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The recombination mechanisms leading to amplified spontaneous emission at the true-green wavelength in CH3NH3PbBr3 perovskites
Author(s) -
Davide Priante,
İbrahim Dursun,
Mohd Sharizal Alias,
Dong Shi,
V.A. Melnikov,
Tien Khee Ng,
Omar F. Mohammed,
Osman M. Bakr,
Boon S. Ooi
Publication year - 2015
Publication title -
applied physics letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.182
H-Index - 442
eISSN - 1077-3118
pISSN - 0003-6951
DOI - 10.1063/1.4913463
Subject(s) - photoluminescence , spontaneous emission , wavelength , recombination , perovskite (structure) , excitation , radiative transfer , materials science , exciton , optoelectronics , spectral line , atomic physics , molecular physics , condensed matter physics , chemistry , optics , physics , laser , crystallography , biochemistry , quantum mechanics , astronomy , gene
We investigated the mechanisms of radiative recombination in a CH3NH3PbBr3 hybrid perovskite material using low-temperature, power-dependent (77K), and temperature-dependent photoluminescence (PL) measurements. Two bound-excitonic radiative transitions related to grain size inhomogeneity were identified. Both transitions led to PL spectra broadening as a result of concurrent blue and red shifts of these excitonic peaks. The red-shifted bound-excitonic peak dominated at high PL excitation led to a true-green wavelength of 553nm for CH3NH3PbBr3 powders that are encapsulated in polydimethylsiloxane. Amplified spontaneous emission was eventually achieved for an excitation threshold energy of approximately 350μJ/cm2. Our results provide a platform for potential extension towards a true-green light-emitting device for solid-state lighting and display applications

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