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This work investigates the radiation resistance of high‐performance multi‐component perovskite solar cells (PSCs) for the first time under extreme short‐pulse proton irradiation conditions. The devices are subjected to high‐intensity 170 keV pulsed (150 ns) proton irradiation, with a fluence of up to 1013 p cm−2, corresponding to ≈30 years of operation at low Earth orbit. A complex material characterization of the perovskite active layer and device physics analysis of the PSCs before and after short‐pulse proton irradiation is conducted. The obtained results indicate that the photovoltaic performance of the solar cells experiences a slight deterioration up to 20 % and 50 % following the low 2 × 1012 p cm−2 and high 1 × 1013 p cm−2 proton fluences, respectively, due to increased non‐radiative recombination losses. The findings reveal that multi‐component PSCs are immune even to extreme high‐intense short‐pulse proton irradiation, which exceeds harsh space conditions, including intense coronal ejection events usually associated with solar flares. [ABSTRACT FROM AUTHOR]

Copper oxide is one of the original semiconductor materials employed for solar cells in the early 19th century before Silicon solar cells became popular due to their abundant availability, and eco‐friendly nature. The optoelectronic parameters signify its huge potential in solar cell devices, though it's far from the theoretically predicted performance, provides tremendous scope to improve the solar cell performance by forming different heterojunctions. In this study, we investigated the copper oxide's (CuO) potential as an active layer in thin‐film solar cells theoretically with a new structure consisting of a Glass/ITO/Graphite/CuO/Ni. Furthermore, the charge carrier's generation rate and theoretical thresholds for photovoltaic device efficiency were determined for varying active layer thicknesses by employing a normalized light intensity equivalent to that of the AM1.5 spectrum. The optimized performance of the simulated structure by considering realistic optical parameters of the solar cell was ~24%, obtained for the 500 nm CuO films. The performed theoretical work can help to employ CuO and boost the performance of solar cells experimentally. [ABSTRACT FROM AUTHOR]

The increase in the performance of organic solar cells observed over the past few years has reinvigorated the search for a deeper understanding of the loss and extraction processes in this class of device. A detailed knowledge of the density of free charge carriers under different operating conditions and illumination intensities is a prerequisite to quantify the recombination and extraction dynamics. Differential charging techniques are a promising approach to experimentally obtain the charge carrier density under the aforementioned conditions. In particular, the combination of transient photovoltage and photocurrent as well as impedance and capacitance spectroscopy have been successfully used in past studies to determine the charge carrier density of organic solar cells. In this Tutorial, these experimental techniques will be discussed in detail, highlighting fundamental principles, practical considerations, necessary corrections, advantages, drawbacks, and ultimately their limitations. Relevant references introducing more advanced concepts will be provided as well. Therefore, the present Tutorial might act as an introduction and guideline aimed at new prospective users of these techniques as well as a point of reference for more experienced researchers. [ABSTRACT FROM AUTHOR]

In this study, a comprehensive quantitative analysis of the photodiode (PD) is conducted and photovoltaic (PV) characteristics of organic non‐fullerene PCE10:ITIC‐4F devices before and after exposure to a 150 ns pulse of 170 keV proton irradiation with the fluence of 2·1012 p cm−2 that is equivalent to ≈6 years of operation at a low Earth orbit. While an expected initial performance reduction happened in the photodiode and photovoltaic operation modes, a hitherto unknown self‐healing effect in the organic devices is observed several days after the proton irradiation. The organic bulk‐heterojunction (BHJ) material properties and the multi‐mechanisms recombination processes before and after irradiation and during self‐healing are investigated. This analysis provides a quantitative understanding of the changes occurring in the device physics and points toward the relevant aspects of the self‐healing mechanism related to the dynamics of proton‐induced traps in the bulk of the organic active layer. Ultimately, the synergy of record lightweight features and newly discovered self‐healing of proton‐induced damage in organic PDs and solar cells highlights their great potential for applications in rapidly emerging space technology. [ABSTRACT FROM AUTHOR]

The term 'Solar Cell' is commonly used for Photovoltaics that convert light into electrical energy. However, light can be harvested from various sources not limited to the Sun. This work considers the possibility of harvesting photons from different star types, including our closest neighbor star Proxima Centauri. The theoretical efficiency limits of single junction photovoltaic devices are calculated for different star types at a normalized light intensity corresponding to the AM0 spectrum intensity with AM0 = 1361 W/m2. An optimal bandgap of > 12 eV for the hottest O5V star type leads to 47% Shockley-Queisser photoconversion efficiency (SQ PCE), whereas a narrower optimal bandgap of 0.7 eV leads to 23% SQ PCE for the coldest red dwarf M0, M5.5Ve, and M8V type stars. Organic Photovoltaics (OPVs) are the most lightweight solar technology and have the potential to be employed in weight-restricted space applications, including foreseeable interstellar missions. With that in mind, the Sun's G2V spectrum and Proxima Centauri's M5.5Ve spectrum are considered in further detail in combination with two extreme bandgap OPV systems: one narrow bandgap system (PM2:COTIC-4F, Eg = 1.14 eV) and one wide bandgap system (PM6:o-IDTBR, Eg = 1.62 eV). Semi-empirically modeled JV-curves reveal that the absorption characteristics of the PM2:COTIC-4F blend match well with both the G2V and the M5.5Ve spectrum, yielding theoretical PCEs of 22.6% and 12.6%, respectively. In contrast, the PM6:o-IDTBR device shows a theoretical PCE of 18.2% under G2V illumination that drops sharply to 0.9% under M5.5Ve illumination. [ABSTRACT FROM AUTHOR]

In this review, the current state of materials science and the device physics of semitransparent organic solar cells is summarized. Relevant synthetic strategies to narrow the band gap of organic semiconducting molecules are outlined, and recent developments in the polymer donor and near-infrared absorbing acceptor materials are discussed. Next, an overview of transparent electrodes is given, including oxides, multi-stacks, thin metal, and solution processed electrodes, as well as considerations that are unique to ST-OPVs. The remainder of this review focuses on the device engineering of ST-OPVs. The figures of merit and the theoretical limitations of ST-OPVs are covered, as well as strategies to improve the light utilization efficiency. Lastly, the importance of creating an in-depth understanding of the device physics of ST-OPVs is emphasized and the existing works that answer fundamental questions about the inherent changes in the optoelectronic processes in transparent devices are presented in a condensed way. This last part outlines the changes that are unique for devices with increased transparency and the resulting implications, serving as a point of reference for the systematic development of next-generation ST-OPVs. [ABSTRACT FROM AUTHOR]

The effect of the cross‐coupling catalyst tetrakis(triphenylphosphine)palladium(0) (Pd(PPh3)4) on the performance of a model organic bulk‐heterojunction solar cell composed of a blend of poly([2,6′‐4,8‐di(5‐ethylhexylthienyl)benzo[1,2‐b;3,3‐b]dithiophene]{3‐fluoro‐2[(2‐ethylhexyl)carbonyl]thieno[3,4‐b]thiophenediyl}) (PTB7‐Th) donor and 3,9‐bis(2‐methylene‐((3‐(1,1‐dicyanomethylene)‐6,7‐difluoro)‐indanone))‐5,5,11,11‐tetrakis(4‐hexylphenyl)‐dithieno[2,3‐d:2′,3′‐d′]‐s‐indaceno[1,2‐b:5,6‐b′]dithiophene (IOTIC‐4F) non‐fullerene acceptor is investigated. The effect of intentional addition of different amounts of Pd(PPh3)4 on morphology, free charge carrier generation, non‐geminate bulk trap‐ and surface trap‐assisted recombination as well as bimolecular recombination and charge extraction is quantified. This work shows that free charge carrier generation is affected significantly, while the impact of Pd(PPh3)4 on non‐geminate recombination processes is limited because the catalyst does not facilitate efficient trap‐assisted recombination. The studied system shows substantial robustness towards the addition of Pd(PPh3)4 in small amounts. [ABSTRACT FROM AUTHOR]

Organic (semi)transparent photovoltaics (ST‐OPVs) promise integrated, sustainable, low‐cost energy harvesting solutions. However, current efficiency limitations have to be overcome to make ST‐OPV a competitive technology. In this simulation‐based work, the effect of the selective transparency on the photoelectronic processes in ST‐OPVs is studied and changes in the generation–recombination dynamics and the extraction efficiency are demonstrated that are causally linked to the increased transparency. The study of five model systems with transparent indium tin oxide (ITO) back electrodes and systematically varied extinction coefficients and an opaque cell with Ag back contact allows to quantify these changes in the photoelectronic processes and to address the role of the series and the shunt resistors while keeping all other parameters of the modeled devices identical. The findings demonstrate the increased importance of the active layer quality in ST‐OPVs and indicate that ST‐OPVs benefit from a wider choice of transparent electrode materials. [ABSTRACT FROM AUTHOR]

The relationship of the temperature–light intensity dependence of open‐circuit voltage Voc in nonfullerene‐based organic solar cells with their material characteristics and multimechanism recombination parameters is described. The systematic variation of the effective bandgap Eg,eff and the electrode layers allows the observation of different relative contributions of bimolecular, bulk, and surface trap‐assisted recombination mechanisms. The complementary advantages of the analytical model and the established voltage‐impedance spectroscopy technique provide a useful tool to quantify multimechanism recombination parameters, effective density of states Nc, and energetic disorder σ in organic solar cells under operating conditions. The validity of the proposed model to understand the temperature and light intensity dependent of Voc is shown by applying it to four different donor:nonfullerene acceptor blend systems with conventional or inverted device architectures. [ABSTRACT FROM AUTHOR]

The short‐circuit current (Jsc) of organic solar cells is defined by the interplay of exciton photogeneration in the active layer, geminate and non‐geminate recombination losses and free charge carrier extraction. The method proposed in this work allows the quantification of geminate recombination and the determination of the mobility‐lifetime product (µτ) as a single integrated parameter for charge transport and non‐geminate recombination. Furthermore, the extraction efficiency is quantified based on the obtained µτ product. Only readily available experimental methods (current‐voltage characteristics, external quantum efficiency measurements) are employed, which are coupled with an optical transfer matrix method simulation. The required optical properties of common organic photovoltaic (OPV) materials are provided in this work. The new approach is applied to three OPV systems in inverted or conventional device structures, and the results are juxtaposed against the µτ values obtained by an independent method based on the voltage–capacitance spectroscopy technique. Furthermore, it is demonstrated that the new method can accurately predict the optimal active layer thickness. [ABSTRACT FROM AUTHOR]

The determination of the voltage‐dependent density of free charge carriers via capacitance spectroscopy is considered an important step in the analysis of emerging photovoltaic technologies, such as organic and perovskite solar cells. In particular, an intimate knowledge of the density of free charge carriers is required for the determination of crucial parameters such as the effective mobility, charge carrier lifetime, nongeminate recombination coefficients, average extraction times, and competition factors. Hence, it is paramount to verify the validity of the commonly employed approaches to obtain the density of free charge carriers. The advantages, drawbacks, and limitations of the most common approaches are investigated in detail and strategies to mitigate misleading values are explored. To this end, two types of nonfullerene organic solar cells based on a PTB7‐Th:ITIC‐2F blend and a PM6:Y6 blend, respectively, are used as a case study to assess how subsequent analyses of the nongeminate recombination dynamics depend on the chosen approach to calculate the density of free charge carriers via capacitance spectroscopy. [ABSTRACT FROM AUTHOR]

Abstract: Organic bulk heterojunction (BHJ) solar cells require energetic offsets between the donor and acceptor to obtain high short‐circuit currents (JSC) and fill factors (FF). However, it is necessary to reduce the energetic offsets to achieve high open‐circuit voltages (VOC). Recently, reports have highlighted BHJ blends that are pushing at the accepted limits of energetic offsets necessary for high efficiency. Unfortunately, most of these BHJs have modest FF values. How the energetic offset impacts the solar cell characteristics thus remains poorly understood. Here, a comprehensive characterization of the losses in a polymer:fullerene BHJ blend, PIPCP:phenyl‐C61‐butyric acid methyl ester (PC61BM), that achieves a high VOC (0.9 V) with very low energy losses (Eloss = 0.52 eV) from the energy of absorbed photons, a respectable JSC (13 mA cm−2), but a limited FF (54%) is reported. Despite the low energetic offset, the system does not suffer from field‐dependent generation and instead it is characterized by very fast nongeminate recombination and the presence of shallow traps. The charge‐carrier losses are attributed to suboptimal morphology due to high miscibility between PIPCP and PC61BM. These results hold promise that given the appropriate morphology, the JSC, VOC, and FF can all be improved, even with very low energetic offsets. [ABSTRACT FROM AUTHOR]

Perovskite solar cells have been shown to be of extraordinary radiation hardness, considering high energetic (68 MeV) proton irradiation with doses up to 1013 p cm−2. In this study electrical and photoelectrical properties of perovskite solar cells with and without proton irradiation are analyzed in detail. The results reveal that proton irradiation improves the open circuit voltage, fill factor, and recombination lifetime of photogenerated charge carriers in perovskite solar cells. These enhancements are mainly a result of the lower nonradiative recombination losses in the proton irradiated devices. The proton treatment creates shallow traps, which may be associated with the proton induced point defects due to the displacements of atoms in the inorganic Pb–I framework, which act as unintentional doping sources and partially compensate deep traps originated from the photodegradation of methylammonium molecules. [ABSTRACT FROM AUTHOR]

The light intensity dependence of the main photoelectrical parameters of the nonfullerene small-molecule bulk heterojunction (BHJ) solar cells p-DTS(FBTTh2)2:perylene diimide (T1:PDI) shows that the nongeminate recombination losses play an important role in this system. A simple approach for the quantitative analysis of capacitance spectroscopy data of the organic BHJ solar cells, which allows to determine the density of free charge carriers as a function of applied bias under standard working conditions, is demonstrated. Using the proposed capacitance spectroscopic technique, the nongeminate recombination losses in the T1:PDI solar cells are quantitatively characterized in the scope of the bimolecular- and trap-assisted recombination mechanisms. Their contributions are separately analyzed within a wide range of the applied bias. [ABSTRACT FROM AUTHOR]

The AC properties of high-efficiency ( η = 8.01% under standard 100 mW/cm2 AM1.5 illumination) small-molecule bulk heterojunction (SM BHJ) solar cells (p-DTS(FBTTh2)2/PC70BM) at different DC biases and frequencies of small amplitude (±10 mV) AC signal in the dark at room temperature were investigated in details. We showed the presence of interface states at the heterojunction interface and determined their parameters from the analysis of spectral distributions of real and imaginary components of the measured impedance. The dielectric constant of BHJ εBHJ = 2.9 was determined from the geometrical capacitance of totally depleted BHJ layer. We explained quantitatively the effect of interface states and series resistance on the measured C-V characteristics of the SM BHJ solar cells at both low and high frequencies. The quantitative value of the density of defect states in the bulk N = 1.05 × 1016 cm−3 was determined from the high frequency C-V characteristic corrected by the effect of the series resistance. Copyright © 2015 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]

Non-geminate recombination, as one of the most relevant loss mechanisms in organic and perovskite solar cells, deserves special attention in research efforts to further increase device performance. It can be subdivided into first, second, and third order processes, which can be elucidated by the effects that they have on the time-dependent open-circuit voltage decay. In this study, analytical expressions for the open-circuit voltage decay exhibiting one of the aforementioned recombination mechanisms were derived. It was possible to support the analytical models with experimental examples of three different solar cells, each of them dominated either by first (PBDBT:CETIC-4F), second (PM6:Y6), or third (irradiated CH3NH3PbI3) order recombination. Furthermore, a simple approach to estimate the dominant recombination process was also introduced and tested on these examples. Moreover, limitations of the analytical models and the measurement technique itself were discussed. [ABSTRACT FROM AUTHOR]

Understanding the recombination dynamics of organic and perovskite solar cells has been a crucial prerequisite in the steadily increasing performance of these promising new types of photovoltaics. Surface recombination in particular has turned out to be one of the last remaining roadblocks, which specifically reduces the open circuit voltage. In this study, the relationship between the rate of surface recombination and the density of charge carriers is analyzed, revealing a cubic dependence between these two parameters. This hypothesis is then tested and verified with the recombination dynamics of an organic solar cell known to exhibit significant surface recombination and a high energy proton irradiated CH 3 NH 3 PbI 3 perovskite solar cell during white light illumination. Incidentally, these results can also explain recombination orders exceeding the commonly known threshold for bimolecular recombination that have been observed in some studies without the need for a charge carrier dependent bimolecular recombination coefficient. Image 1 • Surface recombination specifically reduces the open circuit voltage in organic and perovskite solar cells. • A cubic relationship between the rate of surface recombination and the charge carrier density has been derived. • This hypothesis has been successfully tested for organic and perovskite solar cells. • Recombination orders β > 2 can now be explained without charge carrier density dependent k bm. [ABSTRACT FROM AUTHOR]

Halide perovskites are a promising class of novel photoactive materials for their application in flexible photovoltaic devices. Tolerance and stability of devices to various mechanical stresses are important aspects of this technology for its effective and long-term operation. Currently, this aspect has not been fully researched and addressed by the research community. Hence, this work is aimed at studying the effect of mild mechanical stresses (MMSs) induced by convex bending on the behaviour of ITO/ZnO/MAPbI 3 /Spiro-OMeTAD/Au slot-die-coated flexible perovskite solar cells (FPSCs) and investigating the underlying mechanisms leading to performance degradation in devices. The carrier generation, recombination, and extraction processes within FPSCs are investigated before and after the application of MMSs. The obtained results suggest that the photovoltaic performance of the FPSCs deteriorates by up to 50% after convex bending, due to increased non-radiative recombination losses. The results obtained in this work provide some valuable insights into the dynamics of recombination processes in FPSCs exposed to MMSs and can be used for developing new strategies for improving the mechanical stability of devices. [Display omitted] • Flexible perovskite solar cells fabricated by a slot-die coating method. • A comprehensive analysis of the device physics of flexible slot-die-coated perovskite SCs. • Unravelling device physics of slot-die-coated flexible PSCs before and after applying mild mechanical stresses. [ABSTRACT FROM AUTHOR]

In this study, a comprehensive analytical model to quantify the total nongeminate recombination losses, originating from bimolecular as well as bulk and surface trap‐assisted recombination mechanisms in nonfullerene‐based bulk heterojunction organic solar cells is developed. This proposed model is successfully employed to obtain the different contributions to the recombination current of the investigated solar cells under different illumination intensities. Additionally, the model quantitatively describes the experimentally measured open‐circuit voltage versus light intensity dependence. Most importantly, it is possible to calculate the experimental results with the same fitting parameter values from the presented model. The validity of this model is also proven by a combination of other independent, steady‐state, and transient experimental techniques. This new powerful analytical tool will enable researchers in the photovoltaic community to take into account the synergetic contribution from all relevant types of nongeminate recombination losses in different optoelectronic systems and target their analysis of recombination dynamics at any operating voltage. [ABSTRACT FROM AUTHOR]

Comparison of the photovoltaic properties of F3:fullerene bulk heterojunction solar cells (where F3 is a donor molecule of intermediate dimensions) with normal and inverted structures as a function of photoactive layer thickness is carried out by using optical modeling and light‐dependent photoelectrical characterization. The larger short circuit current of inverted devices can be explained by higher light absorption in the active layer, relative to normal devices. However, worse charge extraction conditions and trap‐assisted recombination, in the bulk heterojunction blend in inverted devices, give rise to larger nongeminate recombination losses and an opposite thickness dependence of the short circuit current and fill factor than what is observed in counterparts with the conventional device architecture. A study of F3:PC61BM bulk heterojunction (BHJ) solar cells with normal and inverted structures as a function of the thickness of the active layer is carried out. The larger short circuit current of the thin inverted devices is explained by the higher light absorption in the active layer. However, the thick inverted devices exhibit unoptimized charge collection and trap‐assisted recombination losses. [ABSTRACT FROM AUTHOR]