Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userDirect evidence of strong local ferroelectric ordering in a thermoelectric semiconductor
162
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
It is thought that the proposed new family of multi-functional materials namely the ferroelectric thermoelectrics may exhibit enhanced functionalities due to the coupling of the thermoelectric parameters with ferroelectric polarization in solids. Therefore, the ferroelectric thermoelectrics are expected to be of immense technological and fundamental significance. As a first step towards this direction, it is most important to identify the existing high performance thermoelectric materials exhibiting ferroelectricity. Herein, through the direct measurement of local polarization switching we show that the recently discovered thermoelectric semiconductor $AgSbSe_{2}$ has local ferroelectric ordering. Using piezo-response force microscopy, we demonstrate the existence of nanometer scale ferroelectric domains that can be switched by external electric field. These observations are intriguing as $AgSbSe_{2}$ crystalizes in cubic rock salt structure with centro-symmetric space group (Fm-3m) and therefore no ferroelectricity is expected. However, from high resolution transmission electron microscopy (HRTEM) measurement we found the evidence of local superstructure formation which, we believe, leads to local distortion of the centro-symmetric arrangement in $AgSbSe_{2}$ and gives rise to the observed ferroelectricity. Stereochemically active $5s^{2}$ lone pair of Sb can also give rise to local structural distortion, which creates ferroelectricity in $AgSbSe_{2}$.
rate research
Read More
The direct magnetoelectric (ME) effect resulting from the polarization changes induced in a ferroelectric film by the application of a magnetic field to a ferromagnetic substrate is described using the nonlinear thermodynamic theory. It is shown that the ME response strongly depends on the initial strain state of the film. The ME polarization coefficient of the heterostructures involving Terfenol-D substrates and compressively strained lead zirconate titanate (PZT) films, which stabilize in the out-of-plane polarization state, is found to be comparable to that of bulk PZT/Terfenol-D laminate composites. At the same time, the ME voltage coefficient reaches a giant value of 50 V/(cm Oe), which greatly exceeds the maximum observed static ME coefficients of bulk composites. This remarkable feature is explained by a favorable combination of considerable strain sensitivity of polarization and a low electric permittivity in compressively strained PZT films. The theory also predicts a further dramatic increase of ME coefficients at the strain-induced transitions between different ferroelectric phases.
Ferroelectric materials contain a switchable spontaneous polarization that persists even in the absence of an external electric field. The coexistence of ferroelectricity and metallicity in a material appears to be illusive, since polarization is ill-defined in metals, where the itinerant electrons are expected to screen the long-range dipole interactions necessary for dipole ordering. The surprising discovery of the polar metal, LiOsO3 has generated interest in searching for new polar metals motivated by the prospects of exotic quantum phenomena such as unconventional pairing mechanisms giving rise to superconductivity, topological spin currents, anisotropic upper critical fields, and Mott multiferroics. Previous studies have suggested that the coordination preferences of the Li atom play a key role in stabilizing the polar metal phase of LiOsO3, but a thorough understanding of how polar order and metallicity can coexist remains elusive. Here, we use XUV-SHG as novel technique to directly probe the broken inversion-symmetry around the Li atom. Our results agree with previous theories that the primary structural distortion that gives rise to the polar metal phase in LiOsO3 is a consequence of a sub-Angstrom Li atom displacement along the polar axis. A remarkable agreement between our experimental results and ab initio calculations provide physical insights for connecting the nonlinear response to unit-cell spatial asymmetries. It is shown that XUV-SHG can selectively probe inversion-breaking symmetry in a bulk material with elemental specificity. Compared to optical SHG methods, XUV-SHG fills a key gap for studying structural asymmetries when the structural distortion is energetically separated from the Fermi surface. Further, these results pave the way for time-resolved probing of symmetry-breaking structural phase transitions on femtosecond timescales with element specificity.
We have combined temperature dependent local structural measurements with first principles density functional calculations to develop a three dimensional local structure model of the misfit system [Ca2CoO3][CoO2]1.61 (referred to as Ca3Co4O9) which has a rock salt structure stacked incommensurately on a hexagonal CoO2 lattice. The local structural measurements reveal a low coordination of Co(2)-O bonds in the rock salt layer with large static structural disorder. The temperature dependence of the Co(1)-Co(1) bond correlations in the CoO2 layer are found to be normal above ~75K and with a very small static disorder component. An anomalous enhancement in the Co(1)-Co(1) correlations occurs at the onset of long-range magnetic order. Density functional computations suggest that the reduction of the coordination of Co(2) is due to the formation of chains of Co(2)Ox in the a-b plane linked to the Ca-O layers by c-axis Co(2)-O bonds. The reduced dimensionality introduced by the chain-like structure in the rock salt layer and high atomic order in the C
We present a theoretical study of the electronic thermoelectric power of a semiconductor parabolic quantum well in a magnetic field. The case of a longitudinal magnetic field, with respect to the temperature gradient, has been considered. The calculations were carried out taking into account spin-splitting of the dimensionally quantized electronic energy levels. It has been shown that in the region of strong confinement the thermoelectric power decreases with increasing magnetic field, which is related to the downward shift of the lower Zeeman-split spin subband.
Photoexcitation in solids brings about transitions of electrons/holes between different electronic bands. If the solid lacks an inversion symmetry, these electronic transitions support spontaneous photocurrent due to the topological character of the constituting electronic bands; the Berry connection. This photocurrent, termed shift current, is expected to emerge on the time-scale of primary photoexcitation process. We observed ultrafast time evolution of the shift current in a prototypical ferroelectric semiconductor by detecting emitted terahertz electromagnetic waves. By sweeping the excitation photon energy across the band gap, ultrafast electron dynamics as a source of terahertz emission abruptly changes its nature, reflecting a contribution of Berry connection upon interband optical transition. The shift excitation carries a net charge flow, and is followed by a swing-over of the electron cloud on the sub-picosecond time-scale of electron-phonon interaction. Understanding these substantive characters of the shift current will pave the way for its application to ultrafast sensors and solar cells.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
