QbitSSH v6
QbitSSH v6
QbitSSH v6
If (t1 − t2 )2 < E 2 < (t1 + t2 )2 , the wave number k is sign, sin[(N − 2n)k]. This sign turns out to be that of
real (corresponding to bulk states; this range gives the sin(N k) giving, finally,
energy bands in the continuum limit), whereas outside
−1 n
this range it is complex (any such solution being an edge bulk MX
state, as we will see). For the moment, we will assume k ψ± = sgn(sN ) sN −2n |2n + 1i
is real. n=0
o
Since k → k + π has no effect on the ansatz, k can ± s2n+2 |2n + 2i . (11)
be taken to be in the range (−π/2, π/2]. For any energy
other than E 2 = (t1 ± t2 )2 (a case which can safely be
Let us return now to the solution of (9) for k. Recall
ignored), there are two solutions to (5), which we will
that, if real, k is in the range [0, π/2]. It can be shown
write ±k, where 0 < k < π/2.
that the endpoints (which correspond to E 2 = (t1 ± t2 )2 )
It is useful to write t1 + t2 e±i2k = |E|e±i2ϕ ; like k, can be excluded. Eq. (9) cannot be solved analytically
0 < ϕ < π/2. Then the solution to (4) can be written for k, but it can be solved graphically. The number of
−iϕ solutions in the range (0, π/2) depends, naturally, on the
A e
= , (6) number of sites. More surprisingly, it also depends on the
B ±eiϕ
parameter r. This parameter has a critical value given
by [23]
where here and in what follows the upper (lower) sign is
for the solution of positive (negative) energy. The most N
general solution to the middle components of (2) is given rC ≡ . (12)
N +2
by a sum of (3) with (6) and the same expression with
(k, ϕ) → (−k, −ϕ): If r > rC , there are N/2 solutions of (9) for k in
(0, π/2). Each pair k, −k corresponds to two energy
M −1 n
X eigenstates of the form (11) with equal and opposite en-
C+ e−iϕ ei2nk + C− eiϕ e−i2nk |2n + 1i
|ψ± i = ergies. Thus, there are a total of N solutions, forming a
n=0
o complete set of solutions of (2). Since all these solutions
± C+ eiϕ ei2nk + C− e−iϕ e−i2nk |2n + 2i
(7) have oscillatory behavior as a function of the site index,
they are bulk states, as was mentioned earlier.
where C± are constants. If, however, r < rC , there is one fewer solution of (9)
The first and last components of (2) give in (0, π/2), giving a total of N − 2 solutions. But HSSH
clearly has N eigenvalues and eigenvectors, so two have
yet to be found. The missing solutions have complex
iϕ −i2k −iϕ i2k
e e e e C+
= 0. (8) wave numbers. If we substitute k = π/2 + iκ into (9), we
e−iϕ eiN k eiϕ e−iN k C−
find
As above, a nontrivial solution requires that the determi-
sinh(N κ)
nant vanish, giving the following equation for k, written = r. (13)
in terms of the hopping-parameter ratio r ≡ t1 /t2 and sinh((N + 2)κ)
sj ≡ sin(jk):
This equation cannot be solved analytically, but it is easy
r sN +2 + sN = 0. (9) to see that there are two real, equal and opposite solu-
tions for κ if r < rC and none if r > rC , which is exactly
We will return to the solution of this equation, and the what is needed to make up for the two missing solutions
energy spectrum which follows from (5), shortly. of (2) for k real. Defining κ to be the positive solution,
Solving (8) for C± and substituting in (7) gives the two corresponding solutions of (2), identified with
edge states since they have an exponential nature, turn
bulk MX−1 n out to be:
ψ± = sin (2n + 2)k − 2ϕ |2n + 1i −1
E MX
n=0 edge n
o ψ± = (−) shN −2n |2n + 1i
± sin (2n + 2)k |2n + 2i , (10) n=0
± sh2n+2 |2n + 2i , (14)
where we have noted explicitly that these states, being
oscillatory, are bulk states. The coefficient of |2n + 1i
can be simplified
slightly as follows. First, note that (9) where we have written shj = sinh(jκ).
implies sin (N + 2)k − 2ϕ = 0 which, given the range of The wave numbers are determined by (9) and, if r <
ϕ, then implies 2ϕ = (N + 2)k mod π. Now, modding rC , (13). The energies are then determined by (5). The
by π either has no effect on the coefficient or changes it energy spectrum for N = 20 is displayed as a function of r
by a sign, depending on whether the subtraction is an in Fig. 2. (The energy spectrum has appeared in various
even or odd multiple of π, so the coefficient is, up to a forms in the literature; see for instance [21, 23, 25–29].)
4
Energies (N=20) the band gap (defined in the thermodynamic limit) for
E/t2 r < rC . These are the edge states given by (14).
Describing the states given by (14) as edge states mer-
3
r < rc r > rc its some discussion. On the one hand, the wave number
is complex, so for a sufficiently large system the states
are confined to the edges with a penetration length into
2
the bulk given by l ≡ 1/κ. On the other hand, as r → rC
from below, κ goes to zero and the penetration length
goes to infinity (see Fig. 3). Thus for any finite-size sys-
1
tem and r sufficiently close to rC , the penetration length
is longer than the system size and the state is for all in-
tents and purposes no longer confined to the edges, ren-
r
0.5 1 1.5 2 dering it relatively indistinguishable from the rest of the
states.
rc An approximate analytic solution to (13) can be given
-1
if N is large and/or r is small. One finds
| log r| rN (1 − r2 )
-2 κ= − + O(r2N ). (15)
2 2
The first term becomes dominant rapidly as either N gets
-3 0.8 0.9 1 large or r gets small; in Fig. 3 only that term is included
in the analytic curves.
FIG. 2: Energy spectrum of the SSH hamiltonian as a func- We can derive an approximate analytic expression for
tion of the hopping-parameter ratio r = t1 /t2 for N = 20. the edge-state energies by substituting k = π/2 + iκ into
The solid lines are bulk states for all r; the dashed lines are (5), with κ given by (15). The dominant term in (15)
states which are bulk (edge) states for r > rC (r < rC ). The gives E = 0 (and indeed these states are often erro-
grey areas are the energy bands in the thermodynamic limit neously described as zero-energy states); the energies are
(N → ∞). Notice (see inset) that the edge states are exactly dominated by the second term, giving
at the band edges for r = rC .
E = ±t2 rN/2 (1 − r2 ) + O(rN ), (16)
1 N=20 20 0.3
3
r<1 r>1
n
5 10 15 20
2
-0.5
1
FIG. 7: (color online) Zero-energy edge state (right for r > 1,
left for r < 1) for N = 21. The dotted lines are the expo-
nential envelope functions ± exp[(n/2) log r] (up to normal-
r ization).
0.5 1.0 1.5 2.0
H = W † HSSH VN (23)
FIG. 8: Isolated Qubit
0 VN† H DD
As was mentioned in the introduction, our main inter- As above, the only modification of H DD needed is a term
est is to investigate how the dynamics of a double dot added to the upper-left element. This added term is pro-
is affected by the presence of edge states in an adjoin- portional to the surface Green’s function of HSSH,∞ :
ing system. We therefore consider a system composed
of three parts: the double dot coupled to one end of an ΣSSH,∞ = tC 2 GSSSH,∞ (E) (28)
7
The surface Green’s function GSSSH,∞ is the (N, N ) com- It is useful to define
ponent of the Green’s function of HSSH,∞ defined by q
δ 0 = δ|2 →0 = (1 − 02 )2 + 4τ 2 (33)
2
GSSH,∞ (E − HSSH,∞ ) = 1. (29) 1
λ0± = λ± |2 →0 = 0 + (ΣSSH,∞ ± δ 0 ). (34)
2 2
To determine GSSSH,∞ ,
we write the first row of GSSH,∞
in a form identical to (3) and follow the steps used to Since HSSH,∞ is not Hermitian (reflecting the fact
derive (10). (The current calculation is somewhat eas- that the double dot is not a closed system), the time-
ier because we only need the last component.) Here as dependent Green’s function will have decaying behavior
above, the cases N even and odd must be handled differ- (in contrast with the oscillatory behavior exhibited in
ently. We find (22)) from which the decoherence rate can be extracted
by determining the slowest decay. This determines the
Et2 sN − Σ∞ (t1 sN −2 + t2 sN ) long-term behavior of the double dot.
GSSSH,∞ = (30)
2
t2 (t1 sN +2 + t2 sN ) − Et2 Σ∞ sN However, the time-dependent Green’s function cannot
be evaluated exactly since the very complicated depen-
if N is even and dence of ΣSSH,∞ on E precludes an exact evaluation of
the Fourier transform of GSSSH,∞ .
t2 (t2 sN −1 + t1 sN +1 ) − EΣ∞ sN −1 An analytic approximation can be obtained by noting
GSSSH,∞ = (31)
t1 t2 EsN +1 − t1 Σ∞ (t2 sN +1 + t1 sN −1 ) that the frequencies in the isolated double dot Green’s
function GDD are λ± . Eq. (34) suggests using λ0± instead.
if N is odd. This is not quite correct, since λ0± are energy-dependent.
The surface Green’s functions is shown in Fig. 9 for However, for small coupling between the double dot and
the case where N is odd, where there is an edge state the rest of the system, one can show [4] that to a good
on the right of the SSH chain. This corresponds to case approximation the (now complex) frequencies should be
(d) shown in Fig. 1. The striking feature is the large evaluated at the corresponding poles of the isolated dou-
negative imaginary part of the Green’s function at zero ble dot Green’s function, λ0+ (λ+ ) and λ0− (λ− ). According
energy, corresponding to the large local density of states to this analytic approximation, the decay rates are given
of the right edge state. This large negative imaginary by the imaginary part of the frequencies, and we conclude
part of the surface Green’s function is the main source of that the decoherence time τφ is given by
decoherence for the double dot coupled to the rightmost
site of the SSH chain. −1 1 0
(τφ ) ≈ min − = {ΣSSH,∞ (λ± ) ± δ (λ± )} . (35)
2
This expression makes it clear that there are two contrib-
utors to the decay rate, corresponding to the coupling of
each double dot state to the SSH chain. The slower of
the two rates dominates at long times, so it is this that
−1
determines (τφ ) .
Alternatively, one can determine the decoherence time
by numerically evaluating the Fourier transform of the
Green’s function and extracting the decay constant of the
long-time behavior. All matrix elements will decay with
the same rate. Here we use the off-diagonal element to
compute it. For the Fourier transform, it is important to
use a very small discretization of the energy and we used
∆E ∼ 10−5 (for a bandwidth of 4). The time dependence
FIG. 9: (color online) Line plots of the surface Green’s func- is then evaluated using a fast Fourier transform, which
tion GSSSH,∞ (31) of the right most site as a function of energy, is fitted to multiple exponential decay functions, from
while the dots are obtained by evaluating numerically the full which the slowest decay is extracted at long times.
matrix (25). Here N = 11 and t1 > t2 were used, which
Both methods will be used in what follows; the excel-
corresponds to case (c) in Fig. 9.
lent agreement between the analytic approximation and
numerical evaluation of the decoherence time is a con-
The energy-dependent Green’s function for the dou- vincing post hoc justification of the analytic approxima-
ble dot including the effect of the SSH chain and lead is tion (see Figs. 10 and 11). The parameters in these fig-
obtained in a straightforward manner by the substitution ures were chosen so that one double dot energy is zero
(so that it couples to any SSH edge states, whose ener-
2 → 2 + ΣSSH,∞ ≡ 02 (32) gies are also zero or exponentially small), while the other
double dot energy lies in the SSH continuum. The latter
in (20) (and similar equations for the other components). gives rise to rapid decoherence, so the overall decoherence
8
is determined by whether or not the zero-energy state right edge of the SSH chain (with coupling tC ), the qubit
also decoheres rapidly. In the discussion that follows, will decohere much faster when there is an edge state (N
we therefore focus on the decoherence of the zero-energy odd), while the decoherence rate will be exponentially
state; we will see that this depends strongly on whether suppressed for the gapped N even case. This is what we
or not there is a same-side edge state. see in Fig. 10. Already for N = 80, with the choice of
There are some small deviations between the numerics parameters given in Fig. 10, we see approximately a five-
and analytical solution (35). Most of the small differences decade difference in the decoherence rate between the
can be attributed to extracting numerically the decay odd (one edge state) and the even (no edge states) cases.
rates from a finite time interval of a strongly oscillating Hence, the qubit can act as a very sensitive detector of
function. the edge state.
While we have shown that the coupling of the qubit
to the SSH chain affects its dynamics, the reverse is also
true. The topological nature of the edge states in the
SSH chain is also perturbed. However, the coupling of
the qubit induces a perturbation of the SSH states of
order t2c , which can be neglected for tc 1, which is the
situation we are considering here.
as, more generally, for the implementation of topological Québec via the INTRIQ strategic cluster grant. RM is
quantum computation. grateful for the hospitality of Perimeter Institute where
part of this work was carried out. Research at Perime-
ter Institute is supported by the Government of Canada
Acknowledgments through the Department of Innovation, Science and Eco-
nomic Development and by the Province of Ontario
This work was supported in part by the Natural Sci- through the Ministry of Research, Innovation and Sci-
ence and Engineering Research Council of Canada and ence.
by the Fonds de Recherche Nature et Technologies du
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