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      Two birds with one stone: dual grain-boundary and interface passivation enables >22% efficient inverted methylammonium-free perovskite solar cells

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          Abstract

          We present a dual passivation approach for p–i–n perovskite solar cells using phenethylammonium chloride that simultaneously passivates defects at the grain boundaries and the perovskite/C 60 interface, thus substantially enhancing both V OC and FF.

          Abstract

          Advancing inverted (p–i–n) perovskite solar cells (PSCs) is key to further enhance the power conversion efficiency (PCE) and stability of flexible and perovskite-based tandem photovoltaics. Yet, the presence of defects at grain boundaries and in particular interfacial recombination at the perovskite/electron transporting layer interface induce severe non-radiative recombination losses, limiting the open-circuit voltage ( V OC) and fill factor (FF) of PSCs in this architecture. In this work, we introduce a dual passivation strategy using the long chain alkylammonium salt phenethylammonium chloride (PEACl) both as an additive and for surface treatment to simultaneously passivate the grain boundaries and the perovskite/C 60 interface. Using [2-(9 H-carbazol-9-yl)ethyl]phosphonic acid (2PACz) as a hole transporting layer and a methylammonium (MA)-free Cs 0.18FA 0.82PbI 3 perovskite absorber with a bandgap of ∼1.57 eV, prolonged charge carrier lifetime and an on average 63 meV enhanced internal quasi-Fermi level splitting are achieved upon dual passivation compared to reference p–i–n PSCs. Thereby, we achieve one of the highest PCEs for p–i–n PSCs of 22.7% (stabilized at 22.3%) by advancing simultaneously the V OC and FF up to 1.162 V and 83.2%, respectively. Using a variety of experimental techniques, we attribute the positive effects to the formation of a heterogeneous 2D Ruddlesden–Popper (PEA) 2(Cs 1− x FA x ) n−1 Pb n (I 1− y Cl y ) 3 n+1 phase at the grain boundaries and surface of the perovskite films. At the same time, the activation energy for ion migration is significantly increased, resulting in enhanced stability of the PSCs under light, humidity, and thermal stress. The presented dual passivation strategy highlights the importance of defect management both in the grain boundaries and the surface of the perovskite absorber layer using a proper passivation material to achieve both highly efficient and stable inverted p–i–n PSCs.

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          Surface passivation of perovskite film for efficient solar cells

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            Pseudo-halide anion engineering for α-FAPbI3 perovskite solar cells

            Metal halide perovskites of the general formula ABX3-where A is a monovalent cation such as caesium, methylammonium or formamidinium; B is divalent lead, tin or germanium; and X is a halide anion-have shown great potential as light harvesters for thin-film photovoltaics1-5. Among a large number of compositions investigated, the cubic α-phase of formamidinium lead triiodide (FAPbI3) has emerged as the most promising semiconductor for highly efficient and stable perovskite solar cells6-9, and maximizing the performance of this material in such devices is of vital importance for the perovskite research community. Here we introduce an anion engineering concept that uses the pseudo-halide anion formate (HCOO-) to suppress anion-vacancy defects that are present at grain boundaries and at the surface of the perovskite films and to augment the crystallinity of the films. The resulting solar cell devices attain a power conversion efficiency of 25.6 per cent (certified 25.2 per cent), have long-term operational stability (450 hours) and show intense electroluminescence with external quantum efficiencies of more than 10 per cent. Our findings provide a direct route to eliminate the most abundant and deleterious lattice defects present in metal halide perovskites, providing a facile access to solution-processable films with improved optoelectronic performance.
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              Efficient perovskite solar cells via improved carrier management

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                Author and article information

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                Journal
                EESNBY
                Energy & Environmental Science
                Energy Environ. Sci.
                Royal Society of Chemistry (RSC)
                1754-5692
                1754-5706
                November 10 2021
                2021
                : 14
                : 11
                : 5875-5893
                Affiliations
                [1 ]Light Technology Institute, Karlsruhe Institute of Technology, Engesserstrasse 13, 76131 Karlsruhe, Germany
                [2 ]Institute of Microstructure Technology, Karlsruhe Institute of Technology, Hermann-von Helmholtz-Platz 1, 76344 Eggenstein-Leopoldshafen, Germany
                [3 ]Max Planck Institute for polymer research, department physics at interfaces, Ackermannweg 10, 55128 Mainz, Germany
                [4 ]Technical University of Darmstadt, Department of Materials and Earth Sciences, Surface Science Laboratory, Otto-Berndt-Strasse 3, 64287 Darmstadt, Germany
                [5 ]InnovationLab GmbH, Speyerer Strasse 4, 69115 Heidelberg, Germany
                [6 ]Center for Nanophotonics, AMOLF, 1098 XG Amsterdam, The Netherlands
                [7 ]School of Engineering, The Australian National University, Canberra, 2601, Australia
                [8 ]Institute of Advanced Materials, Universitat Jaume I, 12006 Castelló, Spain
                [9 ]Insitute for Quantum Materials and Technologies, Karlsruhe Institute of Technology, Herrmann-von-Helmholtz-Platz 1, 76344 Eggenstein-Leopoldshafen, Germany
                Article
                10.1039/D1EE01508G
                a90dfbfc-04b0-422e-bdfb-88938a540416
                © 2021

                http://creativecommons.org/licenses/by/3.0/

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