Towards InAs/InGaAs/GaAs Quantum Dot Solar Cells Directly Grown on Si Substrate

This paper reports on an initial assessment of the direct growth of In(Ga)As/GaAs quantum dots (QDs) solar cells on nanostructured surface Si substrate by molecular beam epitaxy (MBE). The effect of inserting 40 InAs/InGaAs/GaAs QDs layers in the intrinsic region of the heterojunction pin-GaAs/n⁺-Si was evaluated using photocurrent spectroscopy in comparison with pin-GaAs/n⁺-Si and pin-GaAs/GaAs without QDs. The results reveal the clear contribution of the QDs layers to the improvement of the spectral response up to 1200 nm. The novel structure has been studied by X ray diffraction (XRD), photoluminescence spectroscopy (PL) and transmission electron microscopy (TEM). These results provide considerable insights into low cost III-V material-based solar cells.     

Efficiency Boost in Dye-Sensitized Solar Cells by Post- Annealing UV-Ozone Treatment of TiO2 Mesoporous Layer

The organic residues on titanium(IV) oxide may be a significant factor that decreases the efficiency of dye-sensitized solar cells (DSSC). Here, we suggest the UV-ozone cleaning process to remove impurities from the surface of TiO₂ nanoparticles before dye-sensitizing. Data obtained from scanning electron microscopy, Kelvin probe, Fourier-transform infrared spectroscopy, and Raman spectroscopy showed that the amounts of organic contamination were successfully reduced. Additionally, the UV-VIS spectrophotometry, spectrofluorometry, and secondary ion mass spectrometry proved that after ozonization, the dyeing process was relevantly enhanced. Due to the removal of organics, the power conversion efficiency (PCE) of the prepared DSSC devices was boosted from 4.59% to 5.89%, which was mostly caused by the increment of short circuit current (J_sc) and slight improvement of the open circuit voltage (V_oc).     

Improving Efficiency of Multicrystalline Silicon and CIGS Solar Cells by Incorporating Metal Nanoparticles

This work studies the use of gold (Au) and silver (Ag) nanoparticles in multicrystalline silicon (mc-Si) and copper-indium-gallium-diselenide (CIGS) solar cells. Au and Ag nanoparticles are deposited by spin-coating method, which is a simple and low cost process. The random distribution of nanoparticles by spin coating broadens the resonance wavelength of the transmittance. This broadening favors solar cell applications. Metal shadowing competes with light scattering in a manner that varies with nanoparticle concentration. Experimental results reveal that the mc-Si solar cells that incorporate Au nanoparticles outperform those with Ag nanoparticles. The incorporation of suitable concentration of Au and Ag nanoparticles into mc-Si solar cells increases their efficiency enhancement by 5.6% and 4.8%, respectively. Incorporating Au and Ag nanoparticles into CIGS solar cells improve their efficiency enhancement by 1.2% and 1.4%, respectively. The enhancement of the photocurrent in mc-Si solar cells is lower than that in CIGS solar cells, owing to their different light scattering behaviors and material absorption coefficients.     

Cesium Doping for Performance Improvement of Lead(II)-acetate-Based Perovskite Solar Cells

Lead(II)-acetate (Pb(Ac)₂) is a promising lead source for the preparation of organolead trihalide perovskite materials, which avoids the use of inconvenient anti-solvent treatment. In this study, we investigated the effect of cesium doping on the performance of Pb(Ac)₂-based perovskite solar cells (PSCs). We demonstrate that the quality of the CH₃NH₃PbI₃ perovskite film was improved with increased crystallinity and reduced pinholes by doping the perovskite with 5 mol% cesium. As a result, the power conversion efficiency (PCE) of the PSCs was improved from 14.1% to 15.57% (on average), which was mainly induced by the significant enhancements in short-circuit current density and fill factor. A PCE of 18.02% was achieved for the champion device of cesium-doped Pb(Ac)₂-based PSCs with negligible hysteresis and a stable output. Our results indicate that cesium doping is an effective approach for improving the performance of Pb(Ac)₂-based PSCs.     

Routes for Metallization of Perovskite Solar Cells

The application of metallic nanoparticles leads to an increase in the efficiency of solar cells due to the plasmonic effect. We explore various scenarios of the related mechanism in the case of metallized perovskite solar cells, which operate as hybrid chemical cells without p-n junctions, in contrast to conventional cells such as Si, CIGS or thin-layer semiconductor cells. The role of metallic nano-components in perovskite cells is different than in the case of p-n junction solar cells and, in addition, the large forbidden gap and a large effective masses of carriers in the perovskite require different parameters for the metallic nanoparticles than those used in p-n junction cells in order to obtain the increase in efficiency. We discuss the possibility of activating the very poor optical plasmonic photovoltaic effect in perovskite cells via a change in the chemical composition of the perovskite and through special tailoring of metallic admixtures. Here we show that it is possible to increase the absorption of photons (optical plasmonic effect) and simultaneously to decrease the binding energy of excitons (related to the inner electrical plasmonic effect, which is dominant in perovskite cells) in appropriately designed perovskite structures with multishell elongated metallic nanoparticles to achieve an increase in efficiency by means of metallization, which is not accessible in conventional p-n junction cells. We discuss different methods for the metallization of perovskite cells against the background of a review of various attempts to surpass the Shockley–Queisser limit for solar cell efficiency, especially in the case of the perovskite cell family.     

BTO-Coupled CIGS Solar Cells with High Performances

In order to improve the power conversion efficiency (PCE) of Cu(In,Ga)Se₂ (CIGS) solar cells, a BaTiO₃ (BTO) layer was inserted into the Cu(In,Ga)Se₂. The performances of the BTO-coupled CIGS solar cells with structures of Mo/CIGS/CdS/i-ZnO/AZO, Mo/BTO/CIGS/CdS/i-ZnO/AZO, Mo/CIGS/BTO/CdS/i-ZnO/AZO, Mo/CIGS/CdS/BTO/i-ZnO/AZO, Mo/CIGS/BTO/i-ZnO/AZO, Mo/CIGS/CdS/BTO/AZO, and Mo/ CIGS/CdS(5 nm)/BTO(5 nm)/i-ZnO/AZO were systematically studied via the SCAPS-1D software. It was found that the power conversion efficiency (PCE) of a BTO-coupled CIGS solar cell with a device configuration of Mo/CIGS/CdS/BTO/AZO was 24.53%, and its open-circuit voltage was 931.70 mV. The working mechanism for the BTO-coupled CIGS solar cells with different device structures was proposed. Our results provide a novel strategy for improving the PCE of solar cells by combining a ferroelectric material into the p-n junction materials.     

Electrochemical Impedance Investigation of Dye-Sensitized Solar Cells Based on Electrospun TiO2 Nanofibers Photoanodes

This work investigates an electrochemical impedance analysis based on synthesized TiO₂ nanofibers (NFs) photoanodes, which were fabricated via electrospinning and calcination. The investigated photoanode substrate NFs were studied in terms of physicochemical tools to investigate their morphological character, crystallinity, and chemical contents via scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS), and X-ray diffraction (XRD) analyses. As a result, the studied photoanode substrate NFs were applied to fabricate dye-sensitized solar cells (DSCs), and the electrochemical impedance analysis (EIS) was studied in terms of equivalent circuit fitting and impacts of N-doping, the latter of which was approved via XPS analysis. N-doping has a considerable role in the enhancement of charge transfers, which could be due to the strong interactions between active-site N atoms and the used photosensitizer.     

Guidelines for the Bandgap Combinations and Absorption Windows for Organic Tandem and Triple-Junction Solar Cells

Organic solar cells have narrow absorption windows, compared to the absorption band of inorganic semiconductors. A possible way to capture a wider band of the solar spectrum—and thus increasing the power conversion efficiency—is using more solar cells with different bandgaps in a row, i.e., a multi-junction solar cell. We calculate the ideal material characteristics (bandgap combinations and absorption windows) for an organic tandem and triple-junction solar cell, as well as their acceptable range. In this way, we give guidelines to organic material designers.     

Impact of Precursor Concentration on Perovskite Crystallization for Efficient Wide-Bandgap Solar Cells

High-crystalline-quality wide-bandgap metal halide perovskite materials that achieve superior performance in perovskite solar cells (PSCs) have been widely explored. Precursor concentration plays a crucial role in the wide-bandgap perovskite crystallization process. Herein, we investigated the influence of precursor concentration on the morphology, crystallinity, optical property, and defect density of perovskite materials and the photoelectric performance of solar cells. We found that the precursor concentration was the key factor for accurately controlling the nucleation and crystal growth process, which determines the crystallization of perovskite materials. The precursor concentration based on Cs_0.05FA_0.8MA_0.15Pb(I_0.84Br_0.16)₃ perovskite was controlled from 0.8 M to 2.3 M. The perovskite grains grow larger with the increase in concentration, while the grain boundary and bulk defect decrease. After regulation and optimization, the champion PSC with the 2.0 M precursor concentration exhibits a power conversion efficiency (PCE) of 21.13%. The management of precursor concentration provides an effective way for obtaining high-crystalline-quality wide-bandgap perovskite materials and high-performance PSCs.     

Recent Advances in Selenophene-Based Materials for Organic Solar Cells

Due to the low cost, light weight, semitransparency, good flexibility, and large manufacturing area of organic solar cells (OSCs), OSCs have the opportunity to become the next generation of solar cells in some specific applications. So far, the efficiency of the OSC device has been improved by more than 20%. The optical band gap between the lowest unoccupied molecular orbital (LUMO) level and the highest occupied molecular orbital (HOMO) level is an important factor affecting the performance of the device. Selenophene, a derivative of aromatic pentacyclic thiophene, is easy to polarize, its LUMO energy level is very low, and hence the optical band gap can be reduced. In addition, the selenium atoms in selenophene and other oxygen atoms or sulfur atoms can form an intermolecular interaction, so as to improve the stacking order of the active layer blend film and improve the carrier transport efficiency. This paper introduces the organic solar active layer materials containing selenium benzene in recent years, which can be simply divided into donor materials and acceptor materials. Replacing sulfur atoms with selenium atoms in these materials can effectively reduce the corresponding optical band gap of materials, improve the mutual solubility of donor recipient materials, and ultimately improve the device efficiency. Therefore, the sulfur in thiophene can be completely replaced by selenium or oxygen of the same family, which can be used in the active layer materials of organic solar cells. This article mainly describes the application of selenium instead of sulfur in OSCs.     

Eco-Friendly Dye-Sensitized Solar Cells Based on Water-Electrolytes and Chlorophyll

Organic solvents used for electrolytes of dye-sensitized solar cells (DSSCs) are generally not only toxic and explosive but also prone to leakage due to volatility and low surface tension. The representative dyes of DSSCs are ruthenium-complex molecules, which are expensive and require a complicated synthesis process. In this paper, the eco-friendly DSSCs were presented based on water-based electrolytes and a commercially available organic dye. The effect of aging time after the device fabrication and the electrolyte composition on the photovoltaic performance of the eco-friendly DSSCs were investigated. Plasma treatment of TiO₂ was adopted to improve the dye adsorption as well as the wettability of the water-based electrolytes on TiO₂. It turned out that the plasma treatment was an effective way of improving the photovoltaic performance of the eco-friendly DSSCs by increasing the efficiency by 3.4 times. For more eco-friendly DSSCs, the organic-synthetic dye was replaced by chlorophyll extracted from spinach. With the plasma treatment, the efficiency of the eco-friendly DSSCs based on water-electrolytes and chlorophyll was comparable to those of the previously reported chlorophyll-based DSSCs with non-aqueous electrolytes.     

5.5 MeV Electron Irradiation-Induced Transformation of Minority Carrier Traps in p-Type Si and Si1−xGex Alloys

Minority carrier traps play an important role in the performance and radiation hardness of the radiation detectors operating in a harsh environment of particle accelerators, such as the up-graded sensors of the high-luminosity hadron collider (HL-HC) at CERN. It is anticipated that the sensors of the upgraded strip tracker will be based on the p-type silicon doped with boron. In this work, minority carrier traps in p-type silicon (Si) and silicon–germanium (Si_1−xGe_x) alloys induced by 5.5 MeV electron irradiation were investigated by combining various modes of deep-level transient spectroscopy (DLTS) and pulsed technique of barrier evaluation using linearly increasing voltage (BELIV). These investigations were addressed to reveal the dominant radiation defects, the dopant activity transforms under local strain, as well as reactions with interstitial impurities and mechanisms of acceptor removal in p-type silicon (Si) and silicon–germanium (SiGe) alloys, in order to ground technological ways for radiation hardening of the advanced particle detectors. The prevailing defects of interstitial boron–oxygen (B_iO_i) and the vacancy–oxygen (VO) complexes, as well as the vacancy clusters, were identified using the values of activation energy reported in the literature. The activation energy shift of the radiation-induced traps with content of Ge was clarified in all the examined types of Si_1−xGe_x (with x= 0–0.05) materials.     

Development of Graphene Nano-Platelet Based Counter Electrodes for Solar Cells

Graphene has been envisaged as a highly promising material for various field emission devices, supercapacitors, photocatalysts, sensors, electroanalytical systems, fuel cells and photovoltaics. The main goal of our work is to develop new Pt and transparent conductive oxide (TCO) free graphene based counter electrodes (CEs) for dye sensitized solar cells (DSSCs). We have prepared new composites which are based on graphene nano-platelets (GNPs) and conductive polymers such as poly (3,4-ethylenedioxythiophene) poly(styrenesulfonate) (PEDOT:PSS). Films of these composites were deposited on non-conductive pristine glass substrates and used as CEs for DSSCs which were fabricated by the “open cell” approach. The electrical conductivity studies have clearly demonstrated that the addition of GNPs into PEDOT:PSS films resulted in a significant increase of the electrical conductivity of the composites. The highest solar energy conversion efficiency was achieved for CEs comprising of GNPs with the highest conductivity (190 S/cm) and n-Methyl-2-pyrrolidone (NMP) treated PEDOT:PSS in a composite film. The performance of this cell (4.29% efficiency) compares very favorably to a DSSC with a standard commercially available Pt and TCO based CE (4.72% efficiency in the same type of open DSSC) and is a promising replacement material for the conventional Pt and TCO based CE in DSSCs.     

Transient Photocurrent Response of Plasmon-Enhanced Polymer Solar Cells with Gold Nanoparticles

In this work, the transient photocurrent of the plasmon-enhanced polymer bulk heterojunction solar cells based on poly(3-hexylthiophene) (P3HT) and [6,6]-Phenyl C₆₁ butyric acid methyl ester (PCBM) is investigated. Two kinds of localized surface plasmon resonance (LSPR) enhanced devices were fabricated by doping the gold nanoparticles (Au NPs) into the anode buffer layer and inserting Au NPs between the anode buffer layer and the active layer. We probed the dynamics of the turn-on and turn-off responses to 400 μs square-pulse optical excitation from the 380 nm and 520 nm light-emitting diodes (LED) driven by an electric pulse generator. The transient photocurrent curves of devices with Au NPs at different positions and under different excitation wavelength are compared and analyzed. The charge trapping/detrapping processes that occurred at the interface of Au NPs and the active layer were observed; these exhibit an overshoot in the initial fast rise of photocurrent response. Our results show that the incorporating position of Au NPs is an important key factor to influence the transient photocurrent behaviors.     

Polythiophenes Comprising Conjugated Pendants for Polymer Solar Cells: A Review

Polythiophene (PT) is one of the widely used donor materials for solution-processable polymer solar cells (PSCs). Much progress in PT-based PSCs can be attributed to the design of novel PTs exhibiting intense and broad visible absorption with high charge carrier mobility to increase short-circuit current density (J_sc), along with low-lying highest occupied molecular orbital (HOMO) levels to achieve large open circuit voltage (V_oc) values. A promising strategy to tailor the photophysical properties and energy levels via covalently attaching electron donor and acceptor pendants on PTs backbone has attracted much attention recently. The geometry, electron-donating capacity, and composition of conjugated pendants are supposed to be the crucial factors in adjusting the conformation, energy levels, and photovoltaic performance of PTs. This review will go over the most recent approaches that enable researchers to obtain in-depth information in the development of PTs comprising conjugated pendants for PSCs.     

Tolerance of Perovskite Solar Cells under Proton and Electron Irradiation

In this work, radiation experiments and simulations were carried out on perovskite solar cells (PSCs). The experimental results show that the PSCs in this work were robust to proton irradiation but more sensitive to electron irradiation, which is different from the results of previous studies. Simulations based on the Monte Carlo method show that the energy loss at the interface was much higher than that in the material bulk, and the interface was more sensitive to electron incidents.     

Overview of the Current State of Gallium Arsenide-Based Solar Cells

As widely-available silicon solar cells, the development of GaAs-based solar cells has been ongoing for many years. Although cells on the gallium arsenide basis today achieve the highest efficiency of all, they are not very widespread. They have particular specifications that make them attractive, especially for certain areas. Thanks to their durability under challenging conditions, it is possible to operate them in places where other solar cells have already undergone significant degradation. This review summarizes past, present, and future uses of GaAs photovoltaic cells. It examines advances in their development, performance, and various current implementations and modifications.     

The Influence of Alkoxy Substitutions on the Properties of Diketopyrrolopyrrole-Phenyl Copolymers for Solar Cells

A previously reported diketopyrrolopyrrole (DPP)-phenyl copolymer is modified by adding methoxy or octyloxy side chains on the phenyl spacer. The influence of these alkoxy substitutions on the physical, opto-electronic properties, and photovoltaic performance were investigated. It was found that the altered physical properties correlated with an increase in chain flexibility. Well-defined oligomers were synthesized to verify the observed structure-property relationship. Surprisingly, methoxy substitution on the benzene spacer resulted in higher melting and crystallization temperatures in the synthesized oligomers. This trend is not observed in the polymers, where the improved interactions are most likely counteracted by the larger conformational possibilities in the polymer chain upon alkoxy substitution. The best photovoltaic performance was obtained for the parent polymer: fullerene blends whereas the modifications on the other two polymers result in reduced open-circuit voltage and varying current densities under similar processing conditions. The current densities could be related to different polymer: fullerene blend morphologies. These results show that supposed small structural alterations such as methoxy substitution already significantly altered the physical properties of the parent polymer and also that oligomers and polymers respond divergent to structural alterations made on a parent structure.     

Spiky Durian-Shaped Au@Ag Nanoparticles in PEDOT:PSS for Improved Efficiency of Organic Solar Cells

The localized surface plasmon resonance (LSPR) effects of nanoparticles (NPs) are effective for enhancing the power conversion efficiency (PCE) of organic solar cells (OSCs). In this study, spiky durian-shaped Au@Ag core-shell NPs were synthesized and embedded in the hole transport layer (HTL) (poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate) (PEDOT:PSS)) of PTB7:PC₇₁BM bulk-heterojunction OSCs. Different volume ratios of PEDOT:PSS-to-Au@Ag NPs (8%, 10%, 12%, 14%, and 16%) were prepared to optimize synthesis conditions for increased efficiency. The size properties and surface morphology of the NPs and HTL were analyzed using field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), and atomic force microscopy (AFM). UV–Vis spectroscopy and current density–voltage (J-V) analysis were used to investigate the electrical performance of the fabricated OSCs. From the results, we observed that the OSC with a volume ratio of 14% (PEDOT:PSS–to–Au@Ag NPs) performed better than others, where the PCE was improved from 2.50% to 4.15%, which is a 66% increase compared to the device without NPs.     

Influence of Tin Doped TiO2 Nanorods on Dye Sensitized Solar Cells

The one-step hydrothermal method was used to synthesize Sn-doped TiO₂ (Sn-TiO₂) thin films, in which the variation in Sn content ranged from 0 to 7-wt % and, further, its influence on the performance of a dye-sensitized solar cell (DSSC) photoanode was studied. The deposited samples were analyzed by X-ray diffraction (XRD) and Raman spectroscopy, which confirmed the existence of the rutile phase of the synthesized samples with crystallite size ranges in between 20.1 to 22.3 nm. In addition, the bare and Sn-TiO₂ thin films showed nanorod morphology. A reduction in the optical band gap from 2.78 to 2.62 eV was observed with increasing Sn content. The X-ray photoelectron spectroscopy (XPS) analysis confirmed Sn⁴⁺ was successfully replaced at the Ti⁴⁺ site. The 3-wt % Sn-TiO₂ based DSSC showed the optimum efficiency of 4.01%, which was superior to 0.87% of bare and other doping concentrations of Sn-TiO₂ based DSSCs. The present work reflects Sn-TiO₂ as an advancing material with excellent capabilities, which can be used in photovoltaic energy conversion devices.