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      Bidirectional Anions Gathering Strategy Afford Efficient Mixed PbSn Perovskite Solar Cells

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          Abstract

          Mixed lead‐tin (PbSn) perovskite solar cells (PSCs) possess low toxicity and adjustable bandgap for both single‐junction and all‐perovskite tandem solar cells. However, the performance of mixed PbSn PSCs still lags behind the theoretical efficiency. The uncontrollable crystallization and the resulting structural defect are important reasons. Here, the bidirectional anions gathering strategy (BAG) is reported by using Methylammonium acetate (MAAc) and Methylammonium thiocyanate (MASCN) as perovskite bulk additives, which Ac escapes from the perovskite film top surface while SCN gathers at the perovskite film bottom in the crystallization process. After the optoelectronic techniques, the bidirectional anions movement caused by the top‐down gradient crystallization is demonstrated. The layer‐by‐layer crystallization can collect anions in the next layer and gather at the broader, enabling a controllable crystallization process, thus getting a high‐quality perovskite film with better phase crystallinity and lower defect concentration. As a result, PSCs treated by the BAG strategy exhibit outstanding photovoltaic and electroluminescent performance with a champion efficiency of 22.14%. Additionally, it demonstrates excellent long‐term stability, which retains ≈92.8% of its initial efficiency after 4000 h aging test in the N 2 glove box.

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          Most cited references41

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          Perovskite solar cells with atomically coherent interlayers on SnO2 electrodes

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            Enhanced photovoltage for inverted planar heterojunction perovskite solar cells

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              Imperfections and their passivation in halide perovskite solar cells

              Perovskite solar cells to date are made of polycrystalline films which contain a high density of defects. Imperfection passivation to reduce non-radiative recombination and suppress ion migration could improve device efficiency and device stability. All highly-efficient organic–inorganic halide perovskite (OIHP) solar cells to date are made of polycrystalline perovskite films which contain a high density of defects, including point and extended imperfections. The imperfections in OIHP materials play an important role in the process of charge recombination and ion migration in perovskite solar cells (PSC), which heavily influences the resulting device energy conversion efficiency and stability. Here we review the recent advances in passivation of imperfections and suppressing ion migration to achieve improved efficiency and highly stable perovskite solar cells. Due to the ionic nature of OIHP materials, the defects in the photoactive films are inevitably electrically charged. The deep level traps induced by particular charged defects in OIHP films are major non-radiative recombination centers; passivation by coordinate bonding, ionic bonding, or chemical conversion have proven effective in mitigating the negative impacts of these deep traps. Shallow level charge traps themselves may contribute little to non-radiative recombination, but the migration of charged shallow level traps in OIHP films results in unfavorable band bending, interfacial reactions, and phase segregation, influencing the carrier extraction efficiency. Finally, the impact of defects and ion migration on the stability of perovskite solar cells is described.
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                Author and article information

                Contributors
                Journal
                Small
                Small
                Wiley
                1613-6810
                1613-6829
                May 2023
                February 25 2023
                May 2023
                : 19
                : 20
                Affiliations
                [1 ] Key Laboratory of Photovoltaic and Energy Conservation Materials Institute of Solid‐State Physics Hefei Institutes of Physical Science Chinese Academy of Science Hefei 230031 China
                [2 ] University of Science and Technology of China Hefei 230026 China
                [3 ] Univ. Grenoble Alpes CEA CNRS INP IRIG/SyMMES STEP Grenoble 38000 France
                Article
                10.1002/smll.202207480
                f78aa820-fca4-4b86-974e-9593162c12e4
                © 2023

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

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