Quantum spin liquid is a disordered magnetic state with fractional spin excitations. Its clearest example is found in an exactly solved Kitaev honeycomb model where a spin flip fractionalizes into two types of anyons, quasiparticles that are neither fermions nor bosons: a pair of gauge fluxes and a Majorana fermion. Here we demonstrate this kind of fractionalization in the Kitaev paramagnetic state of the honeycomb magnet α-RuCl3. The spin-excitation gap measured by nuclear magnetic resonance consists of the predicted Majorana fermion contribution following the cube of the applied magnetic field, and a finite zero-field contribution matching the predicted size of the gauge-flux gap. The observed fractionalization into gapped anyons survives in a broad range of temperatures and magnetic fields despite inevitable non-Kitaev interactions between the spins, which are predicted to drive the system towards a gapless ground state. The gapped character of both anyons is crucial for their potential application in topological quantum computing.
Employing complementary torque magnetometry and electron spin resonance on single crystals of herbertsmithite, the closest realization to date of a quantum kagome antiferromagnet featuring a spin-liquid ground state, we provide novel insight into different contributions to its magnetism. At low temperatures, two distinct types of defects with different magnetic couplings to the kagome spins are found. Surprisingly, their magnetic response contradicts the threefold symmetry of the ideal kagome lattice, suggesting the presence of a global structural distortion that may be related to the establishment of the spin-liquid ground state.
One of the key questions concerning frustrated lattices that has lately emerged is the role of disorder in inducing spin-liquid-like properties. In this context, the quantum kagome antiferromagnets YCu3(OH)6Cl3, which has been recently reported as the first geometrically perfect realization of the kagome lattice with negligible magnetic/non-magnetic intersite mixing and a possible quantumspin-liquid ground state, is of particular interest. However, contrary to previous conjectures, here we show clear evidence of bulk magnetic ordering in this compound below TN = 15 K by combining bulk magnetization and heat capacity measurements, and local-probe muon spin relaxation measurements. The magnetic ordering in this material is rather unconventional in several respects. Firstly, a crossover regime where the ordered state coexists with the paramagnetic state extends down to TN /3 and, secondly, the fluctuation crossover is shifted far below TN . Moreover, persistent spin dynamics that is observed at temperatures as low as T /TN = 1/300 could be a sign of emergent excitations of correlated spin-loops or, alternatively, a sign of fragmentation of each magnetic moment into an ordered and a fluctuating part. arXiv:1904.02878v2 [cond-mat.str-el] 1 Jul 2019
The emergent behavior of spin liquids that are born out of geometrical frustration makes them an intriguing state of matter. We show that in the quantum kagome antiferromagnet ZnCu3(OH)6SO4 several different correlated, yet fluctuating states exist. By combining complementary local-probe techniques with neutron scattering, we discover a crossover from a critical regime into a gapless spin-liquid phase with decreasing temperature. An additional unconventional instability of the latter phase leads to a second, distinct spin-liquid state that is stabilized at the lowest temperatures. We advance such complex behavior as a feature common to different frustrated quantum magnets.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.