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.     

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.     

Single-Component Organic Solar Cells Based on Intramolecular Charge Transfer Photoabsorption

Conjugated donor–acceptor molecules with intramolecular charge transfer absorption are employed for single-component organic solar cells. Among the five types of donor–acceptor molecules, the strong push–pull structure of DTDCPB resulted in solar cells with high J_SC, an internal quantum efficiency exceeding 20%, and high V_OC exceeding 1 V with little photon energy loss around 0.7 eV. The exciton binding energy (EBE), which is a key factor in enhancing the photocurrent in the single-component device, was determined by quantum chemical calculation. The relationship between the photoexcited state and the device performance suggests that the strong internal charge transfer is effective for reducing the EBE. Furthermore, molecular packing in the film is shown to influence photogeneration in the film bulk.     

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.     

Application of Graphene-Related Materials in Organic Solar Cells

Graphene-related materials (GRMs) such as graphene quantum dots (GQDs), graphene oxide (GO), reduced graphene oxide (rGO), graphene nanoribbons (GNRs), and so forth have recently emerged as photovoltaic (PV) materials due to their nanodimensional structure and outstanding properties such as high electrical and thermal conductivity, large specific surface, and unique combination of mechanical strength and flexibility. They can be a crucial part of transparent electrodes, hole/electron transport materials, and active layers in organic solar cells (OSCs). Besides their role in charge extraction and transport, GRMs act as device protectors against environmental degradation through their compact bidimensional structure and offer good durability. This review briefly presents the synthesis methods of GRMs and describes the current progress in GRM-based OSCs. PV parameters (short circuit current, open circuit voltage, power conversion efficiency, and fill factor) are summarized and comparatively discussed for the different structures. The efficiency recently surpassed 15% for an OSC incorporating polymer-modified graphene as a transparent electrode. The long-term stability of OSCs incorporating GRMs is also discussed. Finally, conclusions and the outlook for future investigation into GRM-based devices for PVs are presented.     

Solution Processed PVB/Mica Flake Coatings for the Encapsulation of Organic Solar Cells

Organic photovoltaics (OPVs) die due to their interactions with environmental gases, i.e., moisture and oxygen, the latter being the most dangerous, especially under illumination, due to the fact that most of the active layers used in OPVs are extremely sensitive to oxygen. In this work we demonstrate solution-based effective barrier coatings based on composite of poly(vinyl butyral) (PVB) and mica flakes for the protection of poly (3-hexylthiophene) (P3HT)-based organic solar cells (OSCs) against photobleaching under illumination conditions. In the first step we developed a protective layer with cost effective and environmentally friendly methods and optimized its properties in terms of transparency, barrier improvement factor, and bendability. The developed protective layer maintained a high transparency in the visible region and improved oxygen and moisture barrier quality by the factor of ~7. The resultant protective layers showed ultra-flexibility, as no significant degradation in protective characteristics were observed after 10 K bending cycles. In the second step, a PVB/mica composite layer was applied on top of the P3HT film and subjected to photo-degradation. The P3HT films coated with PVB/mica composite showed improved stability under constant light irradiation and exhibited a loss of <20% of the initial optical density over the period of 150 h. Finally, optimized barrier layers were used as encapsulation for organic solar cell (OSC) devices. The lifetime results confirmed that the stability of the OSCs was extended from few hours to over 240 h in a sun test (65 °C, ambient RH%) which corresponds to an enhanced lifetime by a factor of 9 compared to devices encapsulated with pristine PVB.     

Semiconductor Nanocrystals as Light Harvesters in Solar Cells

Photovoltaic cells use semiconductors to convert sunlight into electrical current and are regarded as a key technology for a sustainable energy supply. Quantum dot-based solar cells have shown great potential as next generation, high performance, low-cost photovoltaics due to the outstanding optoelectronic properties of quantum dots and their multiple exciton generation (MEG) capability. This review focuses on QDs as light harvesters in solar cells, including different structures of QD-based solar cells, such as QD heterojunction solar cells, QD-Schottky solar cells, QD-sensitized solar cells and the recent development in organic-inorganic perovskite heterojunction solar cells. Mechanisms, procedures, advantages, disadvantages and the latest results obtained in the field are described. To summarize, a future perspective is offered.     

Studying the Effect of High Substrate Temperature on the Microstructure of Vacuum Evaporated TAPC: C60 Organic Solar Thin Films

Organic solar cells (OSCs), also known as organic photovoltaics (OPVs), are an emerging solar cell technology composed of carbon-based, organic molecules, which convert energy from the sun into electricity. Key for their performance is the microstructure of the light-absorbing organic bulk heterojunction. To study this, organic solar films composed of both fullerene C₆₀ as electron acceptor and different mole percentages of di-[4-(N,N-di-p-tolyl-amino)-phenyl]-cyclohexane (TAPC) as electron donor were evaporated in vacuum in different mixing ratios (5, 50 and 95 mol%) on an ITO-coated glass substrate held at room temperature and at 110 °C. The microstructure of the C₆₀: TAPC heterojunction was studied by grazing incidence wide angle X-ray scattering to understand the effect of substrate heating. By increasing the substrate temperature from ambient to 110 °C, it was found that no significant change was observed in the crystal size for the C₆₀: TAPC concentrations investigated in this study. In addition to the variation done in the substrate temperature, the variation of the mole percent of the donor (TAPC) was studied to conclude the effect of both the substrate temperature and the donor concentration on the microstructure of the OSC films. Bragg peaks were attributed to C₆₀ in the pure C₆₀ sample and in the blend with low donor mole percentage (5%), but the C₆₀ peaks became nondiscernible when the donor mole percentage was increased to 50% and above, showing that TAPC interrupted the formation of C₆₀ crystals.     

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).     

Solvent Vapor Treatment Effects on Poly(3-hexylthiophene) Thin Films and its Application for Interpenetrating Heterojunction Organic Solar Cells

The solvent vapor treatment (SVT) for poly(3-hexylthiophene) (PAT6) films and its application to interpenetrating heterojunction organic solar cells have been studied. It was found that SVT could improve the crystallinity and electrical characteristics of the PAT6 films. We fabricated organic solar cells with an interpenetrating structure of PAT6 and fullerenes utilizing the SVT process, and discuss the improved performance of the solar cells by taking the film crystallinity, optical properties, and morphology into consideration.     

Improving the Efficiency of Organic Solar Cells upon Addition of Polyvinylpyridine

We report on the efficiency improvement of organic solar cells (OPVs) based on the low energy gap polyfluorene derivative, APFO-3, and the soluble C₆₀ fullerene PCBM, upon addition of a residual amount of poly (4-vinylpyridine) (PVP). We find that the addition of 1% by weight of PVP with respect to the APFO-3 content leads to an increase of efficiency from 2.4% to 2.9%. Modifications in the phase separation details of the active layer were investigated as a possible origin of the efficiency increase. At high concentrations of PVP, the blend morphology is radically altered as observed by Atomic Force Microscopy. Although the use of low molecular weight additives is a routine method to improve OPVs efficiency, this report shows that inert polymers, in terms of optical and charge transport properties, may also improve the performance of polymer-based solar cells.     

Ultrasonically Processed WSe2 Nanosheets Blended Bulk Heterojunction Active Layer for High-Performance Polymer Solar Cells and X-ray Detectors

Two-dimensional (2D) tungsten diselenide (WSe₂) has attracted considerable attention in the field of photovoltaic devices owing to its excellent structure and photoelectric properties, such as ordered 2D network structure, high electrical conductivity, and high mobility. For this test, we firstly prepared different sizes (NS1–NS3) of WSe₂ nanosheets (NSs) through the ultrasonication method and characterized their structures using the field emission scanning electron microscope (FE-SEM), Raman spectroscopy, and X-ray powder diffraction. Moreover, we investigated the photovoltaic performance of polymer solar cells based on 5,7-Bis(2-ethylhexyl)benzo[1,2-c:4,5-c′]dithiophene-4,8-dione(PBDB-T):(6,6)-phenyl-C71 butyric acid methyl ester (PCBM) with different WSe₂ NSs as the active layer. The fabricated PBDB-T:PCBM active layer with the addition of NS2 WSe₂ NSs (1.5 wt%) exhibited an improved power conversion efficiency (PCE) of 9.2%, which is higher than the pure and NS1 and NS3 WSe₂ blended active layer-encompassing devices. The improved PCE is attributed to the synergic enhancement of exciton dissociation and an improvement in the charge mobility through the modified active layer for polymer solar cells. Furthermore, the highest sensitivity of 2.97 mA/Gy·cm² was achieved for the NS2 WSe₂ NSs blended active layer detected by X-ray exposure over the pure polymer, and with the NS1 and NS2 WSe₂ blended active layer. These results led to the use of transition metal dichalcogenide materials in polymer solar cells and X-ray detectors.     

Morphology Control of Monomer–Polymer Hybrid Electron Acceptor for Bulk-Heterojunction Solar Cell Based on P3HT and Ti-Alkoxide with Ladder Polymer

We report the morphology control of a nano-phase-separated structure in the photoactive layer (power generation layer) of organic–inorganic hybrid thin-film solar cells to develop highly functional electronic devices for societal applications. Organic and inorganic–organic hybrid bulk heterojunction solar cells offer several advantages, including low manufacturing costs, light weight, mechanical flexibility, and a potential to be recycled because they can be fabricated by coating them on substrates, such as films. In this study, by incorporating the carrier manager ladder polymer BBL as the third component in a conventional two-component power generation layer consisting of P3HT—the conventional polythiophene derivative and titanium alkoxide—we demonstrate that the phase-separated structure of bulk heterojunction solar cells can be controlled. Accordingly, we developed a discontinuous phase-separated structure suitable for charge transport, obtaining an energy conversion efficiency higher than that of the conventional two-component power generation layer. Titanium alkoxide is an electron acceptor and absorbs light with a wavelength lower than 500 nm. It is highly sensitive to LED light sources, including those used in homes and offices. A conversion efficiency of 4.02% under a 1000 lx LED light source was achieved. Hence, high-performance organic–inorganic hybrid bulk heterojunction solar cells with this three-component system can be used in indoor photovoltaic systems.     

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.     

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.     

Computational Probing of Tin-Based Lead-Free Perovskite Solar Cells: Effects of Absorber Parameters and Various Electron Transport Layer Materials on Device Performance

Tin-based perovskite solar cells have gained global research attention due to the lead toxicity and health risk associated with its lead-based analog. The promising opto-electrical properties of the Tin-based perovskite have attracted researchers to work on developing Tin-based perovskite solar cells with higher efficiencies comparable to lead-based analogs. Tin-based perovskites outperform lead-based ones in areas such as optimal band gap and carrier mobility. A detailed understanding of the effects of each parameter and working conditions on Tin-based perovskite is crucial in order to improve efficiency. In the present work, we have carried out a numerical simulation of a planar heterojunction Tin-based (CH₃NH₃SnI₃) perovskite solar cell employing a SCAPS 1D simulator. Device parameters, namely, the thickness of the absorber layer, the defect density of the absorber layer, working temperature, series resistance, and metalwork function, were exclusively investigated. ZnO was employed as the ETL (electron transport layer) material in the initial simulation to obtain optimized parameters and attained a maximum efficiency of 19.62% with 1.1089 V open circuit potential (V_oc) at 700 nm thickness (absorber layer). Further, different ETL materials were introduced into the optimized device architecture, and the Zn₂SnO₄-based device delivered an efficiency of 24.3% with a V_oc of 1.1857 V. The obtained results indicate a strong possibility to model and construct better-performing perovskite solar cells based on Tin (Sn) with Zn₂SnO₄ as the ETL layer.     

Structural Properties of Zinc Oxide Nanorods Grown on Al-Doped Zinc Oxide Seed Layer and Their Applications in Dye-Sensitized Solar Cells

We fabricated zinc oxide (ZnO) nanorods (NRs) with Al-doped ZnO (AZO) seed layers and dye-sensitized solar cells (DSSCs) employed the ZnO NRs between a TiO₂ photoelectrode and a fluorine-doped SnO₂ (FTO) electrode. The growth rate of the NRs was strongly dependent on the seed layer conditions, i.e., thickness, Al dopant and annealing temperature. Attaining a large particle size with a high crystallinity of the seed layer was vital to the well-aligned growth of the NRs. However, the growth was less related to the substrate material (glass and FTO coated glass). With optimized ZnO NRs, the DSSCs exhibited remarkably enhanced photovoltaic performance, because of the increase of dye absorption and fast carrier transfer, which, in turn, led to improved efficiency. The cell with the ZnO NRs grown on an AZO seed layer annealed at 350 °C showed a short-circuit current density (J_SC) of 12.56 mA/cm², an open-circuit voltage (V_OC) of 0.70 V, a fill factor (FF) of 0.59 and a power conversion efficiency (PCE, η) of 5.20% under air mass 1.5 global (AM 1.5G) illumination of 100 mW/cm².     

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.     

Characteristics of Dye-Sensitized Solar Cells with TiO2 Stripes

A TiO₂ strip array with a thickness of 90 nm was fabricated by photolithography and physical vapor deposition. This work utilized the chemical and physical methods to fabricate the TiO₂ strip array. A porous semiconductor layer made of TiO₂ nanoparticles was coated on the TiO₂ strip array. The TiO₂ strip array has a one-dimensional protrusive structure. The energy conversion efficiency (4.38%) of a dye-sensitized solar cell (DSSC) with the TiO₂ strip array exceeded that (3.20%) of a DSSC without a TiO₂ strip array by 37%. In addition, this result was verified by the electrochemical impedance spectra of the two DSSCs. Therefore, the TiO₂ strip array can be used to increase the energy conversion efficiencies of DSSCs. The large energy conversion efficiency of the DSSC with the TiO₂ strip array arises from the large surface area of the one-dimensional protrusive structure and its specific electron transport paths. The DSSC with the TiO₂ strip array has advantages of economical production cost, easy fabrication, and boosting energy conversion efficiency.     

Current Approach in Surface Plasmons for Thin Film and Wire Array Solar Cell Applications

Surface plasmons, which exist along the interface of a metal and a dielectric, have been proposed as an efficient alternative method for light trapping in solar cells during the past ten years. With unique properties such as superior light scattering, optical trapping, guide mode coupling, near field concentration, and hot-electron generation, metallic nanoparticles or nanostructures can be tailored to a certain geometric design to enhance solar cell conversion efficiency and to reduce the material costs. In this article, we review current approaches on different kinds of solar cells, such as crystalline silicon (c-Si) and amorphous silicon (a-Si) thin film solar cells, organic solar cells, nanowire array solar cells, and single nanowire solar cells.