No abstract

The main drawback of the methylammonium lead halide perovskite solar cells is their degradation in ambient atmosphere. To investigate ambient-air-induced cell degradation, spectral dependencies of open-circuit voltage (VOC), fill factor (FF) and the power conversion efficiency (PCE) have been acquired (for the first time reported in literature).Our custom-made measurement system allowed us to perform measurements of the abovementioned entities in situ directly in vacuum during and after thermal deposition of the electrode. We also studied how these parameters in vacuum changed after cell exposure to ambient air for 85 min (50 nm top electrode) and for 180 min (100 nm top Ag electrode). For fresh CH3NH3PbI3–xClx cell (never been in open air) with very high shunt resistance of 3·107 Ω·cm2 (with practically no shorts and therefore FF could be determined mainly by charge carrier recombination processes) we found that FF in vacuum increased along with an increase of the incident photon energy from 0.55 at 760 nm up to 0.82 at 400 nm. Hypothesis considering hot polaron participation in charge carrier photogeneration and recombination processes as well as another competing hypothesis were offered as possible explanations for the observed FF increase.The kinetics of short-circuit photocurrent EQE with a change in pressure was also investigated. It was also shown that perovskite solar cell degradation could be noticeably reduced by increasing the top Ag electrode thickness to at least 100 nm, which could possibly facilitate the usual encapsulation process.

Development of hybrid organic-inorganic perovskite solar cells (PSC) has been one of the hottest research topics since 2013. Within brief literature review, we would like to achieve two objectives. Firstly, we would like to indicate that a whole set of physical properties, such as high change carrier mobility, very low recombination rates, large carrier life time and diffusion length, large absorption coefficients and very weak exciton binding energies, are defining high power conversion efficiency (PCE) of methyl ammonium lead trihalide SC. The second objective is to draw attention to some, in our opinion, important aspects that previously have not been satisfactory addressed in literature. Although degradation of PSC is widely discussed, processes at very first exposure to ambient conditions after deposition of top electrode are uncovered.

Organometal halide perovskites are promising materials for lowcost, high-efficiency solar cells. The method of perovskite layer deposition and the interfacial layers play an important role in determining the efficiency of perovskite solar cells (PSCs). In the paper, we demonstrate inverted planar perovskite solar cells where perovskite layers are deposited by two-step modified interdiffusion and one-step methods. We also demonstrate how PSC parameters change by doping of charge transport layers (CTL). We used dimethylsupoxide (DMSO) as dopant for the hole transport layer (PEDOT:PSS) but for the electron transport layer [6,6]-phenyl C 61 butyric acid methyl ester (PCBM)) we used N,N-dimethyl-N-octadecyl(3-aminopropyl)trimethoxysilyl chloride (DMOAP).The highest main PSC parameters (PCE, EQE, V OC ) were obtained for cells prepared by the one-step method with fast crystallization and doped CTLs but higher fill factor (FF) and shunt resistance (R sh ) values were obtained for cells prepared by the two-step method with undoped CTLs.