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      Resonantly enhanced multiple exciton generation through below-band-gap multi-photon absorption in perovskite nanocrystals

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          Abstract

          Multi-photon absorption and multiple exciton generation represent two separate strategies for enhancing the conversion efficiency of light into usable electric power. Targeting below-band-gap and above-band-gap energies, respectively, to date these processes have only been demonstrated independently. Here we report the combined interaction of both nonlinear processes in CsPbBr 3 perovskite nanocrystals. We demonstrate nonlinear absorption over a wide range of below-band-gap excitation energies (0.5–0.8 E g). Interestingly, we discover high-order absorption processes, deviating from the typical two-photon absorption, at specific energetic positions. These energies are associated with a strong enhancement of the photoluminescence intensity by up to 10 5. The analysis of the corresponding energy levels reveals that the observed phenomena can be ascribed to the resonant creation of multiple excitons via the absorption of multiple below-band-gap photons. This effect may open new pathways for the efficient conversion of optical energy, potentially also in other semiconducting materials.

          Abstract

          The effects of the combined interplay of below-band-gap multi-photon absorption and multiple exciton generation have not been investigated. Here, the authors show the combined interaction of these processes in perovskite nanocrystals, leading to an enhanced interband photoluminescence emission under resonant conditions.

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          Most cited references26

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          Quantum Dot Solar Cells. Semiconductor Nanocrystals as Light Harvesters†

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            Highly efficient multiple exciton generation in colloidal PbSe and PbS quantum dots.

            We report ultra-efficient multiple exciton generation (MEG) for single photon absorption in colloidal PbSe and PbS quantum dots (QDs). We employ transient absorption spectroscopy and present measurement data acquired for both intraband as well as interband probe energies. Quantum yields of 300% indicate the creation, on average, of three excitons per absorbed photon for PbSe QDs at photon energies that are four times the QD energy gap. Results indicate that the threshold photon energy for MEG in QDs is twice the lowest exciton absorption energy. We find that the biexciton effect, which shifts the transition energy for absorption of a second photon, influences the early time transient absorption data and may contribute to a modulation observed when probing near the lowest interband transition. We present experimental and theoretical values of the size-dependent interband transition energies for PbSe QDs. We present experimental and theoretical values of the size-dependent interband transition energies for PbSe QDs, and we also introduce a new model for MEG based on the coherent superposition of multiple excitonic states.
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              Quantum Size Effect in Organometal Halide Perovskite Nanoplatelets.

              Organometal halide perovskites have recently emerged displaying a huge potential for not only photovoltaic, but also light emitting applications. Exploiting the optical properties of specifically tailored perovskite nanocrystals could greatly enhance the efficiency and functionality of applications based on this material. In this study, we investigate the quantum size effect in colloidal organometal halide perovskite nanoplatelets. By tuning the ratio of the organic cations used, we can control the thickness and consequently the photoluminescence emission of the platelets. Quantum mechanical calculations match well with the experimental values. We find that not only do the properties of the perovskite, but also those of the organic ligands play an important role. Stacking of nanoplatelets leads to the formation of minibands, further shifting the bandgap energies. In addition, we find a large exciton binding energy of up to several hundreds of meV for nanoplatelets thinner than three unit cells, partially counteracting the blueshift induced by quantum confinement. Understanding of the quantum size effects in perovskite nanoplatelets and the ability to tune them provide an additional method with which to manipulate the optical properties of organometal halide perovskites.
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                Author and article information

                Contributors
                Aurora.Manzi@physik.uni-muenchen.de
                feldmann@lmu.de
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                17 April 2018
                17 April 2018
                2018
                : 9
                : 1518
                Affiliations
                [1 ]ISNI 0000 0004 1936 973X, GRID grid.5252.0, Chair for Photonics and Optoelectronics, Department of Physics and Center for NanoScience (CeNS), , Ludwig-Maximilians-Universität, ; Amalienstr. 54, 80799 Munich, Germany
                [2 ]GRID grid.452665.6, Nanosystems Initiative Munich (NIM), ; Schellingstr. 4, 80799 Munich, Germany
                Author information
                http://orcid.org/0000-0002-9040-5719
                http://orcid.org/0000-0001-6168-2509
                http://orcid.org/0000-0002-9816-5596
                Article
                3965
                10.1038/s41467-018-03965-8
                5904181
                29666394
                e8f3bd6c-0fcf-4b22-abcb-a595aea0c3ac
                © The Author(s) 2018

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 28 August 2017
                : 22 March 2018
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