Elucidating the origins of high preferential crystal orientation in quasi‐2D perovskite solar cells

Incorporating large organic cations to form 2D and mixed 2D/3D structures significantly increases the stability of perovskite solar cells. However, due to their low electron mobility, aligning the organic sheets to ensure unimpeded charge transport is critical to rival the high performances of pure 3D systems. While additives such as methylammonium chloride (MACl) can enable this preferential orientation, so far, no complete description exists explaining how they influence the nucleation process to grow highly aligned crystals. Here, by investigating the initial stages of the crystallization, as well as partially and fully formed perovskites grown using MACl, the origins underlying this favorable alignment are inferred. This mechanism is studied by employing 3-fluorobenzylammonium in quasi-2D perovskite solar cells. Upon assisting the crystallization with MACl, films with a degree of preferential orientation of 94%, capable of withstanding moisture levels of 97% relative humidity for 10 h without significant changes in the crystal structure are achieved. Finally, by combining macroscopic, microscopic, and spectroscopic studies, the nucleation process leading to highly oriented perovskite films is elucidated. Understanding this mechanism will aid in the rational design of future additives to achieve more defect tolerant and stable perovskite optoelectronics

Different Device Architectures for Bulk-Heterojunction Solar Cells

We report different solar cell designs which allow a simple electrical connection of subsequent devices deposited on the same substrate. By arranging so-called standard and inverted solar-cell architectures next to each other, a serial connection of the two devices can easily be realized by a single compound electrode. In this work, we tested different interfacial layer materials like polyethylenimine (PEI) and PEDOT:PSS, and silver as a non-transparent electrode material. We also built organic light emitting diodes applying the same device designs demonstrating the versatility of applied layer stacks. The proposed design should allow the preparation of organic bulk-heterojunction modules with minimized photovoltaically inactive regions at the interconnection of individual devices

Conducting PolymerBased Biocomposites Using Deoxyribonucleic Acid (DNA) as Counterion

In this work, the preparation of conducting polymerbased composites using a biological anionic polymer based on salmon deoxyribonucleic acid (DNA) is presented. The most commonly used polymers poly(3,4ethylenedioxythiophene) (PEDOT), as well as polypyrrole, are polymerized in the presence of DNA. Since conjugated polymers are in the polycationic state in their electrically conducting form, the role of the counterion is now fulfilled by the low cost biomolecule DNA as an alternative material, which is also a polyanion thanks to its phosphate chain. The resulting synthesized material is a conducting polymerDNA biocomposite. Such materials are highly attractive for the rising field of bioelectronics and biosensors, especially in organic electrochemical transistors (OECTs) and ion pumps. OECTs made of these conducting polymer biocomposites are fabricated and their electrochemical device operation is compared to the most widely used PEDOT:polystyrenesulfonate.(VLID)4844471Version of recor

Optoelectronic Properties of Layered Perovskite Solar Cells

Herein, the optoelectronic properties of interface-engineered perovskite 2D|3D-heterojunction structure solar cells are reported. The reciprocity theorem is applied to determine the maximum open-circuit voltage (V-oc) the device can deliver under solar illumination. A V-oc of 1.295 V is found, analyzing the measured external quantum efficiency and assuming only radiative recombination. For comparison, the experimental open-circuit voltage found for the studied 2D|3D heterojunctions is 1.15 V. The contribution of nonradiative recombination is explored by measuring the electroluminescence quantum yield. A quantum yield of 0.4% is found at current densities equivalent to 1 sun illumination. This translates into a V-oc loss of approximate to 140 mV, which is in very good agreement with the experimental findings. In addition, the fundamental correlation between luminescence intensity and the chemical potential predicted by the generalized Planck law is confirmed for the photoluminescence measured at different light intensities when the device is operated under open-circuit conditions and for the electroluminescence when operated under a forward bias. The investigations in this study suggest that further efficiency improvements can be achieved by reducing the nonradiative recombination in the studied solar cell. At the same time, a high-performance near IR light emitting diode can be realized.GM

Optoelectronic Properties of Layered Perovskite Solar Cells

Herein, the optoelectronic properties of interfaceengineered perovskite 2D|3Dheterojunction structure solar cells are reported. The reciprocity theorem is applied to determine the maximum opencircuit voltage (Voc) the device can deliver under solar illumination. A Voc of 1.295V is found, analyzing the measured external quantum efficiency and assuming only radiative recombination. For comparison, the experimental opencircuit voltage found for the studied 2D|3D heterojunctions is 1.15V. The contribution of nonradiative recombination is explored by measuring the electroluminescence quantum yield. A quantum yield of 0.4% is found at current densities equivalent to 1sun illumination. This translates into a Voc loss of 140mV, which is in very good agreement with the experimental findings. In addition, the fundamental correlation between luminescence intensity and the chemical potential predicted by the generalized Planck law is confirmed for the photoluminescence measured at different light intensities when the device is operated under opencircuit conditions and for the electroluminescence when operated under a forward bias. The investigations in this study suggest that further efficiency improvements can be achieved by reducing the nonradiative recombination in the studied solar cell. At the same time, a highperformance near IR light emitting diode can be realized.(VLID)4843823Version of recor

Tunable Properties of Nature-Inspired N,N′-Alkylated Riboflavin Semiconductors

A series of novel soluble nature-inspired flavin derivatives substituted with short butyl and bulky ethyl-adamantyl alkyl groups was prepared via simple and straightforward synthetic approach with moderate to good yields. The comprehensive characterization of the materials, to assess their application potential, has demonstrated that the modification of the conjugated flavin core enables delicate tuning of the absorption and emission properties, optical bandgap, frontier molecular orbital energies, melting points, and thermal stability. Moreover, the thin films prepared thereof exhibit smooth and homogeneous morphology with generally high stability over time

Interface passivation using diketopyrrolopyrrole‐oligothiophene copolymer to improve the performance of perovskite solar cells

Abstract The unprecedented increase in power conversion efficiency (PCE) of low‐cost organo‐inorganic halide perovskite solar cells (OIHPSCs) toward its Shockley‐Queisser limit intriguingly has prompted researchers to investigate the disadvantages of these devices. The issue of operational stability is the main hurdle challenging the way forward for commercialization. To address this, various engineering processes like composition, additives, anti‐solvents, bulk and interface passivation, and deposition techniques have been widely applied to manage both extrinsic and intrinsic factors that induce degradation of the OIHPSCs. In this work, we employed interface passivation, which is an efficient approach to reduce nonradiative recombination. An ultrathin layer of electron donor diketopyrrolopyrrole‐oligothiophene copolymer (DPP860) was applied as an interface passivator between the photoactive layer and [6,6]‐phenyl C61 butyric acid methyl ester (PCBM). The role of the interface passivation on optoelectronic properties of the OIHPSCs was assessed using current density versus voltage (J‐V) characteristics, photoluminescence spectroscopy and time‐resolved photoluminescence spectroscopy. The findings show devices treated with DPP860 exhibit enhanced current density (Jsc) and fill factor, attributing for suppressed nonradiative recombination. Moreover, it shows relative improvement in the stability of the device. The results of this finding reveal that using oligothiophene copolymer can enhance the photovoltaic performance and the stability of inverted OIHPSCs in the ambient environment

In Vitro Cytotoxicity of D18 and Y6 as Potential Organic Photovoltaic Materials for Retinal Prostheses

Millions of people worldwide are diagnosed with retinal dystrophies such as retinitis pigmentosa and age-related macular degeneration. A retinal prosthesis using organic photovoltaic (OPV) semiconductors is a promising therapeutic device to restore vision to patients at the late onset of the disease. However, an appropriate cytotoxicity approach has to be employed on the OPV materials before using them as retinal implants. In this study, we followed ISO standards to assess the cytotoxicity of D18, Y6, PFN-Br and PDIN individually, and as mixtures of D18/Y6, D18/Y6/PFN-Br and D18/Y6/PDIN. These materials were proven for their high performance as organic solar cells. Human RPE cells were put in direct and indirect contact with these materials to analyze their cytotoxicity by the MTT assay, apoptosis by flow cytometry, and measurements of cell morphology and proliferation by immunofluorescence. We also assessed electrophysiological recordings on mouse retinal explants via microelectrode arrays (MEAs) coated with D18/Y6. In contrast to PFN-Br and PDIN, all in vitro experiments show no cytotoxicity of D18 and Y6 alone or as a D18/Y6 mixture. We conclude that D18/Y6 is safe to be subsequently investigated as a retinal prosthesis

Lanthanide (Eu, Tb, La)-Doped ZnO Nanoparticles Synthesized Using Whey as an Eco-Friendly Chelating Agent

Strategies for production and use of nanomaterials have rapidly moved towards safety and sustainability. Beyond these requirements, the novel routes must prove to be able to preserve and even improve the performance of the resulting nanomaterials. Increasing demand of high-performance nanomaterials is mostly related to electronic components, solar energy harvesting devices, pharmaceutical industries, biosensors, and photocatalysis. Among nanomaterials, Zinc oxide (ZnO) is of special interest, mainly due to its environmental compatibility and vast myriad of possibilities related to the tuning and the enhancement of ZnO properties. Doping plays a crucial role in this scenario. In this work we report and discuss the properties of undoped ZnO as well as lanthanide (Eu, Tb, and La)-doped ZnO nanoparticles obtained by using whey, a by-product of milk processing, as a chelating agent, without using citrate nor any other chelators. The route showed to be very effective and feasible for the affordable large-scale production of both pristine and doped ZnO nanoparticles in powder form