Gabriele Raino1,2,Nuri Yazdani3,Simon Böhme1,2,Chenglian Zhu1,2,Marta Rossell2,Rolf Erni2,Vanessa Wood3,Ivan Infante4,Maksym Kovalenko1,2
ETH Zurich1,Empa–Swiss Federal Laboratories for Materials Science and Technology2,ETH Zürich3,Istituto Italiano di Tecnologia4
Gabriele Raino1,2,Nuri Yazdani3,Simon Böhme1,2,Chenglian Zhu1,2,Marta Rossell2,Rolf Erni2,Vanessa Wood3,Ivan Infante4,Maksym Kovalenko1,2
ETH Zurich1,Empa–Swiss Federal Laboratories for Materials Science and Technology2,ETH Zürich3,Istituto Italiano di Tecnologia4
Semiconductor quantum dots (QDs) have long been considered artificial atoms, but despite the overarching analogies in the strong energy-level quantization and the single-photon emission capability, their emission spectrum is far broader than typical atomic emission lines. Here,<sup>1</sup> by using ab-initio molecular dynamics for simulating exciton-surface phonon interactions in structurally dynamic CsPbBr<sub>3</sub> QDs, followed by single quantum dot optical spectroscopy, we demonstrate that emission line-broadening in these quantum dots is primarily governed by the coupling of excitons to low-energy surface phonons. Mild adjustments of the surface chemical composition allow for attaining much smaller emission linewidths of 35 - 65 meV (vs. initial values of 70-120 meV), which are on par with the best values known for structurally rigid, colloidal II-VI quantum dots (20 - 60 meV).<br/>Ultra-narrow emission at room temperature is desired for conventional light-emitting devices and paramount for emerging quantum light sources.<br/><br/><b>Reference</b><br/>[1] Rainò, G. et al., Nat. Commun. 13, 2587 (2022).<br/>https://doi.org/10.1038/s41467-022-30016-0