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

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          Abstract

          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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          Author and article information

          Journal
          Nature
          Nature
          Springer Science and Business Media LLC
          1476-4687
          0028-0836
          Apr 2021
          : 592
          : 7854
          Affiliations
          [1 ] Department of Energy Engineering, School of Energy and Chemical Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan, Republic of Korea.
          [2 ] Laboratory of Photonics and Interfaces, Institute of Chemical Sciences and Engineering, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
          [3 ] Laboratory of Photomolecular Science, Institute of Chemical Sciences Engineering, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
          [4 ] Korea Institute of Energy Research (KIER), Ulsan, Republic of Korea.
          [5 ] Laboratory of Computational Chemistry and Biochemistry, Institute of Chemical Sciences and Engineering, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
          [6 ] Laboratory of Magnetic Resonance, Institute of Chemical Sciences and Engineering, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
          [7 ] Shanghai Synchrotron Radiation Facility (SSRF), Zhangjiang Lab, Shanghai Advanced Research Institute, Chinese Academy of Sciences, Shanghai, P. R. China.
          [8 ] Laboratory for Molecular Engineering of Optoelectronic Nanomaterials, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
          [9 ] Department of Chemistry and Research Institute of Basic Sciences, Kyung Hee University, Seoul, Republic of Korea.
          [10 ] Laboratory of Photomolecular Science, Institute of Chemical Sciences Engineering, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland. anders.hagfeldt@uu.se.
          [11 ] Department of Chemistry, Ångström Laboratory, Uppsala University, Uppsala, Sweden. anders.hagfeldt@uu.se.
          [12 ] Korea Institute of Energy Research (KIER), Ulsan, Republic of Korea. kimds@kier.re.kr.
          [13 ] Laboratory of Photonics and Interfaces, Institute of Chemical Sciences and Engineering, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland. michael.graetzel@epfl.ch.
          [14 ] Department of Energy Engineering, School of Energy and Chemical Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan, Republic of Korea. jykim@unist.ac.kr.
          Article
          10.1038/s41586-021-03406-5
          10.1038/s41586-021-03406-5
          33820983
          30229a60-2ae3-4e70-ac58-d5c3aee39185
          History

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