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      Efficient and Stable Inverted Perovskite Solar Modules Enabled by Solid–Liquid Two-Step Film Formation

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          Highlights

          • High-quality large-area perovskite films are prepared using a solid–liquid two-step film formation method combined with CsBr modification for the buried interface and Urea additive for perovskite crystallization.

          • The inverted perovskite solar modules’ performance is enhanced to 20.56% in 61.56 cm 2 with improved stability.

          Supplementary Information

          The online version contains supplementary material available at 10.1007/s40820-024-01408-2.

          Abstract

          A considerable efficiency gap exists between large-area perovskite solar modules and small-area perovskite solar cells. The control of forming uniform and large-area film and perovskite crystallization is still the main obstacle restricting the efficiency of PSMs. In this work, we adopted a solid–liquid two-step film formation technique, which involved the evaporation of a lead iodide film and blade coating of an organic ammonium halide solution to prepare perovskite films. This method possesses the advantages of integrating vapor deposition and solution methods, which could apply to substrates with different roughness and avoid using toxic solvents to achieve a more uniform, large-area perovskite film. Furthermore, modification of the NiO x/perovskite buried interface and introduction of Urea additives were utilized to reduce interface recombination and regulate perovskite crystallization. As a result, a large-area perovskite film possessing larger grains, fewer pinholes, and reduced defects could be achieved. The inverted PSM with an active area of 61.56 cm 2 (10 × 10 cm 2 substrate) achieved a champion power conversion efficiency of 20.56% and significantly improved stability. This method suggests an innovative approach to resolving the uniformity issue associated with large-area film fabrication.

          Supplementary Information

          The online version contains supplementary material available at 10.1007/s40820-024-01408-2.

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          Most cited references48

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          Cation and anion immobilization through chemical bonding enhancement with fluorides for stable halide perovskite solar cells

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            Conformal quantum dot–SnO 2 layers as electron transporters for efficient perovskite solar cells

            Improvements to perovskite solar cells (PSCs) have focused on increasing their power conversion efficiency (PCE) and operational stability and maintaining high performance upon scale-up to module sizes. We report that replacing the commonly used mesoporous–titanium dioxide electron transport layer (ETL) with a thin layer of polyacrylic acid–stabilized tin(IV) oxide quantum dots (paa-QD-SnO 2 ) on the compact–titanium dioxide enhanced light capture and largely suppressed nonradiative recombination at the ETL–perovskite interface. The use of paa-QD-SnO 2 as electron-selective contact enabled PSCs (0.08 square centimeters) with a PCE of 25.7% (certified 25.4%) and high operational stability and facilitated the scale-up of the PSCs to larger areas. PCEs of 23.3, 21.7, and 20.6% were achieved for PSCs with active areas of 1, 20, and 64 square centimeters, respectively. Mesoporous titanium dioxide is commonly used as the electron transport layer in perovskite solar cells, but electron transport layers based on tin(IV) oxide quantum dots could be more efficient, with a better-aligned conduction band and a higher carrier mobility. Kim et al . show that such quantum dots could conformally coat a textured fluorine-doped tin oxide electrode when stabilized with polyacrylic acid. Improved light trapping and reduced nonradiative recombination resulted in a certified power conversion efficiency of 25.4% and high operational stability. In larger-area minimodules, active areas as high as 64 square centimeters maintained certified power conversion efficiencies of more than 20%. —PDS Polymer-stabilized tin oxide nanoparticles suppress recombination at the electron-transport layer–perovskite interface.
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              Stabilizing perovskite-substrate interfaces for high-performance perovskite modules

              The buried interfaces of perovskite solar cells are difficult to alter after synthesis. During manufacture, Chen et al . removed perovskite films with dimethyl sulfoxide solvent from the hole-transfer layer and observed a substantial void fraction that degraded film performance. Replacing most of the dimethyl sulfoxide with carbohydrazide, a lead-coordinating compound with a much higher boiling point, eliminated voids. Such solar cells maintained high power conversion efficiency after 550 hours of operation at 60°C. —PDS A solid-state lead-coordinating compound removed detrimental voids at buried perovskite-substrate interfaces. The interfaces of perovskite solar cells (PSCs) are important in determining their efficiency and stability, but the morphology and stability of imbedded perovskite-substrate interfaces have received less attention than have top interfaces. We found that dimethyl sulfoxide (DMSO), which is a liquid additive broadly applied to enhance perovskite film morphology, was trapped during film formation and led to voids at perovskite-substrate interfaces that accelerated the film degradation under illumination. Partial replacement of DMSO with solid-state carbohydrazide reduces interfacial voids. A maximum stabilized power conversion efficiency (PCE) of 23.6% was realized for blade-coated p-type/intrinsic/n-type (p-i-n) structure PSCs with no efficiency loss after 550-hour operational stability tests at 60°C. The perovskite mini-modules showed certified PCEs of 19.3 and 19.2%, with aperture areas of 18.1 and 50.0 square centimeters, respectively.
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                Author and article information

                Contributors
                jixf@sari.ac.cn
                guan@hirosaki-u.ac.jp
                qfu222@cityu.edu.hk
                alexjen@cityu.edu.hk
                Journal
                Nanomicro Lett
                Nanomicro Lett
                Nano-Micro Letters
                Springer Nature Singapore (Singapore )
                2311-6706
                2150-5551
                2 May 2024
                2 May 2024
                December 2024
                : 16
                : 190
                Affiliations
                [1 ]Graduate School of Science and Technology, Hirosaki University, ( https://ror.org/02syg0q74) 3-Bunkyocho, Hirosaki, 036-8561 Japan
                [2 ]Department of Materials Science and Engineering, Department of Chemistry, Hong Kong Institute for Clean Energy, City University of Hong Kong Kowloon, ( https://ror.org/02zhqgq86) Hong Kong, 999077 People’s Republic of China
                [3 ]GRID grid.9227.e, ISNI 0000000119573309, The Interdisciplinary Research Center, Shanghai Advanced Research Institute, , Chinese Academy of Sciences, ; Shanghai, 201210 People’s Republic of China
                [4 ]GRID grid.9227.e, ISNI 0000000119573309, Shanghai Synchrotron Radiation Facility (SSRF), Zhangjiang Lab, Shanghai Advanced Research Institute, , Chinese Academy of Sciences, ; Shanghai, 201204, People’s Republic of China
                [5 ]JINNENG Clean Energy Technology Ltd., ( https://ror.org/001qb9t53) Jinzhong, 030300 Shanxi People’s Republic of China
                [6 ]Hangzhou Zhongneng Photoelectricity Technology Co., Ltd., Hangzhou, 310018 People’s Republic of China
                [7 ]College of Chemical Engineering and Technology, Taiyuan University of Technology, ( https://ror.org/03kv08d37) Taiyuan, 030024 People’s Republic of China
                [8 ]Institute of Regional Innovation, Hirosaki University, ( https://ror.org/02syg0q74) 3-Bunkyocho, Hirosaki, 036-8561 Japan
                Article
                1408
                10.1007/s40820-024-01408-2
                11065817
                38698298
                6f06e013-916b-4bb4-b82f-ad972e9991bb
                © The Author(s) 2024

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 26 January 2024
                : 20 March 2024
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                © Shanghai Jiao Tong University 2024

                inverted perovskite solar cells,perovskite solar modules,two-step film formation,crystallization,defect passivation

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