Polarization dynamics of solid-state quantum emitters

Fuente: arXiv
Saved in:
Bibliographic Details
Main Authors: 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
Format: Preprint
Published: 2023
Subjects:
Online Access:
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1866910437233131520
author 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
author_facet 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
contents 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.
format Preprint
id arxiv_https___arxiv_org_abs_2303_04732
institution arXiv
publishDate 2023
record_format arxiv
spellingShingle Polarization dynamics of solid-state quantum emitters
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
Quantum Physics
Mesoscale and Nanoscale Physics
Optics
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.
title Polarization dynamics of solid-state quantum emitters
topic Quantum Physics
Mesoscale and Nanoscale Physics
Optics
url https://arxiv.org/abs/2303.04732