arXiv subjects

Daniel Haskel

Publications and source records attributed to Daniel Haskel.

24 records · Page 2Linked to original sources

arXiv2017

Resonant x-ray scattering reveals possible disappearance of magnetic order under hydrostatic pressure in the Kitaev candidate $γ$-Li$_2$IrO$_3$

Honeycomb iridates such as $γ$-Li$_2$IrO$_3$ are argued to realize Kitaev spin-anisotropic magnetic exchange, along with Heisenberg and possibly other couplings. While systems with pure Kitaev interactions are candidates to realize a quantum spin liquid ground state, in $γ$-Li$_2$IrO$_3$ it has been shown that the balance of magnetic interactions leads to the incommensurate spiral spin order at ambient pressure below 38 K. We study the fragility of this state in single crystals of $γ$-Li$_2$IrO$_3$ using resonant x-ray scattering (RXS) under applied hydrostatic pressures of up to 3.0 GPa. RXS is a direct probe of the underlying electronic order, and we observe the abrupt disappearance of the $q$=(0.57, 0, 0) spiral order at a critical pressure $P_c = 1.5\ $GPa with no accompanying change in the symmetry of the lattice. This dramatic disappearance is in stark contrast with recent studies of $β$-Li$_2$IrO$_3$ that show continuous suppression of the spiral order in magnetic field; under pressure, a new and possibly nonmagnetic ground state emerges.

cond-mat.mtrl-sci↗

arXiv2016

Emerging magnetism and anomalous Hall effect in iridate-manganite heterostructures

Strong Coulomb repulsion and spin-orbit coupling are known to give rise to exotic physical phenomena in transition metal oxides. Initial attempts to investigate systems where both of these fundamental interactions are comparably strong, such as 3d and 5d complex oxide superlattices, have revealed properties that only slightly differ from the bulk ones of the constituent materials. Here, we observe that the interfacial coupling between the 3d antiferromagnetic insulator SrMnO3 and the 5d paramagnetic metal SrIrO3 is enormously strong, yielding an anomalous Hall response as the result of charge transfer driven interfacial ferromagnetism. These findings show that low dimensional spin-orbit entangled 3d-5d interfaces provide an avenue to uncover technologically relevant physical phenomena unattainable in bulk materials.

cond-mat.str-el↗

arXiv2016

Combined single crystal polarized XAFS and XRD at high pressure: probing the interplay between lattice distortions and electronic order at multiple length scales in high $T_c$ cuprates

Some of the most exotic material properties derive from electronic states with short correlation length (~10-500 Å), suggesting that the local structural symmetry may play a relevant role in their behavior. Here we discuss the combined use of polarized x-ray absorption fine structure and x-ray diffraction at high pressure as a powerful method to tune and probe structural and electronic orders at multiple length scales. Besides addressing some of the technical challenges associated with such experiments, we illustrate this approach with results obtained in the cuprate La$_{1.875}$Ba$_{0.125}$CuO$_4$, in which the response of electronic order to pressure can only be understood by probing the structure at the relevant length scales.

cond-mat.mtrl-sci↗

arXiv2015

Decoupling of the Antiferromagnetic and Insulating States in Tb doped Sr2IrO4

Sr2IrO4 is a spin-orbit coupled insulator with an antiferromagnetic (AFM) transition at TN=240 K. We report results of a comprehensive study of single-crystal Sr2Ir1-xTbxO4. This study found that mere 3% (x=0.03) tetravalent Tb4+(4f7) substituting for Ir4+ (rather than Sr2+) completely suppresses the long-range collinear AFM transition but retains the insulating state, leading to a phase diagram featuring a decoupling of magnetic interactions and charge gap. The insulating state at x=0.03 is characterized by an unusually large specific heat at low temperatures and an incommensurate magnetic state having magnetic peaks at (0.95, 0, 0) and (0, 0.95, 0) in the neutron diffraction, suggesting a spiral or spin density wave order. It is apparent that Tb doping effectively changes the relative strength of the SOI and the tetragonal CEF and enhances the Hund's rule coupling that competes with the SOI, and destabilizes the AFM state. However, the disappearance of the AFM accompanies no metallic state chiefly because an energy level mismatch for the Ir and Tb sites weakens charge carrier hopping and renders a persistent insulating state. This work highlights an unconventional correlation between the AFM and insulating states in which the magnetic transition plays no critical role in the formation of the charge gap in the iridate.

cond-mat.str-el↗

arXiv2015

Effects of chemical pressure on the magnetic ground states of the osmate double perovskites SrCaCoOsO6 and Ca2CoOsO6

The magnetic ground state in the double perovskite system Sr2-xCaxCoOsO6 changes from an antiferromagnet (x = 0), to a spin glass (x = 1), to a ferrimagnet (x = 2) as the Ca content increases. This crossover is driven by chemical pressure effects that control the relative strength of magnetic exchange interactions. The synthesis, crystal structure, and magnetism of SrCaCoOsO6 and Ca2CoOsO6 are investigated and compared with Sr2CoOsO6. Both compounds adopt a monoclinic crystal structure with rock salt ordering of Co2+ and Os6+ and a-a-b+ octahedral tilting, but the average Co-O-Os bond angle evolves from 158.0(3) degrees in SrCaCoOsO6 to 150.54(9) degrees in Ca2CoOsO6 as the smaller Ca2+ ion replaces Sr2+. While this change may seem minor it has a profound effect on the magnetism, changing the magnetic ground state from antiferromagnetic in Sr2CoOsO6 (TN1 = 108 K, TN2 = 70 K), to a spin glass in SrCaCoOsO6 (Tf1 = 32 K, Tf2 = 13 K), to ferrimagnetic in Ca2CoOsO6 (TC = 145 K). In the first two compounds the observation of two transitions is consistent with weak coupling between the Co and Os sublattices.

cond-mat.str-el↗

arXiv2008

Pressure-induced electronic mixing and enhancement of ferromagnetic ordering in EuX (X=Te, Se, S, O) magnetic semiconductors

The pressure- and anion-dependent electronic structure of EuX (X=Te, Se, S, O) monochalcogenides is probed with element- and orbital-specific X-ray absorption spectroscopy in a diamond anvil cell. An isotropic lattice contraction enhances the ferromagnetic ordering temperature by inducing mixing of Eu 4{\it f} and 5{\it d} electronic orbitals. Anion substitution (Te $\to$ O) enhances competing exchange pathways through spin-polarized anion {\it p} states, counteracting the effect of the concomitant lattice contraction. The results have strong implications for efforts aimed at enhancing FM exchange interactions in thin films through interfacial strain or chemical substitutions.

cond-mat.mtrl-sci↗