Proton Irradiation Tolerance of High-Efficiency Perovskite Absorbers for Space Applications.

Lead halide perovskite single layers with three grain sizes are subjected to proton-beam irradiation in order to assess the durability and radiation tolerance of perovskite solar cells (PSCs) against space radiation. Proton-beam irradiation is chosen because proton beams significantly affect solar cell performance in the space environment. We evaluate the effects of proton beams by focusing on the grain structure, crystal structure, and carrier lifetime of a perovskite single layer by using scanning electron microscopy, X-ray diffraction, photoluminescence (PL) spectra, and time-resolved PL (TRPL). The results show that proton irradiation does not significantly affect the grain structure and crystal structure of perovskite layer; the TRPL results show that the carrier lifetime inside the grain is constant up to a fluence of 1 × 1014 p+/cm2 and decreases significantly at a fluence of 1 × 1015 p+/cm2. Proton-beam radiation tolerance of the grain inside the perovskite layer is dominant in the radiation tolerance of PSCs.

Lead-free perovskite solar cells using Sb and Bi-based A3B2X9 and A3BX6 crystals with normal and inverse cell structures.

Research of CH3NH3PbI3 perovskite solar cells had significant attention as the candidate of new future energy. Due to the toxicity, however, lead (Pb) free photon harvesting layer should be discovered to replace the present CH3NH3PbI3 perovskite. In place of lead, we have tried antimony (Sb) and bismuth (Bi) with organic and metal monovalent cations (CH3NH3+, Ag+ and Cu+). Therefore, in this work, lead-free photo-absorber layers of (CH3NH3)3Bi2I9, (CH3NH3)3Sb2I9, (CH3NH3)3SbBiI9, Ag3BiI6, Ag3BiI3(SCN)3 and Cu3BiI6 were processed by solution deposition way to be solar cells. About the structure of solar cells, we have compared the normal (n-i-p: TiO2-perovskite-spiro OMeTAD) and inverted (p-i-n: NiO-perovskite-PCBM) structures. The normal (n-i-p)-structured solar cells performed better conversion efficiencies, basically. But, these environmental friendly photon absorber layers showed the uneven surface morphology with a particular grow pattern depend on the substrate (TiO2 or NiO). We have considered that the unevenness of surface morphology can deteriorate the photovoltaic performance and can hinder future prospect of these lead-free photon harvesting layers. However, we found new interesting finding about the progress of devices by the interface of NiO/Sb3+ and TiO2/Cu3BiI6, which should be addressed in the future study.

Enhancement of the hole conducting effect of NiO by a N2 blow drying method in printable perovskite solar cells with low-temperature carbon as the counter electrode.

In this article, we demonstrate for the first time a mesoscopic printable perovskite solar cell (PSC) using NiO as the hole transporting material and low-temperature processed carbon as the counter electrode. A single deposition method assisted by N2 blow drying was used for the deposition of MAPbI3 on a TiO2/ZrO2/NiO screen-printed electrode. As the final step a low-temperature processing (i.e. 75 °C) carbon counter layer was fabricated on MAPbI3 by a blade coating method. It is found that the capping layer thickness of MAPbI3 has a significant effect on the device efficiency, especially when NiO is introduced as a hole transporting material into the structure. Electrochemical impedance spectroscopy demonstrates good charge transport characteristics for the device with a thin MAPbI3 capping layer obtained by the N2 blow drying method. Our best performing device demonstrated a remarkable photovoltaic performance with a short-circuit current density (Jsc) of 22.38 mA cm-2, an open circuit voltage (Voc) of 0.97 V, and a fill factor (FF) of 0.50 corresponding to a photo-conversion efficiency (PCE) of 10.83%. Moreover, the un-encapsulated device exhibited advantageous stability over 1000 h in air in the dark.

100 °C Thermal Stability of Printable Perovskite Solar Cells Using Porous Carbon Counter Electrodes.

Many efforts have been made towards improving perovskite (PVK) solar cell stability, but their thermal stability, particularly at 85 °C (IEC 61646 climate chamber tests), remains a challenge. Outdoors, the installed solar cell temperature can reach up to 85 °C, especially in desert regions, providing sufficient motivation to study the effect of temperature stress at or above this temperature (e.g., 100 °C) to confirm the commercial viability of PVK solar cells for industrial companies. In this work, a three-layer printable HTM-free CH3 NH3 PbI3 PVK solar cell with a mesoporous carbon back contact and UV-curable sealant was fabricated and tested for thermal stability over 1500 h at 100 °C. Interestingly, the position of the UV-curing glue was found to drastically affect the device stability. The side-sealed cells show high PCE stability and represent a large step toward commercialization of next generation organic-inorganic lead halide PVK solar cells.

Light stability tests of CH3NH3PbI3 perovskite solar cells using porous carbon counter electrodes.

The CH3NH3PbI3 perovskite solar cells have been fabricated using three-porous-layered electrodes as, 〈glass/F-doped tin oxide (FTO)/dense TiO2/porous TiO2-perovskite/porous ZrO2-perovskite/porous carbon-perovskite〉 for light stability tests. Without encapsulation in air, the CH3NH3PbI3 perovskite solar cells maintained 80% of photoenergy conversion efficiency from the initial value up to 100 h under light irradiation (AM 1.5, 100 mW cm-2). Considering the color variation of the CH3NH3PbI3 perovskite layer, the significant improvement of light stability is due to the moisture-blocking effect of the porous carbon back electrodes. The strong interaction between carbon and CH3NH3PbI3 perovskite was proposed by the measurements of X-ray photoelectron spectroscopy and X-ray diffraction of the porous carbon-perovskite layers.