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      Tin perovskite solar cells with >1,300 h of operational stability in N 2 through a synergistic chemical engineering approach

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          Summary

          Despite the promising properties of tin-based halide perovskites, one clear limitation is the fast Sn +2 oxidation. Consequently, the preparation of long-lasting devices remains challenging. Here, we report a chemical engineering approach, based on adding Dipropylammonium iodide (DipI) together with a well-known reducing agent, sodium borohydride (NaBH 4), aimed at preventing the premature degradation of Sn-HPs. This strategy allows for obtaining efficiencies (PCE) above 10% with enhanced stability. The initial PCE remained unchanged upon 5 h in air (60% RH) at maximum-power-point (MPP). Remarkably, 96% of the initial PCE was kept after 1,300 h at MPP in N 2. To the best of our knowledge, these are the highest reported values for Sn-based solar cells. Our findings demonstrate a beneficial synergistic effect when additives are incorporated, highlight the important role of iodide in the performance upon light soaking, and, ultimately, unveil the relevance of controlling the halide chemistry for future improvement of Sn-based perovskite devices.

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          Highlights

          • Highly efficient and long-lasting unencapsulated Sn-perovskite (Sn-HPs) solar cells

          • Synergistic chemical engineering approach for highly efficient and durable Sn-HPs

          • Elucidation of the photo-electrochemical mechanisms involved in Sn-HPs solar cells

          • Relevance of halide photochemistry in the performance of Sn-HPs solar cells

          Context & scale

          Despite the unprecedented achievements that solar cells based on lead perovskites have experienced in the last decades, they still suffer from essential limitations. Toxicity has been considered a handicap since the commencement of their exploitation. The stability of halide perovskites is far from being comparable to that of silicon. In addition, the photo-electrochemistry that determines their performance, the degradation paths, and the role of the additives employed is not fully understood. Tin-based perovskites alleviate the toxicity associated with lead, and we have developed a synergetic chemical strategy to enhance the performance of devices, giving special emphasis to extending the operational stability. Remarkably, our findings point to the significance of the halides’ chemistry in outlining the device's performance, as well as contribute to unveiling mechanistic details that determine the photo-electrochemical processes that rule the operating principles and degradation reactions.

          Abstract

          Tin-based halide perovskites are promising candidates for the development of highly efficient and low-cost photovoltaics based on low-toxicity materials. Yet, the performance of Sn-HPs solar cells is far below that of other technologies. This work focuses on enhancing the photoconversion efficiencies and extending the operational lifetime of the devices through the beneficial synergy provided by the incorporated additives. Furthermore, crucial mechanistic details that determine the performance of the devices are provided with the aim of bringing this technology one step forward.

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          Most cited references82

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          Organometal halide perovskites as visible-light sensitizers for photovoltaic cells.

          Two organolead halide perovskite nanocrystals, CH(3)NH(3)PbBr(3) and CH(3)NH(3)PbI(3), were found to efficiently sensitize TiO(2) for visible-light conversion in photoelectrochemical cells. When self-assembled on mesoporous TiO(2) films, the nanocrystalline perovskites exhibit strong band-gap absorptions as semiconductors. The CH(3)NH(3)PbI(3)-based photocell with spectral sensitivity of up to 800 nm yielded a solar energy conversion efficiency of 3.8%. The CH(3)NH(3)PbBr(3)-based cell showed a high photovoltage of 0.96 V with an external quantum conversion efficiency of 65%.
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            Efficient hybrid solar cells based on meso-superstructured organometal halide perovskites.

            The energy costs associated with separating tightly bound excitons (photoinduced electron-hole pairs) and extracting free charges from highly disordered low-mobility networks represent fundamental losses for many low-cost photovoltaic technologies. We report a low-cost, solution-processable solar cell, based on a highly crystalline perovskite absorber with intense visible to near-infrared absorptivity, that has a power conversion efficiency of 10.9% in a single-junction device under simulated full sunlight. This "meso-superstructured solar cell" exhibits exceptionally few fundamental energy losses; it can generate open-circuit photovoltages of more than 1.1 volts, despite the relatively narrow absorber band gap of 1.55 electron volts. The functionality arises from the use of mesoporous alumina as an inert scaffold that structures the absorber and forces electrons to reside in and be transported through the perovskite.
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              Lead Iodide Perovskite Sensitized All-Solid-State Submicron Thin Film Mesoscopic Solar Cell with Efficiency Exceeding 9%

              We report on solid-state mesoscopic heterojunction solar cells employing nanoparticles (NPs) of methyl ammonium lead iodide (CH3NH3)PbI3 as light harvesters. The perovskite NPs were produced by reaction of methylammonium iodide with PbI2 and deposited onto a submicron-thick mesoscopic TiO2 film, whose pores were infiltrated with the hole-conductor spiro-MeOTAD. Illumination with standard AM-1.5 sunlight generated large photocurrents (JSC) exceeding 17 mA/cm2, an open circuit photovoltage (VOC) of 0.888 V and a fill factor (FF) of 0.62 yielding a power conversion efficiency (PCE) of 9.7%, the highest reported to date for such cells. Femto second laser studies combined with photo-induced absorption measurements showed charge separation to proceed via hole injection from the excited (CH3NH3)PbI3 NPs into the spiro-MeOTAD followed by electron transfer to the mesoscopic TiO2 film. The use of a solid hole conductor dramatically improved the device stability compared to (CH3NH3)PbI3 -sensitized liquid junction cells.
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                Author and article information

                Contributors
                Journal
                Joule
                Joule
                Joule
                Cell Press
                2542-4351
                20 April 2022
                20 April 2022
                : 6
                : 4
                : 861-883
                Affiliations
                [1 ]Institute of Advanced Materials (INAM), Universitat Jaume I, Av. Sos Baynat, s/n, 12071 Castelló, Spain
                [2 ]UMDO, Instituto de Ciencia de los Materiales, Universidad de Valencia, c/ Catedrático J. Beltrán, 2, 46980 Paterna, Spain
                [3 ]Facultad de Química, Universidad Nacional Autónoma de México, Coyoacán, Ciudad de México 04510, México
                [4 ]MATINÉE: CSIC Associated Unit (ICMM-ICMUV of the University of Valencia), Universidad de Valencia, Valencia, Spain
                Author notes
                []Corresponding author rasanche@ 123456uji.es
                [∗∗ ]Corresponding author sero@ 123456uji.es
                [5]

                Lead contact

                Article
                S2542-4351(22)00095-2
                10.1016/j.joule.2022.02.014
                9097823
                35711469
                2b7cbae1-2e94-4155-b754-2ac28ae15514
                © 2022 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 8 September 2021
                : 29 October 2021
                : 18 February 2022
                Categories
                Article

                tin perovskite solar cells,light-soaking treatment,photoinduced trap-healing effect,ligand-to-metal charge transfer,photo-redox reactivity of tin and iodine,long-term device stability,photovoltaics,lead-free semiconductors,metal halide perovskites

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