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      A 2B n–1 Pb n I 3 n+1 (A = BA, PEA; B = MA; n = 1, 2): Engineering Quantum-Well Crystals for High Mass Density and Fast Scintillators

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          Abstract

          Quantum-well (QW) hybrid organic–inorganic perovskite (HOIP) crystals, e.g., A 2PbX 4 (A = BA, PEA; X = Br, I), demonstrated significant potentials as scintillating materials for wide energy radiation detection compared to their individual three-dimensional (3D) counterparts, e.g., BPbX 3 (B = MA). Inserting 3D into QW structures resulted in new structures, namely A 2BPb 2X 7 perovskite crystals, and they may have promising optical and scintillation properties toward higher mass density and fast timing scintillators. In this article, we investigate the crystal structure as well as optical and scintillation properties of iodide-based QW HOIP crystals, A 2PbI 4 and A 2MAPb 2I 7. A 2PbI 4 crystals exhibit green and red emission with the fastest PL decay time <1 ns, while A 2MAPb 2I 7 crystals exhibit a high mass density of >3.0 g/cm 3 and tunable smaller bandgaps <2.1 eV resulting from quantum and dielectric confinement. We observe that A 2PbI 4 and PEA 2MAPb 2I 7 show emission under X- and γ-ray excitations. We further observe that some QW HOIP iodide scintillators exhibit shorter radiation absorption lengths (∼3 cm at 511 keV) and faster scintillation decay time components (∼0.5 ns) compared to those of QW HOIP bromide scintillators. Finally, we investigate the light yields of iodide-based QW HOIP crystals at 10 K (∼10 photons/keV), while at room temperature they still show pulse height spectra with light yields between 1 and 2 photons/keV, which is still >5 times lower than those for bromides. The lower light yields can be the drawbacks of iodide-based QW HOIP scintillators, but the promising high mass density and decay time results of our study can provide the right pathway for further improvements toward fast-timing applications.

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              Organometal halide perovskites as visible-light sensitizers for photovoltaic cells.

              Two organolead halide perovskite nanocrystals, CH(3)NH(3)PbBr(3) and CH(3)NH(3)PbI(3), were found to efficiently sensitize TiO(2) for visible-light conversion in photoelectrochemical cells. When self-assembled on mesoporous TiO(2) films, the nanocrystalline perovskites exhibit strong band-gap absorptions as semiconductors. The CH(3)NH(3)PbI(3)-based photocell with spectral sensitivity of up to 800 nm yielded a solar energy conversion efficiency of 3.8%. The CH(3)NH(3)PbBr(3)-based cell showed a high photovoltage of 0.96 V with an external quantum conversion efficiency of 65%.
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                Author and article information

                Journal
                J Phys Chem C Nanomater Interfaces
                J Phys Chem C Nanomater Interfaces
                jy
                jpccck
                The Journal of Physical Chemistry. C, Nanomaterials and Interfaces
                American Chemical Society
                1932-7447
                1932-7455
                26 April 2023
                08 June 2023
                : 127
                : 22
                : 10737-10747
                Affiliations
                []Łukasiewicz Research Network-PORT Polish Center for Technology Development , Stabłowicka 147, Wrocław 54-066, Poland
                []Research Group of Advanced Functional Materials and Research Center for Nanoscience and Nanotechnology, Institut Teknologi Bandung , Jl. Ganesha 10, Bandung 40132 Indonesia
                [§ ]Dipartimento di Fisica, Università di Milano-Bicocca , Milan 20126, Italy
                []CERN , Esplanade des Particules 1, 1211 Meyrin, Switzerland
                []Institute of Physics, Faculty of Physics, Astronomy, and Informatics, Nicolaus Copernicus University in Toruń , ul. Grudzia̧dzka 5, 87-100 Toruń, Poland
                [# ]School of Electrical and Electronic Engineering, Nanyang Technological University , Singapore 639798, Singapore
                [% ]Institut Lumière Matière, UMR5306, Université Claude Bernard Lyon1 and CNRS Lyon , 69622 Lyon, France
                [& ]Dipartimento di Chimica Industriale “Toso Montanari”, Università di Bologna , 40136 Bologna, Italy
                Author notes
                Author information
                https://orcid.org/0000-0001-5681-9953
                https://orcid.org/0000-0001-9424-0416
                https://orcid.org/0000-0002-8017-7847
                https://orcid.org/0000-0001-6282-8610
                https://orcid.org/0000-0001-7758-2326
                https://orcid.org/0000-0002-6207-4801
                https://orcid.org/0000-0002-0205-9837
                https://orcid.org/0000-0001-8623-9191
                https://orcid.org/0000-0002-9997-6841
                Article
                10.1021/acs.jpcc.3c00824
                10258843
                d41d5b2c-c2d1-4edd-9304-ceb722080437
                © 2023 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 06 February 2023
                : 17 April 2023
                Funding
                Funded by: H2020 European Research Council, doi 10.13039/100010663;
                Award ID: 101040681
                Funded by: Lukasiewicz Research Network-PORT, doi NA;
                Award ID: NA
                Funded by: Institut Teknologi Bandung, doi 10.13039/501100015689;
                Award ID: 308/IT1.B07.1/TA.00/2023
                Funded by: Ministry of Education - Singapore, doi 10.13039/501100001459;
                Award ID: RG149/19
                Categories
                Article
                Custom metadata
                jp3c00824
                jp3c00824

                Thin films & surfaces
                Thin films & surfaces

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