ترغب بنشر مسار تعليمي؟ اضغط هنا

Terahertz Spin-Orbital Excitations in the paramagnetic state of multiferroic Sr$_2$FeSi$_2$O$_7$

113   0   0.0 ( 0 )
 نشر من قبل Rolando Vald\\'es Aguilar
 تاريخ النشر 2016
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

We studied the novel multiferroic material Sr$_2$FeSi$_2$O$_7$, and found 3 absorption modes above the magnetic ordering transition temperature using time-domain terahertz spectroscopy. These absorption modes can be explained as the optical transitions between the spin-orbit coupling and crystal field split 3d$^6$ Fe$^{2+}$ ground state term in this material. Consideration of the compressed tetrahedral environment of the Fe$^{2+}$ site is crucial to understand the excitations. We point out, however, discrepancies between the single-site atomic picture and the experimental results.

قيم البحث

اقرأ أيضاً

158 - A. A. Aligia , C. Helman 2018
Using maximally localized Wannier functions obtained from DFT calculations, we derive an effective Hubbard Hamiltonian for a bilayer of Sr$_3$Cr$_2$O$_7$, the $n=2$ member of the Ruddlesden-Popper Sr$_{n+1}$Cr$_n$O$_{3n+1}$ system. The model consists of effective $t_{2g}$ orbitals of Cr in two square lattices, one above the other. The model is further reduced at low energies and two electrons per site, to an effective Kugel-Khomskii Hamiltonian that describes interacting spins 1 and pseudospins 1/2 at each site describing spin and orbitals degrees of freedom respectively. We solve this Hamiltonian at zero temperature using pseudospin bond operators and spin waves. Our results confirm a previous experimental and theoretical study that proposes spin ordering antiferromagnetic in the planes and ferromagnetic between planes, while pseudospins form vertical singlets, although the interplane separation is larger than the nearest-neighbor distance in the plane. We explain the physics behind this rather unexpected behavior.
Exotic spin-multipolar ordering in spin transition metal insulators has so far eluded unambiguous experimental observation. A less studied, but perhaps more feasible fingerprint of multipole character emerges in the excitation spectrum in the form of quadrupolar transitions. Such multipolar excitations are desirable as they can be manipulated with the use of light or electric field and can be captured by means of conventional experimental techniques. Here we study single crystals of multiferroic Sr$_2$CoGe$_2$O$_7$, and show that due to its nearly isotropic nature a purely quadrupolar bimagnon mode appears in the electron spin resonance (ESR) spectra. This non-magnetic spin-excitation couples to the electric field of the light and becomes observable for a specific experimental configuration, in full agreement with a theoretical analysis of the selection rules.
80 - L. Wang , J. Werner , A. Ottmann 2018
We investigate magnetoelectric coupling and low-energy magnetic excitations in multiferroic $alpha$-Cu$_2$V$_2$O$_7$ by detailed thermal expansion, magnetostriction, specific heat and magnetization measurements in magnetic fields up to 15~T and by hi gh-field/high-frequency electron spin resonance studies. Our data show negative thermal expansion in the temperature range $leq 200$~K under study. Well-developed anomalies associated with the onset of multiferroic order (canted antiferromagnetism with a significant magnetic moment and ferroelectricity) imply pronounced coupling to the structure. We detect anomalous entropy changes in the temperature regime up to $sim 80$~K which significantly exceed the spin entropy. Failure of Gruneisen scaling further confirms that several dominant ordering phenomena are concomitantly driving the multiferroic order. By applying external magnetic fields, anomalies in the thermal expansion and in the magnetization are separated. Noteworthy, the data clearly imply the development of a canted magnetic moment at temperatures above the structural anomaly. Low-field magnetostriction supports the scenario of exchange-striction driven multiferroicity. We observe low-energy magnetic excitations well below the antiferromagnetic gap, i.e., a ferromagnetic-type resonance branch associated with the canted magnetic moment arising from Dzyaloshinsii-Moriya interactions. The anisotropy parameter $tilde{D}=1.6(1)$~meV indicates a sizeable ratio of DM- and isotropic magnetic exchange.
80 - J. Vit , J. Viirok , L. Peedu 2021
Non-reciprocal directional dichroism assigns an optical diode-like property to non-centrosymmetric magnets, making them appealing for low-dissipation optical devices. However, the direct electric control of this phenomenon at constant temperatures is scarce. In Ba$_2$CoGe$_2$O$_7$, we demonstrate the isothermal electric switch between domains possessing opposite magnetoelectric susceptibilities. Combining THz spectroscopy and multiboson spin-wave analysis, we show that unbalancing the domain population realizes the non-reciprocal light absorption of spin excitations.
252 - M. Zhu , Y. Wang , P. G. Li 2018
We report the magnetic and electronic properties of the bilayer ruthenate Sr$_3$Ru$_2$O$_7$ upon Fe substitution for Ru. We find that Sr$_3$(Ru$_{1-x}$Fe$_x$)$_2$O$_7$ shows a spin-glass-like phase below 4 K for $x$ = 0.01 and commensurate E-type ant iferromagnetically ordered insulating ground state characterized by the propagation vector $q_c$ = (0.25 0.25 0) for $x$ $geq$ 0.03, respectively, in contrast to the paramagnetic metallic state in the parent compound with strong spin fluctuations occurring at wave vectors $q$ = (0.09 0 0) and (0.25 0 0). The observed antiferromagnetic ordering is quasi-two-dimensional with very short correlation length along the $c$ axis, a feature similar to the Mn-doped Sr$_3$Ru$_2$O$_7$. Our results suggest that this ordered ground state is associated with the intrinsic magnetic instability in the pristine compound, which can be readily tipped by the local magnetic coupling between the 3$d$ orbitals of the magnetic dopants and Ru 4$d$ orbitals.
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