QUANTUM STATE

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In quantum mechanics, the 'quantum state' of a system is a set of numbers that fully describe a quantum system. Since quantum theory is non-deterministic, these numbers only relate to the likely outcome of measuring a parameter of the system, such as its energy or angular momentum (see Measurement in quantum mechanics). These numbers are called the quantum numbers of the system.
In classical mechanics, a particle would be described in terms of its position and momentum. In quantum mechanics however, the position and momentum of a particle cannot be exactly measured, so instead, particles are described by a set of quantum numbers that are specific to the system being described. For example, in the case of a single particle in a one dimensional box, the state of a particle can be defined by a single quantum number related to the energy of this particle.
All experimental predictions are based on the quantum state of the system and the quantum operations acting on the state. A fully specified quantum state can be described by a ''state vector'', a wave function, or a complete set of quantum numbers for a specific system. A partially known quantum state, such as an ensemble with some quantum numbers fixed, can be described by a density matrix.

Contents

Conceptual description

The state of a physical system

Quantum states

Schrödinger picture vs. Heisenberg picture

Formalism in quantum physics

Bra-ket notation

Basis states

Superposition of states

Pure and mixed states

Mathematical formulation

Notes

See also

Further reading

Conceptual description

The state of a physical system

The 'state' of a physical system is a complete description of the parameters of the experiment.
To understand this rather abstract notion, it is useful to first explore it in an example from classical mechanics.
Consider an experiment with a (non-quantum) particle of mass $m=1$ which moves freely, and without friction,
in one spatial direction.
We start the experiment at time $t=0$ by pushing the particle with some speed into some direction.
Doing this, we determine the initial position $q$ and the initial momentum
$p$
of the particle. These 'initial conditions' are what characterizes the 'state'
$sigma$ of the system,
formally denoted as $sigma\; =\; (p,q)$. We say that we 'prepare the state' of the system
by fixing its initial conditions.
At a later time $t>0$, we conduct measurements on the particle.
The measurements we can perform on this simple
system are essentially its position $Q(t)$ at time $t$, its momentum $P(t)$,
and combinations of these.
Here $P(t)$ and $Q(t)$ refer to the measurable quantities ('observables')
of the system as such, not the specific results they produce in a certain run of the experiment.
However, knowing the state $sigma$ of the system, we can compute the
''value of the observables in the specific state'', i.e., the results that our measurements will produce,
depending on $p$ and $q$.
We denote these values as $langle\; P(t)$
angle _sigma and $langle\; Q(t)$
angle _sigma.
In our simple example, it is well known that the particle moves with constant velocity; therefore,
$$
langle P(t)
angle _sigma = p, quad
langle Q(t)
angle _sigma = pt+q.

Now suppose that we start the particle with a random initial position and momentum.
(For argument's sake, we may suppose that the particle is pushed away at $t=0$
by some apparatus which is controlled by a random number generator.)
The state $sigma$ of the system is now not described by two numbers
$p$ and $q$, but rather by two probability distributions.
The observables $P(t)$ and $Q(t)$ will produce random results now;
they become random variables, and their values in a single measurement cannot be predicted.
However, if we repeat the experiment sufficiently often,
always preparing the same state $sigma$, we can predict the 'expectation value'
of the observables (their statistical mean) in the state $sigma$. The expectation
value of $P(t)$ is again denoted by $langle\; P(t)$
angle _sigma, etc.
These "statistical" states of the system are called 'mixed states',
as opposed to the 'pure states' $sigma=(p,q)$ discussed further above.
Abstractly, mixed states arise as a statistical mixture of pure states.

Quantum states

In quantum systems, the conceptual distinction between observables and states persists just as described above.
The state $sigma$ of the system is fixed by the way the physicist prepares his experiment
(e.g., how he adjusts his particle source). As above, there is a distinction between pure states and
mixed states, the latter being statistical mixtures of the former.
However, some important differences arise in comparison with classical mechanics.
In quantum theory, ''even pure states show statistical behaviour''.
Regardless of how carefully we prepare the state $$
ho of the system,
measurement results are not repeatable in general, and we must understand the expectation value
$langle\; A$
angle _sigma of an observable $A$ as a statistical mean.
It is this mean that is predicted by physical theories.
For any fixed observable $A$, it is generally
possible to prepare a pure state $sigma\_A$ such that $A$ has a fixed
value in this state: If we repeat the experiment several times, each time
measuring $A$, we will always obtain the same measurement result,
without any random behaviour.
Such pure states $sigma\_A$ are called 'eigenstates' of $A$.
However, it is generally impossible to prepare a simultaneous eigenstate
for ''all'' observables. For example, we cannot prepare a state
such that both the position measurement $Q(t)$
and the momentum measurement $P(t)$
(at the same time $t$) produce "sharp" results;
at least one of them will exhibit random behaviour.
This is the content of the Heisenberg uncertainty relation.
Moreover, in contrast to classical mechanics, it is unavoidable that
''performing a measurement on the system changes its state''.
More precisely: After measuring an observable $A$,
the system will be in an eigenstate of $A$.
This expresses a kind of logical consistency: If we measure $A$ twice in the same
run of the experiment, the measurements being directly consecutive in time, then they will
produce the same results. This has some strange consequences however:
Consider two observables, $A$ and $B$, where $A$ corresponds
to a measurement earlier in time than $B$.
Suppose that the system is in an eigenstate of $B$.
If we measure only $B$, we will not notice statistical behaviour.
If we measure first $A$ and then $B$ in the same run of the experiment,
the system will transfer to an eigenstate of $A$ after the first measurement,
and we will generally notice that the results of $B$ are statistical.
Thus, ''quantum mechanical measurements influence one another'', and it is important
in which order they are performed.
Another feature of quantum states becomes relevant if we consider a physical system that
consists of multiple subsystems; for example, an experiment with two particles rather than one.
Quantum physics allows for certain states, called 'entangled states',
that show certain statistical correlations between measurements on the two particles
which cannot be explained by classical theory. For details, see entanglement.
These entangled states lead to experimentally testable properties (Bell's theorem)
that allow to distinguish between quantum theory and alternative classical (non-quantum) models.

Schrödinger picture vs. Heisenberg picture

In the discussion above, we have taken the observables $P(t)$, $Q(t)$
to be dependent on time, while the state $sigma$ was fixed once at the beginning of the experiment.
This approach is called the 'Heisenberg picture'. One can, equivalently, treat the observables as fixed,
while the state of the system depends on time; that is known as the 'Schrödinger picture'.
Conceptually (and mathematically), both approaches are equivalent; choosing one of them is a matter of convention.
Both viewpoints are used in quantum theory. While non-relativistic quantum mechanics is usually formulated
in terms of the Schrödinger picture, the Heisenberg picture is often preferred in a relativistic context,
that is, for quantum field theory.

Formalism in quantum physics

Bra-ket notation

Paul Dirac invented a powerful and intuitive notation to describe quantum states, known as bra-ket notation. For instance, one can refer to an |''excited atom''> or to $|!!uparrow$
angle for a spin-up particle, hiding the underlying complexity of the mathematical description, which is revealed when the state is ''projected'' onto a coordinate basis. For instance, the simple notation |1s> describes the first hydrogen atom bound state, but becomes a complicated function in terms of Laguerre polynomials and spherical harmonics when projected onto the basis of position vectors |'r'>. The resulting expression ''Ψ''('r')=<'r'|1s>, which is known as the wave function, is a special representation of the quantum state, namely, its projection into position space. Other representations, such as projection into momentum space, are possible. The various representations are simply different expressions of a single physical 'quantum state'.

Basis states

Any quantum state $|psi$
angle can be expressed in terms of a sum of ''basis states'' (also called ''basis kets'') $|k\_i$
angle in the form
:$|\; psi$
angle = sum_i c_i | k_i
angle
where $c\_i$ are the coefficients representing the probability amplitude, such that the absolute square of the probability amplitude, $left\; |\; c\_i$
ight | ^2 is the probability of a measurement in terms of the basis states yielding the state $|k\_i$
angle. The normalization condition mandates that the total sum of probabilities is equal to one,
:$sum\_i\; left\; |\; c\_i$
ight | ^2 = 1.
The simplest understanding of basis states is obtained by examining the quantum harmonic oscillator. In this system, each basis state $|n$
angle has an energy
ight). The set of basis states can be extracted using a construction operator $hat\{a\}^\{dagger\}$ and a destruction operator $hat\{a\}$ in what is called the ladder operator method.

Superposition of states

If a quantum mechanical state $|psi$
angle can be reached by more than one path, then $|psi$
angle is said to be a linear superposition of states. In the case of two paths, if the states after passing through path and path are
:
angle = egin{matrix}rac{1}{sqrt{2}}end{matrix} |0
angle + egin{matrix}rac{1}{sqrt{2}}end{matrix} |1
angle, and
:
angle = egin{matrix}rac{1}{sqrt{2}}end{matrix} |0
angle - egin{matrix}rac{1}{sqrt{2}}end{matrix} |1
angle,
then $|psi$
angle is defined as the normalized linear sum of these two states. If the two paths are equally likely, this yields
:$|psi$
angle = egin{matrix}rac{1}{sqrt{2}}end{matrix}|lpha
angle + egin{matrix}rac{1}{sqrt{2}}end{matrix}|eta
angle = egin{matrix}rac{1}{sqrt{2}}end{matrix}(egin{matrix}rac{1}{sqrt{2}}end{matrix}|0
angle + egin{matrix}rac{1}{sqrt{2}}end{matrix}|1
angle) + egin{matrix}rac{1}{sqrt{2}}end{matrix}(egin{matrix}rac{1}{sqrt{2}}end{matrix}|0
angle - egin{matrix}rac{1}{sqrt{2}}end{matrix}|1
angle) = |0
angle.
Note that in the states
angle and
angle, the two states $|0$
angle and $|1$
angle each have a probability of as obtained by the absolute square of the probability amplitudes, which are and In a superposition, it is the probability amplitudes which add, and not the probabilities themselves. The pattern which results from a superposition is often called an interference pattern. In the above case, $|0$
angle is said to constructively interfere, and $|1$
angle is said to destructively interfere.
For more about superposition of states, see the double-slit experiment.

Pure and mixed states

A ''pure quantum state'' is a state which can be described by a single ket vector, or as a sum of basis states. A ''mixed quantum state'' is a statistical distribution of pure states.
The expectation value $langle\; a$
angle of a measurement $A$ on a pure quantum state is given by
:$langle\; a$
angle = langle psi | A | psi
angle = sum_i a_i langle psi | lpha_i
angle langle lpha_i | psi
angle = sum_i a_i | langle lpha_i | psi
angle |^2 = sum_i a_i P(lpha_i)
where
angle are basis kets for the operator $A$, and is the probability of $|\; psi$
angle being measured in state
angle.
In order to describe a statistical distribution of pure states, or ''mixed state'', the density matrix (or density operator), $$
ho, is used. This extends quantum mechanics to quantum statistical mechanics. The density operator is defined as
:$$
ho = sum_s p_s | psi_s
angle langle psi_s |
where $p\_s$ is the fraction of each ensemble in pure state $|psi\_s$
angle. The ensemble average of a measurement $A$ on a mixed state is given by
:$left\; [\; A$
ight ] = langle overline{A}
angle = sum_s p_s langle psi_s | A | psi_s
angle = sum_s sum_i p_s a_i | langle lpha_i | psi_s
angle |^2 = tr(
ho A)
where it is important to note that two types of averaging are occurring, one being a quantum average over the basis kets of the pure states, and the other being a statistical average over the ensemble of pure states.

Mathematical formulation

For a mathematical discussion on states as functionals, see Gelfand-Naimark-Segal construction. There, the same objects are described in a C
★ -algebraic context.

Notes

# If you are not familiar with the concept of momentum, think of it as being the velocity of the particle. That is fully justified in this context.
# To avoid misunderstandings: Here we mean that $Q(t)$ and $P(t)$ are measured in the same state, but ''not'' in the same run of the experiment.)
# For concreteness' sake, you may suppose that $A=Q(t\_1)$ and $B=P(t\_2)$ in the above example, with $t\_2>t\_1>0$.

See also

★ Quantum harmonic oscillator

★ Bra-ket notation

★ Orthonormal basis

★ Wave function

★ Probability amplitude

★ Density matrix

★ Qubit

Further reading

The concept of quantum states, in particular the content of the section Formalism in quantum physics above, is covered in most standard textbooks on quantum mechanics.
For a discussion of conceptual aspects and a comparison with classical states, see:

★ Lectures on Quantum Theory: Mathematical and Structural Foundations, , Chris J, Isham, Imperial College Press, ,
For a more detailed coverage of mathematical aspects, see:

★ Operator Algebras and Quantum Statistical Mechanics 1, , Ola, Bratteli, Springer, , 2nd edition In particular, see Sec. 2.3.