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The extinction spectra of a three-layered metal nanoshell, which consists of a particle with a dielectric core, a middle Ag (Au) layer, and an outer Au (Ag) shell, have been investigated by means of the Mie theory. With a decrease in the outer shell thickness or the middle layer thickness, the wavelengths of the localized surface plasmon resonance (LSPR) for SiO2–Ag–Au (SiO2–Au–Ag) nanoshells show distinct redshifts and the full widths at half maximum (FWHMs) for the dipole peaks in the extinction spectra decrease first and then increase. We have further investigated the influence of the embedding medium on the LSPRs for SiO2–Ag–Au and SiO2–Au–Ag nanoshells and found that the resonance wavelengths of the particles show redshift and the FWHM of the dipole peak increases with increasing the dielectric constant of the embedding medium. The calculated results indicate that the LSPR of the three-layered gold-silver nanoshells can be controlled to the near-infrared region by changing the geometry, which has practical biomedical application. [ABSTRACT FROM AUTHOR]

Abstract: The electric field enhancements in Au/Ag and Ag/Au core/shell nanoparticles have been investigated by means of quasi-static theory. The maximum enhancements of outside fields for Au/Ag and Ag/Au nanoshells occur along the incident polarization at plasmon resonance wavelength. It is surprised that the largest field enhancement in the shell of Ag/Au nanoshell occurs along the polarization direction, while that for Au/Ag nanoshell is perpendicular to the incident polarization. At off-resonance wavelength 1000 nm, the general shape of the field pattern is similar to that in resonance case except for much weaker amplitude. Furthermore, for the seamless nanoshells, the maximum enhancements of the electric field increase by increasing the shell thickness. As the shell thickness is small, the hot spots play an important role in the enhancement of the local electric field. [Copyright &y& Elsevier]

Abstract: The size effects on SrTiO3 nanoparticles have been investigated by means of Raman spectroscopy with changing the grain size in the range 10–80 nm. The intensities of the first-order polar TO2 and TO4 modes increase as the grain size reduces, suggesting the enhanced interaction of the surface-defect dipoles on the grain boundary. By contrast, the intensities for the first-order nonpolar TO3 mode decrease with reducing the grain size. Further we have found that the Raman frequencies of the vibration modes are very sensitive to the variation of the grain size. The softening of the TO2 and TO3 modes with decreasing the grain size indicates the increase of the Ti–O bond length, which is consistent with the lattice expansion investigated by XRD. We have ascribed the size effects to the negative pressure effects due to the enhanced interaction of the surface-defect dipoles. [Copyright &y& Elsevier]