International Journal of Photoenergy

International Journal of Photoenergy / 2015 / Article
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Thin-Film Photovoltaics 2014

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Research Article | Open Access

Volume 2015 |Article ID 515767 |

Silvio Pierro, Andrea Scuto, Luca Valenti, Marina Foti, Anna Battaglia, Giovanni Mannino, Cosimo Gerardi, Felice Crupi, Salvatore Lombardo, "Measurements and Simulations on the Mechanisms of Efficiency Losses in HIT Solar Cells", International Journal of Photoenergy, vol. 2015, Article ID 515767, 7 pages, 2015.

Measurements and Simulations on the Mechanisms of Efficiency Losses in HIT Solar Cells

Academic Editor: Olindo Isabella
Received01 Oct 2014
Revised17 Feb 2015
Accepted18 Feb 2015
Published08 Jun 2015


We study the electrical and the optical behavior of HIT solar cell by means of measurements and optoelectrical simulations by TCAD simulations. We compare the HIT solar cell with a conventional crystalline silicon solar cell to identify the strengths and weaknesses of the HIT technology. Results highlight different mechanisms of electrical and optical efficiency losses caused by the presence of the amorphous silicon layer. The higher resistivity of the a-Si layers implies a smaller distance between the metal lines that causes a higher shadowing. The worst optical coupling between the amorphous silicon and the antireflective coating implies a slight increase of reflectivity around the 600 nm wavelength.

1. Introduction

The heterostructure with intrinsic thin layer solar cell, so called HIT, is the most promising monocrystalline silicon based technology to enhance the cost/efficiency factor [1]. This assumption is based on the enhancement made by the HIT with respect to a monocrystalline solar cell by the cost reduction introduced by the lower thermal budget, and by the increasing of the open circuit voltage thanks to the heterojunction barrier that decreases the minority current [2]. From the previous considerations we expect a strong increase in the HIT performance with respect to the c-Si technology. The base research-cell efficiencies reported in literature tell us that the efficiency of the HIT solar cell is slightly higher than the efficiency of the microcrystalline bulk solar cell (25.6% of HIT against 25% of bulk microcrystalline) [3]. Subsequent improvements have allowed HIT solar cells to reach the efficiency of 25.6% [4]. Actually, the main focus to increase the HIT efficiency is connected to the surface recombination velocity at amorphous-crystalline interface [5]. In order to further increase the cell efficiency we need to understand the main causes of efficiency losses and how to reduce them.

This paper focuses the attention on the physical aspects that affect the HIT solar cells different from technological aspects as surface passivation or defect densities. For this purpose we compare measurements of bulk crystalline silicon solar cell with the equivalent HIT solar cell. Furthermore, by using a commercial TCAD simulator [6] tuned with device measurements, we intend to investigate the main loss mechanisms for both structures and identify the main problems of the HIT technology.

The remainder of this paper is organized as follows. Section 2 describes the process details of the realized samples and the simulation setup. Section 3 reports the experimental and numerical results and discusses the main phenomena affecting the HIT efficiency. Section 4 reports the conclusions of this work.

2. Experimental Details

The HIT structure is presented in Figure 1. Starting from a p-type CZ wafer, by a HF etching process a front random pyramids texturing is built. A highly doped p-type layer is deposited on the back surface, which is crystallized by a thermal process, forming the back surface field (BSF) layer. The intrinsic and the n-type amorphous layers are deposited by inductively coupled plasma chemical vapour deposition (ICPCVD) on the top surface of the wafer. The aluminum doped zinc oxide (AZO) is used as antireflective coating (ARC) layer and is grown by sputtering. To finalize the structure, the back metallization covers the entire device and is a Ti/Pt/Au multilayer; the top metal is made by screen printing of a silver paste. A double HIT structure was not realized, since the amorphous BSF does not add enhancement on a p-type HIT solar cell [7, 8]. For comparison purpose, we realized the crystalline structure shown in Figure 1. The device parameters of the HIT and the reference structures are reported in Table 1. The key difference between the two structures is the emitter region, which is crystallized by a thermal process in the case of the crystalline structure.


Sheet resistanceΩ/sq147.78
AZO thicknessnm9188
Emitter thicknessnm50
Emitter dopingcm−31 × 1020
n-type a-Si:H thicknessnm10
n-type a-Si:H dopingcm−31 × 1018
i-type a-Si:H thicknessnm5
Emitter/AZO SRVcm/s8.7 × 1042.1 × 104
i/n a-Si SRVcm/s102

Electrical measurements

The electrical simulation setup uses a drift-diffusion model with Fermi statistics, with the Schenk bandgap narrowing model [9] and the Slotboom model for free mobility carrier degradation [10]. The Auger and Radiative recombination has been added as far as the SRH recombination for both bulk and surfaces. For the crystalline solar cell, the surface recombination velocity of c-Si/AZO interface uses the SRH surface recombination model, tuned with literature results [11]; the doping level for both emitter and BSF layers is tuned with spreading resistance measurements on our devices. The HIT solar cell is made by replacing the emitter with the i/n a-Si:H layers. The HIT physical model requires adding the thermionic current and the surface recombination at the amorphous-crystalline interface [12, 13]. The amorphous silicon density of states (DOS) is modeled by three Gaussian distributions, two for the conduction and valence band tails and one for the mid gap defect concentration [13]. The most relevant a-Si:H electrical parameters used in the simulations are reported in Table 2. The optical simulation solves an extended version of the Transfer Matrix Method with diffused and direct light to take into account surface texturing [14, 15]. The coherent light follows the direct path, while the diffused ray follows a scattered function, the so-called angular distribution function [16]. The ratio between the scattered and direct ray is the haze parameter. In the simulation above, the haze parameter has been set to 0.73 and the haze profile follows a square cosine law. The values of refractive index and absorption coefficient for the materials used in the solar cell are consistent with literature data [17].


Electron affinityeV3.9
Electron mobilitycm2V−1s−120
Hole mobilitycm2V−1s−12
DOS in CBcm−32.5 × 1020
DOS in VBcm−32.5 × 1020

Conduction band tail
Traps concentrationcm−31 × 1018
Standard deviation0.08
Capture cross section for ecm−21 × 10−16

Valence band tail
Traps concentrationcm−31 × 1018
Standard deviation0.08
Capture cross section for ecm−21 × 10−19

Mid gap
Traps concentrationcm−31 × 1016
Standard deviation0.15
Capture cross sectioncm−21 × 10−16

3. Results and Discussion

Figure 2 shows the main electrical parameters of HIT and crystalline (subsequently c-Si) solar cells as a function of pitch. According to literature, the open circuit voltage of the HIT cell is greater than c-Si [2]; on the other hand, the short circuit current and the fill factor are lower. This translates into a lower efficiency value of the HIT compared to c-Si, and the difference increases as the pitch increases. Figure 3 shows the optimized pitch distance that reaches the highest efficiency; this value reaches a trade-off between the shadowing losses and the fill factor that show opposite trends as a function of pitch length. Increasing the sun concentration, the pitch distance decreases faster in the c-Si solar cell compared to HIT, thus increasing the efficiency of HIT compared to c-Si. In order to understand the fill factor loss we analyze simulation results for both HIT and c-Si structures at maximum power peak; results are shown in Figure 4, where the black lines are the current path and the color is the current density. It is worth noting that the current flows vertically inside the bulk, while it goes in direction of the contact in both the emitter and the AZO regions. The current direction into the emitter causes an increase of the density current near to the contact, thus increasing the electrostatic potential loss inside the emitter. This effect depends on the pitch width and the emitter resistivity. In order to gain insight on the lateral loss effect, Figure 5 compares the electrostatic potential along the c-Si/a-Si heterointerface for the HIT structure and the electrostatic potential at the p-n junction for the c-Si structure. Moving away from the contact, the potential decreases due to the emitter and AZO resistivity. The potential loss is highly close to the contact due to the higher current density and is higher in the HIT compared to the reference one, due to the higher resistivity of a-Si compared to c-Si. The electrostatic potential at the interface causes an increase in the dark current that decreases the photogenerated current. This effect depends on the operation condition. At short circuit current condition, the dark current is low with respect to the photogenerated current, so the effect can be neglected. By increasing the voltage, the diode current becomes relevant with respect to the photogenerated current, and the effect cannot be neglected anymore. At open circuit voltage, the diode dark current is equal to the photogenerated current, since the dark current depends on the lateral effect; there is an open circuit voltage reduction. This phenomenon is present in both HIT and crystalline devices. As can be seen from Figure 5, the potential variation in the HIT structure is higher than the crystalline solar cell because of the higher emitter resistivity; the higher potential variation produces a decrease in the fill factor and in the open circuit voltage. In order to reduce this effect we need to shrink the pitch, thus causing a higher shadowing that decreases efficiency. The optimum value between lateral losses and shadowing is shown in Figure 3. Because of the previous effect, the HIT solar cell needs a smaller pitch than the c-Si, but with increasing sun concentration this effect tends to decrease, since the c-Si solar cell pitch decreases faster than the HIT and when the two pitch values are the same the HIT efficiency becomes greater than the c-Si one.

Figure 6 shows the reflectivity of the devices for both simulations and measurements. As can be seen, the HIT structure shows a higher reflectivity from 300 nm to 600 nm with respect to the c-Si structure. This reflectivity increase translates into a lower energy absorbed by the solar cell and less energy. Figure 7 shows the difference of spectral power density absorbed by the HIT and c-Si solar cell with respect to the AM1.5G spectral density; this is an optical analysis derived from the overall reflectivity and transmittance; we cannot notice electrical issues and cannot determine which layer adsorbs the light. The optical stack of HIT structure differs from the c-Si structure by the addiction of the two a-Si:H layers, the n-doped and intrinsic layers (stack successfully called a-Si:H) in between the silicon bulk and the AZO layer. From literature we know that a good antireflective layer in between two materials must obey some rules; in particular, the thickness of the layer must ensure the destructive interference of the reflected wave and the refractive index must be as close as possible to the square root of the product of the refractive indices of the two materials. If the layers are more than one, we must use the same rule for the two neighbor materials. Figure 8 shows the refractive index of the c-Si, a-Si:H, and AZO material compared with the optimum refractive index for the case of 1 layer in between c-Si and the air and the case of 2 layers (like HIT structure). As can be seen, the AZO is a good material to use as single inner layer for c-Si solar cell; this ensures a low reflectivity in c-Si solar cell. The a-Si:H shows a refractive index similar to the c-Si for wavelength higher than 550 nm; then the reflectivity in this wavelength range should be approximated to the c-Si solar cell. For smaller frequencies, the a-Si:H and c-Si refractive indices are no more similar; this implies that the optical behavior must follow the model with 2 layers in between the silicon and the air. Under this range, the AZO is still a good material, but the a-Si:H is close enough to the optimum level for wavelength smaller than 400 nm; before this value the worst index matching does not ensure a low reflectivity. This analysis is in good agreement with the optical measurements shown in Figure 6. The integral of the reflectivity value is used as a figure of merit for the system and Figure 9 shows this integral as a function of the a-Si:H layer thickness compared to the structure with no a-Si:H layer. The inset figure shows that the AZO reaches a minimum of reflectivity when its thickness is 91 nm and this value is not dependent on the a-Si:H thickness. The a-Si:H thickness affects the reflectance and there is a maximum of reflectance at 20 nm. This result tells us to use a very thin a-Si:H layer or a greater one. But using a thick layer implies a bigger series resistance and a layer thinner than 5 nm can be a problem for quantum effects [18].

4. Conclusions

In this paper we compared the HIT solar cell with a c-Si solar cell to identify the main problems of the HIT technology. We made measurements and simulation and by comparing the optimized structure for both technologies we noticed two losses differences into HIT. A lower fill factor and a higher reflectivity for the HIT solar cell. The fill factor decrease is due to a higher potential loss along the p-n junction that causes a higher diode current. To prevent this we need to shrink the pitch, causing a higher shadowing. The lower short circuit current is caused by higher reflection losses into HIT. This is caused by the worst optical coupling between the amorphous silicon and the antireflective coating in the wavelength range from 400 nm to 600 nm; we cannot reduce this effect since the reduction is related to optical properties of the amorphous layer; to reduce the reflectivity we must shrink the a-Si layer, but the thickness cannot be smaller than the value in use to prevent quantum effects.

Conflict of Interests

The authors certify that they have no affiliations with or involvement in any organization or entity with any financial interest (such as honoraria; educational grants; participation in speakers’ bureaus; membership, employment, consultancies, stock ownership, or other equity interests; and expert testimony or patent-licensing arrangements) or nonfinancial interest (such as personal or professional relationships, affiliations, knowledge, or beliefs) in the subject matter or materials discussed in this paper.


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Copyright © 2015 Silvio Pierro et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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