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The microscopic mechanism of heavy band formation, relevant for unconventional superconductivity in CeCoIn$_5$ and other Ce-based heavy fermion materials, depends strongly on the efficiency with which $f$ electrons are delocalized from the rare earth sites and participate in a Kondo lattice. Replacing Ce$^{3+}$ ($4f^1$, $J=5/2$) with Sm$^{3+}$ ($4f^5$, $J=5/2$), we show that a combination of crystal field and on-site Coulomb repulsion causes SmCoIn$_5$ to exhibit a $\Gamma_7$ ground state similar to CeCoIn$_5$ with multiple $f$ electrons. Remarkably, we also find that with this ground state, SmCoIn$_5$ exhibits a temperature-induced valence crossover consistent with a Kondo scenario, leading to increased delocalization of $f$ holes below a temperature scale set by the crystal field, $T_v$ $\approx$ 60 K. Our result provides evidence that in the case of many $f$ electrons, the crystal field remains the most important tuning knob in controlling the efficiency of delocalization near a heavy fermion quantum critical point, and additionally clarifies that charge fluctuations play a general role in the ground state of "115" materials., Comment: 12 pages, 5 figures

We report on the structural and superconducting properties of the intermetallic compound BaGaGe. We find that this material undergoes a structural second-order phase transition from the distorted AlB$_2$-type structure (1H, $a$ = 4.3254(2) \r{A}, $c$ = 5.1078(3) \r{A}, P6/mmm) into the CaIn$_2$-type structure (2H, $a$ = 4.3087(3) \r{A}, $c$ = 10.2117(6) \r{A}, P6$_3$/mmc) at a transition temperature of $T_{\rm S}$ = 253 K. We find that the structural phase-transition corresponds to a coherent buckling of the honeycomb layers, which we can interpret as a disorder-to-order transition of the atoms located within this layer. We show that the 2H-BaGaGe phase becomes superconducting at a critical temperature of $T_{\rm c}$ = 2.1 K. The bulk nature of the superconductivity in 2H-BaGaGe is confirmed by means of specific heat measurements, where we determine a value of $\Delta C$/$\gamma T_{\rm c}$ = 1.59, which is close to the expected BCS value in the weak coupling limit.

Diffraction from a lattice of periodically spaced crystals is a topic of current interest because of the great development of self-organised superlattices (SL) of nanocrystals (NC). The self-organisation of NC into SL has theoretical interest, but especially a rich application prospect, as the coherent organisation has large effects on a wide range of material properties. Diffraction is a key method to understand the type and quality of SL ordering. Hereby the characteristic diffraction signature of a SL of NC - together with the characteristic types of disorder - are theoretically explored., Comment: 20 pages, 8 Figures

The van der Waals material CrSBr stands out as a promising two-dimensional magnet. Especially, its high magnetic ordering temperature and versatile magneto-transport properties make CrSBr an important candidate for new devices in the emergent field of two-dimensional magnetic materials. To date, the magnetic and structural properties of CrSBr have not been fully elucidated. Here, we report on the detailed temperature-dependent magnetic and structural properties of this material, by comprehensively combining neutron scattering, muon spin relaxation spectroscopy, synchrotron X-ray diffraction, and magnetization measurements. We evidence that this material undergoes a transition to an A-type antiferromagnetic state below $T_{\rm N} \approx$ 140 K, with a pronounced two-dimensional character as deduced from the determined critical exponent of $\beta \approx $ 0.18. In our analysis of the field-induced metamagnetic transition, we find that the ferromagnetic correlations within the monolayers persist clearly above the N\'eel temperature in this material. Furthermore, we unravel the low-temperature (i.e. $T < T_{\rm N}$) magnetic hidden order within the long-range magnetically ordered state. We find that it is associated to a slowing down of the magnetic fluctuations, accompanied by a continuous reorientation of the internal magnetic field. These take place upon cooling below $T_s$ $\approx$ 100 K, until a spin freezing process occurs at $T$* $\approx$ 40 K. We argue this complex dynamic behavior to reflect a magnetic crossover driven by the in-plane uniaxial anisotropy, which is ultimately caused by the mixed-anion character of the material. Our findings indicate that the magnetic and structural properties of CrSBr widen its potential application as a component for spin-based electronic devices.

The crystal structure and magnetic correlations in triangular antiferromagnet FeGa$_2$S$_4$ are studied by x-ray diffraction, magnetic susceptibility, neutron diffraction and neutron inelastic scattering. We report significant mixing at the cation sites and disentangle magnetic properties dominated by major and minor magnetic sites. The magnetic short-range correlations at 0.77 \AA$^{-1}$ correspond to the major sites and being static at base temperature they evolve into dynamic correlations around 30 - 50 K. The minor sites contribute to the magnetic peak at 0.6 \AA$^{-1}$, which vanishes at 5.5 K. Our analytical studies of triangular lattice models with bilinear and biquadratic terms provide the ratios between exchanges for the proposed ordering vectors. The modelling of the inelastic neutron spectrum within linear spin wave theory results in the set of exchange couplings $J_1=1.7$\,meV, $J_2=0.9$\,meV, $J_3=0.8$\,meV for the bilinear Heisenberg Hamiltonian. However, not all features of the excitation spectrum are explained with this model., Comment: Accepted in Phys. Rev. B

The dynamical properties of free and bound domain-wall excitations in Ising-chain materials have recently become the focus of intense research interest. New materials and spectrometers have made it possible to control the environment of coupled Ising chains by both effective internal and applied external fields, which can be both longitudinal and transverse, and thus to demonstrate how the resulting magnetic phase transitions and the nature of the associated excited states obey fundamental symmetry properties. In RbCoCl$_3$, the weakly coupled Ising chains form a triangular lattice whose frustrated geometry and magnetic ordering transitions at low temperature open new possibilities for the Ising-chain environment. We have investigated the structure and magnetism in RbCoCl$_3$ by high-resolution x-ray diffraction and neutron scattering measurements on powder and single crystal samples between 1.5 K and 300 K. Upon cooling, the Co$^{2+}$ spins develop one-dimensional antiferromagnetic correlations along the chain axis ($c$-axis) below 90 K. Below the first N\'eel temperature, $T_{N1}$ = 28 K, a partial 3D magnetic order sets in, with propagation vector ${\vec k}_1$ = (1/3,1/3,1), the moments aligned along the $c$-axis and every third chain uncorrelated from its neighbours. Only below a second magnetic phase transition at $T_{N2}$ = 13 K does the system achieve a fully ordered state, with two additional propagation vectors: ${\vec k}_2$ = (0,0,1) establishes a "honeycomb" $c$-axis order, in which 1/3 of the chains are subject to a strong effective mean field due to their neighbours whereas 2/3 experience no net field, while ${\vec k}_3$ = (1/2,0,1) governs a small, staggered in-plane ordered moment. We conclude that RbCoCl$_3$ is an excellent material to study the physics of Ising chains in a wide variety of temperature-controlled environments., Comment: 23+3 pages, 10+2 figures, 6+4 tables

Using detailed synchrotron diffraction, magnetization, thermodynamic and transport measurements, we investigate the relationship between the mixed valence of Ir, lattice strain and the resultant structural and magnetic ground states in the geometrically frustrated triple perovskite iridate Ba$_{3}$NaIr$_{2}$O$_{9}$. We observe a complex interplay between lattice strain and structural phase co-existence, which is in sharp contrast to what is typically observed in this family of compounds. The low temperature magnetic ground state is characterized by the absence of long range order, and points towards the condensation of a cluster glass state from an extended regime of short range magnetic correlations.

We investigated the influence of oxygen over-stoichiometry on apical oxygen disorder and magnetic correlations in Nd2NiO4+d (d~0.11) in the temperature range of 2-300 K by means of synchrotron x-ray powder diffraction, neutron single crystal and powder diffraction studies, combined with macroscopic magnetic measurements. In the investigated temperature range, the compound crystalizes in a tetragonal commensurate structure with the P42/ncm space group with excess oxygen atoms occupy the 4b (3/4 1/4 1/4) interstitial sites, coordinated by four apical oxygen atoms. Large and anisotropic thermal displacement parameters are found for equatorial and apical oxygen atoms, which are strongly reduced on an absolute scale compared to the Nd2NiO4.23 phase. Maximum Entropy analysis of the neutron single crystal diffraction data uncovered anharmonic contributions to the displacement parameters of the apical oxygen atoms, toward the nearest vacant 4b interstitial site, related to the phonon assisted oxygen diffusion mechanism. Macroscopic magnetization measurements and neutron powder diffraction studies reveal long-range antiferromagnetic ordering of the Ni-sublattice at TN ~ 53 K with a weak ferromagnetic component along the c-axis, while the long-range magnetic ordering of the Nd-sublattice occurs below 10 K. Temperature dependent neutron diffraction patterns show the appearance of a commensurate magnetic order at TN with the propagation vector k = (100) and the emergence of an additional incommensurate phase below 30 K, while both phases coexist at 2 K. The commensurate magnetic structure is best described by the P42/nc`m` Shubnikov space group. Refined magnetic moments of the Ni and Nd-sites at 2 K are 1.144(76) muB and 1.632(52) muB respectively. A possible origin of the incommensurate phase is discussed and a tentative magnetic phase diagram is proposed.

The anomalous thermal expansion in a layered 3$d$-5$d$ based triple perovskite iridate Ba$_{3}$CoIr$_{2}$O$_{9}$ is investigated using high resolution synchrotron diffraction. Below the magneto-structural transition at 107\,K, the onset of antiferromagnetic order is associated with a monoclinic distortion of the hexagonal structure. Deeper within the magnetically ordered state, a part of the monoclinic phase distorts even further, and both these structural phases co-exist down to the lowest measured temperatures. We observe negative thermal expansion in this phase co-existence regime, which appears to be intimately connected to the temperature driven relative fractions of these monoclinic phases. The significant NTE observed in this system could be driven by magnetic exchange striction, and is of relevance to a number of systems with pronounced spin orbit interactions.

We report a comprehensive investigation of the triple perovskite iridate Ba$_{3}$CoIr$_{2}$O$_{9}$. Stabilizing in the hexagonal $P6_{3}/mmc$ symmetry at room temperature, this system transforms to a monoclinic $C2/c$ symmetry at the magnetic phase transition. On further reduction in temperature, the system partially distorts to an even lower symmetry ($P2/c$), with both these structurally disparate phases coexisting down to the lowest measured temperatures. The magnetic structure as determined from neutron diffraction data indicates a weakly canted antiferromagnetic structure, which is also supported by first-principles calculations. Theory indicates that the Ir$^{5+}$ carries a finite magnetic moment, which is also consistent with the neutron data. This suggests that the putative $J=0$ state is avoided. Measurements of heat capacity, electrical resistance noise and dielectric susceptibility all point towards the stabilization of a highly correlated ground state in the Ba$_{3}$CoIr$_{2}$O$_{9}$ system.

Realisation of the tetragonal phase of $Cs_2CuCl_4$ is possible using specific crystal growth conditions at a temperature below $281K$. This work deals with the comparison of the magnetic susceptibility and the magnetization of this new tetragonal compound with the magnetic behaviour of tetragonal $Cs_2CuCl_{2.9}Br_{1.1}$, $Cs_2CuCl_{2.5}Br_{1.5}$, $Cs_2CuCl_{2.2}Br_{1.8}$ and presents consistent results for such quasi $2-D$ antiferromagnets. Structural investigation at low temperature for $Cs_2CuCl_{2.2}Br_{1.8}$ shows no phase transition. The structure remains in the tetragonal symmetry $I4/mmm$. Furthermore, several magnetic reflections corresponding to the propagation vector $k = (0, 0, 0)$ are observed for this tetragonal compound through neutron diffraction experiments below the magnetic phase transition at $T_N = 11.3K$ confirming its antiferromagnetic nature., Comment: Preprint

Terbium gallium garnet (TGG), Tb$_3$Ga$_5$O$_{12}$, is well known for its applications in laser optics, but also exhibits complex low-temperature magnetism that is not yet fully understood. Its low-temperature magnetic order is determined by means of time-of-flight neutron powder diffraction. It is found to be a multiaxial antiferromagnet with magnetic Tb$^{3+}$ ions forming six sublattices of magnetic moments aligned parallel and anti-parallel to the $\langle100\rangle$ crystallographic directions of the cubic unit cell. The structure displays strong easy-axis anisotropy with respect to a two-fold axis of symmetry in the local orthorhombic environment of the Tb$^{3+}$ sites. The crystal-field splitting within the single-ion ground-state manifold is investigated by inelastic neutron scattering on powder samples. A strong temperature dependence of the quasidoublet ground-state is observed and revised parameters of the crystal-field Hamiltonian are given. The results of bulk magnetic susceptibility and magnetisation measurements are in good agreement with values based on the crystal-field model down to 20~K, where the onset of magnetic correlations is observed., Comment: 15 pages, 12 figures

We study magnetic behaviour of the Yb$^{3+}$ ions on a frustrated pyrochlore lattice in the spinel {\CYS}. The crystal-electric field parameters deduced from high-energy inelastic neutron scattering reveal well-isolated ytterbium ground state doublet with a weakly Ising character. Magnetic order studied by powder neutron diffraction evolves from the $XY$-type antiferromagnetic $\Gamma_5$ state to a splayed ice-like ferromagnet (both with k=0) in applied magnetic field with $B_c$=3 T. Low-energy inelastic neutron scattering identifies weakly dispersive magnetic bands around 0.72 meV starting at $\mid\bf{Q}\mid$ = 1.1 \AA$^{-1}$~ at zero field, which diminish with field and vanish above 3 T. We explain the observed magnetic behaviour in framework of the nearest-neighbour anisotropic exchange model for effective $S=1/2$ Kramers doublets on the pyrochlore lattice. The estimated exchanges position the {\CYS} spinel close to the phase boundary between the $\Gamma_5$ and splayed ferromagnet states, similar to the Yb-pyrochlores suggesting an important role of the competition between these phases., Comment: 24 pages, 7 Figures

Many functional materials are today synthesised in form of nanoparticles displaying preferred orientation effects to some small or large extent. The analysis of diffraction data of such kind of systems is best performed in the framework of the total scattering approach that prescinds from translation symmetry assumptions. We therefore derived modified expressions for the most common total scattering functions, in particular the Debye Scattering Equation (DSE) that yields the texture-averaged differential cross section as a function of atomic coordinates and texture parameters. The modified DSE encodes higher-order even spherical Bessel functions which account for the texture effect. Selection rules arising from experimental geometries and symmetries are discussed. In addition the duality of the texture effect is introduced showing the effects of texture on both the I(Q) and G(r). The paper includes several definitions and appendices which are meant to be useful for those involved in the development of crystallographic computing., Comment: 46 pages, 8 figures, 2 tables, 7 sections, 2 appendices

Calcium carbonate is a model system to investigate the mechanism of solid formation by precipitation from solutions, and it is often considered in the debated classical and non-classical nucleation mechanism. Despite the great scientific relevance of calcium carbonate in different areas of science, little is known about the early stage of its formation. We, therefore, designed contactless devices capable to provide informative investigations on the early stages of the precipitation pathway of calcium carbonate in supersaturated solutions using classical scattering methods such as Wide-Angle X-ray Scattering (WAXS) and Small-Angle X-ray Scattering (SAXS) techniques. In particular, SAXS was exploited for investigating the size of entities formed from supersaturated solutions before the critical conditions for amorphous calcium carbonate (ACC) nucleation are attained. The saturation level was controlled by mixing four diluted solutions (i.e., NaOH, CaCl2, NaHCO3, H2O) at constant T and pH. The scattering data were collected on a liquid jet generated about 75 sec after the mixing point. The data were modeled using parametric statistical models providing insight about the size distribution of denser matter in the liquid jet. Theoretical implications on the early stage of solid formation pathway are inferred., Comment: 31 pages, 10 figures

In this article, a practical procedure for absolute intensity calibration for SAXS studies on liquid microjets is established, using a gold nanoparticle suspension as standard so that the intercept at $Q=0$ of the SAXS scattering curve would provide a scaling reference. In order to get the most precise extrapolation at $Q=0$, we used an extension to the Guinier approximation, with a second-order term in the fit that adapts to a larger $Q$-range., Comment: 13 pages, 1 fig

In spinels ACr2O4 (A=Mg, Zn) realisation of the classical pyrochlore Heisenberg antiferromagnet model is complicated by a strong spin-lattice coupling: the extensive degeneracy of the ground state is lifted by a magneto-structural transition at TN=12.5 K. We study the resulting low-temperature low-symmetry crystal structure by synchrotron x-ray diffraction. The consistent features of x-ray low-temperature patterns are explained by the tetragonal model of Ehrenberg et. al (Pow. Diff. 17, 230( 2002)), while other features depend on sample or cooling protocol. Complex partially ordered magnetic state is studied by neutron diffraction and spherical neutron polarimetry. Multiple magnetic domains of configuration arms of the propagation vectors k1=(1/2 1/2 0), k2=(1 0 1/2) appear. The ordered moment reaches 1.94(3) muB/Cr3+ for k1 and 2.08(3) muB/Cr3+ for k2, if equal amount of the k1 and k2 phases is assumed. The magnetic arrangements have the dominant components along the [110] and [1-10] diagonals and a smaller c-component. By inelastic neutron scattering we investigate the spin excitations, which comprise a mixture of dispersive spin waves propagating from the magnetic Bragg peaks and resonance modes centered at equal energy steps of 4.5 meV. We interpret these as acoustic and optical spin wave branches, but show that the neutron scattering cross sections of transitions within a unit of two corner-sharing tetrahedra match the observed intensity distribution of the resonances. The distinctive fingerprint of cluster-like excitations in the optical spin wave branches suggests that propagating excitations are localized by the complex crystal structure and magnetic orders.

The charge ordered structure of ions and vacancies characterizing rare-earth pyrochlore oxides serves as a model for the study of geometrically frustrated magnetism. The organization of magnetic ions into networks of corner-sharing tetrahedra gives rise to highly correlated magnetic phases with strong fluctuations, including spin liquids and spin ices. It is an open question how these ground states governed by local rules are affected by disorder. In the pyrochlore Tb$_2$Hf$_2$O$_7$, we demonstrate that the vicinity of the disordering transition towards a defective fluorite structure translates into a tunable density of anion Frenkel disorder while cations remain ordered. Quenched random crystal fields and disordered exchange interactions can therefore be introduced into otherwise perfect pyrochlore lattices of magnetic ions. We show that disorder can play a crucial role in preventing long-range magnetic order at low temperatures, and instead induces a strongly-fluctuating Coulomb spin liquid with defect-induced frozen magnetic degrees of freedom., Comment: 18 pages, 4 figures, + Supplementary Information (4 figures)

We present a model of the lattice dynamics of the rare earth titanate pyrochlores R2Ti2O7 (R=Tb, Dy, Ho), which are important materials in the study of frustrated magnetism. The phonon modes are obtained by density functional calculations, and these predictions are verified by comparison with scattering experiments. Single crystal inelastic neutron scattering is used to measure acoustic phonons along high symmetry directions for R=Tb, Ho; single crystal inelastic x-ray scattering is used to measure numerous optical modes throughout the Brillouin zone for R=Ho; and powder inelastic neutron scattering is used to estimate the phonon density of states for R=Tb, Dy, Ho. Good agreement between the calculations and all measurements is obtained, allowing confident assignment of the energies and symmetries of the phonons in these materials under ambient conditions. The knowledge of the phonon spectrum is important for understanding spin-lattice interactions, and can be expected to be transferred readily to other members of the series to guide the search for unconventional magnetic excitations., Comment: 15 pages, 11 figures

In a floating water bridge the total radiation scattering of water stressed by a moderately strong electric field (1mV/nm) was compared to water without an applied electric field using X-ray and small angle neutron scattering. Structure refinement was carried out using the EPSR method and the TIP4P/2005 water model. These results did not reveal a significant difference in the local static structure of water however analysis of the simulation indicated that the modeled local potential energy surface reveals a departure between electrically stressed and unstressed water. The observed differences show that the local environment is changed by the applied electric field although weak relative to the intermolecular coulombic field. When discussing the results we show that the current methods used to simulate the pair potentials are still insufficient to treat such non-equilibrium systems and further simulation techniques have to be developed to properly reconstruct the microscopic dielectric relaxation process.

Recent experimental results have emphasized two aspects of Tb2Ti2O7 which have not been taken into account in previous attempts to construct theories of Tb2Ti2O7: the role of small levels of structural disorder, which appears to control the formation of a long-range ordered state of as yet unknown nature; and the importance of strong coupling between spin and lattice degrees of freedom, which results in the hybridization of crystal field excitons and transverse acoustic phonons. In this work we examine the juncture of these two phenomena and show that samples with strongly contrasting behavior vis-a-vis the structural disorder (i.e. with and without the transition to the ordered state), develop identical magnetoelastic coupling. We also show that the comparison between single crystal and powder samples is more complicated than previously thought - the correlation between lattice parameter (as a measure of superstoichiometric Tb$^{3+}$) and the existence of a specific heat peak, as observed in powder samples, does not hold for single crystals., Comment: 8 pages, 4 figures; resubmitted version

We investigated the crystal structure and lattice excitations of the ternary intermetallic stannide Ca3Ir4Sn13 using neutron and x-ray scattering techniques. For T > T* ~ 38 K the x-ray diffraction data can be satisfactorily refined using the space group Pm-3n. Below T* the crystal structure is modulated with a propagation vector of q = (1/2, 1/2, 0). This may arise from a merohedral twinning in which three tetragonal domains overlap to mimic a higher symmetry, or from a doubling of the cubic unit cell. Neutron diffraction and neutron spectroscopy results show that the structural transition at T* is of a second-order, and that it is well described by mean-field theory. Inelastic neutron scattering data point towards a displacive structural transition at T* arising from the softening of a low-energy phonon mode with an energy gap of Delta(120 K) = 1.05 meV. Using density functional theory the soft phonon mode is identified as a 'breathing' mode of the Sn12 icosahedra and is consistent with the thermal ellipsoids of the Sn2 atoms found by single crystal diffraction data.

We report on combined neutron and resonant x-ray scattering results, identifying the nature of the spin-orbital ground state and magnetic excitations in LuVO3 as driven by the orbital parameter. In particular, we distinguish between models based on orbital Peierls dimerization, taken as a signature of quantum effects in orbitals, and Jahn-Teller distortions, in favor of the latter. In order to solve this long-standing puzzle, polarized neutron beams were employed as a prerequisite in order to solve details of the magnetic structure, which allowed quantitative intensity-analysis of extended magnetic excitation data sets. The results of this detailed study enabled us to draw definite conclusions about classical vs quantum behavior of orbitals in this system and to discard the previous claims about quantum effects dominating the orbital physics of LuVO3 and similar systems., Comment: Phys. Rev. B 91, 161104(R) (2015)

We report synchrotron radiation diffraction and muon spin rotation (muSR) measurements on the frustrated pyrochlore magnet Tb2Ti2O7. The powder diffraction study of a crushed crystal fragment does not reveal any structural change down to 4 K. The muSR measurements performed at 20 mK on a mosaic of single crystals with an external magnetic field applied along a three-fold axis are consistent with published a.c. magnetic-susceptibility measurements at 16 mK. While an inflection point could be present around an internal field intensity slightly above 0.3 T, the data barely support the presence of a magnetization plateau., Comment: To appear in the proceedings of the 13th International Conference on Muon Spin Rotation, Relaxation and Resonance, Grindelwald, Switzerland, 1-6 June 2014

CoAl2O4 spinel with magnetic Co2+ ions on the diamond A-lattice is known to be magnetically frustrated. We compare neutron single crystal diffraction patterns measured in zero and applied magnetic fields with the ones obtained from classical Monte-Carlo models. In simulations we test the influence of various parameters on diffraction patterns: the ratio of nearest-, J1, and next-nearest, J2, neighbor interactions, magnetic field applied along the principal crystallographic directions, and random disorder on the A(Co2+)- and B(Al3+)- sites. We conclude that the models considered so far explain the broadening of magnetic Bragg peaks in zero magnetic field and their anisotropic response to applied magnetic field only partly. As bulk properties of our single crystal are isotropic, we suggest that its microstructure, specifically <111>-twin boundaries, could be a reason of the nonconventional magnetic order in CoAl2O4., Comment: 9 pages, 8 figures

At low temperatures, Tb$_2$Ti$_2$O$_7$ enters a spin liquid state, despite expectations of magnetic order and/or a structural distortion. Using neutron scattering, we have discovered that in this spin liquid state an excited crystal field level is coupled to a transverse acoustic phonon, forming a hybrid excitation. Magnetic and phononlike branches with identical dispersion relations can be identified, and the hybridization vanishes in the paramagnetic state. We suggest that Tb$_2$Ti$_2$O$_7$ is aptly named a "magnetoelastic spin liquid" and that the hybridization of the excitations suppresses both magnetic ordering and the structural distortion. The spin liquid phase of Tb$_2$Ti$_2$O$_7$ can now be regarded as a Coulomb phase with propagating bosonic spin excitations., Comment: 10 pages, 6 figures, supplementary information included

The structure of BaMg1/3Ta2/3O3 (BMT) has been studied using X-ray scattering. The phonons have been measured and the results are similar to those of other materials with the perovskite structure such as PbMg1/3Nb2/3O3 (PMN). The acoustic and lowest energy optic branches were measured but it was not possible to measure the branches of higher energy, possibly this is because they largely consist of oxygen motions. High-resolution inelastic measurements also showed that the diffuse scattering was strictly elastic and not directly related to the phonon spectra. A diffuse scattering was observed in BMT near the (H\pm1/2, K\pm1/2, L\pm1/2) points in the Brillouin zone and this had a characteristic cube shape. This arises from ordering of the B-site ions in BMT. Additional experiments revealed a diffuse scattering in BMT similar in shape to Bragg reflections at wave-vectors of the form (H\pm1/3, K\pm1/3, L\pm1/3). Such reflections were also observed by Lufaso [Chem. Matt. 16 (2004) 2148] from powders and suggest that this structure of BMT consists of 4 differently oriented domains of a trigonal structure and results from a different ordering of the B-site ions from that responsible for the scattering at the (H\pm1/2, K\pm1/2, L\pm1/2) points. The results lead us to suggest that for BMT single crystals the bulk has the properties of a cubic perovskite, whereas the surface may have quite different structure from that of the bulk. This difference resembles the behaviour of cubic relaxors like PMN and PMN doped by PbTiO3, where significant surface effects have been reported., Comment: 14 pages, 6 figures

A quite unusual diffuse scattering phenomenology was observed in the single-crystal X-ray diffraction pattern of cubic perovskite BMT ($\mathrm{BaMg}_{1/3}\mathrm{Ta}_{2/3}\mathrm{O}_3$). The intensity of the scattering is parametrized as a set of cube-like objects located at the centers of reciprocal space unit cells, resembling very broad and cubic-shaped (1/2,1/2,1/2)-satellites. BMT belongs to perovskites of formula AB$'_{1/3}$B$"_{2/3}$O$_{3}$ (A=Mg, B$'=$Ta, B$"=$Mg). The cubes of the intensity can be attributed to the partial correlations of the occupancies of the B site. The pair correlation function is the Fourier transform of the diffuse scattering intensity and the latter's idealized form yields the unusual property of a power-law correlation decay with distance. Up to now this is observed only in a few exotic instances of magnetic order or nematic crystals. Therefore it cannot be classified as a short-range order phenomenon, as in most situations originating diffuse scattering. A Monte-Carlo search in configuration space yielded solutions that reproduce faithfully the observed diffuse scattering. Analysis of the results in terms of the electrostatic energy and the entropy point to this phase of BMT as a metastable state, kinetically locked, which could be the equilibrium state just below the melting point., Comment: 29 pages, 6 figures

We study spin liquid in the frustrated diamond lattice antiferromagnet CoAl2O4 by means of single crystal neutron scattering in zero and applied magnetic field. The magnetically ordered phase appearing below TN=8 K remains nonconventional down to 1.5 K. The magnetic Bragg peaks at the q=0 positions remain broad and their profiles have strong Lorentzian contribution. Additionally, they are connected by weak diffuse streaks along the <111> directions. These observations are explained within the spiral spin liquid model as short-range magnetic correlations of spirals populated at these finite temperatures, as the energy minimum around q=0 is flat and the energy of excited states with q=(111) is low. The agreement is only qualitative, leading us to suspect that microstructure effects are also important. Magnetic field significantly perturbs spin correlations. The 1.5 K static magnetic moment increases from 1.58 mB/Co at zero field to 2.08 mB/Co at 10 T, while the magnetic peaks, being still broad, acquire almost Gaussian profile. Spin excitations are rather conventional spin waves at zero field, resulting in the exchange parameters J1=0.92(1) meV, J2=0.101(2) meV and the anisotropy term D=-0.0089(2) meV for CoAl2O4. The application of a magnetic field leads to a pronounced broadening of the excitations at the zone center, which at 10 T appear gapless and nearly featureless.

The relaxor ferroelectric PbMg_1/3Ta_2/3O_3 was studied by single-crystal neutron and synchrotron x-ray diffraction and its detailed atomic structure has been modeled in terms of static Pb-displacements that lead to the formation of polar nanoregions. Similar to the other members of the Pb-based relaxor family like PbMg_1/3Nb_2/3O_3 or PbZn_1/3Nb_2/3O_3 the diffuse scattering in the [H,0,0]/[0,K,0] scattering plane has a butterfly-shape around the (h,0,0) Bragg reflections and is transverse to the scattering vector for (h,h,0) peaks. In the [H,H,0]/[0,0,L] plane the diffuse scattering is elongated along the <1,1,2> directions and is transverse to the scattering vector for (h,h,h) reflections. We find that a model consisting of correlated Pb-displacements along the <1,1,1>-directions reproduces the main features of the diffuse scattering in PbMg_1/3Ta_2/3O_3 adequately when the correlation lengths between the Pb-ion displacement vectors are longest along the <1,1,1> and <1,-1,0> and shortest along <1,1,-2> directions., Comment: 17 pages, 3 figures, submitted to Phys. Rev. B. Version2: revised with minor corrections

Using neutron powder diffraction and Monte-Carlo simulations we show that a spin-liquid regime emerges at $all compositions in the diamond-lattice antiferromagnets Co(Al1-xCox)2O4. This spin-liquid regime induced by frustration due to the second-neighbour exchange coupling J2, is gradually superseded by antiferromagnetic collinear long-range order (k=0) at low temperatures. Upon substitution of Al3+ by Co3+ in the octahedral B-site the temperature range occupied by the spin-liquid regime narrows and TN increases. To explain the experimental observations we considered magnetic anisotropy D or third-neighbour exchange coupling J3 as degeneracy-breaking perturbations. We conclude that Co(Al1-xCox)2O4 is below the theoretical critical point J2/J1=1/8, and that magnetic anisotropy assists in selecting a collinear long-range ordered ground state, which becomes more stable with increasing x due to a higher efficiency of O-Co3+-O as an interaction path compared to O-Al3+-O.

CuCrS2 is a triangular lattice Heisenberg antiferromagnet with a rhombohedral crystal structure. We report on neutron and synchrotron powder diffraction results which reveal a monoclinic lattice distortion at the magnetic transition and verify a magnetoelastic coupling. CuCrS2 is therefore an interesting material to study the influence of magnetism on the relief of geometrical frustration., Comment: 6 pages, 6 figures, 1 table

We report an investigation into the superconducting and magnetic properties of Fe_{1+y}Se_{x}Te_{1-x} single crystals by magnetic susceptibility, muon spin rotation, and neutron diffraction. We find three regimes of behavior in the phase diagram for 0\leq x\leq 0.5: (i) commensurate magnetic order for x< 0.1, (ii) bulk superconductivity for $x\lesssim 0.1$, and (iii) a range \sim 0.25\leq x\leq 0.45 in which superconductivity coexists with static incommensurate magnetic order. The results are qualitatively consistent with a two-band mean-field model in which itinerant magnetism and extended s-wave superconductivity are competing order parameters., Comment: 4 pages, 4 figures

The structure of a single layer of graphene on Ru(0001) has been studied using surface x-ray diffraction. A surprising superstructure has been determined, whereby 25 x 25 graphene unit cells lie on 23 x 23 unit cells of Ru. Each supercell contains 2 x 2 crystallographically inequivalent subcells caused by corrugation. Strong intensity oscillations in the superstructure rods demonstrate that the Ru substrate is also significantly corrugated down to several monolayers, and that the bonding between graphene and Ru is strong and cannot be caused by van der Waals bonds. Charge transfer from the Ru substrate to the graphene expands and weakens the C-C bonds, which helps accommodate the in-plane tensile stress. The elucidation of this superstructure provides important information in the potential application of graphene as a template for nanocluster arrays., Comment: 9 pages, 3 figures, paper submitted to peer reviewed journal

We report a study of the triangular lattice Heisenberg magnet NiGa2S4 by the positive muon spin rotation and relaxation technique. We unravel three temperature regimes: (i) below T_c = 9.2(2) K a spontaneous static magnetic field at the muon site is observed and the spin dynamics is appreciable: the time scale of the modes we probe is ~ 7 ns; (ii) an unconventional stretched exponential relaxation function is found for T_c < T < T_{cross} where T_{cross} = 12.6 K, which is a signature of a multichannel relaxation for this temperature range; (iii) above T_{cross}, the relaxation is exponential as expected for a conventional compound. The transition at T_c is of the continuous type. It occurs at a temperature slightly smaller than the temperature at which the specific heat displays a maximum at low temperature. This is reminiscent of the behavior expected for the Berezinskii-Kosterlitz-Thouless transition. We argue that these results reflect the presence of topological defects above T_c., Comment: 5 pages, 2 figures. Corrected typo at the end of the abstract