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      Amorphous F‐doped TiO x Caulked SnO 2 Electron Transport Layer for Flexible Perovskite Solar Cells with Efficiency Exceeding 22.5%

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          Abstract

          Flexible perovskite solar cells (f‐PSCs) show great promise in portable‐power applications (e.g., chargers, drones) and low‐cost, scalable productions (e.g., roll‐to‐roll). However, in conventional n–i–p architecture f‐PSCs, the low‐temperature processed metal oxide electron transport layers (ETLs) usually suffer from high resistance and severe defects that limit the power conversion efficiency (PCE) improvement of f‐PSCs. Besides the enhancement in the mobility of metal oxide and passivation for perovskite/ETL interfacial defects reported in previous literature, herein, the electron transport loss between the metal oxide nanocrystallines within the ETL is studied by introducing an amorphous F‐doped TiO x (F‐TiO x) caulked crystalline SnO 2 composite ETL. The F‐TiO x in this novel composite ETL acts as an interstitial medium between adjacent SnO 2 nanocrystallines, which can provide more electron transport channels, effectively passivate oxygen vacancies, and optimize the energy level arrangement, thus significantly enhancing the electron mobility of ETL and reducing the charge transport losses. The composite ETL‐based f‐PSCs achieve a high PCE of 22.70% and good operational stability. Furthermore, a moderate roughness of the composite ETL endows f‐PSCs with superior mechanical reliability by virtue of a strong coupling at the ETL/perovskite interface, by which the f‐PSCs can maintain 82.11% of their initial PCE after 4000 bending cycles.

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          Electron-hole diffusion lengths exceeding 1 micrometer in an organometal trihalide perovskite absorber.

          Organic-inorganic perovskites have shown promise as high-performance absorbers in solar cells, first as a coating on a mesoporous metal oxide scaffold and more recently as a solid layer in planar heterojunction architectures. Here, we report transient absorption and photoluminescence-quenching measurements to determine the electron-hole diffusion lengths, diffusion constants, and lifetimes in mixed halide (CH3NH3PbI(3-x)Cl(x)) and triiodide (CH3NH3PbI3) perovskite absorbers. We found that the diffusion lengths are greater than 1 micrometer in the mixed halide perovskite, which is an order of magnitude greater than the absorption depth. In contrast, the triiodide absorber has electron-hole diffusion lengths of ~100 nanometers. These results justify the high efficiency of planar heterojunction perovskite solar cells and identify a critical parameter to optimize for future perovskite absorber development.
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            Solvent engineering for high-performance inorganic-organic hybrid perovskite solar cells.

            Organolead trihalide perovskite materials have been successfully used as light absorbers in efficient photovoltaic cells. Two different cell structures, based on mesoscopic metal oxides and planar heterojunctions have already demonstrated very impressive advances in performance. Here, we report a bilayer architecture comprising the key features of mesoscopic and planar structures obtained by a fully solution-based process. We used CH3NH3 Pb(I(1-x)Br(x))3 (x = 0.1-0.15) as the absorbing layer and poly(triarylamine) as a hole-transporting material. The use of a mixed solvent of γ-butyrolactone and dimethylsulphoxide (DMSO) followed by toluene drop-casting leads to extremely uniform and dense perovskite layers via a CH3NH3I-PbI2-DMSO intermediate phase, and enables the fabrication of remarkably improved solar cells with a certified power-conversion efficiency of 16.2% and no hysteresis. These results provide important progress towards the understanding of the role of solution-processing in the realization of low-cost and highly efficient perovskite solar cells.
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              Perovskite solar cells with atomically coherent interlayers on SnO2 electrodes

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                Author and article information

                Contributors
                Journal
                Advanced Functional Materials
                Adv Funct Materials
                Wiley
                1616-301X
                1616-3028
                March 2023
                January 03 2023
                March 2023
                : 33
                : 11
                Affiliations
                [1 ] Key Laboratory of Materials Modification by Laser, Ion, and Electron Beams (Ministry of Education) School of Physics Dalian University of Technology Dalian 116024 China
                [2 ] State Key Laboratory of Fine Chemicals School of Chemistry Dalian University of Technology Dalian 116024 China
                [3 ] Hangzhou Zhongneng Optoelectronics Technology Co., Ltd. Hangzhou 310018 China
                [4 ] Physics department The Hong Kong University of Science and Technology Hong Kong 999077 China
                [5 ] Key Laboratory for Precision and Non‐traditional Machining Technology of Ministry of Education Dalian University of Technology Dalian 116024 China
                [6 ] School of Engineering Brown University Providence Rhode Island 02912 USA
                Article
                10.1002/adfm.202213961
                82f0eb08-1b19-4c10-bed8-1f59c8a6b178
                © 2023

                http://onlinelibrary.wiley.com/termsAndConditions#vor

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