اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدMagnetic Order in the Pyrochlore Iridates A2Ir2O7 (A = Y, Yb)
120
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We present results from muon spin relaxation/rotation, magnetization, neutron scattering and transport measurements on polycrystalline samples of the pyrochlore iridates Y2Ir2O7 (Y-227) and Yb2Ir2O7 (Yb-227). Well-defined spontaneous oscillations of the muon asymmetry are observed together with hysteretic behavior in magnetization below 130 K in Yb-227, indicative of commensurate long-range magnetic order. Similar oscillations are observed in Y-227 below 150 K; however the onset of hysteretic magnetization at T = 190 K indicates a transition to an intermediate state lacking long-range order as observed in Nd-227. Our results also show that insulating members of the iridate family have nearly identical magnetic ground states, and that the presence of magnetic A-site species does not play any significant role in altering the ground state properties.
قيم البحث
اقرأ أيضاً
We present resistivity, magnetization, and zero field muon spin relaxation ($mu$SR) data for the pyrochlore iridate materials Nd$_{2-x}$Ca$_{x}$Ir$_{2}$O$_{7}$ ($x = 0, 0.06$, and $0.10$) and Sm$_2$Ir$_2$O$_7$. While Nd$_{2}$Ir$_{2}$O$_{7}$ (Nd227) i
s weakly conducting, Sm$_{2}$Ir$_{2}$O$_{7}$ (Sm227) has slowly diverging resistivity at low temperature. Nd227 and Sm227 exhibit magnetic anomalies at $T_{M} = 105 K$ and $137 K$, respectively. However, zero-field $mu$SR measurements show that long-range magnetic order of the Ir$^{4+}$ sublattice sets in at much lower temperatures ($T_{LRO} sim 8 K$ for Nd227 and $70 K$ for Sm227); both materials show heavily damped muon precession with a characteristic frequency near 9 MHz. The magnetic anomaly at $T_{M}$ in Nd227 is not significantly affected by the introduction of hole carriers by Ca-substitution in the conducting Nd$_{2-x}$Ca$_{x}$Ir$_{2}$O$_{7}$ samples, but the muon precession is fully suppressed for both.
Pyrochlore iridates A2Ir2O7 (A = rare earth elements, Y or Bi) hold great promise for realizing novel electronic and magnetic states owing to the interplay of spin-orbit coupling, electron correlation and geometrical frustration. A prominent example
is the formation of all-in/all-out (AIAO)antiferromagnetic order in the Ir4+ sublattice that comprises of corner-sharing tetrahedra. Here we report on an unusual magnetic phenomenon, namely a cooling-field induced shift of magnetic hysteresis loop along magnetization axis, and its possible origin in pyrochlore iridates with non-magnetic Ir defects (e.g. Ir3+). In a simple model, we attribute the magnetic hysteresis loop to the formation of ferromagnetic droplets in the AIAO antiferromagnetic background. The weak ferromagnetism originates from canted antiferromagnetic order of the Ir4+ moments surrounding each non-magnetic Ir defect. The shift of hysteresis loop can be understood quantitatively based on an exchange-bias like effect in which the moments at the shell of the FM droplets are pinned by the AIAO AFM background via mainly the Heisenberg (J) and Dzyaloshinsky-Moriya (D) interactions. The magnetic pinning is stable and robust against the sweeping cycle and sweeping field up to 35 T, which is possibly related to the magnetic octupolar nature of the AIAO order.
Nonequilibrium many-body dynamics is becoming one of the central topics of modern condensed matter physics. Floquet topological states were suggested to emerge in photodressed band structures in the presence of periodic laser driving. Here we propose
a viable nonequilibrium route without requiring coherent Floquet states to reach the elusive magnetic Weyl semimetallic phase in pyrochlore iridates by ultrafast modification of the effective electron-electron interaction with short laser pulses. Combining textit{ab initio} calculations for a time-dependent self-consistent reduced Hubbard $U$ controlled by laser intensity and nonequilibrium magnetism simulations for quantum quenches, we find dynamically modified magnetic order giving rise to transiently emerging Weyl cones that are probed by time- and angle-resolved photoemission spectroscopy. Our work offers a unique and realistic pathway for nonequilibrium materials engineering beyond Floquet physics to create and sustain Weyl semimetals. This may lead to ultrafast, tens-of-femtoseconds switching protocols for light-engineered Berry curvature in combination with ultrafast magnetism.
The consequences of nonmagnetic-ion dilution for the pyrochlore family Y$_{2}$($M_{1-x}N_{x}$)$_{2}$O$_{7}$ ($M$ = magnetic ion, $N$ = nonmagnetic ion) have been investigated. As a first step, we experimentally examine the magnetic properties of Y$_{
2}$CrSbO$_{7}$ ($x$ = 0.5), in which the magnetic sites (Cr$^{3+}$) are percolative. Although the effective Cr-Cr spin exchange is ferromagnetic, as evidenced by a positive Curie-Weiss temperature, $Theta_mathrm{{CW}}$ = 20.1(6) K, our high-resolution neutron powder diffraction measurements detect no sign of magnetic long range order down to 2 K. In order to understand our observations, we performed numerical simulations to study the bond-disorder introduced by the ionic size mismatch between $M$ and $N$. Based on these simulations, bond-disorder ($x_{b}$ $simeq$ 0.23) percolates well ahead of site-disorder ($x_{s}$ $simeq$ 0.61). This model successfully reproduces the critical region (0.2 < $x$ < 0.25) for the Neel to spin glass phase transition in Zn(Cr$_{1-x}$Ga$_{x}$)$_{2}$O$_{4}$, where the Cr/Ga-sublattice forms the same corner-sharing tetrahedral network as the $M/N$-sublattice in Y$_{2}$($M_{1-x}N_{x}$)$_{2}$O$_{7}$, and the rapid drop in magnetically ordered moment in the Neel phase [Lee $et$ $al$, Phys. Rev. B 77, 014405 (2008)]. Our study stresses the nonnegligible role of bond-disorder on magnetic frustration, even in ferromagnets.
Cubic Y$_{2}$Ti$_{2}$O$_{7}$ single crystals doped with Er$^{3+}$ and Yb$^{3+}$ ions have been studied by the methods of electron spin resonance (ESR) and selective laser spectroscopy. ESR spectra exhibit signals from rare-earth ions that substitute
for yttrium ions in sites with local trigonal symmetry. The $g$ tensor components are determined. The results of optical investigations indicate that impurity centers of several types are formed; the sublevel energies of the ground and excited multiplets of these centers are found. Among the great variety of detected optical centers, the centers that dominate in the formation of ESR spectra are discriminated. An analysis of the experimental data using the exchange-charge model have made it possible to determine the sets of parameters of the crystal field for Er$^{3+}$ and Yb$^{3+}$ ions substituting Y$^{3+}$ ions in regular crystallographic sites in pyrochlore Y$_{2}$Ti$_{2}$O$_{7}$.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
