Open Quantum Systems/Projection Operator Techniques

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Decay into two bands

We consider a two-level systems coupled to an environment consisting of two distinct energy bands. The system is described by the Hamiltonian

H=HS+HE+HI.

The system Hamiltonian HS is an ordinary two-level system with an energy difference of ΔE, according to

HS=ΔE|ee|=ΔEσ+σ,

where we have set the energy of the ground state |g to zero. For the energy bands of the environment, we assume a linear spectrum, i.e,

HE=n1=1N1δεN1n1|n1n1|+n2=1N2(ΔE+δεN2n2)|n2n2|,

where N1 and N2 are the total number of states in each band. The interaction Hamiltonian is given by

HI=n1=1N1n2=1N2λn1,n2(σ+1E)(1S|n1n2|)+H.c.,

i.e., whenever the two-level system is de-excited, an excitation is created in the environment, and vice versa. The matrix elements λn1,n2 are random Gaussianly distributed variables with a variance λ2. In the following, we assume a separation of energy scales according to ΔEδEλ.

This model has some very interesting properties. First of all, the size of the environment is clearly finite, meaning that excitations in the environment may not decay fast enough and the Markov approximation may not be applicable. This is even further strengthened when taking into account that the interaction will lead to very strong correlations between system and environment. At the same time, the weak interaction naturally gives rise to a peturbative expansion.

We proceed by defining a correlated projection operator for the relevant part of the dynamics [1], according to

𝒫ρ=Tr{Π1ρ}1N1Π1+Tr{Π2ρ}1N2Π2=Pe1N1Π1+Pg1N2Π2,

where we have introducted the projectors

Π1=n1=1N11S|n1n1|Π2=n2=1N21S|n2n2|

and Pe and Pg denote the probability to find the two-level system in its excited or ground state, respectively. Because of conservation of probability, we have Pg=1Pe, meaning that the relevant part of the dynamics consists of a single variable!

In the following, we will derive its equation of motion. The second order TCL master equation is given by

𝒫ddtρ=0tds𝒫(t)(s)𝒫ρ,

which in our case can be written as

P˙e1N1Π1+(1P˙e)1N2Π2=0tdsTr{Π1(t)(s)𝒫ρ}1N1Π1+Tr{Π2(t)(s)𝒫ρ}1N2Π2.

since the projection and the time derivative commute. Multiplying with Π1 and taking the trace yields

P˙e=0tdsTr{Π1(t)(s)𝒫ρ}=0tdsTr{Π1[HI(t),[HI(s),Pe1N1Π1+(1Pe)1N2Π2]]}.

Expanding the commutator and making use of the relation ΠiΠj=δijΠi results in

P˙e=0tdsTr{Pe1N1Π1HI(s)HI(t)(1Pe)1N2Π1HI(t)HI(s)+H.c.}.

We can now introduce two relaxation rates γ1,2 describing the transition rates between the two bands. Specifically, we have

γi=1Ni0tdsn1n1|HI(s)HI(t)+H.c|n1.

As the interaction Hamiltonian couples does not contain terms that leave the band index unchanged, we may write the matrix elements as

n1|HI(s)HI(t)+H.c|n1=n2n1|HI(s)|n2n2|HI(t)|n1+c.c..

As we work in the interaction picture, we have

n1|HI(s)|n2n2|HI(t)|n1=exp(iω12s)exp(iω12t)|λn1,n2|2,

where we have introduced the transitions frequencies ω12=δε(n1/N1n2/N2). Using the statistical properties of the interaction Hamiltonian and performing the integration over s finally yields [2]

γi=2λ2Nin1,n2sin(ω12t)ω12.

For the next step, we note that the sinc function appearing in the relaxation rates is a representation of the Dirac δ distribution, i.e.,

πδt(ω12)=limtsin(ω12t)ω12.

Then, at large enough times and small enough couplings [3], we may approximate the rates by

γ12πλ2N1k,lδ(En1En2)=2πλ2N2δεγ22πλ2N1δε.

The equation of motion for the excited state probability then reads

P˙e=(γ2+γ1)Pe+γ2.

Assuming the two-level system is initially in its excited state, the stationary state given by Pes=γ2/(γ1+γ2) is approached in an exponential decay according to

Pe(t)=Pes+γ1γ1+γ2exp[2(γ1+γ2)t].

This solution is in excellent agreement with numerical simulations of the full Schrödinger equation [4].

It is important to stress that this efficient description of such a complex system is only possible because our projection operator correctly captures the essential features of the dynamics. If one choses a different projection operator, say, one without correlations between system and environments, according to

𝒫ρ=TrE{ρ}ρE,

then the second order TCL master equation no longer correctly describes the dynamics, as higher orders are divergent [4].

  1. Template:Cite book
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  4. 4.0 4.1 Cite error: Invalid <ref> tag; no text was provided for refs named Breuer2006