ترغب بنشر مسار تعليمي؟ اضغط هنا

A-type antiferromagnetic order and magnetic phase diagram of the trigonal Eu spin-7/2 triangular-lattice compound EuSn2As2

184   0   0.0 ( 0 )
 نشر من قبل David C. Johnston
 تاريخ النشر 2021
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

The trigonal compound EuSn2As2 was recently discovered to host Dirac surface states within the bulk band gap and orders antiferromagnetically below the Neel temperature TN = 24 K. Here the magnetic ground state of single-crystal EuSn2As2 and the evolution of its properties versus temperature T and applied magnetic field H are reported. Included are zero-field single-crystal neutron-diffraction measurements versus T, magnetization M(H,T), magnetic susceptibility chi(H,T) = M(T)/H, heat capacity Cp(H,T), and electrical resistivity rho(H,T) measurements. The neutron-diffraction and chi(T) measurements both indicate a collinear A-type antiferromagnetic (AFM) structure below TN =23.5(2) K, where the Eu{2+} spins S = 7/2 in a triangular ab-plane layer (hexagonal unit cell) are aligned ferromagnetically in the ab plane whereas the spins in adjacent Eu planes along the c axis are aligned antiferromagnetically. The chi(H{ab},T) and chi(H{c},T) data together indicate a smooth crossover between the collinear AFM alignment and an unknown magnetic structure at H ~ 0.15 T. Dynamic spin fluctuations up to 60 K are evident in the chi(T), Cp(T) and rho(H,T) measurements, a temperature that is more than twice TN. The rho(H,T) of the compound does not reflect a contribution of the topological state, but rather is consistent with a low-carrier-density metal with strong magnetic scattering. The magnetic phase diagrams for both H||c and H||ab in the H-T plane are constructed from the TN(H), chi(H,T), Cp(H,T), and rho(H,T) data.



قيم البحث

اقرأ أيضاً

124 - Sophie De Brion 2010
Using magnetic torque measurement on a NaNiO2 single crystal, we have established the magnetic phase diagram of this triangular compound. It presents 5 different phases depending on the temperature (4 K - 300 K) and magnetic field (0 - 22 T) revealin g several spin reorientations coupled to different magnetic anisotropies.
We used single-crystal x-ray and neutron diffraction to investigate the crystal and magnetic structures of trigonal lattice iridate Ca2Sr2IrO6. The crystal structure is determined to be $Rbar3$ with two distinct Ir sites. The system exhibits long-ran ge antiferromagnetic order below $T_N = 13.1$ K. The magnetic wave vector is identified as $(0,0.5,1)$ with ferromagnetic coupling along the $a$ axis and antiferromagnetic correlation along the $b$ axis. Spins align dominantly within the basal plane along the [1,2,0] direction and tilt 34$^circ$ towards the $c$ axis. The ordered moment is 0.66(3) $mu_B$/Ir, larger than other iridates where iridium ions form corner- or edge-sharing $rm IrO_6$ octahedral networks. The tilting angle is reduced to $approx19^circ$ when a magnetic field of 4.9 Tesla is applied along the $c$ axis. Density functional theory calculations confirm that the experimentally determined magnetic configuration is the most probable ground state with an insulating gap $sim0.5$~eV.
Organic salts represent an ideal experimental playground for studying the interplay between magnetic and charge degrees of freedom, which has culminated in the discovery of several spin-liquid candidates, such as $kappa$-(ET)$_2$Cu$_2$(CN)$_3$ ($kapp a$-Cu). Recent theoretical studies indicate the possibility of chiral spin liquids stabilized by ring-exchange, but the parent states with chiral magnetic order have not been observed in this material family. In this work, we discuss the properties of the recently synthesized $kappa$-(BETS)$_2$Mn[N(CN)$_2$]$_3$ ($kappa$-Mn). Based on analysis of specific heat, magnetic torque, and NMR measurements combined with ab initio calculations, we identify a spin-vortex crystal order. These observations definitively confirm the importance of ring-exchange in these materials, and support the proposed chiral spin-liquid scenario for triangular lattice organics.
Here, we report the synthesis and magnetic properties of a Yb-based triangular-lattice compound LiYbS$_2$. At low temperatures, it features an effective spin-$frac{1}{2}$ state due to the combined effect of crystal electric field and spin orbit coupl ing. Magnetic susceptibility measurements and $^7$Li nuclear magnetic resonance experiments reveal the absence of magnetic long range ordering down to 2~K, which suggests a possible quantum spin liquid ground state. A dominant antiferromagnetic nearest neighbour exchange interaction $J/k_{rm B}simeq$ 5.3~K could be extracted form the magnetic susceptibility. The NMR linewidth analysis yields the coupling constant between the Li nuclei and Yb$^{3+}$ ions which was found to be purely dipolar in nature.
117 - Qiang Luo , Shijie Hu , Bin Xi 2017
Motivated by the recent experiment on a rare-earth material YbMgGaO$_4$ [Y. Li textit{et al.}, Phys. Rev. Lett. textbf{115}, 167203 (2015)], which found that the ground state of YbMgGaO$_4$ is a quantum spin liquid, we study the ground-state phase di agram of an anisotropic spin-$1/2$ model that was proposed to describe YbMgGaO$_4$. Using the density-matrix renormalization group method in combination with the exact diagonalization, we calculate a variety of physical quantities, including the ground-state energy, the fidelity, the entanglement entropy and spin-spin correlation functions. Our studies show that in the quantum phase diagram there is a $120^{circ}$ phase and two distinct stripe phases. The transitions from the two stripe phases to the $120^{circ}$ phase are of the first order. However, the transition between the two stripe phases is not the first order, which is different from its classical counterpart. Additionally, we find no evidence for a quantum spin liquid in this model. Our results suggest that additional terms may be also important to model the material YbMgGaO$_4$. These findings will stimulate further experimental and theoretical works in understanding the quantum spin liquid ground state in YbMgGaO$_4$.
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