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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Gregori, Luca
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Publications (13/13 displayed)
- 2024Combining Trivalent Ion-Doping with Halide Alloying toIncrease the Efficiency of Tin Perovskitescitations
- 2024How Photogenerated I 2 Induces I-Rich Phase Formation in Lead Mixed Halide Perovskitescitations
- 2024Reaction Mechanism of Hydrogen Generation and Nitrogen Fixation at Carbon Nitride/Double Perovskite Heterojunctionscitations
- 2024How Photogenerated I2 Induces I-Rich Phase Formation in Lead Mixed Halide Perovskitescitations
- 2023Defect Engineering to Achieve Photostable Wide Bandgap Metal Halide Perovskitescitations
- 2023The Origin of Broad Emission in ⟨100⟩ Two-Dimensional Perovskites: Extrinsic vs Intrinsic Processes.
- 2023The Origin of Broad Emission in ⟨100⟩ Two-Dimensional Perovskites: Extrinsic vs Intrinsic Processes.
- 2023How Photogenerated I2 Induces I‐rich Phase Formation in Lead Mixed Halide Perovskitescitations
- 2023How Halide Alloying Influences the Optoelectronic Quality in Tin-Halide Perovskite Solar Absorberscitations
- 2022The Origin of Broad Emission in ⟨100⟩ Two-Dimensional Perovskites: Extrinsic vs Intrinsic Processes.
- 2022Role of Terminal Group Position in Triphenylamine-Based Self-Assembled Hole-Selective Molecules in Perovskite Solar Cellscitations
- 2022The Origin of Broad Emission in ⟨100⟩ Two-Dimensional Perovskites: Extrinsic vs Intrinsic Processescitations
- 2022The Origin of Broad Emission in ⟨100»Two-Dimensional Perovskites:Extrinsic vs Intrinsic Processescitations
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article
How Photogenerated I2 Induces I-Rich Phase Formation in Lead Mixed Halide Perovskites
Abstract
<p>Bandgap tunability of lead mixed halide perovskites (LMHPs) is a crucial characteristic for versatile optoelectronic applications. Nevertheless, LMHPs show the formation of iodide-rich (I-rich) phase under illumination, which destabilizes the semiconductor bandgap and impedes their exploitation. Here, it is shown that how I<sub>2</sub>, photogenerated upon charge carrier trapping at iodine interstitials in LMHPs, can promote the formation of I-rich phase. I<sub>2</sub> can react with bromide (Br<sup>−</sup>) in the perovskite to form a trihalide ion I<sub>2</sub>Br<sup>−</sup> (I<sup>δ−</sup>-I<sup>δ+</sup>-Br<sup>δ−</sup>), whose negatively charged iodide (I<sup>δ−</sup>) can further exchange with another lattice Br<sup>−</sup> to form the I-rich phase. Importantly, it is observed that the effectiveness of the process is dependent on the overall stability of the crystalline perovskite structure. Therefore, the bandgap instability in LMHPs is governed by two factors, i.e., the density of native defects leading to I<sub>2</sub> production and the Br<sup>−</sup> binding strength within the crystalline unit. Eventually, this study provides rules for the design of chemical composition in LMHPs to reach their full potential for optoelectronic devices.</p>