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      Electrochemistry and Spectroelectrochemistry of Lead Halide Perovskite Films: Materials Science Aspects and Boundary Conditions

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          Abstract

          The unique optoelectronic properties of lead halide perovskites have triggered a new wave of excitement in materials chemistry during the past five years. Electrochemistry, spectroelectrochemistry, and photoelectrochemistry could be viable tools both for analyzing the optoelectronic features of these materials and for assembling them into hybrid architectures (e.g., solar cells). At the same time, the instability of these materials limits the pool of solvents and electrolytes that can be employed in such experiments. The focus of our study is to establish a stability window for electrochemical tests for all-inorganic CsPbBr 3 and hybrid organic–inorganic MAPbI 3 perovskites. In addition, we aimed to understand the reduction and oxidation events that occur and to assess the damage done during these processes at extreme electrochemical conditions. In this vein, we demonstrated the chemical, structural, and morphological changes of the films in both reductive and oxidative environments. Taking all these results together as a whole, we propose a set of boundary conditions and protocols for how electrochemical experiments with lead halide perovskites should be carried out and interpreted. The presented results will contribute to the understanding of the electrochemical response of these materials and lead to a standardization of results in the literature so that comparisons can more easily be made.

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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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            Electrochemical considerations for determining absolute frontier orbital energy levels of conjugated polymers for solar cell applications.

            Narrow bandgap conjugated polymers in combination with fullerene acceptors are under intense investigation in the field of organic photovoltaics (OPVs). The open circuit voltage, and thereby the power conversion efficiency, of the devices is related to the offset of the frontier orbital energy levels of the donor and acceptor components, which are widely determined by cyclic voltammetry. Inconsistencies have appeared in the use of the ferrocenium/ferrocene (Fc + /Fc) redox couple, as well as the values used for the absolute potentials of standard electrodes, which can complicate the comparison of materials properties and determination of structure/property relationships.
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              Interface energetics in organo-metal halide perovskite-based photovoltaic cells

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                Author and article information

                Journal
                Chem Mater
                Chem Mater
                cm
                cmatex
                Chemistry of Materials
                American Chemical Society
                0897-4756
                1520-5002
                05 December 2017
                13 February 2018
                : 30
                : 3
                : 561-569
                Affiliations
                []Radiation Laboratory, University of Notre Dame , Notre Dame, Indiana 46556, United States
                []Department of Physical Chemistry and Materials Science, University of Szeged , Rerrich Square 1, Szeged, H-6720, Hungary
                [§ ]Department of Chemistry and Biochemistry, University of Notre Dame , Notre Dame, Indiana 46556, United States
                []ELI-ALPS Research Institute , Szeged, Dugonics sq. 13, 6720, Hungary
                Author notes
                [* ](P.V.K.) E-mail: pkamat@ 123456nd.edu .
                [* ](C.J.) E-mail: janaky@ 123456chem.u-szeged.hu .
                Article
                10.1021/acs.chemmater.7b04321
                5828706
                29503507
                7c7a4306-ea90-4939-9045-ea666661fa3b
                Copyright © 2017 American Chemical Society

                This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.

                History
                : 16 October 2017
                : 01 December 2017
                Categories
                Methods/Protocols
                Custom metadata
                cm7b04321
                cm-2017-04321d

                Materials science
                Materials science

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