Abstract
Semiconductor nanocrystal emission polarization is a crucial probe of nanocrystal physics and an essential factor for nanocrystal-based technologies. While the transition dipole moment for the lowest excited state to ground state transition is well characterized, the dipole moment of higher multiexcitonic transitions is inaccessible via most spectroscopy techniques. Here, we realize direct characterization of the doubly excited-state relaxation transition dipole by heralded defocused imaging. Defocused imaging maps the dipole emission pattern onto a fast single-photon avalanche diode detector array, allowing the postselection of photon pairs emitted from the biexciton-exciton emission cascade and resolving the differences in transition dipole moments. Type-I1/2 seeded nanorods exhibit higher anisotropy of the biexciton-to-exciton transition compared to the exciton-to-ground state transition. In contrast, type-II seeded nanorods display a reduction of biexciton emission anisotropy. These findings are rationalized in terms of an interplay between the transient dynamics of the refractive index and the excitonic fine structure.
Original language | English |
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Pages (from-to) | 5417-5423 |
Number of pages | 7 |
Journal | Nano Letters |
Volume | 23 |
Issue number | 12 |
DOIs | |
Publication status | Published - 28 Jun 2023 |
Bibliographical note
Publisher Copyright:© 2023 The Authors. Published by American Chemical Society.
Funding
This research was supported by the Israel Science Foundation (ISF), and the Directorate for Defense Research and Development (DDR&D), Grant No. 3415/21. D.A. gratefully acknowledges support by the VATAT Fellowship for female PhD students in Physics/Math and Computer Science. D.O. is the incumbent of the Harry Weinrebe professorial chair of laser physics.
Funders | Funder number |
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Directorate for Defense Research and Development | 3415/21 |
VATAT | |
Israel Science Foundation |
Keywords
- biexciton
- emission anisotropy
- emission transition dipole
- Heralded Spectroscopy
- single-particle spectroscopy
- SPAD arrays