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      Passivation and process engineering approaches of halide perovskite films for high efficiency and stability perovskite solar cells

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          Abstract

          Recent advances on passivation and morphology engineering approaches adopted to obtain high efficiency and stability in perovskite solar cells are thoroughly reviewed.

          Abstract

          The surface, interfaces and grain boundaries of a halide perovskite film carry critical tasks in achieving as well as maintaining high solar cell performance due to the inherently defective nature across their regime. Passivating materials and felicitous process engineering approaches have significant ramifications in the resultant perovskite film, and the solar cell's overall macroscale properties as they dictate structural and optoelectronic properties. Herein, we exploit a vast number of defect engineering approaches aiming to increase the performance and the stability of perovskite solar cells, especially against humidity, continuous illumination, and heat. This review begins with the perovskite materials' fundamental structural properties followed by the advances made to induce higher stabilization in perovskite solar cells by fine-tuning materials chemistry design parameters. We continue by summarizing defect passivation strategies based on molecular entities' application, including suitable functional groups that enable sufficient surface, bulk and grain boundary passivation, morphology, and crystallinity control. We also present methods to control the density of defects through the variation of processing conditions, solvent annealing and solvent engineering approaches, gas-assisted deposition methods, and use of self-assembled monolayers, as well as colloidal engineering and coordination surface chemistry. Finally, we give our perspective on how a combined understanding of materials chemistry aspects and passivation mechanisms will further develop high-efficiency and stability perovskite solar cells.

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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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              Surface passivation of perovskite film for efficient solar cells

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                Author and article information

                Contributors
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                Journal
                EESNBY
                Energy & Environmental Science
                Energy Environ. Sci.
                Royal Society of Chemistry (RSC)
                1754-5692
                1754-5706
                May 19 2021
                2021
                : 14
                : 5
                : 2906-2953
                Affiliations
                [1 ]Department of Chemical Engineering
                [2 ]Pohang University of Science and Technology (POSTECH)
                [3 ]Pohang
                [4 ]Republic of Korea
                [5 ]Institute of Nanoscience and Nanotechnology
                [6 ]National Center for Scientific Research Demokritos
                [7 ]Attica
                [8 ]Greece
                [9 ]Centre for Electronics Frontiers
                [10 ]Zepler Institute for Photonics and Nanoelectronics
                [11 ]University of Southampton
                [12 ]SO17 1BJ Southampton
                [13 ]UK
                [14 ]Department of Physics
                [15 ]University of Patras
                [16 ]26504 Patras
                [17 ]Helmholtz-Zentrum Berlin für Materialien und Energie
                [18 ]12489 Berlin
                [19 ]Germany
                [20 ]Department of Chemical
                [21 ]Materials and Production Engineering
                [22 ]Group for Molecular Engineering of Functional Materials
                [23 ]Institute of Chemical Sciences and Engineering
                [24 ]École Polytechnique Fédérale de Lausanne (EPFL)
                [25 ]CH-1951 Sion
                [26 ]Switzerland
                Article
                10.1039/D1EE00062D
                9249acff-1b74-47f0-b9d2-fdfadc2216be
                © 2021

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

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