Biomedical subjects

A Kirilyuk

Publications and source records attributed to A Kirilyuk.

13 recordsLinked to original sources

PubMed2006

Voltage-controlled phase matching in quadrupole second-harmonic generation.

We have observed strong phase-matched (PM) quadrupole optical second-harmonic generation (SHG) from nematic liquid crystals that possess inversion symmetry. PM conditions were achieved for two configurations by voltage control of the molecular orientation and thus of the refractive indices. Quadrupole SHG was separated from electric-field-induced dipole-type SHG with the help of time-gated measurements in a pulsed electric field.

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PubMed2006

Direct observation of exchange bias related uncompensated spins at the CoO/Cu interface.

Magnetization-induced optical second harmonic generation (MSHG) from the exchange-biased CoO/Cu-(X)/Fe multilayer shows the presence of pinned uncompensated spins at the CoO/Cu interface. For increasing Cu spacer thickness, the exchange bias measured via the hysteresis loop shift diminishes and disappears at X = 3.5 nm, while the MSHG signal still shows a strong magnetic contribution from the CoO interface. This indicates that the magnetic interaction between Fe and CoO layers is sufficiently strong to induce order in the antiferromagnetic layer even at a spacer thickness for which there is no observable hysteresis loop shift.

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PubMed2005

Observation of giant magnetic linear dichroism in (Ga, Mn) As.

Giant magnetic linear dichroism (MLD) is observed in the ferromagnetic semiconductor Ga(0.98)Mn(0.02)As. The contribution to this effect induced by the spontaneous magnetization can be clearly identified by azimuthal dependencies. The spectral dependence of the effect in the range from 1.4 to 2.4 eV shows that the MLD induced by the spontaneous magnetization is strongly enhanced for excitations from the electronic states that are responsible for the ferromagnetism in this material. This spectral sensitivity and the size of the effect makes MLD a powerful tool for the study of (III, Mn)V alloys and similar novel ferromagnetic semiconductors.

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PubMed2005

Ultrafast non-thermal control of magnetization by instantaneous photomagnetic pulses.

The demand for ever-increasing density of information storage and speed of manipulation has triggered an intense search for ways to control the magnetization of a medium by means other than magnetic fields. Recent experiments on laser-induced demagnetization and spin reorientation use ultrafast lasers as a means to manipulate magnetization, accessing timescales of a picosecond or less. However, in all these cases the observed magnetic excitation is the result of optical absorption followed by a rapid temperature increase. This thermal origin of spin excitation considerably limits potential applications because the repetition frequency is limited by the cooling time. Here we demonstrate that circularly polarized femtosecond laser pulses can be used to non-thermally excite and coherently control the spin dynamics in magnets by way of the inverse Faraday effect. Such a photomagnetic interaction is instantaneous and is limited in time by the pulse width (approximately 200 fs in our experiment). Our finding thus reveals an alternative mechanism of ultrafast coherent spin control, and offers prospects for applications of ultrafast lasers in magnetic devices.

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PubMed2005

Structure determination of small vanadium clusters by density-functional theory in comparison with experimental far-infrared spectra.

The far-infrared vibrational spectra for charged vanadium clusters with sizes of 3-15 atoms have been measured using infrared multiple photon dissociation of Vn+Ar-->Vn(+)+Ar. Using density-functional theory calculations, we calculated the ground state energy and vibrational spectra for a large number of stable and metastable geometries of such clusters. Comparison of the calculated vibrational spectra with those obtained in the experiment allows us to deduce the cluster size specific atomic structures. In several cases, a unique atomic structure can be identified, while in other cases our calculations suggest the presence of multiple isomers.

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PubMed2004

Laser-induced ultrafast spin reorientation in the antiferromagnet TmFeO3.

All magnetically ordered materials can be divided into two primary classes: ferromagnets and antiferromagnets. Since ancient times, ferromagnetic materials have found vast application areas, from the compass to computer storage and more recently to magnetic random access memory and spintronics. In contrast, antiferromagnetic (AFM) materials, though representing the overwhelming majority of magnetically ordered materials, for a long time were of academic interest only. The fundamental difference between the two types of magnetic materials manifests itself in their reaction to an external magnetic field-in an antiferromagnet, the exchange interaction leads to zero net magnetization. The related absence of a net angular momentum should result in orders of magnitude faster AFM spin dynamics. Here we show that, using a short laser pulse, the spins of the antiferromagnet TmFeO3 can indeed be manipulated on a timescale of a few picoseconds, in contrast to the hundreds of picoseconds in a ferromagnet. Because the ultrafast dynamics of spins in antiferromagnets is a key issue for exchange-biased devices, this finding can expand the now limited set of applications for AFM materials.

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PubMed2004

Picosecond dynamics of the photoinduced spin polarization in epitaxial (Ga,Mn)as films.

Static and time-resolved magneto-optical spectra of the ferromagnetic semiconductor (Ga,Mn)As show that a pulsed photoexcitation with a fluence of 10 microJ/cm(2) is equivalent to the application of an external magnetic field of about 1 mT, which relaxes with a decay time of 30 ps. This relaxation is attributed to the spin relaxation of electrons in the conduction band and is found to be not affected by interactions with Mn ions.

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PubMed1996