The outdoor performance monitoring of perovskite modules over 16 weeks is reported. Two different types of active perovskite layers were studied: one type contained formamidinium chloride (FACl) halide additives and the other contained no additives with the main purpose to investigate performance trends during the outdoor exposure of those type of devices. Long-term side-by-side outdoor testing of devices with and without halide additives was not implemented in the past and merits investigation in order to determine the impact of additives on perovskite performance and stability. Although the two types of modules displayed similar initial outdoor performance characteristics, their outdoor performance evolution differed. Different degradation rates between the modules with and without additives were obtained just after field installation. In particular, the modules with additives exhibited higher performance degradation under open-circuit loading conditions between current-voltage (IV) scans. Long-term monitoring of both modules recorded a reduction of the efficiency over the course of the day with subsequent recovery overnight and in many cases during the day. The relative values of performance degradation and overnight recovery were calculated over the timespan of outdoor testing and indicated dominant normalized diurnal performance degradation in one type of modules (without FACl additives) in the range between 15–20% and in the other type of modules (with additives) 5–10%. The dominant normalized performance recovery values found were 25–30% and 5–10%, respectively. Finally, dark lock-in thermography (DLIT) and Raman studies were performed on the exposed devices and revealed differences in hotspot evolution and vibrational modes between the different types of module.
Electron and hole transporting layers play a major role in high-performance and stable organic-based optoelectronic devices. This paper demonstrates detailed device engineering of multi-junction organic photovoltaics built on two different metal oxide-based electron and hole transport (buffer) layers prepared by thermal or solution-processed methods. The main focus is on the device processing parameters as well as practical details of preparation of buffer layers to give the research community a clear, step-by-step recipe to successfully replicate and build series and parallel connected multi-junction solution-based organic solar cells for their needs. Here, the recipes and deposition conditions of two metal oxide buffer layers are presented in detail, based on basic commercially available materials and tools, to achieve well-engineered tandem (multi-junction) solution-processed organic solar cells. The buffer layers have appropriate energy levels for electrical selectivity of anode and cathode electrodes, and they are highly stable and chemically compatible with processing of solution-based polymer solar cells. To demonstrate the engineering steps of multi-junction devices, the PCE10:PC70BM blend is used as the active layer for all subcells. Then, to improve the power conversion efficiency of the single-junction photovoltaic device, PCE10:PC70BM blend is used in combination with DPPx:PC70BM with different absorption spectra for bottom and top subcell active layers. An optimized series tandem device with 10.6% power conversion efficiency is demonstrated. Generally, the device structures reported here can also be used for other types of optoelectronic devices, such as light emitting diodes and photodetectors.