Search results for " diffraction"
showing 10 items of 896 documents
The phase diagram and the magnetic structure of nuclear spins in elemental copper below 60 nK
1992
Abstract The phase diagram for nuclear magnetic order is elemental copper and the corresponding ordering vectors were investigated by neutron diffraction at nanokelvin temperatures. The intermediate phase is characterized by an ordering vector (O 2 3 2/3 . This is the first time that this type of order is observed in an fcc antiferromagnet.
Permanent magnetism in apoferritin-encapsulated Pd nanoparticles
2007
Pd nanoparticles have been prepared within the apoferritin cavity. X-Ray powder diffraction, transmission electronic microscopy and magnetization measurements have been used for characterizing the nanoparticles. The nanoparticles exhibit permanent magnetism at room temperature.
Structural and magnetic characterization of Pd nanoparticles encapsulated in apoferritin
2010
Pd nanoparticles exhibiting permanent magnetism at room temperature have been prepared within the apoferritin cavity. Pd nanoparticles in air and under an inert atmosphere were synthesized to study the influence of the aerobic and anaerobic conditions in the final magnetic properties. The surface of nanoparticles as well as the type of crystalline phase could determine the magnetic properties. X-ray powder diffraction, including Debye-function analysis, transmission electronic microscopy, and magnetization measurements have been used for characterizing the nanoparticles.
Structural and Magnetic Properties of Nickel Oxide Nanopowders
2010
Structure and magnetic properties of nickel oxide (NiO) nanopowders have been studied by X-ray/neutron diffraction, SQUID magnetometer, and micro-Raman spectroscopy. Our diffraction data indicate that at room temperature all NiO powders are antiferromagnetically ordered and have a rhombohedral (R-3m) phase. The SQUID magnetometry and Raman spectroscopy measurements support the presence of the antiferromagnetic ordering.
TEM studies on La2−2xCa1+2xMn2O7 (x=0.5 and 0.25)
2003
The nominal compositions and structures of the compounds La2-2xCa1+2xMn2O7 (x=0.5 and 0.25) prepared by solid-state reaction have been studied by transmission electron microscopy and high-resolution electron microscopy. Besides the observation of the major phase of a two-layer structure in the nominal composition La1.0Ca2.0Mn2O7, the embedded n = 3, n = 4 Ruddlesden-Popper phases and La rich phase in the two-layer structure were observed as defects. No layered structure was observed in the nominal composition La1.5Ca1.5Mn2O7. Instead, a major phase of orthorhombically distorted perovskite, a minor phase of an ideal cubic perovskite, and a small fraction of calcium-oxide were observed in the…
Submicrometer CaCuO2 and Ca2CuO3 particles from bimetallic formate precursors
1992
Abstract CaCuO2 and Ca2CuO3 are readily obtained by thermal decomposition of two new calcium and copper formates, CaCu(HCOO)4 and Ca2Cu(HCOO)6. These chemical-precursor based syntheses, while overcoming problems related to the stoichiometry of the final products, involve very short diffusion path lengths. This, in turn, results in soft treatments yielding pure phases constituted by submicrometer (≈0.4 μm) homogeneous particles.
Quantitative X-Ray Powder Diffraction Analysis of Some Feldspars Used as Raw Material in Ceramics
2001
Synthesis of Nd:YAG nanopowder using the citrate method with microwave irradiation
2010
Abstract Nd:YAG nanopowders were prepared using the Pechini process with microwave irradiation ( MWs ). A reference sample was also prepared using conventional heating. XRD pattern analysis showed that nanopowder obtained by means of conventional heating and calcination for 1 h at 900 °C has a structure made up of the garnet phase together with the hexagonal phase that disappeared after two additional hours of thermal treatment. The MWs powder calcined for 1 h consists of the single garnet phase. SAXS data analysis indicated that nanoparticles are characterized by a sharp interface. TEM investigation showed crystalline particles with remarkable agglomeration in both samples, although a more…
Crystal structures of new ternary compounds in RE–Pt–Pb and RE–Au–Pb systems (RE=rare earth metal)
2012
Abstract The crystal structures of the compounds RE 2 Pt 2 Pb (RE = Y, La, Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu; Mo 2 FeB 2 structure type, space group P 4/ mbm , Pearson code tP10 ), REPtPb (RE = La, Ce, Pr, Nd, Sm; ZrNiAl structure type, space group P 6 ¯ 2 m , Pearson code hP9 ), RE 2 Au 2 Pb (RE = Y, La, Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu; Er 2 Au 2 Sn structure type, space group P 4 2 / mnm , Pearson code tP20 ) and REAuPb (RE = Tm, Yb and Lu) were determined using X-ray powder diffraction.