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      Towards commercialization: the operational stability of perovskite solar cells

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          Abstract

          This review gives insight into the operational stability of perovskite solar cells and provides possible research direction for further improvement.

          Abstract

          Recently, perovskite solar cells (PSCs) have attracted much attention owing to their high power conversion efficiency (25.2%) and low fabrication cost. However, the short lifetime under operation is the major obstacle for their commercialization. With efforts from the entire PSC research community, significant advances have been witnessed to improve the device operational stability, and a timely summary on the progress is urgently needed. In this review, we first clarify the definition of operational stability and its significance in the context of practical use. By analyzing the mechanisms in established approaches for operational stability improvement, we summarize several effective strategies to extend device lifetime in a layer-by-layer sequence across the entire PSC. These mechanisms are discussed in the contexts of chemical reactions, photo-physical management, technological modification, etc., which may inspire future R&D for stable PSCs. Finally, emerging operational stability standards with respect to testing and reporting device operational stability are summarized and discussed, which may help reliable device stability data circulate in the research community. The main target of this review is gaining insight into the operational stability of PSCs, as well as providing useful guidance to further improve their operational lifetime by rational materials processing and device fabrication, which would finally promote the commercialization of 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
                (View ORCID Profile)
                Journal
                CSRVBR
                Chemical Society Reviews
                Chem. Soc. Rev.
                Royal Society of Chemistry (RSC)
                0306-0012
                1460-4744
                November 16 2020
                2020
                : 49
                : 22
                : 8235-8286
                Affiliations
                [1 ]Beijing Key Laboratory for Theory and Technology of Advanced Battery Materials
                [2 ]Key Laboratory of Polymer Chemistry and Physics of Ministry of Education
                [3 ]BIC-ESAT
                [4 ]Department of Materials Science and Engineering
                [5 ]College of Engineering
                [6 ]Experimental Centre for Advanced Materials
                [7 ]School of Materials Science and Engineering
                [8 ]Beijing Institute of Technology
                [9 ]Beijing 100081
                [10 ]P. R. China
                Article
                10.1039/D0CS00573H
                32909584
                37bd3b20-10ec-4921-a57e-705421d4911a
                © 2020

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

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