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Ian R. Fisher

Publications and source records attributed to Ian R. Fisher.

At least 55 records · Page 3Linked to original sources

Expanding the momentum field of view in angle-resolved photoemission systems with hemispherical analyzers

In photoelectron spectroscopy, the measured electron momentum range is intrinsically related to the excitation photon energy. Low photon energies $<10$ eV are commonly encountered in laser-based photoemission and lead to a momentum range that is smaller than the Brillouin zones of most materials. This can become a limiting factor when studying condensed matter with laser-based photoemission. An additional restriction is introduced by widely used hemispherical analyzers that record only electrons photoemitted in a solid angle set by the aperture size at the analyzer entrance. Here, we present an upgrade to increase the effective solid angle that is measured with a hemispherical analyzer. We achieve this by accelerating the photoelectrons towards the analyzer with an electric field that is generated by a bias voltage on the sample. Our experimental geometry is comparable to a parallel plate capacitor and, therefore, we approximate the electric field to be uniform along the photoelectron trajectory. With this assumption, we developed an analytic, parameter-free model that relates the measured angles to the electron momenta in the solid and verify its validity by comparing with experimental results on the charge density wave material TbTe$_3$. By providing a larger field of view in momentum space, our approach using a bias potential considerably expands the flexibility of laser-based photoemission setups.

physics.ins-det↗

Field-tuned ferroquadrupolar quantum phase transition in the insulator TmVO$_{4}$

We report results of low-temperature heat capacity, magnetocaloric effect and neutron diffraction measurements of TmVO$_{4}$, an insulator that undergoes a continuous ferroquadrupolar phase transition associated with local partially-filled $4f$ orbitals of the thulium (Tm$^{3+}$) ions. The ferroquadrupolar transition, a realization of Ising nematicity, can be tuned to a quantum critical point using a magnetic field oriented along the $c$-axis of the tetragonal crystal lattice, which acts as an effective transverse field for the Ising-nematic order. In small magnetic fields, the thermal phase transition can be well-described using a semi-classical mean field treatment of the transverse field Ising model. However, in higher magnetic fields, closer to the field-tuned quantum phase transition, subtle deviations from this semi-classical behavior are observed due to quantum fluctuations. Although the phase transition is driven by the local $4f$ degrees of freedom, the crystal lattice still plays a crucial role, both in terms of mediating the interactions between the local quadrupoles, and in determining the critical scaling exponents, even though the phase transition itself can be described via mean field. In particular, bilinear coupling of the nematic order parameter to acoustic phonons changes the spatial and temporal fluctuations of the former in a fundamental way, resulting in different critical behavior of the nematic transverse-field Ising model as compared to the usual case of the magnetic transverse-field Ising model. Our results establish TmVO$_{4}$ as a model material, and electronic nematicity as a paradigmatic example, for quantum criticality in insulators.

cond-mat.str-el↗

Role of equilibrium fluctuations in light-induced order

Engineering novel states of matter with light is at the forefront of materials research. An intensely studied direction is to realize broken-symmetry phases that are "hidden" under equilibrium conditions but can be unleashed by an ultrashort laser pulse. Despite a plethora of experimental discoveries, the nature of these orders and how they transiently appear remain unclear. To this end, we investigate a nonequilibrium charge density wave (CDW) in rare-earth tritellurides, which is suppressed in equilibrium but emerges after photoexcitation. Using a pump-pump-probe protocol implemented in ultrafast electron diffraction, we demonstrate that the light-induced CDW consists solely of order parameter fluctuations, which bear striking similarities to critical fluctuations in equilibrium despite differences in the length scale. By calculating the dynamics of CDW fluctuations in a nonperturbative model, we further show that the strength of the light-induced order is governed by the amplitude of equilibrium fluctuations. These findings highlight photoinduced fluctuations as an important ingredient for the emergence of transient orders out of equilibrium. Our results further suggest that materials with strong fluctuations in equilibrium are promising platforms to host "hidden" orders after laser excitation.

cond-mat.mtrl-sci↗

Elastocaloric signature of nematic fluctuations

The elastocaloric effect (ECE) is a thermodynamic quantity relating changes in entropy to changes in strain experienced by a material. As such, ECE measurements can provide valuable information about the entropy landscape proximate to strain-tuned phase transitions. For ordered states that break only point symmetries, bilinear coupling of the order parameter with strain implies that the ECE can also provide a window on fluctuations above the critical temperature, and hence, in principle, can also provide a thermodynamic measure of the associated susceptibility. To demonstrate this, we use the ECE to sensitively reveal the presence of nematic fluctuations in the archetypal Fe-based superconductor Ba(Fe$_{1-x}$Co$_{x}$)$_2$As$_2$. By performing these measurements simultaneously with elastoresistivity in a multimodal fashion, we are able to make a direct and unambiguous comparison of these closely related thermodynamic and transport properties, both of which are sensitive to nematic fluctuations. As a result, we have uncovered an unanticipated doping-dependence of the nemato-elastic coupling and of the magnitude of the scattering of low energy quasi-particles by nematic fluctuations -- while the former weakens, the latter increases dramatically with increasing doping.

cond-mat.supr-con↗

Anomalous thermal transport and violation of Wiedemann-Franz law in the critical regime of a charge density wave transition

ErTe$_3$ is studied as a model system to explore thermal transport in a layered charge density wave (CDW) material. We present data from thermal diffusivity, resistivity, and specific heat measurements: There is a sharp decrease in thermal conductivity both parallel and perpendicular to the primary CDW at the CDW transition temperature. At the same time, the resistivity changes more gradually. Correspondingly, while well above and below $T_c$, a consistent description of the thermal transport applies with essentially independent electron and phonon contributions (estimated using the Wiedemann Franz law), in the critical regime no such description is possible; the observed behavior corresponds to a strongly coupled electron-phonon critical `soup.'

cond-mat.str-el↗

Robust superconductivity intertwined with charge density wave and disorder in Pd-intercalated ErTe$_3$

Pd-intercalated ErTe$_3$ is studied as a model system to explore the effect of "intertwined" superconducting and charge density wave (CDW) orders. Despite the common wisdom that superconductivity emerges only when CDW is suppressed, we present data from STM and AC susceptibility measurements that show no direct competition between CDW order and superconductivity. Both coexist over most of the intercalation range, with uniform superconductivity over length scales that exceed the superconducting coherence length. This is despite persisting short-range CDW order and increased scattering from the Pd intercalation. While superconductivity is insensitive to local defects in either of the bi-directional CDWs, vestiges of the Fermi-level distortions are observed in the properties of the superconducting state.

cond-mat.supr-con↗

Nematic quantum criticality in an Fe-based superconductor revealed by strain-tuning

Quantum criticality has been invoked as being essential to the understanding of a wide range of exotic electronic behavior, including heavy Fermion and unconventional superconductivity, but conclusive evidence of quantum critical fluctuations has been elusive in many materials of current interest. An expected characteristic feature of quantum criticality is power law behavior of thermodynamic quantities as a function of a non-thermal tuning parameter close to the quantum critical point (QCP). In the present work, we observe power law behavior of the critical temperature of the coupled nematic/structural phase transition as a function of uniaxial stress in a representative family of Fe-based superconductors. Our measurements provide direct evidence of quantum critical nematic fluctuations in this material. Furthermore, these quantum critical fluctuations are not confined within a narrow regime around the QCP, but extend over a wide range of temperatures and tuning parameters.

cond-mat.str-el↗

Imaging Nematic Transitions in Iron-Pnictide Superconductors with a Quantum Gas

The SQCRAMscope is a recently realized Scanning Quantum CRyogenic Atom Microscope that utilizes an atomic Bose-Einstein condensate to measure magnetic fields emanating from solid-state samples. The quantum sensor does so with unprecedented DC sensitivity at micron resolution from room-to-cryogenic temperatures. An additional advantage of the SQCRAMscope is the preservation of optical access to the sample: Magnetometry imaging of, e.g., electron transport may be performed in concert with other imaging techniques. This multimodal imaging capability can be brought to bear with great effect in the study of nematicity in iron-pnictide high-temperature superconductors, where the relationship between electronic and structural symmetry-breaking resulting in a nematic phase is under debate. Here, we combine the SQCRAMscope with an in situ microscope that measures optical birefringence near the surface. This enables simultaneous and spatially resolved detection of both bulk and near-surface manifestations of nematicity via transport and structural deformation channels, respectively. By performing the first local measurement of emergent resistivity anisotropy in iron pnictides, we observe sharp, nearly concurrent transport and structural transitions. More broadly, these measurements demonstrate the SQCRAMscope's ability to reveal important insights into the physics of complex quantum materials.

cond-mat.str-el↗

Interplay of Charge Density Wave States and Strain at the Surface of CeTe$_{2}$

We use scanning tunneling microscopy (STM) to study charge density wave (CDW) states in the rare-earth di-telluride, CeTe$_{2}$. In contrast to previous experimental and first-principles studies of the rare-earth di-tellurides, our STM measurements surprisingly detect a unidirectional CDW with $\textit{q}$ ~ 0.28 $\textit{a}$*, which is very close to what is found in experimental measurements of the related rare-earth tri-tellurides. Furthermore, in the vicinity of an extended sub-surface defect, we find spatially-separated as well as spatially-coexisting unidirectional CDWs at the surface of CeTe$_{2}$. We quantify the nanoscale strain and its variations induced by this defect, and establish a correlation between local lattice strain and the locally-established CDW states. Our measurements probe the fundamental properties of a weakly-bound two-dimensional Te-sheet, which experimental and theoretical work has previously established as the fundamental component driving much of the essential physics in both the rare-earth di- and tri-telluride compounds.

cond-mat.mtrl-sci↗

High resolution time- and angle-resolved photoemission spectroscopy with 11 eV laser pulses

Performing time and angle resolved photoemission spectroscopy (tr-ARPES) at high momenta necessitates extreme ultraviolet laser pulses, which are typically produced via high harmonic generation (HHG). Despite recent advances, HHG-based setups still require large pulse energies (hundreds of $μ$J to mJ) and their energy resolution is limited to tens of meV. Here, we present a novel 11 eV tr-ARPES setup that generates a flux of $5\times10^{10}$ photons/s and achieves an unprecedented energy resolution of 16 meV. It can be operated at high repetition rates (up to 250 kHz) while using input pulse energies down to 3 $μ$J. We demonstrate these unique capabilities by simultaneously capturing the energy and momentum resolved dynamics in two well-separated momentum space regions of a charge density wave material ErTe$_3$. This novel setup offers opportunity to study the non-equilibrium band structure of solids with exceptional energy and time resolutions at high repetition rates.

cond-mat.mtrl-sci↗

Phase transition preceding magnetic long-range order in the double perovskite Ba2NaOsO6

Recent theoretical studies [Chen et al., Phys. Rev. B 82, 174440 (2010), Ishizuka et al., Phys. Rev. B 90, 184422 (2014)] for the magnetic Mott insulator Ba2NaOsO6 have proposed a low-temperature order parameter that breaks lattice rotational symmetry without breaking time reversal symmetry leading to a nematic phase just above magnetic ordering temperature. We present high-resolution calorimetric and magnetization data of the same Ba2NaOsO6 single crystal and show evidence for a weakly field-dependent phase transition occurring at a temperature of Ts ~ 9.5K, above the magnetic ordering temperature of Tc ~ 7.5K. This transition appears as a broadened step in the low-field temperature dependence of the specific heat. The evolution of the phase boundary with applied magnetic field suggests that this phase coincides with the phase of broken local point symmetry seen in high field NMR experiments [Lu et al., Nat.\ Comm. 8 14407 (2017)]. Furthermore, the magnetic field dependence of the specific heat provides clear indications for magnetic correlations persisting at temperatures between Tc and Ts where long-range magnetic order is absent giving support for the existence of the proposed nematic phase.

cond-mat.str-el↗

Light-Induced Charge Density Wave in LaTe$_3$

When electrons in a solid are excited with light, they can alter the free energy landscape and access phases of matter that are beyond reach in thermal equilibrium. This accessibility becomes of vast importance in the presence of phase competition, when one state of matter is preferred over another by only a small energy scale that, in principle, is surmountable by light. Here, we study a layered compound, LaTe$_3$, where a small in-plane (a-c plane) lattice anisotropy results in a unidirectional charge density wave (CDW) along the c-axis. Using ultrafast electron diffraction, we find that after photoexcitation, the CDW along the c-axis is weakened and subsequently, a different competing CDW along the a-axis emerges. The timescales characterizing the relaxation of this new CDW and the reestablishment of the original CDW are nearly identical, which points towards a strong competition between the two orders. The new density wave represents a transient non-equilibrium phase of matter with no equilibrium counterpart, and this study thus provides a framework for unleashing similar states of matter that are "trapped" under equilibrium conditions.

cond-mat.mtrl-sci↗

Imaging anisotropic vortex dynamics in FeSe

Strong vortex pinning in FeSe could be useful for technological applications and could provide clues about the coexistence of superconductivity and nematicity. To characterize the pinning of individual, isolated vortices, we simultaneously apply a local magnetic field and image the vortex motion with scanning SQUID susceptibility. We find that the pinning is highly anisotropic: the vortices move easily along directions that are parallel to the orientations of twin domain walls and pin strongly in a perpendicular direction. These results are consistent with a scenario in which the anisotropy arises from vortex pinning on domain walls and quantify the dynamics of individual vortex pinning in FeSe.

cond-mat.supr-con↗

Signatures of Anelastic Domain Relaxation in Ba(Fe$_{1-x}$Co$_{x}$)$_{2}$As$_{2}$ Investigated by Mechanical Modulation of Resistivity

The resistive response of Ba(Fe$_{1-x}$Co$_{x}$)$_{2}$As$_{2}$ to AC mechanical deformation is considered in the multi-domain state. This resistance change depends both upon the anelastic relaxation of domain walls and upon the relation between resistance and the domain wall configuration. Samples are adhered to the surface of a piezoelectric stack, which is driven by an AC voltage while the AC modulation of the sample resistance is measured. As the response time of electrons is faster than that of the lattice, the phase difference $ϕ$ between the AC resistance modulation and the AC deformation of the piezoelectric is entirely due to anelastic relaxation effects in the sample. An expression is derived for relating $ϕ$ to a sample's complex compliance, $J(ω)$, in this experimental configuration. Measurements of Ba(Fe$_{1-x}$Co$_{x}$)$_{2}$As$_{2}$ for x= (0.025, 0.052) reveal a peak in the out-of-phase resistivity modulation in the orthorhombic antiferromagnetic state well below the Neél temperature $T_N$ and structural transition $T_S$. Meanwhile, for a composition that is tetragonal at all temperatures, x=0.07, the resistance modulation remains entirely in phase over the same temperatures, establishing domain motion as a probable cause of the observed effects in the samples that do undergo the tetragonal-to-orthorhombic transition. Fits are provided of $\tanϕ$ for a sample with x=0.025 for various amplitude excitations on the piezoelectric stack, from which the apparent activation energy $E_a$ for domain wall motion is found to decreases with increasing amplitude of the deformation along the $[110]_T$ axis. We find $\frac{dE_a}{d\varepsilon^0_{[110,110]_T}} = -1115\pm 196$ eV with $E_a = 9.09 \pm 0.74 \times 10^{-3}$ eV in the zero strain limit if we assume linearity over the entire range of strain amplitudes.

cond-mat.str-el↗

Disorder Induced Suppression of CDW Long Range Order: STM Study of Pd-intercalated ErTe3

Pd-intercalated ErTe3 is studied as a model system for the interplay between a bidirectional two component charge density wave (CDW) state and disorder. Using scanning tunneling microscopy (STM), we show that introducing Pd-intercalants (i.e. disorder) disrupts the long-range order of both CDW states via the creation of dislocations, which appear associated with each CDW separately. While for weak disorder both CDW states continue to coexist throughout the sample, with no "domains" of one CDW direction or another, increasing Pd concentration has a stronger effect on the secondary CDW state, manifested in higher density of dislocations. Vestiges of the two distinct CDW phases persist to intercalation levels much above where signatures of the original phase transition are totally suppressed. This study therefore presents a first look into the disruption of multiple 2D strong-coupling CDW states by the proliferation of dislocations.

cond-mat.str-el↗

AC Elastocaloric effect as a probe for thermodynamic signatures of continuous phase transitions

Studying the response of materials to strain can elucidate subtle properties of electronic structure in strongly correlated materials. So far, mostly the relation between strain and resistivity, the so called elastoresistivity, has been investigated. The elastocaloric effect is a second rank tensor quantity describing the relation between entropy and strain. In contrast to the elastoresistivity, the elastocaloric effect is a thermodynamic quantity. Experimentally, elastocaloric effect measurements are demanding since the thermodynamic conditions during the measurement have to be well controlled. Here we present a technique to measure the elastocaloric effect under quasi adiabatic conditions. The technique is based on oscillating strain, which allows for increasing the frequency of the elastocaloric effect above the thermal relaxation rate of the sample. We apply the technique to Co-doped iron pnictide superconductors and show that the thermodynamic signatures of second order phase transitions in the elastocaloric effect closely follow those observed in calorimetry experiments. In contrast to the heat capacity, the electronic signatures in the elastocaloric effect are measured against a small phononic background even at high temperatures, establishing this technique as a powerful complimentary tool for extracting the entropy landscape proximate to a continuous phase transition.

cond-mat.mtrl-sci↗

Dynamical slowing down in an ultrafast photo-induced phase transition

Complex systems, which consist of a large number of interacting constituents, often exhibit universal behavior near a phase transition. A slowdown of certain dynamical observables is one such recurring feature found in a vast array of contexts. This phenomenon, known as critical slowing down, is well studied mostly in thermodynamic phase transitions. However, it is less understood in highly nonequilibrium settings, where the time it takes to traverse the phase boundary becomes comparable to the timescale of dynamical fluctuations. Using transient optical spectroscopy and femtosecond electron diffraction, we studied a photo-induced transition of a model charge-density-wave (CDW) compound, LaTe$_3$. We observed that it takes the longest time to suppress the order parameter at the threshold photoexcitation density, where the CDW transiently vanishes. This finding can be quantitatively captured by generalizing the time-dependent Landau theory to a system far from equilibrium. The experimental observation and theoretical understanding of dynamical slowing down may offer insight into other general principles behind nonequilibrium phase transitions in many-body systems.

cond-mat.str-el↗

Symmetric and antisymmetric strain as continuous tuning parameters for electronic nematic order

We report the separate response of the critical temperature of the nematic phase transition $T_{\rm S}$ to symmetric and antisymmetric strains for the prototypical underdoped iron pnictide Ba(Fe$_{0.975}$Co$_{0.025}$)$_2$As$_2$. This decomposition is achieved by comparing the response of $T_{\rm S}$ to uniaxial stress and hydrostatic pressure. In addition to quantifying the two distinct linear responses to symmetric strains, we find a quadratic variation of $T_{\rm S}$ as a response to antisymmetric strains $ε_{\rm B_{1g}}$=$\frac{1}{2}$($ε_{\rm xx}$-$ε_{\rm yy}$), exceeding the non linear response to symmetric strains by at least two orders of magnitude. These observations establish orthogonal antisymmetric strain as a powerful tuning parameter for nematic order.

cond-mat.mtrl-sci↗