Search

Impacts of hydrogen annealing on crystallographic characterization, electronic structure, and optical, photocatalytic, and magnetic properties of polycrystalline Zn1−xCoxO (x = 0.01–0.06) samples have been considered. Structural analyses based on powder X-ray diffraction, Rietveld refinement, and Raman spectroscopy prove all materials having the P63mc wurtzite-type structure. The Co-doping and hydrogenation changed the concentration of Zn– and O–related defects whose energy levels occupy the band gap. This also enhanced photocatalytic performance of hydrogenated samples with x > 0.02. X-ray and UV–Vis absorption analyses indicate the substitution of Co2+ for Zn2+ in the wurtzite-type ZnO lattice, leading to irregularly changed the unit-cell parameters. While all the as-prepared samples are paramagnetic, the hydrogenated ones exhibit weak ferromagnetism. Ferromagnetic (FM) ordering increases when x increases, particularly for x ≥ 0.02. According to the results achieved from studying crystalline and electronic structures, we believe that oxygen-vacancies-mediated interactions between Co2+ ions and H–Co–H exchange dimers enhanced FM ordering in hydrogenated Zn1−xCoxO. Computational investigations have also indicated that the magnetization value of H–Zn1−xCoxO is influenced by the positioning of the H dopant, meaning that the couplings between Co and H play an essential role in establishing FM order in H–Zn1−xCoxO. [ABSTRACT FROM AUTHOR]

We have investigated the hydrogen-annealing influence on the crystalline and electronic structures, and magnetic properties of La2/3Ca1/3MnO3 (LCMO). The results have indicated that the annealing at 700 and 900°C (labeled as LCMO-700 and LCMO-900, respectively) readily reduced single-phase LCMO, resulting in a complex phase composition of several isostructural oxygen-deficient perovskite-type phases coexisting with the Ruddlesden-Popper (La/Ca)2MnO4-type phase. While a Mn3+/Mn4+ mixed valence is present in LCMO, the hydrogenannealed samples mainly have Mn2+ and Mn3+ ions. Under such circumstance, large changes in magnetic parameters have been recorded, such as remarkable decreases in values of the magnetization, the Curie temperature (from 251 K for the as-prepared LCMO through 240 K for LCMO700 to ³221 K for LCMO-900), and the magnetic-entropy change. Particularly, the crystal and electronic-structure changes also enhance the magnetic inhomogeneity, resulting in a strong development of the Griffiths phase, and cause the first-to-second-order phase transformation. These results reflect the instability of the LCMO perovskite-type manganite versus hydrogenation. [ABSTRACT FROM AUTHOR]

We have prepared Zn1−xCoxS nanoparticles (NPs) and studied their local-geometric, electronic, and magnetic properties. X-ray diffraction analyses have indicated that NPs with average crystallite sizes of 2.2 ∼ 2.9 nm are single phase and crystallize in the zincblende-type structure. Cobalt ions with oxidation state + 2 (Co2+) replaced for Zn2+ and almost unchanged the zincblende-type structure of the ZnS host lattice. Interestingly, all samples show room-temperature ferromagnetism and ferromagnetic order increases with increasing Co content (x) in Zn1−xCoxS NPs. With the results obtained from analyzing the local-geometric structures at Zn and Co K-edges and photoluminescence spectra, we believe that ferromagnetism in Zn1−xCoxS NPs is related to intrinsic defects and exchange interactions between Co2+ ions. We have also reviewed the recent studies on ZnS-based dilute-magnetic materials. [ABSTRACT FROM AUTHOR]