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.
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http://dx.doi.org/10.1021/acsami.8b07346 | DOI Listing |
Sci Rep
January 2025
Facultad de Química, Materiales-Energía, Universidad Autónoma de Querétaro, Santiago de Querétaro, C.P.76010, Querétaro, México.
ABSchalcogenide perovskites (CPs) are emerging as promising alternatives to lead halide perovskites due to their unique properties. However, their bandgap exceeds the Shockley-Queisser limit. By substituting S with Se, the bandgap is significantly reduced, shifting it from the visible into the near-infrared region.
View Article and Find Full Text PDFOrg Lett
January 2025
State Key Laboratory for Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials, Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, Fujian 361005, People's Republic of China.
KOBu-promoted [3 + 2] cycloaddition of dimethyl sulfoxide (DMSO) with fullerenes has been developed for facile and efficient one-pot synthesis of 1,2,3,4-cyclic sulfoxide-fused [60]/[70]fullerene dihydrides, which offers a versatile platform for the site-selective preparation of various fullerene multiadducts with a wide range of functional groups. The utility of these tetra-functionalized fullerenes is demonstrated by the successful application as electron-transport materials in perovskite solar cells.
View Article and Find Full Text PDFEES Solar
January 2025
Department of Chemical Engineering and Biotechnology, University of Cambridge Cambridge CB3 0AS UK.
Thermal co-evaporation of halide perovskites is a solution-free, conformal, scalable, and controllable deposition technique with great potential for commercial applications, particularly in multi-junction solar cells. Monolithic triple-junction perovskite solar cells have garnered significant attention because they can achieve very high efficiencies. Nevertheless, challenges arise in fabricating these devices, as they require multiple layers and precise current matching across complex absorber stacks.
View Article and Find Full Text PDFRSC Adv
January 2025
Department of Electrical Engineering, Sarhad University of Information Technology Peshawar 25000 Pakistan.
The growing demand for efficient, stable, and environmentally friendly photovoltaic technologies has motivated the exploration of nontoxic perovskite materials such as KGeCl. However, the performance of KGeCl-based perovskite solar cells (PSCs) depends heavily on the compatibility of charge transport layers (CTLs) and optimization of device parameters. In this study, six PSC configurations were simulated using SCAPS-1D software, incorporating CTLs such as Alq, CSTO, VO, PB, and SbS.
View Article and Find Full Text PDFAdv Mater
January 2025
College of Chemistry, Nanchang University, Nanchang, 330031, China.
A strong n-type perovskite layer is crucial in achieving high open-circuit voltage (V) and power conversion efficiency (PCE) in the p-i-n solar cells, as the weak n-type perovskites result in a loss of V, and the p-type perovskites contain numerous electron traps that cause the severe carrier recombination. Here, three types of perylene diimide (PDI) based small molecule dopants with different dimensions, including 1D-PDI, 2D-PDI, and 3D-PDI are designed, to produce heavier n-type perovskites. The PDI-based molecules with Selenium atoms have a strong electron-donating ability, effectively enlarging the quasi-Fermi level splitting within the perovskites.
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