1. Introduction
In quantum field theory, field commutators vanish outside the light cone, as expected from relativistic causality considerations [
1]. However, it is well known that vacuum field correlations in general do not vanish for space-like separations; this is not in contradiction with relativistic causality since a nonvanishing field correlation function does not allow the possibility of a superluminal transmission of information [
2,
3,
4,
5,
6].
The fact that quantum vacuum fluctuations, for example in the case of the electromagnetic field, possess nonvanishing correlations between spacetime points separated by a space-like interval can, however, have profound conceptual implications and physical consequences. Examples are inducing correlations between quantum objects in causally disconnected regions of spacetime [
3,
7] and determining radiation-mediated (van der Waals and Casimir-Polder) interactions between atoms [
8,
9,
10,
11,
12], even in dynamical (time-dependent) conditions [
13]. Dispersion interactions are thus an indirect evidence of the existence of vacuum fluctuation and of their spectral and spatial correlation features. Direct measurements of the vacuum fluctuations of the quantum electric field have been reported, as well as their dependence on the space-time volume sampled [
14].
Recently, some experiments have been able to demonstrate the existence of vacuum field correlations between non-causally connected space-time points, exploiting electro-optic sampling [
7,
15]. Previous theoretical achievements on vacuum fluctuations and their spatial correlations, and the experimental possibility of proving their existence, make it very important to analyze in detail their properties and physical consequences, as well as their relevance on observable physical effects. Very recently, the possibility of experimentally probing and individually separating vacuum field fluctuations and source radiation contributions exploiting electro-optic sampling has been also proposed [
16].
The experimental results and theoretical proposals above are currently giving a strong theoretical and experimental boost and relevance to studying the physical features of vacuum field correlations, including their nonlocality, in both stationary and nonstationary conditions, as well as their effects on different quantum systems and observable quantities.
The existence of zero-point field fluctuations is one of the most prominent predictions of the quantum theory of the electromagnetic field, and quantum fields in general; even in the ground state of the free field, the electric and magnetic fields fluctuate around their vanishing average value, as a consequence of the Heisenberg uncertainty principle resulting from the noncommutativity of components of the electric and magnetic field operators [
17]. These fluctuations are at the origin of many important observable effects, such as the spontaneous decay of an excited atom in vacuum, the Lamb shift, and the Casimir and Casimir–Polder forces between neutral objects in vacuum [
11,
17,
18,
19,
20].
In this paper, we review relevant properties of the electromagnetic and scalar field vacuum fluctuations, both in the vacuum and in the presence of field sources. We consider both equilibrium and nonequilibrium conditions. Specifically, we investigate and review their space-time correlations in both static and dynamical conditions, their role in static and dynamical radiation-mediated effects such as two- and many-body dispersion interactions (van der Waals and Casimir–Polder), as well as their nonlocal properties and consequent relation with entanglement between field and matter observables [
8,
9,
13,
21,
22,
23,
24,
25].
This paper is organized as follows. In
Section 2, we first introduce the equal-time vacuum field correlations in the field ground state, both for the massless scalar field and the electromagnetic field, stressing their nonlocal features. We then discuss how they are modified by the presence of a polarizable body such as a ground- or excited-state atom, considering a stationary configuration. In
Section 3, we investigate how Casimir–Polder dispersion interactions between two or three atoms give an indirect evidence of the nonlocal features of the spatial field correlations. In
Section 4, we consider nonstationary cases, when the interacting system starts from a nonequilibrium configuration, discussing in detail the time evolution of the nonlocal spatial correlations of the electric field. We then investigate how this leads to dynamical three-body Casimir–Polder interactions, both in the case of three bare ground-state atoms and when one of the three atoms is initially in a bare excited state.
Section 5 is devoted to our conclusive remarks.
2. Stationary Vacuum Field Correlations
We first discuss the vacuum field correlations for the massless relativistic scalar field and for the electromagnetic field, in a stationary case, specifically the vacuum state. Let us first consider a massless real scalar field; the field operator is given by [
26]
where
,
V is the quantization volume, the annihilation and creation operators
and
satisfy the usual bosonic commutation rules, and periodic boundary conditions are used. We have
, where
is the vacuum state of the field defined as
for all
. The equal-time vacuum correlation function is easily obtained as
In the continuum limit,
,
, Equation (
2) becomes
where an exponential regularization factor
, with
, has been introduced. After the integration over
k, taking
, we have (for
)
This relation shows the existence of nonlocal spatial field correlations outside the light cone, as well as a divergence on the light cone (even if Equation (
4) is an equal-time correlation function, it can be easily extended to the general case).
Similar considerations hold for the electromagnetic field, that is the main point of this paper. We are mainly interested to the nonrelativistic quantum electrodynamical case, and in this case it is convenient to work in the Coulomb gauge,
. The expressions of the vector potential, electric field and magnetic field operators are (Gauss units) [
17]
where
is a unit vector along the direction of the wavevector
,
(
) are polarization unit vectors, assumed real, and
.
In the vacuum state, defined by
for any
, we have
,
, and the vacuum equal-time correlation function for the Fourier components of the (transverse) electric field is easily found as
where
and from now on the Einstein’s convention of repeated indices is used. For the sum over the polarizations, we have used
In the continuum limit,
,
, after integration over
, we obtain the equal-time vacuum spatial correlation for the components of the electric field
where
is a component of the unit vector
.
Similarly to the massless scalar field case, Equation (
8) shows that vacuum fluctuations of the electric field have nonlocal spatial correlations (i.e., they do not vanish outside the light cone) [
3,
27].
There are also vacuum nonlocal correlations between components of the magnetic field, as well as between components of the electric and magnetic fields. For the magnetic-magnetic correlation, we have
where, for the sum over the polarizations, we have used
Equation (
9), after summation over
in the continuum limit gives, for the spatial correlation of the magnetic field, the same expression (
8) for the electric field case
Finally, for the electric-magnetic case we obtain
where for the sum over polarizations we have used
and
is the totally antisymmetric Levi–Civita symbol [
19]. Analogously,
In the continuum limit, the angular
integration of (
12) yields
that is purely imaginary [
27]. The electric–magnetic correlation function (
14), after polarization sum and angular integration, yields the same expression of the first one, Equation (
15), but with the opposite sign. Therefore the symmetrized e-m vacuum correlation function vanishes.
In the next section, we will discuss the deep relation between vacuum field correlation functions, also in the presence of field sources or in dynamical situations, with van der Waals and Casimir–Polder interactions between atoms or in general electrically and magnetically polarizable bodies.
Spatial field correlations are modified by the presence of boundary conditions [
28,
29] or field sources, an atom or a polarizable body for example [
21,
22]. In the latter case, we speak of dressed spatial field correlations. Let us assume that an atom A is placed at
, and
is its dipole moment operator. The Hamiltonian of the system, in the multipolar coupling scheme and within the dipole approximation, is
where
and
are, respectively, the free atom and the free field Hamiltonians,
is the dipole moment operator of the atom A and
is the electric field operator evaluated at the position
of the atom (it is indeed the transverse displacement field, that outside the field source coincides with the total electric field) [
11,
17,
30,
31,
32]. We just mention that also macroscopic boundary condition yield changes to the spatial correlations of the electromagnetic field and related physical phenomena [
28,
29,
32,
33,
34]. Very recently, spatial field correlations of the massless scalar field between points at the opposite side of a movable perfect mirror (thus subjected to quantum fluctuations of its position) have been investigated [
35].
Due to the atom-field interaction, the non-interacting ground state
, where
indicates the ground state of the atom A and
the vacuum field state, is not an eigenstate of the total Hamiltonian
H. At the second order in the atom-field coupling, the true (interacting) ground state
of the system can be obtained by time-independent perturbation theory in the form [
8,
12,
22]
where
and
are eigenstates of
in the form of a tensor product of the atomic state
n and one- and two-photon Fock states, respectively; also,
is a normalization factor. In the above equations,
m,
n indicate a complete set of atomic states,
are the matrix elements of the electric dipole moment operator of atom A, and
are atomic transition frequencies from the ground state. Equation (
17) shows that the dressed ground state is not separable in the atom and field space state, and the atom is surrounded by a cloud of virtual photons [
36,
37]. A similar situation occurs for a physical nucleon where, in the framework of generalized parton distributions, the bare nucleon is surrounded by a cloud of virtual mesons, and an expression analogous to (
17) is indeed obtained [
38].
We can now evaluate the equal-time correlation function between modes of the electric field [
22]
where c.c. stands for the complex conjugate and, for the sake of simplicity, without loss of generality, we have assumed that the dipole matrix elements are real, that is
.
The first term in the RHS of (
19), apart from the polarization sum, is essentially the same in (
6), which is the
bare correlation function, while the second term gives the contribution due to the presence of atom A, yielding the
dressed correlation function. Equation (
19) shows that in the presence of an atom, contrarily to the bare vacuum case, also different field modes become correlated. In the next section, we will discuss in detail the importance of this point in the non-additive three-body van der Waals and Casimir–Polder dispersion interaction between ground state atoms [
21,
22,
23].
Summation of (
19) over the field modes yields the dressed spatial correlation function of the complete electric field at two different points of space and equal time:
where the first term is the same given in Equation (
8), that is the bare correlation function, and the second term is the (dressing) correction due to the presence of the ground-state atom A. The latter term involves polarization sum (see (
7)) and angular integrations that can be easily performed using
where we have defined the following differential operator:
and the apex
R indicates the coordinate with respect to which the derivatives are taken. After straightforward algebra, we obtain the second term in (
20) at the second order in the atom–field coupling in the form of a double frequency integration:
where
and
. Performing first the integration over
and then that over
, we finally obtain
where
is the auxiliary function of the sine and cosine integral functions,
and
, respectively [
39]. Equation (
24) shows that the dressing part of the correlation function is monotonically decreasing with the distance, with a characteristic distance scale given by
. Asymptotically, for
, we have
[
39]. Thus, Equation (
24) asymptotically scales with the inverse seventh power of the distance from the atom A; this
distance scaling should be compared with the
scaling of the bare vacuum fluctuations in (
8). In the next section, we will discuss the relevance of this property for the non-additive three-body Casimir–Polder interaction between ground-state atoms or molecules in the far-zone (retarded) regime.
Equations (
17)–(
19) have been obtained for a ground-state atom. If we consider the case of an atom in one of its excited states, in the continuum limit there is an extra contribution from the frequency integrations due to the resonance pole [
23]. In this case, for simplicity we consider a two-level atom with transition frequency
, located at
, and interacting with the quantum electromagnetic field through the Hamiltonian (
16).
and
indicate the ground and excited state of atom A, with energy
and
, respectively. The bare excited state is then
. We assume to consider timescales shorter than the lifetime of the excited state, and thus we neglect the spontaneous decay of the atom. The second-order interacting excited state is then [
8,
23]
where
is a normalization factor. The presence of a pole at
, related to the possibility of a real transition from the excited to the ground state, should be noted; we will see that its presence has important consequences on the spatial correlations of the field and on the three-body Casimir–Polder interaction when an excited atom is involved.
Analogously to the ground-state case, we can now evaluate the spatial correlation function relative to two modes of the electric field on the dressed state (
25), and we obtain, up to the second order in the atom-field coupling (we are assuming that the matrix elements
are real) [
23]
With a procedure analogous to the previous ground-state case we can now obtain, in the continuum limit, the following expression for the spatial correlation function of the complete electric field
where
is the bare spatial correlation (
8) and the dressing correlation
has a structure analogous to that of the ground-state case previously considered. The main difference is the presence of a pole at
in the frequency integration path, as it is evident from Equation (
26), yielding a resonant contribution to the correlation function. The final result is [
23]
where PV indicates the Principal Value of the integral. This equation contains two terms. Comparison of (
27) with (
24) shows that the first term has a similar structure as in the case of the ground state and includes contributions from all field modes; the second term in (
27) is a new one, originating from the resonant pole at
and shows spatial oscillations with a scale given by
[
23].
4. Dressed Dynamical Field Correlations and Dynamical Three-Body Casimir–Polder Forces
The considerations on dressed field correlations in the previous sections refer to static (time-independent) situations. Also, the case with one excited atom was considered for short times, so that its spontaneous decay can be neglected. In this section, we will address dynamical nonstationary situations, when the system starts from a nonequilibrium configuration. We will address relevant aspects of the building up in time of nonlocal spatial field correlations, as well as dynamical time-dependent three-body Casimir–Polder interactions. We will show that relevant nonlocal features appear in the time evolution and build-up of the field spatial correlations, and how they manifest in the consequent time-dependent dispersion (van der Waals and Casimir–Polder) interactions between three (or more) atoms. This suggests that dynamical dispersion interactions could provide a way to probe these nonlocal nonequilibrium field correlations, similarly to the stationary case of previous section.
We first concentrate on the nonstationary spatial field correlations when an atom (A) is present, in both cases of an initially bare ground-state atom and an initially bare excited-state atom. In such cases, the initial state at
is a nonequilibrium state, being an eigenstate of the unperturbed Hamiltonian and not of the total Hamiltonian: thus, they will evolve in time. The atom–field Hamiltonian is given by (
16).
4.1. Dynamical Ground-State Correlations
We consider an atom A interacting with the quantum electromagnetic field via the dipolar interaction Hamiltonian (
16). We assume that at
the system is prepared in the noninteracting (bare) ground state
, where
is the ground state of the atom and
is the photon vacuum. Differently from
Section 2, here we use a time-dependent approach in order to study the time evolution of the correlation function starting from our nonequilibrium initial state. We work in the Heisenberg representation, and solve by iteration up to the second order the Heisenberg equations for the field operators
where the apex indicates the perturbative order. From the explicit iterative solution (
37) we can obtain the corresponding iterative solution for the electric field operator in the Heisenberg representation [
24,
50]
that we will exploit to obtain the equal-time electric-field spatial correlations in a two-level approximation for the atom, that is
. Here,
,
and
are the pseudospin operators for atom A. Also,
are the matrix elements of the atomic electric dipole operator between the excited state
and the ground state
, with energy
and
, respectively. We will, however, assume, as before, that the dipole matrix elements are real, so that
, In the pseudospin formalism, the atomic Hamiltonian is
, where
.
Writing down the Heisenberg equations of motion for the field and atomic operators and solving them up to the second order in the atom-field coupling, we can finally obtain an explicit expression of the two-mode correlation function of the electric field operator in the initial bare ground state
[
24]
where
ℜ stands for the real part and we have defined the function
Equation (
39) clearly shows that different field modes, initially uncorrelated, acquire with time a correlation consequent to their mutual interaction with the atom (contrarily to the case of the field bare vacuum).
We also obtain the two-point and equal-time nonstationary spatial correlation function for the complete electric field, given by
(first-order terms vanish) [
8,
50]. After some lengthy algebraic calculations, we find the following expressions of the single terms in (
41)
where
,
, and
is the Heaviside step function [
24]. Also,
is the differential operator defined in (
22).
The first term in (
41), explicitly given in the first line of (
42), coincides with the time-independent correlation in the bare ground state, as discussed in
Section 2 (see Equation (
8)); all other terms in (
41) and (
42) describe the time evolution of the correlation function during the dynamical self-dressing process of the atom, and are a main object of investigation in this section.
Some intriguing physical considerations are made in order to physically understand the behavior of the dynamical spatial correlations we have obtained. For the sake of clarity, we separately consider the various contributions in the expressions above.
The second contribution in (
41) and (
42) is the product of the retarded dipole fields from atom A in points
and
(the operator
in (
38)) [
50]; the presence of the two
functions expresses that this contribution to spatial correlation vanishes outside the light cone centered on atom A: it is different from zero only if both points
and
are inside the causality sphere of A, in full agreement with relativistic causality. However, since
can be larger than
even if both
and
are smaller than
, the correlation can be nonvanishing even for two points
r and
that are not causally connected each other; this peculiar behavior is possible because the fields in both points are causally connected with the “source” atom A. This behavior clearly shows a nonlocal feature of dynamical spatial field correlations during the atomic dressing.
The contribution of the other terms in (
41) and (
42), involving the zeroth- and second-order electric field operators, shows a quite different and peculiar behavior. It is different from zero even if just one of the two points
and
is inside the causality sphere of atom A, notwithstanding the other point can be outside of it. Mathematically, this is related to the fact that this term arises from a product of the second-order field generated by atom A (the operator
in (
38)) and the free field (the operator
in (
38)): the first one is causally connected with A while the second one is source independent (i.e., it is the free field at time
t). In other words, this contribution to the spatial correlation function at a generic time
t, can be nonvanishing even for points separated by a space-like interval, provided at least one of them is inside the causality sphere of A.
We can conclude that nonstationary field correlations, during the evolution of the atom-field system starting from our nonequilibrium configuration at , have peculiar nonlocal features. An important point, in our opinion, is understanding whether such nonlocal features can manifest or be observed, at least indirectly, in observable physical quantities. In the next section, we will show how these nonlocal features can indeed manifest in the dynamical three-body Casimir–Polder dispersion interactions between atoms or, in general, polarizable bodies.
4.2. Dynamical Excited-State Correlations
We now investigate the case when atom A, approximated as a two-level system, is initially in its bare excited state , with field in its bare vacuum state . Also in this case the initial state is a nonequilibrium state, and we expect a dynamical change of the spatial correlation function of the electric field; moreover, new aspects should appear with respect to the ground-state case, due to resonance effects related to the possibility of emission of a real photon. The calculation proceeds similarly to the ground-state case of the previous subsection, using the same iterative-solution method for the Heisenberg equations of motion of the field and atom operators, and then evaluating the electric-field spatial correlation in the bare excited state of atom A and the field vacuum state, . We consider time shorter than the lifetime of the excited state and thus we can neglect its spontaneous decay; however, contrarily to the ground-state case, a resonance pole in the frequency integrations is present in this case, yielding a new contribution to the correlation function.
After lengthy algebraic calculations, we obtain that the spatial correlation function of the electric field can indeed be separated in two contributions, a resonant one and a nonresonant one,
The nonresonant term is found to be the same of that for the ground-state atom, Equations (
41) and (
42), with an opposite sign, that is
. The resonant term, resulting from the pole at
, is given by [
24]
For the nonresonant contribution, the same physical considerations about its nonlocal features given in the previous subsection for the ground-state case apply, in particular that it is in general different from zero if one of the two points is inside the causality sphere of A, even if the other point is outside the causality sphere. In other words, the presence of the excited atom manifests itself in the two-point spatial correlation even if one point is outside the causality sphere of A, provided the other point is inside, and whatever the distance between the two points is. The resonant contribution (
44) shows, as expected, oscillations in space with a scale given by the atomic transition wavelength
; it is not vanishing provided both points are causally connected with the atom A, that is if
, even in the case they are not causally connected with each other (that is,
).
We wish to stress that the nonlocal features of the dynamical spatial correlations we have discussed in this section are totally consistent with relativistic causality, of course, because correlations cannot transport information.
4.3. Dynamical Three-Body Casimir–Polder Interactions
In this subsection, we briefly analyze some consequence of the nonlocal character of the dynamical field correlations investigated in the previous subsections, specifically in dynamical Casimir–Polder three-body interactions, extending the stationary case of the previous section to nonstationary situations.
Our starting point is the relation between the spatial correlations of a quantum field, specifically of the electric field, and the dispersive two- and three-body Casimir–Polder forces, as discussed in
Section 3. Here, we mainly consider three-body interactions in nonstationary conditions, both in the case of three bare ground-state atoms and in the case of one bare excited atom and two ground-state atoms; we thus extend our methods and results for stationary three-body interactions, presented in
Section 3, to the dynamical case, on the basis of the dynamical dressed field correlations obtained in the previous subsections.
We assume to have one atom (A) in and two other ground-state atoms (B and C) in and . We consider both cases of atom A initially in its bare ground state and in its bare excited state.
We first consider the case of atom A initially
in its bare ground state and the field in the vacuum state. As already mentioned, this is a nonstationary condition, because bare states are not eigenstates of the complete Hamiltonian. We start evaluating the interaction energy between atoms B and C during the self-dressing of atom A assuming, as mentioned, the state of the interacting system field-(atom A) in the nonequilibrium bare state
. We evaluate this interaction energy exploiting the expression (
34), extended to the present nonstationary situation by substituting the two-mode correlation function of the electric field with its time-dependent expression, Equation (
39). After lengthy algebraic calculations, we can obtain the explicit analytical expression of the dynamical interaction energy, that at a generic time
is given by [
13]
where
is the function giving the sign of the variable
x,
is the Heaviside step function and
,
,
are the distances between the atoms defined in
Section 3.2.
Several physical considerations relevant to nonlocality and causality can be made starting from (
45), in different specific situations.
Let us first assume that both atoms B and C are inside the causality sphere of A. In such a case, it is possible to show from (
45) that, after a transient period when the interaction energy is time-dependent, it settles to a stationary value [
13], that coincides with that found with the time-independent approach of
Section 3.2. This also shows the self-consistency of our time-dependent approach.
A remarkable and unexpected result is when at least one of the two atoms B and C is outside the light-cone of A, i.e., when
and/or
; evaluating (
45) in this case it follows that
can be nonvanishing, and that the interaction between B and C can be affected by A, clearly showing a nonlocal behavior of the three-body dispersion energy due to the nonlocality of the dynamical correlation function of the electric field; more details on the ranges of the relevant parameters
,
,
t in which this occurs can be found in [
13].
A relevant quantity worth of investigation is the symmetrized dynamical interaction energy, given by
where the role of the three atoms is exchanged in the symmetrization (for a more detailed discussion of the difference between the time-dependent interaction energies (
45) and (
46), in particular in relation with their measurement, see [
51]). Its expression can be directly obtained from (
45). We will discuss here only its main features relevant to the indirect manifestation of the nonlocality of dressed field correlations in three-body dispersion interactions, aspect we are mainly interested to.
Firstly, after a transient, it is possible to show that the dynamical interaction energy (
46) settles to its stationary equilibrium value (similarly to (
45)), as given by (
36) or by a direct sixth-order perturbative calculation [
11,
44,
45,
47].
Secondly, although (
46) vanishes if each atom is outside the causality sphere of the other two, i.e.,
, it nevertheless shows relevant nonlocal aspects: for example, for times such that one atom (A, for example) is not causally connected with the other two atoms (B and C), while B and C are causally connected to each other, situation represented by the conditions
,
,
, the dynamical three-body interaction (
45) is not vanishing. In other word, this observable interaction energy manifests a nonlocal behavior, ultimately related to the nonlocal features of the dynamical spatial correlations of the electric field, since it is not vanishing even if one atom is outside the causality sphere of the other two [
13,
51].
Similar considerations can be made in the nonstationary case in which one of the three atoms (A) is initially in its bare excited state with the field in its vacuum state, using the dynamical excited state field correlations given in (
43). In this case, the main difference with the previous case is the presence of the resonant term (
44) in the spatial correlation function of the electric field. This extra term finally yields the following additional contribution to the dynamical three-body interaction energy [
24]:
where the same notation of the previous cases have been used. The resonant contribution (
47) at time
t is not vanishing only if both atoms B and C are inside the light cone of A, i.e.,
and
even if they can be causally disconnected each other, for example if
, showing also in this case some nonlocal aspect of the resonant term of the interaction energy.
Finally, we wish to mention that similar considerations about the nonlocal features of the three-body component of the dynamical dispersion interaction between three atoms can be obtained by evaluating them exploring effective Hamiltonians [
40,
49], as discussed in detail in [
13,
24,
51] also with reference to the measurement of the three-body component of dispersion interactions which involves the overall system and thus it is intrinsically nonlocal.