Von Neumann Picture§
Lindblad master equation is built upon von newmann picture which is somewhat just schrodinger picture but for the full density state operator, thus in somesense it is a more complete schordinger euqation. Thus, let's derive the von numann equation very quickly and easily. First of all, a general state can be written as a sum of pure state, which is
ρ=i∑pi∣ψi⟩⟨ψi∣
Thus
ρ˙=i∑pi(∣ψi⟩˙⟨ψi∣+∣ψi⟩⟨ψi∣˙)
Where if we apply the Schrodinger equation now, here, we get
ρ˙=iℏ1i∑pi(H^∣ψi⟩⟨ψi∣−∣ψi⟩⟨ψi∣H^)=iℏ1(H^i∑pi∣ψi⟩⟨ψi∣−i∑pi∣ψi⟩⟨ψi∣H^)=iℏ1[H^,ρ]
Or, although non standard, but personally feels more appropiete since we are comparing it to the schrodinger equation, we will write it as
iℏρ˙=[H^,ρ]
Where the schrodinger equation is
iℏ∣ψ⟩˙=H^∣ψ⟩
The setup§
Now, to derive the master equation, we note that everything is derived in the interaction frame and then translate back to the lab frame as before with RWA. Thus, in the rotating from, our hamiltonian is
H^=k,λ∑gk,λA^k,λei(ωeg−ωk)t+gk,λ∗A^k,λ†ei(ωk−ωeg)t
Applying the Von Neumann equation,
iℏρ˙=[H^,ρ]
Let's change it's form so that we can take approximation from there. By integration, we note that the density matrix can be evaluated as
iℏρ(t)=iℏρ0+∫0t[H^(t′),ρ(t′)]dt′
Thus, the Von neumann equation becomes
iℏρ˙ρ˙=[H^,ρ0+iℏ1∫0t[H^,ρ]dt]=iℏ1[H^,ρ0]−ℏ21∫0t[H^(t),[H^(t′),ρ(t′)]]dt′
Born Approximation§
- We assume The bath and the system interact weakly, such that their state can be factorized approximately
ρ(t)=ρS(t)⊗ρB(t)
Where S and B stands for System and Bath. And ρB(t) is approximatly constant
- Also, as it is constant, we assume ⟨B⟩=0, in the terminology of density matrices, it is Tr(Bρ)=0.
- In Born approximation, we also take Markov approximation
Thus, now, to make use of everything of here, let's take the trace of system B,
ρ˙S(t)=iℏ1TrB[H^,ρ0]−ℏ21∫0tTrB[H^(t),[H^(t′),ρ(t′)]]dt′
Then, because H is bilinear upon S and B, where in this case S=σ, B=b, A=S⊗B, by assumption 2, the first order terms must vanish to 0. And we use assumption 3 onto that integral, Thus
ρ˙S=−ℏ21∫0∞TrB[H^(t),[H^(t−τ),ρ(t)]]dτ
Where it is not obvious here, but the first markov approximation ( take t′=t on the density matrix ) is justified because we already assumed that the time we are interested is below the decay timescale, which is very small. And on the second markov approximation ( substituting τ=t−t′ and then making the upper limit ∞ ) is justified because there will be the correlation function TrB(H(t)H(t−τ)ρ) appearing on all 4 terms after exanding the commutation, and the coorelation should drops to zero at large time differences, also below the decay time scale.
The Lindblad Master Equation§
The rest of the math are the same as previous derivation for spontanuos emission, thus it will be omitted here. The conclusion after transforming back to the schrodinger frame are
ρ˙S=−ℏi[H^S,ρS]+γDσ^−(ρS)DL(ρ)=LρL†−21{L†L,ρ}
Notice, everything now is in the system frame, the bath is simplied to just giving a way to decay and we didn't need to deal with interaction terms from here.
Adjoint Lindblad Master Equation§
With
⟨O⟩˙=Tr(Oρ˙)
We direclty use the Lindblad Master Equation on it.
The first term gives,
−ℏiTr(O[H^,ρ])=−ℏiTr(OH^ρ−OρH^)=−ℏiTr(OH^ρ−H^Oρ)=−ℏiTr([O,H^]ρ)
The dissipation term gives,
γTr(ODL(ρ))=γTr(OLρL†−21OL†Lρ−21OρL†L)=γTr(L†OLρ−21OL†Lρ−21L†LOρ)=γTr(DL†(O)ρ)DL†(O)=L†OL−21{L†L,O}
Thusm easily we can see
⟨O⟩˙=Tr([−ℏi[O,H^]+γDL†(O)]ρ)
Now, if we change to the Heisenberg frame, the expectation value should not change, but who stays constant have changed. Now ρ stays constant and the operator changes, so in Heisenberg frame, we get
O˙=−ℏi[O,H^]+γDL†(O)
This is the adjoint equation.
Purcell effect ( again )§
From the equationes, we note ⟨σ+σ−⟩=Pe , we can get
P˙e=ig⟨aσ+−a†σ−⟩−γPe
Then we assume
- a weak excitation ( σz=−1 )
- adiabatic elimination, a˙=0
- weak correlation limit between atom and field ⟨aσ⟩=⟨a⟩⟨σ⟩
- κ≫g
P˙e=−(γ+κ4g2)Pe
When with the same assumption but κ≪g, we get
P˙e=−2γPe