Browsing by Subject "Solar cell"

Now showing 1 - 9 of 9

Open Access
Absorption enhancement in InGaN-based photonic crystal-implemented solar cells
(SPIE, 2012-07-26) Gundogdu, T. F.; Gokkavas, M.; Özbay, Ekmel
We investigate the absorption characteristics of InGaN solar cells with high indium (0.8) content and a one-dimensional periodic nano-scale pattern (implemented) in the InGaN layer theoretically. The short-circuit current of our InGaN-based solar cell structure is calculated for different lattice constant, etch depth, and fill factor values. A substantial increase in the absorption (17.5% increase in short-circuit current) is achieved when the photonic crystal pattern is thoroughly optimized. (c) 2012 Society of Photo-Optical Instrumentation Engineers (SPIE). [DOI: 10.1117/1.JNP.6.061603]
Open Access
Analysis of the mosaic defects in graded and non graded InxGa1‐xN solar cell structures
(Süleyman Demirel Üniversitesi, 2017) Kars Durukan, İ.; Öztürk, M. K.; Özçelik, S.; Özbay, Ekmel
In this study, graded (A) InxGa1‐xN (10.5 ≤ x ≤ 18.4) and non graded (B) InxGa1‐xN (13.6 ≤ x ≤ 24.9) samples are grown on c‐oriented sapphire substrate using the Metal Organic Chemical Vapour Deposition (MOCVD) technique. The structural, optical and electrical features of the grown InGaN/GaN solar cell structures are analyzed using High Resolution X‐Ray Diffraction (HRXRD), Photoluminescense (PL), Ultraviolet (UV), current density and potential (JV) measurements. According to the HRXRD results; it is determined that the InGaN layer of the graded structure has a lower FWHM (Full width at half maximum) value. From the PL measurements, it is observed that the GaN half‐width peak value of the graded sample is narrower and the InGaN peak width value of the graded sample is larger. From UV measurements, that the graded sample has a greater band range. JV measurements determine that the performance of the graded structure is higher.
Open Access
A baseball-bat-like CdTe/TiO2 nanorods-based heterojunction core–shell solar cell
(Elsevier, 2013) Karaagac, H.; Parlak, M.; Aygun, L. E.; Ghaffari, M.; Bıyıklı, Necmi; Okyay, Ali Kemal
Rutile TiO2 nanorods on fluorine-doped thin oxide glass substrates via the hydrothermal technique were synthesized and decorated with a sputtered CdTe layer to fabricate a core-shell type n-TiO2/p-CdTe solar cell. Absorbance spectrum verified the absorption contribution of both TiO2 and CdTe to the absorption process. The solar cell parameters, such as open circuit voltage, short circuit current density, fill factor and power conversion efficiency were found to be 0.34 V, 1.27 mA cm-2, 28% and 0.12%, respectively. .
Open Access
Enhancement of polycrystalline silicon solar cells efficiency using indium nitride particles
(Institute of Physics Publishing Ltd., 2015) Alkis, S.; Chowdhury, F. I.; Alevli, M.; Dietz, N.; Yalızay, B.; Aktürk, S.; Nayfeh, A.; Okyay, Ali Kemal
In this work, we present a hybrid indium nitride particle/polycrystalline silicon solar cell based on 230 nm size indium nitride particles (InN-Ps) obtained through laser ablation. The solar cell performance measurements indicate that there is an absolute 1.5% increase (Δη) in the overall solar cell efficiency due to the presence of InN-Ps. Within the spectral range 300-1100 nm, improvements of up to 8.26% are observed in the external quantum efficiency (EQE) and increases of up to 8.75% are observed in the internal quantum efficiency (IQE) values of the corresponding solar cell. The enhancement in power performance is due to the down-shifting properties of the InN-Ps. The electrical measurements are supplemented by TEM, Raman, UV/VIS and PL spectroscopy of the InN-Ps. © 2015 IOP Publishing Ltd.
Open Access
Investigation of lithium salts-nonionic surfactant lyotropic liquid crystalline mesophases in a dye sensitized solar cell as gel electrolyte
(2015-09) Yılmaz, Ezgi
Liquid crystals are one of the most widely studied and used materials in chemistry. The properties of liquid crystals make them interesting to research also for various electrochemical applications. In this context, lithium salts such as LiI, LiCl, LiBr, and LiNO3 can be assembled using non-ionic surfactants into lyotropic liquid crystalline (LLC) mesophases[1], [2] and used as gel electrolytes in various applications. In this work, the LLC mesophases of LiI with and without other lithium salts (such as LiCl, LiBr, and LiNO3) were prepared using 10-lauryl ether (C12H25(CH2CH2O)10OH, denoted as C12EO10) and characterized using the FT-IR (Fourier Transform Infrared Spectroscopy), Raman spectroscopy, XRD (X-Ray Diffraction), POM (Polarized Optical Microscopy), and AC conductivity measurements. Beside from single salt-surfactant mesophases, we also prepared LiI/I2 redox couple in an LLC phase with the help of a non-ionic surfactant and they were also characterized using the same techniques. We found out that the mesophases can be prepared as gels by directly mixing salt and surfactant with certain amounts of water or as solutions using excess solvent (such as water, ethanol, or acetonitrile) that can be evaporated to form the LLC mesophases. The water content of both sets of samples is the same upon exposing to the atmosphere for a certain time and it only depends on the salt amount and humidity under the ambient conditions (around room temperature and 20-25 % RH). The required water/salt ratio for a stable mesophase is around 3.0 which, it is much lower than the water needed to dissolve those salts in an aqueous media. The water/salt mole ratio closely follows the Hofmeister series of anions, where the water amount order is as follows; LiCl>LiBr>LiI>LiNO3, however, the AC ionic conductivity follows a different order; LiNO3>LiCl>LiBr>LiI. Adding I2 by 1/10 mole ratio of the LiI into the media does not change the properties of the mesophases. The AC conductivity increases with increasing salt and water content of the mesophases with a typical conductivity of around 0.1 to 1.0 mS/cm-1. The mesophases are also stable in a very broad temperature (below 0 °C to 60-130 °C) and salt concentration (2-10 salt/surfactant mole ratio) ranges. Finally, the LiI/I2 mesophases were used as gel-electrolytes in dye sensitized solar cells (DSSCs) as gel-electrolytes and redox couples. A set of samples were prepared with different ratios of the LiI:I2 redox couple (such as, 1:0.1, 1:0.2, 2:0.2, 2:0.3, 3:0.2, 3:0.3, 4:0.4, and 5:0.5) and the solar performances were tested in a DSSC, which contains N719 dye sensitized TiO2 anode and Pt cathode using a solar simulator. However, the LLC phases have gel like structure and it is hard to infiltrate the gel into the pores of dye modified nano-TiO2 films. To overcome the diffusion problem, the gel-electrolytes were also prepared as a solution in excess water, ethanol or acetonitrile that evaporates upon infiltration over time. In addition to this, by changing the procedure of preparing the TiO2 paste, improvement on results was also obtained. The DSSC provides 0.2 % efficiencies with 0.50 fill factors when gel-electrolytes are used. Since water is used for preparing the LLC phases, we had always lower Voc values. However, when it is prepared as a solution with excess ethanol, it provides up to 3.33 % efficiencies with 9.58 mA/cm2 short circuit current and 0.6 V open circuit voltage. Also, new procedure for preparing the TiO2 paste provides us even higher Voc values such as 0.76 V, which is unusual for the water based LLC electrolytes in this area.
Open Access
Investigation on lithium salt - surfactant lyotropic liquid crystalline mesophases: characterization, role of water, and electrochemical behaviors
(2021-09) Topuzlu, Ezgi Yılmaz
In this thesis, lyotropic liquid crystalline (LLC) mesophases of lithium salts (LiCl, LiBr, LiNO3, LiSCN, LiI, LiI/I2, and LiH2PO4) and 10-lauryl ether (C12H25(OCH2CH2)10OH, C12EO10) have been investigated and the LiI/I2 LLC mesophases was used as gel electrolyte in a dye sensitized solar cell (DSSC). The LLC mesophases of LiCl, LiBr, LiNO3, LiSCN, and LiH2PO4 salts were prepared in a broad range of salt concentrations and found that the mesophases of LiCl, LiBr, LiNO3, and LiSCN salts are stable between 2 and 10 salt/surfactant mole ratios. The LiI-C12EO10 samples undergo meso-crystallization over a 3 mole ratio and not investigated at high salt mole ratios. The LiH2PO4-C12EO10 LLC samples are semi stable and leach out salt crystals upon aging because they cannot hold sufficient water; the water holding capacity and stability of the LiH2PO4 mesophases can be improved by adding various amount of H3PO4 that prevents salt crystallization by increasing the water content of the mesophase. Therefore, this thesis was divided into three main chapters, the first chapter is on the role of water in the LLC mesophases of LiCl, LiBr, LiNO3, and LiSCN. The second chapter is on the LiH2PO4 LLC mesophases, and addition of H3PO4 to prevent crystal formation. And the last one is about the use of the LiI/I2 LLC mesophase as gel electrolyte in DSSCs. The mesophases were obtained by evaporating clear solutions of all ingredients. First, they were fully characterized by using Attenuated Total Reflectance-Fourier Transform Infrared (ATR-FTIR), Raman, and UV-Vis absorption spectroscopy, X-ray diffraction (XRD), AC conductivity, gravimetric measurements, and polarized optical microscope (POM) imaging to identify structural and electrical properties and water up takes of the mesophases. The water evaporation has been monitored by gravimetric, spectroscopic, and conductivity measurements. The water evaporation rate follows a 2/3 power of the evaporated water weight. After complete water evaporation, the LiCl and LiBr systems keep a similar amount of water in their mesophases (typically 3-8 water/Li+, depending on the humidity condition). However, the LiSCN and LiNO3 systems keep a significantly lower amount of water inside their mesophase (1.5-5 water/Li+ depending on the humidity condition). Water has a critical role in forming the lithium salt-surfactant mesophases and their structural properties. To investigate the role of water, humidity-dependent measurements have been carried by using gravimetry, spectroscopy, AC conductivity, and POM techniques. The gravimetric and spectroscopic data show that the H2O/Li+ mole ratio increases linearly by 0.08-0.09 per humidity. Increasing water amount in the mesophases improves their ionic conductivities with at least a factor of two when the humidity was changed from 20 % to 40 %. The water/Li+ mole ratios, water-ion, water-water, water-surfactant, and ion-surfactant interactions strongly depend on the counter anions of the lithium salts and closely follows the Hofmeister series of anions, such that the water molecules are strongly held in the LiCl mesophase but weakly held in the LiNO3 and LiSCN. Controlling the humidity over the lithium salt-surfactant mesophases is a promising way of tuning the properties of the LLC mesophases as needed. Furthermore, mixing two different lithium salts may also improve/adjust the water amount in the gel-phases. For instance, adding LiCl to LiNO3 mesophase increases the final water content in the mesophase and, therefore, the conductivity. Controlling the water amount in the mesophase can be beneficial for the use of the lithium salt-surfactant mesophases in various electrochemical applications. The LiH2PO4 mesophase has also been extensively investigated by changing the salt/surfactant mole ratio and found out that it forms at high humidity but is unstable at lower humidity. The LiH2PO4-mesophase undergoes a phase change by leaching out first surfactant and then the salt crystals. Increasing the salt amount in the mesophase can postpone the salt crystallization but it cannot stop completely. However, the LiH2PO4 mesophases can also be stabilized by adding H3PO4 that holds an extensive amount of water. The LiH2PO4-H3PO4 mesophase forms a buffer LLC mesophase that can be used in electrochemical devices as gel-electrolytes where constant pH is needed. The LiI-I2 redox couple was also prepared in LLC mesophase, characterized by the above approaches, and used in a DSSC as gel-electrolyte. To investigate the importance of the water content in the mesophase different humidity levels were tested for gelation. It was shown that 40 % humidity is the best since it increases the efficiency of DSSC from 3.67 % to 5.36 %. Further increase in the humidity level causes dye detachment and free iodine formation; therefore, the efficiency of DSSC start to decline. Altering how to introduce dye and electrolyte over the working electrode, such as introducing dye and electrolyte simultaneously and carrying gelation at 40 % humidity, results a further increase in the cell efficiency to 7.32 %, which is the highest efficiency achieved for an LLC gel electrolyte in DSSC.
Open Access
Nanosecond pulsed laser ablated sub-10 nm silicon nanoparticles for improving photovoltaic conversion efficiency of commercial solar cells
(Institute of Physics Publishing Ltd., 2017) Rasouli, H. R.; Ghobadi, A.; Ghobadi, T. G. U.; Ates, H.; Topalli, K.; Okyay, Ali Kemal
In this paper, we demonstrate the enhancement of photovoltaic (PV) solar cell efficiency using luminescent silicon nanoparticles (Si-NPs). Sub-10 nm Si-NPs are synthesized via pulsed laser ablation technique. These ultra-small Si nanoparticles exhibit photoluminescence (PL) character tics at 425 and 517 nm upon excitation by ultra-violet (UV) light. Therefore, they can act as secondary light sources that convert high energetic photons to ones at visible range. This down-shifting property can be a promising approach to enhance PV performance of the solar cell, regardless of its type. As proof-of-concept, polycrystalline commercial solar cells with an efficiency of ca 10% are coated with these luminescent Si-NPs. The nanoparticle-decorated solar cells exhibit up to 1.64% increase in the external quantum efficiency with respect to the uncoated reference cells. According to spectral photo-responsivity characterizations, the efficiency enhancement is stronger in wavelengths below 550 nm. As expected, this is attributed to down-shifting via Si-NPs, which is verified by their PL characteristics. The results presented here can serve as a beacon for future performance enhanced devices in a wide range of applications based on Si-NPs including PVs and LED applications.
Open Access
Scattering analysis of silver nanoparticles for solar cell applications using integral equations
(IEEE, 2018) Uysal, İsmail Enes; Ülkü, H. A.; Bağcı, H.; Gülseren, Oğuz
Plasmonic nanoparticles (NPs) can be used to improve the efficiency of solar cells. Analysis of electromagnetic scattering from NPs is often carried out under the assumptions that they reside in air and have 'ideal' shapes (sphere, cube, etc.) However, in a realistic setup, nanoparticles are fabricated on a substrate and their shape and size cannot be controlled precisely. In this work, a surface integral equation solver is used to accurately characterize the scattering from a realistic system, where silver hemispheres of varying sizes are fabricated on an indium tin-oxide substrate. Results obtained by the solver are compared to the experimental results obtained for a similar system.
Open Access
Thickness dependence of solar cell efficiency in transition metal dichalcogenides MX2 (M: Mo, W; X: S, Se, Te)
(Elsevier, 2020) Özdemir, Burak; Barone, V.
Bulk transition metal dichalcogenides are indirect gap semiconductors with optical gaps in the range of 0.7–1.6 eV, which makes them suitable for solar cell applications. In this work, we study the electronic structure, optical properties, and the thickness dependence of the solar cell efficiencies of MX2 (M: Mo, W; X: S, Se, Te) with density functional theory and GW + BSE. Through this analysis, we find a change in solar cell efficiency trends at slab thicknesses of 3 μm. For thin films solar cells (thicknesses smaller than 3 μm), the tellurides present the highest efficiencies (about 20% for a 100 nm thick slab). In contrast, for thicknesses greater than 3 μm, our results indicate that a maximum solar cell efficiency can be achieved in WS2. For instance, a 100 μm slab of WS2 presents a solar cell efficiency of 36.3%, making this material a promising candidate for solar cell applications.