The master equations for bistability in the bad cavity limit in an atomic system is solved when the number of atoms N is not more than 45. A detailed comparison is made of results from Fokker-Planck equations and from the master equation. The validity of the decorrelation approximation for the master equation is examined.
In the general framework of the system size expansion of Van Kampen and Kubo, we consider the Fokker-Planck equation for a model of absorptive bistability in the bad-cavity limit. The physical system is described by the reduced atomic density operators after adiabatic elimination of the cavity field variables. Mapping of the master equation into c-number form according to the normal-ordering mapping scheme yields known results for the atomic fluctuations and correlation functions; however, it also leads to a Fokker-Planck equation with a non-positive-definite diffusion matrix. The symmetrical-order-mapping scheme eliminates this difficulty. The leading contribution to the system size expansion yields a Fokker-Planck equation for the symmetrical-ordered density function having a positive-definite diffusion matrix. The atomic expectation values and fluctuations previously derived from the quantum Langevin equations emerge naturally from this Fokker-Planck equation.
A generalized Fokker-Planck equation is used to study the problem of single-atom optical bistability in the good-cavity limit. The effects of quantum fluctuations are investigated by linearizing fluctuations around the steady-state value. It is shown that in the good-cavity limit, quantum fluctuations are relatively small, and hence there exist both absorptive and dispersive single-atom bistability. By comparing our single-atom Fokker-Planck equation with the N-atom Fokker-Planck equation, we find that in the good-cavity limit, these two different Fokker-Planck equations reduce to identical equations. We therefore come to an important conclusion that the results obtained from the many-atom Fokker-Planck equation in the good-cavity limit are also valid for a single atom. \textcopyright{} 1996 The American Physical Society.
Spontaneous emission from a system of N identical two-level atoms is considered using a master equation recently derived by the author. The master equation describing the time evolution of the phase-space distribution function associated with the reduced density operator of the atomic system is obtained. This master equation, which is of the type of a Fokker-Planck equation, is used to derive the equation of motion for the mean values of various atomic operators characterizing the physical properties of the system. This leads to a hierarchy of equations, which is decoupled by making a suitable approximation. The intensity of the spontaneously emitted radiation is then calculated. Next, the spontaneous emission from geometrically small systems is considered. For this case, the master equation is solved exactly, and an exact expression for the radiation rate is obtained. The exact solution of the master equation is also used to calculate the normally ordered correlation functions for the electric field. Section V deals with the spontaneous emission from a system of harmonic oscillators, the size of the system being small compared to a wavelength. The master equation for this problem is also solved exactly, and it is shown that this system also leads to superradiant emission in some cases, e.g., if all the oscillstors are excited initially to some coherent state ∣z0〉.
In Chapter 9, we derived the master equation for a reduced density operator of a two-level atom coupled to a multi-mode vacuum field. We have seen that the master equation is an operator type equation that, in general, is not easy to solve. We have illustrated the solution of the master equation by representing the density operator in the basis of the two states of the two-level atom. The purpose of the representation of the master equation was to obtain c-number differential equations that are equivalent to the operator equations, but are more readily soluble.