Structural, optical, magnetic properties and energy-band structure of MFe2O4 (M = Co, Fe, Mn) nanoferrites prepared by co-precipitation technique.

MFe2O4 (M = Co, Fe, Mn) nanoparticles were successfully formed through the chemical co-precipitation technique. X-ray diffraction, scanning electron microscopy, and energy-dispersive X-ray analysis were used to investigate samples' structural properties. The investigated structural properties included phases formed, crystallite size, cation distribution, hopping length, bond length, bond angle, edge length, and shared and unshared octahedral edge length. Scanning electron micrographs of the prepared samples demonstrated well-defined crystalline nanoparticles. The grain diameter was 15, 9, and 34 nm for CoFe2O4, Fe3O4, and MnFe2O4, respectively. The energy-dispersive X-ray analysis confirmed the existence of every element (Co, Fe, and O) and no discernible impurities in the samples. The optical properties were studied in detail through photoluminescence (PL) spectroscopy and Raman spectroscopy. The presence of active modes in Raman spectra confirmed the spinel structure of the MFe2O4 nanoparticles. The direct bandgap energy estimated through UV-visible spectroscopy was about 2.59-2.64 eV, corresponding with the energy-band structures of the octahedral site (1.70 eV) and the tetrahedral site (0.9 eV). This result was further confirmed by PL emission spectra. Based on Mie theory and UV-visible and PL spectral data, the mechanism of photothermal characterization for MFe2O4 nanoparticles was determined. Investigating the changes in temperature of magnetic parameters including coercivity, squareness ratio, and saturation magnetization for MFe2O4 samples showed the dominant influence of ion distribution and A-A, A-B, and B-B exchange interactions. This study also showed that strong anisotropy and weak dipolar interaction tended to increase the coercivity and squareness ratio of CoFe2O4. Conversely, weaker anisotropy and stronger dipolar interaction corresponded with the small coercivity and squareness ratio of Fe3O4 and MnFe2O4 samples.

Determination of the crystalline size of hexagonal La1-xSrxMnO3 (x = 0.3) nanoparticles from X-ray diffraction - a comparative study.

The electronic, magnetic, optical and elastic properties of nanomaterials are governed partially by the crystallite size and crystal defects. Here, the crystalline size of hexagonal La1-xSrxMnO3 (x = 0.3) nanoparticles was determined using various methods. Single-phase La0.7Sr0.3MnO3 nanopowders were produced after 10 h of milling in a commercial high-energy SPEX 8000D shaker mill, and then they were heated at 700 °C and 800 °C to study the effect of calcined temperature on the crystallization of nanoparticles. The modified Scherrer, Williamson-Hall, size-strain, and Halder-Wagner methods were used to determine the crystallite sizes and the elastic properties, such as intrinsic strain, stress, and energy density, from the X-ray diffraction peak broadening analysis. The obtained results were then compared with one another. The difference in crystallite sizes calculated from the different methods was due to the different techniques.

The effect of MnCO3 on the gain coefficient for the 4I13/2 → 4I15/2 transition of Er3+ ions and near-infrared emission bandwidth flatness of Er3+/Tm3+/Yb3+ co-doped barium zinc silicate glasses.

The roles of Mn2+ ions in the MnCO3 compound, leading to the formation of an Mn2+-Yb3+ dimer and affecting the gain coefficient for the 4I13/2 → 4I15/2 transition of Er3+ ions and near-infrared (NIR) emission bandwidth flatness of Er3+/Tm3+/Yb3+ co-doped in SiO2-ZnO-BaO (SZB) barium zinc silicate glasses, were investigated in this work. The composition of all elements from the original raw materials that exist in the host glasses was determined using energy-dispersive X-ray spectroscopy (EDS). Under the excitation of a 980 nm laser diode (LD), the NIR emission of Er3+/Tm3+/Yb3+-co-doped SZB glasses produced a bandwidth of about 430 nm covering the O, E, and C bands. The effects of Mn2+ ions and the Mn2+-Yb3+ dimer on the gain coefficient for the 4I13/2 → 4I15/2 transition of Er3+ ions and bandwidth flatness of NIR emission of Er3+/Tm3+-co-doped and Er3+/Tm3+/Yb3+-co-doped SZB glasses were also assigned. The optimal molar concentration of Mn2+ ions was determined such that the NIR bandwidth flatness of Er3+/Tm3+/Yb3+-co-doped SZB glasses was the flattest. In addition, the role of Mn2+ ions in reducing the gain coefficient for the 4I13/2 → 4I15/2 transition of Er3+ ions was also calculated and discussed.

Influence of structure phase transition on the thermoelectric properties of Cu2Se1-x Te x liquid-like compounds.

Copper chalcogenide Cu2(Se,Te) compounds are well known as typical p-type thermoelectric materials with a figure of merit (ZT) that can be optimized by the ratio of Se : Te. Here, by using the mechanical alloying and solid-state reaction methods, Te was substituted into Se sites within Cu2Se as the formula Cu2Se1-x Te x (x = 0.1, 0.2, 0.25, and 0.3). The observed changes in structural phase, grain morphologies, and grain size were recorded by XRD and FE-SEM imaging with the appearance of the secondary phase of Cu2Te, with a Te content of x = 0.25. The layered structure morphology was observed more clearly at the high Te content. The electrical conductivity was greatly increased with enriched Te content while the maximum Seebeck coefficient was obtained in the Cu2Se0.75Te0.25 sample. Accordingly, a power factor value of up to 9.84 µW cm-1 K-2 at 773 K was achieved. The appearance of a Cu2Te phase with a Te content of 0.25 created a structural phase transition which results in a ZT value of 1.35 at 773 K in the Cu2Se0.75Te0.25 sample.

Influence of Co-Doping on Magnetic Properties and Magnetocaloric Effect of Fe-Co-Zr-Cu-B Melt-Spun Ribbons.

In this work, we investigated magnetic properties and magnetocaloric effect in Fe90-xCoxZr7Cu1B2 (x = 0, 1, 2, 3 and 4) melt-spun ribbons. The ribbons were prepared by using a melt-spinning method with a tangential velocity of a copper wheel of 40 m·s-1. The obtained ribbons are almost amorphous. The alloys exhibit typical soft magnetic behavior with low coercivity at room temperature. A minor replacement of Fe by Co gives an increment in Curie temperature (TC) of the alloys to higher temperatures. The TC of the alloys increases from 242 to 342 K with an increase of x from 0 to 4. Maximum magnetic entropy change, ΔSm max, of the alloys, was found to be larger than 0.7 J·kg-1·K-1 in a magnetic field change ΔH of 12 kOe for all the concentrations of Co. High refrigerant capacitys (RC >100 J ·kg-1 with ΔH = 12 kOe) at room temperature region have been obtained for the alloys. The large magnetocaloric effect near room temperature suggests that the alloys can be considered as magnetic refrigerants in the range of 250-350 K.

A hybrid design of Ag-decorated ZnO on layered nanomaterials (MgAC) with photocatalytic and antibacterial dual-functional abilities.

In this work, Ag@ZnO and Ag@ZnO/MgAC photocatalysts were synthesized using a simple two-step electrochemical method by the addition of magnesium aminoclay (MgAC) as a great stabilizer and a Lewis base, which could donate electrons for reduction of Ag+ and Zn2+ ions, facilitating uniform formation as well as effective inhibition of aggregation of Ag@ZnO nanoparticles (NPs) on the MgAC matrix. Ag@ZnO and Ag@ZnO/MgAC were investigated for photocatalytic degradation of MB and their antibacterial efficiencies. Ag@ZnO/MgAC showed excellent photocatalytic MB degradation with a performance of 98.56% after 80 min of visible-light irradiation and good antibacterial activity against Salmonella (Sal) and Staphylococcus aureus (S. aureus) bacterial strains, providing promising high application potential. Herein, different from the bare ZnO NPs, for Ag@ZnO/MgAC nanocomposites, Ag@ZnO NPs functioned as an effective photocatalyst under visible light illumination, in which, incorporated Ag atoms in the ZnO crystal structure caused the increase in a larger number of lattice defect sites. Benefiting from the strong surface plasmon resonance (SPR) effect of Ag and energy band matching between ZnO and Ag, the visible light absorption capacity and the separation of the photogenerated charge carriers were promoted. Therefore, the MB degradation efficiency of Ag@ZnO/MgAC was considerably accelerated in the presence of produced radicals from visible light illumination.

The structural transition of bimetallic Ag-Au from core/shell to alloy and SERS application.

It is well-known that Ag-Au bimetallic nanoplates have attracted significant research interest due to their unique plasmonic properties and surface-enhanced Raman scattering (SERS). In recent years, there have been many studies on the fabrication of bimetallic nanostructures. However, controlling the shape, size, and structure of bimetallic nanostructures still has many challenges. In this work, we present the results of the synthesis of silver nanoplates (Ag NPls), and Ag-Au bimetallic core/shell and alloy nanostructures, using seed-mediated growth under green LED excitation and a gold salt (HAuCl4) as a precursor of gold. The results show that the optical properties and crystal structure strongly depend on the amount of added gold salt. Interestingly, when the amount of gold(x) in the sample was less than 0.6 µmol (x < 0.6 µmol), the structural nature of Ag-Au was core/shell, in contrast x > 0.6 µmol gave the alloy structure. The morphology of the obtained nanostructures was investigated using the field emission scanning electron microscopy (FESEM) technique. The UV-Vis extinction spectra of Ag-Au nanostructures showed localized surface plasmon resonance (LSPR) bands in the spectral range of 402-627 nm which changed from two peaks to one peak as the amount of gold increased. Ag-Au core/shell and alloy nanostructures were utilized as surface enhanced Raman scattering (SERS) substrates to detect methylene blue (MB) (10-7 M concentration). Our experimental observations indicated that the highest enhancement factor (EF) of about 1.2 × 107 was obtained with Ag-Au alloy. Our detailed investigations revealed that the Ag-Au alloy exhibited significant EF compared to pure metal Ag and Ag-Au core/shell nanostructures. Moreover, the analysis of the data revealed a linear dependence between the logarithm of concentration (log C) and the logarithm of SERS signal intensity (log I) in the range of 10-7-10-4 M with a correlation coefficient (R 2) of 0.994. This research helps us understand better the SERS mechanism and the application of Raman spectroscopy on a bimetallic surface.

Chiral zirconia magnetic microspheres as a new recyclable selector for the discrimination of racemic drugs.

Separation of enantiomers of a chiral compound is one of the most interesting and challenging tasks because of their identical physical and chemical properties. Magnetic materials possessing chiral functionality on their surface can not only exhibit magnetic properties but also recognize chirality. Fe3O4@ZrO2 core-shell nano-materials have not been reported previously for chiral separation of racemates. Zirconia has been shown to be the most stable oxide mechanically, thermally and chemically, and shows better physical and chemical properties among inorganic metal oxides. The present work explores core-shell microspheres consisting of a Fe3O4 magnetic core covered by a zirconia shell (Fe3O4@ZrO2) which are immobilized with cellulose tris(3,5-dimethylphenylcarbamate) to get chiral zirconia magnetic microspheres (CZMMs). As-synthesized CZMMs have been applied for the separation of racemic chiral drugs and the results indicate the CZMMs are potential chiral nanomaterials for enantioseparations. Most importantly the synthesized CZMMs have shown an excellent recyclability and can be used for further chiral separations of different kinds of racemates.