arXiv subjects

J. W. Lynn

Publications and source records attributed to J. W. Lynn.

At least 73 records · Page 4Linked to original sources

arXiv2010

Interplay between Fe and Nd magnetism in NdFeAsO single crystals

The structural and magnetic phase transitions have been studied on NdFeAsO single crystals by neutron and x-ray diffraction complemented by resistivity and specific heat measurements. Two low-temperature phase transitions have been observed in addition to the tetragonal-to-orthorhombic transition at T_S = 142 K and the onset of antiferromagnetic (AFM) Fe order below T_N = 137 K. The Fe moments order AFM in the well-known stripe-like structure in the (ab) plane, but change from AFM to ferromagnetic (FM) arrangement along the c direction below T* = 15 K accompanied by the onset of Nd AFM order below T_Nd = 6 K with this same AFM configuration. The iron magnetic order-order transition in NdFeAsO accentuates the Nd-Fe interaction and the delicate balance of c-axis exchange couplings that results in AFM in LaFeAsO and FM in CeFeAsO and PrFeAsO.

cond-mat.supr-con↗

arXiv2010

Soft phonons and structural phase transition in superconducting Ba0.59K0.41BiO3

We have observed a softening of phonons and a structural phase transition in a superconducting Ba0.59K0.41BiO3 (Tc = 31 K) single crystal using elastic and inelastic neutron scattering measurements. The soft phonon occurs for the [111] transverse acoustic mode at the zone boundary. The phonon energies in this vicinity are found to continuously decrease with decreasing temperature from above room temperature to 200 K, where a structural phase transition from cubic to tetragonal symmetry occurs. The overall results are consistent with previous data that reported phonon softening and a (0.5, 0.5, 0.5) type superstructure in several Ba1-xKxBiO3 systems. However, we also find weak (0.5, 0.5, 0) type superstructure peaks that reveal an additional component to the modulation. No significant change related to the superconductivity was observed for the soft phonon energies or linewidths.

cond-mat.supr-con↗

arXiv2010

Origin of Electric Field Induced Magnetization in Multiferroic HoMnO3

We have performed polarized and unpolarized small angle neutron scattering experiments on single crystals of HoMnO3 and have found that an increase in magnetic scattering at low momentum transfers begins upon cooling through temperatures close to the spin reorientation transition at TSR ~ 40 K. We attribute the increase to an uncompensated magnetization arising within antiferromagnetic domain walls. Polarized neutron scattering experiments performed while applying an electric field show that the field suppresses magnetic scattering below T ~ 50 K, indicating that the electric field affects the magnetization via the antiferromagnetic domain walls rather than through a change to the bulk magnetic order.

cond-mat.str-el↗

arXiv2009

Cd-doping effects in Ce2MIn8 (M = Rh and Ir) heavy fermion compounds

Low temperature magnetic properties of Cd-doped Ce2MIn8 (M = Rh and Ir) single crystals are investigated. Experiments of temperature dependent magnetic susceptibility, heat capacity and electrical resistivity measurements revealed that Cd-doping enhances the antiferromagnetic (AFM) ordering temperature from TN = 2.8 K (x = 0) to TN = 4.8 K (x = 0.21) for Ce2RhIn8-xCdx and induces long range AFM ordering with TN = 3.8 K (x = 0.21) for Ce2IrIn8-xCdx. Additionally, X-ray and neutron magnetic scattering studies showed that Cd-doped samples present below TN a commensurate antiferromagnetic structure with a propagation vector (1/2,1/2,0). The resolved magnetic structures for both compounds indicate that the Cd-doping tends to rotate the direction of the ordered magnetic moments toward the ab-plane. This result suggests that the Cd-doping affects the Ce3+ ground state single ion anisotropy modifying the crystalline electrical field (CEF) parameters at the Ce3+ site. Indications of CEF evolution induced by Cd-doping were also found in the electrical resistivity measurements. Comparisons between our results and the general effects of Cd-doping on the related compounds CeMIn5 (M = Co, Rh and Ir) confirms the claims that the Cd-doping induced electronic tuning is the main effect favoring AFM ordering in these compounds.

cond-mat.str-el↗

arXiv2009

Collapse of the hyperfine magnetic field at the Ru site in ferromagnetic rare earth intermetallics

The Mössbauer Effect(ME) is frequently used to investigate magnetically ordered systems. One usually assumes that the magnetic order induces a hyperfine magnetic field, $B_{hyperfine}$, at the ME active site. This is the case in the ruthenates, where the temperature dependence of $B_{hyperfine}$ at $^{99}$Ru sites tracks the temperature dependence of the ferromagnetic or antiferromagnetic order. However this does not happen in the rare-earth intermetallics, GdRu$_2$ and HoRu$_2$. Specific heat, magnetization, magnetic susceptibility, Mössbauer effect, and neutron diffraction have been used to study the nature of the magnetic order in these materials. Both materials are found to order ferromagnetically at 82.3 and 15.3 K, respectively. Despite the ferromagnetic order of the rare earth moments in both systems, there is no evidence of a correspondingly large $B_{hyperfine}$ in the Mössbauer spectrum at the Ru site. Instead the measured spectra consist of a narrow peak at all temperatures which points to the absence of magnetic order. To understand the surprising absence of a transferred hyperfine magnetic field, we carried out {\it ab initio} calculations which show that spin polarization is present only on the rare-earth site. The electron spin at the Ru sites is effectively unpolarized and, as a result, $B_{hyperfine}$ is very small at those sites. This occurs because the 4$d$ Ru electrons form broad conduction bands rather than localized moments. These 4$d$ conduction bands are polarized in the region of the Fermi energy and mediate the interaction between the localized rare earth moments.

cond-mat.str-el↗

arXiv2009

Electronic self-organization in the single-layer manganite $\rm Pr_{\it 1-x}Ca_{\it 1+x}MnO_4$

We use neutron scattering to investigate the doping evolution of the magnetic correlations in the single-layer manganite $\rm Pr_{\it 1-x}Ca_{\it 1+x}MnO_4$, away from the $x=0.5$ composition where the CE-type commensurate antiferromagnetic (AF) structure is stable. We find that short-range incommensurate spin correlations develop as the system is electron doped ($x<0.5$), which coexist with the CE-type AF order. This suggests that electron doping in this system induces an inhomogeneous electronic self-organization, where commensurate AF patches with $x=0.5$ are separated by electron-rich domain walls with short range magnetic correlations. This behavior is strikingly different than for the perovksite $\rm Pr_{\it 1-x}Ca_{\it x}MnO_3$, where the long-range CE-type commensurate AF structure is stable over a wide range of electron or hole doping around $x=0.5$.

cond-mat.str-el↗

arXiv2009

Coupled magnetic and ferroelectric domains in multiferroic Ni3V2O8

Electric control of multiferroic domains is demonstrated through polarized magnetic neutron diffraction. Cooling to the cycloidal multiferroic phase of Ni3V2O8 in an electric field (E) causes the incommensurate Bragg reflections to become neutron spin polarizing, the sense of neutron polarization reversing with E. Quantitative analysis indicates the E-treated sample has handedness that can be reversed by E. We further show close association between cycloidal and ferroelectric domains through E-driven spin and electric polarization hysteresis. We suggest that definite cycloidal handedness is achieved through magneto-elastically induced Dzyaloshinskii-Moriya interactions.

cond-mat.str-el↗

arXiv2009

Temperature, magnetic field, and pressure dependence of the crystal and magnetic structures of the magnetocaloric compound Mn1.1Fe0.9(P0.8Ge0.2)

Neutron powder diffraction studies of the crystal and magnetic structures of the magnetocaloric compound Mn1.1Fe0.9(P0.8Ge0.2) have been carried out as a function of temperature, applied magnetic field, and pressure. The data reveal that there is only one transition observed over the entire range of variables explored, which is a combined magnetic and structural transformation between the paramagnetic to ferromagnetic phases (Tc~255 K for this composition). The structural part of the transition is associated with an expansion of the hexagonal unit cell in the direction of the a- and b-axes and a contraction of the c-axis as the FM phase is formed, which originates from an increase in the intra-layer metal-metal bond distance. The application of pressure is found to have an adverse effect on the formation of the FM phase since pressure opposes the expansion of the lattice and hence decreases Tc. The application of a magnetic field, on the other hand, has the expected effect of enhancing the FM phase and increasing Tc. We find that the substantial range of temperature/field/pressure coexistence of the PM and FM phases observed is due to compositional variations in the sample. In-situ high temperature diffraction measurements were carried out to explore this issue, and reveal a coexisting liquid phase at high temperatures that is the origin of this variation. We show that this range of coexisting phases can be substantially reduced by appropriate heat treatment to improve the sample homogeneity.

cond-mat.mtrl-sci↗

arXiv2009

Lattice distortion and magnetic quantum phase transition in CeFeAs(1-x)P(x)O

We use neutron scattering to show that replacing the larger arsenic with smaller phosphorus in CeFeAs(1-x)P(x)O simultaneously suppresses the AF order and orthorhombic distortion near x = 0.4, providing evidence for a magnetic quantum critical point. Furthermore, we find that the pnictogen height in iron arsenide is an important controlling parameter for their electronic and magnetic properties, and may play an important role in electron pairing and superconductivity.

cond-mat.supr-con↗

arXiv2009

Magnetic ordering in electronically phase separated Sr/O co-doped La(2-x)Sr(x)CuO(4+y)

We present results of magnetic neutron diffraction experiments on the co-doped super-oxygenated La(2-x)Sr(x)CuO(4+y) (LSCO+O) system with x=0.09. The spin-density wave has been studied and we find long-range incommensurate antiferromagnetic order below T_N coinciding with the superconducting ordering temperature T_c=40 K. The incommensurability value is consistent with a hole-doping of n_h~1/8, but in contrast to non-superoxygenated La(2-x)Sr(x)CuO(4) with hole-doping close to n_h ~ 1/8 the magnetic order parameter is not field-dependent. We attribute this to the magnetic order being fully developed in LSCO+O as in the other striped lanthanum-cuprate systems.

cond-mat.supr-con↗

arXiv2009

Intrinsic Localized Modes Observed in the High Temperature Vibrational Spectrum of NaI

Inelastic neutron measurements of the high-temperature lattice excitations in NaI show that in thermal equilibrium at 555 K an intrinsic mode, localized in three dimensions, occurs at a single frequency near the center of the spectral phonon gap, polarized along [111]. At higher temperatures the intrinsic localized mode gains intensity. Higher energy inelastic neutron and x-ray scattering measurements on a room-temperature NaI crystal indicate that the creation energy of the ground state of the intrinsic localized mode is 299 meV.

cond-mat.str-el↗

arXiv2008

Magnetic structures of quaternary intermetallic borocarbides RCo2B2C (R=Dy, Ho, Er)

The magnetic structures of the title compounds have been studied by neutron diffraction. In contrast to the isomorphous RNi2B2C compounds wherein a variety of exotic incommensurate modulated structures has been observed, the magnetic structure of ErCo2B2C is found to be collinear antiferromagnet with k=((1/2),0,(1/2)) while that of HoCo2B2C and DyCo2B2C are observed to be simple ferromagnets. For all studied compounds, the moments are found to be confined within the basal plane and their magnitudes are in good agreement with the values obtained from the low-temperature isothermal magnetization measurements. The absence of modulated magnetic structures in the RCo2B2C series (for ErCo2B2C, verified down to 50 mK) is attributed to the quenching of the Fermi surface nesting features.

cond-mat.str-el↗

arXiv2008

Synthesis and magnetic characterization of TmCo2B2C

A new quaternary intermetallic borocarbide TmCo2B2C has been synthesized via a rapid-quench of an arc-melted ingot. Elemental and powder-diffraction analyses established its correct stoichiometry and single-phase character. The crystal structure is isomorphous to that of TmNi2B2C(I4/mmm) and is stable over the studied temperature range. Above 7 K, the paramagnetic state follows the modified Curie-Weiss behavior (X=C/(T-theta)+X0 wherein X0=0.008(1) emu/mole and the temperature-dependent term reflecting the paramagnetism of the Tm subsystem: ueff=7.6(2) uB [in agreement with the expected value for a free Tm3+ ion] and theta = -4.5(3) K. Long range ferromagnetic order of the Tm sublattice is observed to develop around ~1 K. No superconductivity is detected in TmCo2B2C down to 20 mK, a feature which is consistent with the general trend in the RCo2B2C series. Finally, the influence of the rapid-quench process on the magnetism (and superconductivity) of TmNi2B2C will be discussed and compared to that of TmCo2B2C.

cond-mat.str-el↗

arXiv2008

Polaron formation in the optimally doped ferromagnetic manganites La0.7Ba0.3MnO3 and La0.7Ba0.3MnO3

The nature of the polarons in the optimally doped colossal magnetoresistive (CMR) materials La0.7Ba0.3MnO3 (LBMO) and La0.7Sr0.3MnO3 (LSMO) is studied by elastic and inelastic neutron scattering. In both materials, dynamic nanoscale polaron correlations develop abruptly in the ferromagnetic state. However, the polarons are not able to lock-in to the lattice and order, in contrast to the behavior of La0.7Ca0.3MnO3. Therefore ferromagnetic order in LBMO and LSMO survives their formation, explaining the conventional second order nature of the ferromagnetic--paramagnetic transition. Nevertheless, the results demonstrate that the fundamental mechanism of polaron formation is a universal feature of these ferromagnetic perovskite manganites.

cond-mat.str-el↗

arXiv2008

Lattice collapse and quenching of magnetism in CaFe2As2 under pressure: A single crystal neutron and x-ray diffraction investigation

Single crystal neutron and high-energy x-ray diffraction have identified the phase lines corresponding to transitions between the ambient-pressure tetragonal (T), the antiferromagnetic orthorhombic (O) and the non-magnetic collapsed tetragonal (cT) phases of CaFe2As2. We find no evidence of additional structures for pressures up to 2.5 GPa (at 300 K). Both the T-cT and O-cT transitions exhibit significant hysteresis effects and we demonstrate that coexistence of the O and cT phases can occur if a non-hydrostatic component of pressure is present. Measurements of the magnetic diffraction peaks show no change in the magnetic structure or ordered moment as a function of pressure in the O phase and we find no evidence of magnetic ordering in the cT phase. Band structure calculations show that the transition results in a strong decrease of the iron 3d density of states at the Fermi energy, consistent with a loss of the magnetic moment.

cond-mat.supr-con↗

arXiv2008

First-order magnetic and structural phase transitions in Fe$_{1+y}$Se$_x$Te$_{1-x}$

We use bulk magnetic susceptibility, electronic specific heat, and neutron scattering to study structural and magnetic phase transitions in Fe$_{1+y}$Se% $_x$Te$_{1-x}$. Fe$_{1.068}$Te exhibits a first order phase transition near 67 K with a tetragonal to monoclinic structural transition and simultaneously develops a collinear antiferromagnetic (AF) order responsible for the entropy change across the transition. Systematic studies of FeSe$%_{1-x}$Te$_x$ system reveal that the AF structure and lattice distortion in these materials are different from those of FeAs-based pnictides. These results call into question the conclusions of present density functional calculations, where FeSe$_{1-x}$Te$_x$ and FeAs-based pnictides are expected to have similar Fermi surfaces and therefore the same spin-density-wave AF order.

cond-mat.supr-con↗

arXiv2008

Magnetic switching and phase competition in the multiferroic antiferromagnet $\rm Mn_{1-x}Fe_xWO_4$

Elastic neutron scattering is used to study the spin correlations in the multiferroic $\rm Mn_{1-x}Fe_{x}WO_4$ with $x=0.035, 0.05$ and 0.10. The noncollinear, incommensurate (ICM) magnetic structure associated with the ferroelectric (FE) phase in pure $\rm MnWO_4$ is suppressed at $x=0.035$ and completely absent at $x=0.10$. The ICM spin order and FE phase can be restored by applying a magnetic field along the spin easy-axis. The low-$T$ commensurate magnetic structure extends in both H/T with increasing Fe concentration. The systematic evolution of the magnetic and electric properties indicates that the noncollinear ICM spin order results from competing magnetic interactions and its stabilization can be tuned by the internal ($x$) or external (magnetic field) perturbations.

cond-mat.str-el↗

arXiv2008

Pressure-induced volume-collapsed tetragonal phase of CaFe2As2 as seen via neutron scattering

Recent investigations of the superconducting iron-arsenide families have highlighted the role of pressure, be it chemical or mechanical, in fostering superconductivity. Here we report that CaFe2As2 undergoes a pressure-induced transition to a non-magnetic, volume "collapsed" tetragonal phase, which becomes superconducting at lower temperature. Spin-polarized total-energy calculations on the collapsed structure reveal that the magnetic Fe moment itself collapses, consistent with the absence of magnetic order in neutron diffraction.

cond-mat.supr-con↗