Chemical Inhomogeneity Research Articles

Near-theoretical strength and deformation stabilization achieved via grain boundary segregation and nano-clustering of solutes

Grain boundary hardening and precipitation hardening are important mechanisms for enhancing the strength of metals. Here, we show that these two effects can be amplified simultaneously in nanocrystalline compositionally complex alloys (CCAs), leading to near-theoretical strength and large deformability. We develop a model nanograined (TiZrNbHf)98Ni2 alloy via thermodynamic design. The Ni solutes, which has a large negative mixing enthalpy and different electronegativity to Ti, Zr, Nb and Hf, not only produce Ni-enriched local chemical inhomogeneities in the nanograins, but also segregate to grain boundaries. The resultant alloy achieves a 2.5 GPa yield strength, together with work hardening capability and large homogeneous deformability to 65% compressive strain. The local chemical inhomogeneities impede dislocation propagation and encourage dislocation multiplication to promote strain hardening. Meanwhile, Ni segregates to grain boundaries and enhances cohesion, suppressing the grain growth and grain boundary cracking found while deforming the reference TiZrNbHf alloy. Our alloy design strategy thus opens an avenue, via solute decoration at grain boundaries combined with local chemical inhomogeneities inside the grains, towards ultrahigh strength and large plasticity in nanostructured alloys.

Ferroelectric tungsten bronze-based ceramics with high-energy storage performance via weakly coupled relaxor design and grain boundary optimization

A multiscale regulation strategy has been demonstrated for synthetic energy storage enhancement in a tetragonal tungsten bronze structure ferroelectric. Grain refining and second-phase precipitation (perovskite phase) are introduced in the BaSrTiNb2-xTaxO9 ceramics by regulating the composition and sintering process. Disordered polarization and distribution, chemical inhomogeneity, and insulating boundary layers are achieved to provide the fundamental structural origin of the relaxation characteristic, high breakdown strength, and superior energy storage performance. Thus, an ultrahigh energy storage density of 12.2 J cm−3 with an low energy consumption was achieved at an electric field of 950 kV cm−1. This is the highest known energy storage performance in tetragonal tungsten bronze-based ferroelectric. Notably, this ceramic shows remarkable stability over frequency, temperature, and cycling electric fields. This work brings new material candidates and structure design for developing of energy storage capacitors apart from the predominant perovskite ferroelectric ceramics.

The impact of chemical inhomogeneity in calcinated powders on grain growth behavior and piezoelectric properties of lead-free KNN-based ceramic

Despite outstanding electromechanical properties are achieved in KNN-based ceramics, unstable reproducibility of piezoelectric properties remains a challenge to industrial production, owing to a lack of in-depth understanding of grain growth behavior and chemical homogenization throughout the overall solid-state synthesis process. Herein, a significant chemical heterogeneity behavior was found in calcinated 0.957K0.48Na0.52Nb0.96Sb0.04O3-0.04Bi0.5Na0.5ZrO3-0.003CaZrO3 powders owing to non-uniform diffusion and competitive chemical reaction among multicomponent reactants. The chemical heterogeneity is significantly alleviated by modulating calcination temperatures and ball-milling the calcinated powders. Furthermore, it was demonstrated that the heterogeneous calcinated powder with different particle size distribution plays a significant role in grain growth behavior and chemical homogenization of bulk ceramics. Finally, we obtained uniform grain size distribution and preferable chemical homogeneity in ceramics with the calcination of 900 oC and undergone twice ball milling, which exhibit superior piezoelectric properties (d33=368 pC/N, kp=0.52). This work provides an effective paradigm to ameliorate the inferior reproducibility of KNN-based ceramics by effectively regulating the processing condition during solid-state synthesis.

STUDY OF THE INFLUENCE OF THE CHEMICAL COMPOSITION OF RAILWAY AXLE STEEL ON THE UNIFORMITY OF THE FINAL MICROSTRUCTURE

The relevance of the work. For modern railway transport, increasing the strength and operational reliability of rolling stock parts, in particular railway axles, is an urgent task. It is known that the inhomogeneity of the distribution of chemical elements in the structure of structural grade carbon steels is formed mainly during their crystallization and may subsequently affect the final structural state and set of properties. Purpose. Study of the influence of the chemical composition of steels for railway axles on the uniformity of the structure. Methodology. Experimental ingots of different chemical compositions with different amounts and ratios of the main chemical elements within the range of OS and EA1N were produced in laboratory conditions. The grain structure was studied on microsections after etching with nital. Chemical inhomogeneity (“traces” of the dendritic structure) − the distribution of chemical elements in the microstructure of cast samples was detected by etching in a hot solution of sodium picrate. Metallographic analysis was performed on a light (optical) microscope “Axiovert 200 M MAT” manufactured by “Carl Zeiss”. The results. The effect of changing the chemical composition of carbon steel, which is intended for the manufacture of railway axles, on the peculiarities of the formation of ferrite-pearlite heterogeneity and grain size is determined. It is shown that in samples of steels corresponding to the EA1N brand with a lower carbon content, the distribution of phases is uneven. The mechanism of formation of such a structure is explained from the point of view of two theories. In samples of steels with an average carbon content, which correspond to steel of the OS grade, the distribution of the pearlite and ferrite phases is more uniform, the relationship between the size and the degree of darkening of the pearlite areas with the order of the former dendritic branches has been established. Based on the results of the quantitative analysis of the final grain structure, it was established that OS steel with an average carbon content at different Mn/Si ratios has a more uniform grain structure. EA1N steel with a lower carbon content has a pronounced grain size, with an increase in the Mn/Si ratio, the largest maximum of the dependence of the distribution shifts to a larger grain size (smaller number). Practical results. Increasing the homogeneity of the final microstructure contributes to increasing the plasticity and viscosity of steel, which directly affects the reliability and durability of railway axles.

The rates and host galaxies of pair-instability supernovae through cosmic time: predictions from BPASS and IllustrisTNG

ABSTRACT Pair-instability supernovae (PISNe) have long been predicted to be the final fates of near-zero-metallicity very massive stars ($Z \lt Z_\odot /3$, M$_\mathrm{ZAMS} \gtrsim 140\, \text{M}_\odot$). However, no definite PISN has been observed to date, leaving theoretical modelling validation open. To investigate the observability of these explosive transients, we combine detailed stellar evolution models for PISNe formation, computed from the binary population and spectral synthesis code suite, bpass, with the star formation history of all individual computational elements in the Illustris-TNG simulation. This allows us to compute comic PISN rates and predict their host galaxy properties. Of particular importance is that IllustrisTNG galaxies do not have uniform metallicities throughout, with metal-enriched galaxies often harbouring metal-poor pockets of gas where PISN progenitors may form. Accounting for the chemical inhomogeneities within these galaxies, we find that the peak redshift of PISNe formation is $z=3.5$ instead of the value of $z=6$ when ignoring chemical inhomogeneities within galaxies. Furthermore, the rate increases by an order of magnitude from 1.9 to 29 PISN Gpc$^{-3}$ yr$^{-1}$ at $z=0$, if the chemical inhomogeneities are considered. Using state-of-the-art theoretical PISN light curves, we find an observed rate of 13.8 (1.2) visible PISNe per year for the Euclid-Deep survey, or 83 (7.3) over the 6-yr lifetime of the mission when considering chemically inhomogeneous (homogenous) systems. Interestingly, only 12 per cent of helium PISN progenitors are sufficiently massive to power a superluminous supernova event, which can potentially explain why PISN identification in time-domain surveys remains elusive and progress requires dedicated strategies.

Self-chemophoresis in the thin diffuse interface approximation

Self-chemophoresis is an appealing and quite successful interpretation of the motility exhibited by certain chemically active colloidal particles suspended in a solution of their ‘fuel’: the particle has a phoretic response to self-generated, rather than externally imposed, inhomogeneities in the chemical composition of the solution. The postulated mechanism of chemophoresis is the interaction of the particle (via an adsorption potential) with the chemical inhomogeneities in the surrounding medium. When the range of this interaction is much smaller than any other relevant scale in the system, the (translational and rotational) phoretic velocities can be described in terms of a phoretic coefficient and a slip fluid velocity at the surface of the particle. Using the case of a spherical particle as a simple and physically insightful example, here we exploit an integral representation of the rigid-body motion to critically re-examine this framework. The systematic analysis highlights two steps in the approximation: first the thin–layer approximation (very large particle size), and subsequently a lubrication approximation (slow variation of the adsorption potential along the tangential direction). We also discuss how these approximations could be relaxed and the effect of this on the particle's motion.

Effect of chemical inhomogeneity on the structure and properties of the two-layer TiAl-based coating obtained by non-vacuum electron beam cladding: Experimental investigations and density functional theory simulations

Non-vacuum electron beam cladding is a highly effective technology for producing protective coatings on metal workpieces. In this study, the 3.8 mm thick TiAl-based coating with Cr and Nb additions was obtained on the Ti alloy substrate in two passes of the electron beam. To evaluate inhomogeneity of the two-layer coating, energy-dispersive synchrotron X-ray diffraction (EDSXRD) in combination with energy-dispersive X-ray spectroscopy (EDX) was applied. It was found that in the direction from the top of the coating to the substrate, the dilution of the cladding layers with Ti increased. It influenced the phase constitution of the coating and led to a variation in the chemical composition of different phases (α2-Ti3Al, β-phase, and TiN). The properties of the first (lower) and the second (upper) cladding layers were evaluated separately. The upper layer exhibited greater oxidation resistance than the lower one due to the presence of the γ-phase, which has superior high-temperature stability compared to the α2-Ti3Al phase, predominant in the coating. The influence of varying chemical composition on the oxidation resistance was also estimated using density functional theory (DFT) simulations. It was found that decrease in Al content in the α2 phase leads to an increase in oxygen absorption energy. This could potentially result in a decrease in oxidation resistance. Wear resistance of the first and the second cladding layers was at the same level mainly due to the low contribution of minor phases. Additionally, DFT simulations show that the variations in chemical composition of the major phase (Ti3Al) are not likely to impact the coating wear resistance.

Design, microstructure, wear and corrosion behaviors of laser clad FeNiCoCrMo0.3Nbx hypoeutectic high entropy alloys coatings

FeNiCoCrMo0.3Nbx (x = 0.15, 0.40 and 0.55 in molar ratio) hypoeutectic high entropy alloys (HEAs) coatings are prepared by laser cladding (LC) designed by binary eutectic composition strategy. Nbx HEAs coatings present FCC + Laves duplex. Under the joint action of various strengthening mechanisms, the average microhardness of Nb0.15, Nb0.40 and Nb0.55 coatings is as high as 480.5 ± 7, 510.2 ± 6 and 540.6 ± 5 HV0.2, respectively. The unique fluctuating oxide film of the HEAs coatings plays a role in reducing wear, with the specific wear rates of 0.37 × 10−4, 0.22 × 10−4 and 0.18 × 10−4 mm3/Nm for Nb0.15, Nb0.40, and Nb0.55 cladding layers, respectively. The Nbx HEAs coatings displayed excellent corrosion resistance in 0.5 M H2SO4 solution. For Nb0.15 and Nb0.40 HEAs coatings, the increase of Nb promotes the formation of passivation film and improves corrosion resistance. However, the higher dislocation density intensifies the chemical inhomogeneity of the alloy due to excessive addition of Nb, which is not conducive to the corrosion resistance of Nb0.55 HEAs coating. The Nb0.40 cladding layer exhibits better corrosion resistance, and the Icorr is only 1.24 ± 0.6 μA/cm2. Combined with Mott-Schottky (M-S) test, the carrier densities (ND) of three HEAs coatings are increased in the order of Nb0.40 (1.09 × 1021 cm−3) < Nb0.15 (1.83 × 1021 cm−3) < Nb0.55 (3.57 × 1021 cm−3), indicating that the strong protective passivation film is also a key factor to achieve better corrosion resistance.

Synthesis and Characterization of Epitaxially-Fused Quantum Dot Superlattices at the Single Grain Limit

Epitaxially-fused superlattices of colloidal quantum dots (QD epi-SLs) may exhibit electronic minibands and high-mobility charge transport, but doing so requires epi-SLs with extremely high degrees of spatial and chemical (compositional) uniformity. In this talk, I will discuss both our efforts to understand and improve the epi-SL formation process, as well as recent charge transport studies on single epi-SL grains.Epi-SLs are synthesized from a parent SL structure, typically composed of QDs with long insulating ligands. Over the past several years, we have developed insight into the physical and chemical mechanisms by which this parent SL structure is converted into an epi-SL. I will present detailed, multi-model structural characterization of the SL structures, which unveils the astonishing choreographic process by which millions of QDs rotate and translate, in concert, to form the epi-SL.This structural transformation is initiated by chemical changes to the QD ligand layer, usually through manual introduction of liquids into the SL film. Mechanistic studies into this ligand-exchange process reveal a multi-step chemical sequence that initiates with a simple acid-base reaction. We exploit this insight to fabricate epi-SLs by means of photochemical triggering (using ultraviolet illumination) rather than alternative “hands-on” techniques which suffer from poor experimental control and pronounced chemical inhomogeneity and structural damage in the films. The use of light to trigger the SL conversion process enables much finer control in both the temporal and spatial domains, opening the door to much larger-area SL films and direct photopatterning of epi-SLs.In the latter portion of the talk, I will present recent work charge transport studies in individual, highly-ordered PbSe QD epi-SL grains. One technical challenge in making these devices is the inherent mismatch in using traditional microfabrication techniques to make single-grained devices of air-sensitive materials. Here, we demonstrate the air-free fabrication of microscale field-effect transistors (μ-FETs) with channels consisting of single PbSe QD epi-SL grains (~ 1 -10 µm grain sizes) and analyze charge transport phenomena in these samples. The devices exhibit p-channel or ambipolar transport with a hole mobility as high as 3.5 cm2 V–1 s–1 at 290 K and 6.5 cm2 V–1 s–1 at 170–220 K, one order of magnitude larger than that of previous QD solids.

Exploring high-performance environmental barrier coatings for rare earth silicates: A combined approach of first principles calculations and machine learning

RE2Si2O7 is promising materials for environmental barrier coating (EBC), but the vast phase space poses challenges for the screening of RE2Si2O7. It follows that a combined approach of first principles calculations and machine learning is proposed for this problem, with establishing a comprehensive database comprising β-, γ- and δ-RE2Si2O7 (RE=La–Lu, Y, Sc) and correlating their mechanical/thermal properties on structural characteristics. It is revealed the [O3Si–O–SiO3] structure and polyhedron distortion affect mechanical properties of RE2Si2O7, while criteria for selecting RE2Si2O7 with low thermal conductivity are identified, including complex crystal structures, chemical bond inhomogeneity, and strong non-harmonic lattice vibrations. Also, the machine learning model accurately predicts the coefficient of thermal expansion (CTE) and minimum thermal conductivity (λmin) of RE2Si2O7, with volume and mass variations identified as critical factors, respectively. This integrated approach efficiently screens RE2Si2O7 for EBC application and enables rapid assessments of their thermal properties.

Exploring the ultra-hot Jupiter WASP-178b

Despite recent progress in the spectroscopic characterization of individual exoplanets, the atmospheres of key ultra-hot Jupiters (UHJs) still lack comprehensive investigations. These include WASP-178b, one of the most irradiated UHJs known to date. We observed the dayside emission signal of this planet with CRIRES+ in the spectral K band. By applying the cross-correlation technique and a Bayesian retrieval framework to the high-resolution spectra, we identified the emission signature of 12CO (S/N = 8.9) and H2O (S/N = 4.9), and a strong atmospheric thermal inversion. A joint retrieval with space-based secondary eclipse measurements from TESS and CHEOPS allowed us to refine our results on the thermal profile and thus to constrain the atmospheric chemistry, yielding a solar to super-solar metallicity (1.4 ± 1.6 dex) and a solar C/O ratio (0.6 ± 0.2). We infer a significant excess of spectral line broadening and identify a slight Doppler-shift between the 12CO and H2O signals. These findings provide strong evidence for a super-rotating atmospheric flow pattern and suggest the possible existence of chemical inhomogeneities across the planetary dayside hemisphere. In addition, the inclusion of photometric data in our retrieval allows us to account for stellar light reflected by the planetary atmosphere, resulting in an upper limit on the geometric albedo (0.23). The successful characterization of WASP-178b’s atmosphere through a joint analysis of CRIRES+, TESS, and CHEOPS observations highlights the potential of combined studies with space- and ground-based instruments and represents a promising avenue for advancing our understanding of exoplanet atmospheres.

Magnetic skin effect in Pb(Fe _{1/2}$ Nb _{1/2}$ )O3

Relaxor-ferroelectrics display exceptional dielectric properties resulting from the underlying random dipolar fields induced by strong chemical inhomogeneity. An unusual structural aspect of relaxors is a skin-effect where the near-surface region in single crystals exhibit structures and critical phenomena that differ from the bulk. Relaxors are unique in that this skin effect extends over a macroscopic lengthscale of ∼100 μm whereas usual surface layers only extend over a few unit cells (or ∼nm). We present a muon spectroscopy study of Pb(Fe _{1/2} Nb _{1/2} )O3 (PFN) which displays ferroelectric order, including many relaxor-like dielectric properties such as a frequency broadened dielectric response, and antiferromagnetism with spatially short-range polar correlations and hence can be termed a multiferroic. In terms of the magnetic behavior determined by the Fe3+ ( S=5/2 , L ≈ 0) ions, PFN has been characterized as a unique example of a ‘cluster spin-glass’. We use variable momentum muon spectroscopy to study the depth dependence of the slow magnetic relaxations in a large 1 cm3 crystal of PFN. Zero-field positive muon spin relaxation is parameterized using a stretched exponential, indicative of a distribution of relaxation rates of the Fe3+ spins. This bandwidth of frequencies changes as a function of muon momentum, indicative of a change in the Fe3+ relaxation rates as a function of muon implantation depth in our single crystal. Using negative muon elemental analysis, we find small-to-no measurable change in the Fe3+/Nb5+ concentration with depth implying that chemical concentration alone cannot account for the change in the relaxational dynamics. PFN displays an analogous magnetic skin effect reported to exist in the structural properties of relaxor-ferroelectrics.

New solvothermal flow synthesis of strontium titanate nanoparticles based on the use of acetylacetonate precursors in water/ethanol mixture

In this study, strontium titanate (SrTiO3) nanoparticles were obtained utilizing a one-step supercritical continuous solvothermal synthesis process involving acetylacetonate precursors for both strontium and titanium cations instead of the historical alkoxide ones. These precursors are expensive, difficult to access (especially for strontium isopropoxyde) and inadequately stable, forcing the use of a glove box and controlled atmospheres, which is not the case for acetylacetonates. Pure SrTiO3 nanoparticles with a crystallite size of roughly 20 nm were successfully synthesized. In addition to the cubic structure of SrTiO3, FTIR revealed surface functions that are typical of "wet" processes, while Raman spectroscopy showed the activation of non-centrosymmetric modes brought on by non-linear contributions. The nanoparticles show a faceted shape and are stable at elevated temperatures (up to 800 °C), according to in-situ high temperature XRD measurements. However, due to a chemical deficiency in strontium, titanium dioxide (TiO2) phases are formed at higher temperatures. In-situ high temperature HRTEM investigations showed the existence of two populations of particles, with a better stability for the bigger-sized particles after thermal treatment as well as the sintering and restructuring of the smallest ones. Also, the microscopy results suggest the possibility of a chemical inhomogeneity within the crystallites. Overall, this study offers important new knowledge on the physicochemical characteristics of the synthesized SrTiO3 nanoparticles and their thermal stability using a novel supercritical continuous solvothermal approach based on the use of acetylacetonate precursors.

Temperature and field dependencies of the magnetization of ferrimagnetic Gd-Co films: Chemical inhomogeneity or spin-flop transition

Magnetic properties of amorphous Gd-Co ferrimagnetic films prepared by magnetron sputtering have been studied for various thicknesses. In a certain temperature range close to the magnetic compensation temperature, triple hysteresis loops and the characteristic features of the tempera-ture dependencies of magnetization were observed for all samples under consideration. Two-layer film model with an inhomogeneous chemical composition and a spin-flop transition scenario in two sub-lattice ferrimagnet was employed for understanding the origins of these phenomena. Within the framework of the spin-flop transition, the inter sub-lattice exchange coupling constant was estimated using various methods.

Excitation mechanisms of C II optical permitted lines in ionized nebulae

Context. Carbon is the fourth most abundant element in the universe and its distribution is critical to understanding stellar evolution and nucleosynthesis. In optical studies of ionized nebulae, the only way to determine the C/H abundance is by using faint C II recombination lines (RLs). However, these lines give systematically higher abundances than their collisionally excited counterparts, observable at ultraviolet (UV) wavelengths. Therefore, a proper understanding of the excitation mechanisms of the faint permitted lines is crucial for addressing this long-standing abundance discrepancy (AD) problem. Aims. In this study, we investigate the excitation mechanisms of C II lines λλ3918, 3920, 4267, 5342, 6151, 6462, 7231, 7236, 7237, and 9903. Methods. We use the DEep Spectra of Ionized REgions Database (DESIRED) that contains spectra of H II regions, planetary nebulae and other objects to analyze the fluorescence contributions to these lines and the accuracy of the atomic recombination data used to model the C+ ion. Results. We find that C II λλ4267, 5342, 6151, 6462, and 9903 arise exclusively from recombinations with no fluorescent contributions. In addition, the recombination theory for these lines is consistent with the observations. Our findings show that the AD problem for C2+ is not due to fluorescence in the widely used C II lines or errors in their atomic parameters, but to other phenomena such as temperature variations or chemical inhomogeneities. On the other hand, C II λλ3918, 3920, 6578, 7231, 7236, 7237 have important fluorescent contributions, which are inadvisable for tracing the C2+ abundances. We also discuss the effects of possible inconsistencies in the atomic effective recombination coefficients of C II λλ6578, 7231, 7236, and 7237.

Strain performance and thickness-induced asymmetry in SrTiO3 doped BNT-based lead-free ferroelectrics from nonergodic to ergodic phase

Changes in the relaxation state can greatly affect the electric-field induced strain response in bismuth sodium titanate-based materials. In this work, the strain performances from nonergodic relaxation (NER) to ergodic relaxation (ER) phase transition are investigated by introducing SrTiO3 in (Bi0·5Na0.5)0.98(La0·5Li0.5)0.02TiO3. The solid solutions of perovskite are achieved in all compositions. The ferroelectric to the relaxation phase transition is revealed based on the characteristic peak shape in XRD and temperature dependence of the dielectric properties. The weakened hysteresis of electric-field induced polarization and strain curves results from the creation of localized random fields due to the coexistence of multiple A-site ions, disrupting the ferroelectric long-range ordering at a higher SrTiO3 dopant. The formation of polar nanodomain is promoted and accompanied by the transition from the NER to the ER state. Meanwhile, chemical inhomogeneity is deduced by the anomalous variation in the conduction mechanism and surface state of elemental environments. Asymmetric strain behavior is obtained upon reducing the sample thickness to 0.2 mm, especially pronounced in components with stronger ferroelectricity, where highly asymmetric strain is dominated by surface effect and generated by the non-180° domain switching of the upper and lower surface layers. These features provide insights into the design of strain properties in lead-free piezoelectric ceramics.

Microstructure and Mechanical Properties of Ti-6Al-4V In Situ Alloyed with 3 wt% Cr by Laser Powder Bed Fusion

This work studied the microstructure and mechanical properties of Ti-6Al-4V in situ alloyed with 3 wt% Cr by laser powder bed fusion (LPBF). Specimens with a relative density of 99.14 ± 0.11% were produced, showing keyhole and lack of fusion pores. Due to incomplete mixing of the components during melting, chemical inhomogeneities were observed in the solidified material. The addition of Cr promoted thermal supercooling during solidification and induced a reduction in the primary β grain size in the longitudinal direction and a weakening of the otherwise strong ⟨100⟩β texture, both typical issues for Ti-6Al-4V produced by LPBF. The primary β at first transformed martensitically to α’, but by preheating the substrate plate to 500 °C and cyclically reheating the material by melting subsequent layers, in situ martensite decomposition was achieved, resulting in a fine lamellar α + β microstructure. In addition, the B19 phase was detected in the β matrix, presumably caused by Fe impurities in the Cr powder feedstock. Specimens exhibited a hardness of 402 ± 18 HV10, and an excellent ultimate tensile strength of 1450 ± 22 MPa at an elongation at break of 4.5 ± 0.2%.

Understanding the impacts of L12 nanoprecipitates on the electrochemical and passive behavior of CoCrNiAlTi-type high-entropy alloys

This work investigated the effects of L12 nanoprecipitates on the electrochemical corrosion behavior and passive film characteristics of CoCrNiAlTi-type high-entropy alloys (HEAs) in chloride-containing solutions. Compared with the single-phase recrystallized alloys, the precipitation of the L12 phase destabilized surface passive films, thus deteriorating the localized corrosion resistance and increasing the metastable pitting activities of the L12-strengthened HEA. Influenced by the L12-induced chemical inhomogeneities, the increase of Cr(OH)3 content in passive films together with the high galvanic corrosion tendency between the two phases was considered as the main reason for the increased susceptibility of the L12-strengthened alloys to localized corrosion attacks.

Unveiling high resistivity mechanism in (0.8-x)BaTiO3-0.2BiScO3-x(Bi0.5Li0.5)TiO3 ceramics with good dielectric temperature-stability

Focusing on the high resistivity together with low intrinsic conduction in BaTiO3–BiMeO3 materials, it can contribute to the development of reliable high-temperature capacitor materials. In this work, x(Bi0·5Li0.5)TiO3-(0.8-x)BaTiO3-0.2BiScO3 (where x ranges from 0 to 0.2) ceramics were fabricated by a solid reaction method. The temperature stability of dielectric permittivity and resistance are improved significantly by the introduce of (Bi0·5Li0.5)TiO3 (referred to as BL) compared to BaTiO3–BiMeO3. The composition discrepancy due to chemical inhomogeneity can be determined by SEM and EDS mapping although XRD exhibit a single perovskite phase. The characteristics of distinct conductivity behaviors in micro-regions was measured by kelvin probe force microscopy (KPFM). The non-stoichiometry gives rise to two kinds of defects for charge compensation: an ionic compensation and oxygen-vacancy compensation in different grains. The increase of the hopping activation energy of charged carries enhances the high-temperature resistance of the system. The sample of x = 0.15 shows very good temperature stability of dielectric permittivity in the temperature range from 200 °C to 400 °C, and that of x = 0.1 exhibits the highest resistivity of 3.6 MΩ cm at 570 °C. The proposed method gives an efficient strategy for improving the dielectric temperature stability and insulation by the special defect compensation in the perovskite oxides.

Oxidized structure and Compositional properties of 1144 phase FBS by analytical electron microscopy

The 1144 phase (Ae1A1Fe4As4) shows a strong advantage of engineering fabrication among Fe (Iron)-based superconductor (FBS) family due to the robustness of its superconducting properties with respect to chemical inhomogeneities, granted by its uniform crystalline-layered structure. This regularity is furthermore associated to crystalline defects capable of acting as efficient pinning centers, from which high critical currents can achieved at high fields. Like other FBS phases, its lossless current-carrying capability can be remarkably degraded by distractions at grain boundaries (GBs). GB oxidation is an issue of upmost importance to the realization of the practical FBS application for high field (> 20T) magnet. In this study, we explore oxidized grain boundary and intrinsic grain structural properties of 1144 polycrystalline samples by applying analytical electron microscopy such as atomic resolution scanning transmission electron microscopy and atom probe tomography. These structural properties of samples produced by a mechanochemically assisted synthesis are evaluated following the degradation of superconducting properties due to oxidation. We observe a strong correlation between the contamination at grain boundaries and the decrease of transport properties of the bulk sample, while the crystallin structure seems to be not affected by the oxidation.