Colloidal 2D PbX (X = S, Se, Te) nanocrystals are innovative materials pushing the boundaries of quantum confinement by combining crystal thicknesses down to a monolayer with additional confinement in the lateral dimension. These flat PbSe quantum dots (fQDs) exhibit telecommunication band photoluminescence (1.43–0.83 eV), which is highly interesting for fiber optic information processing. With scanning tunneling microscopy/spectroscopy (STM/STS), we probe single-layer-defined fQD populations down to one monolayer, showing an in-gap state free QD-like density of states in excellent agreement with theoretical tight-binding (TB) calculations. Cryogenic ensemble spectra match STS/STM and TB calculations and exhibit the contribution of mono-, bi-, and trilayers to the photoluminescence. Comparing the electronic band gaps with the optical ones, we derive exciton binding energies as high as 600 meV for PbSe monolayers. Our results allow for a target-oriented synthesis of a new class of QDs with record binding energies and precisely tailored optical properties at technologically relevant wavelengths.

Mechanisms by which excitons and charge carriers can funnel and recombine in 2D multi-layered MAPbBr3 Ruddlesden-Popper perovskite nanosheets are missing. This femtosecond transient absorption spectr...