Crystalline Phase Transformation Research Articles

Enhanced electroactive β‐phase and dielectric properties in P(VDF‐HFP) composite flexible films through doping with three calcium chloride salts: CaCl2, CaCl2·2H2O, and CaCl2·6H2O

AbstractFlexible dielectric films with a high dielectric constant, utilizing P(VDF‐HFP)/salt composites, were manufactured through the solution casting method. In this work, we studied the impacts of three calcium chloride salts—CaCl2, CaCl2·2H2O, and CaCl2·6H2O—on the surface morphology, crystalline phase transformation, mechanical properties, and dielectric responses of the P(VDF‐HFP) copolymer. The detailed structure and properties of all samples were assessed via scanning electron microscope (SEM), atomic force microscopy (AFM), Fourier transform infrared spectroscopy (FTIR), X‐ray diffraction (XRD), tensile testing, and LCR meter analysis. The experimental results demonstrated that the addition of calcium salts to the P(VDF‐HFP) composites induced a visibly microporous morphology, with the porosity and surface roughness of the composites gradually increasing with salt content. In comparison to the pure P(VDF‐HFP) film, the composite films exhibited decreased stiffness and heightened flexibility. Furthermore, a higher β‐phase fraction and notable enhancements in the dielectric constant resulting from the inclusion of calcium salts were observed. Consequently, the P(VDF‐HFP) composite filled with 3 wt% of CaCl2·6H2O demonstrated the highest capability for promoting the β‐phase fraction and dielectric constant, achieving values of 98.33% and 21.49% (at 10 Hz), respectively.

Treatment of chromium-containing sludge using sintering and ironmaking combined technology: A risk-reducing strategy for environmental impact

The efficient, safe and eco-friendly disposal of the chromium-containing sludge (CCS) has attracted an increasing concern. In this study, Co-processing of CCS was developed via employing sintering and ironmaking combined technology for its harmless disposal and resource utilization. Crystalline phase and valence state transformation of chromium (Cr), technical feasibility assessment, leaching risk, characteristics of sintered products, and pollutant release during CCS co-processing were investigated through a series of laboratory-scale sintering pot experiments and large scale industrial trials. The results showed that the content of Cr(VI) in sintered products first increased then decreased with increasing temperature ranges of 300 °C–800 °C, and reached a maximum of 2189.64 mg/kg at 500 °C. 99.99% of Cr(VI) can be reduced to Cr(III) at above 1000 °C, which was attributed to the transformation of the Cr(VI)-containing crystalline phases (such as, MgCrO4 and CaCrO4) to the (Mg, Fe2+)(Cr, Al, Fe3+)2O4. The industrial trial results showed that adding 0.5 wt‰ CCS to sintering feed did not have adverse effects on the properties of the sintered ore and the plant's operating stability. The tumbler index of sinter was above 78% and the leaching concentrations of TCr (0.069 mg/L) was significantly lower than the Chinese National Standard of 1.0 mg/L (GB5085.3–2007). The TCr contents of sintering dust and blast furnace gas (BFG) scrubbing water were less than 0.19 wt‰ and 0.11 mg/L, respectively, which was far below the regulatory limit (1.5 mg/L, GB13456-2012). The mass balance evaluation results indicated that at least 89.9% of the Cr in the CCS migrated into the molten iron in the blast furnace (BF), which became a useful supplement to the molten iron. This study provided a new perspective strategy for the safe disposal and resource utilization of CCS in iron and steel industry.

Elemental partitioning-mediated crystalline-to-amorphous phase transformation under quasi-static deformation

The transformation induced plasticity phenomenon occurs when one phase transforms to another one during plastic deformation, which is usually diffusionless. Here we present elemental partitioning-mediated crystalline-to-amorphous phase transformation during quasi-static plastic deformation, in an alloy in form of a Cr-Ni-Co (crystalline)/Zr-Ti-Nb-Hf-Ni-Co (amorphous) nanolaminated composite, where the constitute elements of the two phases have large negative mixing enthalpy. Upon plastic deformation, atomic intermixing occurs between adjacent amorphous and crystalline phases due to extensive rearrangement of atoms at the interfaces. The large negative mixing enthalpy among the constituent elements promotes amorphous phase transformation of the original crystalline phase, which shows different composition and short-range-order structure compared with the other amorphous phase. The reduced size of the crystalline phase shortens mean-free-path of dislocations, facilitating strain hardening. The enthalpy-guided alloy design based on crystalline-to-amorphous phase transformation opens up an avenue for the development of crystal-glass composite alloys with ultrahigh strength and large plasticity.

Crystalline phase transformation of Sr-Fe based oxygen carriers modulate the cyclic performance for syngas and CO coproduction in chemical looping ethanol reforming coupled with CO2 splitting

The chemical looping reforming coupled with CO2 splitting (CLR-CS) offers a promising solution for syngas production and simultaneous decomposition of CO2. In this study, the Sr-Fe based oxygen carriers (OCs) were evaluated in CLR-CS using ethanol as fuel. The presence of Sr significantly improved the oxidation performance of iron oxides. The Sr element in fresh Sr-Fe based OCs mainly formed two crystal phases, including SrFe12O19 and Sr4Fe6O13. Increasing the amount of Sr element made it easier to form Sr4Fe6O13 crystal phase. The Sr4Fe6O13 was favorable for syngas production, due to the higher surface oxygen vacancy formation energy with a range of 3.13–3.37 eV. However, the lower oxygen transfer capacity (OTC) of Sr4Fe6O13 resulted in a lower CO yield in the of stage of CO2 decomposition. Compared with Sr4Fe6O13, SrFe12O19 exhibited the higher OTC and the higher reactivity of lattice oxygen, which was preferable to produce more CO2 in the stage of ethanol reforming in fuel reactor. During the cycle tests, the crystalline phase of SrFe12O19 didn’t regenerate under the CO2 atmosphere but transformed into Sr4Fe6O13. It was attributed to the lower energy barrier of CO2 oxidation on the oxygen defect surface of Sr4Fe6O13. The phase transformation of SrFe12O19 accompanied the formation of Fe3O4. The excessive Fe3O4 had poor stability and inactivated easily due to sintering and agglomeration in Sr1Fe4 and Sr1Fe6 samples. The Sr1Fe2, namely the molar ratio of SrO to Fe2O3 of 1:2, exhibited the better performance for syngas (0.291 Nm3/kg OC) and CO (0.141 Nm3/kg OC) coproduction at 800 °C. Additionally, the Sr1Fe2 presented an excellent cyclic stability in 30 cycles due to the suitable proportion of Sr4Fe6O13 and iron oxides formed, which maintained a high syngas yield and avoided sintering of iron oxides. Overall, the Sr1Fe2 is a promising OC candidate in CLR-CS process.

Insights into the Structural Evolution Process of Na/ZnFe2O4 Spinel Catalyst in CO2 Hydrogenation

AbstractThe CO2 hydrogenation to olefins process over Fe‐based catalysts offer a promising route for the production of high‐value chemicals from non‐fossil route. Herein, we present a Na promoted ZnFe2O4 spinel catalyst and their structural evolution from fresh state to reduction and to reaction period was elucidated. The clear phase segregation between Fe and Zn occurred after reduction/reaction because of crystalline phase transformation in the order of ZnFe2O4→ZnO+Fe7C3+χ‐Fe5C2→FeO+ZnO+Fe7C3+χ‐Fe5C2. The formation of iron carbide phases (Fe7C3 and χ‐Fe5C2) was enhanced dramatically by Na promoter. The adjacent Na promoter increase the electron density in Fe−Zn interfaces and enhance its ability to dissociate CO* to form adsorbed CHx* species, thus promoting the formation of olefins. This Na promoted rich electronic Fe−Zn interfaces alters the balance between iron oxides and iron carbides on the catalyst surface, which accelerate the chain growth reaction and facilitate the coupling efficiency of tandem reaction. The various catalysts were characterized by N2 physisorption, SEM, HR‐TEM, HAADF‐STEM, ex‐situ /in situ XRD, Mössbauer spectra, ICP, in situ XPS, and operando DRIFTs.

“Tailoring thermal stability and in-plane magnetic anisotropy of CoFeB alloy thin films via growth conditions engineering”

The present work investigates the influence of growth conditions on the magneto-structural properties of magnetron-sputtered CoFeB alloy thin films. Films grown at room temperature (RT) are soft magnetic (coercivity <9 Oe), show amorphous microstructure, and possess a distinct uniaxial magnetic anisotropy (UMA) in the film plane. The amorphous microstructure and UMA persist up to a growth temperature (Ts) of 300 °C. CoFeB film grown at Si (100) substrate shows amorphous to crystalline phase transformation at Ts = 500 °C. In contrast, under the same growth conditions, the CoFeB film prepared on the SiO2 substrate maintains an amorphous structure up to Ts = 500 °C. The difference in the microstructures was explained in terms of the out-diffusion of B to the interfacial layer and segregation near the substrate for the films having crystalline and amorphous structure, respectively. On both the substrates Addition of W buffer layer facilitated the growth of smooth and nanocrystalline CoFeB films at Ts ∼300 °C. Upon crystallization, UMA evolution with a simultaneous increase in the coercive field is interpreted in terms of joint effect of random anisotropy model and surface/interface roughness-induced magnetization reversal mechanism. Unlike post-annealing, the CoFeB films prepared at high temperature shows superior thermal stability against crystallization. The relationship between the soft magnetic performance, UMA evolution, and thermal stability of CoFeB films with the growth conditions is established. The study reveals the role of growth condition engineering, to obtain CoFeB thin films with controlled microstructure and magnetic performance, which is crucial for designing the spintronics devices.

Laser doping of n-type 4H-SiC with boron using solution precursor for mid-wave infrared optical properties

Laser doping of n-type 4H-silicon carbide (SiC) semiconductor substrates with boron (B) using a pulsed Nd:YAG laser (λ = 1064 nm) is reported. An aqueous boric acid solution was used as a boron precursor. A simple theoretical heat transfer model was employed to select the laser processing parameters, i.e., laser power and laser-substrate interaction time, and determine the appropriate temperature to dope 4H-SiC substrates. The selected processing parameters ensured that the temperature at the laser-substrate interaction zone was below the SiC peritectic temperature to prevent any crystalline phase transformations in SiC. Fourier-transform infrared spectrometry was conducted to determine the optical properties of both undoped and boron-doped 4H-SiC substrates within the mid-wave infrared (MWIR) wavelength range (3–5 μm). Boron atoms create an acceptor energy level at 0.29 eV above the valence band in the 4H-SiC bandgap, which corresponds to λ = 4.3 μm. Boron-doped 4H-SiC substrate exhibited reduced reflectance and increased absorptance for the MWIR range. An absorption peak at λ = 4.3 μm was detected for the doped substrate. This confirmed the creation of the acceptor energy level in the 4H-SiC bandgap and, thus, doping of 4H-SiC with boron. A notable decrease in the refractive index, i.e., from 2.87 to 2.52, after laser doping of n-type 4H-SiC with boron was achieved.

A Dual Encapsulation Strategy for High-Temperature Micro PCM Particles with High Cyclic Durability.

Addressing critical issues such as high-temperature corrosion, leakage, degradation, and subpar cyclic performance is imperative for phase change materials (PCMs), prompting the development of appropriate encapsulation techniques to surmount these challenges. In this study, a dual encapsulation strategy is proposed for high-temperature micro PCM particles. Al-Si core is microencapsulated via the "solvent evaporation-heating curing" method. Subsequently, TiO2 is employed as the skeleton material for form-stable encapsulation of PCM microcapsules by "cold pressed sintering". Detailed analysis of the crystalline phase transformation mechanism in the sintering synthesis pathway of TiO2 underscore its potential as a robust structural material with exceptional thermal stability. Furthermore, the incorporation of hexagonal boron nitride (hBN) results in a substantial enhancement of the thermal conductivity of the composites, increasing by 121.1-131.3%. The prepared form-stable phase change microcapsules (FSPCMs) are subjected to 5000 thermal cycles in the air atmosphere. There is no observed PCM leakage or composite ruptures in the FSPCM. Moreover, the oxidized mass gain is merely 3.3%, signifying exceptional oxidation resistance. Thermophysical analysis indicates that FSPCM can retain 91.3% of the enthalpy after 2000 cycles, with over 80% preservation after 5000 cycles, underscoring its remarkable cyclic thermal durability.

Addition of ceramic waste for the preparation of VA-based alkali-activated material with high temperature resistance

This study prepares volcanic ash (VA)-blast furnace slag (S) based alkali-activated materials (AAM) with the addition of ceramic waste for exposure to high temperatures (1000 °C). The temperature resistance of alkali-activated materials were described by measuring their surface morphology, gel structure and thermal damage degree, through NMR and UPV tests. At calcination temperature of 800 °C, the VA-based alkali-activated materials with ceramic waste shows ultrasonic velocity of 1962 m/s and a porosity of 17.30 %, indicating the prevention from gel structural collapse. As low calcination temperatures (≤600 °C), ceramic waste only functions as filler materials and reduces compressive strength of the alkali-activated materials. While at calcination temperature of 800 °C, there is an activity generated by the transformation of crystalline phases into amorphous phases in the ceramic waste, thus participates the alkali-activated reaction and increases compressive strength of the alkali-activated materials. At 1000 °C, the collapse of skeleton of the alkali-activated material is induced by thermal incompatibility of the matrix and thermal compression.

Air‐Stable Atomically Encapsulated Crystalline‐Crystalline Phase Transitions in In2Se3

AbstractThe layered semiconductor In2Se3 has a low temperature crystalline–crystalline (α → β) phase transformation with distinct electrical properties that make it a promising candidate for phase change memory. Here, using scanning tunneling microscopy, correlative in situ micro‐Raman, and electrical measurements, it is shown that the β phase can persist in bulk crystals at room temperature in non‐oxidative environments. Of particular note, the stability of β phase crystals in ambient conditions under encapsulation of graphene and similar passivation layers, is reported for the first time. The strategy of encapsulation to ensure the persistence of β phase overlaps with efforts to passivate switching materials. It is further demonstrated that degradation from the elevated temperatures required for the phase change is slowed through examination of Raman signatures. These results demonstrate an alternative method of phase manipulation with a new stabilization of β‐In2Se3 in ambient conditions potentially extendable to other polymorphic materials, and the importance of passivation in In2Se3 memory devices.

Effect of Calcination Temperature on the Powder of Freshwater Snail Shells (Sulcospira testudinaria) Properties

Gastropod shells, such as those from the freshwater snail (Sulcospira testudinaria), have garnered interest as potential sources of calcium precursors. These shells are rich in calcium carbonate (CaCO3), which can be thermally decomposed into calcium oxide (CaO) through calcination. However, more information is needed on optimizing calcium extraction from the Sulcospira testudinaria (SST) shells. This study aims to investigate the influence of calcination temperature on the characteristics of powder of these shells. The study involves two sample treatments: uncalcined shells and shells calcined at temperatures ranging from 500°C to 1100°C for 1 hour. Fourier transform infrared spectroscopy (FTIR) analysis of uncalcined shell powder revealed the presence of aragonite functional groups within the CaCO3 structure. X-ray diffraction (XRD) analysis provided insights into the transformation of crystalline phases of CaCO3, starting from aragonite to calcite and eventually to calcium oxide, explaining the material's weight loss during calcination. The conversion of aragonite to calcite occurs between 500°C and 700°C, while optimal decomposition into CaO is achieved at 1000°C. X-ray fluorescence (XRF) analysis indicated reduced impurities in the samples post-calcination. Scanning electron microscopy (SEM) detailed the morphological characteristics of the shell powders, highlighting temperature-dependent surface features. In conclusion, the optimal calcination temperature for extracting calcium from SST shells is 1000°C. The resulting calcium oxide can be a valuable precursor for various material applications. This research contributes to the efficient utilization of biowaste resources, emphasizing the potential of freshwater snail shells in the sustainable production of calcium-derived materials.

Study on performance and mechanism of foamed ceramics based on lead fuming furnace slag

This paper proposes a new method for preparing lightweight and thermally insulated foamed ceramics via direct high-temperature foaming using lead fuming furnace slag as the major material, quartz sand as the texturizer, borax as the flux, and AlN as the foaming agent. The effects of the chemical composition and sintering process parameters on the crystalline phase transformation, pore structure, and properties of the foamed ceramics were investigated. The foaming mechanism during sintering was also examined using TG-DSC analysis and pore morphology analyses. These results indicate that the slag content strongly affects the formation of the pore structure. Different sintering parameters can modify the pore structure, and a single crystalline phase (CaSiO3) was generated during the sintering process. Under the optimum conditions, the foamed ceramics showed the best overall performance with the bulk density, apparent porosity, average pore size, thermal conductivity, and compressive strength of 0.221 g cm−3, 84.53 %, 1.10 mm, 0.1100 W/(m·K), and 2.52 MPa, respectively. Its excellent porous structure and low thermal conductivity make it suitable as a thermal insulation material in building partition walls.

Revealing the effect of crystallinity and oxygen vacancies of Fe-Co phosphate on oxygen evolution for high-current water splitting

Strategically tuning the composition and structure of transition metal phosphates (TMPs) holds immense promise in the development of efficient oxygen evolution reaction (OER) electrocatalysts. However, the effect of crystalline phase transformation for TMPs on the catalytic OER activity remains relatively uncharted. In this study, we have deftly orchestrated the reaction process of anion-etched precursor to induce the amorphization process of FeCo-POx from crystalline to amorphous states. The as-obtained amorphous FeCo-POx (A-FeCo-POx) exhibited an optimized OER performance with a low overpotential of 270 mV at a current density of 10 mA cm−2, which could be attributed to the flexibility of its amorphous structure and the synergistic effect of oxygen vacancies. Moreover, when incorporated into an overall water splitting (OWS) device configured as A-FeCo-POx(+)||Pt/C(–), it displayed long-term solid stability, sustaining operation for 300 h at a current density of 200 mA cm−2. This work not only provides valuable insights into understanding the transformation from crystalline to amorphous states, but also establishes the groundwork for the practical utilization of amorphous nanomaterials in the field of water splitting.

Effect of Phosphoric Acid on the Preparation of α-Hemihydrate Gypsum Using Hydrothermal Method.

The effects of phosphoric acid (H3PO4) in pressurized aqueous solution on the dehydration of CaSO4·2H2O to form α-hemihydrate gypsum (α-HH) phase and the regulation of crystal shape were studied in this paper in order to provide guidance for the low-cost and high-value utilization of phosphogypsum. The results showed that H3PO4 can significantly accelerate the formation rate of the α-HH phase and that it did not participate in the formation of the α-HH phase in the form of eutectic phosphorus during crystalline phase transformation. In terms of crystal shape regulation, H3PO4 can impact the effect of a citric acid crystal regulator on α-HH crystal shape regulation. The more H3PO4 added, the greater the aspect ratio of α-HH. Accordingly, the water consumption and 2 h dry compressive strength of α-HH products were gradually increased and decreased with an increase in H3PO4 content, respectively. Despite this, the compressive strength of α-HH can still meet the requirements of the α20 grade in JC/T 2038-2010 "α High Strength Gypsum" in China when the H3PO4 content was limited to less than 0.4%.

Photocatalytic Degradation of 1,4-Dioxane by Heterostructured Bi2O3/Cu-MOF Composites

Photocatalysts exhibiting high activity for the degradation of 1,4-dioxane (1,4-D) have been a subject of intense focus due to their high toxicity and challenging degradability. Bismuth oxide (Bi2O3) is recognized as an ideal photocatalyst; however, there have been limited studies on its effectiveness in 1,4-D degradation. It is crucial to address the issue of low photocatalytic efficiency attributed to the instability and easy recombination of photogenerated electrons and holes in Bi2O3 upon photoexcitation. In this study, Cu-MOF and oxygen vacancy were utilized to improve the 1,4-D photocatalytic degradation efficiency of Bi2O3 by preparing Bi2O3, Bi2O3/Cu-MOF, Bi2O3−x, and Bi2O3−x/Cu-MOF. The results revealed that the incorporation of Cu-MOF induced a larger specific surface area, a well-developed pore structure, and a smaller particle size in Bi2O3, facilitating enhanced visible light utilization and an improved photoelectron transfer rate, leading to the highest photocatalytic activity observed in Bi2O3/Cu-MOF. In addition, oxygen vacancies were found to negatively affect the photocatalytic activity of Bi2O3, mainly due to the transformation of the β-Bi2O3 crystalline phase into α-Bi2O3 caused by oxygen vacancies. Further, the synergistic effect of MOF and oxygen vacancies did not positively affect the photocatalytic activity of Bi2O3. Therefore, the construction of heterojunctions using Cu-MOF can significantly enhance the efficiency of degradation of 1,4-D, and Bi2O3/Cu-MOF appears to be a promising photocatalyst for 1,4-D degradation. This study opens new avenues for the design and optimization of advanced photocatalytic materials with improved efficiency for the treatment of recalcitrant organic pollutants.

Experimental study of delayed ettringite formation under geothermal high-temperature environment

The geothermal high-temperature environment will potentially damage engineering, which is mainly reflected in the expansion cracking caused by delayed ettringite formation (DEF). The solution method was used to simulate the temperature and humidity coupled liquid-phase environment of ettringite formation, investigate the temperature limit of ettringite generation in concrete pore solution, and analyze the effect of gypsum admixture on DEF under a geothermal environment. The results show that the high temperature has a promoting effect on ettringite generation from the early hydration of cement, and the high temperature causes the AFt generated early to be gradually converted into AFm as the curing age increases. 70–75 °C is the key temperature interval for the transformation of the AFt crystalline phase into the AFm crystalline phase, and it is recommended that the core temperature of concrete during hardening be controlled below 60 °C to avoid the potential risk of AFt decomposing into AFm in large quantities and DEF. The sulfate content of the Portland cement used in the high-temperature region should be strictly controlled, and the amount of gypsum used should not exceed 4%.

Residual stress associated with crystalline phase transformation of 3–6 mol% yttria-stabilized zirconia ceramics induced by mechanical surface treatments

Monolithic dental prostheses made of 3–6 mol% yttria-stabilized zirconia (3–6YSZ) have gained popularity owing to their improved material properties and semi-automated fabrication processes. In this study, we aimed to evaluate the influence of mechanical surface treatments, such as polishing, grinding, and sandblasting, on the residual stress of 3–6YSZ used for monolithic prostheses in association with crystalline phase transformation. Plate specimens were prepared from five dental zirconia blocks: Aadva Zirconia ST (3YSZ), Aadva Zirconia NT (6YSZ), Katana HT (4YSZ), Katana STML (5YSZ), and Katana UTML (6YSZ). The specimens were either polished using 1, 3, or 9 μm diamond suspensions, ground using 15, 35, or 55 μm diamond discs, or sandblasted at 0.2, 0.3, or 0.4 MPa. The residual stress, crystalline phase, and hardness were analyzed using the cosα method, X-ray diffraction (XRD), and Vickers hardness test, respectively. Additionally, we analyzed the residual stress on the surfaces of monolithic zirconia crowns (MZCs) made of 4YSZ, 5YSZ, and 6YSZ, which were processed using clinically relevant procedures, including manual grinding, followed by polishing using a dental electric motor on the external surface, and sandblasting on the internal surface. Residual stress analysis demonstrated that grinding and sandblasting, particularly the latter, resulted in the generation of compressive residual stress on the surfaces of the plate specimens. XRD revealed that the ground and sandblasted specimens contained a larger amount of the rhombohedral phase than that of the polished specimens, which may be a cause of the residual stress. Sandblasting significantly increased the Vickers hardness compared to polishing, which may possibly be due to the generation of compressive residual stress. In the case of MZCs, compressive residual stress was detected not only on the sandblasted surface, but also on the polished surface. The difference in the residual stress between the plate and crown specimens may be related to the force applied during the automated and manual grinding and polishing procedures. Further studies are required to elucidate the effects of the compressive residual stress on the clinical performance of MZCs.

Phase-change-driven tuning of linear and nonlinear optical properties of Te/As2Se3 bilayer thin films for optoelectronic applications

The present work reports the amorphous-crystalline phase transformation by interdiffusion of Te into the As2Se3 matrix with annealing at various temperatures (100, 150, and 200 °C). Te/As2Se3 bilayer thin films were prepared by electron beam evaporation under high vacuum conditions. The amorphous nature of As2Se3 thin film was confirmed from the X-ray diffraction study. The presence of small peaks in Te/As2Se3 thin film indicates the As4Te4 (monoclinic) and As2Se3 (monoclinic) phases, confirming the amorphous to crystalline phase transformation upon Te interdiffusion and subsequent annealing. The impact of Te top layer deposition on the vibrational modes were also observed from the Raman spectroscopy. The formation of Te agglomerates is confirmed from the morphological analysis which disappeared with further annealing. Furthermore, the water contact angle measurements have provided insight into surface interaction mechanisms of these materials. The linear and nonlinear optical properties were changed upon interdiffusion of Te as observed from UV–Visible spectroscopy. The increase in Eu indicated an increase in disorder hence the decrease in the bandgap. The 3rd order nonlinear susceptibility (χ3) and nonlinear refractive index (n2) increased with annealing. The tuning of linear and nonlinear optical properties by annealing can be used in various optoelectronic applications. Specifically, the phase transformation behaviour of Te/As2Se3 bilayer thin films enables their utilization in phase-change material-based optoelectronic devices.

Optical coherence tomography (OCT) for the analysis of zirconia crystalline phase transformation

This study aimed to validate the Optical coherence tomography (OCT) for the analysis of the transformed zone of two dental zirconia-based materials after hydrothermal ageing and correlate the values with biaxial flexural strength. Kinetics of tetragonal to monoclinic phase transformation (t→m) was calculated. X-ray diffraction (XRD) results showed a sigmoidal transformation rate over time due to the limited X-ray maximum penetration depth. Scanning electron microscope (SEM) and OCT showed a linear relationship between the thickness of the transformed layer and the ageing time. The apparent activation energy was 104.5 kJ/mol and 106.7 kJ/mol (SEM) and 106 kJ/mol and 99.4 kJ/mol (OCT) for the infrastructure and monolithic dental zirconia, respectively. Mechanical strength decreased after 150 h. of ageing at 150 °C for both materials showing a correlation with the depth of the transformed zone observed by OCT. Therefore, both monoclinic phase percentage and the depth of the transformed layer are critical concerning zirconia mechanical properties upon hydrothermal ageing. OCT is a non-destructive, fast, innovative, and accurate method for the analysis of zirconia's t→m phase transformation depth kinetics after hydrothermal ageing.

Amorphous-crystalline phase transformation induced changes in linear and non-linear optical properties of Te/As2Se3 bilayer thin films

The current work describes the amorphous state to crystalline state transition upon diffusion of the top Te layer into the bottom As2Se3 layer at 200 °C annealing temperature. The Te/As2Se3 bilayer thin films were prepared by electron beam (e-beam) evaporation technique. The XRD study confirms the amorphous to crystalline phase transformation. The UV–Visible spectroscopy data shows significant changes in both linear and non-linear optical properties due to the diffusion of Te into As2Se3 upon thermal annealing. The phase transformation behaviour of the Te/As2Se3 bilayer thin films can be utilized in various optoelectronic applications.