اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدMagnetic field control of charge structures in the magnetically disordered phase of the multiferroic LuFe$_2$O$_4$
94
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
Using neutron diffraction, we have studied the magnetic field effect on charge structures in the charge-ordered multiferroic material LuFe$_2$O$_4$. An external magnetic field is able to change the magnitude and correlation lengths of the charge valence order even before the magnetic order sets in. This affects the dielectric and ferroelectric properties of the material and induces a giant magneto-electric effect. Our results suggest that the magneto-electric coupling in LuFe$_2$O$_4$ is likely due to magnetic field effect on local spins, in clear contrast to the case in most other known multiferroic systems where the bulk magnetic order is important.
قيم البحث
اقرأ أيضاً
The reflectivity of a large LuFe(2)O(4) single crystal has been measured with the radiation field either perpendicular or parallel to the c axis of its rhombohedral structure, from 10 to 500K, and from 7 to 16000 cm-1. The transition between the two-
dimensional and the three-dimensional charge order at T_(CO) = 320 K is found to change dramatically the phonon spectrum in both polarizations. The number of the observed modes above and below T_(CO), according to a factor-group analysis, is in good agreement with a transition from the rhombohedral space group R{bar 3}m to the monoclinic C2/m. In the sub-THz region a peak becomes evident at low temperature, whose origin is discussed in relation with previous experiments.
We investigated the series of temperature and field-driven transitions in LuFe$_2$O$_4$ by optical and M{o}ssbauer spectroscopies, magnetization, and x-ray scattering in order to understand the interplay between charge, structure, and magnetism in th
is multiferroic material. We demonstrate that charge fluctuation has an onset well below the charge ordering transition, supporting the order by fluctuation mechanism for the development of charge order superstructure. Bragg splitting and large magneto optical contrast suggest a low temperature monoclinic distortion that can be driven by both temperature and magnetic field.
Oxides containing iridium ions display a range of magnetic and conducting properties that depend on the delicate balance between interactions and are controlled, at least in part, by the details of the crystal architecture. We have used muon-spin rot
ation ($mu$SR) to study the local field in four iridium oxides, Ca$_4$IrO$_6$, Ca$_5$Ir$_3$O$_{12}$, Sr$_3$Ir$_2$O$_7$ and Sr$_2$IrO$_4$, which show contrasting behavior. Our $mu$SR data on Ca$_4$IrO$_6$ and Ca$_5$Ir$_3$O$_{12}$ are consistent with conventional antiferromagnetism where quasistatic magnetic order develops below $T_{rm N}=13.85(6)$ K and 7.84(7) K respectively. A lower internal field is observed for Ca$_5$Ir$_3$O$_{12}$, as compared to Ca$_4$IrO$_6$ reflecting the presence of both Ir$^{4+}$ and Ir$^{5+}$ ions, resulting in a more magnetically dilute structure. Muon precession is only observed over a restricted range of temperature in Sr$_3$Ir$_2$O$_7$, while the Mott insulator Sr$_2$IrO$_4$ displays more complex behavior, with the $mu$SR signal containing a single, well-resolved precession signal below $T_{rm N}=230$,K, which splits into two precession signals at low temperature following a reorientation of the spins in the ordered state.
The low-temperature magnetic phase diagram of the multiferroic system FeTe$_2$O$_5$Br down to 300 mK and up to 9 T is presented. Short-range magnetic correlations within the crystal layers start to develop already at $sim$50 K, i.e., far above $T_{N1
} sim$ 11.0 K, where the system undergoes a magnetic phase transition into the high-temperature incommensurate (HT-ICM) phase. Only 0.5 K lower, at $T_{N2}$, the system undergoes a second phase transition into the low-temperature incommensurate amplitude-modulated (LT-ICM) phase accompanied by a spontaneous electric polarization. When the magnetic field is applied, the transition temperatures shift depending on the field orientation. In the case of $B||b$ and $B >$ 4.5 T, the HT-ICM phase disappears along with the electric polarization in the LT-ICM phase. The field dependence of the magnetic transition temperatures is explained in the context of the magnetic susceptibility behavior. Similarities and differences between the novel amplitude-modulated and well-established helicoidal magnetoelectrics are discussed.
We performed elastic neutron scattering measurements on the charge- and magnetically-ordered multiferroic material LuFe(2)O(4). An external electric field along the [001] direction with strength up to 20 kV/cm applied at low temperature (~100 K) does
not affect either the charge or magnetic structure. At higher temperatures (~360 K), before the transition to three-dimensional charge-ordered state, the resistivity of the sample is low, and an electric current was applied instead. A reduction of the charge and magnetic peak intensities occurs when the sample is cooled under a constant electric current. However, after calibrating the real sample temperature using its own resistance-temperature curve, we show that the actual sample temperature is higher than the thermometer readings, and the intensity reduction is entirely due to internal sample heating by the applied current. Our results suggest that the charge and magnetic orders in LuFe(2)O(4) are unaffected by the application of external electric field/current, and previously observed electric field/current effects can be naturally explained by internal sample heating.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
