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The results of study of the behavior of surface plasmon polaritons in the layered structure of a VO2‒SiO2-graphene-based hyperbolic metasurface under the influence of an external magnetic field before and at the beginning of the phase transition of vanadium dioxide are presented. As a result of calculations, it is shown how the isofrequency contour of surface plasmons changes taking into account the different direction of the external magnetic field. It is also shown how an external magnetic field affects the direction of static magnetization caused by the inverse Faraday effect. This work can offer additional ways to control the behavior of surface plasmons, as well as become the basis for the study of new self-adjusting structures. [ABSTRACT FROM AUTHOR]

Mixed-stacked organic molecular compounds near the neutral-ionic phase boundary, represented by tetrathiafulvalene-p-chloranil (TTF-CA), show a unique phase transition from a paraelectric neutral (N) phase to a ferroelectric ionic (I) phase when subjected to decreasing temperature or applied pressure, which is called an NI transition. This NI transition can also be induced by photoirradiation, in which case it is known as a prototypical 'photoinduced phase transition'. In this paper, we focus on the ultrafast electron and molecular dynamics in the transition between the N and I states induced by irradiation by a femtosecond laser pulse and a terahertz electric-field pulse in TTF-CA. In the first half of the paper, we review the photoinduced N-to-I transition in TTF-CA studied by femtosecond-pump-probe reflection spectroscopy. We show that in the early stage of the transition, collective charge transfers occur within 20 fs after the photoirradiation, and microscopic one-dimensional (1D) I domains are produced. These ultrafast I-domain formations are followed by molecular deformations and displacements, which play important roles in the stabilization of photogenerated I domains. In the photoinduced I-to-N transition, microscopic 1D N domains are also produced and stabilized by molecular deformations and displacements. However, the time characteristics of the photoinduced N-to-I and I-to-N transitions in the picosecond time domain are considerably different from each other. In the second half of this paper, we review two phenomena induced by a strong terahertz electric-field pulse in TTF-CA: themodulation of a ferroelectric polarization in the I phase and the generation of a large macroscopic polarization in the N phase. [ABSTRACT FROM AUTHOR]

We report the observation of a Skyrmion lattice in the chiral multiferroic insulator Cu2OSeO3 using Cu L3-edge resonant soft x-ray diffraction. We observe the unexpected existence of two distinct Skyrmion sublattices that arise from inequivalent Cu sites with chemically identical coordination numbers but different magnetically active orbitals. The Skyrmion sublattices are rotated with respect to each other, implying a long wavelength modulation of the lattice. The modulation vector is controlled with an applied magnetic field, associating this moirélike phase with a continuous phase transition. Our findings will open up a new class of science involving manipulation of quantum topological states. [ABSTRACT FROM AUTHOR]

Negative capacitance (NC) in a planar W-doped VO2 micro-switch was observed at room temperature in the low-frequency range 1 kHz-10 MHz. The capacitance changed from positive to negative values as the W-doped VO2 active layer switched from semiconducting to metallic state under applied voltage. In addition, a capacitance-voltage hysteresis was observed as the applied voltage was cycled from -35 to 35V. These observations suggest that NC results from the increase of the electrically induced conductivity in the active layer. This NC phenomenon could be exploited in advanced multifunctional devices including ultrafast switches, field-effect transistors and memcapacitive systems. [ABSTRACT FROM AUTHOR]

Photoinduced phase transitions are of special interest in condensed matter physics because they can be used to change complex macroscopic material properties on the ultrafast timescale. Cooperative interactions between microscopic degrees of freedom greatly enhance the number and nature of accessible states, making it possible to switch electronic, magnetic or structural properties in new ways. Photons with high energies, of the order of electron volts, in particular are able to access electronic states that may differ greatly from states produced with stimuli close to equilibrium. In this study we report the photoinduced change in the lattice structure of a charge and orbitally ordered Nd0.5Sr0.5MnO3 thin film using picosecond time-resolved X-ray diffraction. The photoinduced state is structurally ordered, homogeneous, metastable and has crystallographic parameters different from any thermodynamically accessible state. A femtosecond time-resolved spectroscopic study shows the formation of an electronic gap in this state. In addition, the threshold-like behaviour and high efficiency in photo-generation yield of this gapped state highlight the important role of cooperative interactions in the formation process. These combined observations point towards a 'hidden insulating phase' distinct from that found in the hitherto known phase diagram. [ABSTRACT FROM AUTHOR]

Correlated electron materials can undergo a variety of phase transitions, including superconductivity, the metal–insulator transition and colossal magnetoresistance. Moreover, multiple physical phases or domains with dimensions of nanometres to micrometres can coexist in these materials at temperatures where a pure phase is expected. Making use of the properties of correlated electron materials in device applications will require the ability to control domain structures and phase transitions in these materials. Lattice strain has been shown to cause the coexistence of metallic and insulating phases in the Mott insulator VO2. Here, we show that we can nucleate and manipulate ordered arrays of metallic and insulating domains along single-crystal beams of VO2 by continuously tuning the strain over a wide range of values. The Mott transition between a low-temperature insulating phase and a high-temperature metallic phase usually occurs at 341 K in VO2, but the active control of strain allows us to reduce this transition temperature to room temperature. In addition to device applications, the ability to control the phase structure of VO2 with strain could lead to a deeper understanding of the correlated electron materials in general. [ABSTRACT FROM AUTHOR]

The transient nanoscale dynamics of materials on femtosecond to picosecond timescales is of great interest in the study of condensed phase dynamics such as crack formation, phase separation and nucleation, and rapid fluctuations in the liquid state or in biologically relevant environments. The ability to take images in a single shot is the key to studying non-repetitive behaviour mechanisms, a capability that is of great importance in many of these problems. Using coherent diffraction imaging with femtosecond X-ray free-electron-laser pulses we capture time-series snapshots of a solid as it evolves on the ultrafast timescale. Artificial structures imprinted on a Si3N4 window are excited with an optical laser and undergo laser ablation, which is imaged with a spatial resolution of 50 nm and a temporal resolution of 10 ps. By using the shortest available free-electron-laser wavelengths and proven synchronization methods this technique could be extended to spatial resolutions of a few nanometres and temporal resolutions of a few tens of femtoseconds. This experiment opens the door to a new regime of time-resolved experiments in mesoscopic dynamics. [ABSTRACT FROM AUTHOR]

A general nomenclature applicable to the phases that form in any sequence of transitions in the solid state has been recommended by an IUCr Working Group [Acta Cryst.(1998). A54, 1028-1033]. The six-field notation of the first Report, hereafter I, was applied to the case of structural phase transitions, i.e. to transformations resulting from temperature and/or pressure changes between two crystalline (strictly periodic) phases involving modifications to the atomic arrangement. Extensive examples that illustrate the recommendations were provided. This second Report considers, within the framework of a similar six- field notation, the more complex nomenclature of transitions involving magnetic phases, incommensurate phases and transitions that occur as a function of composition change. Extension of the nomenclature to the case of phases with less clearly established relevance to standard schemes of transition in equilibrium systems, namely polytype phases, radiation-induced and other transient phases, quasicrystalline phases and their transitions is recommended more tentatively. A uniform notation for the translational periodicity, propagation vector or wavevector for magnetic and/or incommensurate phases, substances is specified. The notation adopted for incommensurate phases, relying partly on the existence of an average structure, is also consistent with that for commensurate phases in a sequence. The sixth field of the nomenclature is used to emphasize the special features of polytypes and transient phases. As in illustrative examples are provided for each category of phase sequence. [ABSTRACT FROM AUTHOR]

In this article, we present a comprehensive review on recent research progress in design and fabrication of active tunable metamaterials and devices based on phase transition of VO2. Firstly, we introduce mechanisms of the metal-to-insulator phase transition (MIPT) in VO2 investigated by ultrafast THz spectroscopies. By analyzing the THz spectra, the evolutions of MIPT in VO2 induced by different external excitations are described. The superiorities of using VO2 as building blocks to construct highly tunable metamaterials are discussed. Subsequently, the recently demonstrated metamaterial devices based on VO2 are reviewed. These metamaterials devices are summarized and described in the categories of working frequency. In each working frequency range, representative metamaterials based on VO2 with different architectures and functionalities are reviewed and the contributions of the MIPT of VO2 are emphasized. Finally, we conclude the recent reports and provide a prospect on the strategies of developing future tunable metamaterials based on VO2. [ABSTRACT FROM AUTHOR]

We review some recent advances in the use of optical fields at terahertz frequencies to drive the lattice of complex materials. We will focus on the control of low energy collective properties of solids, which emerge on average when a high frequency vibration is driven and a new crystal structure induced. We first discuss the fundamentals of these lattice rearrangements, based on how anharmonic mode coupling transforms an oscillatory motion into a quasi-static deformation of the crystal structure. We then discuss experiments, in which selectively changing a bond angle turns an insulator into a metal, accompanied by changes in charge, orbital and magnetic order. We then address the case of light induced non-equilibrium superconductivity, a mysterious phenomenon observed in some cuprates and molecular materials when certain lattice vibrations are driven. Finally, we show that the dynamics of electronic and magnetic phase transitions in complex-oxide heterostructures follow distinctly new physical pathways in case of the resonant excitation of a substrate vibrational mode. [ABSTRACT FROM AUTHOR]

The coexistence of ferromagnetic and antiferromagnetic phases and their role in the photoinduced insulator-to-metal transition in Pr1-xCaxMnO3 are revealed via ultrafast resonant x-ray diffraction and broadband optical reflectivity measurements. The antiferromagnetic scattering signal and ferromagnetically sensitive reflectivity measurements show similar, strongly temperature dependent time scales. We attribute the common dynamics to an activation barrier between the equilibrium insulating phase and the photoinduced metallic phase related to interactions between the phase-separated ferromagnetic and antiferromagnetic insulating phases. [ABSTRACT FROM AUTHOR]

Epitaxial La0.7Sr0.3MnO3 (LSMO) thin films, with different thicknesses ranging from 20 to 330 nm, were deposited on (1 0 0)-oriented strontium titanate (STO) substrates by pulsed laser deposition, with their structure and morphology characterized at room temperature. The magnetic and electric transport properties of the as-processed thin films reveal an abnormal behaviour in the temperature dependent magnetization M(T) below the antiferrodistortive STO phase transition (TSTO), and also an anomaly in the magnetoresistance and electrical resistivity close to the same temperature. Films with thickness ≤100 nm show an in-excess magnetization and pronounced changes in the coercivity due to the interface-mediated magnetoelastic coupling with antiferrodistortive domain wall movement occurring below TSTO. However, in thicker LSMO thin films, an in-defect magnetization is observed. This reversed behaviour can be understood with the emergence in the upper layer of the film, of a columnar structure needed to relax the elastic energy stored in the film, which leads to randomly oriented magnetic domain reconstructions. For enough high-applied magnetic fields, as thermodynamic equilibrium is reached, a full suppression of the anomalous magnetization occurs, wherein the temperature dependence of the magnetization starts to follow the expected Brillouin behaviour. [ABSTRACT FROM AUTHOR]