Nature Communications (Nov 2024)

A green solvent enables precursor phase engineering of stable formamidinium lead triiodide perovskite solar cells

  • Benjamin M. Gallant,
  • Philippe Holzhey,
  • Joel A. Smith,
  • Saqlain Choudhary,
  • Karim A. Elmestekawy,
  • Pietro Caprioglio,
  • Igal Levine,
  • Alexandra A. Sheader,
  • Esther Y-H. Hung,
  • Fengning Yang,
  • Daniel T. W. Toolan,
  • Rachel C. Kilbride,
  • Karl-Augustin Zaininger,
  • James M. Ball,
  • M. Greyson Christoforo,
  • Nakita K. Noel,
  • Laura M. Herz,
  • Dominik J. Kubicki,
  • Henry J. Snaith

DOI
https://doi.org/10.1038/s41467-024-54113-4
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 14

Abstract

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Abstract Perovskite solar cells (PSCs) offer an efficient, inexpensive alternative to current photovoltaic technologies, with the potential for manufacture via high-throughput coating methods. However, challenges for commercial-scale solution-processing of metal-halide perovskites include the use of harmful solvents, the expense of maintaining controlled atmospheric conditions, and the inherent instabilities of PSCs under operation. Here, we address these challenges by introducing a high volatility, low toxicity, biorenewable solvent system to fabricate a range of 2D perovskites, which we use as highly effective precursor phases for subsequent transformation to α-formamidinium lead triiodide (α-FAPbI3), fully processed under ambient conditions. PSCs utilising our α-FAPbI3 reproducibly show remarkable stability under illumination and elevated temperature (ISOS-L-2) and “damp heat” (ISOS-D-3) stressing, surpassing other state-of-the-art perovskite compositions. We determine that this enhancement is a consequence of the 2D precursor phase crystallisation route, which simultaneously avoids retention of residual low-volatility solvents (such as DMF and DMSO) and reduces the rate of degradation of FA+ in the material. Our findings highlight both the critical role of the initial crystallisation process in determining the operational stability of perovskite materials, and that neat FA+-based perovskites can be competitively stable despite the inherent metastability of the α-phase.