An official website of the United States government
Abstract Multi-photon entangled graph states are a fundamental resource in quantum communication networks, distributed quantum computing, and sensing. These states can in principle be created deterministically from quantum emitters such as optically active quantum dots or defects, atomic systems, or superconducting qubits. However, finding efficient schemes to produce such states has been a long-standing challenge. Here, we present an algorithm that, given a desired multi-photon graph state, determines the minimum number of quantum emitters and precise operation sequences that can produce it. The algorithm itself and the resulting operation sequence both scale polynomially in the size of the photonic graph state, allowing one to obtain efficient schemes to generate graph states containing hundreds or thousands of photons.
more »
« less
This content will become publicly available on January 1, 2026
Caught in a trap: how to capture a quantum dot
Many new quantum technologies will rely on the precise manipulation of single photons; however, most light sources produce photons randomly. Quantum dots, which can reliably produce single photons, may provide a solution. From Virginia Commonwealth University and Vanderbilt University in the US, Dr Nathaniel Kinsey and Dr Justus Ndukaife are developing a device that can trap quantum dots and enhance their photon emission rates, paving the way for new quantum technologies.
more »
« less
- Award ID(s):
- 2322891
- PAR ID:
- 10621519
- Publisher / Repository:
- Futurum
- Date Published:
- Journal Name:
- Futurum
- ISSN:
- 2632-8399
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
The utility of colloidal semiconductor quantum dots as a source of photons and charge carriers for photonic and photovoltaic applications has created a large field of research focused on tailoring and broadening their functionality beyond what an exciton can provide. One approach towards expanding the range of characteristics of photons and charge carriers from quantum dots is through doping impurity ions ( e.g. Mn 2+ , Cu + , and Yb 3+ ) in the host quantum dots. In addition to the progress in synthesis enabling fine control of the structure of the doped quantum dots, a mechanistic understanding of the underlying processes correlated with the structure has been crucial in revealing the full potential of the doped quantum dots as the source of photons and charge carriers. In this review, we discuss the recent progress made in gaining microscopic understanding of the photophysical pathways that give rise to unique dopant-related luminescence and the generation of energetic hot electrons via exciton-to-hot electron upconversion.more » « less
-
null (Ed.)Hybrid materials comprised of inorganic quantum dots functionalized with small-molecule organic chromophores have emerged as promising materials for reshaping light's energy content. Quantum dots in these structures can serve as light harvesting antennas that absorb photons and pass their energy to molecules bound to their surface in the form of spin-triplet excitons. Energy passed in this manner can fuel upconversion schemes that use triplet fusion to convert infrared light into visible emission. Likewise, triplet excitons passed in the opposite direction, from molecules to quantum dots, can enable solar cells that use singlet fission to circumvent the Shockley–Queisser limit. Silicon QDs represent a key target for these hybrid materials due to silicon's biocompatibility and preeminence within the solar energy market. However, while triplet transfer from silicon QDs to molecules has been observed, no reports to date have shown evidence of energy moving in the reverse direction. Here, we address this gap by creating silicon QDs functionalized with perylene chromophores that exhibit bidirectional triplet exciton transfer. Using transient absorption, we find triplet transfer from silicon to perylene takes place over 4.2 μs while energy transfer in the reverse direction occurs two orders of magnitude faster, on a 22 ns timescale. To demonstrate this system's utility, we use it to create a photon upconversion system that generates blue emission at 475 nm using photons with wavelengths as long as 730 nm. Our work shows formation of covalent linkages between silicon and organic molecules can provide sufficient electronic coupling to allow efficient bidirectional triplet exchange, enabling new technologies for photon conversion.more » « less
-
Abstract A key obstacle for all quantum information science and engineering platforms is their lack of scalability. The discovery of emergent quantum phenomena and their applications in active photonic quantum technologies have been dominated by work with single atoms, self‐assembled quantum dots, or single solid‐state defects. Unfortunately, scaling these systems to many quantum nodes remains a significant challenge. Solution‐processed quantum materials are uniquely positioned to address this challenge, but the quantum properties of these materials have remained generally inferior to those of solid‐state emitters or atoms. Additionally, systematic integration of solution‐processed materials with dielectric nanophotonic structures has been rare compared to other solid‐state systems. Recent progress in synthesis processes and nanophotonic engineering, however, has demonstrated promising results, including long coherence times of emitted single photons and deterministic integration of emitters with dielectric nano‐cavities. In this review article, these recent experiments using solution‐processed quantum materials and dielectric nanophotonic structures are discussed. The progress in non‐classical light state generation, exciton‐polaritonics for quantum simulation, and spin‐physics in these materials is discussed and an outlook for this emerging research field is provided.more » « less
-
Quantum information processing demands efficient quantum light sources (QLS) capable of producing high-fidelity single photons or entangled photon pairs. Single epitaxial quantum dots (QDs) have long been proven to be efficient sources of deterministic single photons; however, their production via molecular-beam epitaxy presents scalability challenges. Conversely, colloidal semiconductor QDs offer scalable solution processing and tunable photoluminescence but suffer from broader linewidths and unstable emissions. This leads to spectrally inseparable emission from exciton (X) and biexciton (XX) states, complicating the production of single photons and triggered photon pairs. Here, we demonstrate that colloidal semiconductor quantum shells (QSs) achieve significant spectral separation (~ 75-80 meV) and long temporal stability of X and XX emissive states, enabling the observation of exciton-biexciton bunching in colloidal QDs. Our low-temperature single-particle measurements show cascaded XX-X emission of single photon pairs for over 200 seconds, with minimal overlap between X and XX features. The X-XX distinguishability allows for an in-depth theoretical characterization of cross-correlation strength, placing it in perspective with photon pairs of epitaxial counterparts. These findings highlight a strong potential of semiconductor quantum shells for applications in quantum information processing.more » « less
