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. 2021 Nov 23;12(12):1435. doi: 10.3390/mi12121435

Nanoresonator Enhancement of Majorana-Fermion-Induced Slow Light in Superconducting Iron Chains

Huajun Chen 1
Editor: Patrice Salzenstein1
PMCID: PMC8705128  PMID: 34945284

Abstract

We theoretically investigate Fano resonance in the absorption spectrum of a quantum dot (QD) based on a hybrid QD-nanomechanical resonator (QD–NR) system mediated by Majorana fermions (MFs) in superconducting iron (Fe) chains. The absorption spectra exhibit a series of asymmetric Fano line shapes, which are accompanied by the rapid normal phase dispersion and induce the optical propagation properties such as the slow light effect under suitable parametric regimes. The results indicated that the slow light induced by MFs can be obtained under different coupling regimes and different detuning regimes. Moreover, we also investigated the role of the NR, and the NR behaving as a phonon cavity enhances the slow light effect.

Keywords: Majorana fermions, nanomechanical resonator, quantum dot, slow light

1. Introduction

Majorana fermions (MFs) have witnessed significant progress in the past few decades in condensed matter systems due to their potential applications in decoherence-free quantum computation and quantum information processing [1] because they obey non-Abelian statistics. Although proposed originally as a model for neutrinos, MFs have recently been predicted to occur as quasi-particle bound states in engineered solid state systems [2], such as semiconducting nanowire/superconductor (SNW/SC) hybrid structure [3,4,5,6], ferromagnetic atomic chains on a superconductor [7], iron-based superconductor hybrid devices [8], topological superconductors [9,10], and topological insulator structures [11]. To observe Majorana-like signatures in the hybrid solid-state systems, a few significant and representative experimental schemes have been proposed, such as the zero-bias peaks (ZBPs) in tunneling spectroscopy [3,4,5,6,7], the Josephson effect [12], Coulomb blockade spectroscopy [9], and the spin-resolved measurements [13].

On the other hand, due to the significant progress in modern nanoscience and nanotechnology, artificial atoms, i.e., quantum dots (QDs) [14], indicate the ideal intermediary to detect and investigate MFs both theoretically [15,16,17,18,19] and experimentally [20]. We found that QDs are always treated as only a resonant level [15,16,17,18,19] in the detection of MFs with QDs in the electrical domain. Different from the previous schemes for detecting MFs, we presented an optical scheme for probing MFs with QD treated as a two-level system (TLS) and driven by the optical pump–probe technology [21,22], which may provide a potential supplement for detecting MFs. In order to investigate MF-induced coherent optical propagation, such as the slow light effect, we designed a hybrid QD–SNW/SC ring device [23,24], and to reach the enhanced coherent optical spectra, we considered putting the QD into a nanomechanical resonator (NR) system [21,22]. However, the NR enhancement of the coherent optical propagation, such as the fast and slow light effects [25,26,27] mediated by MFs, have not yet been explored to the best of our knowledge.

In this paper, motivated by the above-mentioned optical schemes for detecting MFs, we investigated the Fano resonance and slow light in the hybrid system discussed in [22], where a two-level QD was implanted in an NR to probe MFs in ferromagnetic atomic chains on a superconductor. Previous works for detecting MFs by optical means have shown that both the linear [22] and nonlinear [21] optical spectra are enhanced significantly when the NR is introduced. In the present paper, we first investigated the absorption spectra of the QD in the hybrid QD–NR system and the iron chains on the superconducting Pb surface, as shown in Figure 1, under different system parameters including the QD–MF coupling strength β, the QD–NR coupling strength g, the Majorana–pump field detuning ΔM, and the exciton–pump field detuning Δc. Especially, the absorption spectra display a series of asymmetric Fano line shapes when considering QD–MF coupling, which can be illustrated using the interference effect with the dressed state theory. Due to Fano resonances being characterized by a rapid, steeper dispersion, the group velocity index ng of light pulses can be accelerated and decreased significantly, which correspond to the negative and positive dispersion, respectively, and then reach the fast and slow light effects. Second, we investigated the slow light effect by numerically calculating the group delay of the probe field around the transparency window accompanied by the steep phase dispersion, and we found that a tunable and controllable slow light propagation can be achieved by manipulating the parametric regimes. Moreover, the slow light effect was enhanced significantly compared with previous work [24] because, here, the NR was introduced in the present system, which acts as a phonon cavity, enhancing the slow light effect.

Figure 1.

Figure 1

(a) The schematic of the hybrid device, where a two-level QD is coupled to a nearby MF in the iron chains on the superconducting Pb surface. (b) The QD driven by two-tone fields is embedded in an NR.

2. Model and Theory

2.1. The Hamiltonian of the System

The schematic setup studied in this work is shown in Figure 1, where iron (Fe) chains are overlaid on the superconducting Pb(110) surface [7], and we employed a two-level QD driven by two-tone fields to investigate the coherent optical properties mediated by MFs [23]. To obtain the enhanced coherent optical properties, we considered that the two-level QD is implanted in an NR system to make up a hybrid QD–NR system [22]. Here, based on the hybrid system as shown in Figure 1, we investigated MF-induced coherent optical propagation. The QD was treated as a TLS consisting of the ground state g and the single exciton state e in the hybrid QD–NR system, and HQD=ωexSz with the exciton frequency ωex is the Hamiltonian of the QD, where Sz and S± are the pseudospin operators with commutation relations Sz,S±=±S± and S+,S=2Sz. For the NR [28,29], which can be characterized by a harmonic oscillator with Hamiltonian HNR=ωmb+b (where b and ωm are the annihilation operator and frequency of the phonon mode), due to the thickness of the beam being much smaller than its width, and then, the lowest-energy resonance corresponding to the fundamental flexural mode will constitute the phonon mode. In the hybrid QD–NR system [28], the flexion induces extensions and compressions, and then, the longitudinal strain will modify the energy of the electronic states of QDs via deformation potential coupling with the coupled Hamiltonian Hcou=ωmβSz(b++b) with the coupling strength β [28]. As a result, we obtain the Hamiltonian of the hybrid QD–NR system as:

HQDNR=ωexSz+ωmb+b+ωmβSz(b++b). (1)

For the QD–MF coupling, due to each MF being its own antiparticle, then an operator γ with γ=γ and γ2=1 is introduced to describe MFs. We obtain that the Hamiltonian of the QD couples to the nearby MF γ1 as follows [15,16,17,18,19,21,22,23,24]:

HQDMF=iϵMγ1γ2/2+ig(SS+)γ1, (2)

where the first term in Equation (2) is the interaction of the two MFs in Fe chains on the superconducting Pb. ϵM=ωMel/ξ is the coupling energy with l being the length of the Fe chains and ξ the superconducting Pb coherent length with Majorana frequency ωM. If the length l is large enough, we find the coupling energy ϵMel/ξ0. Therefore, we need to discuss the two cases, i.e., ϵM0, termed coupled Majorana edge states, and ϵM=0, termed uncoupled Majorana edge states. The second one in Equation (2) gives the near by MFs γ1 coupled to the QD with the coupling strength β, which relate to the distance of the QD and superconducting device. For simplicity, we introduce the regular fermion creation and annihilation operators f and f with the anti-commutative relation f,f=1; thus, according to the relation of γ1=f+f and γ2=i(ff), Majorana operator γ can be transformed into the regular fermion operator f. Then, the second term in Equation (2) reduces to ig(SfS+f) by neglecting the non-conservation terms of energy ig(SfS+f+) based on the rotating wave approximation [30]. Therefore, Equation (2) can be reduced to:

HQDMF=ΔM(ff1/2)+ig(SfS+f). (3)

When the hybrid QD–NR system is driven by two-tone fields [31], the Hamiltonian of QD coupled to the two fields is given by [32]:

HDriQD=μεp(S+eiωct+Seiωct)μεs(S+eiωst+Seiωst), (4)

where μ is the dipole moment of the exciton, ωc (ωs) is the strong pump (weak probe) field frequency, and εc and εs are the slowly varying envelope of the pump field and probe field, respectively. In a rotating frame of frequency ωp, we obtain the total Hamiltonian of the system as:

H=ΔcSz+ωmb+b+ωmβSz(b++b)+ΔM(ff1/2)+ig(SfS+f)Ωc(S++S)μεs(S+eiδt+Seiδt), (5)

where Δc=ωexωc (δ=ωsωc, ΔM=ωMωc) is the detuning of the exciton frequency (probe field, the MF frequency) from the pump frequency. Ωc=μεc/ is the Rabi frequency of the pump field.

2.2. Quantum Langevin Equations

According to the Heisenberg equation of motion iρ/t=[ρ,H] (ρ=Sz, S, f, Q), we can obtain the Heisenberg–Langevin equations (H-LEs) of the operators with the corresponding noise and damping terms as follows:

S˙z=Γ1(Sz+1/2)g(Sf+S+f)+iΩc(S+S)+(iμεs/)(S+eiδtSeiδt), (6)
S˙=[(iΔc+ωmβQ)+Γ2]S+2gSzf2iΩcSz2iμεsSzeiδt/+τ^(t), (7)
f˙=(iΔM+κM/2)f+gS+ς^(t), (8)
Q¨+γmQ˙+ωm2Q=2ωm2βSz+ξ^(t), (9)

where Γ1 (Γ2) is the exciton spontaneous emission rate (dephasing rate), Q=b+b is the position operator, and γm (κM) is the decay rate of the NR (MF). τ^(t) is the δ-correlated Langevin noise operator with zero mean and obeys the correlation function τ^(t)τ^(t)δ(tt). ς^ and ξ^ represent the Langevin force arising from the interaction between the Majorana modes and the environment [22,33].

We introduce the perturbation theory: ρ=ρ0+δρ, then ρ0 (i.e., S0z, S0, and f0) means the steady parts and δρ (i.e., δSz, δS, and δf) indicates the fluctuation ones. Substituting the perturbation method into Equations (6)–(9), we obtain the steady-state solutions of the variables as follows:

Γ1(w0+1)+2g(S0f0*+S0*f0)=2iΩc(S0S0*), (10)
(iΔc+Γ2)S0=2(gf0iΩc), (11)
(iΔM+κM/2)f0=gS0,Q0=βw0, (12)

which determine the steady-state population inversion (w0=2S0z) of the exciton as follows:

Γ1(w0+1)(Ξ1Ξ2+β2w02Ξ3)+4w0Γ2Ωpu2Ξ1=0. (13)

where Ξ1=ΔM2+κM2/4, Ξ2=(Δc2+Γ22+ωm2g4w022ωmΔcg2w0), Ξ3=β22ωmΔMg2+2ΔcΔMΓ2κM, and Δc=Δc+ωmβQ0. As all the pump fields are assumed to be sufficiently strong, all the operators can be identified with their expectation values under the mean-field approximation Qc=Qc [34], and after being linearized by neglecting nonlinear terms in the fluctuations, the H-LEs for the expectation values are:

δS˙z=Γ1δSzg(S0δf+S0*δf+f0*δS+f0δS+)+iΩp(δS+δS)+iμεs(S0*eiδtS0eiδt), (14)
δS˙=(iΔc+Γ2)δS2iΩcδS+2g(f0δS+S0δf)iμεsw0eiδt, (15)
δf˙=(iΔM+κM/2)δf+gδS, (16)
δQ¨+γmδQ˙+ωm2δQ=2ωm2βδSz. (17)

2.3. Coherent Optical Spectrum

In order to solve the equation set of the above H-LEs, we make the ansatz [32] δρ=ρ+eiδt+ρeiδt. Solving the equation set and working to the lowest order in εs, but to all orders in εp, we obtain the linear optical susceptibility as χeff(1)(ωs)=μS+(ωs)/εs=Σ1χ(1)(ωs) with Σ1=μ2/(Γ2), and then, the dimensionless linear susceptibility χ(1)(ωs) is given by:

χ(1)(ωpr)=[(Π4*+Λ1Π3*)Π1Λ3iw0Π4*]Γ2Π2Π4*Λ1Λ2Π1Π3*, (18)

where Σ1=g/(iΔM+κM/2iδ), Σ2=g/(iΔM+κM/2iδ), η=2βωm2/(δ2+iδγmωm2), Λ1=[iΩcg(f0+S0Σ2*)]/(Γ1iδ), Λ2=[iΩcg(f0*+S0*Σ1)]/(Γ1iδ), Λ3=iS0*/(Γ1iδ), Π1=2(gf0iΩc)iωmβS0η, Π2=i(Δcδ+ωmβQ0)+Γ2gw0Σ1Λ2Π1, Π3=2(gf0iΩc)iωmβS0η*, Π4=i(Δc+δ+ωmβQ0)+Γ2gw0Σ2Λ3Π3. The imaginary and real parts of χ(1)(ωpr) indicate absorption and dissipation, respectively.

2.4. Group Velocity Index

As the light group velocity as [35,36] υg=c/[n+ωs(dn/dωs)] where n1+2πχeff(1), then we obtain:

c/υg=1+2πRe[χeff(1)(ωs)]ωs=ωex+2πωsRe(dχeff(1)/dωs)ωs=ωex. (19)

Obviously, when Re[χeff(1)(ωs)]ωs=ωex=0, the dispersion is steeply positive or negative and the group velocity is significantly reduced or increased. We further define the group velocity index ng as:

ng=cυg1=cυgυg=2πωexρμ2Γ2Re(dχeff(1)dωs)ωs=ωex=Γ2ΣRe(dχeff(1)dωs)ωs=ωex, (20)

where Σ=2πωexρμ2/Γ22. One can observe the slow light if ng>0 and the superluminal light when ng<0 [37]. For the parameters of the hybrid QD–NR system [28], the exciton relaxation rate (the exciton dephasing rate Γ2) Γ1=0.3 GHz (Γ2=0.15 GHz). The parameters NR are (ωn, M, Qf)=(1.2 GHz, 5.3×1018 kg, 3×104), where ωm, M, and Qf are the resonator frequency, the effective mass, and the quality factor of the NR, respectively. The decay rate of the NR is γm=ωm/Qf=40 kHz, and the coupling strength is β=0.06. The parameters of MFs [3,4,5,6,24], the QD–MFs coupling strength g=0.1 GHz, the decay rate of the MFs κM=0.1 MHz, Γ1=0.3 GHz, Γ2=0.15 GHz, and Ωp2=0.1(GHz)2.

3. Numerical Results and Discussion

There are two kinds of coupling in the hybrid system, i.e., the QD–MF coupling and the QD–NR coupling, as shown in Figure 1, and in the QD–MF coupling regime, ΔM=0 or ΔM0, i.e., the uncoupled Majorana edge state or coupled Majorana edge state will also influence the coherent optical properties, so it is necessary to investigate the coherent optical spectra under different parameters and coupling regimes. Figure 2 shows the absorption spectra of the QD as a function of probe–exciton detuning Δs=ωsωex at the red detuning (Δc=ωm) for different parameters and coupling regimes. In Figure 2(a1,a2), we give the absorption spectra under ΔM=0 and ΔM0, respectively, for the parameters of g=0, β=0, and Δc=ωm, i.e., there are no QD–MF coupling (g=0) and QD–NR coupling (β=0), and only the QD is driven by a pump laser and a probe laser, then the absorption spectra show a Lorentz peak. In Figure 2(b1,b2), we consider the QD–MF coupling (g0) without considering the QD–NR coupling (β=0). In the uncoupled Majorana edge state (ΔM=0), the absorption spectrum not only shows a Lorentz peak around Δs=0, but also presents a sideband peak at Δs=ωm (ωm=1.2 GHz), as shown in Figure 2(b1). In the coupled Majorana edge state (ΔM0, such as ΔM=0.2 GHz), the absorption spectrum also displays a Lorentz peak around Δs=0; however, the sideband peak at Δs=ωm in Figure 2(b1) is split into two peaks located at ωm+ΔM (−1.4 GHz) and ωmΔM (−1.0 GHz), respectively, as shown in Figure 2(b2). In Figure 2(c1,c2), we not only consider the QD–MF coupling (g0), but also consider the QD–NR coupling (β0). In the case of ΔM=0, the absorption spectrum as shown in Figure 2(c1) shows the same result as shown in Figure 2(b1), i.e., in the uncoupled Majorana edge state (ΔM=0), the role of the QD–NR coupling (β0) is feeble and can be neglected. However, in the coupled Majorana edge state (ΔM=0.2 GHz), if the QD–MF coupling (g0) and the QD–NR coupling (β0) simultaneously exist in the system, as shown in Figure 2(c2), we find that not only the absorption spectrum at Δs=0 displays a Fano resonance (an asymmetric splitting), but also the sideband peak at Δs=ωm shows a splitting located at ωm+ΔM and ωmΔM, respectively. For the Fano resonance around Δs=0 in the absorption spectrum, the physical origin of this result is due to the QD–MF coherent interaction, and a dressed state theory was introduced to interpret this physical phenomenon [38]. Therefore, the coupled Majorana edge state (ΔM0) combined with the QD–MF coupling and the QD–NR coupling will together influence the absorption spectrum, and then, it is necessary to research the role of the coupled Majorana edge state in the following.

Figure 2.

Figure 2

(a1,a2) The absorption spectra versus the probe–exciton detuning Δs for the parameters of g=0, β=0, Δc=ωm under the condition of ΔM=0 and ΔM0, respectively. (b1,b2) The absorption spectra versus Δs for the parameters of g=0.1 GHz, β=0, Δc=ωm under the condition of ΔM=0 and ΔM0, respectively. (c1,c2) The absorption spectra versus Δs for the parameters of g=0.1 GHz, β=0.06, Δc=ωm under the condition of ΔM=0 and ΔM0, respectively.

In Figure 3, we further present the absorption and dispersion profiles as a function of the probe detuning Δs at the parameters of g=0.1 GHz, β=0.06, and Δc=ωm for several different Majorana–pump detuning ΔM. The left parts show the absorption, and we can find that the Fano resonance induced by QD–MF coupling at Δs=0 appear in the absorption spectra and the sideband peak induced by QD–NR coupling at Δs=ωm is split into two peaks. With increasing the detuning ΔM from ΔM=0.2 GHz to ΔM=1.4 GHz, in the two split peaks distributing in two sides of Δs=ωm, the left peak located at ωm+ΔM moves to the left, while the right peak located at ωmΔM moves to the right. The right parts plot the dispersion, and we show that the evolutionary process of the dispersion as a function of Δs with increasing detuning ΔM from ΔM=0.2 GHz to ΔM=1.4 GHz, which combines the absorption, will induce the slow light effect because the dispersion manifests a positive steep slope around Δs=0. The details of the absorption and dispersion around Δs=0 are displayed in the following figures.

Figure 3.

Figure 3

(Left) The absorption versus Δs for several different detuning ΔM. (Right) The dispersion versus Δs for several different detuning ΔM. The other parameters are g=0.1 GHz, β=0.06, Δc=ωm, and Ωc2=0.1 (GHz)2.

Then, in Figure 4a, we take ΔM=0.6 GHz as an example; the red curve shows the details of the absorption in Figure 3 around Δs=0; the absorption spectrum presents Fano resonance, and the Fano shape is related to the detuning ΔM. The blue curve plots the details of the dispersion in Figure 3 around Δs=0, and the dispersion is deep. However, no matter how the detuning ΔM changes, there is still an invariant result, i.e., the dispersion shows a positive steep slope around Δs=0. Therefore, we also investigated the Fano resonance-induced coherent optical propagation properties, as shown in Figure 4b. In Figure 4b, we plot the group velocity index ng versus the QD–MF coupling g for four different Rabi frequencies Ωc2 under the parameters of β=0.06, ΔM=0.6 GHz, and Δc=ωm. We can see that the group velocity index ng behaves as the slow light effect, and the process of the evolution of the group velocity index ng is related to the QD–MF coupling g.

Figure 4.

Figure 4

(a) The absorption and dispersion as a function of Δs at fixed ΔM=0.6 GHz. (b) The group velocity index ng versus the QD–MF coupling g for four different Rabi frequencies Ωc2 under the parameters of β=0.06, ΔM=0.6 GHz, and Δc=ωm.

Subsequently, in Figure 5a, we further investigate the absorption spectra as a function of Δs for three different QD–MF coupling g under the parameters of β=0.06, ΔM=0.6 GHz, Δc=ωm, and Ωc2=0.1 (GHz)2, and we found that the splitting width of the absorption spectra is enhanced with increasing the QD–MF coupling g. Figure 5b displays the process of the evolution of the dispersion for three QD–MF coupling g, and the inset is the detail part around Δs=0. We can obtain that the dispersion shows a positive steep slope around Δs=0, which results in the slow light effect. Therefore, in Figure 5c, we plot the group velocity index ng as a function of the Rabi frequency Ωc2 for ΔM=0 and ΔM0, respectively, at fixed QD–MF coupling g=0.05 GHz, and it is obvious that the group velocity index ng gradually increases and reaches a maximum, then decays to almost a zero value with increasing Rabi frequency Ωc2, both at the coupled Majorana edge state (ΔM0) and uncoupled Majorana edge state (ΔM=0). If we consider a bigger QD–MF coupling, such as g=0.15 GHz, as shown in Figure 5d, we can find that the slow light effect (i.e., the process of the evolution of the group velocity index ng) is more remarkable in the coupled Majorana edge state (ΔM=0.6 GHz) than in ΔM=0.

Figure 5.

Figure 5

(a,b) The absorption and dispersion as a function of Δs for three different QD–MF coupling g under the parameters of β=0.06, ΔM=0.6 GHz, Δc=ωm, and Ωc2=0.1 (GHz)2. (c,d) The group velocity index ng versus Ωc2 for QD–MF coupling g=0.05 GHz and g=0.15 GHz, respectively.

Except the QD–MF coupling g, the pump–exciton detuning Δc and the QD–NR coupling β can also affect the slow light effect. In Figure 6a, we give the absorption spectra as a function of Δs for three different pump–exciton detuning Δc under the parameters of β=0.06, g=0.1 GHz, ΔM=0.6 GHz, and Ωc2=0.1 (GHz)2, and it is clear that the absorption spectra show the mode-splitting behavior around Δs=0 and that a transparent window (i.e., the zero absorption depth, as shown in the inset in Figure 6a) also appears in the absorption spectra. Figure 6b displays the dispersion for three different Δc, and the dispersion has a positive steep slope around Δs=0, as shown in the inset in Figure 6b. Thus, in Figure 6c, we plot the group velocity index ng as a function of Ωc2 for three Δc at ΔM=0.6 GHz, and we can see that the slow light effect is more obvious in Δc=ωm than in Δcωm. We also investigated the role of the NR in the hybrid system that influences the slow light. The previous work demonstrated that the NR will behave as a phonon cavity, enhancing the coherent optical spectrum. Then, in Figure 6d, we compare the case of β=0 (no QD–NR coupling) and β0 (the QD–NR coupling strength β=0.06). If there is no QD–NR coupling, the slow light effect induced by MFs is demonstrated in a hybrid semiconductor/superconductor ring device [24], and it is similar to the result of the green curve in Figure 6d. However, if the QD–NR coupling is taken into consideration, such as the purple curve in Figure 6d, we can find that the group velocity index ng manifesting the slow light is enhanced significantly compared with the condition of no QD–NR coupling. Finally, by controlling the detuning regimes and the coupling regimes, the slow light can be reached in the hybrid system.

Figure 6.

Figure 6

(a,b) The absorption and dispersion versus Δs for three Δc under the parameters of β=0.06, g=0.1 GHz, ΔM=0.6 GHz, and Ωc2=0.1 (GHz)2; the insets are their details. (c) ng as a function of Ωc2 for three Δc at ΔM=0.6 GHz. (d) ng versus Ωc2 in the condition of β=0 and β0, respectively.

4. Conclusions

In conclusion, we demonstrated the coherent optical propagation properties in a hybrid device, which includes a QD driven by a pump field and a probe field implanted into an NR coupled to nearby MFs in superconducting iron (Fe) chains, and we investigated the absorption spectra of the probe field under different detuning regimes (such as pump–exciton detuning Δc and Majorana–pump detuning ΔM) and different coupling regimes (such as QD–MF coupling g and QD–NR coupling β). When the QD couples to nearby MFs, a Fano resonance can be obtained in the absorption spectra, which accompany the rapid phase dispersion inducing the slow light effect. The results showed that the group velocity index can be controlled by the QD–MF coupling, which can reach the slow light effect. Moreover, the NR was considered, which behaved as a phononic cavity, leading to an enhanced slow light effect.

Funding

Hua-Jun Chen was supported by the National Natural Science Foundation of China (Grants Nos. 11647001 and 11804004). The project was funded by the China Postdoctoral Science Foundation (Grant No. 2020M681973) and the Anhui Provincial Natural Science Foundation (Grant No. 1708085QA11).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The author declares that there are no competing interests.

Footnotes

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