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Register a new userExamining the surface phase diagram of IrTe$_2$ with photoemission
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In the transition metal dichalcogenide IrTe$_2$, low-temperature charge-ordered phase transitions involving Ir dimers lead to the occurrence of stripe phases of different periodicities, and nearly degenerate energies. Bulk-sensitive measurements have shown that, upon cooling, IrTe$_2$ undergoes two such first-order transitions to $(5times1times5)$ and $(8times1times8)$ reconstructed phases at $T_{c_1}sim 280$~K and $T_{c_2}sim 180$~K, respectively. Here, using surface sensitive probes of the electronic structure of IrTe$_2$, we reveal the first-order phase transition at $T_{c_3}=165$~K to the $(6times1)$ stripes phase, previously proposed to be the surface ground state. This is achieved by combining x-ray photoemission spectroscopy and angle-resolved photoemission spectroscopy, which give access to the evolution of stripe domains and a particular surface state, the energy of which is dependent on the Ir dimer length. By performing measurements over a full thermal cycle, we also report the complete hysteresis of all these phases.
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Strain is ubiquitous in solid-state materials, but despite its fundamental importance and technological relevance, leveraging externally applied strain to gain control over material properties is still in its infancy. In particular, strain control over the diverse phase transitions and topological states in two-dimensional (2D) transition metal dichalcogenides (TMDs) remains an open challenge. Here, we exploit uniaxial strain to stabilize the long-debated structural ground state of the 2D topological semimetal IrTe$_2$, which is hidden in unstrained samples. Combined angle-resolved photoemission spectroscopy (ARPES) and scanning tunneling microscopy (STM) data reveal the strain-stabilized phase has a 6x1 periodicity and undergoes a Lifshitz transition, granting unprecedented spectroscopic access to previously inaccessible type-II topological Dirac states that dominate the modified inter-layer hopping. Supported by density functional theory (DFT) calculations, we show that strain induces a charge transfer strongly weakening the inter-layer Te bonds and thus reshaping the energetic landscape of the system in favor of the 6x1 phase. Our results highlight the potential to exploit strain-engineered properties in layered materials, particularly in the context of tuning inter-layer behavior.
We present a combined angle-resolved photoemission spectroscopy and low-energy electron diffraction (LEED) study of the prominent transition metal dichalcogenide IrTe$_2$ upon potassium (K) deposition on its surface. Pristine IrTe$_2$ undergoes a series of charge-ordered phase transitions below room temperature that are characterized by the formation of stripes of Ir dimers of different periodicities. Supported by density functional theory calculations, we first show that the K atoms dope the topmost IrTe$_2$ layer with electrons, therefore strongly decreasing the work function and shifting only the electronic surface states towards higher binding energy. We then follow the evolution of its electronic structure as a function of temperature across the charge-ordered phase transitions and observe that their critical temperatures are unchanged for K coverages of $0.13$ and $0.21$~monolayer (ML). Using LEED, we also confirm that the periodicity of the related stripe phases is unaffected by the K doping. We surmise that the charge-ordered phase transitions of IrTe$_2$ are robust against electron surface doping, because of its metallic nature at all temperatures, and due to the importance of structural effects in stabilizing charge order in IrTe$_2$.
In the quest to realize a quantum spin liquid (QSL), magnetic long-range order is hardly welcome. Yet it can offer deep insights into a complex world of strong correlations and fluctuations. Much hope was placed in the cubic pyrochlore Yb$_2$Ti$_2$O$_7$ as a putative U(1) QSL but a new class of ultra-pure single crystals make it abundantly clear the stoichiometric compound is a ferromagnet. Here we present a detailed experimental and theoretical study of the corresponding field-temperature phase diagram. We find it to be richly anisotropic with a critical endpoint for $vec{B},parallel,langle 100rangle$, while field parallel to $langle 110 rangle$ and $langle 111 rangle$ enhances the critical temperature by up to a factor of two and shifts the onset of the field-polarized state to finite fields. Landau theory shows that Yb$_2$Ti$_2$O$_7$ in some ways is remarkably similar to pure iron. However, it also pinpoints anomalies that cannot be accounted for at the classical mean-field level including a dramatic enhancement of $T_{mathrm{C}}$ and reentrant phase boundary by fields with a component transverse to the easy axes, as well as the anisotropy of the upper critical field in the quantum limit.
The low-temperature magnetic phase diagram of the multiferroic system FeTe$_2$O$_5$Br down to 300 mK and up to 9 T is presented. Short-range magnetic correlations within the crystal layers start to develop already at $sim$50 K, i.e., far above $T_{N1} sim$ 11.0 K, where the system undergoes a magnetic phase transition into the high-temperature incommensurate (HT-ICM) phase. Only 0.5 K lower, at $T_{N2}$, the system undergoes a second phase transition into the low-temperature incommensurate amplitude-modulated (LT-ICM) phase accompanied by a spontaneous electric polarization. When the magnetic field is applied, the transition temperatures shift depending on the field orientation. In the case of $B||b$ and $B >$ 4.5 T, the HT-ICM phase disappears along with the electric polarization in the LT-ICM phase. The field dependence of the magnetic transition temperatures is explained in the context of the magnetic susceptibility behavior. Similarities and differences between the novel amplitude-modulated and well-established helicoidal magnetoelectrics are discussed.
We explore the field-temperature phase diagram of the XY pyrochlore antiferromagnet Er$_2$Ti$_2$O$_7$, by means of magnetization and neutron diffraction experiments. Depending on the field strength and direction relative to the high symmetry cubic directions $[001], [1bar{1}0]$ and $[111]$, the refined field induced magnetic structures are derived from the zero field $psi_2$ and $psi_3$ states of the $Gamma_5$ irreducible representation which describes the ground state of XY pyrochlore antiferromagnets. At low field, domain selection effects are systematically at play. In addition, for $[001]$, a phase transition is reported towards a $psi_3$ structure at a characteristic field $H_c^{001}=$ 43 mT. For $[1bar{1}0]$ and $[111]$, the spins are continuously tilted by the field from the $psi_2$ state, and no phase transition is found while domain selection gives rise to sharp anomalies in the field dependence of the Bragg peaks intensity. For $[1bar{1}0]$, these results are confirmed by high resolution inelastic neutron scattering experiments, which in addition allow us to determine the field dependence of the spin gap. This study agrees qualitatively with the scenario proposed theoretically by Maryasin {it et al.} [Phys. Rev. B {bf 93}, 100406(R) (2016)], yet the strength of the field induced anisotropies is significantly different from theory.
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