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Mechanochemical synthesis of stable, quantum-confined CsPbBr3 perovskite nanocrystals with blue-green emission and high PLQY
Author(s) -
Ankit Goyal,
Emmanouela Andrioti,
Yingying Tang,
Qian Zhao,
Kaibo Zheng,
Kateřina Dohnalova Newell,
Peter Schall
Publication year - 2022
Publication title -
journal of physics materials
Language(s) - English
Resource type - Journals
ISSN - 2515-7639
DOI - 10.1088/2515-7639/ac618f
Subject(s) - photoluminescence , quantum yield , materials science , perovskite (structure) , nanocrystal , quantum dot , halide , stokes shift , spectroscopy , optoelectronics , light emitting diode , luminescence , nanotechnology , optics , chemistry , physics , crystallography , inorganic chemistry , fluorescence , quantum mechanics
Cesium lead halides are a family of bright, visible-light emitting materials with near-unity photoluminescence quantum yield (PLQY) in nanocrystals (NCs). The usual way to achieve visible light-emission tunability is by mixing halides, which often leads to phase separation and poor stability. While the NCs should also show size-dependent PL emission, reports on strong quantum confinement in these materials are scarce. Here, we report the synthesis of quantum-confined cesium lead bromide (CsPbBr 3 ) NCs via a facile, environment-friendly, and scalable high-energy mechanochemical synthesis route. The PLQY measured is ∼85%, even after 90 days of synthesis, and the emission wavelength is shifted from green, 520 nm, to blue, 460 nm by quantum confinement in NCs of size 3–5 nm. Micro-PL optical spectroscopy and atomic force microscopy confirm the size tunability of PL on a single-dot scale. Our work demonstrates the potential of mechanochemical synthesis in the medium-scale production of bright luminescent quantum-confined NCs that could be extended to other materials as well.

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