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      Lewis acid/base approach for efficacious defect passivation in perovskite solar cells

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          Abstract

          The Lewis acid/base passivation strategy and its effects on energy level alignment, recombination kinetics, hysteresis behavior and operational stability for efficient perovskite solar cells are comprehensively reviewed.

          Abstract

          Halide perovskite solar cells (PSCs) have been materialized as a hotspot in the next-generation photovoltaic technology due to their low-cost manufacturing process and high-efficiency characteristics. However, the defects within the bulk or in the grain boundaries and surface hinder ambipolar charge transport as non-radiative recombination centers. Efficacious defect passivation is therefore highly desired for high-efficiency and stable PSCs. Herein, a feasible Lewis acid/base passivation strategy and its effects on energy level alignment, recombination kinetics, hysteresis behavior and operational stability for efficient PSCs are comprehensively reviewed. These additives have been widely used to coordinate with unwanted defects and form Lewis adducts by dative bonds, where the Lewis acid contributes to passivate negatively charged defects ( e.g., under-coordinated I ions and Pb–I anti-sites) and the Lewis base plays a significant role in passivating positively charged defects ( e.g., under-coordinated Pb 2+ and Pb 2+ interstitials), whereas zwitterions could passivate negatively and positively charged defects simultaneously. This highly executable Lewis adduct passivation would enable scalable deposition techniques for efficient and stable PSCs like inkjet printing, doctor-blade coating, screen printing, laser pattering and roll-to-roll deposition. Additionally, we also discuss the prospects of the maturity of this passivation strategy towards upscaling manufacture of perovskite photovoltaic and related optoelectronic devices.

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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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            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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              Solar cells. Electron-hole diffusion lengths > 175 μm in solution-grown CH3NH3PbI3 single crystals.

              Long, balanced electron and hole diffusion lengths greater than 100 nanometers in the polycrystalline organolead trihalide compound CH3NH3PbI3 are critical for highly efficient perovskite solar cells. We found that the diffusion lengths in CH3NH3PbI3 single crystals grown by a solution-growth method can exceed 175 micrometers under 1 sun (100 mW cm(-2)) illumination and exceed 3 millimeters under weak light for both electrons and holes. The internal quantum efficiencies approach 100% in 3-millimeter-thick single-crystal perovskite solar cells under weak light. These long diffusion lengths result from greater carrier mobility, longer lifetime, and much smaller trap densities in the single crystals than in polycrystalline thin films. The long carrier diffusion lengths enabled the use of CH3NH3PbI3 in radiation sensing and energy harvesting through the gammavoltaic effect, with an efficiency of 3.9% measured with an intense cesium-137 source.
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                Author and article information

                Contributors
                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                June 30 2020
                2020
                : 8
                : 25
                : 12201-12225
                Affiliations
                [1 ]School of Materials and Energy
                [2 ]University of Electronic Science and Technology of China
                [3 ]Chengdu
                [4 ]China
                [5 ]Center for Excellence in Nanoscience (CAS)
                [6 ]Key Laboratory of Nanosystem and Hierarchical Fabrication (CAS)
                [7 ]National Center for Nanoscience and Technology
                [8 ]Beijing 100190
                Article
                10.1039/D0TA03957H
                fca366b4-4a43-4dbb-bb32-d801f8ec44f3
                © 2020

                http://rsc.li/journals-terms-of-use

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