The structure and mechanical properties of Cr-based Cr-Ti alloy films

Previous studies have dealt with Cr and its alloy films that exhibit promising characteristics as surface modification layers for antiwear, anticorrosive, and decorative applications. However, the effect of Ti alloying on the structure and mechanical properties of Cr films has not been studied. This work aimed to the structure and mechanical properties of Cr-Ti alloy films in the Cr-rich side. To this end, pure Cr, Cr-6 at.% Ti, Cr-11 at.% Ti, Cr-16 at.% Ti, and Cr-21 at.% Ti alloy films were prepared by magnetron sputtering, and the structure and mechanical properties of the films were evaluated. The results indicated that all the films exhibited a Cr-based growth with body-centered cubic structure, and increasing the Ti content decreased the (110) orientation growth of Cr basis. Ti alloying increased the hardness of the films, while leaded to a monotonic decrease in the modulus of the films. The first-principles method was employed to demonstrate that the reduced modulus was determined by the Ti alloying degree, rather than the orientation evolution of the films. The analysis of H/E value suggested that the wear resistance of the films was improved by Ti alloying. The mechanical properties of present Cr-Ti alloy films, and other Cr-based alloy films or metallic glasses in publications were compared and discussed. We proposed that Ti alloying is a considerable way to explore advanced mechanical properties of Cr-based alloy films.

Neutron diffraction study of the Ti1-xMoxC alloy

In this work, the crystal structure and (RMSD) root-mean-square displacement of atoms in new cubic refractory interstitial alloys Ti0.74Mo0.26C and Ti0.70Mo0.30C were determined by neutron diffraction. These alloys are obtained by powder metallurgy by sintering fine powders of cubic titanium carbides TiC and molybdenum MoC. The values of the RMSD of atoms in these alloys, obtained by the methods of least squares and full-profile analysis from the neutron diffraction data, turned out to be identical. They turned out to be much larger than in the stoichiometric TiC alloy, which has a similar cubic structure and close geometric parameters of atoms with the Ti0.74Mo0.26C and Ti0.70Mo0.30C alloys. These alloys were explained by the occurrence of large static distortions in the lattice of the Ti0.70Mo0.30C alloy due to the differences in the masses and atomic radii of the titanium and molybdenum elements.

Exploring High-Pressure Transformations in Low-Z (H2, Ne) Hydrates at Low Temperatures

The high pressure structural behavior of H2 and Ne clathrate hydrates with approximate composition H2/Ne·~4H2O and featuring cubic structure II (CS-II) was investigated by neutron powder diffraction using the deuterated analogues at ~95 K. CS-II hydrogen hydrate transforms gradually to isocompositional C1 phase (filled ice II) at around 1.1 GPa but may be metastably retained up to 2.2 GPa. Above 3 GPa a gradual decomposition into C2 phase (H2·H2O, filled ice Ic) and ice VIII’ takes place. Upon heating to 200 K the CS-II to C1 transition completes instantly whereas C1 decomposition appears sluggish also at 200 K. C1 was observed metastably up to 8 GPa. At 95 K C1 and C2 hydrogen hydrate can be retained below 1 GPa and yield ice II and ice Ic, respectively, upon complete release of pressure. In contrast, CS-II neon hydrate undergoes pressure-induced amorphization at 1.9 GPa, thus following the general trend for noble gas clathrate hydrates. Upon heating to 200 K amorphous Ne hydrate crystallizes as a mixture of previously unreported C2 hydrate and ice VIII’.

Synthesis, Characterization, and NH3 Sensing Properties of (Zn0.7 Mn0.3-x Cex Fe2O4) Nano-Ferrite

This study includes the preparation of novel nano ferrite (Zn0.7 Mn0.3-x Cex Fe2O4) by using the auto combustion technique. For the following molar values, the percentage x was calculated: 0.0, 0.05, 0.1, 0.15, 0.2, 0.25, and 0.3. The nano-ferrite was calcined for 2 hours at 500°C. The energy dispersive x-ray spectroscopy (EDX), X-ray diffraction (XRD) and field emission scanning electron microscopy FE-SEM was used to examine structural, morphological, and sensing properties. The spinel cubic structure was revealed by XRD findings. The particle distribution was shown to contain voids by FE-SEM. The testing of sensing characteristics to NH3 gas indicated that the synthesized nano-ferrite has a small response time ranging from (15.3-25.2) s as well as a small recovery time between (36-58.5) s, also has a higher sensitivity of about 72.23%.

Cobalt Ferrite Nanocomposite as Electrochemical Sensor for The Detection of Guanine, Uric Acid and Their Mixture

Cobalt ferrite nanocomposite was synthesized and characterized by analytical techniques such as FESEM, EDS and XRD. The average crystallite size was found to be in the range of 10–12 nm with a cubic structure. Further, the nanocomposite was used for the detection of guanine (GU) and uric acid (UA) and found to be an efficient electrode modifier. The lower limit of detection for GU and UA was found to be 300 nM and 400 nM, respectively

Facile Synthesis of Pd-Ir Nanocubes for Biosensing

Displaying extremely high peroxidase-like activity and uniform cubic structure enclosed by (100) facets, Pd-Ir nanocubes are an attractive nanomaterial for bioanalysis. However, there exists a great challenge to deposit atomic layers of Ir on the surface of Pd nanocubes due to the relatively low energy barrier of homogeneous nucleation of Ir atoms compared to heterogeneous nucleation. Here, a simple and surfactant-free approach is presented to synthesize Pd-Ir nanocubes with atomic Ir shell thickness in an aqueous solution at room temperature. Biomolecules such as antibodies and nucleic acids have free access to the surface of Pd-Ir nanocubes. Applications of Pd-Ir nanocubes in immunoassays and aptamer-based biosensors are realized, exploiting the excellent peroxidase activity and fluorescence quenching ability of Pd-Ir nanocubes. This work makes a significant step forward towards the practical utility of Pd-Ir nanocubes in bioanalysis.