Considering second-order terms in time-dependent perturbation expansions, the role of the nonresonant part is pointed out and explained using a simple property of the generalized function ζ(x); the results are shown to be independent of the preparation function f(t).
We now consider systems for which the Hamiltonian contains time-dependent interaction terms. In such cases we cannot reduce the time-dependent Schro¨dinger equation to an eigenvalue equation. However, if the time-dependent terms can be regarded as small perturbations, we can develop a form of perturbation theory that can be used to calculate the effects of time-dependent terms. Consider a system for which the Hamiltonian may be written as the sum of a dominant unperturbed part Hˆ0 and a small perturbation Hˆ ′ as Hˆ = Hˆ0 + λHˆ ′(t) , (10.1.1) where the unperturbed Hamiltonian Hˆ0 is independent of time, whereas the perturbation Hˆ ′ may depend on time. The parameter 0 < λ < 1 has been introduced to keep track of various orders of approximations as in the case of time-independent perturbation theory discussed in Chapter 8. The basic idea is that a small perturbation to the Hamiltonian will produce a small change in the wave function. For a time-dependent perturbation, this change means that a system, initially in a particular eigenstate of Hˆ0, will find itself in a time-dependent admixture of the eigenstates. Thus the time-dependent perturbation causes the system to undergo transition to different eigenstates of Hˆ0. So for time-dependent perturbations our interest lies in calculating the probabilities for transition to different states.
Exactly solvable models in quantum mechanics are very rare.However, perturbation theory is a powerful tool to research the complex quantum systems and is widely used in theoretical physics and chemistry.For the particle weakly perturbed by the surrounding environment, its energy eigenstate and eigenvalue are separately calculated up to the first-order and second-order perturbation approximations in the undergraduate textbook of quantum mechanics.Whereas in reality, we have to calculate the high-order perturbation correction terms occasionally.Along the same lines of the low-order perturbation correction terms of energy eigenvalues and eigenstate for stationary state perturbation theory in the non-degenerate case, the third-order and fourth-order perturbation correction terms are strictly attained in this paper.Moreover, it points out the essence of perturbation theory and provides its derivation ideas.Students are no longer afraid of tedious derivation and can derive any-order perturbation correction.These results can serve as an extension and supplement for the quantum mechanics textbooks.Furthermore, it is very helpful for students to deeply understand quantum perturbation theory.
We study universal features in the shape dependence of entanglement entropy in the vacuum state of a conformal field theory (CFT) on R1,d−1 . We consider the entanglement entropy across a deformed planar or spherical entangling surface in terms of a perturbative expansion in the infinitesimal shape deformation. In particular, we focus on the second order term in this expansion, known as the entanglement density. This quantity is known to be non-positive by the strong-subadditivity property. We show from a purely field theory calculation that the non-local part of the entanglement density in any CFT is universal, and proportional to the coefficient C T appearing in the two-point function of stress tensors in that CFT. As applications of our result, we prove the conjectured universality of the corner term coefficient CTσ=24π2 in d = 3 CFTs, and the holographic Mezei formula for entanglement entropy across deformed spheres.