Heralded Spectroscopy of Highly Luminescent, confined CsPbI3 nanorods: synthesis, enhanced stability, anisotropic emission
DIPANWITA ROY a, Daniel Amgar a, Gur Lubin a, Dan Oron a
a Weizmann Institute of Science, Herzl St. 234, Rehovot, Israel
Proceedings of International Conference on Emerging Light Emitting Materials (EMLEM23)
Peyia, Cyprus, 2023 November 13th - 15th
Organizers: Grigorios Itskos, Maksym Kovalenko and Maryna Bodnarchuk
Poster, DIPANWITA ROY, 050
Publication date: 18th August 2023

Colloidal lead halide perovskite (LHP) nanocrystals (NCs) can be considered a promising class of quantum light emitter for the next generation of optoelectronic devices. Anisotropic shapes of LHP NCs play an important role in their optical properties. Thus, it is highly required to implement an in-depth study of structure and property correlations. There have been plenty of reports on the CsPbBr3 nanoplatelets (NPs), nanowires (NWs), and a few investigations on the CsPbBr3 NRs. Semiconductor NRs offer a linearly polarized light emission. Thus, the 1D anisotropy along with strong confinement make these structures interesting for further study.[1]

In this study, CsPbI3 NRs have been synthesized based on an improved chemical transformation method where the addition of water to Cs4PbI6 NCs induces transformation to CsPbI3 NRs with different controlled aspect ratios and photoluminescence quantum yields (PLQY) of up to 80%. Previously, the instability of NRs hampered their detailed study leaving a gap in the detailed discussion of geometry-specific optical properties. However, we have developed a synthesis scheme for strong confined CsPbI3 NRs with increasing stability that enables further structural and optical study.

NRs are known to emit linearly polarized light, indicating the existence of dipole moment along with the long axis of the NRs.[1] Optical anisotropy can originate both from the asymmetry of the crystal lattice, or the habit of the finite crystal. In this work, we wish to explore the emission anisotropy of inorganic LHP NRs using a newly developed approach that combines defocused imaging with heralded spectroscopy of single NRs.[2] For this we have used an innovative single photon avalanche diode (SPAD) array onto which the out-of-focus dipole emission pattern can be imaged, and resolved in time and space, allowing the direct observation and quantification of the difference between the emission transition dipole of the first and second excited states revealing multi-excitonic interactions in single perovskite NRs.[1-2]

The authors would like to thank Daniel for assisting with the measurements and characterization of the SPAD23 detector and Gur for the fruitful discussion and technical support in the SPAD23 system and Miri Kazes for assistance with supporting experiments.

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