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D. P. Chen

Publications and source records attributed to D. P. Chen.

16 recordsLinked to original sources

Higgs mode and its decay in a two dimensional antiferromagnet

Condensed-matter analogs of the Higgs boson in particle physics allow insights into its behavior in different symmetries and dimensionalities. Evidence for the Higgs mode has been reported in a number of different settings, including ultracold atomic gases, disordered superconductors, and dimerized quantum magnets. However, decay processes of the Higgs mode (which are eminently important in particle physics) have not yet been studied in condensed matter due to the lack of a suitable material system coupled to a direct experimental probe. A quantitative understanding of these processes is particularly important for low-dimensional systems where the Higgs mode decays rapidly and has remained elusive to most experimental probes. Here, we discover and study the Higgs mode in a two-dimensional antiferromagnet using spin-polarized inelastic neutron scattering. Our spin-wave spectra of Ca$_2$RuO$_4$ directly reveal a well-defined, dispersive Higgs mode, which quickly decays into transverse Goldstone modes at the antiferromagnetic ordering wavevector. Through a complete mapping of the transverse modes in the reciprocal space, we uniquely specify the minimal model Hamiltonian and describe the decay process. We thus establish a novel condensed matter platform for research on the dynamics of the Higgs mode.

cond-mat.str-el

Soft spin-amplitude fluctuations in a Mott-insulating ruthenate

Magnetism in transition-metal compounds (TMCs) has traditionally been associated with spin degrees of freedom, because the orbital magnetic moments are typically largely quenched. On the other hand, magnetic order in 4f- and 5d-electron systems arises from spin and orbital moments that are rigidly tied together by the large intra-atomic spin-orbit coupling (SOC). Using inelastic neutron scattering on the archetypal 4d-electron Mott insulator Ca$_2$RuO$_4$, we report a novel form of excitonic magnetism in the intermediate-strength regime of the SOC. The magnetic order is characterized by ``soft'' magnetic moments with large amplitude fluctuations manifested by an intense, low-energy excitonic mode analogous to the Higgs mode in particle physics. This mode heralds a proximate quantum critical point separating the soft magnetic order driven by the superexchange interaction from a quantum-paramagnetic state driven by the SOC. We further show that this quantum critical point can be tuned by lattice distortions, and hence may be accessible in epitaxial thin-film structures. The unconventional spin-orbital-lattice dynamics in Ca$_2$RuO$_4$ identifies the SOC as a novel source of quantum criticality in TMCs.

cond-mat.str-el

Domain Wall Conductivity in Oxygen Deficient Multiferroic YMnO3 Single Crystals

The transport properties of domain walls in oxygen deficient multiferroic YMnO3 single crystals have been probed using conductive atomic force microscopy and piezoresponse force microscopy. Domain walls exhibit significantly enhanced conductance after being poled in electric fields, possibly induced by oxygen vacancy ordering at domain walls. The electronic conduction can be understood by the Schottky emission and Fowler-Nordheim tunnelling mechanisms. Our results show that the domain wall conductance can be modulated through band structure engineering by manipulating ordered oxygen vacancies in the poling fields.

cond-mat.mtrl-sci

Spin dynamics in the pseudogap state of a high-temperature superconductor

The pseudogap is one of the most pervasive phenomena of high temperature superconductors. It is attributed either to incoherent Cooper pairing setting in above the superconducting transition temperature Tc, or to a hidden order parameter competing with superconductivity. Here we use inelastic neutron scattering from underdoped YBa(2)Cu(3)O(6.6) to show that the dispersion relations of spin excitations in the superconducting and pseudogap states are qualitatively different. Specifically, the extensively studied "hour glass" shape of the magnetic dispersions in the superconducting state is no longer discernible in the pseudogap state and we observe an unusual "vertical" dispersion with pronounced in-plane anisotropy. The differences between superconducting and pseudogap states are thus more profound than generally believed, suggesting a competition between these two states. Whereas the high-energy excitations are common to both states and obey the symmetry of the copper oxide square lattice, the low-energy excitations in the pseudogap state may be indicative of collective fluctuations towards a state with broken orientational symmetry predicted in theoretical work.

cond-mat.supr-con

Electronic texture of the thermoelectric oxide Na0.75CoO2

From 59Co and 23Na NMR, we demonstrate the impact of the Na+ vacancy ordering on the cobalt electronic states in Na0.75CoO2: at long time scales, there is neither a disproportionation into 75 % Co3+ and 25 % Co4+ states, nor a mixed-valence metal with a uniform Co3.25+ state. Instead, the system adopts an intermediate configuration in which 30 % of the lattice sites form an ordered pattern of localized Co3+ states. Above 180 K, an anomalous mobility of specific Na+ sites is found to coexist with this electronic texture, suggesting that the formation of the latter may contribute to stabilizing the Na+ ordering. Control of the ion doping in these materials thus appears to be crucial for fine-tuning of their thermoelectric properties.

cond-mat.str-el

Doping induced magnetic clusters and Co spin state transition in Na_xCoO_2 with 0.78<x<.97

By muon spin rotation we investigated the magnetic properties of a series of highly Na doped NaxCoO2 single crystals with 0.78(1) 0.04 until they yield a bulk magnetic state near x=0.78. Evidence for a strong (likely geometrical) frustration of the magnetic order is obtained from the anomalous doping dependence of the spin fluctuation rate (above the ordering temperature) which is strongly enhanced at x=0.78 as compared to x=0.97.

cond-mat.supr-con

Spin singlet pairing in the superconducting state of NaxCoO2\cdot1.3H2O: evidence from a ^{59}Co Knight shift in a single crystal

We report a ^{59}Co Knight shift measurement in a single crystal of the cobalt oxide superconductor Na_{x}CoO_2\cdot1.3H_2O (T_c=4.25 K). We find that the shift due to the spin susceptibility, K^s, is substantially large and anisotropic, with the spin shift along the a-axis K^s_a being two times that along the c-axis K^s_c. The shift decreases with decreasing temperature (T) down to T\sim100 K, then becomes a constant until superconductivity sets in. Both K^s_a and K^s_c decrease below T_c. Our results indicate unambiguously that the electron pairing in the superconducting state is in the spin singlet form.

cond-mat.supr-con

Anomalous electronic Raman scattering in Na_xCoO_2 H_2O

Raman scattering experiments on Na_{x}CoO_2 yH_2O single crystals show a broad electronic continuum with a pronounced peak around 100 cm-1 and a cutoff at approximately 560 cm-1over a wide range of doping levels. The electronic Raman spectra in superconducting and non-superconducting samples are similar at room temperature, but evolve in markedly different ways with decreasing temperature. For superconducting samples, the low-energy spectral weight is depleted upon cooling below T* sim 150K, indicating a opening of a pseudogap that is not present in non-superconducting materials. Weak additional phonon modes observed below T* suggest that the pseudogap is associated with charge ordering.

cond-mat.str-el

Non-magnetic insulator state in Na1CoO2 and phase separation of Na vacancies

Crystallographic, magnetic and NMR properties of a NaxCoO2 single crystal with x~1 are presented. We identify the stoichiometric Na1CoO2 phase, which is shown to be a non-magnetic insulator, as expected for homogeneous planes of Co3+ ions with S=0. In addition, we present evidence that, because of slight average Na deficiency, chemical and electronic phase separation leads to a segregation of Na vacancies into the well-defined, magnetic, Na0.8CoO2 phase. The importance of phase separation is discussed in the context of magnetic order for x~0.8 and the occurrence of a metal-insulator transition for x->1.

cond-mat.str-el

Magnetic ordering and spin waves in $\bf Na_{0.82}CoO_2$

Na$_x$CoO$_2$, the parent compound of the recently synthesized superconductor Na$_x$CoO$_2$:$y$H$_2$O, exhibits bulk antiferromagnetic order below $\sim20$ K for 0.75 $\leq x \leq$ 0.9. We have performed neutron scattering experiments in which we observed Bragg reflections corresponding to A-type antiferromagnetic order in a Na$_{0.82}$CoO$_2$ single crystal and characterized the corresponding spin-wave dispersions. The spin waves exhibit a strongly energy-dependent linewidth. The in-plane and out-of-plane exchange constants resulting from a fit to a nearest-neighbor Heisenberg model are similar in magnitude, which is unexpected in view of the layered crystal structure of Na$_{x}$CoO$_2$. Possible implications of these observations are discussed.

cond-mat.str-el

Study of intercalation and deintercalation of Na_xCoO_2 yH_2O single crystals

Single crystals of NaxCoO2 with beta-phase (x=0.55, 0.60 and 0.65), alpha'-phase (x=0.75) and alpha-phase (x=0.9, 1.0) have been grown by the floating zone technique. The Na-extraction and hydration were carried out for the alpha'-sample to get superconducting phase of NaxCoO2.yH2O (x~0.3, y~1.3). Hydrated single crystals exhibit cracked layers perpendicular to the c-axis due to a large expansion when the water is inserted into the structure. A study of intercalation/deintercalation was performed to determine the stability of the hydrated phase and effects of hydration on the structure of the compound. X-ray diffraction and Thermogravimetric experiments are used to monitor the process of water molecules accommodated in and removed from the crystal lattice. The initial intercalation process takes place with two-water molecules corresponding to y=0.6) inserted in a formula unit, followed by a group of four (y=1.3) to form a cluster of Na(H2O)4. Thermogravimetric analysis suggests that the deintercalation occurs with the removal of the water molecules one by one from the hydrated cluster at elevated temperatures of approximately 50, 100, 200 and 300 C, respectively. Our investigations reveal that the hydration process is dynamic and that water molecule inter- and deintercalation follow different reaction paths in an irreversible way.

cond-mat.str-el

Phonon scattering and stability of Na_0.5CoO_2

Raman scattering experiments have been performed on Na_xCoO_2 as function of temperature at the composition x=0.5 where a structural instability and a metal-insulator transition have been observed. Three additional phonon modes are observed compared to samples with larger x. An in-situ annealing study (T_max=550 K) with the initial presence of water vapor at ambient conditions reveals an irreversible structural instability of this composition.

cond-mat.str-el

Two-Dimensional Geometry of Spin Excitations in the High Temperature Superconductor YBa2Cu3O6+x

The fundamental building block of the copper oxide superconductors is a Cu4O4 square plaquette. In most of these materials, the plaquettes are slightly distorted and form a rectangular lattice. An influential theory predicts that high-temperature superconductivity is nucleated in "stripes" aligned along one of the axes of this lattice. This theory had received strong support from experiments that appeared to indicate a one-dimensional character of the magnetic excitations in the high temperature superconductor YBa2Cu3O6.6. Here we report neutron scattering data on "untwinned" YBa2Cu3O6+x crystals, in which the orientation of the rectangular lattice is maintained throughout the entire volume. Contrary to the earlier claim, we demonstrate that the geometry of the magnetic fluctuations is two-dimensional. Rigid stripe arrays therefore appear to be ruled out over a wide range of doping levels in YBa2Cu3O6+x, but the data may be consistent with liquid-crystalline stripe order.

cond-mat.str-el

Bulk antiferromagnetism in $\bf Na_{0.82}CoO_2$ single crystals

Susceptibility, specific heat, and muon spin rotation measurements on high-quality single crystals of $\rm Na_{0.82}CoO_2$ have revealed bulk antiferromagnetism with Néel temperature $\rm T_N = 19.8 \pm 0.1$ K and an ordered moment perpendicular to the $\rm CoO_2$ layers. The magnetic order encompasses nearly 100% of the crystal volume. The susceptibility exhibits a broad peak around 30 K, characteristic of two-dimensional antiferromagnetic fluctuations. The in-plane resistivity is metallic at high temperatures and exhibits a minimum at $\rm T_N$.

cond-mat.str-el

The crystal growth and characterization of NaxCoO2 and NaxCoO2yH2O

A systematic study of NaxCoO2 (x=0.50 - 0.90) and NaxCoO2 yH(D)2O (x=0.26 - 0.42, y=1.3) has been performed to determine phase stability and the effect of hydration on the structural and superconducting properties of this system. We show that a careful control of the Na deintercalation process and hydration dynamics is possible in single crystals of this system. Furthermore, we give experimental evidence that the dependence of the superconducting transition temperature on Na content is much weaker than reported earlier. Implications of this effect for the understanding of the superconducting phase diagram are discussed.

cond-mat.supr-con

Charge ordering and magneto-polarons in Na$_{0.82}$CoO$_2$

Using spectral ellipsometry, we have measured the dielectric function of a Na$_{0.82(2)}$CoO$_2$ crystal that exhibits bulk antiferromagnetism with T$_{N}$=19.8 K. We identify two prominent transitions as a function of temperature. The first one at 280 K involves marked changes of the electronic and the lattice response that are indicative of charge ordering in the CoO$_{2}$ layers. The second transition coincides with T$_{N}$=19.8 K and reveals a sizeable spin-charge coupling. The data are discussed in terms of charge ordering and formation of magneto-polarons due to a charge-induced spin-state transition of adjacent Co$^{3+}$ ions.

cond-mat.str-el