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1.
Phys Rev Lett ; 128(11): 117203, 2022 Mar 18.
Artigo em Inglês | MEDLINE | ID: mdl-35363007

RESUMO

Nanodiamonds with embedded nitrogen-vacancy (NV) centers have emerged as promising magnetic field sensors, as hyperpolarizing agents in biological environments, as well as efficient tools for spin mechanics with levitating particles. These applications currently suffer from random environmental interactions with the diamond which implies poor control of the N-V direction. Here, we predict and report on a strong diamagnetism of a pure spin origin mediated by a population inversion close to a level crossing in the NV center electronic ground state. We show control of the sign of the magnetic susceptibility as well as angle locking of the crystalline axis of a microdiamond along an external magnetic field, with bright perspectives for these applications.

2.
Nature ; 580(7801): 56-59, 2020 04.
Artigo em Inglês | MEDLINE | ID: mdl-32238930

RESUMO

Observing and controlling macroscopic quantum systems has long been a driving force in quantum physics research. In particular, strong coupling between individual quantum systems and mechanical oscillators is being actively studied1-3. Whereas both read-out of mechanical motion using coherent control of spin systems4-9 and single-spin read-out using pristine oscillators have been demonstrated10,11, temperature control of the motion of a macroscopic object using long-lived electronic spins has not been reported. Here we observe a spin-dependent torque and spin-cooling of the motion of a trapped microdiamond. Using a combination of microwave and laser excitation enables the spins of nitrogen-vacancy centres to act on the diamond orientation and to cool the diamond libration via a dynamical back-action. Furthermore, by driving the system in the nonlinear regime, we demonstrate bistability and self-sustained coherent oscillations stimulated by spin-mechanical coupling, which offers the prospect of spin-driven generation of non-classical states of motion. Such a levitating diamond-held in position by electric field gradients   under vacuum-can operate as a 'compass' with controlled dissipation and has potential use in high-precision torque sensing12-14, emulation of the spin-boson problem15 and probing of quantum phase transitions16. In the single-spin limit17 and using ultrapure nanoscale diamonds, it could allow quantum non-demolition read-out of the spin of nitrogen-vacancy centres at ambient conditions, deterministic entanglement between distant individual spins18 and matter-wave interferometry16,19,20.

3.
Phys Rev Lett ; 121(5): 053602, 2018 Aug 03.
Artigo em Inglês | MEDLINE | ID: mdl-30118282

RESUMO

We report on observations of Ramsey interferences and spin echoes from electron spins inside a levitating macroscopic particle. The experiment is realized using nitrogen-vacancy (NV) centers hosted in a micron-sized diamond stored in a Paul trap both under atmospheric conditions and under vacuum. Spin echoes are used to show that the Paul trap preserves the coherence time of the embedded electron spins for more than microseconds. Conversely, the NV spin is employed to demonstrate high angular stability of the diamond even under vacuum. These results are significant steps towards strong coupling of NV spins to the rotational mode of levitating diamonds.

4.
Phys Rev Lett ; 116(4): 043603, 2016 Jan 29.
Artigo em Inglês | MEDLINE | ID: mdl-26871331

RESUMO

We demonstrate coherent population trapping of a single nuclear spin in a room-temperature solid. To this end, we exploit a three-level system with a Λ configuration in the microwave domain, which consists of nuclear spin states addressed through their hyperfine coupling to the electron spin of a single nitrogen-vacancy defect in diamond. Moreover, the Λ-scheme relaxation is externally controlled through incoherent optical pumping and separated in time from consecutive coherent microwave excitations. Such a scheme allows us (i) to monitor the sequential accumulation of population into the dark state and (ii) to reach a novel regime of coherent population trapping dynamics for which periodic arrays of dark resonances can be observed, owing to multiple constructive interferences. This Letter offers new prospects for quantum state preparation, information storage in hybrid quantum systems, and metrology.

5.
Phys Rev Lett ; 110(13): 133602, 2013 Mar 29.
Artigo em Inglês | MEDLINE | ID: mdl-23581319

RESUMO

We perform a high-resolution real-time readout of the motion of a single trapped and laser-cooled Ba+ ion. By using an interferometric setup, we demonstrate a shot-noise-limited measurement of thermal oscillations with a resolution of 4 times the standard quantum limit. We apply the real-time monitoring for phase control of the ion motion through a feedback loop, suppressing the photon recoil-induced phase diffusion. Because of the spectral narrowing in the phase-locked mode, the coherent ion oscillation is measured with a resolution of about 0.3 times the standard quantum limit.

6.
Phys Rev Lett ; 110(8): 083603, 2013 Feb 22.
Artigo em Inglês | MEDLINE | ID: mdl-23473144

RESUMO

A scheme for entangling distant atoms is realized, as proposed in the seminal paper by [C. Cabrillo et al., Phys. Rev. A 59, 1025 (1999)]. The protocol is based on quantum interference and detection of a single photon scattered from two effectively one meter distant laser cooled and trapped atomic ions. The detection of a single photon heralds entanglement of two internal states of the trapped ions with high rate and with a fidelity limited mostly by atomic motion. Control of the entangled state phase is demonstrated by changing the path length of the single-photon interferometer.

7.
Phys Rev Lett ; 107(13): 133002, 2011 Sep 23.
Artigo em Inglês | MEDLINE | ID: mdl-22026849

RESUMO

By tightly focusing a laser field onto a single cold ion trapped in front of a far-distant dielectric mirror, we could observe a quantum electrodynamic effect whereby the ion behaves as the optical mirror of a Fabry-Pérot cavity. We show that the amplitude of the laser field is significantly altered due to a modification of the electromagnetic mode structure around the atom in a novel regime in which the laser intensity is already changed by the atom alone. We propose a direct application of this system as a quantum memory for single photons.

8.
Clin Exp Dermatol ; 36(7): 782-7, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-21507037

RESUMO

BACKGROUND: EDNRB gene variants were reported to be associated with melanoma risk in French patients, with the S305N variant showing the highest frequency. AIM: To verify the S305N association with melanoma risk in an independent larger French population (378 patients, 389 controls); to investigate the role of EDNRB variants in melanoma risk in an Italian population (133 patients, 118 controls); and to explore the association of CDKN2A or CDK4 mutations with the S305N EDNRB variant in a subgroup of patients (59 French, 12 Italian) with a suspected hereditary predisposition to melanoma (familial melanoma, sporadic multiple primary melanoma or melanoma associated with pancreatic cancer). METHODS: The S305N variant was genotyped in the French population, while the EDNRB gene in the Italian population was entirely sequenced. RESULTS: Overall, there was no significant difference in the frequency of the S305N variant between patients with sporadic melanoma and controls in either the French or the Italian population. However, a significantly higher S305N allele frequency was detected in French patients with a suspected hereditary predisposition to melanoma compared with controls (P = 0.04). In addition, in this subgroup of patients, the S305N allele was also significantly associated with the presence of CDKN2A mutations (P = 0.04). CONCLUSIONS: Our results showed no evidence of association of the S305N EDNRB polymorphism with sporadic melanoma risk in either the French or Italian populations, but there was an indication that EDNRB might be a melanoma-predisposing gene in French patients with a suspected hereditary predisposition to melanoma.


Assuntos
Predisposição Genética para Doença , Melanoma/genética , Receptor de Endotelina B/genética , Neoplasias Cutâneas/genética , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Alelos , Estudos de Casos e Controles , Estudos de Coortes , Feminino , França , Frequência do Gene , Genes p16 , Humanos , Itália , Masculino , Pessoa de Meia-Idade , Polimorfismo Genético , Análise de Sequência de DNA , Adulto Jovem
9.
Opt Lett ; 35(7): 1091-3, 2010 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-20364227

RESUMO

Photon echo schemes are excellent candidates for high efficiency coherent optical memory. They are capable of high-bandwidth multipulse storage, pulse resequencing and have been shown theoretically to be compatible with quantum information applications. One particular photon echo scheme is the gradient echo memory (GEM). In this system, an atomic frequency gradient is induced in the direction of light propagation leading to a Fourier decomposition of the optical spectrum along the length of the storage medium. This Fourier encoding allows precision spectral manipulation of the stored light. In this Letter, we show frequency shifting, spectral compression, spectral splitting, and fine dispersion control of optical pulses using GEM.

10.
Phys Rev Lett ; 105(15): 153604, 2010 Oct 08.
Artigo em Inglês | MEDLINE | ID: mdl-21230903

RESUMO

In this Letter, we report an absorption spectroscopy experiment and the observation of electromagnetically induced transparency from a single trapped atom. We focus a weak and narrow band Gaussian light beam onto an optically cooled 138Ba+ ion using a high numerical aperture lens. Extinction of this beam is observed with measured values of up to 1.35%. We demonstrate electromagnetically induced transparency of the ion by tuning a strong control beam over a two-photon resonance in a three-level Λ-type system. The probe beam extinction is inhibited by more than 75% due to population trapping.

11.
Phys Rev Lett ; 101(20): 203601, 2008 Nov 14.
Artigo em Inglês | MEDLINE | ID: mdl-19113339

RESUMO

We investigate the properties of a recently proposed gradient echo memory (GEM) scheme for information mapping between optical and atomic systems. We show that GEM can be described by the dynamic formation of polaritons in k space. This picture highlights the flexibility and robustness with regards to the external control of the storage process. Our results also show that, as GEM is a frequency-encoding memory, it can accurately preserve the shape of signals that have large time-bandwidth products, even at moderate optical depths. At higher optical depths, we show that GEM is a high fidelity multimode quantum memory.

12.
Opt Lett ; 33(20): 2323-5, 2008 Oct 15.
Artigo em Inglês | MEDLINE | ID: mdl-18923610

RESUMO

We propose a photon echo quantum memory scheme using detuned Raman coupling to long-lived ground states. In contrast to previous three-level schemes based on controlled reversible inhomogeneous broadening that use sequences of pi pulses, the scheme does not require accurate control of the coupling dynamics to the ground states. We present a proof-of-principle experimental realization of our proposal using rubidium atoms in a warm vapor cell. The Raman resonance line is broadened using a magnetic field that varies linearly along the direction of light propagation. Inverting the magnetic field gradient rephases the atomic dipoles and re-emits the light pulse in the forward direction.

13.
Br J Dermatol ; 159(4): 968-73, 2008 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-18717677

RESUMO

We report the case of an 83-year-old French woman with multiple melanomas showing a severe DNA repair deficiency, corrected after transfection by XPC cDNA. Two biallelic mutations in the XPC gene are reported: an inactivating frameshift mutation in exon 15 (c.2544delG, p.W848X) and a missense mutation in exon 11 (c.2108 C>T, P703L). We demonstrate that these new mutations are involved in the DNA repair deficiency and confirm the diagnosis of xeroderma pigmentosum from complementation group C (XP-C). We speculate that the coexistence of a MC1R variant may be involved in the phenotype of multiple melanomas and that the unusual long-term survival may be related to a lower ultraviolet radiation exposure and to a regular clinical follow-up. This patient appears to be the first French Caucasian XP-C case and one of the oldest living patients with XP reported worldwide.


Assuntos
Reparo do DNA/genética , Proteínas de Ligação a DNA/genética , Mutação da Fase de Leitura/genética , Melanoma/genética , Mutação de Sentido Incorreto/genética , Neoplasias Primárias Múltiplas/genética , Neoplasias Cutâneas/genética , Xeroderma Pigmentoso/genética , Idoso de 80 Anos ou mais , Feminino , Humanos , Melanoma/patologia , Neoplasias Primárias Múltiplas/patologia , Fenótipo , Neoplasias Cutâneas/patologia , Sobreviventes , População Branca , Xeroderma Pigmentoso/patologia
14.
Opt Express ; 16(10): 7369-81, 2008 May 12.
Artigo em Inglês | MEDLINE | ID: mdl-18545442

RESUMO

We demonstrate experimentally the delay of squeezed light and entanglement using Electromagnetically Induced Transparency (EIT) in a rubidium vapour cell. We perform quadrature amplitude measurements of the probe field and find no appreciable excess noise from the EIT process. From input squeezing of 3.2+/-0.5 dB at low sideband frequencies, we observed the survival of 2.0+/-0.5 dB of squeezing at the EIT output. By splitting the squeezed light on a beam-splitter, we generated biased entanglement between two beams. We transmit one of the entangled beams through the EIT cell and correlate the quantum statistics of this beam with its entangled counterpart. We experimentally observed a 2.2+/-0.5 micros delay of the biased entanglement and obtained a preserved degree of wavefunction inseparability of 0.71+/-0.01, below the unity value for separable states.


Assuntos
Campos Eletromagnéticos , Óptica e Fotônica , Físico-Química/métodos , Desenho de Equipamento , Gases , Luz , Teoria Quântica , Fatores de Tempo
15.
Phys Rev Lett ; 100(2): 023601, 2008 Jan 18.
Artigo em Inglês | MEDLINE | ID: mdl-18232866

RESUMO

We present a simple quantum memory scheme that allows for the storage of a light field in an ensemble of two-level atoms. The technique is analogous to the NMR gradient echo for which the imprinting and recalling of the input field are performed by controlling a linearly varying broadening. Our protocol is perfectly efficient in the limit of high optical depths and the output pulse is emitted in the forward direction. We provide a numerical analysis of the protocol together with an experiment performed in a solid state system. In close agreement with our model, the experiment shows a total efficiency of up to 15%, and a recall efficiency of 26%. We suggest simple realizable improvements for the experiment to surpass the no-cloning limit.

16.
Phys Rev Lett ; 97(18): 183601, 2006 Nov 03.
Artigo em Inglês | MEDLINE | ID: mdl-17155542

RESUMO

Using electromagnetically induced transparency (EIT), it is possible to delay and store light in atomic ensembles. Theoretical modeling and recent experiments have suggested that the EIT storage mechanism can be used as a memory for quantum information. We present experiments that quantify the noise performance of an EIT system for conjugate amplitude and phase quadratures. It is shown that our EIT system adds excess noise to the delayed light that has not hitherto been predicted by published theoretical modeling. In analogy with other continuous-variable quantum information systems, the performance of our EIT system is characterized in terms of conditional variance and signal transfer.

19.
Eur J Clin Invest ; 31(5): 382-8, 2001 May.
Artigo em Inglês | MEDLINE | ID: mdl-11380589

RESUMO

BACKGROUND: Haemochromatosis is a common genetic disorder, inherited as an autosomal recessive trait that results in a progressive accumulation of iron in most tissues of the body. Positive association studies have been recently published between cardiovascular diseases and heterozygosity for the major mutation C282Y in the haemochromatosis gene HFE. METHODS: In the present work, we have determined the HFE genotypes for C282Y and H63D in subjects from two case-control studies: the ECTIM and GENIC studies, designed to identify genetic variants associated with myocardial and brain infarction, respectively. In addition, we tested whether HFE mutations were associated with the degree of arteriosclerosis assessed non-invasively by Doppler ultrasonography on the carotid and femoral arteries, in a group of apparently healthy individuals (the AXA Study). RESULTS: The prevalence of 282Y, and 63D allele carriers, did not differ between cases and controls in the ECTIM and in the GENIC studies, while 63D but not 282Y carriers were more numerous among subjects with atherosclerotic plaques in the AXA Study. CONCLUSIONS: These three studies do not provide consistent evidence supporting the hypothesis that HFE mutations are associated with an increased risk of cardiovascular disease and with the development of arteriosclerosis.


Assuntos
Doenças Cardiovasculares/genética , Predisposição Genética para Doença/genética , Antígenos HLA/genética , Hemocromatose/genética , Antígenos de Histocompatibilidade Classe I/genética , Proteínas de Membrana , Mutação/genética , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Arteriosclerose/diagnóstico por imagem , Arteriosclerose/epidemiologia , Arteriosclerose/genética , Ácido Aspártico/genética , Infarto Encefálico/epidemiologia , Infarto Encefálico/genética , Doenças Cardiovasculares/epidemiologia , Estudos de Casos e Controles , Cisteína/genética , Feminino , França/epidemiologia , Genótipo , Hemocromatose/epidemiologia , Proteína da Hemocromatose , Histidina/genética , Humanos , Masculino , Pessoa de Meia-Idade , Infarto do Miocárdio/epidemiologia , Infarto do Miocárdio/genética , Irlanda do Norte/epidemiologia , Polimorfismo Genético/genética , Prevalência , Estudos Prospectivos , Tirosina/genética , Ultrassonografia , Reino Unido/epidemiologia
20.
Br J Haematol ; 112(1): 51-4, 2001 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-11167783

RESUMO

Hereditary hyperferritinaemia cataract syndrome (HHCS) is characterized by hyperferritinaemia without iron overload. It is essential to differentiate true iron accumulation from HHCS as these patients rapidly develop iron-deficient anaemia when subjected to phlebotomies. The diagnosis of HHCS relies on the identification of point mutations or deletions present in the iron-responsive element of the first exon of the L-ferritin gene. However, many samples referred for diagnosis of putative HHCS are normal. To avoid unnecessary DNA sequencing, we have developed a diagnosis strategy based on the screening of the target DNA region by denaturing gradient gel electrophoresis. This method enabled the accurate identification of 11 different previously known mutations. This strategy will be of interest for family studies or for the screening of large series of patients.


Assuntos
Catarata/genética , Ferritinas/sangue , Regiões 5' não Traduzidas , Análise Mutacional de DNA/métodos , Eletroforese em Gel de Poliacrilamida/métodos , Humanos , Mutação , Síndrome
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