• Nenhum resultado encontrado

Plasmon-polariton fractal spectra in quasiperiodic photonic crystals with graphene

N/A
N/A
Protected

Academic year: 2021

Share "Plasmon-polariton fractal spectra in quasiperiodic photonic crystals with graphene"

Copied!
8
0
0

Texto

(1)

LETTER

Plasmon-polariton fractal spectra in quasiperiodic photonic crystals with

graphene

To cite this article: M. S. Vasconcelos and M. G. Cottam 2019 EPL 128 27003

(2)

doi: 10.1209/0295-5075/128/27003

Plasmon-polariton fractal spectra in quasiperiodic photonic

crystals with graphene

M. S. Vasconcelos1,2 and M. G. Cottam1

1 Department of Physics and Astronomy, University of Western Ontario - London, Ontario N6A 3K7, Canada 2 Escola de Ciˆencias e Tecnologia, Universidade Federal do Rio Grande do Norte - 59078-900, Natal-RN, Brazil

received 13 May 2019; accepted in final form 24 October 2019 published online 9 December 2019

PACS 78.67.Wj – Optical properties of graphene

PACS 78.67.Pt – Multilayers; superlattices; photonic structures; metamaterials PACS 61.44.Br – Quasicrystals

Abstract – In this work we study the plasmon-polariton spectra in one-dimensional photonic

crys-tals based on the Fibonacci, Thue-Morse and double-period sequences, where we have graphene at the interface of one of the constituent building blocks (A = SiO2/graphene, B = SiO2). The dispersion relations for each quasicrystal are numerically calculated by using a transfer-matrix approach. The spectra of these structures are shown to be fractals (for the bulk bands distri-bution), obeying a power law in a particular frequency region and these are induced specifically by the quasiperiodic ordering in the unit cells of each system studied. We also report a strong dependence of the width of the bulk bands on the wave vector for this particular frequency region, whereas for large wave vectors the fractal properties in these spectra are absent.

Copyright c EPLA, 2019

Introduction. – Fractals have been one of the most

fascinating areas of research over the last forty years [1]. Nowadays, we have studies and applications of fractals in many different areas, like condensed-matter physics [2], engineering [3,4], metamaterials [5], and biology [6]. Specifically, their quantum effects were recently studied including transport [7], optical [8] and plasmonic [9] prop-erties of regular fractal structures (Sierpinski carpet and gasket), and their power-law energy level spacing distri-butions [10]. However, there exists a very special one-dimensional system that exhibits fractal spectra as one of its main characteristics: the so-called 1D quasiperiodic system. Interest in such systems started with the discov-ery of quasiperiodic crystalline (or quasicrystalline) alloys in 1982 by Shechtman et al. [11]. It emerged that qua-sicrystals corresponded to an intermediate system between ordered and random systems, like amorphous materials. Today quasicrystals are well recognized as a natural exten-sion of the notion of a crystal to structures with quasiperi-odic (QP), instead of periquasiperi-odic, arrangements of atoms [12,13]. A more recent updated definition of quasicrys-tals with dimensionality n (n = 1, 2 or 3) is that they can also be defined as a projection of a periodic structure in a higher-dimensional space mD, where m > n [14]. Quasicrystals, therefore, represent a special class of deter-ministic aperiodic structures, exhibiting fractal properties

in their spectra [15], with a distinct appearance for each chain [16], even for different excitations [17–19].

The pioneering work of Merlin et al. [20] on one-dimensional quasicrystals (1D-QC) structures, called quasiperiodic superlattices, has become the standard. We may define two distinct building blocks, each of which car-ries the necessary physical information, and then they are arranged according to a particular sequence. For example, they can be described in terms of a series of generations that obey the relation of particular recursion. In this work, we consider the building blocks A as silica (SiO2) with

graphene in one of its interfaces, and the building blocks B are composed only by silica. Our choice here is intentional for a study of the quasiperiodicity induced by the graphene sheets in their plasmon-polariton spectra. A previous work on Fibonacci 1D-QC [21] with graphene at all in-terfaces focussed only on the band distribution and trans-mission spectra induced by the quasiperiodic organization of the dielectric layers at normal and oblique incidence. It is well known [18,19,22] that our type of choice illustrates more clearly the fractal nature in the spectra. On the other hand, the fractal, that was introduced by Mandel-brot [23] to characterize geometrical figures that are not defined in the Euclidian geometry, exhibits very interest-ing properties that can appear in diverse fields ranginterest-ing from DNA [24] to the edges of Saturn’s rings [25].

(3)

M. S. Vasconcelos and M. G. Cottam

Graphene is a 2D material that consists of a flat sheet of carbon atoms, arranged in a hexagonal lattice and form-ing a monoatomic layer [26]. Its very special electronic structure reveals an exotic “zero bandgap” and it exhibits semiconductor properties when doped [27]. Also, in doped graphene we should have collective excitations such as plasmons, and plasmon-polaritons [28] with interesting op-tical characteristics in a similar way to surface plasmons on metal surfaces [29]. These interesting properties make graphene ideal for the study of metamaterials in the in-frared and terahertz regions [30]. These optical properties of graphene give us several applications in photonics [31] and plasmonics [32].

Polaritons are mixed excitations of a photon (light) and a crystal excitation. In 1D dielectric photonic crys-tals (PCs) we can use Maxwell’s equations to study these modes at long wavelengths (typically wave vectors below 103m−1 [22,33]). In this limit the electric and magnetic fields may extend beyond the boundaries of a PC. These fields couple with the excitations in the neighbouring (as well as the same) layers in a PC. Through Bloch’s theo-rem, we can understand that these collective excitations characterize the PC. Specifically, if we have a 2D electron gas at interfaces in these systems, the collective modes are

plasmon-polaritons. They are described by a Bloch wave

number Q for the direction normal to the interfaces. The propagation of a polariton mode corresponds to Q lying within a new Brillouin zone associated with the PC pe-riodicity, 0 ≤ |Q| ≤ π/L, where L is the unit cell size of the PC. For completeness, we will study here the sur-face modes of a semi-infinite PC (formed by truncating an infinite PC by an external surface). The reduction of symmetry can lead to the appearance of so-called surface polaritons.

The development of graphene-based devices in the ter-ahertz regime is currently attractive following the dis-covery that the surface plasmon polaritons supported by graphene sheets can be tuned in the terahertz regime by adjusting the external gate voltage or chemical doping. Recently, the production of terahertz (THz) radiation by a relatively low-energy electron beam directed onto the top of graphene layers was recently proposed as a new THz source (for a review see [34]). In this approach, sur-face plasmon polaritons with resonance frequencies in the THz range can be excited by an incident beam of moving electrons with speeds of less than 10 percent of the light speed. In this context, the present work can give insights into this new emerging field called graphene plasmonics.

Specifically we study the plasmon-polariton spectra in 1D photonic crystals generated by the Fibonacci, Thue-Morse and double-period sequences, where we have graphene at the interface of one of the constituents of its building blocks. This work is organized as follows. In the next section we present the general theory of plasmon-polaritons for dielectric or semiconductor multilayers with graphene sheets in the interfaces, and we apply this theory to our present case, showing the transfer matrix for each

Fig. 1: (a) The A and B building blocks considered here, taken as SiO2, with  = 2.2, and dA = dB = 10 μm. (b) The lay-ered geometry illustrated for the third-generation Fibonacci se-quence (ABAAB ) showing graphene sheets at some interfaces. In the case of a semi-infinite array with a surface at z = 0 the external medium is denoted as C.

1D-QC structure. Then we show the numerical results, il-lustrating the important role of the graphene sheets in the fractal spectra, and also we contrast it with other studies about the Fibonacci case. Finally we present the conclu-sions of this work.

Theory. – We consider a 1D-QC with building blocks A and B juxtaposed in a fashion that is determined

ac-cording to a chosen quasiperiodic sequence to form a lay-ered structure. The individual building blocks A and B are layers of a dielectric material (chosen as SiO2 with dielectric constant ) having thicknesses dA and dB,

re-spectively, as in fig. 1(a). One interface of building block

A is taken to have a monolayer of graphene (with thickness

negligible compared with dA), whereas B has no graphene

layer.

The graphene monolayers can be modelled as having a frequency-dependent optical conductivity, which includes both the intraband (σintra) and interband (σinter)

contri-butions (see [35] and references therein). The interband contribution plays the leading role around the absorption limit, ¯hω ≈ 2μc, while the intraband contribution is im-portant at low frequencies compared with μc/¯h, giving a

competing effect. Here, we are considering the form taken by the optical conductivity in the THz regime [36].

Following [37] we consider a periodic alternation of unit cells, where the arrangement of A and B layers are cho-sen to correspond to a quasiperiodic sequence, which may be either Fibonacci, Thue-Morse or double-period. For example, in fig. 1(b) we show the third-generation Fi-bonacci sequence. Initially, we consider an infinitely ex-tended structure, for which Bloch’s theorem is applicable, and then the effects of an external surface are introduced. Only p-polarization will be considered here, since the ef-fects of the graphene are more evident in this case [38].

(4)

Dispersion relations: general multilayer. In order to obtain the plasmon-polariton bulk modes of the infinite PC, we utilise Maxwell’s equations within each dielectric medium. For the transverse magnetic modes (TM or p-polarization) within medium A (or B) of the m-th layer, the electric field component is

Exj(m) = exp(ikxx − iωt){A(m)1j exp[ikzj(z − zm)] + A(m)2j exp[−ikzj(z − zm)]}, (1)

where kzj= (jω2/c2− k2x)1/2 with kxbeing the in-plane

component of the wave vector (parallel to the x-y plane),

ω is the angular frequency, j is the dielectric function in medium j and c is the velocity of the light in vacuum. The constants A(m)1j and A(m)2j (j = A or B; m = 1, 2, . . . ) are amplitudes for forward- and backward-travelling waves, respectively. Using H = (0c2/iω)∇ × E, the

correspond-ing magnetic-field component in medium A ( or B) can be calculated. We consider the magnetic permeability μj = 1 in each medium. Also we have used ∇ · D = 0 to relate

the amplitudes of the electric and magnetic fields. By applying the electromagnetic boundary conditions, requiring the continuity of the tangential component of the electric field and the discontinuity of the magnetic field to be equal to the current density J = σ(ω) E, at the

interfaces z = (n − 1)L + dA and z = nL, we can relate the electromagnetic fields for cell n to those for cell n + 1. After re-expressing the amplitudes in terms of those for index n (recall that m labels the individual layers, while

n labels the unit cells), we obtain

⎛ ⎝A(n)1j A(n)2j⎠ = M ⎛ ⎝A(n+1)1j A(n+1)2j⎠ , (2)

where j = A or B, depending on the quasiperiodic se-quence. For the periodic case this matrix is simply given by M = MAMABMBMBA, with Mαβ(Mγ) correspond-ing to the electromagnetic propagation across the inter-face α|β (across the medium γ), where α, β and γ denote

A or B. These matrices are [35]

Mαβ=1 2 ⎡ ⎢ ⎢ ⎣ 1 + βkzα αkzβ + σα 1 βkzα αkzβ + σα 1−βkzα αkzβ − σα 1 + βkzα αkzβ − σα ⎤ ⎥ ⎥ ⎦ , (3) = exp(−ik) 0 0 exp(ikzγdγ) , (4)

with σα = σkzα/α0ω . Although the quasiperiodic structures have no translational symmetry, we use the periodicity of the unit cell through the application of Bloch’s theorem. We consider that this model describes the quasiperiodicity when the number of generation goes

to infinity (called the thermodynamic limit [39]). There-fore, the implicit dispersion relation for the bulk plasmon-polariton modes is (see, e.g., [22,33,39])

cos(QL) = 1/2 Tr(M ), (5)

where M is a unimodular matrix and Tr denotes the trace. For the surface modes we consider a semi-infinite PC with the geometry as in fig. 1(b). The region z < 0 is assumed to be a dielectric medium C with electric field

ExC(0)= [A(0)1Cexp(kCz)] exp(ikxx − iωt), (6) where kC= (kx2− Cω2/c2)1/2. The previous

electromag-netic boundary conditions apply at z = 0. For simplicity, we assume k2x > Cω2/c2 so that kC takes only real and positive values. The localized surface plasmon-polaritons correspond to decaying solutions for the amplitudes of the electromagnetic fields with respect to the distance from the surface plane z = 0. Therefore, we can find the im-plicit dispersion relation for the surface modes [22,35] as

M22+ M21/λ = exp(βL) = M11+ M12λ, (7) where Mi,j (i, j = 1, 2) are the elements of the matrix M

defined in eq. (2), and λ = (r − σC+ 1)/(r + σC− 1) is a

surface-dependent parameter. We have defined the ratio

r = A/C, with σC= σkx/(iC0ω). Also, here we choose

kC ≈ kx, only in the surface case, following [40].

Dispersion relations: one-dimensional quasicrystals.

We now apply the above formalism to the bulk and surface plasmon-polaritons in aperiodic (Fibonacci, Thue-Morse, and double-period) structures. First the Fibonacci struc-ture can be constructed by juxtaposing the two building blocks A and B so that the n-th generation is given by the interactive rule Sn = Sn−1Sn−2, for n ≥ 2 , with S0= B

and S1 = A. Also, it can be constructed by applying the

inflation rules A → AB and B → A for each generation, starting with A. The Fibonacci generations are S0 = A,

S1 = B, S2 = AB, S3 = ABA, etc. The number of the building blocks increases according to the Fibonacci num-ber, Fl = Fl−1+ Fl−2 (with F0 = F1= 1). The transfer matrices are

a) for S1= A and S2= AB

TS1 = MAMAA; TS2= MAMABMBMBA; (8) b) for S3= ABA

TS3 = MAMABMBMBAMAMAA= TS2TS1; (9) c) for any higher generation (n ≥ 2)

TSn= TSn−1TSn−2. (10)

Knowing the initial transfer matrices TS1 and TS2, we can determine the transfer matrix of any generation. Another way to obtain the same result (for bulk modes) is through a study of the trace map of TSn [41].

(5)

M. S. Vasconcelos and M. G. Cottam

The Thue-Morse sequence at the n-th stage is defined by Sn = Sn−1Sn−1+ (n ≥ 1), where Sn+ = Sn−1+ Sn−1, with S0 = A and S0+ = B. Alternatively we can employ the

transformations steps A → AB , B → BA. The number of building blocks increases as 2n−1. The first stages for Thue-Morse generations are S1 = A, S2 = AB, S3 =

ABA, . . . , and the transfer matrices for each generation

can be calculated by induction using a) for S2= AB

TS2 = MAMABMBMBA= Tα2MBA, (11) where

2= MAMABMB, 2 = MBMBAMA; (12) b) for S3= ABBA

TS3 = MAMABMBMBBMBMBAMAMAA

= Tα2MBBTβ2MAA= Tα3MAA (13)

where Tα3 = Tα2MBBTβ2 and Tβ3 = Tβ2MAATα2; c) for any generation n (n ≥ 2)

TSn= 

TαnMBA, for n even,

TαnMAA, for n odd,

(14)

with

Tαn= 

Tαn−1MABTβn−1, for n even,

Tαn−1MBBTβn−1, for n odd,

(15)

and

Tβn= 

Tβn−1MBATαn−1, for n even,

Tβn−1MAATαn−1, for n odd.

(16)

We can define a similar rule for the double-period se-quence, where the n-th stages are found from the recur-sion relations Sn = Sn−1Sn−2Sn−2 (n ≥ 1), with S1= A and S2 = AB. Alternatively the transformation rules

A → AB, B → AA can be applied. The double-period

generations are S1= A, S2= AB, S2= ABAA, etc. The

number of building blocks for this sequence increase like 2n−1. The transfer matrix for the 2nd generation S1= A

is found in the same way as in the Fibonacci case, i.e., a) for S1= A and S2= AB

TS1 = MAMAA; TS2= MAMABMBMBA; (17) b) for 3rd generation we have

TS3 = MAMABMBMBAMAMAAMAMAA

= TS2TS1TS1; (18)

c) for any generation n ≥ 3

TSn= TSn−1TSn−2TSn−2. (19)

Numerical results. – We present numerical examples

to illustrate the results for the plasmon-polariton spec-tra that can propagate in the quasiperiodic structures described in the last section. We consider the dielectric media in building blocks A and B to be SiO2with  = 2.2 appropriate for THz frequencies [42]. Also we choose the temperature T = 300 K and μc= 0.2 eV for the graphene sheets [35]. We ignore the role of absorption since it is typically small in SiO2for other distinct crystalline forms and composition [43] in the temperature and frequencies of interest in this work. The other physical parameters used here are dA= dB= 10 μm. We consider medium C to be

vacuum (C = 1). All the frequencies encountered here are

in the THz range. We should comment that the use of the transfer-matrix method (TMM) is computationally more efficient for our purpose than the use of more accurate methods such as the Finite Element Method or Boundary Element Method, where it would be necessary to access large-scale computational facilities, like clusters, etc. By using TMM we can employ a simple personal computer.

The plasmon-polariton spectra for the quasiperiodic Fibonacci, Thue-Morse, and double-period PCs are presented in figs. 2(a) and 4(a), respectively. Here the sur-face modes are represented by the black lines, while the bulk bands are characterized by the shaded areas, which are bounded by the conditions QL = 0 and QL = π (at which the cosine factor in eq. (5) is ±1). The results presented in those figures are in accordance with those found in the literature for the periodic case, including the so-called graphene-induced gap [35], for normal incidence (kxdA= 0). The surface modes lie outside the bulk bands, subject to the constraint k2x> Cω2/c2. This means that

any surface mode in these plots lies to the right of the vacuum light line (VLL) given by ω = ckx/√0. For

ref-erence, we also show the dielectric light line (DLL) for the PC given by ω = ckx/√.

In fig. 2(a) for the spectrum for the 6th Fibonacci generation we have 8 building blocks A and 5 building blocks B. We can note two well-defined regions for the bulk plasmon-polariton spectrum, for frequencies above and below ω ≈ 1.34 THz. For ω below about 1.34 THz and for kxdA ≈ 0 there is a large gap, sometimes called

the graphene-induced gap [44,45], which extends out to the DLL of SiO2. For kxdA values to the right of the DLL we have many bulk bands which start at the ori-gin and eventually merge into three narrow bands that will join in a straight line with a constant group velocity for high values of kxdA (not shown here). We can in-fer that these bands are induced by the graphene sheets at interfaces in building blocks A. In fact, the effect of the optical conductivity is expected to be stronger at low frequencies [36]. Therefore, for frequencies greater than

ω ≈ 1.34 THz and wave vectors kxdA to the left of the DLL, we have only the quasiperiodic effects induced by the dielectric layers (except for a shift in all spectra, when compared with [22,33,46,47]), which is well known (see [48] to compare with the normal incidence case).

(6)

n

Fig. 2: (a) Plasmon-polariton bulk and surface dispersion rela-tion for the quasiperiodic n = 6 Fibonacci 1D-QC. The straight lines VLL and DLL represent the vacuum (dashed line) and the dielectric (dotted line) light lines, respectively. (b) Distribution of bandwidths for the plasmon-polaritons as a function of the Fibonacci generation number n.

We see (to the right of the DLL) that the number of bulk bands is equal to the number of building blocks A and to the Fibonacci number F5 = 8. It is a general property that this number is always equal to the Fibonacci number of the n − 1 generation. Also in this region, there are 12 surface modes in total. There is one between the VLL and DLL, and the others are at the right of DLL between the bulk bands, except for one close to kxdA ≈ 1.31 and ω ≈ 1.53 THz that has a very interesting behaviour. This

mode starts at kxdA ≈ 1.02 and ω ≈ 1.47 and “crosses”

its adjacent surface and bulk modes. For higher values

kxdA it merges with another surface branch. The cross-ing (or anti-crosscross-ing) effects between surfaces modes have been a subject of intense studies over decades (for a re-view see [49]). It has been shown that in crossing ef-fects we have one or several modes coexisting at the same frequency and wave vector. Moreover, their dispersion curves appear to be closely spaced, just as in our case. At the point(s) of their convergence the curve(s) can in-tersect, merge with each other or split apart [50], i.e., the waves modes are either not coupled or the coupling is negligible. The anti-crossing effect that can appear in the system that we are studying is related to there being signif-icant coupling between the modes, resulting in the modes

Fig. 3: Log-log plot of the total width of the allowed regions Δ as a function of the Fibonacci number Fn.

type transformation and/or energy exchange between the waves. Such modes can appear between waves of the same or different nature, and, in particular, a “mixing” between surface, guided and bulk modes can occur [51]. The effect can appear in metallic thin films, where specifically it is linked with the strong coupling between surfaces modes rather like two coupled harmonic oscillators [49]. We can infer here that we have an anti-crossing effect and it is related with the quasiperiodic organization of the Fi-bonacci (or other) sequence in the PC. In other words, the Fibonacci sequence will cause a strong coupling be-tween electromagnetic fields of the plasmon-polariton sur-face modes (mainly due to building blocks A), in such a way that we have a strong coupling in a specific point,

kxdA≈ 1.11 and ω ≈ 1.53 THz, in the dispersion relation

for n = 6.

The distribution of the bandwidths for Fibonacci PCs is shown up to the 9th generation (a unit cell with 55 A and 34 B building blocks) in fig. 2(b), for kxdA = 0.5. One can observe that the forbidden and allowed frequencies are a function of the generation number n. As expected, for large n, the allowed band distribution gets narrower, with the behaviour becoming like a guided mode (some-times called a localized mode) for large n. It forms the fa-mous Cantor set (or Cantor dust) in this limit (also found in [17–19]). In fact, the total width of the total width of the allowed frequency bands goes down as a power law Δ∼ Fn−δ, where Fn is the Fibonacci number and the

ex-ponent δ is a function of the in-plane wave vector kxdAas we can see in fig. 3. Here we show a log-log plot indicating the power laws for three different values of kxdA, namely 0.5, 0.75 and 1.0.

The Thue-Morse quasiperiodic 4th generation is shown in fig. 4(a). Here, as previously, we have two well-defined regions for the plasmon-polariton spectrum. For the re-gion to the right of the DLL, the number of bulk bands increases as 2n−2, which is the number of building blocks

A. For wave vectors kxdA at the right of the DLL there are bands which start at the origin and merge into three narrow bands (guided modes), that will join in a straight line with a constant group velocity for high values of kxdA

(7)

M. S. Vasconcelos and M. G. Cottam

Fig. 4: (a) As in fig. 2, but for Thue-Morse 1D-QC. The straight lines VLL and DLL represent the vacuum light line (dashed line) and the dielectric light line (dotted line), respectively. (b) Distribution of bandwidths for the plasmon-polaritons as a function of the generation number n.

(not shown here). The surface modes lie between the bulk bands and, as in the previous case, we have also the anti-crossing surfaces modes at kxdA ≈ 0.82 and ω ≈ 1.31.

Again, this is induced by the quasiperiodic organization of the graphene sheets. The bandwidth distribution, forming the so-called Cantor set when the generation number goes to infinity, is presented in fig. 4(b), for kxdA = 0.5. We go up to the 7th generation, which means a unit cell with 25A and B building blocks. The total allowed bandwidth

Δ has power law as Δ∼ (2n)−δ, where δ depends on the wave vector kxdA (like in fig. 3), but for δ vs. 2n, where we now find δ = 0.250, 0.555, and 1.067 for the same value of kxdA shown in fig. 3.

Finally, the plasmon-polariton spectrum was studied for the double-period quasiperiodic structures up to the 4th generation (not shown here due to the similarity to the Thue-Morse case). We have found also two well-defined regions for the plasmon-polariton spectrum. For the sur-face modes we may identify two anti-crossing effects, and we do not find a surface mode between the VLL and DLL, as previously. For the forbidden and allowed regions we have a similar behaviour to the previous case in fig. 3(b), including the scaling Δ∼ (2n)−δ, where again the expo-nent δ is a function of the wave vector kxdA.

Conclusions. – In this work we have presented a

gen-eral theory for the propagation of plasmon-polaritons in 1Q-PC with graphene sheets in one of the building blocks. The spectra are illustrated in figs. 2 and 4. We have stud-ied physical properties related to the quasiperiodicity of the systems and their self-similarity behaviour, whose frac-tality can be described by the power laws (see fig. 3 and the text). Also, we presented a discussion for the bulk and surfaces modes for low frequencies. We stress here the interesting properties (mainly in surfaces modes) that arise when we considered the quasiperiodicity induced by the graphene (figs. 2(a) and 4(a)). The localization (the decrease of the bandwidths when the sequence order tends to infinity) of the spectra is expressed by the distribution of their bandwidths shown in figs. 2(b) and 4(b).

The main experimental techniques to probe these results are inelastic (Raman) light scattering and Attenuated To-tal Reflection (ATR) of the light. In Raman scattering a grating spectrometer is used to detect the scattered light with a typical shift between 0.6 a 500 meV in the frequency of the scattered light [52]. This makes this technique highly suited to probe the plasmon-polariton spectra. Fur-ther, the ATR spectroscopy is simpler to implement, but there is less precision in detecting the modes. The struc-tures proposed here can be experimentally fabricated, fol-lowing [53] where the authors obtained a graphene-based 1D photonic crystal, as confirmed by Raman spectra and optical image of CVD, and demonstrated the excitation of surface modes using a prism coupling technique. Also, Zhang et al. [54] presented an approach to synthesize a high-quality single layer of graphene on a SiO2 substrate using Cu-vapor–assisted chemical vapor deposition. On the other hand, one should mention that another way to probe the self-similarity and fractal spectra of these ape-riodic structures in 2D is to consider dark-field scatter-ing spectroscopy to investigate the scatterscatter-ing properties of two-dimensional plasmonic lattices based on the aperi-odic sequences presented here (for a review see [55,56]).

∗ ∗ ∗

MSV thanks the Department of Physics and Astron-omy at the University of Western Ontario for hospital-ity during his sabbatical as visiting professor. This study was financed in part by the Coordena¸c˜ao de Aperfeioa-mento de Pessoal de N´ıvel Superior (CAPES) of Brasil (Finance Code 88881.172293/2018-01) and the Natural Sciences and Engineering Research Council (NSERC) of Canada (grant RGPIN-2017-04429).

REFERENCES

[1] Bercioux D. and I˜niguez A., Nat. Phys.,15 (2019) 111. [2] Kempkes S. N., Slot M. R., Freeney S. E., Zevenhuizen S. J. M., Vanmaekelbergh D., Swart I. and Smith C. M., Nat. Phys.,15 (2019) 127.

[3] Sivia J. S., Kaur G. and Sarao A. K., Wireless Pers. Commun.,95 (2017) 4269.

(8)

[4] De Nicola F., Puthiya Purayil N. S., Spirito D., Miscuglio M., Tantussi F., Tomadin A., De Angelis F., Polini M., Krahne R. and Pellegrini V., ACS Photon.,5 (2018) 2418.

[5] Moeini S. and Cui T. J., Ann. Phys. (Berlin), 531 (2019) 1800134.

[6] Rothemund P. W. K., Papadakis N. and Winfree E., PLOS Biol.,2 (2004) e424.

[7] van Veen E., Yuan S., Katsnelson M. I., Polini M. and Tomadin A., Phys. Rev. B, 93 (2016) 115428. [8] van Veen E., Tomadin A., Polini M., Katsnelson

M. I.and Yuan S., Phys. Rev. B,96 (2017) 235438. [9] Westerhout T., van Veen E., Katsnelson M. I. and

Yuan S., Phys. Rev. B,97 (2018) 205434.

[10] Iliasov A. A., Katsnelson M. I. and Yuan S., Phys. Rev. B,99 (2019) 075402.

[11] Shechtman D., Blech I., Gratias D. and Cahn J. W., Phys. Rev. Lett., 53 (1984) 1951.

[12] Levine D. and Steinhardt P. J., Phys. Rev. Lett., 53 (1984) 2477.

[13] Maci´a E., ISRN Condens. Matter Phys., 2014 (2014) 165943.

[14] Valy Vardeny Z., Nahata A. and Agrawal A., Nat. Photon.,7 (2013) 177.

[15] Vasconcelos M. and Albuquerque E., Phys. B: Con-dens. Matter, 222 (1996) 113.

[16] Vasconcelos M. S. and Albuquerque E. L., Phys. Rev. B,59 (1999) 11128.

[17] Albuquerque E. L. and Cottam M. G., Solid State Commun.,81 (1992) 383.

[18] de Medeiros F. F., Albuquerque E. L., Vasconcelos M. S. and Mauriz P. W., J. Phys.: Condens. Matter,19 (2007) 496212.

[19] Vasconcelos M. S., Albuquerque E. L. and Mariz A. M., J. Phys.: Condens. Matter, 10 (1998) 5839. [20] Merlin R., Bajema K., Clarke R., Juang F. Y. and

Bhattacharya P. K., Phys. Rev. Lett.,55 (1985) 1768. [21] Namdar A., Onsoroudi R. F., Khoshsima H. and

Sahrai M., Superlattices Microstruct.,115 (2018) 78. [22] Albuquerque E. L. and Cottam M. G., Phys. Rep.,

233 (1993) 67.

[23] Mandelbrot B. B., Proc. Natl. Acad. Sci. U.S.A., 72 (1975) 3825.

[24] Metze K., Expert Rev. Mol. Diagnost., 13 (2013) 719. [25] Li J. and Starzewski M. O., SpringerPlus,4 (2015) 158. [26] Geim A. K. and Novoselov K. S., Nat. Mater.,6 (2007)

183.

[27] Novoselov K. S., Geim A. K., Morozov S. V., Jiang D., Katsnelson M. I., Grigorieva I. V., Dubonos S. V. and Firsov A. A., Nature (London),

438 (2005) 197.

[28] Xiao S., Zhu X., Li B.-H. and Mortensen N. A., Front. Phys.,11 (2016) 117801.

[29] Hwang E. H. and Das Sarma S., Phys. Rev. B, 75 (2007) 205418.

[30] Low T. and Avouris P., ACS Nano,8 (2014) 1086. [31] Sule N., Willis K. J., Hagness S. C. and Knezevic I.,

Phys. Rev. B,90 (2014) 045431.

[32] Ni G. X., McLeod A. S., Sun Z., Wang L., Xiong L., Post K. W., Sunku S. S., Jiang B.-Y., Hone J., Dean C. R., Fogler M. M.and Basov D. N., Nature, 557 (2017) 530.

[33] Cottam M. G. and Tilley D., Introduction to Surface and Superlattice Excitations, 2nd edition (CRC Press) 2004.

[34] Gonc¸alves P. A. D.and Peres N. M. R., An Introduc-tion to Graphene Plasmonics (World Scientific) 2016. [35] Vasconcelos M. S. and Cottam M. G., J. Phys. D:

Appl. Phys.,52 (2019) 285104.

[36] Madani A. and Entezar S. R., Phys. B: Condens. Mat-ter,431 (2013) 1.

[37] Vasconcelos M. S. and Albuquerque E. L., Phys. Rev. B,57 (1998) 2826.

[38] Bludov Y. V., Ferrira A., Peres N. M. R. and Vasilevskiy M. I., Int. J. Mod. Phys. B, 27 (2013) 1341001.

[39] Albuquerque E. L. and Cottam M. G., Polaritons in Periodic and Quasiperiodic Structures (Elsevier Science) 2004.

[40] Constantinou N. C. and Cottam M. G., J. Phys. C: Solid State Phys.,19 (1986) 739.

[41] Kohmoto M., Kadanoff L. P. and Tang C., Phys. Rev. Lett.,50 (1983) 1870.

[42] Li Y., Qi L., Yu J., Chen Z., Yao Y. and Liu X., Opt. Mater. Express,7 (2017) 1228.

[43] Davies C. L., Patel J. B., Xia C. Q., Herz L. M. and Johnston M. B., J. Infrared Millim. Terahertz Waves,

39 (2018) 1236.

[44] Depine R. A., Graphene Optics: Electromagnetic Solu-tion of Canonical Problems (Morgan & Claypool Publish-ers) 2016.

[45] Costa C. H., Vasconcelos M. S., Fulco U. L. and Albuquerque E. L., Opt. Mater.,72 (2017) 756. [46] Silva E., Costa C., Vasconcelos M. and Anselmo D.,

Opt. Mater.,89 (2019) 623 .

[47] Fan Y., Wei Z., Li H., Chen H. and Soukoulis C. M., Phys. Rev. B,88 (2013) 241403.

[48] Vasconcelos M. S., Albuquerque E. L. and Mariz A. M., J. Phys.: Condens. Matter,10 (1998) 5839. [49] T¨orm¨a P. and Barnes W. L., Rep. Prog. Phys., 78

(2014) 013901.

[50] Agranovich V. M., Litinskaia M. and Lidzey D. G., Phys. Rev. B,67 (2003) 085311.

[51] Tuz V. R., Fesenko V. I., Fedorin I. V., Sun H.-B. and Shulga V. M., Superlattices Microstruct., 103 (2017) 285.

[52] Olego D., Pinczuk A., Gossard A. C. and Wiegmann W., Phys. Rev. B,25 (1982) 7867.

[53] Sreekanth K. V., Zeng S., Shang J., Yong K. T. and Yu T., Sci. Rep.,2 (2012) 737.

[54] Zhang W., Zhang L., Zhang H., Song L., Ye Q. and Cai J., Mater. Res. Express, 5 (2018) 125601.

[55] Gopinath A., Boriskina S. V., Feng N.-N., Reinhard B. M.and Negro L. D., Nano Lett.,8 (2008) 2423. [56] Dal Negro L., Wang R. and Pinheiro F. A., Crystals,

Referências

Documentos relacionados

Não poderia deixar de agradecer ao “Bond do Capurro” meus colegas de mestrado, pela amizade e pelas mensagens de incentivo nos momentos desanimadores deste percurso (sobrevivemos

Base of wings not extremely narrow; hindwing with one apparent anal vein; in forewing CuP beyond axillary angle distant from anal margin; costal margin dark

(Ç) Em Volta Redonda hâ indûstria

Bártlová (2016) divide em três campos independentes, que são: os jogos matemáticos, os quebra-cabeças matemáticos e os problemas recreativos. Assim, ela descreve cada um

Em termos gerais, a técnica de marcação de munições pelo complexo [EuPIC3NMK3] revelou-se promissora para a análise de resíduos de disparos de armas de fogo, possibilitando

 Utilização de um planejamento experimental para estudar a influência dos parâmetros na reação: razão molar óleo/acetato de metila; quantidade de catalisador em relação à

Na Seção 2.2 são destacados a arquitetura do middleware Ginga e abordados aspectos importantes sobre a programação de aplicações para a TV Digital, com ênfase nas linguagens NCL

Emissão de NH3 observada pela incubação de diferentes materiais torta de mamona – TM, gliricídia – GL e bagaço de cana – BC obtida pelo método de captura conjunta de CO2 e de