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Entanglement Between A Two-Level System and A Quantum Harmonic Oscillator
Entanglement Between A Two-Level System and A Quantum Harmonic Oscillator
Entanglement Between A Two-Level System and A Quantum Harmonic Oscillator
Kwan-yuet Ho∗
Department of Physics, University of Maryland, College Park, MD 20742
(Dated: January 2, 2008)
The entanglement between a Pauli-like two-level system and a quantum harmonic oscillator en-
hanced by an interaction between them and a δ-pulse sequence is studied, with the decoherence
due to their coupling with a Markovian bath. Without the Markovian bath, the entanglement is
enhanced to maximum possible values. With the Markovian bath, the entanglement is enhanced up
to some time and then dissipated, with the system in thermal equilibrium with the Markovian bath
after a very long time. The time for achieving the maximum entanglement shows discontinuous
jumps over the parameters of decoherence.
arXiv:0801.0310v2 [quant-ph] 16 Apr 2008
for n is any positive integers and τ0 = ωπ0 . This δ-pulse With the density matrix of the whole system in the
sequence gives the effects of putting −iσx in the calcula- interaction picture given by ρ(t), its time evolution is
tion, and it flips the spin of the two-level system. This given by the following dynamical equation
delta function is an approximation of such flipping pulse
and is valid is such a pulse is much stronger than the
energy spacing of the quantum harmonic oscillator ~ω0
[6].
Both the two-level system and the oscillator is coupled
to a Markovian bath by the following interaction: dρ(t) 1
= [V (t), ρ(t)]. (11)
dt i~
X ǫz ǫz
HB = ~ g1k (bk † σ− e−i(νk + ~ )t + σ+ bk ei(νk + ~ )t()4)
k
X
+~ g2k (bk † ae−i(νk −ω0 )t + a† bk ei(νk −ω0 )t ),
k
V (t) = H̃JC (t) + H̃t (t) + H̃B (t), (7) ρs (t) = T rB (ρ(t)). (12)
where
λ0
H̃I (t) = − (ae−iω0 t + a† eiω0 t )σz , (8)
2
π X ǫz ǫz
While tracing out, the bath term (10) is expanded up
H̃t (t) = ~ δ(t − nτ0 )(ei ~ t σ− + e−i ~ t σ+ ), (9)
2 n to second order. Suppose the bath is stationary and the
X dissipation does not depend on the memory, i.e., the dis-
H̃B (t) = ~ g1k (bk † σ− + σ+ bk ) sipation is said to be Markovian. Markovian approxima-
k
X tion is taken and finally a master equation is derived [12].
+~ g2k (bk † a + a† bk ). (10) So the final equation is given as
k
dρs (t)
= iα0 ω0 e−iω0 t (aσz ρs (t) − ρs (t)aσz ) + eiω0 t (a† σz ρs (t) − ρs (t)a† σz )
dt
Γ
−n̄σ (σ− σ+ ρs (t) − 2σ+ ρs (t)σ− + ρs (t)σ− σ+ )
2
Γ
−(n̄σ + 1) (σ+ σ− ρs (t) − 2σ− ρs (t)σ+ + ρs (t)σ+ σ− )
2
C
−n̄r (aa ρs (t) − 2a† ρs (t)a + ρs (t)aa† )
†
2
C
−(n̄r + 1) (a† aρs (t) − 2aρs (t)a† + ρs (t)a† a) (13)
2
πX h ǫz ǫz
ǫz ǫz
i
−i δ (t − nτ0 ) ei ~ t σ− + e−i ~ t σ+ ρs (t) − ρs (t) ei ~ t σ− + e−i ~ t σ+ ,
2 n
With the master equation, the time evolution of the well. Yet the negativity is still a good measure of entan-
system consisting only the two-level system and the os- glement for mixed states.
cillator can be evaluated. In this paper, both the participation ratio and nega-
tivity will be used as a measure to measure the entangle-
ment.
III. QUANTIFYING ENTANGLEMENT
where where
1 1 − |α+(−1)n̄n 2nα0 |2
|±i = √ (| ↑i ± | ↓i), P↑↑ (α, α∗ , nτ0 ) = e r , (31)
2 2πn̄r
1 1 ( n̄1 +2)4n2 α0 2 − |α| 2
√
1 − e−4|α̃(t,nτ0 )|2 1 − |α−(−1)n̄n 2nα0 |2
N = . (27) P↓↓ (α, α∗ , nτ0 ) = e r . (34)
2 2πn̄r
The negativity (27) is plotted as shown in Fig. 2. The participation ratios at t = nτ0 with respect to the
When the system just starts to evolve for some small two-level system and the oscillator are then given respec-
t, there are some overlapping between the two coher- tively by
ent states associated with | ↑i and | ↓i. As time 2
goes on, the coherent states gets further apart and Kσ (nτ0 ) = , (35)
1 + exp [−16n2 α0 2 (1 + 2n̄r )]
h−(−1)n α̃(t, nτ0 )|(−1)n α̃(t, nτ0 )]i ≈ 0, and thus system
become more entangled. The negativity approaches its 2(1 + 2n̄r )
Kr (nτ0 ) = i. (36)
saturated (maximum) value of 21 and the participation
h 2α 2
1 + exp − 16n 0
(1+2n̄r )
ratio 2.
If the initial state is a thermal ground state at temper- As time goes on, Kσ → 2 and Kr → 2(1 + 2n̄r ). The
ature T given in terms of density matrix as discrepancy comes from the fact that the state is a mixed
state.
| ↑i + | ↓i h↑ | + h↓ |
ρI (0) = √ · √ The density matrix of the state can be computed at
2 2 any time by solving the master equation (13). This can
∞ be done numerically, but P↑↑ (α, α∗ , t) and P↓↓ (α, α∗ , t)
" #
~ω0 r~ω
−k T − k T0
X
⊗ (1 − e B ) e B |rihr| can also be computed analytically and so is Kr , given by
r=0
|α ∓ (−1)(n+1) α̃(t, nτ0 )|2
1
| ↑i + | ↓i h↑ | + h↓ |
∗
= √ · √ P↑↑/↓↓ (α, α , t) = exp − ,
2 2 πn̄r n̄r
Z (37)
⊗ d2 α · P0 (α, α∗ )|αihα|, (28) where α̃(t, nτ0 ) is defined in (24). The reduced density
matrix of the quantum oscillator side is
where P0 (α, α∗ ) is the P -representation of the thermal Z
state and is equal to ρr (t) = d2 α · [P↑↑ (α, α∗ , t) + P↓↓ (α, α∗ , t)]|αihα|
Z
1 − |α| d2 α · P (α, α∗ , t)|αihα|.
2
P0 (α, α∗ ) = e n̄r , (29) = (38)
πn̄r
The participation ratio of the oscillator side can be eval-
where the average boson distribution for the oscillator uated directly by
given by (15). When T = 0, the state becomes the pure
ground state |0ih0| which can be again manipulated as 1
Z Z
shown previously for α = 0. As in appendix A, by (A5), = d2 α d2 α′ P (α, α∗ , t)P (α′ , α′∗ , t)
Kr
the state can be calculated analytically at t = nτ0 as 2
−|α′ |2 +α∗ α′ +αα′∗
·e−|α| , (39)
Z
ρ(nτ0 ) = | ↑ih↑ | ⊗ d2 α · P↑↑ (α, α∗ , nτ0 )|αihα| and is found to be
2
Z
+ | ↑ih↓ | ⊗ d2 α · P↑↓ (α, α∗ , nτ0 )|αihα| Kr (t) = h 2
i. (40)
Z 1 + exp − 4|α̃(t,nτ
2n̄r +1
0 )|
where the upper sign denote the term for P↑↑ and the
lower sign for P↓↓ . The last term of (13) just switches
the spin at time t = nτ0 where τ0 = ωπ . Between these
switches, the state can be fully described by the Fokker-
Planck equations (41). The solutions to these two equa-
tions can be found using the Green’s function of the
Fokker-Planck equation, as listed in the appendix B. If
the initial state is a ground state, then the Glauber-
Sudarshan representation of the oscillator at any time
nτ0 ≤ t < (n + 1)τ0 is given by
VI. CONCLUSION
It is worth to note that the time tmax to achieve By σx D(α0 σz )σx = D† (α0 σz ) and
iπa† a −iπa† a †
this maximum negativity decreases as the decoherence e D(α0 σz )e = D (α0 σz ), we have
strength increases, with some jumps at a number of †
points as shown in figure 6. The jump can be explained D (2nα0 σz ) for even n
U (nτ0 ) = † . (A4)
by observing the time evolution of the entanglement with iσx e−iπa a D† (2nα0 σz ) for odd n
different values of Γ(= C). As Γ increases, the graph
As a result, if the system is a pure state desccribed by
of the time evolution of the entanglement shifted down-
kets, the initial state |ψ0 i will evolve to
wards continuously as shown in figure 7. Unlike the time
evolution of the entanglement while there is no decoher- U (nτ0 )|ψ0 i.
ence which increases monotonically (as in figure 2), there
are some ripples in the variation as time goes on when And if it is a mixed state, the state is described by density
decoherence due to a thermal bath is present. The max- matrices and at t = nτ0 the matrix is given by
imum negativity Nmax still decreases continuously as Γ †
increases, but the time tmax to achieve this maximum get D (2nα0 σz )ρ0 D(2nα0 σz ), for even n
† †
a jump because of these ripples, as shown in the magni- ρ(nτ0 ) = σx e−iπa a D† (2nα0 σz )ρ0 D(2nα0 σz )eiπa a σx , .
fied graph of the time variation of negativity in figure 8. for odd n
(A5)
8
APPENDIX B: GREEN’S FUNCTION OF THE for the upper sign denotes the spin-up and the lower sign
FOKKER-PLANCK EQUATION the spin-down. Then it can be proved that
C
The Fokker-Planck equations (41) can be solved with w(t, nτ0 ) = (−1)n e− 2 nτ0 w(t − nτ0 , 0), (B3)
the use of Green’s function [19]. Suppose at time t = nτ0 ,
the state is given by P↑↓ (α, α∗ , nτ0 ), the state at any time where
nτ0 ≤ t < (n + 1)τ0 is then given by C
e−(iω0 + 2 )(t−nτ0 ) − 1
w(t − nτ0 , 0) = ±(−1)n α0 ω0 eiω0 t .
P↑↑/↓↓ (α, α∗ , nτ0 ≤ t < (n + 1)τ0 ) (B1) ω0 − i C2
Z (B4)
= ds α · P (α, α∗ , t|α′ , α′∗ , nτ0 )P↑↓ (α′ , α′∗ , nτ0 ),