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      A strategic review on processing routes towards highly efficient perovskite solar cells

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          Abstract

          An organic–inorganic perovskite is comprised of an organic cation (CH 3NH 3 +, FAI, or Cs), a metal cation (Pb 2+ or Sn 2+) and a halide (I , Cl , or Br ) molecule.

          Abstract

          An organic–inorganic perovskite is comprised of an organic cation (CH 3NH 3 +, FAI, or Cs), a metal cation (Pb 2+ or Sn 2+) and a halide (I , Cl , or Br ) molecule. Precursor salts containing these cations, molecules and halide ions dissolved in solvents are used to prepare perovskite films. Perovskite film formation takes place through the reaction of precursor elements, which is assisted by various processing conditions such as thermal annealing, moisture and solvent treatment. This review focuses on various perovskite formation and crystallization routes with respect to processing parameters including the precursor solvent, solvent mixture, temperature, time, formation of solvent led-intermediate complex species, doping and humidity. Adding water as the dopant to the precursor solvent and exposure to moisture from atmospheric humidity to improve perovskite film quality are also discussed. Processing conditions and crystallization processes are described in correlation with the perovskite film morphology, crystallinity, defects, charge transport and device performance. This article will aim to highlighting recent findings in the selection of solvents in the crystallization of perovskite films, solvent induced intermediate phases, and effects of water in assisting perovskite crystallization for improved film quality and device performance. The review will also present various structural and nanoscale characterization techniques that have been used to probe solvent based intermediate species transformation processes to the perovskite phase and understand the effects in correlation with device performance.

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          Most cited references65

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          Highly Reproducible Perovskite Solar Cells with Average Efficiency of 18.3% and Best Efficiency of 19.7% Fabricated via Lewis Base Adduct of Lead(II) Iodide.

          High efficiency perovskite solar cells were fabricated reproducibly via Lewis base adduct of lead(II) iodide. PbI2 was dissolved in N,N-dimethyformamide with equimolar N,N-dimethyl sulfoxide (DMSO) and CH3NH3I. Stretching vibration of S═O appeared at 1045 cm(-1) for bare DMSO, which was shifted to 1020 and 1015 cm(-1) upon reacting DMSO with PbI2 and PbI2 + CH3NH3I, respectively, indicative of forming the adduct of PbI2·DMSO and CH3NH3I·PbI2·DMSO due to interaction between Lewis base DMSO and/or iodide (I(-)) and Lewis acid PbI2. Spin-coating of a DMF solution containing PbI2, CH3NH3I, and DMSO (1:1:1 mol %) formed a transparent adduct film, which was converted to a dark brown film upon heating at low temperature of 65 °C for 1 min due to removal of the volatile DMSO from the adduct. The adduct-induced CH3NH3PbI3 exhibited high charge extraction characteristics with hole mobility as high as 3.9 × 10(-3) cm(2)/(V s) and slow recombination rate. Average power conversion efficiency (PCE) of 18.3% was achieved from 41 cells and the best PCE of 19.7% was attained via adduct approach.
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            Recent Advances in Bulk Heterojunction Polymer Solar Cells.

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              CH3NH3PbI3 perovskite/fullerene planar-heterojunction hybrid solar cells.

              All-solid-state donor/acceptor planar-heterojunction (PHJ) hybrid solar cells are constructed and their excellent performance measured. The deposition of a thin C60 fullerene or fullerene-derivative (acceptor) layer in vacuum on a CH3 NH3 PbI3 perovskite (donor) layer creates a hybrid PHJ that displays the photovoltaic effect. Such heterojunctions are shown to be suitable for the development of newly structured, hybrid, efficient solar cells. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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                Author and article information

                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                2018
                2018
                : 6
                : 6
                : 2406-2431
                Affiliations
                [1 ]Center for Advanced Photovoltaics
                [2 ]Electrical Engineering and Computer Science Department
                [3 ]South Dakota State University
                [4 ]Brookings
                [5 ]USA
                [6 ]Hefei National Laboratory for Physical Sciences at Microscale
                [7 ]Key Laboratory of Materials for Energy Conversion
                [8 ]Chinese Academy of Sciences
                [9 ]Department of Materials Science and Engineering
                [10 ]Synergetic Innovation Center of Quantum Information & Quantum Physics
                Article
                10.1039/C7TA08277K
                9f9096f5-f4d3-4084-b80f-e8a538b85759
                © 2018

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

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