4.6 Article

Fundamentals of tin iodide perovskites: a promising route to highly efficient, lead-free solar cells

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 9, Issue 19, Pages 11812-11826

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ta01573g

Keywords

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Funding

  1. Fondazione di Sardegna [2F20000210007]
  2. project PRIN 2017 TOPSPIN - Italian Ministry of University
  3. Deutsche Forschungsgemeinschaft (DFG) [408012143]
  4. Materials for Sustainability (Mat4Sus) program of The Netherlands Organization for Scientific Research (NWO) [739.017.005]
  5. Italian MIUR [PON04a2 00490]
  6. PRACE [2019204911]

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Hybrid tin-iodide perovskites are studied as a lead-free replacement for lead-iodide perovskites, and theoretical analysis reveals that they exhibit comparable or even superior photoconversion efficiency when compared to lead perovskites, especially in thick-layer limit. This is attributed to the smaller absorption cross section and smaller band gap of tin-based materials, which are very close to the ideal Shockley-Queisser limit. The rate of photoluminescence emission is found to be extremely sensitive to the absorption spectral weight at the band extrema, with different B-factors observed for different tin-based perovskites. Additionally, the impact of Urbach energy and hole doping on the properties of these materials is described in detail.
Hybrid tin-iodide perovskites are investigated as potential lead-free replacement of the lead-iodide perovskites; however, the intrinsic operational limit of these systems has not been described in detail, so far. In this work we combine advanced ab initio calculations with XRD and absorption measurements to lay out the fundamentals of formamidinium (FASnI(3)) and methylammonium (MASnI(3)) tin iodide perovskites, in comparison with the lead-halide MAPbI(3) prototype. Our theoretical analysis reveals that the tin-based materials display an intrinsic photoconversion efficiency on a par with the lead perovskites, and even superior in the thick-layer limit, where the theoretical PCE reaches 30.5% for lead-halides, and 32.3% for tin-halides under AM1.5G illumination; this is the result of two competing factors: a smaller absorption cross section at the onset for stannates, and their smaller band gap of 1.36 eV, thus very close to the ideal Shockley-Queisser limit. We found the rate of photoluminescence emission extremely sensitive to the absorption spectral weight at the band extrema, resulting in B-factor as different as 7.6 x 10(-9) s(-1) cm(3) for MASnI(3) and 0.4 x 10(-10) s(-1) cm(3) for FASnI(3). The additional impact of Urbach energy and hole doping, giving rise to large Burstein-Moss effect, is described in detail.

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