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1.
Phys Rev Lett ; 101(13): 133601, 2008 Sep 26.
Artigo em Inglês | MEDLINE | ID: mdl-18851447

RESUMO

Using electromagnetically induced transparency in a cesium vapor, we demonstrate experimentally that the quantum state of a light beam can be mapped into the long-lived Zeeman coherences of an atomic ground state. Two noncommuting variables carried by light are simultaneously stored and subsequently read out, with no noise added. We compare the case where a tunable single sideband is stored independently of the other one to the case where the two symmetrical sidebands are stored using the same electromagnetically induced transparency window.

2.
Phys Rev Lett ; 97(2): 023605, 2006 Jul 14.
Artigo em Inglês | MEDLINE | ID: mdl-16907444

RESUMO

We show that strong squeezing and entanglement can be generated at the output of a cavity containing atoms interacting with two fields in a coherent population trapping situation, on account of a nonlinear Faraday effect experienced by the fields close to a dark-state resonance in a cavity. Moreover, the cavity provides a feedback mechanism allowing to reduce the quantum fluctuations of the ground state spin, resulting in strong steady state spin squeezing.

3.
Eur Phys J E Soft Matter ; 9(5): 427-34, 2002 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-15011089

RESUMO

The macroscopic shape of liquid-crystalline elastomers strongly depends on the order parameter of the mesogenic groups. This order can be manipulated if photo-isomerisable groups, e.g. containing N=N bonds, are introduced into the material. We have explored the large photo-mechanical response of such an azobenzene-containing nematic elastomer at different temperatures, using force and optical birefringence measurements, and focusing on fundamental aspects of population dynamics and the related speed and repeatability of the response. The characteristic time of "on" and "off" regimes strongly depends on temperature, but is generally found to be very long. We were able to verify that the macroscopic relaxation of the elastomer is determined by the nematic order dynamics and not, for instance, by the polymer network relaxation.

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