The first decade of colloidal perovskite quantum dots: Quo Vadis?
Maksym Kovalenko a b
a Swiss Federal Institute of Technology Zurich (ETH Zurich), 8093 Zurich, Switzerland
b Empa-Swiss Federal Laboratories for Materials Science and Technology, 8600 Dübendorf, Switzerland
Materials for Sustainable Development Conference (MATSUS)
Proceedings of MATSUS Spring 2025 Conference (MATSUSSpring25)
Photophysics of metal halide perovskites: from fundamentals to emerging applications - #PeroLight
Sevilla, Spain, 2025 March 3rd - 7th
Organizers: Ivan Scheblykin and Yana Vaynzof
Keynote, Maksym Kovalenko, presentation 672
DOI: https://doi.org/10.29363/nanoge.matsusspring.2025.672
Publication date: 16th December 2024

This year marks the first decade of colloidally synthesized lead halide perovskite quantum dots (LHP QDs), defining QDs as size- and shape-uniform ensembles with tunable quantum confinement and single-photon emission. Gradually, during this period, practically the entire compositional within a general formula APbX3 was thoroughly studied, with A being cesium (Cs), methylammonium (MA), formamidinium (FA), and azeridinium (AZ) was produced as high-quality nanocrystals. This journey is, arguably, at its very beginning. The LHP QDs are vastly different from conventional, more covalent semiconductors – they are ionic compounds with much lower formation energies, entropically stabilized, and structurally dynamic. The design of surface capping ligands turned out to be decisive for their stabilization at the nanoscale and for taming their photophysics. Currently, LHP NCs are prototyped as primary green emitters for television displays owing to facile and scalable production, higher emissivity-per-mass under blue excitation, and narrow emission linewidth. Their excitonic characteristics exceed initial expectations in many regards, opening opportunities as quantum light sources. In particular, at cryogenic temperatures, LHP QDs exhibit long excitonic coherence times, which start to match the fast sub-100 ps radiative rates. Both characteristics are optimized, to our surprise, in larger CsPbX3 QDs beyond the quantum confinement, namely, 20-40 nm, owing to the single-photon superradiance effect (giant oscillator strength at the single-exciton per NC regime). Single-component and multicomponent QD superlattices exhibit collective emission, known as superfluorescence, characterized by the oscillating, ultrafast (10-30 ps) radiative decays. This presentation will walk you through both the most essential progress over this first decade, including our current work, and outline future prospects.

© FUNDACIO DE LA COMUNITAT VALENCIANA SCITO
We use our own and third party cookies for analysing and measuring usage of our website to improve our services. If you continue browsing, we consider accepting its use. You can check our Cookies Policy in which you will also find how to configure your web browser for the use of cookies. More info