With the aim of fully utilizing the low processing temperatures of perovskite solar cells, significant progress in replacing high temperature processed TiO₂ by various low-temperature solution processed electron transporting layers (LT-ETLs) was recently reported. Here, recent progress in the development of LT-ETLs for regular planar structure perovskite solar cells, which is essential for achieving high efficiency in parallel to avoiding hysteresis, is reviewed. In addition, the application of a novel hysteresis-free LT-ETLs for regular planar perovskite solar cells in our laboratory is briefly discussed. By incorporating a low temperature processed WO_x nanoparticular layer in combination with a mixed fullerene functionalized self-assembled monolayers (SAMs), a regular, planar structure, and hysteresis-free perovskite solar cell with a maximum efficiency of almost 15% can be fabricated.

Semitransparent organic photovoltaic (OPV) cells promise applications in various transparent architectures where their opaque counterparts cannot contribute. Realizing practical applications of this technology requires the manufacturing of large-area modules without significant performance loss compared to the lab-scale devices. In this work, efficient semitransparent OPV modules based on ultrafast laser patterning on both glass and flexible substrates are reported. Solution-processed metallic silver nanowires (AgNWs) are used as transparent top electrodes. The efficient low-ohmic contact of the interconnects between the top AgNWs and the bottom electrode in combination with high-precision laser beam positioning system allow to fabricate semitransparent modules with high electrical fill factor of ≈63% and a remarkable geometric fill factor exceeding 95%, respectively. These results represent an important progress toward upscaling of high-performance OPV modules with reduced production costs.

Length of the terminal alkyl chains at dicyanovinyl (DCV) groups of two dithienosilole (DTS) containing small molecules (DTS(Oct)₂-(2T-DCV-Me)₂ and DTS(Oct)₂-(2T-DCV-Hex)₂ ) is investigated to evaluate how this affects the molecular solubility and blend morphology as well as their performance in bulk heterojunction organic solar cells (OSCs). While the DTS(Oct)₂-(2T-DCV-Me)₂ (a solubility of 5 mg mL⁻¹) system exhibits both high short circuit current density (J _sc) and high fill factor, the DTS(Oct)₂-(2T-DCV-Hex)₂ (a solubility of 24 mg mL⁻¹) system in contrast suffers from a poor blend morphology as examined by atomic force morphology and grazing incidence X-ray scattering measurements, which limit the photovoltaic properties. The charge generation, transport, and recombination dynamics associated with the limited device performance are investigated for both systems. Nongeminate recombination losses in DTS(Oct)₂-(2T-DCV-Hex)₂ system are demonstrated to be significant by combining space charge limited current analysis and light intensity dependence of current–voltage characteristics in combination with photogenerated charge carrier extraction by linearly increasing voltage and transient photovoltage measurements. DTS(Oct)₂-(2T-DCV-Me)₂ in contrast performs nearly ideal with no evidence of nongeminate recombination, space charge effects, or mobility limitation. These results demonstrate the importance of alkyl chain engineering for solution-processed OSCs based on small molecules as an essential design tool to overcome transport limitations.

A systematic study on the effect of various cathode buffer layers on the performance and stability of solution-processed small-molecule organic solar cells (SMOSCs) based on tris{4-[5-(1,1-dicyanobut-1-en-2-yl)-2,2-bithiophen-5-yl]phenyl}amine (N(Ph-2T-DCN-Et)₃):6,6-phenyl-C71-butyric acid methyl ester (N(Ph-2T-DCN-Et)₃:PC₇₀BM) is presented. The power conversion efficiency (PCE) in these systems can be significantly improved from approximately 4% to 5.16% by inserting a metal oxide (ZnO) layer between the active layer and the Al cathode instead of an air-sensitive Ba or Ca layer. However, the low work-function Al cathode is susceptible to chemical oxidation in the atmosphere. Here, an amine group functionalized fullerene complex (DMAPA-C₆₀) is inserted as a cathode buffer layer to successfully modify the interface towards ZnO/Ag and active layer/Ag functionality. For devices with ZnO/DMAPA-C₆₀/Ag and DMAPA-C₆₀/Ag cathodes the PCEs are improved from 2.75% to 4.31% and to 5.40%, respectively, compared to a ZnO/Ag device. Recombination mechanisms and stability aspects of devices with various cathodes are also investigated. The significant improvement in device performance and stability and the simplicity of fabrication by solution processing suggest this DMAPA-C₆₀-based interface as a promising and practical pathway for developing efficient, stable, and roll-to-roll processable SMOSCs.

Replacing halogenated solvents in the processing of organic solar cells by green solvents is a required step before the commercialization of this technology. With this purpose, some attempts have been made, although a general method is yet to be developed. Here, the potential of the Hansen solubility parameters (HSP) analysis for the design of green ink formulations for solution-processed active layer in bulk heterojunction photovoltaic devices based on small molecules is demonstrated. The motivation of moving towards organic small molecules stems from their lower molecular weight and more definite structure which makes them more likely to be dissolved in a wider variety of organic solvents. In the first step, the HSP of selected active materials are determined, namely, the star-shaped D-π-A tris{4-[5′′-(1,1-dicyanobut-1-en-2-yl)-2,2′-bithiophen-5-yl]phenyl}amine N(Ph-2T-DCN-Et)₃ small molecule and fullerene derivative [6,6]-phenyl-C₇₁-butyric acid methyl ester (PC₇₀BM). Secondly, computer simulations based on HSP allow the prediction of suitable green solvents for this specific material system. The most promising green solvents, according to the simulations, are then used to fabricate solar cell devices using pristine solvents and two solvents mixtures. These devices show power conversion efficiencies around 3.6%, which are comparable to those obtained with halogenated solvents. This good performance is a result of the sufficient solubility achieved after a successful prediction of good (green) solvents.

Organic photovoltaic (OPV) solar cells that can be simply processed from solution are in the focus of the academic and industrial community because of their enormous potential to reduce cost. One big challenge in developing a fully solution-processed OPV technology is the design of a well-performing electrode system, allowing the replacement of ITO. Several solution-processed electrode systems were already discussed, but none of them could match the performance of ITO. Here, we report efficient ITO-free and fully solution-processed semitransparent inverted organic solar cells based on silver nanowire (AgNW) electrodes. To demonstrate the potential of these AgNW electrodes, they were employed as both the bottom and top electrodes. Record devices achieved fill factors as high as 63.0%, which is comparable to ITO based reference devices. These results provide important progress for fully printed organic solar cells and indicate that ITO-free, transparent as well as non-transparent organic solar cells can indeed be fully solution-processed without losses.

Bulk heterojunction based polymer:fullerene solar cells have attracted intensive research interest both in academic and industrial communities in the last two decades, mainly related to their potential low-cost production process. A power conversion efficiency of over 10% has been reported recently, making the commercialization of this clean and cheap solar energy convertor a realistic prospect for the near future. The intrinsic features of semitransparency and color tunability of the thin polymeric photoactive films are the greatest asset for polymer solar cells. Recently, aesthetic semitransparent polymer solar cells (ST-PSCs) that can be integrated into transparent windows, roofs, glass and other semitransparent architectural elements have received much attention. In this perspective paper, we present the progress in achieving high performance ST-PSCs, discuss the requirements for transparent electrodes, focusing on alternatives to tin-doped indium oxide, and address the challenges ahead to make ST-PSC viable for real applications. © 2013 Society of Chemical Industry

Solution processed silver nanowire (Ag NW) films are introduced as transparent electrodes for thin-film solar cells. Ag NW electrodes were processed by doctor blade-coating on glass substrates at moderate temperatures (less than 100 °C). The morphological, optical, and electrical characteristics of these electrodes were investigated as a function of processing parameters. For solar-cell application, Ag NW electrodes with an average transparency of 90% between 450 and 800 nm and a sheet resistivity of ≈10 Ω per square were chosen. The performance of poly(3-hexylthiophen-2,5-diyl):[6,6]-phenyl-C61-butyric acid methyl ester (P3HT:PCBM) solar cells on Ag NW electrodes was found to match the performance of otherwise identical cells on indium tin oxide. Overall, P3HT:PCBM solar cells with an efficiency of 2.5% on transparent Ag NW electrodes have been realized.

Solution-processed bulk heterojunction organic photovoltaic (OPV) devices have gained serious attention during the last few years and are established as one of the leading next generation photovoltaic technologies for low cost power production. This article reviews the OPV development highlights of the last two decades, and summarizes the key milestones that have brought the technology to today’s efficiency performance of over 7%. An outlook is presented on what will be required to drive this young photovoltaic technology towards the next major milestone, a 10% power conversion efficiency, considered by many to represent the efficiency at which OPV can be adopted in wide-spread applications. With first products already entering the market, sufficient lifetime for the intended application becomes more and more critical, and the status of OPV stability as well as the current understanding of degradation mechanisms will be reviewed in the second part of this article.