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

arXiv:2602.22677

Quantum-Optically Resolving the Number of Colloidal Quantum Dots in a Subwavelength Volume

Zhi-Bo Ni, Jia-Wang Yu, Jiong-Zhao Li, Xiao-Tian Cheng, Mei-Na Jiang, Zi-Xuan Song, Xiao-Qing Zhou, Wei Fang, Chen-Hui Li, Feng Liu, Xing Lin, Chao-Yuan Jin

quant-phphysics.opticsSubmitted Feb 26, 2026• Announced Feb 27, 2026• 0 citations
arXivHTMLPDF

Abstract

The number resolution of solid-state artificial atoms is of fundamental interest for the study of quantum few-body systems, yet remains experimentally challenging. Quantum optical experiments offer a non-invasive approach which links up macroscopic measurements with the quantity of quantum emitters. In this work, we propose a time-domain quantum optical methodology for the strict numbering of colloidal CdSe/CdS/ZnS quantum dots (QDs) confined in subwavelength-size polystyrene capsules. The non-polarized, homogeneously broadened emission of colloidal QDs in the subwavelength volume satisfies the description of Dicke's superradiance of identical quantum emitters. An analytic relation describes the numerical dependence of the second-order photon correlation on the number and the collective lifetime of emitters, yielding an experimental counting range of colloidal QDs from one to ten. This work provides a robust pathway for the non-invasive numbering of artificial atoms and the investigation of collective light-matter interactions at the nanoscale.

Comments
25 pages, 7 figures. Main text includes methods

Related papers

Quantum-Optically Resolving the Number of Colloidal Quantum Dots in a Subwavelength Volume

Chaoyuan Jin, Zhibo Ni

Abstract The number resolution of solid-state artificial atoms is of fundamental interest for the study of quantum few-body systems, yet remains experimentally challenging. Quantum optical experiments offer a non-invasive approach which links up macroscopic measurements with the quantity of quantum emitters. In this work, we propose a time-domain quantum optical methodology for the strict numbering of colloidal CdSe/CdS/ZnS quantum dots (QDs) confined in subwavelength size polystyrene capsules. The non-polarized, homogeneously broadened emission of colloidal QDs in the subwavelength volume satisfies the description of Dicke’s superradiance of identical quantum emitters. An analytic relation describes the numerical dependence of the second-order photon correlation on the number and the collective lifetime of emitters, yielding an experimental counting range from one to ten. This work provides a robust pathway for the non-invasive numbering of artificial atoms and the investigation of collective light-matter interactions at the nanoscale.

•Mar 10, 2026•0 citations

In-Situ Quantum Optical Measurement for Colloidal Quantum Dots Confined in an Optical Trap

Zhi-Bo Ni, Jiong-Zhao Li, Jia-Wang Yu +7 more

While optical manipulation of atomic arrays has reached a high degree of precision and scalability, the stable optical confinement of solution-based artificial atoms like colloidal quantum dots (CQDs) remains hindered by weak trapping forces and thermal fluctuations. High-intensity trapping often compromises the quantum properties of these emitters, creating a significant trade-off between mechanical stability and optical integrity. To overcome this, we propose encapsulating CQDs within a transparent polymer matrix, thereby increasing the effective interaction volume and optical restoring force without altering the emitters themselves. This strategy allows for stable spatial confinement under standard experimental conditions, as evidenced by the direct resolution of positional fluctuations through photoluminescence imaging and trajectory tracking. With averaged position fluctuations below 20 nm, the intrinsic emission spectra and photoluminescence decay dynamics remain largely unaffected, and photon-correlation measurements confirm the full preservation of single-photon emission. These findings establish a robust method for the controlled confinement of colloidal quantum emitters and in-situ quantum-optical measurements for future advancements in quantum-optical manipulation of artificial atoms.

physics.opticsCross-listedarXiv:2609.16692•Sep 16, 2026

En route to nanoscopic quantum optical imaging: counting emitters with photon-number-resolving detectors

Shuo Li, Wenchao Li, Vladislav V. Yakovlev +2 more

The fundamental understanding of biological pathways requires minimally invasive nanoscopic optical resolution imaging. Many approaches to high-resolution imaging rely on localization of single emitters, such as fluorescent molecules or quantum dots. Additionally, the exact determination of the number of such emitters in an imaging volume is essential for a number of applications; however, in standard intensity-based microscopy it is not possible to determine the number of individual emitters within a diffraction limited spot without initial knowledge of system parameters. Here we explore how quantum measurements of the emitted photons using photon number resolving detectors can be used to address this challenging task. In the proposed new approach, the problem of counting emitters reduces to the task of determining differences between the emitted photon distribution and the Poisson limit. We show that quantum measurements of the number of photons emitted from an ensemble of emitters enable the determination of both the number of emitters and the probability of emission. This method can be applied for any type of single-photon emitters. The scaling laws of this new approach are presented by the Cramer-Rao Lower Bounds, and this technique has great potential in quantum optical imaging with nanoscopic resolution.

arXiv:2110.03893•Optics Express•Mar 21, 2022•7 citations

Few-Body Decay Dynamics in Colloidal CsPbI3 Quantum-Dot Clusters

Emma Daggett, Christian M. Lange, Nicholas Favate +7 more

Colloidal perovskite quantum dots combine bright emission with the ability to self- assemble into closely spaced structures, enabling radiative dynamics to be studied from isolated emitters to few-dot clusters. Here, we characterize CsPbI3 perovskite quan- tum dots from isolated emitters to self-assembled clusters containing up to ten dots. We estimate the number of emitters in each cluster using a combination of photon autocorrelation, blinking statistics, and emission brightness. Compared with isolated dots, clusters containing two or more emitters exhibit biexponential decay, with a short lifetime that decreases with emitter number and an additional long-lived component. Photon-correlation Fourier spectroscopy shows that the single-dot emission remains far from the lifetime-limited regime. Nevertheless, we observe emitter-number-dependent decay dynamics even in this low-coherence regime. Together, these measurements es- tablish self-assembled perovskite quantum-dot clusters as a platform for studying how collective optical behavior emerges between the single-emitter and ensemble limits

quant-pharXiv:2609.07892•Sep 9, 2026

Many-Body Super- and Subradiance in Ordered Atomic Arrays

Alec Douglas, Lin Su, Michal Szurek +7 more

When quantum emitters couple indistinguishably to light, they can synchronize into a collective light matter system with radiative properties profoundly different from those of independent particles. To date, the resulting collective effects have largely been confined to point like or homogeneous ensembles. Here, we open access to a qualitatively new collective regime by realizing geometrically ordered, spatially extended atom arrays with subwavelength spacing. This establishes a fundamentally new platform in which collective emission is no longer confined to a single Dicke mode but instead emerges from an ordered network of photon mediated interactions. We find that 2D atom arrays undergo strong super and subradiant emission. Despite subwavelength spacing, we achieve site resolved imaging and directly observe the buildup of spatial correlations, demonstrating the transformation of cooperative decay into a strongly correlated many-body process. We observe extensive scaling of superradiance, uncover superradiant revivals, and reveal the ferromagnetic nature of superradiance and the antiferromagnetic nature of subradiance. Our results realize a novel programmable platform for exploring and utilizing dissipative many-body quantum physics, opening new possibilities for photon capture, storage, and atom photon entanglement.

quant-pharXiv:2604.11795•Apr 14, 2026•0 citations

Heralded Emission Detection in InAs/ZnSe Quantum Dot Solids Using Time-Correlated Photons

Tsao, Chieh, Xiang Li, Alex Hinkle +4 more

Harnessing quantum correlations between photons is an emerging frontier in optical spectroscopy, yet experimental demonstrations have largely remained limited to molecular systems at room temperature. Here, we investigate heralded emission detection (HED) under continuous-wave entangled-photon excitation of near-infrared (NIR)-emitting colloidal III-V quantum dot (QD) solids at low temperatures. We demonstrate the advantages of superconducting nanowire single-photon detectors (SNSPDs) for high time resolution ($\sim$72 ps) and large-area NIR avalanche photodiodes (APDs) for high emission count rates ($\sim$2000 cps). Second-order photon-correlation analysis reveals exciton lifetimes and fine-structure energy splittings. These results establish NIR colloidal QDs as a bright, tunable model system for quantum-light spectroscopy and highlight their compatibility with optical cavities as a further experimental control parameter.

arXiv:2509.11704•Sep 15, 2025•0 citations
The number resolution of solid-state artificial atoms is of fundamental interest for the study of quantum few-body systems, yet remains experimentally challenging. Quantum optical experiments offer a non-invasive approach which links up macroscopic measurements with the quantity of quantum emitters. In this work, we propose a time-domain quantum optical methodology for the strict numbering of colloidal CdSe/CdS/ZnS quantum dots (QDs) confined in subwavelength-size polystyrene capsules. The non-polarized, homogeneously broadened emission of colloidal QDs in the subwavelength volume satisfies the description of Dicke's superradiance of identical quantum emitters. An analytic relation describes the numerical dependence of the second-order photon correlation on the number and the collective lifetime of emitters, yielding an experimental counting range of colloidal QDs from one to ten. This work provides a robust pathway for the non-invasive numbering of artificial atoms and the investigation of collective light-matter interactions at the nanoscale.
Abstract The number resolution of solid-state artificial atoms is of fundamental interest for the study of quantum few-body systems, yet remains experimentally challenging. Quantum optical experiments offer a non-invasive approach which links up macroscopic measurements with the quantity of quantum emitters. In this work, we propose a time-domain quantum optical methodology for the strict numbering of colloidal CdSe/CdS/ZnS quantum dots (QDs) confined in subwavelength size polystyrene capsules. The non-polarized, homogeneously broadened emission of colloidal QDs in the subwavelength volume satisfies the description of Dicke’s superradiance of identical quantum emitters. An analytic relation describes the numerical dependence of the second-order photon correlation on the number and the collective lifetime of emitters, yielding an experimental counting range from one to ten. This work provides a robust pathway for the non-invasive numbering of artificial atoms and the investigation of collective light-matter interactions at the nanoscale.
While optical manipulation of atomic arrays has reached a high degree of precision and scalability, the stable optical confinement of solution-based artificial atoms like colloidal quantum dots (CQDs) remains hindered by weak trapping forces and thermal fluctuations. High-intensity trapping often compromises the quantum properties of these emitters, creating a significant trade-off between mechanical stability and optical integrity. To overcome this, we propose encapsulating CQDs within a transparent polymer matrix, thereby increasing the effective interaction volume and optical restoring force without altering the emitters themselves. This strategy allows for stable spatial confinement under standard experimental conditions, as evidenced by the direct resolution of positional fluctuations through photoluminescence imaging and trajectory tracking. With averaged position fluctuations below 20 nm, the intrinsic emission spectra and photoluminescence decay dynamics remain largely unaffected, and photon-correlation measurements confirm the full preservation of single-photon emission. These findings establish a robust method for the controlled confinement of colloidal quantum emitters and in-situ quantum-optical measurements for future advancements in quantum-optical manipulation of artificial atoms.
The fundamental understanding of biological pathways requires minimally invasive nanoscopic optical resolution imaging. Many approaches to high-resolution imaging rely on localization of single emitters, such as fluorescent molecules or quantum dots. Additionally, the exact determination of the number of such emitters in an imaging volume is essential for a number of applications; however, in standard intensity-based microscopy it is not possible to determine the number of individual emitters within a diffraction limited spot without initial knowledge of system parameters. Here we explore how quantum measurements of the emitted photons using photon number resolving detectors can be used to address this challenging task. In the proposed new approach, the problem of counting emitters reduces to the task of determining differences between the emitted photon distribution and the Poisson limit. We show that quantum measurements of the number of photons emitted from an ensemble of emitters enable the determination of both the number of emitters and the probability of emission. This method can be applied for any type of single-photon emitters. The scaling laws of this new approach are presented by the Cramer-Rao Lower Bounds, and this technique has great potential in quantum optical imaging with nanoscopic resolution.
Colloidal perovskite quantum dots combine bright emission with the ability to self- assemble into closely spaced structures, enabling radiative dynamics to be studied from isolated emitters to few-dot clusters. Here, we characterize CsPbI3 perovskite quan- tum dots from isolated emitters to self-assembled clusters containing up to ten dots. We estimate the number of emitters in each cluster using a combination of photon autocorrelation, blinking statistics, and emission brightness. Compared with isolated dots, clusters containing two or more emitters exhibit biexponential decay, with a short lifetime that decreases with emitter number and an additional long-lived component. Photon-correlation Fourier spectroscopy shows that the single-dot emission remains far from the lifetime-limited regime. Nevertheless, we observe emitter-number-dependent decay dynamics even in this low-coherence regime. Together, these measurements es- tablish self-assembled perovskite quantum-dot clusters as a platform for studying how collective optical behavior emerges between the single-emitter and ensemble limits
When quantum emitters couple indistinguishably to light, they can synchronize into a collective light matter system with radiative properties profoundly different from those of independent particles. To date, the resulting collective effects have largely been confined to point like or homogeneous ensembles. Here, we open access to a qualitatively new collective regime by realizing geometrically ordered, spatially extended atom arrays with subwavelength spacing. This establishes a fundamentally new platform in which collective emission is no longer confined to a single Dicke mode but instead emerges from an ordered network of photon mediated interactions. We find that 2D atom arrays undergo strong super and subradiant emission. Despite subwavelength spacing, we achieve site resolved imaging and directly observe the buildup of spatial correlations, demonstrating the transformation of cooperative decay into a strongly correlated many-body process. We observe extensive scaling of superradiance, uncover superradiant revivals, and reveal the ferromagnetic nature of superradiance and the antiferromagnetic nature of subradiance. Our results realize a novel programmable platform for exploring and utilizing dissipative many-body quantum physics, opening new possibilities for photon capture, storage, and atom photon entanglement.
Harnessing quantum correlations between photons is an emerging frontier in optical spectroscopy, yet experimental demonstrations have largely remained limited to molecular systems at room temperature. Here, we investigate heralded emission detection (HED) under continuous-wave entangled-photon excitation of near-infrared (NIR)-emitting colloidal III-V quantum dot (QD) solids at low temperatures. We demonstrate the advantages of superconducting nanowire single-photon detectors (SNSPDs) for high time resolution ($\sim72ps)andlarge−areaNIRavalanchephotodiodes(APDs)forhighemissioncountrates(72 ps) and large-area NIR avalanche photodiodes (APDs) for high emission count rates (72ps)andlarge−areaNIRavalanchephotodiodes(APDs)forhighemissioncountrates(\sim$2000 cps). Second-order photon-correlation analysis reveals exciton lifetimes and fine-structure energy splittings. These results establish NIR colloidal QDs as a bright, tunable model system for quantum-light spectroscopy and highlight their compatibility with optical cavities as a further experimental control parameter.