4.8 Article

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

Journal

NATURE
Volume 592, Issue 7854, Pages 381-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41586-021-03406-5

Keywords

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Funding

  1. Swiss National Supercomputing Centre (CSCS)
  2. EPFL computing center (SCITAS)
  3. Technology Development Program to Solve Climate Changes of the National Research Foundation (NRF) - Ministry of Science, ICT & Future Planning [2020M1A2A2080746]
  4. Ulsan National Institute of Science & Technology (UNIST) [1.200030.01]
  5. Development Program of the Korea Institute of Energy Research (KIER) [C0-2401, C0-2402]
  6. Swiss National Science Foundation [200020_178860, 200020_185092]
  7. NCCR MUST
  8. Swiss National Science Foundation, project 'Fundamental studies of dye-sensitized and perovskite solar cells' [200020_185041]
  9. European Union [881603]
  10. King Abdulaziz City for Science and Technology (KACST)
  11. Swiss National Science Foundation (SNF) [200020_185092] Funding Source: Swiss National Science Foundation (SNF)

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The research introduces a new concept of using formate anion to suppress defects in metal halide perovskite films and enhance film crystallinity, leading to improved efficiency and stability of solar cells.
Metal halide perovskites of the general formula ABX(3)-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 photovoltaics(1-5). Among a large number of compositions investigated, the cubic a-phase of formamidinium lead triiodide (FAPbI(3)) hasemerged as the most promising semiconductor for highly efficient and stable perovskite solar cells(6-9), and maximizing the performance of this material in such devices is of vital importance for the perovskite researchcommunity. 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. Theresulting 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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