X-ray Diffraction Peak Intensity Research Articles

Interfacial reaction behavior between ferromagnetic CoFeB and the topological insulator Sb2Te3

The successful prevention of interfacial reactions between ferromagnetic materials and topological insulators (TIs) is crucial for the realization of reliable spintronic devices using TIs. To this end, we investigated the magnetic properties and interfacial reaction behavior of a bilayer structure composed of ferromagnetic CoFeB and TI Sb2Te3. The effects of including a MgO interlayer was also investigated. Ferromagnetic resonance (FMR) studies showed a remarkably weak resonance peak for the sample annealed at 400 °C for the 2-nm-thick interlayer, and finally, no resonance peak for a film below 1 nm in thickness was observed. X-ray diffraction (XRD) results demonstrated that the Sb2Te3 peak intensities started to decrease upon annealing at 200 °C and completely disappeared for annealing temperatures >400 °C. Hard X-ray photoelectron spectroscopy (HAXPES) results also support that the core-level peaks of Sb and Te split upon annealing at temperatures >200 °C, suggesting the dissociation of Sb2Te3. These results indicate that Sb2Te3 and CoFeB react at the interface during annealing, resulting in a loss of the ferromagnetic properties of the CoFeB layer. Meanwhile, a sample containing a 3-nm-thick MgO layer retained its original Sb2Te3/MgO/CoFeB structure even after annealing at 400 °C, as evidenced by its unchanged XRD peak intensity and FMR spectrum. We expect that our findings will be highly valuable in developing TI-based spintronic devices.

Lattice variation as a function of concentration and grain size in MgO–NiO solid solution system

The study aimed to understand how changes in crystal's size affect the lattice parameters and crystal structure of Mg1-xNixO solid solution for six X values ranging from x = 0 to x = 1. Mg1-xNixO was synthesized via two different wet-chemical techniques: the sol-gel and the microwave hydrothermal method, both followed by calcination at different temperatures of 673, 873, 1073, 1273 and 1473 K. As annealing caused grain growth, the varied temperature range allowed to examine a wide range of grain sizes. The lattice parameters and x values were determined from XRD (X-ray diffraction) peak positions and intensities respectively. The grain size was evaluated by XRD line profile analysis and supported by SEM (scanning electron microscope) observations. At the temperatures of 673 and 873 K grain size was in the nanometric range and from 1073 K and above grain size was in the micrometric range. A non-monotonic lattice variation versus grain size was found for each concentration. When grain size decreased there was a slight contraction, however for grain size in the nanometric range there was a severe lattice expansion. Both lattice parameter changes were explained by two effects acting together: contraction due to surface stress and expansion due to weakening of the ionic bonding at nanocrystalline particles. In this current research study, the lattice parameter was mapped in two dimensions: concentration and grain size. The findings of this study provided valuable insights into the lattice variation in the MgO–NiO solid solution system.

Synthesis of strontium oxide-zinc oxide nanocomposites by Co-precipitation method and its application for degradation of malachite green dye under direct sunlight

Photocatalysts workable under direct sunlight are the safe and cost-effective option for water purification. The nanocomposites of strontium oxide and zinc oxide (SZ NCs) were synthesized using coprecipitation method. The respective precursors of SZ NCs were subjected to alkaline hydrolysis and subsequently thermally treated to yield SZ NCs. The SZ NCs with different ZnO composition was synthesized by varying the concentration of ZnO precursor from 0.2 to 1 M. The structural properties of SZ NCs evaluated using X-Ray diffraction (XRD), Thermogravimetric analysis (TGA), and Differential thermal analysis DTA). The optical properties of SZ NCs studied using ultraviolet–visible (UV–Vis) spectroscopic study. The trend observed in the intensity of XRD peaks indicated the occurrence of Zn doping in the crystalline lattice of SrO and the formation of SrO–ZnO composite. Upon incorporation of 1 M of ZnO precursor, the grain size of the SrO was decreased from 49.3 to 27.6 nm. The weight loss in the thermal analysis indicates the removal of carbonates from the sample upon heating and shows the formation of an oxide structure. UV–Vis spectra confirmed that the presence of SrO enhanced the sunlight absorption of SZ NCs. The increase in the composition of ZnO precursors increased the bandgap of SrO (2.09 eV) to the level of ZnO (3.14 eV). SZ NCs exhibited heterostructure morphology, where the nanosized domains with varying shapes (layered and rod-like) were observed. Under direct sunlight conditions, SZ NCs prepared using 1 M/0.6 M of SrO/ZnO precursors exhibited 15–20 % higher photocatalytic efficiency than neat SrO and ZnO. In precise, 1 mg of this SZ NC was degraded 98 % of malachite green dye dissolved in water (10 ppm) under direct sunlight. Additionally, the thermal stability results showed that 18 % decomposition was obtained due to the degradation impurities in SrO/ZnO catalysts and the XRD results revealed that no structural change is obtained in SrO/ZnO photocatalysts after stability test. The SZ NCs can be effectively used as safe and economic sunlight photocatalysts for water purification in remote areas without the electricity.

Uncooled mid-wavelength InAsSb/AlAsSb heterojunction photodetectors

A mid-wavelength p–B–i–n infrared photodetector constituting ternary alloys of an InAs0.9Sb0.1 absorber and an AlAs0.05Sb0.95 electron barrier was demonstrated to operate at room temperature. The results of high-resolution x-ray diffraction (XRD) analysis indicate the high crystalline quality of the barriode detector structure, grown via molecular beam epitaxy, as supported by the strong XRD peak intensity of InAsSb and its corresponding defect density as low as ∼2.0 × 108 cm−2. The dark current of the barriode detector remained diffusion-limited in the 280–300 K temperature range, and generation–recombination became dominant at 220–260 K owing to the deep-level traps in the depletion region of the absorber and near the lattice-mismatched heterointerface of AlAsSb/InAsSb. Two distinct shallow traps in the InAsSb absorber were identified through Laplace deep-level transient spectroscopy with the activation energies of Et1 = 20 meV and Et2 = 46 meV. The Et1 trap is associated with the hole localization states induced by the alloy disorder of InAsSb, whereas the Et2 trap originated from a point defect of In vacancies in InAsSb. At 300 K, the barriode detector exhibited a 90% cutoff wavelength of 5.0 μm, a peak current responsivity of 0.02 A/W, and a dark current density of 1.9 × 10−3 A/cm2 under a bias voltage of −0.3 V, providing a high specific detectivity of 8.2 × 108 cm Hz1/2/W.

Characterization of Starch Physicochemical Properties and Grain Transcriptome Reveal the Mechanism for Resistant Starch Accumulation

Understanding the physicochemical properties of starch during grain development and the mechanism for resistant starch (RS) accumulation will provide useful information for improving the RS content of wheat. The grains from wheat mutant lines with high RS contents and their corresponding wild-type control were analyzed to characterize the structural and physicochemical properties of wheat starch. A transcriptomic analysis was used to analyze the differentially expressed genes (DEGs) involved in RS accumulation. The results showed that the RS content increased with grain development, along with the total starch content, but a larger increase was observed in the middle and later stages of grain filling. The X-ray diffraction peak intensity and relative crystallinity of starch exhibited the lowest and highest values at 10 days after anthesis, respectively. Regarding the thermal properties of starch, the peak temperature and conclusion temperature generally decreased with grain development; however, the enthalpy values showed no apparent regularity. Compared to control cultivar ZM22, the RS639 and RS683 lines with high RS contents showed high amylose contents and high relative crystallinity and a large proportion of 2.0~9.8 µm starch granules. Furthermore, the transcriptomics analysis revealed that the average relative expression of the glucan-branching enzyme (GBE) α-1,4 glucan phosphorylase (Pho) and starch synthase (SS) in ZM22 was 2.47-, 2.70-, and 2.56-fold higher than that in RS639, respectively; which indicates that the downregulation of the expression of genes encoding GBE, Pho, and SS in wheat grain promotes the accumulation of RS.

Drug-Facilitated Crystallization of Spray-Dried CD-MOFs with Tunable Morphology, Porosity, And Dissolution Profile.

Metal-organic frameworks (MOFs) with versatile functionalities have applications in environmental science, sensor separation, catalysis, and drug delivery. In particular, MOFs used in drug delivery should be biodegradable and easy to control. In this study, spray-dried cyclodextrin-based MOFs (CD-MOFs) with tunable crystallinity, porosity, and dissolution properties were fabricated. The spray-drying precursor properties, such as ethanol volume ratio, incubation time, and precursor concentration, were optimized for controlled crystallization. On the basis of the morphology, X-ray diffraction peak intensity, and specific surface areas of the spray-dried CD-MOF products, they were categorized as amorphous, partially crystalline, and highly crystalline. An active pharmaceutical ingredient ketoconazole (KCZ) was introduced into the precursor to prepare KCZ-containing CD-MOFs. The surface areas of these products were greater by 3-fold (292 m2/g) than that of the plain CD-MOF (94.1 m2/g) prepared using the same parameters. The presence of KCZ in the hydrophobic cavity between the two γ-CD molecules was correlated to the CD-MOF crystal growth. Additionally, CD-MOF particles exhibited different dissolution behaviors on the basis of the position of KCZ in the MOF. These spray-dried CD-MOFs with tunable morphology, specific surface area, and dissolution could have potential applications in various fields.

Synthesis and characterization of copper oxide nanoparticles: its influence on corn (Z. mays) and wheat (Triticum aestivum) plants by inoculation of Bacillus subtilis.

Nanotechnology is now playing an emerging role in green synthesis in agriculture as nanoparticles (NPs) are used for various applications in plant growth and development. Copper is a plant micronutrient; the amount of copper oxide nanoparticles (CuONPs) in the soil determines whether it has positive or adverse effects. CuONPs can be used to grow corn and wheat plants by combining Bacillus subtilis. In this research, CuONPs were synthesized by precipitation method using different precursors such as sodium hydroxide (0.1M) and copper nitrate (Cu(NO3)2) having 0.1M concentration with a post-annealing method. The NPs were characterized through X-ray diffraction (XRD), scanning electron microscope (SEM), and ultraviolet (UV) visible spectroscopy. Bacillus subtilis is used as a potential growth promoter for microbial inoculation due to its prototrophic nature. The JAR experiment was conducted, and the growth parameter of corn (Z. mays) and wheat (Triticum aestivum) was recorded after 5days. The lab assay evaluated the germination in JARs with and without microbial inoculation under CuONP stress at different concentrations (25 and 50mg). The present study aimed to synthesize CuONPs and systematically investigate the particle size effects of copper (II) oxide (CuONPs) (< 50nm) on Triticum aestivum and Z. mays. In our results, the XRD pattern of CuONPs at 500°C calcination temperature with monoclinic phase is observed, with XRD peak intensity slightly increasing. The XRD patterns showed that the prepared CuONPs were extremely natural, crystal-like, and nano-shaped. We used Scherrer's formula to calculate the average size of the particle, indicated as 23nm. The X-ray diffraction spectrum of synthesized materials and SEM analysis show that the particles of CuONPs were spherical in nature. The results revealed that the synthesized CuONPs combined with Bacillus subtilis used in a field study provided an excellent result, where growth parameters of Z. Mays and Triticum aestivum such as root length, shoot length, and plant biomass was improved as compared to the control group.

Hydrothermal Modification of Chabazite for the Fixation of Cesium Ions

During the accident at the Fukushima Dai-ichi Nuclear Power Plant at March 2011, radioactive cesium (137Cs), which has a long half-life of about 30 years, was released into the environment around the plant. Therefore, methods for the recovery and fixation of 137Cs are required. The CHA-type zeolite, chabazite, has high Cs+ selectivity; Cs+ ions have a diameter of approximately 0.36 nm and can thus enter into and be adsorbed by chabazite, which contains pores with diameters of 0.38 nm. However, some Cs+ ions in the large pores may be released by cation exchange in solutions with a high cation concentration. The ANA-type zeolite (ANA) has pores with 0.28 nm diameters, which are smaller than the diameter of Cs+ ions. ANA is synthesized by an alkaline hydrothermal treatment of natural zeolites such as clinoptilolite, mordenite, and chabazite. This hydrothermal modification may be useful for the fixation of Cs+. In the present study, the modification of chabazite exchanged with Cs+ to produce ANA by hydrothermal treatment was investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDX), and the solution stability of Cs+ in the ANA was also evaluated using inductively coupled plasma-mass spectrometry (ICP-MS). Modification of chabazite exchanged with Cs+ to produce single-phase ANA was confirmed in a 1.0 mol/L NaOH solution held at 200 °C for 3 to 144 h. The intensity of XRD peaks corresponding to (211) and (220) planes decreased with increasing Cs+ concentration. SEM observations showed that the ANA crystals had a trapezohedral shape and a size of about 5 µm. EDX analysis of ANA crystals confirmed the presence of Cs+. The amount of Cs+ eluted from ANA in a 0.6 mol/L NaCl solution was less than 1.7%.

Enhancing Resistant Starch Content of High Amylose Rice Starch through Heat-Moisture Treatment for Industrial Application.

The objective of the present study is to enhance the resistant starch (RS) content of high amylose rice starch with heat–moisture treatment (HMT) for industrial application. The optimized HMT condition for achieving the highest RS content established using response surface methodology (RSM) was a temperature of 100 °C, moisture content of 24.2%, and a time of 11.5 h. Upon HMT, the RS content increased from 32.1% for native starch to 46.4% in HMT starch with optimized condition. HMT of the starches reduced the solubility and swelling power. The surface of HMT starch granules was more irregular than native starch. The X-ray diffraction (XRD) peak intensity at 2θ = 5° was greatly reduced by HMT, and the peaks at 22.7° and 24.2° were merged. HMT increased the gelatinization temperature and reduced the gelatinization enthalpy. HMT provides a method for the production of high-yield RS2 with high amylose rice starch in industrial application.

The Effects of Hydrochloric Acid Pretreatment on Different Types of Clay Minerals

Clay minerals are common in geological samples and are useful paleoclimate and sediment provenance proxies. Acid pretreatment is the most common method for the separation and purification of clay minerals. Given that hydrochloric acid (HCl) can dissolve chlorite and distinguish it from kaolinite, the HCl digestion method is used to simplify the routine method of clay mineral analysis. However, there have been few studies of the effects of acid digestion on different clay minerals in the context of extracting paleoclimate indicators. In this study, we used illite, chlorite, kaolinite, and two types of smectite to assess the effects of pretreatment with different HCl concentrations at variable temperatures. Our results show that chlorite is the most soluble clay mineral in HCl and can be effectively dissolved in HCl with concentrations of &gt;1 N. The variable crystal structure of smectite affects its solubility in HCl. Ca-rich smectite, which has more cation substitution of octahedral Al, can be dissolved with HCl. However, Na-rich smectite, which has less cation substitution for octahedral Al, is hardly dissolved in HCl of any concentration or at any temperature. Illite can be partly dissolved in HCl, and the threshold beyond which dissolution occurs is 5 N HCl at 70 °C. Kaolinite is relatively difficult to dissolve in HCl. Given that the HCl digestion method uses the peak intensity of the bulk sample X-ray diffraction (XRD) analysis, whereas the routine method uses the peak area of clay particles, we compared the results of clay mineral quantification and the paleoclimate proxy obtained using the two methods for synthetically prepared mixed and natural clay samples. The results obtained with the HCl digestion method are less accurate than those obtained with the routine method because of the dissolution of illite and smectite in HCl. Therefore, the HCl pretreatment method is not suitable for clay mineral analysis in paleoclimate studies. The present results provide reference data for future studies that employ the acid dissolution pretreatment of clay mineral samples to acquire and quantify paleoclimate proxies.

Phase Transition between Crystalline Variants of Ordinary Ice.

Water is one of the most abundant molecules on Earth. However, this common and "simple" material has more than 18 different phases, which poses a great challenge to theoretically study the nature of water and ice. We designed two reaction coordinates that can distinguish between water and various ice states and used them to efficiently sample all possible states of the system in all-atom molecular dynamics simulation at ambient temperature and pressure. Various structural and thermodynamics properties, including the water-ice phase diagrams, can thus be calculated. We also present a simple model that successfully explains the thermodynamic stability of different ice states. Our work provides effective methods and data for theoretical studies of different phases of water and ice.

Effects of Energetic Carbon-Cluster Ion Irradiation on Lattice Structures of EuBa2Cu3O7−x Oxide Superconductor

C-axis-oriented EuBa2Cu3O7−x oxide films that were 100 nm thick were irradiated with 0.5 MeV C monoatomic ions, 2 MeV C4 cluster ions and 4 MeV C8 cluster ions at room temperature. Before and after the irradiation, X-ray diffraction (XRD) measurement was performed using Cu-Ka X-ray. The c-axis lattice constant increased almost linearly as a function of numbers of irradiating carbon ions, but it rarely depended on the cluster size. Cluster size effects were observed in the XRD peak intensity and the XRD peak width. With increasing the cluster size, the decrease in peak intensity becomes more remarkable and the peak width increases. The experimental result implies that the cluster ions with a larger size provide a more localized energy deposition in a sample, and cause larger and more inhomogeneous lattice disordering. As such, local and large lattice disordering acts as a pinning center for quantum vortex; energetic carbon-cluster ion irradiation will be effective for the increment in the critical current of EuBa2Cu3O7−x superconductors.

Solution combustion synthesis of FeCr 2 O 4 powders for pigment applications: Effect of fuel type

Solution combustion synthesis of iron chromite was reported using iron(III) nitrate nonahydrate and chromium(III) nitrate nonahydrate as starting materials, as well as glycine, urea, citric acid, and ethylene glycol as fuels. The influence of fuel type on the structure, molecular, microstructure as well as chromatic properties of samples was investigated. The X-ray diffraction (XRD) patterns showed that unlike themodynamical prediction, glycine fuel led to strongest combustion and consequent highest XRD peak intensities and lower lattice parameters. Moreover, the change of fuel type and mixing of fuels affected XRD data. Fourier transform infrared analysis showed that the band position of Cr–O and Fe–O bonds were shifted to higher frequencies by using of fuels with weaker combustion reactions. In addition, scanning electron micrographs showed that different morphologies of FeCr2O4 particles were obtained depending on the fuel type and ratios. Energy-dispersive X-ray spectroscopy analysis of the samples showed that oxygen concentration of samples was less than that of stoichiometric ratio of FeCr2O4 due to local reducing atmosphere. Furthermore, chromatic properties of the powders showed that the pigment synthesized with glycine fuel has a better and lighter grayish brown color than the other ones and can be used as a suitable industrial candidate to create a brown color in the ceramic glaze.

Formation efficiency of soil organic matter from plant litter is governed by clay mineral type more than plant litter quality

Plant litters incorporated in soils are decomposed by microorganisms and partially transformed into soil organic matter (SOM) through mineral-organic association and physical protection in soil aggregates. Few studies have linked the effects of clay mineralogy and plant litter quality on controlling the formation efficiency of SOM. Using model soils, the objectives of this study were (1) to determine the effects of clay mineral type and plant litter quality on soil respiration dynamics, and formation efficiency of SOM, physical fractions, and chemical and microbial compositions of SOM at the end of a 120-day incubation; (2) to unravel SOM protection mechanisms and extents by specific clay minerals; and (3) to understand the key role of clay minerals relative to plant litter quality in controlling SOM formation. The changes in X-ray diffraction peak intensity (in terms of peak height) of the clay minerals during incubation and after H2O2 treatment provided evidence for surface adsorption by vermiculite and pore entrapment by kaolinite and illite assemblages. The SOM protection extent parameter, defined based on accumulative soil respiration dynamics, explained well the variation of the formation efficiency of mineral associated SOM (MAOM) and, to a lesser extent, that of occluded particulate SOM (oPOM) in aggregates. 90–96% of plant litter-derived C was protected in the vermiculite material and 33–60% in the pure kaolinite and illite materials. The pure vermiculite material showed the greatest fractions of MAOM and oPOM, the highest relative abundances of O–alkyls and anomeric from carbohydrates in the MAOM fraction. < 1% of plant litter-derived C was transformed into microbial biomass and residues, and fungal residues only were associated with the pure vermiculite material. These results suggested that plant litter incorporated into the soil was decomposed mainly through the ex vivo modification pathway and transformed into SOM through both mineral-organic association and physical protection pathways. Plant litter-derived C was likely protected through mineral-organic association from the earlier stages of decomposition by vermiculite than kaolinite and illite, resulting in more plant carbohydrates associated with vermiculite. Therefore, clay minerals determined SOM formation pathways and played a greater role in controlling SOM formation efficiency than plant litter quality.

Properties of AZO thin films prepared by stationary and rotating RF magnetized plasma sputtering source

The aluminum-doped zinc oxide (AZO) films were deposited with a star-shaped plasma using a high-density radio frequency (RF) magnetized sputtering source to develop well-consistent target utilization. The deposited AZO film characteristics were investigated using stationary and rotational modes with a velocity of 40 rpm, Ar pressure of 1.0 Pa, and RF power of 40 W with a deposition time of 1.0 h. The deposition rate profile of stationary mode with a roughness of ±30.18% was more fluctuating than that of rotational mode with a roughness of ±10.90%. The lowest electrical resistivities of the AZO films were obtained as 3.8 × 10−4 and 3.6 × 10−4 Ω cm at r = 0 mm for the stationary and rotational modes, respectively. According to the AFM and SEM results, the surface profile of the rotational mode grown AZO film was more uniform and smoother than that of the stationary mode. The intensity of x-ray diffraction peaks (002) of the grown AZO film was decreased from the center to the edge of the vessel. Most of the films showed two broad Raman peaks at about 274 and 575 cm−1, representing additional mode and longitudinal optical phonons of the wurtzite ZnO crystal. All the AZO films showed a high transmittance in the visible range, and the average transmittance of the AZO films in the visible range was ∼84%.

Evaluation of the Effect of Deposition pH on the Physico-chemical Properties of Electrochemically Deposited Cadmium Telluride for Photovoltaic Device Applications

Two-electrode (2E) configuration was successfully utilised in the electrochemical deposition of cadmium telluride (CdTe) on fluorine-doped tin oxide (FTO) substrate with the main emphasis on the electrolytic bath pH. The electrochemical deposition pH explored is within the range of (1.00 to 6.00)±0.02 for the aqueous electrolyte comprising of tellurium oxide (TeO2) and cadmium nitrate (Cd(NO3)2) which are the respective precursors of Te and Cd. The optical, structural, morphological, compositional, and electrical properties of the electroplated CdTe thin-films were respectively explored using UV-Vis spectrophotometry, X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray (EDX), and photoelectrochemical (PEC) cell measurements. The optical characterisation show that the CdTe samples exhibit dissimilar absorbance depending on the growth pH for both the as-deposited layers and post-growth treated CdTe layers. A decrease in the absorption edge slope and dip in the bandgap was observed away from pH2. The bandgap of the post-growth treated CdTe layers showed enhancement as it leans towards 1.45 eV, with the trend retention of absorption edge slope, similar to the as-deposited CdTe layers. The electrodeposited CdTe thin-films show a dominant orientation along the cubic (111) CdTe plane, while both the the calculated crystallite size and the XRD peak intensity Pi decreases with the electroplating pH outside the (2.00 to 3.00)±0.02 range. The EDX analyses depicts an alteration in the ratio of Cd to Te atomic percentage relative to the pH of the electrolyte. Comparatively high Te atomic ratio was observed at lower pH values and vice versa with increase alkalinity of the electrolyte. The obtained morphology depicts that the underlying FTO layers are well covered with a gradual reduction in the grain size of the CdTe observable away from pH value (2.00 and 3.00). The photoelectrochemical cell study depicts that the conduction type of the CdTe layers can also be attributed to the CdTe-electrolytic bath pH value.

Evaluation of the Effect of Deposition pH on the Physico-chemical Properties of Electrochemically Deposited Cadmium Telluride for Photovoltaic Device Applications

Two-electrode (2E) configuration was successfully utilised in the electrochemical deposition of cadmium telluride (CdTe) on fluorine-doped tin oxide (FTO) substrate with the main emphasis on the electrolytic bath pH. The electrochemical deposition pH explored is within the range of (1.00 to 6.00)±0.02 for the aqueous electrolyte comprising of tellurium oxide (TeO2) and cadmium nitrate (Cd(NO3)2) which are the respective precursors of Te and Cd. The optical, structural, morphological, compositional, and electrical properties of the electroplated CdTe thin-films were respectively explored using UV-Vis spectrophotometry, X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray (EDX), and photoelectrochemical (PEC) cell measurements. The optical characterisation show that the CdTe samples exhibit dissimilar absorbance depending on the growth pH for both the as-deposited layers and post-growth treated CdTe layers. A decrease in the absorption edge slope and dip in the bandgap was observed away from pH2. The bandgap of the post-growth treated CdTe layers showed enhancement as it leans towards 1.45 eV, with the trend retention of absorption edge slope, similar to the as-deposited CdTe layers. The electrodeposited CdTe thin-films show a dominant orientation along the cubic (111) CdTe plane, while both the the calculated crystallite size and the XRD peak intensity Pi decreases with the electroplating pH outside the (2.00 to 3.00)±0.02 range. The EDX analyses depicts an alteration in the ratio of Cd to Te atomic percentage relative to the pH of the electrolyte. Comparatively high Te atomic ratio was observed at lower pH values and vice versa with increase alkalinity of the electrolyte. The obtained morphology depicts that the underlying FTO layers are well covered with a gradual reduction in the grain size of the CdTe observable away from pH value (2.00 and 3.00). The photoelectrochemical cell study depicts that the conduction type of the CdTe layers can also be attributed to the CdTe-electrolytic bath pH value.

Growth evolution and infrared response of thermally dewetted Au nano-structures for bolometric applications

This paper discusses the growth and characterization of thermally dewetted gold nanostructures for enhanced infrared absorption in bolometer applications. The Au nanostructures are fabricated by solid-state dewetting of ultrathin (18 nm) Au film on Si substrate. The duration of dewetting is varied from 1 min to 30 min. The Au film exhibited the highest X-ray diffraction (XRD) peak intensity along the (111) plane; while the Au nanostructure showed the rising XRD peak along the (220) plane with the dewetting duration. The dewetting process also yielded grain growth and recrystallization of Au nanostructure. The effect of the dewetting on surface morphologies of the Au nanostructure is studied. The Au nanostructures exhibited broadband infrared absorption in the 500–6500 cm−1 range. The sample dewetted for 10 min exhibited up to 200% enhanced absorbance (with respect to the silicon substrate) in the IR range due to the well-suited dimensions of the nanostructures. The hypothesis is also substantiated by examining the plasmonic response of the nanostructure by simulation.

Impact of ionizing radiation on structural, dielectric, and piezoelectric properties of Sr modified PZT

Ion irradiation effects on piezoceramic (Pb0.94 Sr0.04) (Zr0.52 Ti0.48)O3 (PSZT) are investigated by using 4 MeV carbon (C), 9 MeV copper (Cu), and 20 MeV gold (Au) ions. The energies of incident ions are selected in order to target the same range of all incident ions in the material, while producing different amounts of vacancies. The ion irradiation is performed with fluences of 1×1013, 1×1014, and 1×1015 ions/cm2 using Tandem Pelletron accelerator (5UDH-2). Post irradiation changes in PSZT are investigated via various structural, dielectric, and piezoelectric measurement techniques. Results divulge that the irradiation process disturbs the crystallinity along with reduction in X-ray diffraction (XRD) peak intensities owing to strain induced structural defects. A small decrease in dielectric constant is observed due to trapped charges, which screen the depolarization after irradiation. However, a significant decrease is detected in piezoelectric charge coefficients (d33) and piezoelectric voltage coefficients (g33) due to switching of micro domains of PSZT as a result of energy observed during irradiation process. These results indicate that ion irradiation has damaging effects on the properties of PSZT. The discussed information may be utilized to assess performance of PSZT based devices under radiation rich environments such as space.

Morphology, pasting, and structural characteristics of potato starch/xanthan gum blend by critical melting and freeze-thawing treatment

An aqueous suspension of native potato starch (PS)/xanthan gum (XG) mixture was subjected to physical treatments, including critical melting (mild heating, MH; partial gelatinization, PG) and freeze-thawing (FT) treatments. The Physical treatments significantly changed the morphology, pasting, and structural characteristics of potato starch compared with the simple aqueous blending of PS and XG. Microscopy revealed that the starch granules partially melted and some of the melted granules aggregated into a cluster after critical melting and FT treatment. The overall intensity of X-ray diffraction peaks and relative crystallinity also decreased obviously after treatment, indicating partial disruption of the starch inner structure. Both XG addition and physical treatment decreased the solubility index, swelling power, and water holding capacity of starch after physical treatments. Moreover, the final viscosity (from 2988 to about 5000 mPa s) and shear stability (from 3542 to about 200 mPa s) of starch paste were substantially increased by the physical treatments. The critical melting caused the leaching of soluble starch, which induced the formation of starch/XG aggregate matrix attached to the surface of starch granules during FT treatment, contributing to the starch property modification. While the formation of these matrices might also be the reason for the increased thickness of the starch semi-crystalline lamellar structure.