Organic photovoltaics (OPV) represent a thin‐film PV technology that offers attractive prospects for low‐cost and aesthetically appealing (colored, flexible, uniform, semitransparent) solar cells that are printable on large surfaces. In bulk heterojunction (BHJ) OPV devices, organic electron donor and acceptor molecules are intimately mixed within the photoactive layer. Since 2005, the power conversion efficiency of said devices has increased substantially due to insights in the underlying physical processes, device optimization, and chemical engineering of a vast number of novel light‐harvesting organic materials, either small molecules or conjugated polymers. As Nature itself has developed porphyrin chromophores for solar light to energy conversion, it seems reasonable to pursue artificial systems based on the same types of molecules. Porphyrins and their analogues have already been successfully implemented in certain device types, notably in dye‐sensitized solar cells, but they have remained largely unexplored in BHJ organic solar cells. Very recent successes do show, however, the strong (latent) prospects of porphyrinoid semiconductors as light‐harvesting and charge transporting materials in such devices. Here, an overview on the state‐of‐the‐art of porphyrin‐based solution‐processed BHJ OPV is provided and insights are given into the pathways to follow and hurdles to overcome toward further improvements of porphyrinic materials and devices.

For almost sixty years, solar energy for space applications has relied on inorganic photovoltaics, evolving from solar cells made of single crystalline silicon to triple junctions based on germanium and III-V alloys. The class of organic-based photovoltaics, which ranges from all-organic to hybrid perovskites, has the potential of becoming a disruptive technology in space applications, thanks to the unique combination of appealing intrinsic properties (e.g. record high specific power, tunable absorption window) and processing possibilities. Here, we report on the launch of the stratospheric mission OSCAR, which demonstrated for the first time organic-based solar cell operation in extraterrestrial conditions. This successful maiden flight for organic-based photovoltaics opens a new paradigm for solar electricity in space, from satellites to orbital and planetary space stations.Nevertheless, already in the fields of aerospace[3] and of organic and hybrid semiconductors [4,5], the specific power (W/kg) was proposed as a valid figure of merit to evaluate PV technologies for space missions. In this regard, Organic Solar Cells (OSCs) and hybrid organic-inorganic Perovskite Solar Cells (PSCs) -termed together as HOPV, Hybrid and Organic PhotoVoltaicsgreatly outperform their inorganic counterparts [4,5]. They represent two novel branches of PV technologies, which saw their rise during the last decade (last few years in the case of PSCs) thanks to their potentially very low production costs. The high absorbance of the photo-active layers in HOPVs allows for efficient light collection within a few hundred nanometers of material, which leads to thicknesses one or two orders of magnitude lower than those of inorganic thin PVs. The rest of the layers making up the solar cell stacks are either as thin as or thinner than the absorbers, and the only thickness (and hence mass) limitation comes from substrate and encapsulation, which can consist of micrometers thick flexible plastic foil [4,5]. The specific power reached to date for perovskite (23 kW/kg) [4] and organic (10 kW/kg)[5] solar cells is thus over 20

Conjugated polyelectrolyte (CPE) interfacial layers present a powerful way to boost the I-V characteristics of organic photovoltaics. Nevertheless, clear guidelines with respect to the structure of high-performance interlayers are still lacking. In this work, impedance spectroscopy is applied to probe the dielectric permittivity of a series of polythiophene-based CPEs. The presence of ionic pendant groups grants the formation of a capacitive double layer, boosting the charge extraction and device efficiency. A counteracting effect is the diminishing affinity with the underlying photoactive layer. To balance these two effects, we found copolymer structures containing nonionic side chains to be beneficial.

In the field of polymer solar cells, improving photovoltaic performance has been the main driver over the past decade. To achieve high power conversion efficiencies, a plethora of new photoactive donor polymers and fullerene derivatives have been developed and blended together in bulk heterojunction active layers. Simultaneously, further optimization of the device architecture is also of major importance. In this respect, we report on the use of specific types of electron transport layers to boost the inherent I–V properties of polymer solar cell devices, resulting in a considerable gain in overall photovoltaic output. Imidazolium‐substituted polythiophenes are introduced as appealing electron transport materials, outperforming the currently available analogous conjugated polyelectrolytes, mainly by an increase in short‐circuit current. The molecular weight of the ionic polythiophenes has been identified as a crucial parameter influencing performance.