Numerical Investigation of Tunable Plasmonic Tweezers based on Graphene Stripes

We are proposing tunable plasmonic tweezers, consisting two parallel graphene stripes, which can be utilized to effectively trap and sort nanoparticles. We show that by electrostatically tuning the chemical potential of a graphene stripe by about 100 meV (equivalent to ΔVG ≈ 4.4 V), the plasmonic force can be switched efficiently, without a need to switch the laser intensity. This enables high speed and low power switching with a large number of switching cycles. By applying two independent and appropriate gate bias voltages to the stripes, the direction of the plasmonic force can be reversed, which leads to separation of nanoparticles that satisfy the trapping conditions. Numerical simulations show that the potential depths obtained for polystyrene nanoparticles of refractive index n = 1.5717 and radii r ≥ 50 nm is deeper than −10 kBT , confirming the ability of the proposed system to effectively separate such nanoparticles. This capability holds for smaller nanoparticles with larger refractive indices. Finally, performing thermal simulations, we have demonstrated that the heat induced by the illumination increases the fluid temperature by at most 9 °C, having negligible effect on the trapping mechanism. The proposed system opens up new possibilities in developing tunable on-chip manipulation devices, suitable for biological applications.

Here, we have designed a plasmonic force switch in mid-IR range, benefiting from surface plasmons in graphene stripes for sorting nanoparticles.
The Proposed Structure and Operation Principle. Figure 1 shows a 3D schematic representation (a), and top view (b) of the proposed system. It consists of two 100 nm wide graphene stripes on SiO 2 , separated by a 100 nm spacing. This spacing isolates the stripes electrostatically and enables us to control their chemical potential independently by applying different gate bias voltages (V G 1,2 ). The zoomed-in view displays the structure cross-section, in which each of the two graphene stripes is topped by a 10-nm thick SiO 2 layer that separates the stripe from its top gold (Au) gate contact. As can be seen from the figure, the system is divided into two regions -i.e., the detection and the sorting regions. Polystyrene particles are tagged by two different fluorescence labels (red and green), before being injected into the microfluidic channel via the sample inlet. The injected particles are focused, hydrodynamically, to a line of single particles moving along the channel midline 5,19,29 . Then, they are envisioned by fluorescence microscopy while passing through the detection region 28 , where they can be identified by their colored labels. Next, in the sorting region, appropriate bias voltages (V G 1 and V G 2 ) are applied to the graphene stripes to adjust the chemical potentials, according to the data achieved from the detection region. Meanwhile, graphene stripes are normally illuminated in the sorting region, by a plane wave with linear polarization along the stripes widths. For the red (green) particles, V G 1 (V G 2 ) is switched on, so that the field enhancement occurs on the stripe 1 (2), where the localized SPs are excited. We intentionally chose the polarization direction of the incident light to be along the stripes widths, so that the localized SPs are excited due to the confinement of the graphene stripes in y-direction. Since the incident light is illuminated normally and the x component of the wave vector is zero (k x = 0), the generated localized SPs are not expected to propagate along the x axis. Hence, the optical force has no x-component to affect the particles movement along the x-direction. The gradient component of the plasmonic force pushes down the red (green) particles toward the stripe 1 (2) while passing through the sorting region, until they exit from the outlet 1 (2). Nonetheless, if the trapping conditions are not satisfied, the untrapped particles continue to move along the channel midline (x-direction) without deflection, exiting from outlet 3. The proposed design enables us to electrostatically switch the direction of gradient force and sort the particles according to their fluorescent labels. This technique allows the force switching by a low voltage electrical gating, without a need to switch the laser intensity. High speed and low power switching, in addition to enabling a large number of switching cycles, are among other advantages of this configuration.
Simulation Method. To elaborate the proposed system quantitatively, numerical simulations were conducted using 3D finite difference time domain technique, using the perfectly matched layer boundary condition. Graphene is considered to be a single 2D layer, whose optical surface conductivity can be derived using Dyadic Green's function 30 : where e is electron charge,  is the reduced Planck's constant, is the Fermi-Dirac distribution, k B is the Boltzmann's constant, ω is the angular frequency, μ c is the graphene chemical potential, μμ is the phenomenological scattering rate, μ e is the electron mobility, 10 m/s f 6 υ ≈ is the Fermi velocity in graphene, and T is the temperature. The first and the second integrals in Equation 1 refer to the intraband and interband transitions, respectively. It can be observed that optical surface conductivity of graphene, therewith its plasmonic behavior, can be controlled by modulating μ c , via electrostatic gating.
The gate voltage V G 1 (V G 2 ) needed to create appropriate chemical potential in a graphene stripe is calculated using a simple parallel plate capacitor model 31 . According to this model, the applied voltage V changes the charge carrier density n of a graphene stripe: where ε d and t d are the dielectric constant and the thickness of the gate oxide and V 0 is the offset voltage caused by natural doping. This leads to a shift in the chemical potential of the graphene stripe: From Equations 2 and 3, the gate voltage needed to create a determined chemical potential in each of the stripes is calculated: The average optical force exerted on a particle is evaluated using the surface integral: where t T r ( , ) is the Maxwell stress tensor, ε and μ are the medium permittivity and permeability, E and H are the electric and magnetic field intensity vectors, r and t represent the position vector and time, and n is the unitary vector normal to the surface that encloses the volume Ω. This volume is assumed to be a cubic box surrounding the particle that moves along with the particle in order to consider the displacements.

Numerical Results and Discussions
To design an efficient plasmonic force system, first, we studied the effect of different system's parameters on the plasmonic field distribution. For this purpose, as we have pointed out earlier, a laser light is illuminated to a single graphene stripe at normal incidence. The laser light is assumed to be a plane wave with linear polarization along the width of the stripe. The substrate and the fluid containing polystyrene nanoparticles are considered to be glass (n g = 1.52) and water (n w = 1.33), respectively. Figure 2(a) shows mode intensity map normalized with respect to the incident light intensity ( E E / 0 2 ), probed at 10 nm above the graphene stripe, as the incident wavelength and the chemical potential are varied (8.4 ≤ λ ≤ 9.6 μm and 550 ≤ μ c ≤ 800 meV). As can be observed in this figure, the electromagnetic field is enhanced due to surface plasmon excitation at specific wavelengths and chemical potentials. Figure 2(b) displays the normalized mode intensity profiles for three different wavelengths versus the chemical potential. As shown in this figure, by tuning the chemical potential, at any of the three given wavelengths, the related field intensity can be switched from its minimum to maximum value and vice versa. Henceforth, we assume the incident wavelength to be 9 μm, so we can simply switch between its ON state (nearly maximum field intensity) and OFF state (less than 10% of the maximum) by switching the chemical potential between 700 and 600 meV respectively. Considering the 10-nm thick SiO 2 as the gate oxide and using Equation 4, one can easily in the applied gate voltage can lead to 100 meV shift in the chemical potential of the graphene stripe.
To investigate the sorting functionality of our proposed double graphene stripe system, the normalized field distribution in the y − z plane (at x = 0) and in the x − y plane (at = z 10 nm) are calculated. The results are shown in Fig. 3(a),(b), respectively. As can be observed from these figures, the bias voltages V G 1 and V G 2 are adjusted such that the stripe 1 is ON and the stripe 2 is OFF. In other words, the SPs are excited on the surface of the stripe 1. The results for the case, in which the metallic gates are biased such that the stripe 1 is OFF and the stripe 2 is ON are the mirror images of those shown in Fig. 3(a),(b), with respect to the − x z plane (y = 0). In the latter case, the particles are pulled towards the stripe 2. As shown in Fig. 3, the field intensity is non-uniform across the stripe width (y-direction). It is maximum near the edges and sharply drops across the stripe width. Meanwhile, the same data reveal that the field intensity along the stripe (x-direction) is uniform. Thus, the plasmonic gradient force along the stripe is expected to be zero. Besides, since the wave vector of the incident beam has no x-component, we expect the x-component of the net plasmonic force to be zero.
For an incident light of intensity I 20 mW/ m 2 μ = , the components of the force exerted on a polystyrene nanoparticle of radius = r 50 nm and refractive index n 1 5717 = .
are calculated. The results for the biasing condition in which stripe 1 is ON and stripe 2 is OFF are shown in Fig. 4(a). Those for the biasing condition in which stripe 1 is OFF and stripe 2 is ON are the mirror images of the data shown in Fig. 4(a), with respect to y 0 = . As shown in this figure, the z-component of the plasmonic force above the stripe 1 is negative (F 0 z < ), pushing the nanoparticle toward the graphene surface with a peak strength (|F z | max ≈ 2.5 pN) located at the stripe midline ( = − y 100 nm indicated by the vertical dashes). Moreover, this figure shows that as one moves across the width of the stripe 1, from the left to the right of the horizontal axis, the y-component of the plasmonic force (F y ) starts from its maximum value (|F y | max ≈ 0.55 pN) at the stripe left edge y ( 150 nm) = − , decreasing toward zero at the stripe midline where the nanoparticle might be trapped, and continue to decrease until it reaches its largest negative value F F ( ) y y min m ax = − at the stripe right edge = − y ( 5 0 nm). As a consequence, a potential well across the stripe 1 is formed that can trap the particle above the stripe, if equals − k T 10 B or deeper. Moreover, the blue bullets in Fig. 4(a) show that the x-component of the plasmonic force is zero (F 0 x = ), allowing the fluid flow to push the trapped particle toward the outlet 1 for this case. When the biasing condition is reversed, the potential formed across the stripe 2 may trap the particle above the stripe, and the fluid flow pushes the trapped particle toward the outlet 2. If the potential depth is, however, shallower than − k T 10 B , the trapping condition is not fulfilled and fluid flow pushes the untrapped particles toward the outlet 3. Figure 4(b) shows the profiles of the potential energies along the y-direction for the same biasing condition as for Fig. 4(a). These profiles are obtained by the integral ∫ F dy y above and across the graphene stripes widths. As shown in this figure, when the intensity of the incident light is I 20 mW/ m 2 μ = , the depth of the potential well is slightly deeper than k T 10 B − , enough for a stable trap that can overcome the thermal oscillations of particles 1 . The trapped particles y-positions, for the given operating condition are indicated by the vertical dashes. As explained earlier, the only force affecting the particles movements along the channel is due to the fluid flow. Hence, the trapped particles move along the stripe that is ON, before exiting from the corresponding outlet 1(2).
Next, we have investigated the effect of the particle size and refractive index on trapping conditions. of radii r 40, 50, and 60 nm = are shown in Fig. 5(a). It can be observed that the larger the particle radius, the stronger the plasmonic force exerted on it and hence the deeper the resulting potential well across the stripe that is ON. However, there is a limit in increasing the particle size. As the particle's diameter becomes larger than the stripe width, the portion of the particle volume that can effectively interact with the plasmonic field is decreased, decreasing the potential depth as a consequence. Moreover, Fig. 5(a) also reveal that the given operating condition in the presence of polystyrene nanoparticles with radii < r 50 nm cannot create potential wells deep enough to trap the particles effectively. Figure 5(b,c) illustrate the numerical results obtained for similar nanoparticles with refractive indices of = n 2 and 3, respectively. Comparison of potential profiles for particles of the same radii but different refractive indices demonstrates that the larger the refractive index, the stronger the plasmonic force exerted on the particle and the deeper the resulting potential well across the stripe that is ON. The laser intensity used for the stable trapping in this research is comparable to that of the recently proposed graphene-based plasmonic tweezers 22 as well as other metal plasmonic structures [32][33][34] . Higher intensities have also been used with the aid of appropriate heat sinks to overcome the thermal effects 35 . Moreover, high thermal conductivity ) in addition to its extremely low power absorption quickly removes the generated heat 36 . It has also been numerically shown that the same laser intensity generates much less heat in graphene surrounding nanoholes than it generates in a gold layer surrounding nanoholes 21 . Nonetheless, to elaborate the thermal behavior of the proposed system, we have carried out the heat transfer and convection calculations in the − y z plane = x ( 0), using finite element method with open boundary condition at T 20 C 0 =°. We also considered no-slip boundary condition at z = 0 that assumes a zero fluid velocity close to the interface between the fluid and the substrate. Colored pattern in Fig. 6 represents the spatial distribution of the fluid temperature and the arrows directions and colors together define the fluidic convection velocity vectors, when the stripe 1 in ON and μ = I 20 mW/ m 2 . As can be observed from this figure, the maximum temperature above the stripe 1 that is ON reaches to 29 °C.
Using the data shown in Fig. 6, we can estimate the stochastic Langevin force, F th that is responsible for Brownian motion of the particles, from its correlation function, Here, k B , T, and r 6 γ πη = are the Boltzmann constant, the fluid temperature, and the drag coefficient, in which η is the fluid viscosity. The delta function t t ( ) δ − ′ states that there is no correlation between the force in time t and any other instants of time 18,37 . As an example, the maximum Langevin force that may be exerted on a 50-nm particle with the achieved thermal conditions (Fig. 6) is on the order of a few fNs that is about three orders of magnitude smaller than the calculated optical force maxima. Moreover, the fluidic convection velocity vectors, shown in Fig. 6, indicate that the temperature gradient leads to a convective fluid flow around the bright spot that may adversely affect the trapping and sorting operation. However, the effective force on a spherical particle due to this convective flow has been obtained using the Stokes' drag force equation in which v is the fluidic convection velocity vector 38 . Considering the maximum velocity observed in Fig. 6, the effective force due to the convection is also negligible as compared with the optical force maxima. Also, in a spatial temperature gradient, a particle is subjected to thermophoretic force that can be approximately determined by F v = − ∇ is the steady state thermophoretic velocity acquired by a particle drifting along the temperature gradient T ∇ , and D T is the thermophoretic mobility 18,38,39 . The amounts of D T for different aqueous particle suspensions have been measured in numerous experiments and is reported to vary in a range within . Assuming a uniform temperature gradient of T 10 K m 1 μ ∇ = − , the thermophoretic force becomes about two orders of magnitude smaller than the optical force maxima 41 . Hence, these infinitesimally negligible Langevin, thermophoretic and Stokes' drag forces has insignificant effects on the performance of the designed plasmonic tweezers.

Conclusion
In this paper, we have presented a tunable plasmonic nanoparticle sorting system based on two parallel graphene stripes. Each of the 100-nm wide graphene stripes has been biased independently, to control its chemical potential via electrostatic gating. Simulations show that by altering the chemical potentials of the two stripes, the direction  of the plasmonic force exerted on nanoparticles moving in the microfluidic channel is reversed. Injected polystyrene particles, which are hydrodynamically focused in the centerline of the channel, are separated by appropriate electrical gating and are collected through either of the two designated outlets, if the trapping conditions are satisfied. Otherwise, the untrapped particles continue to move with the fluid along the channel midline, flowing out from the third outlet. It is shown that altering the gate voltage about 4.4 V results in potential depth variation of about −10 k B T for a polystyrene nanoparticle of radius = r 50 nm and refractive index n 1 5717 = .
. The potential depth and hence, the trapping stability can be improved by using larger polystyrene nanoparticles or smaller nanoparticles with higher refractive indices. Moreover, performing thermal simulations have shown that the heat induced by the 20 mW/μm 2 illumination elevates the fluid temperature by at most 9 °C that has infinitesimally negligible effect on the plasmonic trapping mechanism. The proposed design enables us to electrically switch the direction of the exerted plasmonic force and actively sort the particles.