The interaction between a coherently oscillating radiation field, such as is generally encountered in micro-wave experiments, and a number of similar atomic systems coupled to the field through their electric dipole moments is analyzed for the case of resonance between atomic system and field, with both the field and molecules treated quantum-mechanically. Expressions are derived for the expectation value of field strength and the energy, and comparison between the two makes it possible to distinguish between coherent and incoherent parts of the energy, the former having its counterpart in the expectation value of the field strength, while the latter has no such counterpart. Terms corresponding to induced and spontaneous emission are identified, and it is shown that the latter includes both coherent and incoherent components. Special situations related to masers and to the coherence of spontaneous radiation are discussed. The distinction between the behavior of correlated and uncorrelated states is examined, and it is shown that both the coherent emission from uncorrelated states and the incoherent emission from correlated states may be proportional to the square of the number of molecules. The phase of the field is predictable for the coherent emission but unpredictable for the incoherent emission.
The interaction between a coherently oscillating radiation field, such as is generally encountered in micro-wave experiments, and a number of similar atomic systems coupled to the field through their electric dipole moments is analyzed for the case of resonance between atomic system and field, with both the field and molecules treated quantum-mechanically. Expressions are derived for the expectation value of field strength and the energy, and comparison between the two makes it possible to distinguish between coherent and incoherent parts of the energy, the former having its counterpart in the expectation value of the field strength, while the latter has no such counterpart. Terms corresponding to induced and spontaneous emission are identified, and it is shown that the latter includes both coherent and incoherent components. Special situations related to masers and to the coherence of spontaneous radiation are discussed. The distinction between the behavior of correlated and uncorrelated states is examined, and it is shown that both the coherent emission from uncorrelated states and the incoherent emission from correlated states may be proportional to the square of the number of molecules. The phase of the field is predictable for the coherent emission but unpredictable for the incoherent emission.
The interaction between the electromagnetic field and a number of identical atomic systems, individually characterized by an electric dipole moment and two energy levels, is analyzed for the case where the atomic systems are inside a lossy cavity and exposed to a coherent driving field, resonance being assumed between atomic system, cavity, and driving field.The problem of introducing loss into a quantum-mechanical formalism is treated first. Formal operator expressions are obtained for the field variables which include the absorption and the fluctuation (both thermal and quantum-mechanical) effects of the loss mechanism. Expectation values are then obtained for the field strength and the field energy which are valid for times short compared to the lifetime of the excited state. It is shown that the spontaneous-emission energy in the field increases initially as the square of the time and approaches a steady-state value after a transient period which is of the order of the cavity relaxation time. The induced emission contains two parts: incoherent emission induced by the thermal field, and coherent emission induced by the driving field. The incoherent induced-emission energy has the same time dependence as the spontaneous-emission energy, and the ratio of the former to the latter is the number of photons in the thermal (inducing) field. The coherent induced-emission energy does not approach a steady-state value, but, after a transient period, increases linearly with the time. The ratio of the coherent induced-emission energy to the spontaneous-emission energy is equal, initially, to the number of photons in the driving-field energy, but becomes $\ensuremath{\beta}t$ times as large after the transient period, where $\ensuremath{\beta}$ is the reciprocal of the cavity relaxation time.The expectation value of the rate of energy emission by the atomic systems is also obtained. It is shown that the ratio of the downward to the upward transition probabilities has the well-known value of n(n+1), where n is the field energy in units of the photon energy, only in the absence of a coherent field.
The theory developed in the first two articles of this series, dealing with the interaction between the electromagnetic field in a cavity resonator and a number of two-level molecules, is generalized to include a Gaussian spread in the molecular frequency. The center of the molecular frequency distribution coincides with the cavity resonant frequency. There is a coherent driving field in the cavity at the same frequency, and cavity loss is taken into account.Using the formalism previously developed for a quantum-mechanical field in a lossy cavity, expressions are obtained by means of second-order perturbation theory for the expectation values of the field strength and field energy in the cavity, and of the power loss by the molecules. It is shown that the parts of the field energy resulting from induced and spontaneous emission, respectively, initially increase as the square of the time and approach steady-state values after (different, in general) transient periods, each of which is determined by two time constants: cavity relaxation time and inverse molecular frequency spread.It is also shown that both the induced and spontaneous emission power radiated by the molecules increase initially linearly with the time and approach steady-state values after transient periods. For the induced emission power, the transient period is determined by only one time constant, the inverse molecular frequency spread, while for the spontaneous emission power it is determined both by the inverse molecular frequency spread and the cavity relaxation time. The ratio of induced to spontaneous emission is initially n, and approaches a steady-state value $n{[\mathrm{exp}({r}^{2})(1\ensuremath{-}\mathrm{erf}r)]}^{\ensuremath{-}1},$ where n is the driving field energy in units of the photon energy, and r is the ratio of the cavity resonance width to molecular frequency spread. The seeming inconsistency of this value with the classical value of the ratio of the Einstein coefficients is discussed.
In the previous articles of this series, dealing with the interaction between a number of molecules and the electromagnetic field in a resonant cavity, both the molecules and the field were treated by perturbation theory. The perturbation restriction on the field is removed in the present article, allowing large changes in the field, but the molecules are still assumed to undergo a small change during the time under consideration. The justification for this type of analysis, involving the generalization of the conventional concepts of induced and spontaneous emission, the applicability to a molecular amplifier during the buildup period, and the re-examination of a calculation by Serber and Townes concerning the fundamental limits of molecular amplification, is discussed.Two different molecular distributions are considered. In one (the resonant case) all molecules have the same frequency as the cavity, and in the other (the nonresonant case) there is a uniform frequency distribution. The molecules are assumed to be initially in an emissive state. Several types of driving fields are considered. Expressions are obtained for the field operators by the solution of a Volterra integral equation, and expectation values are obtained for the field strength and field energy.In the resonant case, both the coherent and incoherent fields increase exponentially after a sufficiently long time, no matter how small the initial gain is. Their ratio becomes constant and is equal to the number of photons in the driving field only in the absence of dissipation. An interesting related result is the fact that the signal-to-noise ratio for constant signal input power increases as the cavity dissipation increases. An estimate of the total time for which the theory is valid is obtained from a consideration of the energy emitted by the molecules. Contact is made with perturbation theory for sufficiently small gain and short time.In the nonresonant case the effect of the molecules is shown to be that of a negative dissipation. In contrast to the resonant case, the gain becomes exponential only if the negative dissipation exceeds, in absolute value, the true dissipation. The ratio of induced to spontaneous emission is, in this case also, equal to the number of photons in the driving field only in the absence of disipation. However, the signal-to-noise ratio for constant input power drops with increasing cavity dissipation.
A semiclassical radiation theory is developed in which the spontaneous emission field of a two-level atom is a quantum entity represented by atomic operators acting in the Hilbert space of the atomic states. The theory is applied to an investigation of the coherence properties of spontaneous emission. It is found that incoherent and coherent components can be identified in the emission field, the former dominating in the early stages of the decay from the excited state and the latter dominating in the later stages or in the emission from a weakly excited atom. The single-atom coherence properties are shown to lead to well-known superradiance phenomena in the spontaneous emission from an assembly of similar atoms. The paper does not use the theory of quantum electrodynamics; it builds on knowledge at the undergraduate level of classical radiation theory and the quantum mechanics of atoms.
The problem of induced and spontaneous emission is investigated for an atomic two-level system with incident beams of radiation which are either in a coherent state or in a stationary state (contain a definite number of photons). The treatment is fully quantum-mechanical, and is confined to the case where the frequency spectrum of the incident beam is narrow compared to the natural linewidth of the system. It is shown that, under such conditions, the spontaneous emission for frequencies within the narrow band of the incident radiation is sharply reduced compared to the prediction of the natural lineshape. It is shown that a hole is burned in the natural lineshape within the narrow frequency band, thus effectively quenching the spontaneous emission at some frequency within the band. This effect is shown to occur both for the coherent and stationary beams. Quantities proportional to the induced and spontaneous probability amplitudes and the lifetimes are computed for times comparable to and long compared to the free lifetime of the state. An expression is found for the spectrum of the emergent radiation in terms of these quantities. Its physical meaning is briefly discussed. The density operator of the field for all times is given.
Conceptual problems in quantum optics are investigated by a study of the physical significance of various types of description of the field of a single mode. The descriptions are examined through the effect of the field on matter. Both undamped and damped modes are considered, the descriptions being those of various degrees of precision in classical and quantum-mechanical formalisms. The matter consists of a large number of "molecules," and the interaction is studied by means of low-order perturbation theory. Formal expressions are obtained for the energy interchange between field and molecules in terms of the zeroth-order (uncoupled) operators, with the effect of the commutation properties of the field variables explicitly separated from that of the excitation of the field, in second order. The significance of taking expectation values of the operator results is discussed, and it is concluded that this procedure is justified only when the experiment under consideration involves an averaging process; thus, the molecular variables should be averaged, but not necessarily those of the field. Conditions under which the averaging process is justified are considered, and it is reasoned that, when such a process is not justified, a statistical description of the field can result only in a statistical description of the interaction process. Results of various field descriptions are compared, and it is shown that for induced emission and for spontaneous emission from coherently oscillating molecules, classical and quantum-mechanical fields are equivalent. However, for a self-consistent theory of spontaneous emission from molecules that are not oscillating coherently, the quantum-mechanical commutation properties of the field are essential if the molecules are treated quantum-mecahnically, and the field must be treated classically if the molecules are treated classically; the type of description used for the excitation of the field is inconsequential. Photoelectric emission is examined, and, within the approximation framework used, shown to be accurately described by a classical treatment of the field. It is pointed out that there does not necessarily exist a connection between "photon statistics," that is, the statistics associated with an ensemble of fields, and photocurrent fluctuations in one or more detectors coupled to the same field.