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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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Bouchez, Guillaume
CentraleSupélec
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Topics
Publications (7/7 displayed)
- 2018Hybrid halide perovskites: a new semiconductor for photovoltaics and light emission
- 2018Experimental determination of fire degradation kinetic for an aeronautical polymer composite materialcitations
- 2017Excitonic Emission and Electron-Phonon coupling in Organic-Inorganic Lead Iodide Perovskite single crystals
- 2017Excitonic Emission and Electron-Phonon coupling in Organic-Inorganic Lead Iodide Perovskite single crystals
- 2016Optical properties of 3D hybrid organic perovskites monocrystals
- 2016Narrow Linewidth Excitonic Emission in Organic-Inorganic Lead Iodide Perovskite Single Crystalscitations
- 2016Excitonic Emission in Organic-Inorganic Lead Iodide Perovskite single crystals
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article
Narrow Linewidth Excitonic Emission in Organic-Inorganic Lead Iodide Perovskite Single Crystals
Abstract
International audience ; Hybrid perovskite thin films have demonstrated impressive performance for solar energy conversion and optoelectronic applications. However, further progress will benefit from a better knowledge of the intrinsic photophysics of materials. Here, the temperature-dependent emission properties of CH3NH3PbI3 single crystals are investigated and compared to those of thin polycrystalline films by means of steady-state and time-resolved photoluminescence spectroscopy. Single crystals photoluminescence present a sharp excitonic emission at high energy, with full width at half maximum of only 5 meV, assigned to free excitonic recombination. We highlight a strong thermal broadening of the free excitonic emission, due to exciton–LO-phonon coupling. The emission turned to be very short-lived with a subnanosecond dynamics, mainly induced by the fast trapping of the excitons. The free excitonic emission is completely absent of the thin film spectra, which are dominated by trap state bands.