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      One-step solution deposition of CsPbBr 3 based on precursor engineering for efficient all-inorganic perovskite solar cells

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          Abstract

          A novel strategy of adopting cesium acetate and methylammonium acetate increases the concentration of CsPbBr 3 precursor solution assisting one-step deposition.

          Abstract

          All-inorganic CsPbBr 3 perovskite solar cells (PSCs) are attracting tremendous interest owing to their outstanding stability, especially under high temperature and humidity atmospheres. Limited by the low solubility of CsBr in most common solvents, it is still a great challenge to prepare high-quality CsPbBr 3 films with sufficient thickness for PSC applications by the convenient one-step solution method. Herein, a novel precursor engineering strategy with the use of cesium acetate (CsAc) and ionic liquid methylammonium acetate (MAAc) is developed to increase the concentration of the CsPbBr 3 precursor solution to 1.0 M and form uniform and high coverage CsPbBr 3 films with large sized crystalline grains. The formation mechanism for this high-quality CsPbBr 3 films is mainly due to tailoring the crystallization kinetics by MAAc. Correspondingly, high light-harvesting capacity and suppressed trap state related charge recombination are realized in the resultant PSCs. The champion CsPbBr 3 PSCs achieve an efficiency of 7.37% ( J SC = 7.40 mA cm −2, V OC = 1.22 V, and FF = 0.841). This device has also displayed good stability with negligible decay over a period of 1500 h under an ambient atmosphere with 30–35% relative humidity.

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          Most cited references56

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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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              Sequential deposition as a route to high-performance perovskite-sensitized solar cells.

              Following pioneering work, solution-processable organic-inorganic hybrid perovskites-such as CH3NH3PbX3 (X = Cl, Br, I)-have attracted attention as light-harvesting materials for mesoscopic solar cells. So far, the perovskite pigment has been deposited in a single step onto mesoporous metal oxide films using a mixture of PbX2 and CH3NH3X in a common solvent. However, the uncontrolled precipitation of the perovskite produces large morphological variations, resulting in a wide spread of photovoltaic performance in the resulting devices, which hampers the prospects for practical applications. Here we describe a sequential deposition method for the formation of the perovskite pigment within the porous metal oxide film. PbI2 is first introduced from solution into a nanoporous titanium dioxide film and subsequently transformed into the perovskite by exposing it to a solution of CH3NH3I. We find that the conversion occurs within the nanoporous host as soon as the two components come into contact, permitting much better control over the perovskite morphology than is possible with the previously employed route. Using this technique for the fabrication of solid-state mesoscopic solar cells greatly increases the reproducibility of their performance and allows us to achieve a power conversion efficiency of approximately 15 per cent (measured under standard AM1.5G test conditions on solar zenith angle, solar light intensity and cell temperature). This two-step method should provide new opportunities for the fabrication of solution-processed photovoltaic cells with unprecedented power conversion efficiencies and high stability equal to or even greater than those of today's best thin-film photovoltaic devices.
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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
                October 8 2019
                2019
                : 7
                : 39
                : 22420-22428
                Affiliations
                [1 ]College of Materials and Energy
                [2 ]South China Agricultural University
                [3 ]Guangzhou 510642
                [4 ]China
                Article
                10.1039/C9TA08465G
                05a6bcb5-c096-44c4-bb76-6918c296f1b3
                © 2019

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

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