger, Bohm and Everett and others, argued that the wave function must have an objective, physical existence. Einstein thought that a complete description of physical reality should refer directly to physical space and time, as distinct from the wave function, which refers to an abstract mathematical space.

Period 3 element

From Wikipedia, the free encyclopedia
https://en.wikipedia.org/wiki/Period_3_element

A period 3 element is one of the chemical elements in the third row (or period) of the periodic table of the chemical elements. The periodic table is laid out in rows to illustrate recurring (periodic) trends in the chemical behaviour of the elements as their atomic number increases: a new row is begun when the periodic table skips a row and a chemical behaviour begins to repeat, meaning that elements with similar behaviour fall into the same vertical columns. The third period contains eight elements: sodium, magnesium, aluminium, silicon, phosphorus, sulfur, chlorine and argon. The first two, sodium and magnesium, are members of the s-block of the periodic table, while the others are members of the p-block. All of the period 3 elements occur in nature and have at least one stable isotope.

Atomic structure

In a quantum mechanical description of atomic structure, this period corresponds to the buildup of electrons in the third (n = 3) shell, more specifically filling its 3s and 3p subshells. There is a 3d subshell, but—in compliance with the Aufbau principle—it is not filled until period 4. This makes all eight elements analogs of the period 2 elements in the same exact sequence. The octet rule generally applies to period 3 in the same way as to period 2 elements, because the 3d subshell is normally non-acting.

Elements

Elements by number

Element	#	Symbol	Block	Electron configuration
Sodium	11	Na	s-block	[Ne] 3s1
Magnesium	12	Mg	s-block	[Ne] 3s2
Aluminium	13	Al	p-block	[Ne] 3s2 3p1
Silicon	14	Si	p-block	[Ne] 3s2 3p2
Phosphorus	15	P	p-block	[Ne] 3s2 3p3
Sulfur	16	S	p-block	[Ne] 3s2 3p4
Chlorine	17	Cl	p-block	[Ne] 3s2 3p5
Argon	18	Ar	p-block	[Ne] 3s2 3p6

Sodium

Main article: Sodium

Sodium (symbol Na) is a soft, silvery-white, highly reactive metal and is a member of the alkali metals; its only stable isotope is ²³Na. It is an abundant element that exists in numerous minerals such as feldspars, sodalite and rock salt. Many salts of sodium are highly soluble in water and are thus present in significant quantities in the Earth's bodies of water, most abundantly in the oceans as sodium chloride.

Many sodium compounds are useful, such as sodium hydroxide (lye) for soapmaking, and sodium chloride for use as a deicing agent and a nutrient. The same ion is also a component of many minerals, such as sodium nitrate.

The free metal, elemental sodium, does not occur in nature but must be prepared from sodium compounds. Elemental sodium was first isolated by Humphry Davy in 1807 by the electrolysis of sodium hydroxide.

Magnesium

Main article: Magnesium

Magnesium (symbol Mg) is an alkaline earth metal and has common oxidation number +2. It is the eighth most abundant element in the Earth's crust and the ninth in the known universe as a whole. Magnesium is the fourth most common element in the Earth as a whole (behind iron, oxygen and silicon), making up 13% of the planet's mass and a large fraction of the planet's mantle. It is relatively abundant because it is easily built up in supernova stars by sequential additions of three helium nuclei to carbon (which in turn is made from three helium nuclei). Due to the magnesium ion's high solubility in water, it is the third most abundant element dissolved in seawater.

The free element (metal) is not found naturally on Earth, as it is highly reactive (though once produced, it is coated in a thin layer of oxide [see passivation], which partly masks this reactivity). The free metal burns with a characteristic brilliant white light, making it a useful ingredient in flares. The metal is now mainly obtained by electrolysis of magnesium salts obtained from brine. Commercially, the chief use for the metal is as an alloying agent to make aluminium-magnesium alloys, sometimes called "magnalium" or "magnelium". Since magnesium is less dense than aluminium, these alloys are prized for their relative lightness and strength.

Magnesium ions are sour to the taste, and in low concentrations help to impart a natural tartness to fresh mineral waters.

Aluminium

Main article: Aluminium

Aluminium (symbol Al) or aluminum (American English) is a silvery white member of the boron group of chemical elements and a p-block metal classified by some chemists as a post-transition metal. It is not soluble in water under normal circumstances. Aluminium is the third most abundant element (after oxygen and silicon), and the most abundant metal, in the Earth's crust. It makes up about 8% by weight of the Earth's solid surface. Aluminium metal is too reactive chemically to occur natively. Instead, it is found combined in over 270 different minerals. The chief ore of aluminium is bauxite.

Aluminium is remarkable for the metal's low density and for its ability to resist corrosion due to the phenomenon of passivation. Structural components made from aluminium and its alloys are vital to the aerospace industry and are important in other areas of transportation and structural materials. The most useful compounds of aluminium, at least on a weight basis, are the oxides and sulfates.

Silicon

Main article: Silicon

Silicon (symbol Si) is a group 14 metalloid. It is less reactive than its chemical analog carbon, the nonmetal directly above it in the periodic table, but more reactive than germanium, the metalloid directly below it in the table. Controversy about silicon's character dates from its discovery: silicon was first prepared and characterized in pure form in 1824, and given the name silicium (from Latin: silicis, flints), with an -ium word-ending to suggest a metal. However, its final name, suggested in 1831, reflects the more chemically similar elements carbon and boron.

Silicon is the eighth most common element in the universe by mass, but very rarely occurs as the pure free element in nature. It is most widely distributed in dusts, sands, planetoids and planets as various forms of silicon dioxide (silica) or silicates. Over 90% of the Earth's crust is composed of silicate minerals, making silicon the second most abundant element in the Earth's crust (about 28% by mass) after oxygen.

Most silicon is used commercially without being separated, and indeed often with little processing of compounds from nature. These include direct industrial building use of clays, silica sand and stone. Silica is used in ceramic brick. Silicate goes into Portland cement for mortar and stucco, and combined with silica sand and gravel, to make concrete. Silicates are also in whiteware ceramics such as porcelain, and in traditional quartz-based soda–lime glass. More modern silicon compounds such as silicon carbide form abrasives and high-strength ceramics. Silicon is the basis of the ubiquitous synthetic silicon-based polymers called silicones.

Elemental silicon also has a large impact on the modern world economy. Although most free silicon is used in the steel refining, aluminum-casting, and fine chemical industries (often to make fumed silica), the relatively small portion of very highly purified silicon that is used in semiconductor electronics (< 10%) is perhaps even more critical. Because of wide use of silicon in integrated circuits, the basis of most computers, a great deal of modern technology depends on it.

Phosphorus

Main article: Phosphorus

Phosphorus (symbol P) is a multivalent nonmetal of the nitrogen group, phosphorus as a mineral is almost always present in its maximally oxidized (pentavalent) state, as inorganic phosphate rocks. Elemental phosphorus exists in two major forms—white phosphorus and red phosphorus—but due to its high reactivity, phosphorus is never found as a free element on Earth.

The first form of elemental phosphorus to be produced (white phosphorus, in 1669) emits a faint glow upon exposure to oxygen – hence its name given from Greek mythology, Φωσφόρος meaning "light-bearer" (Latin: Lucifer), referring to the "Morning Star", the planet Venus. Although the term "phosphorescence", meaning glow after illumination, derives from this property of phosphorus, the glow of phosphorus originates from oxidation of the white (but not red) phosphorus and should be called chemiluminescence. It is also the lightest element to easily produce stable exceptions to the octet rule.

The vast majority of phosphorus compounds are consumed as fertilizers. Other applications include the role of organophosphorus compounds in detergents, pesticides and nerve agents and matches.

Sulfur

Main article: Sulfur

Sulfur (symbol S) is an abundant multivalent nonmetal, one of chalcogens. Under normal conditions, sulfur atoms form cyclic octatomic molecules with chemical formula S₈. Elemental sulfur is a bright yellow crystalline solid when at room temperature. Chemically, sulfur can react as either an oxidant or a reducing agent. It oxidizes most metals and several nonmetals, including carbon, which leads to its negative charge in most organosulfur compounds, but it reduces several strong oxidants, such as oxygen and fluorine.

In nature, sulfur can be found as the pure element and as sulfide and sulfate minerals. Elemental sulfur crystals are commonly sought after by mineral collectors for their brightly-colored polyhedron shapes. Being abundant in native form, sulfur was known in ancient times, mentioned for its uses in ancient Greece, China and Egypt. Sulfur fumes were used as fumigants, and sulfur-containing medicinal mixtures were used as balms and antiparasitics. Sulfur is referenced in the Bible as brimstone in English, with this name still used in several nonscientific terms. Sulfur was considered important enough to receive its own alchemical symbol. It was needed to make the best quality of black gunpowder, and the bright yellow powder was hypothesized by alchemists to contain some of the properties of gold, which they sought to synthesize from it. In 1777, Antoine Lavoisier helped convince the scientific community that sulfur was a basic element, rather than a compound.

Elemental sulfur was once extracted from salt domes, where it sometimes occurs in nearly pure form, but this method has been obsolete since the late 20th century. Today, almost all elemental sulfur is produced as a byproduct of removing sulfur-containing contaminants from natural gas and petroleum. The element's commercial uses are primarily in fertilizers, because of the relatively high requirement of plants for it, and in the manufacture of sulfuric acid, a primary industrial chemical. Other well-known uses for the element are in matches, insecticides and fungicides. Many sulfur compounds are odiferous, and the smell of odorized natural gas, skunk scent, grapefruit, and garlic is due to sulfur compounds. Hydrogen sulfide produced by living organisms imparts the characteristic odor to rotting eggs and other biological processes.

Chlorine

Main article: Chlorine

Chlorine (symbol Cl) is the second-lightest halogen. The element forms diatomic molecules under standard conditions, called dichlorine. It has the highest electron affinity and the one of highest electronegativity of all the elements; thus chlorine is a strong oxidizing agent.

The most common compound of chlorine, sodium chloride (table salt), has been known since ancient times; however, around 1630, chlorine gas was obtained by the Belgian chemist and physician Jan Baptist van Helmont. The synthesis and characterization of elemental chlorine occurred in 1774 by Swedish chemist Carl Wilhelm Scheele, who called it "dephlogisticated muriatic acid air", as he thought he synthesized the oxide obtained from the hydrochloric acid, because acids were thought at the time to necessarily contain oxygen. A number of chemists, including Claude Berthollet, suggested that Scheele's "dephlogisticated muriatic acid air" must be a combination of oxygen and the yet undiscovered element, and Scheele named the supposed new element within this oxide as muriaticum. The suggestion that this newly discovered gas was a simple element was made in 1809 by Joseph Louis Gay-Lussac and Louis-Jacques. This was confirmed in 1810 by Sir Humphry Davy, who named it chlorine, from the Greek word χλωρός (chlōros), meaning "green-yellow".

Chlorine is a component of many other compounds. It is the second most abundant halogen and 21st most abundant chemical element in Earth's crust. The great oxidizing power of chlorine led it to its bleaching and disinfectant uses, as well as being an essential reagent in the chemical industry. As a common disinfectant, chlorine compounds are used in swimming pools to keep them clean and sanitary. In the upper atmosphere, chlorine-containing molecules such as chlorofluorocarbons have been implicated in ozone depletion.

Argon

Main article: Argon

Argon (symbol Ar) is the third element in group 18, the noble gases. Argon is the third most common gas in the Earth's atmosphere, at 0.93%, making it more common than carbon dioxide. Nearly all of this argon is radiogenic argon-40 derived from the decay of potassium-40 in the Earth's crust. In the universe, argon-36 is by far the most common argon isotope, being the preferred argon isotope produced by stellar nucleosynthesis.

The name "argon" is derived from the Greek neuter adjective ἀργόν, meaning "lazy" or "the inactive one", as the element undergoes almost no chemical reactions. The complete octet (eight electrons) in the outer atomic shell makes argon stable and resistant to bonding with other elements. Its triple point temperature of 83.8058 K is a defining fixed point in the International Temperature Scale of 1990.

Argon is produced industrially by the fractional distillation of liquid air. Argon is mostly used as an inert shielding gas in welding and other high-temperature industrial processes where ordinarily non-reactive substances become reactive: for example, an argon atmosphere is used in graphite electric furnaces to prevent the graphite from burning. Argon gas also has uses in incandescent and fluorescent lighting, and other types of gas discharge tubes. Argon makes a distinctive blue–green gas laser.

Biological roles

Sodium is an essential element for all animals and some plants. In animals, sodium ions are used against potassium ions to build up charges on cell membranes, allowing transmission of nerve impulses when the charge is dissipated; it is therefore classified as a dietary inorganic macromineral.

Magnesium is the eleventh most abundant element by mass in the human body; its ions are essential to all living cells, where they play a major role in manipulating important biological polyphosphate compounds like ATP, DNA, and RNA. Hundreds of enzymes thus require magnesium ions to function. Magnesium is also the metallic ion at the center of chlorophyll, and is thus a common additive to fertilizers. Magnesium compounds are used medicinally as common laxatives, antacids (e.g., milk of magnesia), and in a number of situations where stabilization of abnormal nerve excitation and blood vessel spasm is required (e.g., to treat eclampsia).

Despite its prevalence in the environment, aluminium salts are not known to be used by any form of life. In keeping with its pervasiveness, it is well tolerated by plants and animals. Because of their prevalence, potential beneficial (or otherwise) biological roles of aluminium compounds are of continuing interest.

Silicon is an essential element in biology, although only tiny traces of it appear to be required by animals, though various sea sponges need silicon in order to have structure. It is much more important to the metabolism of plants, particularly many grasses, and silicic acid (a type of silica) forms the basis of the striking array of protective shells of the microscopic diatoms.

Phosphorus is essential for life. As phosphate, it is a component of DNA, RNA, ATP, and also the phospholipids that form all cell membranes. Demonstrating the link between phosphorus and life, elemental phosphorus was historically first isolated from human urine, and bone ash was an important early phosphate source. Phosphate minerals are fossils. Low phosphate levels are an important limit to growth in some aquatic systems. Today, the most important commercial use of phosphorus-based chemicals is the production of fertilizers, to replace the phosphorus that plants remove from the soil.

Sulfur is an essential element for all life, and is widely used in biochemical processes. In metabolic reactions, sulfur compounds serve as both fuels and respiratory (oxygen-replacing) materials for simple organisms. Sulfur in organic form is present in the vitamins biotin and thiamine, the latter being named for the Greek word for sulfur. Sulfur is an important part of many enzymes and in antioxidant molecules like glutathione and thioredoxin. Organically bonded sulfur is a component of all proteins, as the amino acids cysteine and methionine. Disulfide bonds are largely responsible for the mechanical strength and insolubility of the protein keratin, found in outer skin, hair, and feathers, and the element contributes to their pungent odor when burned.

Elemental chlorine is extremely dangerous and poisonous for all lifeforms, and is used as a pulmonary agent in chemical warfare; however, chlorine is necessary to most forms of life, including humans, in the form of chloride ions.

Argon has no biological role. Like any gas besides oxygen, argon is an asphyxiant.