We consider a non-Hermitian Hamiltonian in order to effectively describe a two-level system (TLS) coupled to a generic dissipative environment. The total Hamiltonian of the model is obtained by adding a general anti-Hermitian part, depending on four parameters, to the Hermitian Hamiltonian of a tunneling TLS. The time evolution is formulated and derived in terms of the normalized density operator of the model, different types of decays are revealed and analyzed. In particular, the population difference and coherence are defined and calculated analytically. We have been able to mimic various physical situations with different properties, such as dephasing, vanishing population difference and purification.
The purpose of this dissertation is to review the salient features of non-Hermitian quantum mechanics. An introduction to Hermitian quantum mechanics is included to make this review as accessible as possible. Attempts at formulating a consistent physical theory are introduced, before examining non-Hermitian theories’ uses as convenient computational frameworks. Particular emphasis is placed on recent developments in open quantum systems that utilise non-Hermitian Hamiltonians. Chapter four introduces a logic that maps a non-Hermitian Hamiltonian onto a non-Hamiltonian algebra that has a Hermitian Hamiltonian. This was put forward by Sergi, who then goes on to show its application to a two level system. The time evolution is then derived in terms of the density matrix model. This system can then be used to analyse different types of decay such as coherence and population difference. This serves to illustrate the usefulness of the approach.
We investigate the non-Hermitian Hamiltonian which governs the system including two-level atom and electromagnetical field with a circular polarization vector. We find the Hamiltonian by using dipole approximation and rotating wave approximation (RWA), which lead to a non-Hermitian Hamiltonian. We solve the time-independent non-Hermitian Hamiltonian and obtain real eigenvalues of energy for this system. Finally, by solving the Schrodinger equation in the pseudo interaction picture, we show that our results and the results of Jaynes‐Cummings (JC) Hamiltonian are in excellent agreement.
In principle, non-Hermitian quantum equations of motion can be formulated using as a starting point either the Heisenberg’s or the Schrdinger’s picture of quantum dynamics. Here it is shown in both cases how to map the algebra of commutators, defining the time evolution in terms of a non-Hermitian Hamiltonian, onto a non-Hamiltonian algebra with a Hermitian Hamiltonian. The logic behind such a derivation is reversible, so that any Hermitian Hamiltonian can be used in the formulation of non-Hermitian dynamics through a suitable algebra of generalized (non-Hamiltonian) commutators. These results provide a general structure (a template) for non-Hermitian equations of motion to be used in the computer simulation of open quantum systems dynamics.
The construction of physical occupation and transition probabilities in non-Hermitian, effective-Hamiltonian models of coupled near-resonant discrete states which decay to a continuum is analyzed. We consider for definiteness the particular physical example of atomic multiphoton ionization. The possibility of finite duration and arbitrary modulation of this interaction, and of the subsequent ionization and/or decay, in such a system allows us to invoke "adiabatic switching" considerations in conventional
S-matrix theory. The effective Hamiltonian $\stackrel{^}{H}(t)$ is derived for both stationary and time-dependent Schr\"odinger equations. These derivations yield the same effective $\stackrel{^}{H}(t)$, and further reveal that this operator is associated with discrete-state-projected "incoming" scattering states. The Hermitian conjugate operator ${\stackrel{^}{H}}^{\ifmmode\dagger\else\textdagger\fi{}}(t)$ is similarly shown to be associated with discrete-state "outgoing" scattering states. This shows that effective-Hamiltonian theories are intrinsically
S-matrix theories. This fact, in turn, is employed to construct transition amplitudes. The possibility of resonance in the atom-field interaction requires that both the projected incoming states and projected outgoing states be employed in this construction. The projected incoming and outgoing states in the (discrete) bound space are quite conveniently described by effective time-dependent Schr\"odinger equations, supplemented by initial- and final-state boundary conditions. The fact of independent-exponential decay from each mode throughout the history of the interaction, for an arbitrary initial superposition state, in the adiabatic limit, suggests a practical construction for intermediate-time bound-state probabilities. This construction permits the formal definition of individual-state probabilities, which satisfy a generalized adiabatic theorem, and leads to the satisfying result that the total bound-state probability at all intermediate times is the sum of complex-mode probabilities. In marked contrast to the conventional norm-of-state definition of nonionization probability, this sum does not have oscillations at intermediate times, in the limit of adiabatic modulation of the interaction. Superposition-state probabilities, however, exhibit oscillations at intermediate times. The resulting non-Hermitian quantum dynamics is especially suited, and even essential, for an accurate description of near-resonance ionization. Precise matching of the time-dependent $\stackrel{^}{H}(t)$ and ${\stackrel{^}{H}}^{\ifmmode\dagger\else\textdagger\fi{}}(t)$ with bases of their instantaneous eigenstates is required by approximate unitarity in the discrete decaying space, for a consistent theory. We illustrate these considerations in a general way in the context of resolvent-operator techniques. The implementation of the theory in both its time-dependent and stationary-state formulations is presented in an Appendix, for the completely general two-state non-Hermitian Hamiltonian. The results of these formulations are found to agree, in the adiabatic limit, to all orders in the non-Hermitian interaction. The utility of direct diagonalization of the effective $\stackrel{^}{H}(t)$, advocated by Armstrong and Baker, is transparent. The overall context of interpretation of their earlier work is, however, significantly altered. Similar considerations apply for nonswitchable interactions, such as for
K-meson decays. These results represent a practical generalization of quantum mechanics to non-Hermitian systems. The utility, and the necessity, of such a generalization has considerable theoretical interest, and direct experimental implications.
With a view to obtaining further insight into the nature of eigenvalues and eigenfunctions of a stationary state one-dimensional Schrödinger equation corresponding to a non-Hermitian Hamiltonian H ( x , p ) we investigate the ground-state solutions for a variety of potentials within the framework of an extended complex phase space characterized by x = x 1 + i p 2 , p = p 1 + i x 2 , where ( x 1 , p 1 ) and ( x 2 , p 2 ) are real and considered as canonical pairs. The analyticity property of the eigenfunction alone is found sufficient to throw light on the nature of eigenvalues and eigenfunctions for different systems. It is noted that the imaginary part of the eigenvalue, E i , turns out to be zero for all potentials V ( x ) with real couplings whereas it turns out to be nonzero for the case when the couplings are complex. The prescription is also extended to study the excited states. The problems related to the normalization of the eigenfunction and the boundary conditions to be used within this framework are also discussed.