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A method for work-function evaluation is proposed, based on recording the shift of x-ray photoelectron signals from a surface irradiated by low-energy electrons. The method is capable of measuring samples with very low conductivity, poor back contacts, and high dielectric constants. The method is also applicable to magnetic materials and can be particularly effective for studies of multilayer and heterogeneous systems. [ABSTRACT FROM AUTHOR]

We report the development, testing, and demonstration of a setup for modulation excitation spectroscopy experiments at the Inner Shell Spectroscopy beamline of National Synchrotron Light Source - II. A computer algorithm and dedicated software were developed for asynchronous data processing and analysis. We demonstrate the reconstruction of X-ray absorption spectra for different time points within the modulation pulse using a model system. This setup and the software are intended for a broad range of functional materials which exhibit structural and/or electronic responses to the external stimulation, such as catalysts, energy and battery materials, and electromechanical devices. [ABSTRACT FROM AUTHOR]

Highly sensitive laser interferometer was built to measure electromechanical coupling in Gd-doped ceria Ce0.9Gd0.1O2-x thin films in the frequency range up to 20 kHz. Spurious resonances due to substrate bending were avoided by the special mounting of the film in the center of substrate. Compact design allowed to reach high vertical resolution of about 0.2 pm. Electrostriction coefficient measured in 1 µm thick Ce0.9Gd0.1O2-x film was 4.3x10-21m²/V² and slightly decreased with frequency till the extensional resonance of the substrate at about 20 kHz occurred. As expected, the displacement varied as a square of applied voltage without any sign of saturation. A comparison with ceramics showed much higher electrostriction coefficient in the latter in the same frequency range. [ABSTRACT FROM AUTHOR]

We propose an extension of the periodic temperature change (Chynoweth) technique for the measurement of pyroelectric coefficient in the case of a pyroelectric thin film on an insulating (non-conductive) substrate. The modified technique adequately determines the pyroelectric coefficient of the film if its thickness is known. The method determines the pyroelectric coefficient of the substrate even if it is much smaller than that of the film. The method overestimates the thickness of the pyroelectric film and can be used as an estimate only. If the thickness of the pyroelectric film is not known, the method gives a product of the pyroelectric coefficient of the film and its thickness. [ABSTRACT FROM PUBLISHER]

Nonthermal crystallization of amorphous barium titanate (BTO) was initiated by a monochromatic x-ray microbeam from a synchrotron radiation source. Following x-ray exposure, micron-sized BTO single crystals with a true square pyramid shape appeared on the surface of an amorphous BTO substrate-free film. The location and size of the areas in which crystal growth appeared fit well the x-ray microbeam path and size, respectively. A plausible mechanism of x-ray induced initiation of nonthermal crystallization in BTO is proposed. The observed phenomenon holds promise for materials engineering at nanoscale and crystallization of amorphous materials in situations where heating must be avoided. [ABSTRACT FROM AUTHOR]

We show that substrate-free crystallized barium titanate (BaTiO[SUB3]) films adopt a hexagonal structure, whereas substrate-supported films assume the commonly observed tetragonal phase. However, in contrast to the known hexagonal BaTiO[SUB3], the substrate-free crystallized films demonstrate a small but measurable pyroelectric effect, and do not exhibit phase transitions in the 25-423 K temperature range. Thus the substrate-free crystallized BaTiO[SUB3] represents a heretofore unreported crystallographic modification of BaTiO[SUB3]. [ABSTRACT FROM AUTHOR]

We investigated the local environment of the Ce and Gd ions in one of the most important oxygen ion conductors, the CeO2-Gd2O3 solid solution, using Lm edge extended x-ray absorption fine structure (EXAFS) spectroscopy and x-ray absorption near edge spectroscopy (XANES). The average Gd-O distance, as deduced by EXAFS, decreases gradually with increasing Gd content, whereas a sharp decrease in the average Ce-O distance occurs at 25 mol% Gd, accompanying the appearance of structural features characteristic of double fluorite symmetry. An abrupt change in the local environment of Ce, rather than of Gd, is also supported by the XANES spectra. Efforts at stabilizing the oxygen conducting Fm-3m phase in CeO2-Gd2O3 solid solutions should therefore concentrate on tailoring the local environment of the Ce ion. We further suggest that our data may provide an explanation for the recently discovered giant électrostriction effect in Ce0.8Gd0.2O1.9. Since this composition is at the limit of stability of the fluorite phase, local distortions in Ce0.8Gd0.2O1.9 may be modulated by an external electric field more readily than those of the other solid solutions. [ABSTRACT FROM AUTHOR]

This study introduces a novel iterative Bragg peak removal with automatic intensity correction (IBR-AIC) methodology for X-ray absorption spectroscopy (XAS), specifically addressing the challenge of Bragg peak interference in the analysis of crystalline materials. The approach integrates experimental adjustments and sophisticated post-processing, including an iterative algorithm for robust calculation of the scaling factor of the absorption coefficients and efficient elimination of the Bragg peaks, a common obstacle in accurately interpreting XAS data, particularly in crystalline samples. The method was thoroughly evaluated on dilute catalysts and thin films, with fluorescence mode and large-angle rotation. The results underscore the technique's effectiveness, adaptability and substantial potential in improving the precision of XAS data analysis. While demonstrating significant promise, the method does have limitations related to signal-to-noise ratio sensitivity and the necessity for meticulous angle selection during experimentation. Overall, IBR-AIC represents a significant advancement in XAS, offering a pragmatic solution to Bragg peak contamination challenges, thereby expanding the applications of XAS in understanding complex materials under diverse experimental conditions., (open access.)

Compositionally complex oxides (CCOs) or high-entropy oxides (HEOs) are new multielement oxides with unexplored physical and functional properties. In this work, we report fluorite structure-derived compositionally complex zirconia with composition Zr 1- x (Gd 1/5 Pr 1/5 Nd 1/5 Sm 1/5 Y 1/5 ) x O 2-δ ( x = 0.1 and 0.2) synthesized in solid-state reaction route and sintered via hot pressing at 1350 °C. We explore the evolution of these oxides' structural, microstructural, mechanical, electrical, and electromechanical properties regarding phase separation and sintering mechanisms. Highly dense ceramics are achieved by bimodal mass diffusion, composing nanometric tetragonal and micrometric cubic grains microstructure. The material exhibits an anomalously large electrostriction response exceeding the M 33 value of 10 -17 m 2 /V 2 at room temperature and viscoelastic properties of primary creep in nanoindentation measurement under fast loading. These findings are strikingly similar to those reported for doped ceria and bismuth oxide derivates, highlighting the presence of a large concentration of point defects linked to structural distortion and anelastic behavior, which are characteristics of nonclassical ionic electrostrictors.

The local environments of Sc and Y in predominantly ⟨002⟩ textured, Al 1- x Do x N (Do = Sc, x = 0.25, 0.30 or Y, x = 0.25) sputtered thin films with wurtzite symmetry were investigated using X-ray absorption (XAS) and photoelectron (XPS) spectroscopies. We present evidence from the X-ray absorption fine structure (XAFS) spectra that, when x = 0.25, both Sc 3+ and Y 3+ ions are able to substitute for Al 3+ , thereby acquiring four tetrahedrally coordinated nitrogen ligands, i.e., coordination number (CN) of 4. On this basis, the crystal radius of the dopant species in the wurtzite lattice, not available heretofore, could be calculated. By modeling the scandium local environment, extended XAFS (EXAFS) analysis suggests that when x increases from 0.25 to 0.30, CN for a fraction of the Sc ions increases from 4 to 6, signaling octahedral coordination. This change occurs at a dopant concentration significantly lower than the reported maximum concentration of Sc (42 mol % Sc) in wurtzite (Al, Sc)N. XPS spectra provide support for our observation that the local environment of Sc in (Al, Sc)N may include more than one type of coordination., Competing Interests: The authors declare no competing financial interest., (© 2024 The Authors. Published by American Chemical Society.)

Raman spectroscopy is applied for non-destructive characterization of strain in crystalline thin films. The analysis makes use of the numerical value of the mode Grüneisen parameter γ , which relates the fractional change in the frequency of a Raman-active vibrational mode and the strain-induced fractional change in the unit cell volume. When in-plane, compressive biaxial strain in aliovalent doped CeO 2 -films is relieved by partial substrate removal, the films exhibit values of γ for the F 2g vibrational mode which are ∼30% of the literature values for bulk ceramics under isostatic stress. This discrepancy has been attributed to a negative contribution from the anelastic (time-dependent) mechanical properties of aliovalent-doped ceria. Here we propose a way to "separate" anelastic and elastic contributions to the F 2g mode Grüneisen parameter. Mechanically elastic yttria (Y 2 O 3 ) films on Ti/SiO 2 /Si substrate serve as "control". The values of γ calculated from the change in frequency of the ∼375 cm -1 F 2g Raman-active mode are close to the literature values for bulk yttria under isostatic stress. This work should serve to provide a protocol for characterization of selective sensitivity to different strain components of doped ceria thin films.

Electrostrictors, materials developing mechanical strain proportional to the square of the applied electric field, present many advantages for mechanical actuation as they convert electrical energy into mechanical, but not vice versa. Both high relative permittivity and reliance on Pb as the key component in commercial electrostrictors pose serious practical and health problems. Here we describe a low relative permittivity (<250) ceramic, Zr x Ce 1-x O 2 (x < 0.2), that displays electromechanical properties rivaling those of the best performing electrostrictors: longitudinal electrostriction strain coefficient ~10 -16 m 2 /V 2 ; relaxation frequency ≈ a few kHz; and strain ≥0.02%. Combining X-ray absorption spectroscopy, atomic-level modeling and electromechanical measurements, here we show that electrostriction in Zr x Ce 1-x O 2 is enabled by elastic dipoles produced by anharmonic motion of the smaller isovalent dopant (Zr). Unlike the elastic dipoles in aliovalent doped ceria, which are present even in the absence of an applied elastic or electric field, the elastic dipoles in Zr x Ce 1-x O 2 are formed only under applied anisotropic field. The local descriptors of electrostrictive strain, namely, the cation size mismatch and dynamic anharmonicity, are sufficiently versatile to guide future searches in other polycrystalline solids., (© 2023. The Author(s).)

This work reports that the octahedral hydrated Al 3+ and Mg 2+ ions operate within electrolytic cells as kosmotropic (long-range order-making) "ice makers" of supercooled water (SCW). 10 -5 M solutions of hydrated Al 3+ and Mg 2+ ions each trigger, near the cathode (-20 ± 5 V), electro-freezing of SCW at -4 °C. The hydrated Al 3+ ions do so with 100% efficiency, whereas the Mg 2+ ions induce icing with 40% efficiency. In contrast, hydrated Na + ions, under the same experimental conditions, do not induce icing differently than pure water. As such, our study shows that the role played by Al 3+ and Mg 2+ ions in water electro-freezing is impacted by two synchronous effects: (1) a geometric effect due to the octahedral packing of the coordinated water molecules around the metallic ions, and (2) the degree of polarization which these two ions induce and thereby acidify the coordinated water molecules, which in turn imparts them with an ice-like structure. Long-duration molecular dynamics (MD) simulations of the Al 3+ and Mg 2+ indeed reveal the formation of "ice-like" hexagons in the vicinity of these ions. Furthermore, the MD shows that these hexagons and the electric fields of the coordinate water molecules give rise to ultimate icing. As such, the MD simulations provide a rational explanation for the order-making properties of these ions during electro-freezing.

Electro-chemo-mechanical (ECM) coupling refers to mechanical deformation due to electrochemically driven compositional change in a solid. An ECM actuator producing micrometre-size displacements and long-term stability at room temperature was recently reported, comprising a 20 mol% Gd-doped ceria (20GDC), a solid electrolyte membrane, placed between two working bodies made of TiO x /20GDC (Ti-GDC) nanocomposites with Ti concentration of 38 mol%. The volumetric changes originating from oxidation or reduction in the local TiO x units are hypothesized to be the origin of mechanical deformation in the ECM actuator. Studying the Ti concentration-dependent structural changes in the Ti-GDC nanocomposites is therefore required for (i) understanding the mechanism of dimensional changes in the ECM actuator and (ii) maximizing the ECM response. Here, the systematic investigation of the local structure of the Ti and Ce ions in Ti-GDC over a broad range of Ti concentrations using synchrotron X-ray absorption spectroscopy and X-ray diffraction is reported. The main finding is that, depending on the Ti concentration, Ti atoms either form a cerium titanate or segregate into a TiO 2 anatase-like phase. The transition region between these two regimes with Ti(IV) concentration between 19% and 57% contained strongly disordered TiO x units dispersed in 20GDC containing Ce(III) and Ce(IV) and hence rich with oxygen vacancies. As a result, this transition region is proposed to be the most advantageous for developing ECM-active materials., (open access.)

Design of pyroelectric crystals decoupled from piezoelectricity is not only a topic of scientific curiosity but also demonstrates effects in principle that have the potential to be technologically advantageous. Here we report a new method for the design of such materials. Thus, the co-doping of centrosymmetric crystals with tailor-made guest molecules, as illustrated by the doping of α-glycine with different amino acids (Threonine, Alanine and Serine). The polarization of those crystals displays two distinct contributions, one arising from the difference in dipole moments between guest and host and the other from the displacement of host molecules from their symmetry-related positions. These contributions exhibit different temperature dependences and response to mechanical deformation. Thus, providing a proof of concept for the ability to design pyroelectric materials with reduced piezoelectric coefficient (d 22 ) to a minimal value, below the resolution limit of the method (<0.005 pm/V)., (© 2022 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH.)

A protocol for successfully depositing [001] textured, 2−3 µm thick films of Al0.75Sc0.25N, is proposed. The procedure relies on the fact that sputtered Ti is [001]-textured α-phase (hcp). Diffusion of nitrogen ions into the α-Ti film during reactive sputtering of Al0.75,Sc0.25N likely forms a [111]-oriented TiN intermediate layer. The lattice mismatch of this very thin film with Al0.75Sc0.25N is ~3.7%, providing excellent conditions for epitaxial growth. In contrast to earlier reports, the Al0.75Sc0.25N films prepared in the current study are Al-terminated. Low growth stress (<100 MPa) allows films up to 3 µm thick to be deposited without loss of orientation or decrease in piezoelectric coefficient. An advantage of the proposed technique is that it is compatible with a variety of substrates commonly used for actuators or MEMS, as demonstrated here for both Si wafers and D263 borosilicate glass. Additionally, thicker films can potentially lead to increased piezoelectric stress/strain by supporting application of higher voltage, but without increase in the magnitude of the electric field.

Electrostriction is a property of dielectric materials whereby an applied electric field induces a mechanical deformation proportional to the square of that field. The magnitude of the effect is usually minuscule (<10 -19  m 2  V -2 for simple oxides). However, symmetry-breaking phenomena at the interfaces can offer an efficient strategy for the design of new properties 1,2 . Here we report an engineered electrostrictive effect via the epitaxial deposition of alternating layers of Gd 2 O 3 -doped CeO 2 and Er 2 O 3 -stabilized δ-Bi 2 O 3 with atomically controlled interfaces on NdGaO 3 substrates. The value of the electrostriction coefficient achieved is 2.38 × 10 -14  m 2  V -2 , exceeding the best known relaxor ferroelectrics by three orders of magnitude. Our theoretical calculations indicate that this greatly enhanced electrostriction arises from coherent strain imparted by interfacial lattice discontinuity. These artificial heterostructures open a new avenue for the design and manipulation of electrostrictive materials and devices for nano/micro actuation and cutting-edge sensors., (© 2022. The Author(s), under exclusive licence to Springer Nature Limited.)

ConspectusThe ability to control the icing temperature of supercooled water (SCW) is of supreme importance in subfields of pure and applied sciences. The ice freezing of SCW can be influenced heterogeneously by electric effects, a process known as electrofreezing. This effect was first discovered during the 19th century; however, its mechanism is still under debate. In this Account we demonstrate, by capitalizing on the properties of polar crystals, that heterogeneous electrofreezing of SCW is a chemical process influenced by an electric field and specific ions. Polar crystals possess a net dipole moment. In addition, they are pyroelectric, displaying short-lived surface charges at their hemihedral faces at the two poles of the crystals as a result of temperature changes. Accordingly, during cooling or heating, an electric field is created, which is negated by the attraction of compensating charges from the environment. This process had an impact in the following experiments. The icing temperatures of SCW within crevices of polar crystals are higher in comparison to icing temperatures within crevices of nonpolar analogs. The role played by the electric effect was extricated from other effects by the performance of icing experiments on the surfaces of pyroelectric quasi-amorphous SrTiO 3 . During those studies it was found that on positively charged surfaces the icing temperature of SCW is elevated, whereas on negatively charged surfaces it is reduced. Following investigations discovered that the icing temperature of SCW is impacted by an ionic current created within a hydrated layer on top of hydrophilic faces residing parallel to the polar axes of the crystals. In the absence of such current on analogous hydrophobic surfaces, the pyroelectric effect does not influence the icing temperature of SCW. Those results implied that electrofreezing of SCW is a process influenced by specific compensating ions attracted by the pyroelectric field from the aqueous solution. When freezing experiments are performed in an open atmosphere, bicarbonate and hydronium ions, created by the dissolution of atmospheric CO 2 in water, influence the icing temperature. The bicarbonate ions, when attracted by positively charged pyroelectric surfaces, elevate the icing temperature, whereas their counterparts, hydronium ions, when attracted by the negatively charged surfaces reduce the icing temperature. Molecular dynamic simulations suggested that bicarbonate ions, concentrated within the near positively charged interfacial layer, self-assemble with water molecules to create stabilized slightly distorted "ice-like" hexagonal assemblies which mimic the hexagons of the crystals of ice. This occurs by replacing, within those ice-like hexagons, two hydrogen bonds of water by C-O bonds of the HCO 3 - ion. On the basis of these simulations, it was predicted and experimentally confirmed that other trigonal planar ions such as NO 3 - , guanidinium + , and the quasi-hexagonal biguanidinium + ion elevate the icing temperature. These ions were coined as "ice makers". Other ions including hydronium, Cl - , and SO 4 -2 interfere with the formation of ice-like assemblies and operate as "ice breakers". The higher icing temperatures induced within the crevices of the hydrophobic polar crystals in comparison to the nonpolar analogs can be attributed to the proton ordering of the water molecules. In contrast, the icing temperatures on related hydrophilic surfaces are influenced both by compensating charges and by proton ordering.