Origin of the Enhanced Photoluminescence Quantum Yield in MAPbBr3 Perovskite with Reduced Crystal Size AITranslate
Abstract AITranslate
Methylammonium lead bromide perovskite (MAPbBr3) has been widely investigated for applications in visible perovskite light-emitting diodes (LEDs). Fine-tuning of the morphology and of the crystal size, from the microscale down to the quantum confinement regime, has been used to increase the photoluminescence quantum yield (PLQY). However, the physical processes underlying the PL emission of this perovskite remain unclear. Here, we elucidate the origin of the PL emission of polycrystalline MAPbBr3 thin films by different spectroscopic techniques. We estimate the exciton binding energy, the reduced exciton effective mass, and the trap density. Moreover, we confirm the coexistence of free carriers and excitons, quantifying their relative population and mutual interaction over a broad range of excitation densities. Finally, the enhanced PLQY upon crystal size reduction to the micro- and nanometer scale in the presence of additives is attributed to favored excitonic recombination together with reduced surface trapping thanks to efficient passivation by the additives.
KeyWords AITranslate
Basic Information:
DOI:https://doi.org/10.1021/acsenergylett.8b00475
Chinese Library Classification Number:
Citation Information:
Methylammonium lead bromide perovskite (MAPbBr3) has been widely investigated for applications in visible perovskite light-emitting diodes (LEDs). Fine-tuning of the morphology and of the crystal size, from the microscale down to the quantum confinement regime, has been used to increase the photoluminescence quantum yield (PLQY). However, the physical processes underlying the PL emission of this perovskite remain unclear. Here, we elucidate the origin of the PL emission of polycrystalline MAPbBr3 thin films by different spectroscopic techniques. We estimate the exciton binding energy, the reduced exciton effective mass, and the trap density. Moreover, we confirm the coexistence of free carriers and excitons, quantifying their relative population and mutual interaction over a broad range of excitation densities. Finally, the enhanced PLQY upon crystal size reduction to the micro- and nanometer scale in the presence of additives is attributed to favored excitonic recombination together with reduced surface trapping thanks to efficient passivation by the additives.
quote
| GB/T 7714-2015 | [1] Nikolaos Droseros, Giulia Longo, Jan C. Brauer, et al. ACS Energy Letters, 2018(3). DOI:10.1021/acsenergylett.8b00475. |
| MLA | [1] Nikolaos Droseros, et al., ACS Energy Letters, no. 3, 2018, https://doi.org/10.1021/acsenergylett.8b00475. |
| APA | [1] Nikolaos Droseros, Giulia Longo, Jan C. Brauer, Michele Sessolo, Henk J. Bolink, & Natalie Banerji. (2018). ACS Energy Letters(3). https://doi.org/10.1021/acsenergylett.8b00475 |
| IEEE | [1] Nikolaos Droseros, Giulia Longo, Jan C. Brauer, Michele Sessolo, Henk J. Bolink, and Natalie Banerji, ACS Energy Letters, no. 3, 2018, doi: 10.1021/acsenergylett.8b00475. |
