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1.
Europium (Eu+) ions were confined in a Paul trap and detected by non-destructive method. Storage time of Eu+ ions achieved in vacuum was improved by orders of magnitude employing buffer gas cooling. The experimentally detected signal
was fitted to the ion response signal and the total number of ions trapped was estimated. It is found that the peak signal
amplitude as well as the product of FWHM and the peak signal amplitude is proportional to the total number of trapped ions.
The trapped ion secular frequency was swept at different rates and its effect on the absorption line profile was studied both
experimentally and theoretically. 相似文献
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Lay Gaik Teoh 《Journal of Sol-Gel Science and Technology》2012,62(1):47-51
Mesoporous CeO2 and yttrium doped CeO2 (YDC) were prepared by a sol–gel process and characterized by a variety of techniques. XRD patterns showed that the undoped
and doped samples had a cubic fluorite structure. The grain size decreased from 24.8 to 6.1 nm at 500 °C for pure CeO2 and YDC, respectively. N2 adsorption–desorption isotherms showed that the samples possessed typical mesopore characteristics. The BET specific surface
area of the samples increased from 23.04 to 151.49 m2/g for 300 °C calcination after mesoporous CeO2 was doped with Y. It is found that the introduction of Y can inhibit the grain growth, and the presence of the pores also
can be related to this obstacle to grain growth. These results are of great significance for the control of porous microstructure,
crystallinity, and applications for the development of nanostructured mesoporous materials. 相似文献
7.
Bilge Gurun David G. Bucknall Yonathan S. Thio Chin Ching Teoh Eileen Harkin‐Jones 《Journal of Polymer Science.Polymer Physics》2011,49(9):669-677
A unique in situ multiaxial deformation device has been designed and built specifically for simultaneous synchrotron small angle X‐ray scattering (SAXS) and wide angle X‐ray scattering (WAXS) measurements. SAXS and WAXS patterns of high‐density polyethylene (HDPE) and HDPE/clay nanocomposites were measured in real time during in situ multiaxial deformation at room temperature and at 55 °C. It was observed that the morphological evolution of polyethylene is affected by the existence of clay platelets as well as the deformation temperature and strain rate. Martensitic transformation of orthorhombic into monoclinic crystal phases was observed under strain in HDPE, which is delayed and hindered in the presence of clay nanoplatelets. From the SAXS measurements, it was observed that the thickness of the interlamellar amorphous region increased with increasing strain, which is due to elongation of the amorphous chains. The increase in amorphous layer thickness is slightly higher for the nanocomposites compared to the neat polymer. © 2011 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2011 相似文献
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H.-K. Fun O. Shawkataly S.-G. Teoh 《Acta Crystallographica. Section C, Structural Chemistry》1990,46(12):2329-2331
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Naser E. Eltayeb Siang G. Teoh Eny Kusrini Rohana Adnan H.K. Fun 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2010,75(1):453-457
A new Mn(III) complex, [MnCl(H2O)(L)]·H2O·C2H5OH, where L = 2,2′-{1,2-phenylenebis[nitrilomethylylidene]}bis(6-methoxyphenolate), has been synthesized and characterized by single-crystal X-ray diffraction. There is a good agreement between calculated and experimental structural data. The complex is crystallized in orthorhombic with space group Pbca. The Mn1 atom is coordinated with one Schiff base ligand, one water molecule and one chloride anion, forming a six-coordination number. The electronic and fluorescence spectra of the complex were also studied. 相似文献
10.
A series of Zn(II)-Schiff bases I, II and III complexes were synthesized by reaction of o-phenylenediamine with 3-methylsalicylaldehyde, 4-methylsalicylaldehyde and 5-methylsalicylaldehyde. These complexes were characterized using FT-IR, UV-Vis, Diffuse reflectance UV-Vis, elemental analysis and conductivity. Complex III was characterized by XRD single crystal, which crystallizes in the triclinic system, space group P-1, with lattice parameters a?=?9.5444(2) Å, b?=?11.9407(2) Å, c?=?21.1732(3) Å, V?=?2390.24(7) Å3, D c ?=?1.408 Mg m?3, Z?=?4, F(000)?=?1050, GOF?=?0.981, R1?=?0.0502, wR2?=?0.1205. Luminescence property of these complexes was investigated in DMF solution and in the solid state. Computational study of the electronic properties of complex III showed good agreement with the experimental data. 相似文献