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How Halide Alloying Influences the Optoelectronic Quality in Tin-Halide Perovskite Solar Absorbers AITranslate

Center for Nano Science and Technology @PoliMi, Istituto Italiano di Tecnologia;Center for Nano Science and Technology @PoliMi, Istituto Italiano di Tecnologia; University of Naples Federico II;Center for Nano Science and Technology @PoliMi, Istituto Italiano di Tecnologia;Computational Laboratory for Hybrid/Organic Photovoltaics (CLHYO); University of Perugia; King Saud University; University of Naples Federico II; Italy|SKKU Institute of Energy Science and Technology (SIEST) Sungkyunkwan University; King Saud University
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Publisher: ACS
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Abstract AITranslate

Halide alloying in tin-based perovskites allows for photostable bandgap tuning between 1.3 and 2.2 eV. Here, we elucidate how the band edge energetics and associated defect activity impact the optoelectronic properties of this class of materials. We find that by increasing the bromide:iodide ratio, a simultaneous destabilization of acceptor defects (tin vacancies and iodine interstitials) and stabilization of donor defects (iodine vacancies and tin interstitials) occurs, with strong changes arising for Br contents exceeding 50%. This translates into a decreased doping which is, however, accompanied by a higher density of nonradiative recombination channels. Films with high Br content show a high degree of disorder and trap state densities, with the best optoelectronic quality being found for Br contents of around 33%. These observations match the open circuit voltage trend of tin-based mixed halide perovskite solar cells, supporting the relevance of optoelectronic properties and chemistry of defects to optimize wide-bandgap tin perovskite devices.

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DOI:https://doi.org/10.1021/acsenergylett.3c01241

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Citation Information:

Halide alloying in tin-based perovskites allows for photostable bandgap tuning between 1.3 and 2.2 eV. Here, we elucidate how the band edge energetics and associated defect activity impact the optoelectronic properties of this class of materials. We find that by increasing the bromide:iodide ratio, a simultaneous destabilization of acceptor defects (tin vacancies and iodine interstitials) and stabilization of donor defects (iodine vacancies and tin interstitials) occurs, with strong changes arising for Br contents exceeding 50%. This translates into a decreased doping which is, however, accompanied by a higher density of nonradiative recombination channels. Films with high Br content show a high degree of disorder and trap state densities, with the best optoelectronic quality being found for Br contents of around 33%. These observations match the open circuit voltage trend of tin-based mixed halide perovskite solar cells, supporting the relevance of optoelectronic properties and chemistry of defects to optimize wide-bandgap tin perovskite devices.

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GB/T 7714-2015 [1] Felix J. Berger, Isabella Poli, Ece Aktas, et al. ACS Energy Letters, 2023(8). DOI:10.1021/acsenergylett.3c01241.
MLA [1] Felix J. Berger, et al., ACS Energy Letters, no. 8, 2023, https://doi.org/10.1021/acsenergylett.3c01241.
APA [1] Felix J. Berger, Isabella Poli, Ece Aktas, Samuele Martani, Daniele Meggiolaro, Luca Gregori, Munirah D. Albaqami, Antonio Abate, Filippo De Angelis, & Annamaria Petrozza. (2023). ACS Energy Letters(8). https://doi.org/10.1021/acsenergylett.3c01241
IEEE [1] Felix J. Berger, Isabella Poli, Ece Aktas, Samuele Martani, Daniele Meggiolaro, Luca Gregori, Munirah D. Albaqami, Antonio Abate, Filippo De Angelis, and Annamaria Petrozza, ACS Energy Letters, no. 8, 2023, doi: 10.1021/acsenergylett.3c01241.