Room Temperature Optical Properties of Single Perovskite Quantum Dots
Gabriele Raino a b, Franziska Krieg a b, Maryna I. Bodnarchuk b, Maksym V. Kovalenko a b
a ETH Zurich, Laboratory of Inorganic Chemistry, Department of Chemistry & Applied Biosciences, Vladimir-Prelog-Weg, 1, Zürich, Switzerland
b Laboratory for Thin Films and Photovoltaics, Empa – Swiss Federal Laboratories for Materials Science and Technology, Dübendorf, Switzerland, Überland Strasse, 129, Dübendorf, Switzerland
Proceedings of Internet Conference for Quantum Dots (iCQD)
Online, Spain, 2020 July 14th - 17th
Organizers: Quinten Akkerman, Raffaella Buonsanti, Zeger Hens and Maksym Kovalenko
Invited Speaker, Gabriele Raino, presentation 008
Publication date: 3rd July 2020

 

Lead-halide perovskite APbX3 (A=Cs or organic cation; X=Cl, Br, I) nanocrystals (NCs) are subject of intense research due to their exceptional properties as both classical [1] and quantum light sources [2-4]. Many challenges often faced with this material class concern the long-term optical stability, a serious intrinsic issue connected with the labile and polar crystal structure of APbX3 compounds. When conducting spectroscopy at a single particle level, due to the highly enhanced contaminants (e.g., water molecules, oxygen) over NC ratio, deterioration of NC optical properties occurs within tens of seconds, with typically used excitation power densities (1-100 W/cm2), and in ambient conditions.

 

Here [5], we demonstrate that choosing a suitable polymer matrix is of paramount importance for obtaining stable spectra from a single NC and for suppressing the dynamic photoluminescence (PL) blueshift. In particular, polystyrene (PS), the most hydrophobic amongst four tested polymers, leads to the best optical stability, one-to-two orders of magnitude higher than that obtained with poly-(methyl methacrylate) (PMMA), a common polymeric encapsulant containing polar ester groups. Molecular mechanics simulations based on a force-field approximation corroborate the hypothesis that PS affords for a denser molecular packing at the NC surface. These findings underscore the often-neglected role of the sample preparation methodologies for the assessment of the optical properties of perovskite NCs at a single-particle level and guide the further design of robust single photon sources operating at room temperature. 

 

 

  

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