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I. INTRODUCTION
1
has the energy h̄ωa obeys the following exact integro- (uncertainty) of |ei to ∆t, the interval between measure-
differential equation ments (Fig. 3),
Z t
′ Eq. (5) =⇒ ∆E∆t ∼ h̄. (8)
α̇ = − dt′ eiωa (t−t ) Φ(t − t′ )α(t′ ). (1)
0
More generally, in Eq. (8) ∆t = 1/ν, where ν is a charac-
Here α(t) = he|Ψ(t)ieiωa t , h̄ωa is the energy of |ei, and teristic rate of measurements. With this definition, Eq.
(8) holds both for ideal and nonideal (realistic) measure-
ments. Relation (8) comes about since measurements
X
Φ(t) = h̄−2 he|V e−iH0 t/h̄ V |ei = h̄−2 |Vej |2 e−iωj t (2)
j
(projections) dephase level |ei, analogously to phase ran-
domization by collisions, which induce a linewidth that
is the reservoir correlation function, expressed by Vej = is equal to the collision rate ν.
he|V |ji, where |ji (6= |ei) are H0 eigenvectors with eigen-
values h̄ωj . e V
Equation (1) is exactly soluble, but it is enough to con-
sider its short-time behavior by setting α(t) ≈ α(0) = 1 e V
in the integral of (1). This yields the expression hν
meas.
Z t
′ ′ ′ iωa t′
α(t) = 1 − dt (t − t )Φ(t )e , (3)
0 FIG. 3. Measurements broaden level |ei, analogously to
phase randomization by collisions at rate ν, being drastically
in which all powers of t (phase factors!) are included and changing its decay into the reservoir.
interferences between various decay channels may occur.
By contrast, the standard quadratic expansion in t for the
population [3,4] ρee (t) = |α(t)|2 ≈ 1−t2 /τZ2 , in which the G
Zeno time τZ = h̄/(he|H 2 |ei − he|H|ei2 )1/2 is the inverse
a
variance of the energy in |ei, may often fail, as discussed F
below. This is where we essentially differ from standard ν
treatments. How does this difference show up?
Consider instantaneous measurements – projections on ωM ωa ω
|ei interrupting its decay at intervals τ . We can use our γ free
Decay rate
2
the spectrum G(ω) by a δ-function, with a constant C More generally, under condition (9), the QZE scaling
being the integrated spectrum, of R occurs for any G(ω) such that
Z G(ω) → 0 at ω → ∞. (15)
C = G(ω)dω = hV 2 i. (10)
Conditions (9) and (15) ensure the QZE scaling only
for sufficiently large measurement rates and do not always
This approximation becomes exact in the case of resonant imply a monotonous decrease of R as ν increases (see Fig.
Rabi oscillations (ΓR = 0, ωa = ωM ), which explains 4). The latter behavior, which is what one usually has
why the QZE is observable in Itano’s experiment [7] for in mind in discussions of the QZE, is obtained only in
any ν. More generally, this approximation holds for any special situations. For instance, it occurs when G(ω) is
G(ω) that falls off faster than 1/ω on the wings. Then a peak and ωa is within its width ΓR , i.e.,
our universal expression yields the most general result for
the QZE, namely that R decreases with ν: |ωa − ωM | <
∼ ΓR . (16)
R ≈ 2C/ν, (11)
G
where we defined generally F
G(ω) = A|ω − ωc |−β for s(ω − ωc ) ≫ ΓR (13) b) The opposite to the QZE scaling is obtained when-
ever ωa is significantly detuned from the nearest maxi-
and G(ω) is cut off or diminishes fast for s(ω − ωc ) < ΓR . mum of G(ω) at ωm , so that G(ωa ) ≪ G(ωm ). In the
Here ωc is the cutoff frequency, 0 < β < 1, θ() is the unit limit (Fig. 5 - inset):
step function, and s can equal 1 or −1. For instance,
Eq. (13) approximately holds near the waveguide cutoff ν ≪ |ωm − ωa |. (17)
(s = 1, β = 1/2) or the vibrational Debye cutoff (s = −1, the rate R grows with ν, since the dephasing function
β = 1/2). The QZE scaling for a reservoir response (13) F (ω) is then probing more of the rising part of G(ω) in
is found to be the convolution. This limit implies the anti-Zeno effect
(AZE) of decay acceleration by frequent measurements.
R = Bν −β . (14) Physically, this means that, as the energy uncertainty
increases with the measurement rate ν, the state decays
Here B = [2β π/ cos(πβ/2)Γ(2 + β)]A, where Γ() is the into more and more channels, whose weight G(ω) is pro-
gamma-function [20] (in particular, B = (8π 1/2 /3)A for gressively larger.
β = 1/2). Equation (14) holds for a sufficiently weak Remarkably, we may impose condition (10) in any
coupling (A ≪ ν β+1 ) and under condition (9), where, in reservoir that is not spectrally flat. This reveals the uni-
the case of (13), ωM is replaced by ωm or, equivalently, versality of the AZE, which we noted already for radiative
ωc . decay in cavities [16].
3
As an example, consider the coupling spectrum of the in the case of Eq. (13). The quantity νQZE may turn out
form to be much greater than the boundary ν1 of the QZE-
scaling regime (see below).
G(ω) = Aω η , 0 < ω < ωC , The value of νQZE given by Eq. (23a) was identified
G(ω) = 0 otherwise, (18) with the reciprocal “jump time”, i.e., the maximal time
interval between measurements for which the decay rate
so that ωa ≪ ωC . Using the Lorentzian F (ω) (27), as ob- is appreciably changed [21]. However, the correct value
tained for realistic (continuous) measurements (see Sec. of the reciprocal jump time is rather δa , which may be
III), one obtains from Eq. (5) that for ν ≪ ωC smaller by many orders of magnitude than νQZE . In
the special case of ideal instantaneous measurements and
2πA(ωa2 + ν 2 )η/2 sin ηχ a Lorentzian or Lorentzian-like G(ω), the genuine-QZE
R= (0 < η < 1), (19a)
sin ηπ condition (22) reduces to that of Ref. [22].
These considerations apply (with some limitations) to
2 hydrogenic radiative decay (spontaneous emission), for
ωC
−1 ωa
R = A ν ln + ω a π + 2 tan (η = 1) which G(ω) can be calculated exactly [23]:
ωa2 + ν 2 ν
αω
(19b) G(ω) = . (24)
[1 + (ω/ωB )2 ]4
4
b) Continuous measurements. These measurements ωa :
should not be confused with the limit of vanishing inter-
vals between successive continuous projections discussed 1 ν
F (ω) = . (27)
by Misra and Sudarshan. This limit is unphysical, corre- π (ω − ωa )2 + ν 2
sponding to an infinite energy spread h̄ν. In contrast, re-
Thus, qualitatively, there is no essential distinction be-
alistic continuous measurements, though monitoring the
tween different frequent measurements: ideal projections,
state incessantly, still require a finite time for completing
impulsive measurements, and continuous measurements.
an observation, i.e., they have a finite effective rate ν.
γu
tion into a “reservoir” created by the phase-randomizing
Ωp element (polarization rotator) controlled by a noisy field
(see Fig. 7) [24].
Let us first assume constant phase jumps ∆ϕ at the
polarization rotator. Uninterrupted evolution then corre-
sponds to Rabi oscillations of the horizontal polarization
e probability (for θ = 1):
FIG. 6. The Cook scheme: see text for explanations. This decay is slower than Rabi oscillations, signifying the
QZE. Imperfect (weak) measurements (0 < θ < 1) yield
for small phase jumps [(∆ϕ)2 ≪ (1 − θ)2 ] an exponential
e/o polarization decay
rotator PBS 2(∆ϕ)2
∆ϕ Ph (t = nτr ) = exp − 2 t , (30)
cos ∆ϕ |h> τr ν
5
B2 ΓR
G(ω) ≈ , (34)
πτr2 Γ2R + ω 2
i.e. a Lorentzian of width ΓR = (1 − γ)/τr . For highly 0.8
anticorrelated jumps (γ ≈ −1) the “reservoir” spectrum
is a sum of two shifted Lorentzians, 0.6 γ=0.7
Decay rate R
X B2 Γ′R
G(ω) ≈ (35) 0.4
j=±1
πτr2 Γ′R 2 + (π/τr + jω)2
0
-40 -20 0 20 40
Frequency
0.2 0.08
γ=−0.7
0.15 0.06
G, F
0.1 0.04
0.05 0.02
0 0
-40 -20 0 20 40 0 2 4 6 8 10
Frequency Measurement interval
FIG. 12. The AZE trend for the decay rate R (in units
FIG. 9. Idem, for anticorrelated phase jumps.
of τ0−1 ) in a “washboard” potential (Fig. 11) as a func-
tion of the scaled measurement interval τ /τ0 (ωg = 10/τ0 ,
If G(ω) is peaked at ω = 0 (the high-correlation case M 2 a/8h̄2 kL
3
= 0.01, where M is the mass of the atom).
γ ≈ 1), then perfect measurements (θ = 0), correspond-
ing to a flat F (ω), will reduce R, causing the QZE trend,
as compared to weak measurements (θ ≈ 1), correspond-
ing to a narrow spectral profile
1 ν
F (ω) ≈ , (36)
π ν 2 + ω2
with ν = (1 − θ)/τr (see Fig. 8).
The opposite (AZE) trend holds if G(ω) is peaked at
ω = ±π/τr (the highly anti-correlated case, γ ≈ −1)
(Fig. 9). The two trends are illustrated in Fig. 10.
6
TABLE I.
Process References τQZE τAZE
Radiative decay in a cavity Kofman & Kurizki [16] ns ns
Radiative decay Kofman & Kurizki [14] does not exist ps (Rydberg transition)
in open space fs (optical transition)
Photon polarization Kofman, Kurizki 10 ns 10 ns
decay via random & Opatrny [24]
modulation in a cavity
Transmission of tunneling Japha & Kurizki [26] ? ns
emitting atoms
Atomic tunneling Wilkinson et al. [25] 0.01 µs µs
(escape) from
“washboard” (accelerated)
periodic potential
Electron tunneling in Silvestrini et al. [27] ?
current-biased SQUID 10 ns
(“washboard” potential)
Nuclear β-decay Kofman & Kurizki [14] does not exist 10−18 s
Near-threshold Lewenstein fs ms
photodetachment & Rza̧żewski [17]
V. ATOM ESCAPE (DECAY) BY TUNNELING Our simple universal formula (5) results in general cri-
FROM ACCELERATED POTENTIAL teria for the QZE:
(i) It can only occur in systems with spectral width be-
Theoretical and experimental studies by Raizen et al. low the resonance energy.
[25] have shown that cold atoms trapped in an acceler- (ii) It is principally unattainable in open-space radiative
ated (“washboard”-shaped) periodic potential tunnel out or nuclear β-decay, because the required measurement
(Fig. 11) non-exponentially, at times t <
∼ τ0 ≡ ωg /(kL a), rates would cause the creation of new particles.
where h̄ωg is the band gap which equals approximately (iii) Contrary to the widespread view, frequent measure-
half the potential well depth, a the acceleration and kL ments can be chosen to accelerate essentially any decay
the wave number of the laser creating this potential. Our process. Hence, the anti-Zeno effect should be far more
prediction is that AZE should arise for measurement in- ubiquitous than the QZE.
tervals τ ≫ 1/ωg and QZE for τ ≪ 1/ωg . These trends A variety of systems have been shown to be promising
are plotted in Fig. 12. Figure 13 shows (in the logarith- candidates for experimental studies of the AZE, which is
mic scale) the decay law P0 (t) = |α(t)|2 for short times almost always much more accessible than the QZE.
(the solid curve). The two curves in Fig. 13 intersect at
the time τQZE = 2/νQZE , so that the genuine QZE occurs
7
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