ترغب بنشر مسار تعليمي؟ اضغط هنا

Criterion of multi-switching stability for magnetic nanoparticles

90   0   0.0 ( 0 )
 نشر من قبل Fabrizio Porrati
 تاريخ النشر 2007
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

We present a procedure to study the switching and the stability of an array of magnetic nanoparticles in the dynamical regime. The procedure leads to the criterion of multi-switching stability to be satisfied in order to have stable switching. The criterion is used to compare various magnetic-field-induced switching schemes, either present in the literature or suggested in the present work. In particular, we perform micromagnetic simulations to study the magnetization trajectories and the stability of the magnetization after switching for nanoparticles of elliptical shape. We evaluate the stability of the switching as a function of the thickness of the particles and the rise and fall times of the magnetic pulses, both at zero and room temperature. Furthermore, we investigate the role of the dipolar interaction and its influence on the various switching schemes. We find that the criterion of multi-switching stability can be satisfied at room temperature and in the presence of dipolar interactions for pulses shaped according to CMOS specifications, for switching rates in the GHz regime.



قيم البحث

اقرأ أيضاً

In order to control and tailor the properties of nanodots, it is essential to separate the effects of quantum confinement from those due to the surface, and to gain insight into the influence of preparation conditions on the dot physical properties. We address these issues for the case of small Ge clusters (1-3 nm), using a combination of empirical and first-principles molecular dynamics techniques. Our results show that over a wide temperature range the diamond structure is more stable than tetragonal, ST12-like structures for clusters containing more than 50 atoms; however, the magnitude of the energy difference between the two geometries is strongly dependent on the surface properties. Based on our structural data, we propose a mechanism which may be responsible for the formation of metastable ST12 clusters in vapor deposition experiments, by cold quenching of amorphous nanoparticles with unsaturated, reconstructed surfaces.
We investigated the reversible ferromagnetic (FM) behavior of pure and Co doped CeO2 nanopowders. The as-sintered samples displayed an increasing paramagnetic contribution upon Co doping. Room temperature FM is obtained simply by performing thermal t reatments in vacuum at temperatures as low as 500^{circ}C and it can be switched off by performing thermal treatments in oxidizing conditions. The FM contribution is enhanced as we increase the time of the thermal treatment in vacuum. Those systematic experiments establish a direct relation between ferromagnetism and oxygen vacancies and open a path for developing materials with tailored properties.
We report evidence of the magnetization reversal in nanoparticles by surface acoustic waves (SAWs). The experimental system consists of isolated magnetite nanoparticles dispersed on a piezoelectric substrate. Magnetic relaxation from a saturated stat e becomes significantly enhanced in the presence of the SAW at a constant temperature of the substrate. The dependence of the relaxation on SAW power and frequency has been investigated. The effect is explained by the effective ac magnetic field generated by the SAW in the nanoparticles.
The magnetic behavior of $Fe_{3-x}O_4$ nanoparticles synthesized either by high-temperature decomposition of an organic iron precursor or low-temperature co-precipitation in aqueous conditions, is compared. Transmission electron microscopy, X-ray abs orption spectroscopy, X-ray magnetic circular dichroism and magnetization measurements show that nanoparticles synthesized by thermal decomposition display high crystal quality and bulk-like magnetic and electronic properties, while nanoparticles synthesized by co-precipitation show much poorer crystallinity and particle-like phenomenology, including reduced magnetization, high closure fields and shifted hysteresis loops. The key role of the crystal quality is thus suggested since particle-like behavior for particles larger than about 5 nm is only observed when they are structurally defective. These conclusions are supported by Monte Carlo simulations. It is also shown that thermal decomposition is capable of producing nanoparticles that, after further stabilization in physiological conditions, are suitable for biomedical applications such as magnetic resonance imaging or bio-distribution studies.
We report the magnetic properties of magnetic nano-composite, consisting of different quantity of NiFe2O4 nanoparticles in polymer matrix. The nanoparticles exhibited a typical magnetization blocking, which is sensitive on the variation of magnetic f ield, mode of zero field cooled/field cooled experiments and particle quantity in the matrix. The samples with lower particle quantity showed an upturn of magnetization down to 5 K, whereas the blocking of magnetization dominates at lower temperatures as the particle quantity increases in the polymer. We examine such magnetic behaviour in terms of the competitive magnetic ordering between core and surface spins of nanoparticles, taking into account the effect of inter-particle (dipole-dipole) interactions on nanoparticle magnetic dynamics.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا