Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

Single quantum emitters: resonance fluorescence and emission enhancement

Samuele Grandi

Published Apr 1, 2017• 2 citations
Publisher

Abstract

Single photons are highly desirable for encoding, sending and processing quantum information. Suitable engineering of single quantum emitters and their environment can lead to a reliable single photon source and to mediated photon-photon interactions, essential assets for quantum communication and computation purposes. Dye molecules, our chosen single quantum emitter, have attracted much attention in recent years due to their high photostability and narrow emission lines. In this thesis I present a detailed analysis of the optical properties of single dibenzoterrylene molecules in an anthracene matrix. Single photon emission is demonstrated at room and cryogenic temperatures. In the latter case, an analysis of the second-order correlation function of the emission of a single molecule is studied at various temperatures. The data agree with a full solution of the optical Bloch equations over a wide range of temperature, and provide some insight into the dephasing process of the molecules. I then present a technique for integrating single dye molecules with nano-photonic devices. These are hybrid plasmonic waveguides, designed to guide light and to enhance the interaction with a single emitter by a tight confinement of the waveguide mode. Single molecules are deposited over the waveguides and a first evidence of coupling is presented. I conclude with proposed improvements to the optical setup and to the deposition methods. Finally, I present another type of integrated device, where the light matter interaction is enhanced by inserting single quantum emitters into coupled optical resonators. The theoretical description for the case of resonant two-photon absorption from single atoms in coupled photonic crystal cavities is developed. I conclude by proposing a possible realisation of this system, and describing the first steps towards the fabrication of such a device.

DOI
10.25560/48463

Related papers

Photostable molecules on chip: integrated single photon sources for quantum technologies (Conference Presentation)

Costanza Toninelli, Pietro Lombardi, Anna P. Ovvyan +8 more

Efficient quantum light sources and non-linear optical elements at the few photon level are the basic ingredients for most applications in nano and quantum technologies. On the other hand, a scalable platform for quantum ICT typically requires reliable light matter interfaces and on-chip integration. In this work we demonstrate the potential of a novel hybrid technology which combines single organic molecules as quantum emitters and dielectric chips [1]. Dibenzoterrylene molecules in anthracene crystals (DBT:Ac) are particularly suitable quantum systems for this task, since they exhibit long-term photostability in thin samples [2], easy fabrication methods and life-time limited emission at cryogenic temperatures [3]. We demonstrate at room temperature the emission of single photons from DBT molecules into ridge waveguides with a branching ratio up to 40%. The overall single-photon source efficiency, including emission into the guided mode, propagation losses, and emission into a quasi-gaussian mode in free space, is estimated around 16%. These results are competitive with state-of-the-art single photon emission into propagating guided modes from solid state systems [4], while offering a novel platform with unprecedented versatility. References [1] P. Lombardi et al., Arxiv: 1701.00459v1 (2017). [2] C. Toninelli et al., Opt. Express 18, 6577 (2010). [3] A. A. L. Nicolet et al., ChemPhysChem 8, 1929 (2007). [4] I. Zadeh et al., Nano Lett. 16, 2289 (2016); R. S. Daveau et al., Arxiv: 1610.08670v1 (2016). [5] J. Hwang et. al., New J. Phys. 13, 085009 (2011); H.-W. Lee et al., Phys. Rev. A 63, 012305 (2000).

Quantum Photonic Devices•Oct 3, 2017•0 citations

Preparation and testing of organic dye molecules as single photon sources on a chip

Claudio Polisseni

The physical realisation of a photonic quantum computer requires a reliable, fast, ondemand source of single indistinguishable photons. A promising candidate for one of these sources is a single dye molecule in a solid state matrix placed within the evanescent field of a photonic waveguide. This thesis explores the possibility of coupling of single dibenzoterrylene (DBT) molecules in an anthracene matrix to a silicon nitride waveguide at room temperature. I first discuss the theory by which photons from a DBT molecule can be evanescently coupled to a ridge waveguide. I present a novel growth method to form DBT-doped anthracene crystals which is very promising for applications to photonic devices. I discuss the methodology and the theory of such growth. I describe the confocal microscope I developed and used to image and characterise the emission of the single DBT molecules embedded in these crystals. My measurements show that the molecules are extremely stable single quantum emitters with a well-de ned polarization relative to the crystal axes. Measurements of the saturation intensity at room temperature allow me to estimate that a single DBT molecule could deliver at least 1012 photons before bleaching. This method of growth was used to deposit DBT molecules on top of a silicon nitride ridge waveguide. The results of the coupling experiment are shown. These include confocal images, saturation and lifetime measurements. The coupling efficiency is calculated and compared to what was simulated. The challenges of such structures are then presented. To tackle these challenges I deposited the molecules on top of lithium niobate and in silicon nitride slots. I conclude with a proposal for constructing the best photonic structure which would guarantee an easy deposition of the molecules and high coupling efficiencies.

•Jun 1, 2017•0 citations

Organic molecules as single-photon sources

Alexey Shkarin, Stephan Götzinger

The development of single-photon sources has been nothing but rapid in recent years, with quantum emitter-based systems showing especially impressive progress. In this article, we give an overview of the developments in single-photon sources based on single molecules. We will introduce polycyclic hydrocarbons as the most commonly used emitter systems for the realization of an organic solid-state single-photon source. At cryogenic temperatures this special class of fluorescent molecules demonstrates remarkable optical properties such as negligible dephasing, indefinite photostability, and high photon rates, which make them attractive as fundamental building blocks in emerging quantum technologies. To better understand the general properties and limitations of these molecules, we discuss sample preparation and relevant emitter parameters such as absorption and emission spectra, lifetime, and dephasing. We will also give an overview of light extraction strategies as a crucial part of a single-photon source. Finally, we conclude with a look into the future, displaying current challenges and possible solutions.

quant-pharXiv:2602.17428•Feb 20, 2026

Coherent Coupling of Single Molecules to Microresonators

Alexey Shkarin, Dominik Rattenbacher, Jan Renger +3 more

Many interesting proposals in quantum optics and light-matter interaction rely on having multiple quantum emitters well-coupled to a single mode of light. Of particular interest are cases where several identical emitters couple to a one-dimensional (1D) photonic medium. Recently, we presented such a system by evanescent coupling of organic dye molecules to the same guided mode of an on-chip subwavelength waveguide [1]. While this coupling allowed us to demonstrate up to 7.5% transmission extinction of the propagating light by a single molecule, it is still not sufficient for achieving higher-order effects such as photon-mediated interaction of multiple emitters coupled to the same waveguide.

Conference on Lasers and Electro-Optics Europe & European Quantum Electronics Conference (CLEO/Europe-EQEC)•Jun 1, 2019•0 citations

Photostable molecules on chip: Integrated single photon sources for quantum technologies

Pietro Lombardi, Anna P. Ovvyan, Sofia Pazzagli +8 more

Summary form only given. Efficient quantum light sources and non-linear optical elements at the few photon level are the basic ingredients for most applications in nano and quantum technologies. On the other hand, a scalable platform for quantum information and communication typically requires reliable light matter interfaces and on-chip integration. In this work we demonstrate the potential of a novel hybrid technology which combines single organic molecules as quantum emitters and dielectric chips, consisting of ridge waveguides and grating far-field couplers [1].Here the emitters are integrated by spin-coating onto the photonic chip. We demonstrate at room temperature the emission of single photons from DBT molecules into ridge waveguides with a branching ratio up to 40%. The overall single-photon source efficiency, including emission into the guided mode, propagation losses, and emission into a quasi-gaussian mode in free space, is estimated around 16%. These results are competitive with state-of-the-art single photon emission into propagating guided modes from solid state systems [4], while offering a novel platform with unprecedented versatility. Single waveguided photons can be readily processed on-chip or efficiently extracted into a quasi-gaussian mode in free space. We also discuss options to further improve the collection efficiency and applications to quantum optics [5] and to study manybody-induced quantum correlation effects [6].

arXiv:1701.00459•Conference on Lasers and Electro-Optics Europe & European Quantum Electronics Conference (CLEO/Europe-EQEC)•Jun 1, 2017•1 citation

A bright single photon source: Strong coupling of a single molecule to a plasmonic nano-antenna cavity

Raúl Izquierdo López

Single photon emitters are quantum light sources that can enable a variety of quantum based technologies such as quantum information or quantum random number generation, among others. These single photon emitters can have their brightness increased by coupling to a plasmonic cavity. In this work, this possibility is addressed by spin coating anthracene crystals hosting dibenzoterrylene (DBT) molecules on top of Au dipolar nanoantenna arrays. Thin anthracene crystals covering a big fraction of the nanoantenna arrays were achieved, on which confocal fluorescence microscopy and time correlated single photon counting have been used to characterize the emitters. A time gating based analysis has been used to separate the nanoantenna luminescence from the fluorescence of the DBT molecules, obtaining lifetime values from coupled and uncoupled molecules. A set of 149 coupled molecules and 158 uncoupled molecules was represented in a histogram, showing a distribution from whose mean values the lifetime of DBT molecules (t=4.37 ns) was acquired, as well as a mean lifetime reduction of 2.4 times and a maximum lifetime reduction of 7 times.

•Jul 23, 2019•0 citations
Single photons are highly desirable for encoding, sending and processing quantum information. Suitable engineering of single quantum emitters and their environment can lead to a reliable single photon source and to mediated photon-photon interactions, essential assets for quantum communication and computation purposes. Dye molecules, our chosen single quantum emitter, have attracted much attention in recent years due to their high photostability and narrow emission lines. In this thesis I present a detailed analysis of the optical properties of single dibenzoterrylene molecules in an anthracene matrix. Single photon emission is demonstrated at room and cryogenic temperatures. In the latter case, an analysis of the second-order correlation function of the emission of a single molecule is studied at various temperatures. The data agree with a full solution of the optical Bloch equations over a wide range of temperature, and provide some insight into the dephasing process of the molecules. I then present a technique for integrating single dye molecules with nano-photonic devices. These are hybrid plasmonic waveguides, designed to guide light and to enhance the interaction with a single emitter by a tight confinement of the waveguide mode. Single molecules are deposited over the waveguides and a first evidence of coupling is presented. I conclude with proposed improvements to the optical setup and to the deposition methods. Finally, I present another type of integrated device, where the light matter interaction is enhanced by inserting single quantum emitters into coupled optical resonators. The theoretical description for the case of resonant two-photon absorption from single atoms in coupled photonic crystal cavities is developed. I conclude by proposing a possible realisation of this system, and describing the first steps towards the fabrication of such a device.
Efficient quantum light sources and non-linear optical elements at the few photon level are the basic ingredients for most applications in nano and quantum technologies. On the other hand, a scalable platform for quantum ICT typically requires reliable light matter interfaces and on-chip integration. In this work we demonstrate the potential of a novel hybrid technology which combines single organic molecules as quantum emitters and dielectric chips [1]. Dibenzoterrylene molecules in anthracene crystals (DBT:Ac) are particularly suitable quantum systems for this task, since they exhibit long-term photostability in thin samples [2], easy fabrication methods and life-time limited emission at cryogenic temperatures [3]. We demonstrate at room temperature the emission of single photons from DBT molecules into ridge waveguides with a branching ratio up to 40%. The overall single-photon source efficiency, including emission into the guided mode, propagation losses, and emission into a quasi-gaussian mode in free space, is estimated around 16%. These results are competitive with state-of-the-art single photon emission into propagating guided modes from solid state systems [4], while offering a novel platform with unprecedented versatility. References [1] P. Lombardi et al., Arxiv: 1701.00459v1 (2017). [2] C. Toninelli et al., Opt. Express 18, 6577 (2010). [3] A. A. L. Nicolet et al., ChemPhysChem 8, 1929 (2007). [4] I. Zadeh et al., Nano Lett. 16, 2289 (2016); R. S. Daveau et al., Arxiv: 1610.08670v1 (2016). [5] J. Hwang et. al., New J. Phys. 13, 085009 (2011); H.-W. Lee et al., Phys. Rev. A 63, 012305 (2000).
The physical realisation of a photonic quantum computer requires a reliable, fast, ondemand source of single indistinguishable photons. A promising candidate for one of these sources is a single dye molecule in a solid state matrix placed within the evanescent field of a photonic waveguide. This thesis explores the possibility of coupling of single dibenzoterrylene (DBT) molecules in an anthracene matrix to a silicon nitride waveguide at room temperature. I first discuss the theory by which photons from a DBT molecule can be evanescently coupled to a ridge waveguide. I present a novel growth method to form DBT-doped anthracene crystals which is very promising for applications to photonic devices. I discuss the methodology and the theory of such growth. I describe the confocal microscope I developed and used to image and characterise the emission of the single DBT molecules embedded in these crystals. My measurements show that the molecules are extremely stable single quantum emitters with a well-de ned polarization relative to the crystal axes. Measurements of the saturation intensity at room temperature allow me to estimate that a single DBT molecule could deliver at least 1012 photons before bleaching. This method of growth was used to deposit DBT molecules on top of a silicon nitride ridge waveguide. The results of the coupling experiment are shown. These include confocal images, saturation and lifetime measurements. The coupling efficiency is calculated and compared to what was simulated. The challenges of such structures are then presented. To tackle these challenges I deposited the molecules on top of lithium niobate and in silicon nitride slots. I conclude with a proposal for constructing the best photonic structure which would guarantee an easy deposition of the molecules and high coupling efficiencies.
The development of single-photon sources has been nothing but rapid in recent years, with quantum emitter-based systems showing especially impressive progress. In this article, we give an overview of the developments in single-photon sources based on single molecules. We will introduce polycyclic hydrocarbons as the most commonly used emitter systems for the realization of an organic solid-state single-photon source. At cryogenic temperatures this special class of fluorescent molecules demonstrates remarkable optical properties such as negligible dephasing, indefinite photostability, and high photon rates, which make them attractive as fundamental building blocks in emerging quantum technologies. To better understand the general properties and limitations of these molecules, we discuss sample preparation and relevant emitter parameters such as absorption and emission spectra, lifetime, and dephasing. We will also give an overview of light extraction strategies as a crucial part of a single-photon source. Finally, we conclude with a look into the future, displaying current challenges and possible solutions.
Many interesting proposals in quantum optics and light-matter interaction rely on having multiple quantum emitters well-coupled to a single mode of light. Of particular interest are cases where several identical emitters couple to a one-dimensional (1D) photonic medium. Recently, we presented such a system by evanescent coupling of organic dye molecules to the same guided mode of an on-chip subwavelength waveguide [1]. While this coupling allowed us to demonstrate up to 7.5% transmission extinction of the propagating light by a single molecule, it is still not sufficient for achieving higher-order effects such as photon-mediated interaction of multiple emitters coupled to the same waveguide.
Summary form only given. Efficient quantum light sources and non-linear optical elements at the few photon level are the basic ingredients for most applications in nano and quantum technologies. On the other hand, a scalable platform for quantum information and communication typically requires reliable light matter interfaces and on-chip integration. In this work we demonstrate the potential of a novel hybrid technology which combines single organic molecules as quantum emitters and dielectric chips, consisting of ridge waveguides and grating far-field couplers [1].Here the emitters are integrated by spin-coating onto the photonic chip. We demonstrate at room temperature the emission of single photons from DBT molecules into ridge waveguides with a branching ratio up to 40%. The overall single-photon source efficiency, including emission into the guided mode, propagation losses, and emission into a quasi-gaussian mode in free space, is estimated around 16%. These results are competitive with state-of-the-art single photon emission into propagating guided modes from solid state systems [4], while offering a novel platform with unprecedented versatility. Single waveguided photons can be readily processed on-chip or efficiently extracted into a quasi-gaussian mode in free space. We also discuss options to further improve the collection efficiency and applications to quantum optics [5] and to study manybody-induced quantum correlation effects [6].
Single photon emitters are quantum light sources that can enable a variety of quantum based technologies such as quantum information or quantum random number generation, among others. These single photon emitters can have their brightness increased by coupling to a plasmonic cavity. In this work, this possibility is addressed by spin coating anthracene crystals hosting dibenzoterrylene (DBT) molecules on top of Au dipolar nanoantenna arrays. Thin anthracene crystals covering a big fraction of the nanoantenna arrays were achieved, on which confocal fluorescence microscopy and time correlated single photon counting have been used to characterize the emitters. A time gating based analysis has been used to separate the nanoantenna luminescence from the fluorescence of the DBT molecules, obtaining lifetime values from coupled and uncoupled molecules. A set of 149 coupled molecules and 158 uncoupled molecules was represented in a histogram, showing a distribution from whose mean values the lifetime of DBT molecules (t=4.37 ns) was acquired, as well as a mean lifetime reduction of 2.4 times and a maximum lifetime reduction of 7 times.