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      Reducing nonradiative recombination in perovskite solar cells with a porous insulator contact

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          Abstract

          Inserting an ultrathin low-conductivity interlayer between the absorber and transport layer has emerged as an important strategy for reducing surface recombination in the best perovskite solar cells. However, a challenge with this approach is a trade-off between the open-circuit voltage ( V oc ) and the fill factor (FF). Here, we overcame this challenge by introducing a thick (about 100 nanometers) insulator layer with random nanoscale openings. We performed drift-diffusion simulations for cells with this porous insulator contact (PIC) and realized it using a solution process by controlling the growth mode of alumina nanoplates. Leveraging a PIC with an approximately 25% reduced contact area, we achieved an efficiency of up to 25.5% (certified steady-state efficiency 24.7%) in p-i-n devices. The product of V oc × FF was 87.9% of the Shockley-Queisser limit. The surface recombination velocity at the p-type contact was reduced from 64.2 to 9.2 centimeters per second. The bulk recombination lifetime was increased from 1.2 to 6.0 microseconds because of improvements in the perovskite crystallinity. The improved wettability of the perovskite precursor solution allowed us to demonstrate a 23.3% efficient 1-square-centimeter p-i-n cell. We demonstrate here its broad applicability for different p-type contacts and perovskite compositions.

          Through thick but not thin

          To maintain high charge carrier conductivity in perovskite solar cells, the passivating layer is usually very thin (~1 nanometer) to enable electron tunneling. However, this approach limits efficiency because it creates a trade-off between open-circuit voltage and fill factor and challenges in fabricating thin films from solution over large areas. Peng et al . grew a thick (~100 nanometer) dielectric mask formed by depositing alumina nanoplates and thus created random nanoscale openings for carrier transport. This layer reduced nonradiative recombination and boosted power conversion efficiencies from 23 to 25.5% compared with a conventional passivation layer. —PDS

          Abstract

          A solution-processed thick dielectric mask with nanoscale openings can maintain both open-circuit voltage and fill factor.

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          Most cited references84

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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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            Surface passivation of perovskite film for efficient solar cells

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              Pseudo-halide anion engineering for α-FAPbI3 perovskite solar cells

              Metal halide perovskites of the general formula ABX3-where A is a monovalent cation such as caesium, methylammonium or formamidinium; B is divalent lead, tin or germanium; and X is a halide anion-have shown great potential as light harvesters for thin-film photovoltaics1-5. Among a large number of compositions investigated, the cubic α-phase of formamidinium lead triiodide (FAPbI3) has emerged as the most promising semiconductor for highly efficient and stable perovskite solar cells6-9, and maximizing the performance of this material in such devices is of vital importance for the perovskite research community. Here we introduce an anion engineering concept that uses the pseudo-halide anion formate (HCOO-) to suppress anion-vacancy defects that are present at grain boundaries and at the surface of the perovskite films and to augment the crystallinity of the films. The resulting solar cell devices attain a power conversion efficiency of 25.6 per cent (certified 25.2 per cent), have long-term operational stability (450 hours) and show intense electroluminescence with external quantum efficiencies of more than 10 per cent. Our findings provide a direct route to eliminate the most abundant and deleterious lattice defects present in metal halide perovskites, providing a facile access to solution-processable films with improved optoelectronic performance.
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                Author and article information

                Contributors
                Journal
                Science
                Science
                American Association for the Advancement of Science (AAAS)
                0036-8075
                1095-9203
                February 17 2023
                February 17 2023
                : 379
                : 6633
                : 683-690
                Affiliations
                [1 ]Hefei National Research Center for Physical Sciences at the Microscale, CAS Key Laboratory of Materials for Energy Conversion, Department of Materials Science and Engineering, University of Science and Technology of China, Hefei 230026, China.
                [2 ]Chemical and Biological Engineering, University of Colorado, Boulder, CO 80309, USA.
                [3 ]Institute of Energy, Hefei Comprehensive National Science Center, Hefei 230051, China.
                Article
                10.1126/science.ade3126
                36795834
                486dd54f-930d-4e22-8806-93f518c22ce1
                © 2023

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