| Autor: |
Kumar, Anand, Samaner, Çağlar, Cholsuk, Chanaprom, Matthes, Tjorben, Paçal, Serkan, Oyun, Yağız, Zand, Ashkan, Chapman, Robert J., Saerens, Grégoire, Grange, Rachel, Suwanna, Sujin, Ateş, Serkan, Vogl, Tobias |
| Rok vydání: |
2023 |
| Předmět: |
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| Zdroj: |
ACS Nano 18 (7), 5270-5281 (2024) |
| Druh dokumentu: |
Working Paper |
| DOI: |
10.1021/acsnano.3c08940 |
| Popis: |
Quantum emitters in solid-state crystals have recently attracted a lot of attention due to their simple applicability in optical quantum technologies. The polarization of single photons generated by quantum emitters is one of the key parameters that play a crucial role in the applications, such as quantum computation that uses the indistinguishability of photons. However, the degree of single photon polarization is typically quantified using time-averaged photoluminescence intensity of single emitters, which provides limited information about the dipole properties in solids. In this work, we use single defects in hexagonal boron nitride and nanodiamond as efficient room-temperature single photon sources to reveal the origin and the temporal evolution of dipole orientation in solid-state quantum emitters. The angle of excitation and emission dipoles relative to the crystal axes are determined experimentally and then calculated using density functional theory, which results in characteristic angles for every specific defect that can be used as an efficient tool for defect identification and understanding their atomic structure. Moreover, the temporal polarization dynamics reveal a strongly modified linear polarization visibility that depends on the excited state decay time of individual excitation. This effect can be traced back potentially to the excitation of excess charges in the local crystal environment. Understanding such hidden time-dependent mechanisms can further be used to improve the performance of polarization-sensitive experiments, in particular that of quantum communication with single photon emitters. |
| Databáze: |
arXiv |
| Externí odkaz: |
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