Rapid progress achieved on perovskite solar cells raises the expectation for their further development toward practical applications. Moisture sensitivity of perovskite materials is one of the major obstacles which limits the long-term durability of the perovskite solar cells, especially in outdoor operation where rainfall and water accumulation on the solar panels often occur. Micro/nanopinholes within the functional layers of the devices usually lead to water vapor penetration, thus subsequent decomposition of perovskites, and finally poor device performance and shortened operational lifetime. In this work, low-temperature atomic layer deposition (ALD) technique was utilized to incorporate pinhole-free metal oxide layers (TiO and AlO) into an inverted perovskite solar cell consisting of indium tin oxide/NiO/perovskite/PCBM/TiO/Ag. The interface properties between the inserted TiO layer and the perovskite layer were investigated by X-ray photoelectron spectroscopy. The results showed that TiO ALD fabrication process had made negligible degradation to the perovskite layer. The TiO layer can significantly reduce interfacial charge recombination loss, improve interfacial contact, and enhance water resistance. A maximum power conversion efficiency (PCE) of 18.3% was achieved for devices with TiO interface layers. A stacked AlO encapsulation layer was designed and deposited on top of the devices to further improve device stability under harsh environmental conditions. The encapsulated devices with the best performance retained 97% of the initial PCE after being stored in ambient condition for a thousand hours. They also showed great water resistance, and no significant degradation in terms of PCE and photocurrent of the devices was observed after they were immersed in deionized water for as long as 2 h. Our approach offers a promising way of developing highly efficient and stable perovskite solar cells under real-world operational conditions.
Solar cells based on organometal hybrid perovskites have exhibited promising commercialization potential owing to their high efficiency and low-cost manufacturing. However, the poor outdoor operational stability of perovskite solar cells restricted their practical application, and moisture permeation and organic compounds volatilization are realized as the main factors accelerating performance degradation. Herein, we developed a composite encapsulation, by sequentially depositing a compact Al 2 O 3 layer and a hydrophobic 1H,1H,2H,2H-perfluorodecyltrichlorosilane layer on the completed device, to efficiently circumvent vapor permeability. Thus, the stability of the encapsulated perovskite solar cells was systematically investigated under simulated operational conditions. It was found that the MAPbI 3 perovskite was prone to decay into solid PbI 2 and organic vapor at high temperature or upon light illumination, and the decomposition was reversible in a well-encapsulated environment, resulting in reversible performance degradation and recovery. The enhanced thermal stability was ascribed to the competition between the perovskite decomposition and reverse synthesis. The as-prepared high-quality, multilayered encapsulation scheme demonstrated superior sealing property, and no obvious performance decline was observed when the device was stored under ambient air, continuous light illumination, double 85 condition (85 °C, 85% humidity), or even water immersion. Therefore, this work paves the way for a scalable and robust encapsulation strategy feasible to hybrid perovskite optoelectronics in a reproducible manner.
Background: Pyrrolizidine alkaloids (PAs) are probably the most common plant constituents that poison livestock, wildlife, and humans worldwide. Riddelliine is isolated from plants grown in the western United States and is a prototype of genotoxic PAs. Riddelliine was used to investigate the genotoxic effects of PAs via analysis of gene expression in the target tissue of rats in this study. Previously we observed that the mutant frequency in the liver of rats gavaged with riddelliine was 3-fold higher than that in the control group. Molecular analysis of the mutants indicated that there was a statistically significant difference between the mutational spectra from riddelliine-treated and control rats.
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