ترغب بنشر مسار تعليمي؟ اضغط هنا

Canted ferrimagnetism and giant coercivity in the non-stoichiometric double perovskite La2Ni1.19Os0.81O6

91   0   0.0 ( 0 )
 نشر من قبل Hai Feng
 تاريخ النشر 2018
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

The non-stoichiometric double perovskite oxide La2Ni1.19Os0.81O6 was synthesized by solid state reaction and its crystal and magnetic structures were investigated by powder x-ray and neutron diffraction. La2Ni1.19Os0.81O6 crystallizes in the monoclinic double perovskite structure (general formula A2BBO6) with space group P21/n, where the B site is fully occupied by Ni and the B site by 19 % Ni and 81 % Os atoms. Using x-ray absorption spectroscopy an Os4.5+ oxidation state was established, suggesting presence of about 50 % paramagnetic Os5+ (5d3, S = 3/2) and 50 % non-magnetic Os4+ (5d4, Jeff = 0) ions at the B sites. Magnetization and neutron diffraction measurements on La2Ni1.19Os0.81O6 provide evidence for a ferrimagnetic transition at 125 K. The analysis of the neutron data suggests a canted ferrimagnetic spin structure with collinear Ni2+ spin chains extending along the c axis but a non-collinear spin alignment within the ab plane. The magnetization curve of La2Ni1.19Os0.81O6 features a hysteresis with a very high coercive field, HC = 41 kOe, at T = 5 K, which is explained in terms of large magnetocrystalline anisotropy due to the presence of Os ions together with atomic disorder. Our results are encouraging to search for rare earth free hard magnets in the class of double perovskite oxides.



قيم البحث

اقرأ أيضاً

We present a comprehensive theory of the temperature- and disorder-dependence of half-metallic ferrimagnetism in the double perovskite Sr$_2$FeMoO$_6$ (SFMO) with $T_c$ above room temperature. We show that the magnetization $M(T)$ and conduction elec tron polarization $P(T)$ are both proportional to the magnetization $M_S(T)$ of localized Fe spins. We derive and validate an effective spin Hamiltonian, amenable to large-scale three-dimensional simulations. We show how $M(T)$ and $T_c$ are affected by disorder, ubiquitous in these materials. We suggest a way to enhance $T_c$ in SFMO without sacrificing polarization.
As they combine decent mobilities with extremely long carrier lifetimes, organic-inorganic perovskites have opened a whole new field in opto-electronics. Measurements of their underlying electronic structure, however, are still lacking. Using angle-r esolved photoelectron spectroscopy, we measure the valence band dispersion of single-crystal CH$_3$NH$_3$PbBr$_3$. The dispersion of the highest energy band is extracted applying a modified leading edge method, which accounts for the particular density of states of organic-inorganic perovskites. The surface Brillouin zone is consistent with bulk-terminated surfaces both in the low-temperature orthorhombic and the high-temperature cubic phase. In the low-temperature phase, we find a ring-shaped valence band maximum with a radius of 0.043 {AA}$^{-1}$, centered around a 0.16 eV deep local minimum in the dispersion of the valence band at the high-symmetry point. Intense circular dichroism is observed. This dispersion is the result of strong spin-orbit coupling. Spin-orbit coupling is also present in the room-temperature phase. The coupling strength is one of the largest reported so far.
179 - R.O. Kuzian , V.V. Laguta , 2013
We show that a superstructure of antiferromagnetically interacting Fe$^{3+}$ ($S=5/2$) ions in double perovskites AFe$_{1/2}$M$_{1/2}$O$_{3}$ exhibits a ferrimagnetic ordering below $T_{fe} approx 5.6J_1$ ($J_1/k_B sim 50$~K), which is close to room temperature. Small clusters of the same structure exhibit a superparamagnetic behavior at $T lesssim T_{fe}$. The possibility of formation of such clusters explains the room-temperature (superpara)magnetism in 3$d$-metal based oxides.
We report the low-temperature properties of phase-pure single crystals of the half-Heusler compound CuMnSb grown by means of optical float-zoning. The magnetization, specific heat, electrical resistivity, and Hall effect of our single crystals exhibi t an antiferromagnetic transition at $T_{mathrm{N}} = 55~mathrm{K}$ and a second anomaly at a temperature $T^{*} approx 34~mathrm{K}$. Powder and single-crystal neutron diffraction establish an ordered magnetic moment of $(3.9pm0.1)~mu_{mathrm{B}}/mathrm{f.u.}$, consistent with the effective moment inferred from the Curie-Weiss dependence of the susceptibility. Below $T_{mathrm{N}}$, the Mn sublattice displays commensurate type-II antiferromagnetic order with propagation vectors and magnetic moments along $langle111rangle$ (magnetic space group $R[I]3c$). Surprisingly, below $T^{*}$, the moments tilt away from $langle111rangle$ by a finite angle $delta approx 11^{circ}$, forming a canted antiferromagnetic structure without uniform magnetization consistent with magnetic space group $C[B]c$. Our results establish that type-II antiferromagnetism is not the zero-temperature magnetic ground state of CuMnSb as may be expected of the face-centered cubic Mn sublattice.
Single crystal neutron diffraction, inelastic neutron scattering, bulk magnetization measurements, and first-principles calculations are used to investigate the magnetic properties of the honeycomb lattice $rm Tb_2Ir_3Ga_9$. While the $Rln2$ magnetic contribution to the low-temperature entropy indicates a $rm J_{eff}=1/2$ moment for the lowest-energy crystal-field doublet, the Tb$^{3+}$ ions form a canted antiferromagnetic structure below 12.5 K. Due to the Dzyalloshinskii-Moriya interactions, the Tb moments in the $ab$ plane are slightly canted towards $b$ by $6^circ$ with a canted moment of 1.22 $mu_{rm B} $ per formula unit. A minimal $xxz$ spin Hamiltonian is used to simultaneously fit the spin-wave frequencies along the high symmetry directions and the field dependence of the magnetization along the three crystallographic axes. Long-range magnetic interactions for both in-plane and out-of-plane couplings up to the second nearest neighbors are needed to account for the observed static and dynamic properties. The $z$ component of the exchange interactions between Tb moments are larger than the $x$ and $y$ components. This compound also exhibits bond-dependent exchange with negligible nearest exchange coupling between moments parallel and perpendicular to the 4$f$ orbitals. Despite the $J_{{rm eff}}=1/2$ moments, the spin Hamiltonian is denominated by a large in-plane anisotropy $K_z sim -1$ meV. DFT calculations confirm the antiferromagnetic ground state and the substantial inter-plane coupling at larger Tb-Tb distances.
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