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Improving the long-term stability of perovskite solar cells is critical to the deployment of this technology. Despite the great emphasis laid on stability-related investigations, publications lack consistency in experimental procedures and parameters reported. It is therefore challenging to reproduce and compare results and thereby develop a deep understanding of degradation mechanisms. Here, we report a consensus between researchers in the field on procedures for testing perovskite solar cell stability, which are based on the International Summit on Organic Photovoltaic Stability (ISOS) protocols. We propose additional procedures to account for properties specific to PSCs such as ion redistribution under electric fields, reversible degradation and to distinguish ambient-induced degradation from other stress factors. These protocols are not intended as a replacement of the existing qualification standards, but rather they aim to unify the stability assessment and to understand failure modes. Finally, we identify key procedural information which we suggest reporting in publications to improve reproducibility and enable large data set analysis.

Tandem architectures are one of the most promising concepts towards superior power conversion efficiencies of organic solar cells. An accurate determination of the power conversion efficiency requires correction of the spectral mismatch and thus relies on accurate external quantum efficiency (EQE) spectra. Due to the series connection of 2 subcells in the tandem architecture, the EQE of the tandem solar cell reproduces the EQE of one subcell if an appropriate bias light is chosen to selectively illuminate and hence forward bias the other subcell. The resulting internal voltage drop is then compensated by applying an external voltage to the tandem solar cell. In this work, we use impedance spectroscopy to accurately predict the minimum bias light intensity and the external voltage to enable accurate EQE measurements on both subcells. We exemplify this procedure on organic tandem solar cells comprising spectrally complementary absorbers and suggest an extended protocol for future measurements of the EQE.

The photoactive layers of the most efficient organic solar cells comprise blends of at least two organic semiconductors (a donor and an acceptor) to form a bulk-heterojunction. For high-performance, the bulk-heterojunction film must have the donors and acceptors distributed at a distance of no more than the exciton diffusion length to yield efficient exciton splitting. In addition, the donor and acceptor domains must provide percolation pathways for efficient charge carrier transport to the electrodes. Today, state-of-the-art solution processing methods use environmentally, Novel additives have been used to the stabilization of P3HT:ICBA nanoparticle dispersions. Said additives were not reducing the efficiency of organic solar cells built from the stabilized dispersions.

Tandem architectures are one of the most promising concepts towards superior power conversion efficiencies of organic solar cells. An accurate determination of the power conversion efficiency requires correction of the spectral mismatch and thus relies on accurate external quantum efficiency (EQE) spectra. Due to the series connection of 2 subcells in the tandem architecture, the EQE of the tandem solar cell reproduces the EQE of one subcell if an appropriate bias light is chosen to selectively illuminate and hence forward bias the other subcell. The resulting internal voltage drop is then compensated by applying an external voltage to the tandem solar cell. In this work, we use impedance spectroscopy to accurately predict the minimum bias light intensity and the external voltage to enable accurate EQE measurements on both subcells. We exemplify this procedure on organic tandem solar cells comprising spectrally complementary absorbers and suggest an extended protocol for future measurements of the EQE.

The rapidly increasing power conversion efficiencies of organic solar cells are an important prerequisite towards low cost photovoltaic fabricated in high throughput. In this work we suggest indane as non-halogenated replacement for the commonly used halogenated solvent o-dichlorobenzene. Indane was blended with the higher volatile solvents chloroform or toluene or o-xylene in order to improve wettability and to reduce drying time. The combination of high volatile solvents with the less volatile host solvent indane allows for an increased fabrication speed due to a reduction of the overall drying time and provides films with good light absorption behavior and high polymer crystallinity. For the solvent mixture toluene-indane, solar cell performance is comparable to the o-dichlorobenzene reference device indicating this mixture as a suitable replacement for increased productivity without drawbacks in nanomorphology as investigated by atomic force microscopy (AFM) and grazing incidence X-ray diffraction (GIXD). This study provides a fundamental understanding on solvent mixture drying kinetics and can aid the ink formulation.