Intrinsic Lead Ion Emissions in Zero-Dimensional Cs4PbBr6 Nanocrystals
Mohammed, Omar F.
KAUST DepartmentChemical Science Program
Functional Nanomaterials Lab (FuNL)
KAUST Catalysis Center (KCC)
KAUST Solar Center (KSC)
Material Science and Engineering Program
Physical Science and Engineering (PSE) Division
Ultrafast Laser Spectroscopy and Four-dimensional Electron Imaging Research Group
Online Publication Date2017-11-15
Print Publication Date2017-12-08
Permanent link to this recordhttp://hdl.handle.net/10754/626646
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AbstractWe investigate the intrinsic lead ion (Pb2+) emissions in zero-dimensional (0D) perovskite nanocrystals (NCs) using a combination of experimental and theoretical approaches. The temperature-dependent photoluminescence experiments for both “nonemissive” (highly suppressed green emission) and emissive (bright green emission) Cs4PbBr6 NCs show a splitting of emission spectra into high- and low-energy transitions in the ultraviolet (UV) spectral range. In the nonemissive case, we attribute the high-energy UV emission at approximately 350 nm to the allowed optical transition of 3P1 to 1S0 in Pb2+ ions and the low-energy UV emission at approximately 400 nm to the charge-transfer state involved in the 0D NC host lattice (D-state). In the emissive Cs4PbBr6 NCs, in addition to the broad UV emission, we demonstrate that energy transfer occurs from Pb2+ ions to green luminescent centers. The optical phonon modes in Cs4PbBr6 NCs can be assigned to both Pb–Br stretching and rocking motions from density functional theory calculations. Our results address the origin of the dual broadband Pb2+ ion emissions observed in Cs4PbBr6 NCs and provide insights into the mechanism of ionic exciton–optical phonon interactions in these 0D perovskites.
CitationYin J, Zhang Y, Bruno A, Soci C, Bakr OM, et al. (2017) Intrinsic Lead Ion Emissions in Zero-Dimensional Cs4PbBr6 Nanocrystals. ACS Energy Letters 2: 2805–2811. Available: http://dx.doi.org/10.1021/acsenergylett.7b01026.
SponsorsThis work was supported by the King Abdullah University of Science and Technology (KAUST). We acknowledge the IT Research Computing Team and Supercomputing Laboratory at KAUST for their computational and storage resources, as well as their gracious assistance. The work at Georgia Tech has been supported by the Office of Naval Research (Award No. N00014-17-1-2208). C.S. and A.B. acknowledge support from the Ministry of Education (Grant No. MOE2016-T1-1-164) and the National Research Foundation (Grant No. NRF-CRP14-2014-03) of Singapore. We also thank Haoze Yang for assistance in sample preparation and absorption spectra measurements.
PublisherAmerican Chemical Society (ACS)
JournalACS Energy Letters