Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userNegative-vector-chirality 120$^circ$ spin structure in the defect- and distortion-free quantum kagome antiferromagnet YCu$_3$(OH)$_6$Cl$_3$
96
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
The magnetic ground state of the ideal quantum kagome antiferromagnet (QKA) has been a long-standing puzzle, mainly because perturbations to the nearest-neighbor isotropic Heisenberg Hamiltonian can lead to various fundamentally different ground states. Here we investigate a recently synthesized QKA representative YCu$_3$(OH)$_6$Cl$_3$, where perturbations commonly present in real materials, like lattice distortion and intersite ion mixing, are absent. Nevertheless, this compound enters a long-range magnetically ordered state below $T_N=15$ K. Our powder neutron diffraction experiment reveals that its magnetic structure corresponds to a coplanar $120^circ$ state with negative vector spin chirality. The ordered magnetic moments are suppressed to $0.42(2)mu_B$, which is consistent with the previously detected spin dynamics persisting to the lowest experimentally accessible temperatures. This indicates either a coexistence of magnetic order and disorder or the presence of strong quantum fluctuations in the ground state of YCu$_3$(OH)$_6$Cl$_3$. The origin of the magnetic order is sought in terms of Dzyaloshinskii-Moriya magnetic anisotropy and further-neighbor isotropic exchange interactions.
rate research
Read More
We studied the magnetic properties of YCu$_3$(OH)$_6$Br$_2$[Br$_{1-x}$(OH)$_{x}$] ($x$ = 0.33 and 0.45), where Cu$^{2+}$ ions form two-dimensional kagome layers. There is no magnetic order down to 50 mK while the Curie-Weiss temperature is in the order of -100 K. At zero magnetic field, the low-temperature specific heat shows a $T^2$ dependence. Above 2 T, a linear-temperature dependence term in specific heat emerges, and the value of $gamma = C/T$ increases linearly with the field. Furthermore, the magnetic susceptibility tends to a constant value at $T = 0$. Our results suggest that the magnetic ground state of YCu$_3$(OH)$_6$Br$_2$[Br$_{1-x}$(OH)$_{x}$] is consistent with a Dirac quantum-spin-liquid state with linearly dispersing spinon strongly coupled with emergent gauge field, which has long been theoretically proposed as a candidate ground state in the two-dimensional kagome Heisenberg antiferromagnetic system.
Spin liquids are exotic phases of quantum matter challenging Landaus paradigm of symmetry-breaking phase transitions. Despite strong exchange interactions, spins do not order or freeze down to zero temperature. While well-established for 1D quantum antiferromagnets, in higher dimension where quantum fluctuations are less acute, realizing and understanding such states represent major issues, both theoretical and experimental. In this respect the simplest nearest-neighbor Heisenberg antiferromagnet Hamiltonian on the highly frustrated kagome lattice has proven to be a fascinating and inspiring model. The exact nature of its ground state remains elusive and the existence of a spin-gap is the first key-issue to be addressed to discriminate between the various classes of proposed spin liquids. Here, through low-temperature Nuclear Magnetic Resonance (NMR) contrast experiments on high quality single crystals, we single out the kagome susceptibility and the corresponding dynamics in the kagome archetype, the mineral herbertsmithite, ZnCu$_3$(OH)$_6$Cl$_2$. We firmly conclude that this material does not harbor any spin-gap, which restores a convergence with recent numerical results promoting a gapless Dirac spin liquid as the ground state of the Heisenberg kagome antiferromagnet.
Experimental studies of high-purity kagome-lattice antiferromagnets (KAFM) are of great importance in attempting to better understand the predicted enigmatic quantum spin-liquid ground state of the KAFM model. However, realizations of this model can rarely evade magnetic ordering at low temperatures due to various perturbations to its dominant isotropic exchange interactions. Such a situation is for example encountered due to sizable Dzyaloshinskii-Moriya magnetic anisotropy in YCu$_3$(OH)$_6$Cl$_3$, which stands out from other KAFM materials by its perfect crystal structure. We find evidence of magnetic ordering also in the distorted sibling compound Y$_3$Cu$_9$(OH)$_{18}$[Cl$_8$(OH)], which has recently been proposed to feature a spin-liquid ground state arising from a spatially anisotropic kagome lattice. Our findings are based on a combination of bulk susceptibility, specific heat, and magnetic torque measurements that disclose a Neel transition temperature of $T_N=11$~K in this material, which might feature a coexistence of magnetic order and persistent spin dynamics as previously found in YCu$_3$(OH)$_6$Cl$_3$. Contrary to previous studies of single crystals and powders containing impurity inclusions, we use high-purity single crystals of Y$_3$Cu$_9$(OH)$_{18}$[Cl$_8$(OH)] grown via an optimized hydrothermal synthesis route that minimizes such inclusions. This study thus demonstrates that the lack of magnetic ordering in less pure samples of the investigated compound does not originate from the reduced symmetry of spin lattice but is instead of extrinsic origin.
We report a new kagome quantum spin liquid candidate Cu$_3$Zn(OH)$_6$FBr, which does not experience any phase transition down to 50 mK, more than three orders lower than the antiferromagnetic Curie-Weiss temperature ($sim$ 200 K). A clear gap opening at low temperature is observed in the uniform spin susceptibility obtained from $^{19}$F nuclear magnetic resonance measurements. We observe the characteristic magnetic field dependence of the gap as expected for fractionalized spin-1/2 spinon excitations. Our experimental results provide firm evidence for spin fractionalization in a topologically ordered spin system, resembling charge fractionalization in the fractional quantum Hall state.
In an ideal classical pyrochlore antiferromagnet without perturbations, an infinite degeneracy at a ground state leads to absence of a magnetic order and spin-glass transition. Here we present Na$_3$Mn(CO$_3$)$_2$Cl as a new candidate compound where classical spins are coupled antiferromagnetically on the pyrochlore lattice, and report its structural and magnetic properties.The temperature dependences of the magnetic susceptibility and heat capacity, and the magnetization curve are consistent with those of an $S$ = 5/2 pyrochlore lattice antiferromagnet with nearest-neighbor interactions of 2 K. Neither an apparent signature of a spin-glass transition nor a magnetic order is detected in magnetization and heat capacity measurements, or powder neutron diffraction experiments. On the other hand, an antiferromagnetic short-range order from the nearest neighbors is evidenced by the $Q$-dependence of the diffuse scattering which develops around 0.85 AA$^{-1}$. A high degeneracy near the ground state in Na$_3$Mn(CO$_3$)$_2$Cl is supported by the magnetic entropy estimated as almost 4 J K$^{-2}$ mol$^{-1}$ at 0.5 K.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
