Graphene Coupler
Graphene Coupler
Graphene Coupler
, where
(R)
+i
(I)
is a linear frequency-dependent surface con-
ductivity of graphene. Each isolated graphene layer supports
localized surface plasmons with the TM polarization.
4,6
When
losses are neglected, the magnetic eld of these plasmon modes
has the form
H
(0)
1,2
= A
1,2
h
1,2
(x)e
ik
0
z
y
0
, (2)
with the transverse mode prole given by
h
1,2
(x) = ik
0
_
_
e
|xd/2|
_
1, x > d/2,
1, x < d/2,
(3)
where the upper and lower signs correspond to the subscripts 1
and 2 and are associated with the layers located at x = d/2
and x = d/2, respectively (cf. Fig. 1), = k
0
_
2
, and
the normalized wave number is found from the dispersion
relation
2
k
0
_
=
4
(I)
. (4)
045443-1 1098-0121/2013/88(4)/045443(5) 2013 American Physical Society
SMIRNOVA, GORBACH, IORSH, SHADRIVOV, AND KIVSHAR PHYSICAL REVIEW B 88, 045443 (2013)
FIG. 1. (Color online) Schematic of a nonlinear graphene coupler
composed of two layers of graphene. The color pattern demonstrates
how a plasmon beam excited in the top layer tunnels to the bottom
layer (numerical results not to scale). The bottomlayer (which we call
layer 1) and top layer (layer 2) are located in the planes x = d/2
and x = d/2, respectively.
To describe the propagation of nonlinear plasmons in this
double-layer graphene structure, we use the slowly varying
envelope approximation usually employed in the physics of op-
tical solitons.
20
To be more specic, for our problemwe study a
weakly dissipative case when
(R)
(I)
. This dissipation is
low when the frequency of the plasmons and Fermi energy
of graphene satisfy the relations h < 1.67E
F
(
(I)
> 0),
k
B
T E
F
.
21
We also neglect spatial dispersion, which is valid
for h E
F
.
21
To utilize the asymptotic expansion approach, we assume
that (i) nonlinear correction to the conductivity is small, (ii)
waves are localized in the y direction, and their width is such
that diffraction remains weak, and (iii) evanescent coupling
between plasmons excited in different graphene layers is small.
Under these assumptions, the induced current can be taken in
the form
18
J = E
= ( +
NL
|E
|
2
)E
NL
=
3
4
_
3 +
2
_
,
where
3
is the third-order nonlinear conductivity of
graphene.
22
To develop a consistent perturbation theory, we
further assume that in the resulting equations the terms
responsible for the above mentioned effects are of the same
order of smallness. Now we formally introduce a small
parameter ,
2
= max
_
(R)
(I)
NL
|E
|
2
(I)
,(k
0
)
2
,e
k
0
(
2
)d
_
,
and derive the equations for slowly varying plasmon ampli-
tudes. We rewrite Maxwells equations (1) as follows:
E
1,2
= ik
0
H
1,2
,
(5)
H
1,2
= ik
0
E
1,2
+
4
c
(x d/2) (E
1,2
+E
2,1
),
so that the superpositions E = E
1
+E
2
and H = H
1
+H
2
satisfy the original equations. Then, developing a perturbation
theory, the solutions of Eqs. (5) are sought in the form of the
following asymptotic series:
H
1,2y
=
_
A
1,2
(
2
z,y)h
1,2
(x)
+
2
H
(2)
1,2
(
2
z,y,x) +
_
e
ik
0
z
=
_
A
1,2
(z,y)h
1,2
(x) +H
(2)
1,2
(z,y,x) +
_
e
ik
0
z
,
H
1,2z
=
_
H
(1)
1,2
(
2
z,y,x)
+
3
H
(3)
1,2
(
2
z,y,x) +
_
e
ik
0
z
=
_
H
(1)
1,2
(z,y,x) +H
(3)
1,2
(z,y,x) +
_
e
ik
0
z
. (6)
The zero-order term in returns the identity for the
unperturbed plasmons (2)(4). The correction H
(1)
1,2
of the rst
order in is determined from H
1,2
= 0 as
H
(1)
1,2
=
i
k
0
A
1,2
y
h(x).
In the order of
2
we obtain
d
2
H
(2)
1,2
dx
2
+k
2
0
(
2
)H
(2)
1,2
4
c
i
(I)
(x d/2)E
(2)
1,2z
=F
1,2
,
F
1,2
=
_
2ik
0
A
1,2
z
+
2
A
1,2
y
2
_
h
1,2
(x)
+
4
c
(x d/2)(
(R)
+
NL
|A
1,2
|
2
)A
1,2
+
4
c
i
(I)
(x d/2)A
2,1
e
d
, (7)
where
is the derivative of the Diracs delta function, and the
corrections
E
(2)
1,2z
=
i
k
0
H
(2)
1,2
x
(8)
are continuous at x = d/2.
Then, applying the Fredholm theorem,
23
which states
that the solution for the correction H
(2)
1,2
is nondiverging if
the eigenmodes of the homogeneous equation for H
(2)
1,2
are
orthogonal to the perturbation, we nally derive the nonlinear
equations for the slowly varying envelopes A
1,2
of the TM-
polarized plasmons propagating in each layer,
2ik
0
_
A
1,2
z
+ A
1,2
_
+
2
A
1,2
y
2
+g|A
1,2
|
2
A
1,2
= QA
2,1
,
(9)
where
=
2
c
(R)
(
2
)
3/2
k
0
,
g =
4
c
(
2
)
3/2
i
NL
k
2
0
, (10)
Q =
4
c
e
d
(I)
(
2
)
3/2
k
2
0
,
are a linear absorption parameter, and nonlinear and coupling
coefcients, respectively. Remarkably, Eqs. (9), along with
the correct analytical expressions for the effective coefcients
(10), can be obtained in the order O(
2
) of the perturbation
045443-2
NONLINEAR SWITCHING WITH A GRAPHENE COUPLER PHYSICAL REVIEW B 88, 045443 (2013)
expansion by using the substitution
k
0
= k
0
+
_
i
1
2k
0
2
y
2
_
+
in the modied dispersion relation (4), which in the presence
of the second layer takes the form
2
k
0
_
=
4
(I)
i
_
(R)
+
NL
|A
1
|
2
+i
(I)
e
d
A
2
A
1
_
+
_
. (11)
III. NONLINEAR SWITCHING
In the framework of the nonlinear amplitude equations
(9) disregarding losses and beam diffraction, we can analyze
different types of TM-polarized eigenmodes of a nonlinear
double-layer graphene waveguide. For further calculations,
we employ the following expressions for the graphene
conductivity:
10,18,22
=
ie
2
h
_
1
+i
intra
+
1
4
ln
2
2 +
_
, (12a)
3
= i
3
32
e
2
h
(eV
F
)
2
h
2
E
4
F
3
, (12b)
where = h/E
F
,
intra
= h/(E
F
intra
), for the doping level of
E
F
= 0.1 eV, = 1 ( = 2/k
0
12.4 m),
intra
= 10 ps,
24
the Fermi velocity in graphene V
F
c/300, = 4, and take
the separation between the layers as d = 28 nm. We take quite
a large relaxation time and discuss the implications of this
choice below.
We nd that three types of nonlinear modes can propagate
in this double-layer graphene coupler, namely, a symmetric (S)
mode with A
1
= A
2
, an antisymmetric (AS) mode with A
1
=
A
2
, and an asymmetric (A) mode with A
1
= A
2
, similar to
the case of a nonlinear dimer.
25
These modes are presented
in Fig. 2 through their (a), (b) transverse proles and (c)
power-dependent shift of the nonlinear propagation constant.
In the linear regime, only symmetric (S) and antisymmetric
(AS) modes exist. However, above a critical power level, a
symmetry breaking occurs in this nonlinear system when a
different, asymmetric branch (A) emerges, and it describes
the nonlinear states where the power is not distributed equally
between the lower and upper graphene layers. The asymmetric
mode bifurcates at the point p from the antisymmetric
branch, and it is stable, being characterized by a predominant
energy concentration in the vicinity of one of the layers. The
AS mode becomes unstable above the critical power.
Next, we focus our attention on the power-controlled
switching of plasmon beams between the layers and study nu-
merically the propagation of a sech-like input beam launched
into the upper layer (as shown in Fig. 1). The input beam is
selected to be the fundamental solution of a single (uncoupled)
nonlinear equation, and it describes a spatial soliton.
19
For
a peak power density of 6 W/m, the soliton beam width is
about 50 nm. This signicant subwavelength localization is
supported by the large Kerr nonlinearity of graphene.
18,19
0 2 4 6
0
5
10
Guided Power Density (W/m)
k
0
1
)
AS
S
A
p
(c)
14 14
A
(b)
x (nm)
14 14
2
1
0
1
2
AS
S
E
z
(
a
.
u
.
)
(a)
x (nm)
FIG. 2. (Color online) (a), (b) Examples of the transverse mode
proles for symmetric (S), antisymmetric (AS), and asymmetric (A)
modes propagating in the double-layer graphene shown for the E
z
component. (c) Shift of the nonlinear propagation constant vs the
mode power density in the guided plasmon mode propagating in the
z direction. Solid and dashed lines correspond to stable and unstable
branches, respectively.
In Fig. 3, we compare the corresponding switching charac-
teristics of the nonlinear graphene coupler for the continuous
plasmons (whose amplitude is constant along y) (dashed
curve) and for the beams of a nite extent including the soliton
switching (solid curves). The coupler length is selected at the
half-beat length L = /(2Q), when in the linear regime the
input power transfers completely into the second layer.
20
Apart
from an increase of the threshold power density, two regimes
of the coupler operation can be clearly distinguished.
0 2.5 5 7.5 10
0
0.2
0.4
0.6
Input Peak Power Density (W/m)
T
r
a
n
s
m
i
s
s
i
o
n
L
N
FIG. 3. (Color online) Switching characteristics of the nonlinear
graphene coupler. Shown is a fraction of the power transmitted in the
pumped layer for a cw (dashed curve) and soliton input beam (solid
curve) in a half-beat-length coupler as a function of the input peak
power density. Dashed-dotted curve: Calculated relative fractional
output power emerging fromthe other layer in the continuous plasmon
regime.
045443-3
SMIRNOVA, GORBACH, IORSH, SHADRIVOV, AND KIVSHAR PHYSICAL REVIEW B 88, 045443 (2013)
(a)
z
(
m
)
upper layer
0
0.9
1.8
lower layer
(b)
0
0.3
0.6
(c)
y (m)
z
(
m
)
0.2 0 0.2
0
0.9
1.8
(d)
W/m
y (m)
0.2 0 0.2
0
3
6
FIG. 4. (Color online) Spatial distribution of the power density in
the layers of the nonlinear graphene coupler for different input peak
power densities: (a), (b) Linear regime, P
in
= 0.6 W/m and (c), (d)
nonlinear regime, P
in
= 6 W/m, corresponding to the points marked
in Fig. 3 as L and N, respectively.
For relatively small input powers, in the so-called linear
regime, the plasmon beam of the upper layer couples to the
lower layer and tunnels almost completely [see Figs. 4(a) and
4(b)]. For higher values of the input power, the energy transfer
between the layers becomes inhibited, and we observe the
nonlinear regime when the plasmon beamremains in the upper
layer [see Figs. 4(c) and 4(d)]. Importantly, the dissipation
does not inhibit switching but it modies the slope of the
curves and the asymptotic value of the switching curve not
achieving unity, as shown in Fig. 3. Therefore, the beam may
be effectively routed between the graphene layers by changing
its input power.
From the power ow (6 W/m) and knowing the plasmon
structure, we estimate the maximum amplitude of the electric
eld on graphene layer at 7 10
6
V/m, which is below the
graphene breakdown threshold.
26
In our simulations, however,
we assumed low loss graphene, with a relaxation time of
10 ps. Such relaxation times were observed in several works
with multilayer structures,
24,27
however, typical single-layer
graphene reported so far experimentally usually exhibits
relaxation times of the order of 0.1 ps. Such graphene with
higher losses will have a shorter plasmon propagation length,
and it will require larger, and probably unachievable, light
intensities. Therefore, we suggest that high quality, low loss
graphene will potentially be suitable for creating nonlinear
couplers.
Further, we discuss the case when two in-phase beams of
an identical shape are launched into both layers, being shifted
(a)
z
(
m
)
upper layer
0
0.9
1.8
lower layer
(b)
0
0.3
0.6
(c)
y (m)
z
(
m
)
0.2 0 0.2
0
0.9
1.8
(d)
W/m
y (m)
0.2 0 0.2
0
3
6
FIG. 5. (Color online) Plasmon beam routing in the nonlinear
graphene coupler. Spatial distribution of the power density in the
layers of the nonlinear graphene coupler for different input peak
power densities: (a), (b) Linear regime, P
in
= 0.6 W/m and (c), (d)
nonlinear regime, P
in
= 6 W/m.
initially by a half of their width with respect to each other. In
the linear regime, the power exchange between the layers leads
to the effective attraction between the centers of mass of the
beams, as can be seen in Figs. 5(a) and 5(b). However, in the
strongly nonlinear regime the energy exchange is suppressed
and the mutual interaction of optical solitons generated in
the two different layers is accompanied by their repulsion, as
shown in Figs. 5(c) and 5(d).
IV. CONCLUSIONS
We have studied analytically and numerically the propa-
gation of nonlinear electromagnetic waves in a double-layer
graphene structure. We have revealed that this structure can
operate as an efcient planar nonlinear coupler, demonstrating
the switching of light between two different layers of graphene.
We have studied the nonlinear effects in this graphene coupler
for both continuous plasmons and subwavelength spatial
solitons, and described the symmetry breaking and nonlinear
switching with various opportunities for optical beam control
and manipulation at the nanoscale.
ACKNOWLEDGMENTS
The work was supported by the Australian Research
Council, the Engineering and Physical Research Council of
the UK under EP/K009397/1, and the Ministry of Education
and Science of the Russian Federation. The authors thank Y.
Bludov and P. Belov for useful discussions.
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