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Design of high performance and low resistive loss graphene solar cells

A Correction to this article was published on 28 January 2021

This article has been updated


Despite metallic plasmonic excitations can enhance the performance of ultra-thin solar cells however these so-called plasmonic solar cells suffer from a large resistive (Ohmic) loss caused by metallic elements. In this work, we report on a new design that uses graphene nanoribbons (GNRs) in a two-dimensional (2D) grating form at the top of the semiconductor-on-insulator (SOI) solar cells aimed to reduce the resistive loss. The results showed that GNRs can remarkably reduce the resistive loss compared to the SOI cell with Ag nanograting, while keeping all other cell’s parameters, comparable with those of Ag SOI cell. Optical absorption and short-circuit current density of the graphene cells showed, respectively, enhancements of 18 and 1.7 times when optimizations were done with respect to width and the grating period. Our calculations showed that the graphene solar cells dissipate at most 5% of incident sunlight power as narrow and tiny peaks around 508 nm, which is noticeably lower than those of Ag solar cells with high and broad band peaks with the maximum values of 29% at 480 nm and 24% at 637 nm.


Nowadays, the huge decrease in fossil energy resources and high cost of pollution control has forced scientists to search for sustainable energy sources. During the years, different methods have been introduced. Among them, the most important one that guarantees a clean and environmentally friendly technique, has benefited from the photovoltaic effect [1, 2]. In spite of huge research which has been accomplished on solar cell topic, however, there are limitations on the massive production of solar cells. Regarding to this fact that the sunlight radiation covers almost a broad spectrum range, mainly from 290 nm in ultraviolet regime to 3200 nm in mid infrared one, for absorbing long wavelength photons, those which lie in near to mid infrared spectrum regime, thick absorption layers are needed [3]. Increasing the Si wafer thickness not only imposes additional cost, but also can cause junk recombinations, because of a short electron diffusion length [1, 2, 4, 5]. At least, one can name three types of recombination: the electron jumps back from conduction band to valence band and recombines with a hole while a photon is emitted. This process is called band-to-band recombination, or radiative recombination. Reed-Shockley-Hall (RSH) recombination is assisted by trap energy levels in band gap. Auger recombination is a process in which an electron and a hole recombine in a band-to-band transition, but the resulting energy is given off to another electron or hole. In the case of hybrid solar cell, mismatch of different crystal lattices may cause a large number of dangling bond at the interface between two different materials. The interface recombination can be viewed as a type of RSH and the interface becomes major limiting factor resulting in rather high interface recombination velocity which thereby lowers the lifetime of carriers.

Due to the aforementioned difficulties, it was a necessity to find an alternative solution to enhance the light absorption in the thin solar cells. For the first time, in order to improve the carrier collection efficiencies, Redfield [6] introduced dielectric waveguide concept to confine and guide the scattered emission in a Si film with a 2 μm thickness. The method used by Redfield means confining the light beams into a dielectric waveguide of a thin solar cell with an effective technique to enhance the light absorption. Yablonovitch, based on the ray optics, presented a statistical procedure toward measuring the enhancement factor for light intensity as 4n2 for bulk absorption and n2 for surface absorption to make the process of solar cell fabrication much more cost effective [7]. Here n is the refractive index of semiconductor film,

Obtaining the highest efficiency in any design and experiment is indeed a precious goal. Authors have innovated various configurations to enhance the quantum efficiency as well as the short-circuit current density of solar cells [8, 9]. For example, all-inorganic composition and suitable band gap of quantum dots (QDs) have been used in Perovskite solar cells to enhance the power conversion efficiency [10]. In the recent years, applying dielectric photonic crystals [3] and periodically patterned metallic structures [11] as back reflectors in order to enhance the electromagnetic energy intensity even beyond 4n2 limit has become a popular trend. Using the plasmonic excitations in the ultra-thin solar cells, one can simultaneously increase the efficiency of solar cells and reduce the cost of film deposition [1, 4, 12,13,14,15,16,17,18] which are two favorite factors in experimental research. Using perovskite–hybrid plasmonic nanostructured, Zhang et al. have explained the role of plasmonic coupling and photonic cavities in enhancing light–matter interactions and manipulating carrier dynamics [19].

There are at least three main schemes for plasmonic structures to be integrated with a solar cell. The first method involves locating the plasmonic elements at the top of the solar cell [13, 20,21,22]. It provides us with two important advantages: improving the optical absorption in absorption layer through scattering of light into it and preventing the reflection back [23]. Embedding the plasmonic structures inside the absorption layer is another approach [24], in which plasmonic nanoparticles act as subwavelength lenses enabling enhancing the light absorption. The third method is to arrange a grating or striped-like plasmonic structures at the back surface of the solar cell [25,26,27]. In this method, surface plasmon polaritons (SPPs) are excited in the absorption layer, leading to an increase in the optical absorption. Furthermore, in this scheme, where plasmoic structures are served as a back contact [28], a short distance provides proper conditions for collecting the charge carrier to be collected.

To support the SPPs in the active layer of a solar cell, it is a crucial need to find the optimum plasmonic material. Although for many years gold and silver have been of the most interesting and extremely popular materials [29, 30], they impose limitations one practical applications such as energy loss from intraband transitions, large Ohmic losses at the optical frequencies caused by electron-electron scattering, electron-ion scattering, and inelastic scattering from defects and grain boundaries [31], lack of tunability, and difficulties during the fabrication process. Since the first investigation on plasmonic effect, silver has been the best choice for visible light applications, because it has the lowest Ohmic loss and a high onset of intraband transitions. For near infrared/terahertz region, gold and copper can be used, but gold is usually preferred over copper since it doesn’t oxidize and is therefore more stable. There are other materials that have lower losses than silver and gold such as sodium and potassium, however these materials are not stable and would therefore not be easy to be used in plasmonic devices. Nevertheless, due to the lack of tunability and difficulties during the fabrication process, they impose limitations on practical applications.

The discovery of graphene and other 2D materials such as hexagonal boron nitride (h-BN), transition metal chalcogenides to a class of monoelemental 2D materials (Si, Ge, Sn, etc.) which happened in “postgraphene age” triggered a wide range of research concerning 2D materials covering metals, semiconductors, and insulators, all with intriguing properties [32,33,34]. It has been shown that strongly confined surface plasmonic excitation in graphene with outstanding properties such as electrical tunability [35], low dissipative losses [36], strong light-matter interactions [37], and extreme field confinement [38,39,40] can be a trustable substitution for noble materials. Compared with plasmons in noble metals, the electronic properties of graphene can be effectively controlled by changing the Fermi energy through the use of a gate voltage, chemical doping, and electric and magnetic fields [28]. Prominent properties of graphene along with its electronic [32,33,34, 41,42,43] and photonic [44,45,46] features have made it an interesting platform for plasmonic waveguiding applications [37, 47,48,49]. However, so far its abilities have been proven more in the terahertz and mid-infrared frequency range [50, 51] rather than optical spectral region [52] (, ( Patel et al. showed that multilayer graphene acts as an efficient transparent conducting electrode in a graphene/Si heterojunction solar cell [53]. Up to 40 layers of n-type graphene, the efficiency found to be constant and enhanced only to 7.62%. After further optimization on the parameters of p-crystalline silicon wafer, a maximum efficiency of 11.23% has been achieved.

In this work, we investigate the impact of graphene nanoribbons (GNRs) on the optical and electrical performance of ultra-thin SOI solar cells and compare the results with those of SOI cells incorporated with Ag nanostrips. Due to the extremely light confinement, high carrier mobility, and zero band gap characterizations, graphene is worth investigating the light absorption in the Si absorber layer by putting GNRs on SOI (G-SiO2-Si-SiO2) cells. Since graphene is a semimetal material, it seems that its special optical properties can help the waveguide-like modes in the optical frequency range to be strongly excited. These modes are not necessarily confined at the graphene/Si interface, but they are expanded in Si throughout. Our results show that these abnormally excitations can help the optical absorption to be increased in the active layer.

To evaluate systematically the cell’s performance, the optical absorption and short-circuit current density enhancements and resistive (Ohmic) loss of G-SiO2-Si-SiO2 solar cells are calculated and compared with those of Ag nanostrips incorporated SOI (Ag-SiO2-Si-SiO2) cells. For Ag-SiO2-Si-SiO2 solar cells, the optimum design which has been reported previously [17, 18] is used. For G-SiO2-Si-SiO2 cells, width and the period of GNRs, which are two key parameters in the performance of proposed structure, are optimized.

Model and theory

The geometry of our proposed solar cell is schematically shown in Fig. 1a which comprises GNRs at the top of a SOI solar cell. A 10 nm buffer SiO2 layer at the bottom of GNRs prevents undesired and strong damping of the surface plasmons resonances due to the Schottky effect [2]. A 50 nm absorption silicon layer is located under SiO2. Si layer is grown on a SiO2 layer with a 240 nm thickness. Figure 1b shows a unit cell of our G-SiO2-Si-SiO2 solar cell. Figure 1c illustrates an Ag-SiO2-Si-SiO2 solar cell in which an Ag nanograting is placed at the top of a SOI solar cell. For simplicity, a unit cell is shown. Ag nanostrip has a triangle cross section with a 60 nm height and an 80 nm base. For Ag nanostrips, experimental data of Johnson and Christy [31] including the real and imaginary parts of refractive indices were utilized. For optical properties of Si layer, we have used its dielectric function given in Ref. [54]. Refractive index of SiO2 is also set to 1.45. Note that the period of G-SiO2-Si-SiO2 and Ag-SiO2-Si-SiO2 solar cells are chosen to be 314 nm, except for Figs. 5 and 6b in which the grating periods are optimized.

Fig. 1
figure 1

a 3D schematic of G-SiO2-Si-SiO2 solar cell. A 10 nm SiO2, a 50 nm absorption layer (Si), and a 240 nm SiO2 substrate are considered. b A detailed unit cell of G-SiO2-Si-SiO2 solar cell. The thickness of GNR is set to 0.5 nm. c A detailed unit cell of Ag-SiO2-Si-SiO2 solar cell. An Ag strip with triangle cross section with 60 nm height and 80 nm width on a 10 nm SiO2, 50 nm absorption layer (Si), and 240 nm SiO2 substrate. For the top and the bottom sides of the unit cell, a perfectly matched layer (PML), and for lateral sides, the periodic boundary condition (PBC) is considered

A plane electromagnetic wave is illuminated from the top side of the simulation frame with a normalized value of unity. To solve the Maxwell’s wave equations and extraction of the solar cell parameters, we have considered only one unit cell with suitable boundary conditions to reduce the runtime and computational machine RAM. To ensure a realistic cell, we have used periodic boundary conditions for the lateral sides to include the periodicity of the structure, as shown in Fig. 1b and c. We have also used a perfectly matched layer (PML) for the top and the bottom sides of the simulation frame. PML boundaries can help diffracted waves to be absorbed properly. The wavelength scan is performed from 250 to 1100 nm with respect to ASTM-G173 and Si band gap (1.1 eV). It is worth mentioning when the imaginary part of the graphene surface conductivity is positive, the graphene layer behaves like a thin metal material and supports only transverse-magnetic (TM) mode [29]. Note also that under the transverse-electric (TE) mode, the graphene (and even Ag and Au with the thicknesses around 1 nm) will not represent any electromagnetic response in the solar cell, since their thickness is much smaller than the wavelength of the incident field. Therefore, in the following, we have only focused on the TM mode. By solving the Maxwell’s wave equations in the unit cell for the transverse-magnetic (TM) mode, the distribution of electric and magnetic fields was obtained. Here, the complex permittivity of graphene is calculated directly by using εg = 1 − g/(ε0ω t) [36], where ε0 is the permittivity of free space, t is the effective thickness of the graphene, and σg is the complex surface conductivity of graphene which depends on the angular frequency, ω, chemical potential, μc, temperature, T, and charge particle scattering rate, Γ = 1/τ, with τ being the relaxation time of charge carriers. Regarding the intraband and interband transitions, the total conductivity of graphene (σg = σinter + σintra) is described according to the local random phase approximation of the Kubo formula [55] which is written as [56]:

$$ {\sigma}_{\operatorname{int} ra}=\frac{2{ie}^2{Tk}_B}{{\mathrm{\hslash}}^2\pi \left(\omega +i/\tau \right)}\ln \left[2\cosh \left(\frac{\mu_c}{2{Tk}_B}\right)\right], $$
$$ {\sigma}_{\operatorname{int} er}=\frac{e^2}{4\pi}\left[\frac{1}{2}+\frac{1}{\pi}\arctan \left(\frac{\mathrm{\hslash}\omega -2{\mu}_c}{2{Tk}_B}\right)\right.\left.-\frac{i}{2\pi}\ln \frac{{\left(\mathrm{\hslash}\omega +2{\mu}_c\right)}^2}{{\left(\mathrm{\hslash}\omega -2{\mu}_c\right)}^2+{\left(2{Tk}_B\right)}^2}\right]. $$

In the above expression, e represents the charge of the electron, kB is the Boltzmann’s constant, and ω is the photon energy. In our calculations, we set the graphene parameters as τ = 5 ps, T = 300 K, and μc = 0.5 eV. Having found the electric and magnetic field distributions, the absorbed power in Si slab can be determined by the following formula [57]:

$$ \nabla .\overrightarrow{S}=\frac{1}{2}\underset{0}{\overset{\infty }{\int }}\omega \operatorname {Im}\left({\varepsilon}_{Si}\right)\;{\left|E\Big(x,y,z\Big)\right|}^2\; dV $$

where \( \overrightarrow{S} \) is Poynting vector, Im(εSi) is the imaginary part of the Si permittivity, and dV = dx dy dy is the differential volume of the absorption layer (Si). According to the absorption power formula, Eq. (3), the integration is taken over the whole absorption layer volume. In our 2D modeling, the cell is assumed to be invariant along the z-direction, so that the electromagnetic field varies only along x and y. Thus dV = l dx dy, where l is the cell length along the z-direction.

Absorption enhancement, Π(λ), is defined as the ratio of power absorbed in the Si layer of the cell with graphene nanoribbon (Ag nanostrip) to that of bare cell. Bare cells do not possess any graphene nanoribbon. Therefore, the absorption enhancement is given by:

$$ \Pi \left(\lambda \right)=\frac{\underset{GNR/ AG\; cell}{\int }{\left|E\left(x,y,\lambda \right)\right|}^2\; dx\; dy}{\underset{bare\kern0.17em cell}{\int }{\left|E\left(x,y,\lambda \right)\right|}^2\; dx\; dy} $$

To perform fully evaluation on the solar cells, the short-circuit current density (JSC) of the proposed structures should also be calculated. JSc is the current density flowing through the solar cell when the voltage over the cells is assumed to be zero. For an ordinary cell, the short-circuit current density is calculated through the integration of the product of solar irradiance, I(λ), and cell spectral response, SR(λ), over the solar wavelength as: \( {J}_{SC}=\underset{0}{\overset{\infty }{\int }}I\left(\lambda \right)\times SR\left(\lambda \right)\; d\lambda \). In this integration, it is assumed that the quantum efficiency is unity, QE = 1, and SR(λ) = /hc, where q is the elementary charge, h is Planck’s constant, and c is the speed of light. Therefore, the JSC enhancement is given as [58]:

$$ {J}_{SC(Enh.)}=\frac{\underset{400}{\overset{800}{\int }}I\left(\lambda \right)\times SR\left(\lambda \right)\times \prod \left(\lambda \right) d\lambda}{\underset{400}{\overset{800}{\int }}I\left(\lambda \right)\times SR\left(\lambda \right) d\lambda} $$

where Π(λ) is the absorption enhancement given by Eq. (4).

The resistive (Ohmic) loss, RL, which is the solar light power converted to the heat in the cell, is an important parameter for a solar cell which, to the best of our knowledge, has not been reported yet in the solar cells decorated with plasmonic elements. Resistive loss can warm the cell through the Ohmic heat in the cell, so it restricts the cell performance. Cell heating through Ohmic loss is an undesired phenomenon which should be considered in designing the plasmonic solar cells. In order to calculate resistive loss, we integrate \( \overrightarrow{J}.\overrightarrow{E} \) (\( \overrightarrow{J} \) is the current density) over the GNR volume as:

$$ {R}_L=\int \overrightarrow{J}.\overrightarrow{E}\; dV $$

Results and discussion

In this section, we present the results of absorption enhancement, short-circuit current density enhancement, and resistive loss of G-SiO2-Si-SiO2 and Ag-SiO2-Si-SiO2solar cells as well as absorption enhancement of hybrid Ag-G-SiO2-Si-SiO2 solar cell. In all schemes, the thickness of the absorption layer (Si) is taken to be the same.

Figure 2 shows the effect of GNR width (W) on the absorption enhancement of G-SiO2-Si-SiO2 solar cell. To compare the results with those of Ag-SiO2-Si-SiO2 one, we have also plotted the absorption enhancement of Ag-SiO2-Si-SiO2 solar cell in this figure. It is seen that the absorption enhancement of G-SiO2-Si-SiO2 cell strongly depends on the GNR width. For example, as W is increased from 150 to 250 nm, the absorption enhancement increases, too. If W is increased further to 280 nm, the absorption enhancement reduces drastically. Therefore, in the rest of this paper, we choose W = 250 nm as the optimum value for GNR width. It is interesting to note that for W = 250 nm, the absorption enhancement has a sharp peak around 508 nm (blue curve in Fig. 2.). This peak is related to the waveguide mode which is excited in Si layer. Figure 3a, which shows the normalized magnetic field distribution, clearly illustrates this mode happens at 508 nm.

Fig. 2
figure 2

The optical absorption enhancement in G-SiO2-Si-SiO2 solar cell for GNR width of W = 150 nm (doted red curve), W = 200 nm (dashed green curve), W = 250 nm (solid blue curve), and W = 280 nm (dot-dashed violet curve). Solid black curve shows this parameter for Ag-SiO2-Si-SiO2 cell

Fig. 3
figure 3

Distribution of normalized magnetic field: a and b are the waveguide and plasmonic-like modes of G-SiO2-Si-SiO2 solar cell corresponding to 508 and 624 nm, respectively, c and d are the waveguide and plasmonic modes of Ag-SiO2-Si-SiO2 solar cell corresponding to 508 and 642 nm, respectively

As the blue curve in Fig. 2 shows, the absorption enhancement in Si layer is much stronger than that of Ag-SiO2-Si-SiO2 cell which happens at 508 nm. From the magnetic field distribution, Fig. 3c, for Ag-SiO2-Si-SiO2 cell, one can conclude that there is no enhanced optical near field for absorption enhancement, because this wavelength is far from the plasmonic resonance wavelength. Interestingly, at this wavelength, the magnetic field is strongly confined and enhanced in the G-SiO2-Si-SiO2 cell (see Fig. 3a). Therefore, due to the special transport properties of graphene, the light energy concentration and near field enhancement occur in the silicon layer. In the visible range, there are also other modes for G-SiO2-Si-SiO2 cell happening at 624 nm and for Ag-SiO2-Si-SiO2 happening at 642 nm, which assist in solar light absorption in Si layer. For G-SiO2-Si-SiO2 cell, we call it plasmonic-like mode, because for graphene, the plasmonic modes excite at Mid-IR or terahertz spectrum region [28]. For Ag-SiO2-Si-SiO2 cell, it is definitly a localized surface plasmonic (LSP) mode, which occurs at 642 nm and is illustrated clearly in Fig. 3d. Although due to the plasmonic mode excitation for Ag-SiO2-Si-SiO2 cell at 642 nm, the absorption enhancement is much higher than that of G-SiO2-Si-SiO2 cell mode at 624 nm, the latter has an enahncement over a wider range of wavelengths (see Fig. 2). For instance, by increasing the wavelength from 510 nm to 600 nm, the absorption enhancement of the Ag-SiO2-Si-SiO2 cell drops down to 1, but for G-SiO2-Si-SiO2 cell, it changes from 1.5 to 1.85. This charactristic will be much more effective in the future calculations for quantities such as short-circuit current density.

In order to enhance even more the light-graphene interaction [50], we have designed a hybrid solar cell by placing GNR between Ag nanostrip and the SOI substrate (Ag-G-SiO2-Si-SiO2), as is schematically shown in the Fig. 4a. Figure 4b represents the absorption enhancement of the proposed hybrid Ag-G-SiO2-Si-SiO2 cell, where different heights of 10, 40, and 60 nm for Ag nanostrips were considered. For comparison, in Fig. 4b, we have also shown the results for solely G-SiO2-Si-SiO2 and Ag-SiO2-Si-SiO2 solar cells. It is found that for an Ag-SiO2-Si-SiO2 cell with a 10 nm height, there is only a single waveguide peak at 506 nm with a 2.2 enhancement in optical absorption. The magnetic field distribution of this mode is shown in Fig. 4c. From the field distribution, it is observed that the electromagnetic field is strongly confined in the Si layer. For this height, there is a very wide peak for optical absorption in the longer wavelengths region, where we have not shown its distribution. As the height of the Ag nanostrip is increased (i.e. when reach h = 40 nm and 60 nm) the absorption enhancement corresponding to the plasmonic mode is arisen. From Fig. 4b we observe that for h = 40 and 60 nm for Ag height, an enhancement of 4.5 and 3.8 is observed for plasmonic mode at 659 nm and 667 nm, respectively (violet and dashed green curves in Fig. 4b). Figure 4d, e, and f show normalized magnetic distributions for hybrid solar cell with an Ag nanostrip with the height of h = 10 nm at (c) 506 nm and (d) 620 nm, and h = 60 nm at (e) 497 nm and (f) 659 nm.

Fig. 4
figure 4

a Detailed structure of a hybrid Ag-G-SiO2-Si-SiO2 cell including GNR with 0.5 nm height and W = 250 nm width and the Ag nanostrip with 80 nm base length and variable heights of h = 10, 40, and 60 nm. b The absorption enhancements of the hybrid cell for h = 10 nm (dashed red curve), 40 nm (dot dashed green curve), and 60 nm (solid doted violet curve) in comparison with a cell comprising solely a G-SiO2-Si-SiO2 cell (solid blue curve) and Ag-SiO2-Si-SiO2 cell (solid black curve). Distribution of the normalized magnetic field of hybrid cell with h = 10 nm at (c) 506 nm and (d) 620, and h = 60 nm at (e) 497 nm and (f) 659 nm

In the following, we optimize the cell’s performance with considering the period of the GNRs and Ag nanostrips. Figure 5a shows the results for optical absorption of G-SiO2-Si-SiO2 cell for different periods. It is observed that by increasing the period of GNRs from 300 nm, the optical absorption is increased. Also, the absorption peaks are shifted toward longer wavelengths. Our calculations show that the optimum period is around 358 nm. Precisely, the G-SiO2-Si-SiO2 solar cell has a peak for optical absorption enhancement at 500 nm with magnitude of 5.67 for P = 300 nm which increases up to 18.37 at 540 nm for P = 358 nm.

Fig. 5
figure 5

Absorption enhancement of a G-SiO2-Si-SiO2 and b Ag-SiO2-Si-SiO2 solar cells for different periods; P = 300 nm (solid violet curve), P = 314 nm (dashed green curve), P = 328 nm (dotted blue curve), P = 340 nm (solid cyan curve), P = 358 nm (dot-dashed black curve), and P = 400 nm (dot-dashed red curve)

From Fig. 5b we observe that the period of the Ag-SiO2-Si-SiO2 cell has more impact on enhancing the optical absorption through waveguide mode rather than plasmonics mode. It is seen that for P = 300 nm, the absorption enhancement corresponding to the waveguide and plasmonic modes occurs at 480 nm and 641 nm with the value of 2.10 and 6.18, respectively. For P = 358 nm, these peaks shift to 537 nm and 654 nm with magnitude of 4.95 and 7.42, respectively. From Fig. 5 a and b, one can conclude that for P = 358 nm, the absorption enhancement for waveguide modes of the G-SiO2-Si-SiO2 cell is much higher than that of the Ag-SiO2-Si-SiO2 cell. However, as it has been discussed earlier, Ag solar cells lead to an increase in optical absorption by their localized surface plasmons (LSP). Therefore, increasing the period of Ag nanograting helps better absorption of incident light due to its multiple peaks, proportional to their LSP modes. However, it is very crucial issue whether or not this absorbed power would cause a stronger short-circuit current density. In this regard, and in order to compare the performance of G-SiO2-Si-SiO2 and Ag-SiO2-Si-SiO2 cells, we have emphasized JSC enhancement, which is the ratio of JSC of the cell with nanostrip (nanoribbon) divided to JSC of the bare cell without nanostrip (nanoribbon).

Figure 6a and b show the short-circuit current density (Jsc) enhancement for G-SiO2-Si-SiO2 and Ag-SiO2-Si-SiO2 solar cells, respectively. In Fig. 6a, we have evaluated the Jsc for various widths of GNRs, where, as we expected, W = 250 nm gives the optimum value. In Fig. 6b we have compared the results of period optimizations of both G-SiO2-Si-SiO2 with W = 250 nm and Ag-SiO2-Si-SiO2 cells. It is seen that as the period is increased, the Jsc for G-SiO2-Si-SiO2 cell also increases. As expected, P = 358 nm is the optimum period for Jsc of G-SiO2-Si-SiO2 solar cell. However, for Ag-SiO2-Si-SiO2 solar cell, various periods (in the range of 314 to 358 nm) give almost the same Jsc. Interestingly, for G-SiO2-Si-SiO2 solar cell with P = 358 nm, two types of cells give more and less the same value.

Fig. 6
figure 6

a Short-circuit current density (JSC) enhancement of G-SiO2-Si-SiO2 solar cell for different widths of GNRs. b JSC enhancement of G-SiO2-Si-SiO2 with the optimum width (left bars) and Ag-SiO2-Si-SiO2 solar cells (right bars) for different periods of P = 314 nm (dark blue bars), P = 328 nm (cyan bars), P = 340 nm (yellow bars), and P = 358 nm (brown bars)

The last important quantity which has been investigated in this work as the highlight prospect is the resistive (Ohmic) loss. This quantity says about an undesired phenomenon which is the main factor of dissipation of useful energy absorbed from the sunlight. To make a comparison, we have calculated the ratio of absorbed power in the GNRs/Ag nanograting layer to the total sunlight power radiated to the cell. We call it as normalized resistive loss (RL). Figure 7 depicts the normalized resistive loss as a function of wavelength for Ag-SiO2-Si-SiO2 (dashed red curve) and G-SiO2-Si-SiO2 solar cells (solid blue curve) in the visible frequency range. It can be observed that the normalized loss of the G-SiO2-Si-SiO2 is much lower than that of the Ag-SiO2-Si-SiO2. It is found that G-SiO2-Si-SiO2 dissipates at most 4.7% of the incident power which happens at 508 nm, but Ag-SiO2-Si-SiO2 generally dissipates much higher solar energy entire the solar spectrum. For instance, at 480 nm and 637 nm, Ag-SiO2-Si-SiO2 dissipates, respectively, up to 29% and 24% of the incident power. This portion naturally is converted to the heat. The very low amount of dissipation for G-SiO2-Si-SiO2 cell is an invaluable point, because heating the solar cell actually reduces the cell’s performance. Therefore, it is safe to say that in the meantime that G-SiO2-Si-SiO2 and Ag-SiO2-Si-SiO2 enhance the solar cell’s electric and optical performance with the same values, GNRs impose noticeably lower energy dissipation in the cell, so it is a better candidate for incorporating in photovoltaic ultra-thin cells. Recently, several experiments have shown that the chemical vapor deposition (CVD) graphene can be used to improve the performance of the solar cells [59, 60]. Indeed, CVD is the primary technique used to obtain large-area graphene sheets, which are usually in high demand for various solar cell applications. In these experiments, the graphene was synthesized on a Cu foil by an atmospheric pressure CVD (APCVD) and then transferred to a glass substrate. The number of graphene layers could be well controlled via altering the H2 flow rate, which also provides a wide selection range of transparency and sheet resistance. In order to provide a better coverage and contact on CdTe solar cell, the graphene was synthesized with a three-dimensional (3D) structure using porous Ni foam as the growth substrate. A similar method was employed to grow graphene and the 3D structure was successfully observed and transferred to CdTe device [61]. The final graphene back contact thickness exceeded 10 μm with an excellent electrical conductivity (550–600 S/cm), which assisted a significant device efficiency improvement up to 9.1%.

Fig. 7
figure 7

The resistive loss of G-SiO2-Si-SiO2 (solid blue curve) and Ag-SiO2-Si-SiO2 (dashed red curve) solar cells


In summary, we have numerically studied the optical absorption and short-circuit current density enhancements and resistive loss of G-SiO2-Si-SiO2 and Ag-SiO2-Si-SiO2 solar cells which are SOI solar cells with, respectively, GNR and Ag nanogratings at the top. We have compared the results of both cells in the visible frequency range. It is found that the performance of the G-SiO2-Si-SiO2 solar cell strongly depends on the width (W) of GNRs and the period (P) of the structure. By optimizing the W and P of the G-SiO2-Si-SiO2 cell, we could achieve the maximum absorption enhancement for GNR solar cell (18.37 at 540 nm) which is three times higher than that of Ag solar cell at this wavelength. It is demonstrated that the GNR cells with optimum W and P can intensify the waveguide mode peak and cause a better confining of the light into the Si layer. However, Ag solar cell has strong absorption enhancement due to conducting the light into the Si layer by its localized surface plasmons (LSP) modes. The result of calculating short-circuit current density enhancement confirmed that the GNR solar cell with optimized W and P can intensify the waveguide modes high enough such that having a same JSC enhancement compared to Ag solar cell, despite their lack of plasmonic behavior in this frequency range. The outstanding point of this work is the low resistive loss of GNR solar cells. Our calculations showed that GNR solar cells dissipate only less than 5% of incident sunlight power inside the SOI cell happening at 508 nm, compared to high values for Ag solar cells which dissipate the solar power up to 29% and 24% happening at, respectively, 480 and 637 nm.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

Change history

  • 28 January 2021

    An amendment to this paper has been published and can be accessed via the original article.


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M. S. and Y. H. would like to thank SCU of Ahvaz for financial supporting this work.


This work has been supported by Deputy of Research and Technology of Shahid Chamran University (SCU) of Ahvaz under the grant number of SCU.SP98.259.

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M.S. has defined the subject of the article and simulated the problem. Y.H. has written the manuscript, checked the results and made full discussion. The author(s) read and approved the final manuscript.

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M.S. is an associate professor of physics in optics and laser at SCU and is currently the manager of Center for Research on Laser and Plasma (CRLP). His research interest is nanophotonic and light-matter interaction.

Y. H. is an assistance professor of physics in condensed matter and is a member of CRLP of SCU. His main interest is optical and electrical properties of two-dimensional materials.

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Correspondence to Mohammad Sabaeian.

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Sabaeian, M., Hajati, Y. Design of high performance and low resistive loss graphene solar cells. J. Eur. Opt. Soc.-Rapid Publ. 16, 14 (2020).

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