Tuning perovskite nanocrystal superlattices for superradiance in the presence of disorder

Author:

Nguyen T. P. Tan1ORCID,Tan Liang Z.2ORCID,Baranov Dmitry3ORCID

Affiliation:

1. M2I Formation, Sophia Antipolis 1 , Mougins 06250, France

2. Molecular Foundry, Lawrence Berkeley National Laboratory 2 , Berkeley, California 94720, USA

3. Division of Chemical Physics, Department of Chemistry, Lund University 3 , P.O. Box, 124, SE-221 00 Lund, Sweden

Abstract

The cooperative emission of interacting nanocrystals is an exciting topic fueled by recent reports of superfluorescence and superradiance in assemblies of perovskite nanocubes. Several studies estimated that coherent coupling is localized to a small fraction of nanocrystals (10−7–10−3) within the assembly, raising questions about the origins of localization and ways to overcome it. In this work, we examine single-excitation superradiance by calculating radiative decays and the distribution of superradiant wave function in two-dimensional CsPbBr3 nanocube superlattices. The calculations reveal that the energy disorder caused by size distribution and large interparticle separations reduces radiative coupling and leads to the excitation localization, with the energy disorder being the dominant factor. The single-excitation model clearly predicts that, in the pursuit of cooperative effects, having identical nanocubes in the superlattice is more important than achieving a perfect spatial order. The monolayers of large CsPbBr3 nanocubes (LNC = 10–20 nm) are proposed as model systems for experimental tests of superradiance under conditions of non-negligible size dispersion, while small nanocubes (LNC = 5–10 nm) are preferred for realizing the Dicke state under ideal conditions.

Funder

Office of Science

European Research Council

Publisher

AIP Publishing

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

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