This work demonstrates anisotropic exciton transport in a nanocrystal superlattice, suggesting new energy engineering possibilities.
Colloidal self-assembly is one strategy for engineering anisotropic properties into otherwise isotropic materials. In this work, we demonstrate anisotropic exciton transport in an A₂B-type superlattice containing columns of 5.3 nm CsPbBr₃ nanocubes assembled into a hexagonal lattice around 6.5 nm LaF₃ nanodisks. Using transient photoluminescence microscopy, we determined that the exciton diffusivity along the fast axis of the superlattice is more than twice as large as that along the slow axis at T = 5 K, but that anisotropy is greatly suppressed at room temperature. Calculations of the diffusivity anisotropy ratio based on Förster theory overestimate the measured values, highlighting the limitations of this theory in completely describing exciton transport. Overall, our results demonstrate how self-assembly of colloidal nanocrystals can be used to engineer directional energy transport, and raise more questions about the microscopic nature of dipole coupling in CsPbBr₃ NC superlattices.
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Sheehan et al. (2026) studied this question.
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