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We present the properties of a new organic $S=1$ chain system $m$-NO$_2$PhBNO (abbreviated BoNO). In this biradical system two unpaired electrons from aminoxyl groups are strongly ferromagnetically coupled ($|J_\text{FM}| \gtrsim 500$ K) which leads to the formation of an effective $S=1$ state for each molecule. The chains of BoNO diradicals propagate along the crystallographic $a$ axis. Temperature dependence of the $g$ factor and electron paramagnetic resonance (EPR) linewidth are consistent with a low-dimensional system with antiferromagnetic interactions. The EPR data further suggest that BoNO is the first known Haldane system with an almost isotropic $g$ factor ($2.0023 \pm 2 \unicode{x2030}$). The magnetization measurements in magnetic fields up to $40$ T and low-field susceptibility, together with $^1$H nuclear magnetic resonance (NMR) spectra, reveal a dominant intrachain antiferromagnetic exchange coupling of $J_\text{1D} = (11.3\pm0.1)$ K, and attainable critical magnetic fields of $\mu_0 H_\text{c1} \approx 2$ T and $\mu_0 H_\text{c2} \approx 33$ T. These measurements therefore suggest that BoNO is a unique Haldane system with extremely small magnetic anisotropy. Present results are crucial for a future in-depth NMR study of the low-temperature Tomonaga-Luttinger liquid (TLL) and magnetic field-induced phases, which can be performed in the entire phase space., Comment: 13 pages, 12 figures

Doping of quantum antiferromagnets is an established approach to investigate the robustness of their ground state against the competing phases. Predictions of doping effects on the ground state of the Shastry-Sutherland dimer model are here verified experimentally on Mg-doped SrCu2(BO3)2. A partial incorporation of Mg2+ on the Cu2+-site in the SrCu2(BO3)2 structure leads to a subtle but systematic lattice expansion with the increasing Mg-doping concentration, which is accompanied by a concomitant decrease in the spin gap, the Curie-Weiss temperature and the peak temperature of the susceptibility. These findings indicate a doping-induced breaking of Cu2+ spin-1/2 dimers which is also corroborated by X-band EPR spectroscopy that points to a systematic increase in intensity of free Cu2+ sites with increasing Mg-doping concentration. Extending the Mg-doping up to nominal x = 0.10 or SrCu1.9Mg0.1(BO3)2, in the magnetisation measurements taken up to 35 T, a suppression of the pseudo-1/8 plateau is found along with a clear presence of an anomaly at an onset critical field H'C0 ~ 9 T. The latter, absent in pure SrCu2(BO3)2, emerges due to the coupling of liberated Cu2+ spin-1/2 entities in the vicinity of Mg-doping induced impurities., Comment: 17 pages, 6 figures

Quasi-one-dimensional electron systems display intrinsic instability towards long-range ordered phases at sufficiently low temperatures. The superconducting orders are of particular interest as they can possess either singlet or triplet pairing symmetry and frequently compete with magnetism. Here we report on muon spin rotation and relaxation ($\mathrm{\mu}$SR) study of Rb$_2$Mo$_3$As$_3$ characterised by one of the highest critical temperatures $T_{\rm c}=10.4\ \mathrm{K}$ among quasi-one-dimensional superconductors. The transverse-field $\mathrm{\mu}$SR signal shows enhanced damping below $T_{\rm c}$ due to the formation of vortex lattice. Comparison of vortex lattice broadening against single gap $s-$, $p-$ and $d-$wave models shows the best agreement for the $s-$wave scenario but with the anomalously small superconducting gap, $\Delta_0$, to $T_{\rm c}$ ratio of $2\Delta_0/k_{\rm B}T_{\rm c}=2.74(1)$. The alternative nodal $p-$wave or $d-$wave scenarios with marginally worse goodness of fit would yield more realistic $2\Delta_0/k_{\rm B}T_{\rm c}=3.50(2)$ and $2\Delta_0/k_{\rm B}T_{\rm c}=4.08(1)$, respectively, and thus they cannot be ruled out when accounting for the superconducting state in Rb$_2$Mo$_3$As$_3$., Comment: 6 pages

We report a metal-insulator transition (MIT) in the half-filled multiorbital antiferromagnet (AF) BaMn$_2$Bi$_2$ that is tunable by a magnetic field perpendicular to the AF sublattices. Instead of an Anderson-Mott mechanism usually expected in strongly correlated systems, we find by scaling analyses that the MIT is driven by an Anderson localization. Electrical and thermoelectrical transport measurements in combination with electronic band calculations reveal a strong orbital-dependent correlation effect, where both weakly and strongly correlated $3d$-derived bands coexist with decoupled charge excitations. Weakly correlated holelike carriers in the $d_{xy}$-derived band dominate the transport properties and exhibit the Anderson localization, whereas other $3d$ bands show clear Mott-like behaviors with their spins ordered into AF sublattices. The tuning role played by the perpendicular magnetic field supports a strong spin-spin coupling between itinerant holelike carriers and the AF fluctuations, which is in sharp contrast to their weak charge coupling.

Vector-chiral (VC) antiferromagnetism is a spiral-like ordering of spins which may allow ferroelectricity to occur due to loss of space inversion symmetry. In this paper we report direct experimental observation of ferroelectricity in the VC phase of $\beta$-TeVO$_4$, a frustrated spin chain system with pronounced magnetic anisotropy and a rich phase diagram. Saturation polarization is proportional to neutron scattering intensities that correspond to the VC magnetic reflection. This implies that inverse Dzyaloshinskii-Moriya mechanism is responsible for driving electric polarization. Linear magnetoelectric coupling is absent, however an unprecedented dependence of electric coercive field on applied magnetic field reveals a novel way of manipulating multiferroic information., Comment: submitted to PRB Letter, 7 pages, 4 figures

A very large negative magnetoresistance (LNMR) is observed in the insulating regime of the antiferromagnet BaMn$_2$Bi$_2$ when a magnetic field is applied perpendicular to the direction of the sublattice magnetization. High perpendicular magnetic field eventually suppresses the insulating behavior and allows BaMn$_2$Bi$_2$ to re-enter a metallic state. This effect is seemingly unrelated to any field induced magnetic phase transition, as measurements of magnetic susceptibility and specific heat did not find any anomaly as a function of magnetic fields at temperatures above $2\,\mathrm{K}$. The LNMR appears in both current-in-plane and current-out-of-plane settings, and Hall effects suggest that its origin lies in an extreme sensitivity of conduction processes of holelike carriers to the infinitesimal field-induced canting of the sublattice magnetization. The LNMR-induced metallic state may thus be associated with the breaking of the antiferromagnetic parity-time symmetry by perpendicular magnetic fields and/or the intricate multi-orbital electronic structure of BaMn$_2$Bi$_2$.

$\beta$-TeVO$_4$ is a frustrated spin 1/2 zig-zag chain system,where spin-density-wave (SDW), vector chiral (VC)and an exotic dynamic spin-stripe phase compete at low temperatures. Here we use torque magnetometry to study the anisotropy of these phases in magnetic fields of up to 5 T. Our results show that the magnetic-field-induced spin reorientation occurs in the SDW and in the spin stripe phases for $\mu_0 H \geq 2$~T. The observed spin reorientation is a new element of the anisotropic phase diagram for the field directions in the $ac$ and $a^*b$ crystallographic planes. The presented results should help establishing the model of anisotropic magnetic interactions, which are responsible for the formation of complex magnetic phases in $\beta$-TeVO$_4$ and similar quantum systems., Comment: Accepted for publication in Physical Review B

The ground state of alkali metals when the particle size decreases from bulk to nanometric atomic clusters is inevitably accompanied by quantum effects that can suppress their pristine metallic state. We demonstrate that the metallic nature of rubidium clusters confined and arrayed in the framework of insulating low-silica X zeolite is preserved. The $^{87}$Rb NMR spin-lattice relaxation assigned to rubidium clusters in supercages shows a Korringa behavior from 190~K down to 10~K, which is compatible with a macroscopic observation of low electrical resistivity. The density of states at the Fermi level is found to be enhanced compared to the analogous sodium case, consistent with a Holstein-Hubbard model of alkali-loaded zeolites., Comment: Extended version showing new data, 4+epsilon pages, 4 figures

We report the discovery of a novel giant magnetoresistance (GMR) phenomenon in a family of BaMn$_{2}$Pn$_{2}$ antiferromagnets (Pn stands for P, As, Sb, and Bi) with a parity-time symmetry. The resistivities of these materials are reduced by $60$ times in magnetic fields ($\vec{H}$'s), thus yielding the GMR of about $-98\%$. The GMR changes systematically along with the Pn elements, hinting that its origin is the spin orbit coupling (SOC) and/or $d$-$p$ orbital hybridization. A positive MR component emerging on top of the negative GMR at low temperatures suggests an orbital-sensitive magnetotransport as $\vec{H}$ suppresses the conduction of the electron-like carriers in the $d$-like band but enhances those of hole-like ones in the $d$-$p$ hybridized band. The anisotropy of the GMR reveals that the electrical conductivity is extremely sensitive to the minute changes in the direction of the antiferromagnetic moments induced by the parity-time breaking $\vec{H}$, which seems to be associated with a magnetoelectric effect in the dynamic regime of conduction electrons. We attribute the observed GMR to the non-trivial low energy band of BMPn's, which is governed by the parity-time symmetry and an magnetic hexadecapole ordering., Comment: 5 figures

We present a study of the static magnetic properties and spin dynamics in Cobalt valence tautomers (VT), molecules where a low-spin (LS) to high-spin (HS) crossover driven by an intramolecular electron transfer can be controlled by the temperature, by the external pressure or by light irradiation. In the investigated complex, a LS-Co(III) ion bound to a dinegative organic ligand can be reversibly converted into the HS-Co(II) bound to a mononegative one. By combining magnetization measurements with Nuclear Magnetic Resonance (NMR) and Muon Spin Relaxation ({\mu}SR), we have investigated the static magnetic properties and the spin dynamics as a function of the temperature. Moreover, the effect of the external pressure as well as of the infrared light irradiation have been explored through magnetometry and NMR measurements to determine the spin dynamics of the HS state. The photoinduced HS state, which can have a lifetime of several hours below 30 K, is characterized by spin dynamics in the MHz range, which persist at least down to 10 K. The application of an external pressure causes a progressive increase of the LS-HS crossover, which reaches room temperature for pressures around 10 kbar.

The layered {\beta}-NaMnO2, a promising Na-ion energy-storage material has been investigated for its triangular lattice capability to promote complex magnetic configurations that may release symmetry restrictions for the coexistence of ferroelectric and magnetic orders. The complexity of the neutron powder diffraction patterns underlines that the routinely adopted commensurate structural models are inadequate. Instead, a single-phase superspace symmetry description is necessary, demonstrating that the material crystallizes in a compositionally modulated q= (0.077(1), 0, 0) structure. Here, Mn3+ Jahn-Teller distorted MnO6 octahedra form corrugated layer stacking sequences of the {\beta}-NaMnO2 type, which are interrupted by flat sheets of the {\alpha}-like oxygen topology. Spontaneous long-range collinear antiferromagnetic order, defined by the propagation vector k= (1/2, 1/2, 1/2), appears below TN1= 200 K. Moreover, a second transition into a spatially modulated proper-screw magnetic state (k+-q) is established at TN2= 95 K, with an antiferromagnetic order parameter resembling that of a two-dimensional (2D) system. The evolution of 23Na NMR spin-lattice relaxation identifies a magnetically inhomogene-ous state in the intermediate T-region (TN2

We report a $^{23}$Na spin-lattice relaxation rate, $T_1^{-1}$, in low-silica X zeolite. $T_1^{-1}$ follows multiple BPP-type behavior as a result of thermal motion of sodium cations in insulating material. The estimated lowest activation energy of 15~meV is much lower than 100~meV observed previously for sodium motion in heavily Na-loaded samples and is most likely attributed to short-distance jumps of sodium cations between sites within the same supercage., Comment: 2 pages, 1 figure, published in JPSJ

The existence of a quantum spin liquid (QSL) in which quantum fluctuations of spins are sufficiently strong to preclude spin ordering down to zero temperature was originally proposed theoretically more than 40 years ago, but its experimental realisation turned out to be very elusive. Here we report on an almost ideal spin liquid state that appears to be realized by atomic-cluster spins on the triangular lattice of a charge-density wave (CDW) state of 1T-TaS$_2$. In this system, the charge excitations have a well-defined gap of $\sim 0.3$ eV, while nuclear magnetic quadrupole resonance and muon spin relaxation experiments reveal that the spins show gapless quantum spin liquid dynamics and no long range magnetic order down to 70~mK. Canonical $T^{2}$ power-law temperature dependence of the spin relaxation dynamics characteristic of a QSL is observed from 200~K to $T_f= 55$ K. Below this temperature we observe a new gapless state with reduced density of spin excitations and high degree of local disorder signifying new quantum spin order emerging from the QSL., Comment: 15 pages, 4 figures, submitted for a publication

We report a systematic nuclear magnetic resonance investigation of the $^{23}$Na spin-lattice relaxation rate, $1/T_1$, in sodium loaded low-silica X (LSX) zeolite, Na$_n$/Na$_{12}$-LSX, for various loading levels of sodium atoms $n$ across the metal-to-insulator crossover. For high loading levels of $n \geq 14.2$, $1/T_1T$ shows nearly temperature-independent behavior between 10 K and 25 K consistent with the Korringa relaxation mechanism and metallic ground state. As the loading levels decrease below $n \leq 11.6$, the extracted density of states (DOS) at the Fermi level sharply decreases, although a residual DOS at Fermi level is still observed even in samples that lack the metallic Drude-peak in the optical reflectance. The observed crossover is a result of a complex loading-level dependence of electric potential felt by the electrons confined to zeolite cages, where the electronic correlations and disorder both play an important role., Comment: 7 pages, 5 figures

Phase inhomogeneity of otherwise chemically homogenous electronic systems is an essential ingredient leading to fascinating functional properties, such as high-$T_c$ superconductivity in cuprates, colossal magnetoresistance in manganites, and giant electrostriction in relaxors. In these materials distinct phases compete and can coexist due to intertwined ordered parameters. Charge degrees of freedom play a fundamental role, although phase-separated ground states have been envisioned theoretically also for pure spin systems with geometrical frustration that serves as a source of phase competition. Here we report a paradigmatic magnetostructurally inhomogenous ground state of the geometrically frustrated $\alpha$-NaMnO$_2$ that stems from the system's aspiration to remove magnetic degeneracy and is possible only due to the existence of near-degenerate crystal structures. Synchrotron X-ray diffraction, nuclear magnetic resonance and muon spin relaxation show that the spin configuration of a monoclinic phase is disrupted by magnetically short-range ordered nanoscale triclinic regions, thus revealing a novel complex state of matter., Comment: version equivalent to the one published in Nature Communications, freely available at http://www.nature.com/ncomms/2014/140129/ncomms4222/full/ncomms4222.html

We report a \^{23}Na and \^{27}Al nuclear magnetic resonance (NMR) investigation of low-silica X (LSX) zeolite with chemical formula Na_{12}Al_{12}Si_{12}O_{48} (Na_{12}-LSX) loaded with n additional guest sodium atoms. Na_{n}/Na_{12}-LSX exhibits an insulator-to-metal transition around n=11.6, which is accompanied by a significant enhancement of bulk magnetic susceptibility. Paramagnetic moments are thermally activated in the metallic Na_{12}/Na_{12}-LSX with an activation energy of around 0.1 eV. At the same time, a new shifted component (SC) appears in the \^{23}Na NMR, whose large and positive NMR shift scales with bulk magnetic susceptibility. Its spin-lattice relaxation rate 1/T_{1} is governed by the fluctuations determined by the same activation energy as obtained from the bulk magnetic susceptibility data. The timescale of these fluctuations is typical for atomic motions, which suggest strong electron-phonon coupling, a hallmark of polaron states. The insulator-to-metal transition in Na_{n}/Na_{12}-LSX is thus discussed within a polaron model., Comment: 7 pages, 6 figures

We study the electronic structure and magnetic interactions in methylamine-intercalated orthorhombic alkali-doped fullerene (CH3NH2)K3C60 within the density functional theory. As in the simpler ammonia intercalated compound (NH3)K3C60, the orthorhombic crystal-field anisotropy \Delta lifts the t1u triple degeneracy at the \Gamma point and drives the system deep into the Mott-insulating phase. However, the computed \Delta and conduction electron bandwidth W cannot alone account for the abnormally low experimental N\'eel temperature, T_N = 11 K of the methylamine compound, compared to the much higher value T_N = 40 K of the ammonia one. Significant interactions between CH3NH2 and C60^{3-} are responsible for the stabilization of particular pseudo-Jahn-Teller fullerene-cage distortions and the ensuing low-spin S = 1/2 state. These interactions also seem to affect the magnetic properties, as interfullerene exchange interactions depend on the relative orientation of pseudo-Jahn-Teller distortions of neighboring C60^{3-} molecules. For the ferro-orientational order of CH3NH2-K^+ groups we find an apparent reduced dimensionality in magnetic exchange interactions, which may explain the suppressed N\'eel temperature. The disorder in exchange interactions caused by orientational disorder of CH3NH2-K^+ groups could further contribute to this suppression., Comment: 8 pages, 5 figures, 1 table

We report on a systematic temperature dependent X-band electron paramagnetic resonance (EPR) study of nano-sized graphite particles prepared by ball-milling. In as-prepared samples a very intense and sharp EPR resonance at $g=2.0035$ has been measured. The EPR linewidth shows a Korringa-like linear temperature dependence arising due to the coexistence and strong exchange coupling of itinerant and localized edge states. With a prolonged aging in inert atmosphere changes in the EPR signal suggest gradual structural reconstruction where the localized edge-states dominate the EPR signal. In this case the EPR spin susceptibility shows a maximum at $\approx 23\, {\rm K}$ indicating the development of antiferromagnetic correlations as expected for the graphene lattice with a bipartite symmetry., Comment: 6 pages, 5 figures; accepted in Phys. Rev. B as regular article

This paper has been withdrawn by the authors as the available data were not sufficient to support the conclusions, Comment: this paper has been withdrawn

A study of an impurity driven phase-transition into a magnetically ordered state in the spin-liquid Haldane chain compound PbNi2V2O8 is presented. Both, macroscopic magnetization as well as 51V nuclear magnetic resonance (NMR) measurements reveal that the spin nature of dopants has a crucial role in determining the stability of the induced long-range magnetic order. In the case of nonmagnetic (Mg2+) doping on Ni2+ spin sites (S=1) a metamagnetic transition is observed in relatively low magnetic fields. On the other hand, the magnetic order in magnetically (Co2+) doped compounds survives at much higher magnetic fields and temperatures, which is attributed to a significant anisotropic impurity-host magnetic interaction. The NMR measurements confirm the predicted staggered nature of impurity-liberated spin degrees of freedom, which are responsible for the magnetic ordering. In addition, differences in the broadening of the NMR spectra and the increase of nuclear spin-lattice relaxation in doped samples, indicate a diverse nature of electron spin correlations in magnetically and nonmagnetically doped samples, which begin developing at rather high temperatures with respect to the antiferromagnetic phase transition., Comment: 10 pages, 7 figures

A comprehensive study of impurity-induced magnetism in nonmagnetically (Mg${}^{2+}$) and magnetically (Co${}^{2+}$) doped PbNi${}_{2}$V${}_{2}$O${}_{8}$ compounds is given, using both macroscopic dc susceptibility and local-probe electron spin resonance (ESR) techniques. Magnetic coupling between impurity-liberated spins is estimated from a linewidth of low-temperature ESR signal in Mg-doped samples. In addition, in the case of magnetic cobalt dopants the impurity-host magnetic exchange is evaluated from the Co-induced contribution to the linewidth in the paramagnetic phase. The experimentally observed severe broadening of the ESR lines in the magnetically doped compounds with respect to nonmagnetic doping is attributed to a rapid spin-lattice relaxation of the Co${}^{2+}$ ions, which results in a bottleneck-type of temperature dependence of the induced linewidth. The exchange parameters obtained from the ESR analysis offer a satisfactory explanation of the observed low-temperature magnetization in doped samples., Comment: 8 pages, 6 figures

X-band ESR measurements on a single crystal of SrCu$_2$(BO$_3$)$_2$ system in a temperature range between 10 K and 580 K are presented. The temperature and angular dependence of unusually broad ESR spectra can be explained by the inclusion of antisymmetric Dzyaloshinsky-Moriya (DM) interaction, which yields by far the largest contribution to the linewidth. However, the well-accepted picture of only out-of-plane interdimer DM vectors is not sufficient for explanation of the observed angular dependence. In order to account for the experimental linewidth anisotropy we had to include sizable in-plane components of interdimer as well as intradimer DM interaction in addition to the out-of-plane interdimer one. The nearest-neighbor DM vectors lie perpendicular to crystal anisotropy c-axis due to crystal symmetry. We also emphasize that above the structural phase transition occurring at 395 K dynamical mechanism should be present allowing for instantaneous DM interactions. Moreover, the linewidth at an arbitrary temperature can be divided into two contributions; namely, the first part arising from spin dynamics governed by the spin Hamiltonian of the system and the second part due to significant spin-phonon coupling. The nature of the latter mechanism is attributed to phonon-modulation of the antisymmetric interaction, which is responsible for the observed linear increase of the linewidth at high temperatures., Comment: 17 pages, 4 figures, submitted to PRB