We present a model compound with a spin-1/2 spatially anisotropic frustrated square lattice, in which three antiferromagnetic interactions and one ferromagnetic interaction are competing. We observe an unconventional gradual increase in the low-tempe
rature magnetization curve reminiscent of the quantum critical behavior between gapped and gapless phases. In addition, the specific heat and electron spin resonance signals indicate one-dimensional characteristics. These results demonstrate quantum critical behavior associated with one dimensionalization caused by frustrated interactions in the spin-1/2 spatially anisotropic square lattice.
Antiferromagnets host exotic quasiparticles, support high frequency excitations and are key enablers of the prospective spintronic and spin-orbitronic technologies. Here, we propose a concept of a curvilinear antiferromagnetism where material respons
es can be tailored by a geometrical curvature without the need to adjust material parameters. We show that an intrinsically achiral one-dimensional (1D) curvilinear antiferromagnet behaves as a chiral helimagnet with geometrically tunable Dzyaloshinskii--Moriya interaction (DMI) and orientation of the N{e}el vector. The curvature-induced DMI results in the hybridization of spin wave modes and enables a geometrically-driven local minimum of the low frequency branch. This positions curvilinear 1D antiferromagnets as a novel platform for the realization of geometrically tunable chiral antiferromagnets for antiferromagnetic spin-orbitronics and fundamental discoveries in the formation of coherent magnon condensates in the momentum space.
We present a model compound for the $S$=1/2 ferromagnetic Heisenberg chain composed of the verdazyl-based complex $[$Zn(hfac)$_2]$$[$4-Cl-$o$-Py-V-(4-F)$_2]$. $Ab$ $initio$ MO calculations indicate a predominant ferromagnetic interaction forming an $
S$=1/2 ferromagnetic chain. The magnetic susceptibility and specific heat indicate a phase transition to an AF order owing to the finite interchain couplings. We explain the magnetic susceptibility and magnetization curve above the phase transition temperature based on the $S$=1/2 ferromagnetic Heisenberg chain. The magnetization curve in the ordered phase is described by a conventional AF two-sublattice model. Furthermore, the obtained magnetic specific heat reproduces the almost temperature-independent behavior of the $S$=1/2 ferromagnetic Heisenberg chain. In the low-temperature region, the magnetic specific heat exhibits $sqrt{T}$ dependence, which is attributed to the energy dispersion in the ferromagnetic chain.
We present a quantu spin liquid state in a spin-1/2 honeycomb lattice with randomness in the exchange interaction. That is, we successfully introduce randomness into the organic radial-based complex and realize a random-singlet (RS) state. All magnet
ic and thermodynamic experimental results indicate the liquid-like behaviors, which are consistent with those expected in the RS state. These results demonstrate that the randomness or inhomogeneity in the actual systems stabilize the RS state and yield liquid-like behavior.
We present the first experimental realization of an $S=2$ ferromagnetic-antiferromagnetic (F-AF) alternating chain in a new Mn-verdazyl complex [Mn(hfac)$_2$]$cdot$($o$-Py-V) [hfac=1,1,1,5,5,5-hexafluoroacetylacetonate; $o$-Py-V=3-(2-pyridyl)-1,5-dip
henylverdazyl]. Through the $ab$ $initio$ molecular orbital calculation, magnetization, and ESR measurements, this compound is confirmed to form an $S=2$ F-AF alternating chain with Ising anisotropy below about 100 K. Furthermore, we find an anomalous change in magnetization at 1/4 of the saturation value, which is probably a manifestation of the quantum nature of the system.
