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      Recent efficient strategies for improving the moisture stability of perovskite solar cells

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          Abstract

          Current popular and efficient strategies to improve the long-term stability regarding protection against moisture in the field of PSCs.

          Abstract

          In the past few years, hybrid organic–inorganic perovskite solar cells (PSCs) have attracted much attention due to their excellent photovoltaic performance and extremely low fabrication costs. The power conversion efficiency (PCEs) of these PSCs has lepts from 3.8% to a verified PCE of 22.1% within just 7 years. However, the limited long-term stability of PSCs still restricts them from industrial applications, and furthermore, chemical decomposition in humid environments has been recognized as a main degradation pathway of perovskite materials. Although encapsulation techniques are usually used in the field of organic photovoltaics to slow down the degradation of organic materials, the key to resolving the degradation issues related to PSCs is to find stable perovskite materials or device architectures capable of achieving long-term stability. This review discusses the current popular strategies for enhancing the stability of PSCs, which are mostly, in general, concerned with modifying the properties of either the perovskite material itself or the charge transport layers. The stability of perovskite materials is usually optimized by compositional engineering with halides and cations. Meanwhile, on the other hand, incorporating inorganic charge transport layers or an interfacial moisture-resistant agent into PSCs are also considered as effective routes to sustain the device stability as well as to retain the performance of PSCs. This review systemically summarizes the recent efficient strategies for improving the long-term stability of PSC devices and provides useful suggestions for further developments in PSC stability.

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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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            Electron-hole diffusion lengths exceeding 1 micrometer in an organometal trihalide perovskite absorber.

            Organic-inorganic perovskites have shown promise as high-performance absorbers in solar cells, first as a coating on a mesoporous metal oxide scaffold and more recently as a solid layer in planar heterojunction architectures. Here, we report transient absorption and photoluminescence-quenching measurements to determine the electron-hole diffusion lengths, diffusion constants, and lifetimes in mixed halide (CH3NH3PbI(3-x)Cl(x)) and triiodide (CH3NH3PbI3) perovskite absorbers. We found that the diffusion lengths are greater than 1 micrometer in the mixed halide perovskite, which is an order of magnitude greater than the absorption depth. In contrast, the triiodide absorber has electron-hole diffusion lengths of ~100 nanometers. These results justify the high efficiency of planar heterojunction perovskite solar cells and identify a critical parameter to optimize for future perovskite absorber development.
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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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                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
                2017
                2017
                : 5
                : 30
                : 15447-15459
                Affiliations
                [1 ]Center for Applied Chemistry
                [2 ]University of Electronic Science and Technology of China
                [3 ]China
                [4 ]State Key Laboratory Electronic Thin Film and Integrated Devices
                Article
                10.1039/C7TA01325F
                a01ac4ca-4507-45e0-9549-e6792bda8dae
                © 2017
                History

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