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1.
Nature ; 606(7912): 75-81, 2022 06.
Artículo en Inglés | MEDLINE | ID: mdl-35650354

RESUMEN

A quantum computer attains computational advantage when outperforming the best classical computers running the best-known algorithms on well-defined tasks. No photonic machine offering programmability over all its quantum gates has demonstrated quantum computational advantage: previous machines1,2 were largely restricted to static gate sequences. Earlier photonic demonstrations were also vulnerable to spoofing3, in which classical heuristics produce samples, without direct simulation, lying closer to the ideal distribution than do samples from the quantum hardware. Here we report quantum computational advantage using Borealis, a photonic processor offering dynamic programmability on all gates implemented. We carry out Gaussian boson sampling4 (GBS) on 216 squeezed modes entangled with three-dimensional connectivity5, using a time-multiplexed and photon-number-resolving architecture. On average, it would take more than 9,000 years for the best available algorithms and supercomputers to produce, using exact methods, a single sample from the programmed distribution, whereas Borealis requires only 36 µs. This runtime advantage is over 50 million times as extreme as that reported from earlier photonic machines. Ours constitutes a very large GBS experiment, registering events with up to 219 photons and a mean photon number of 125. This work is a critical milestone on the path to a practical quantum computer, validating key technological features of photonics as a platform for this goal.

2.
Nature ; 594(7862): 201-206, 2021 06.
Artículo en Inglés | MEDLINE | ID: mdl-34108694

RESUMEN

The performance of light microscopes is limited by the stochastic nature of light, which exists in discrete packets of energy known as photons. Randomness in the times that photons are detected introduces shot noise, which fundamentally constrains sensitivity, resolution and speed1. Although the long-established solution to this problem is to increase the intensity of the illumination light, this is not always possible when investigating living systems, because bright lasers can severely disturb biological processes2-4. Theory predicts that biological imaging may be improved without increasing light intensity by using quantum photon correlations1,5. Here we experimentally show that quantum correlations allow a signal-to-noise ratio beyond the photodamage limit of conventional microscopy. Our microscope is a coherent Raman microscope that offers subwavelength resolution and incorporates bright quantum correlated illumination. The correlations allow imaging of molecular bonds within a cell with a 35 per cent improved signal-to-noise ratio compared with conventional microscopy, corresponding to a 14 per cent improvement in concentration sensitivity. This enables the observation of biological structures that would not otherwise be resolved. Coherent Raman microscopes allow highly selective biomolecular fingerprinting in unlabelled specimens6,7, but photodamage is a major roadblock for many applications8,9. By showing that the photodamage limit can be overcome, our work will enable order-of-magnitude improvements in the signal-to-noise ratio and the imaging speed.


Asunto(s)
Rayos Láser , Iluminación , Microscopía/métodos , Fotones , Teoría Cuántica , Espectrometría Raman , Células/patología , Células/efectos de la radiación , Rayos Láser/efectos adversos , Iluminación/efectos adversos , Microscopía/instrumentación , Fotones/efectos adversos , Relación Señal-Ruido , Espectrometría Raman/instrumentación , Espectrometría Raman/métodos
4.
Opt Express ; 27(13): 18601-18611, 2019 Jun 24.
Artículo en Inglés | MEDLINE | ID: mdl-31252800

RESUMEN

Label-free biosensors are important tools for clinical diagnostics and for studying biology at the single molecule level. The development of optical label-free sensors has allowed extreme sensitivity but can expose the biological sample to photodamage. Moreover, the fragility and complexity of these sensors can be prohibitive to applications. To overcome these problems, we develop a quantum noise limited exposed-core fiber sensor providing robust platform for label-free biosensing with a natural path toward microfluidic integration. We demonstrate the detection of single nanoparticles down to 25 nm in radius with optical intensities beneath known biophysical damage thresholds.

5.
Nano Lett ; 16(12): 7333-7337, 2016 12 14.
Artículo en Inglés | MEDLINE | ID: mdl-27960530

RESUMEN

Single-mode optical nanofibers are a central component of a broad range of applications and emerging technologies. Their fabrication has been extensively studied over the past decade, but imaging of the final submicrometer products has been restricted to destructive or low-precision techniques. Here, we demonstrate an optical scattering-based scanning method that uses a probe nanofiber to locally scatter the evanescent field of a sample nanofibre. The method does not damage the sample nanofiber and is easily implemented by only using the same equipment as in a standard fiber-puller setup. We demonstrate the subnanometer radial resolution at video rates (0.7 nm in 10 ms) on single mode nanofibers, allowing for a complete high-precision profile to be obtained within minutes of fabrication. The method thus enables nondestructive, fast, and precise characterization of optical nanofibers, with applications ranging from optical sensors and cold atom traps to nonlinear optics.

6.
Opt Lett ; 38(9): 1413-5, 2013 May 01.
Artículo en Inglés | MEDLINE | ID: mdl-23632502

RESUMEN

We report on a hitherto unexplored application of squeezed light: for quantum-enhancement of mechanical transduction sensitivity in microcavity optomechanics. Using a toroidal silica microcavity, we experimentally demonstrate measurement of the transduced phase modulation signal in the frequency range 4-5.8 MHz with a sensitivity -0.72(±0.01) dB below the shot noise level. This is achieved for resonant probing in the highly undercoupled regime, by preparing the probe in a weak coherent state with phase squeezed vacuum states at sideband frequencies.

7.
Phys Rev Lett ; 111(18): 180502, 2013 Nov 01.
Artículo en Inglés | MEDLINE | ID: mdl-24237495

RESUMEN

Noise is the main obstacle for the realization of fault-tolerant quantum information processing and secure communication over long distances. In this work, we propose a communication protocol relying on simple linear optics that optimally protects quantum states from non-Markovian or correlated noise. We implement the protocol experimentally and demonstrate the near-ideal protection of coherent and entangled states in an extremely noisy channel. Since all real-life channels are exhibiting pronounced non-Markovian behavior, the proposed protocol will have immediate implications in improving the performance of various quantum information protocols.

8.
Phys Rev Lett ; 109(3): 030402, 2012 Jul 20.
Artículo en Inglés | MEDLINE | ID: mdl-22861828

RESUMEN

Gaussian quantum discord is a measure of quantum correlations in gaussian systems. Using gaussian discord, we quantify the quantum correlations of a bipartite entangled state and a separable two-mode mixture of coherent states. We experimentally analyze the effect of noise addition and dissipation on gaussian discord and show that the former noise degrades the discord, while the latter noise for some states leads to an increase of the discord. In particular, we experimentally demonstrate the near death of discord by noisy evolution and its revival through dissipation.

9.
Nature ; 443(7111): 574-7, 2006 Oct 05.
Artículo en Inglés | MEDLINE | ID: mdl-17006452

RESUMEN

Genes in the major histocompatibility complex (MHC) encode proteins important in activating antigen-specific immune responses. Alleles at adjacent MHC loci are often in strong linkage disequilibrium; however, little is known about the mechanisms responsible for this linkage disequilibrium. Here we report that the human MHC HLA-DR2 haplotype, which predisposes to multiple sclerosis, shows more extensive linkage disequilibrium than other common caucasian HLA haplotypes in the DR region and thus seems likely to have been maintained through positive selection. Characterization of two multiple-sclerosis-associated HLA-DR alleles at separate loci by a functional assay in humanized mice indicates that the linkage disequilibrium between the two alleles may be due to a functional epistatic interaction, whereby one allele modifies the T-cell response activated by the second allele through activation-induced cell death. This functional epistasis is associated with a milder form of multiple-sclerosis-like disease. Such epistatic interaction might prove to be an important general mechanism for modifying exuberant immune responses that are deleterious to the host and could also help to explain the strong linkage disequilibrium in this and perhaps other HLA haplotypes.


Asunto(s)
Epistasis Genética , Antígeno HLA-DR2/genética , Haplotipos/genética , Esclerosis Múltiple/genética , Alelos , Animales , Linfocitos T CD4-Positivos/inmunología , Modelos Animales de Enfermedad , Encefalomielitis Autoinmune Experimental/genética , Encefalomielitis Autoinmune Experimental/patología , Humanos , Desequilibrio de Ligamiento/genética , Ratones , Esclerosis Múltiple/patología
10.
Sci Rep ; 12(1): 1995, 2022 02 07.
Artículo en Inglés | MEDLINE | ID: mdl-35132077

RESUMEN

The structural dynamics of macromolecules is important for most microbiological processes, from protein folding to the origins of neurodegenerative disorders. Noninvasive measurements of these dynamics are highly challenging. Recently, optical sensors have been shown to allow noninvasive time-resolved measurements of the dynamic polarizability of single-molecules. Here we introduce a method to efficiently predict the dynamic polarizability from the atomic configuration of a given macromolecule. This provides a means to connect the measured dynamic polarizability to the underlying structure of the molecule, and therefore to connect temporal measurements to structural dynamics. To illustrate the methodology we calculate the change in polarizability as a function of time based on conformations extracted from molecular dynamics simulations and using different conformations of motor proteins solved crystalographically. This allows us to quantify the magnitude of the changes in polarizablity due to thermal and functional motions.


Asunto(s)
Técnicas Biosensibles/métodos , Sustancias Macromoleculares/química , Simulación de Dinámica Molecular , Proteínas/química , Pliegue de Proteína
11.
Nat Commun ; 3: 1083, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-23011137

RESUMEN

Quantum key distribution enables two remote parties to grow a shared key, which they can use for unconditionally secure communication over a certain distance. The maximal distance depends on the loss and the excess noise of the connecting quantum channel. Several quantum key distribution schemes based on coherent states and continuous variable measurements are resilient to high loss in the channel, but are strongly affected by small amounts of channel excess noise. Here we propose and experimentally address a continuous variable quantum key distribution protocol that uses modulated fragile entangled states of light to greatly enhance the robustness to channel noise. We experimentally demonstrate that the resulting quantum key distribution protocol can tolerate more noise than the benchmark set by the ideal continuous variable coherent state protocol. Our scheme represents a very promising avenue for extending the distance for which secure communication is possible.

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