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      2D/3D heterostructured CsPbI 2Br solar cells: a choice for a monolithic all-perovskite tandem device

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          Abstract

          Improving the performance of CsPbI 2Br PSCs by spinning BABr on 3D CsPbI 2Br films to form 2D/3D heterostructures, and based on this, monolithic all-PTSCs are fabricated, realizing a pioneering exploration for the application of CsPbI 2Br to all-PTSCs.

          Abstract

          All-inorganic CsPbI 2Br perovskite solar cells (PSCs) have attracted intensive attention owing to their suitable bandgaps and excellent photo- and thermal stability, making them promising ideal top cells in high-performance monolithic all-perovskite tandem solar cells (all-PTSCs). However, CsPbI 2Br PSCs are still facing a challenge due to their relatively low power conversion efficiency (PCE) and moisture sensitivity. Herein, a simple and effective in situ growth method was adopted to construct a two-dimensional/three-dimensional (2D/3D) heterostructure by spinning n-butylammonium bromide (BABr) on the top of a 3D CsPbI 2Br perovskite film. The such fabricated high-quality 2D/3D CsPbI 2Br film exhibits excellent hydrophobicity against moisture invasion, and a well-matched energy level with the hole transport layer (HTL) facilitating hole extraction at the perovskite/HTL interface. As a result, the optimized 2D/3D CsPbI 2Br solar cell achieves an excellent PCE of 16.57% with improved stability. Based on this, we developed an all-PTSC having 2D/3D CsPbI 2Br and MAPbI 3 as the optical absorption layer of top and bottom cells, respectively, along with a solution-processed PEDOT:PSS film with high conductivity and high transmittance as the recombination layer. The fabricated all-PTSC exhibits a PCE of 10.22% and an ultrahigh open-circuit voltage of 2.33 V, approaching the sum of the light voltages of the two sub-cells. Benefiting from the outstanding thermal stability and hydrophobicity of 2D/3D CsPbI 2Br, the all-PTSC showed superior stability under heat and air. This work demonstrates that all-inorganic perovskites as the photo-response cores of top cells are appropriate candidates for the fabrication of efficient and stable monolithic all-PTSCs.

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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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            Perovskite solar cells with atomically coherent interlayers on SnO2 electrodes

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              Efficient perovskite solar cells via improved carrier management

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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
                July 19 2022
                2022
                : 10
                : 28
                : 14799-14809
                Affiliations
                [1 ]State Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing 100029, China
                [2 ]Department of Chemical Engineering, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061, USA
                [3 ]School of Chemistry & Chemical Engineering, Queen's University Belfast, Belfast, BT9 5AG, UK
                Article
                10.1039/D2TA03627D
                c6c9391b-17df-43e3-94ae-449685174118
                © 2022

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

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