RESUMEN
This paper presents the use of soft template method to synthesize core and core-shell up-converting nanoparticles usefull for temperature sensing applications. Based on the stock solutions of core ß-NaYF4:Er3+,Yb3+ nanoparticles and involving soft template method without any additional process of surface functionalization, it is possible to directly design the core-shell ß-NaYF4:Er3+,Yb3+@NaYF4 nanoparticles, which can be perfectly dispersed in cyclohexane and surfactants like oleic acid (OA), triethanolamine (TEA) or Cetyltrimethylammonium bromide (CTAB). The morphological, crystalline and elemental characteristics of samples were investigated by Field Emission Scanning Electron Microscopy, X-Ray Diffraction, High Resolution Transmission Electron Microscopy, Selected Area Electron Diffraction patterns and Energy-Dispersive X-Ray Spectroscopy (EDX) measurements. The results showed that the synthesized NaYF4:Er3+,Yb3+@NaYF4 core-shell nanoparticles have roughly spherical shape, pure hexagonal ß phase with core size of about 35 ± 5 nm and shell thickness of about 40 ± 5 nm. It has been shown that the coating of the ß-NaYF4:Er3+,Yb3+ core with NaYF4 shell layer enables to enhance the green upconversion (UC) emission intensities in respect to red one. Under 976 nm excitation, the synthesized ß-NaYF4:2%Er3+,19%Yb3+@NaYF4 core-shell nanoparticles revealed three strong emission bands at 520 nm, 545 nm and 650 nm corresponding to 2H11/2, 4S3/2 and 4F9/2 to 4I15/2 transitions of Er3+ ions with the lifetimes of 215, 193 and 474 µs, respectively. The calculated CIE chromaticity coordinates proved that the emission colour of core-shell nanoparticles was changed from red into yellowish green upon increasing the power density of the 976 nm laser from 0.73 to 9.95 W/cm2. The calculated slopes indicated that in the ß-NaYF4:2%Er3+,19%Yb3+@NaYF4 core-shell nanoparticles, two-photon and three-photon UC processes took place simultaneously. Although the former one is similar as in the case of ß-NaYF4:Er3+,Yb3+ bare core nanoparticles, the latter one, three-photon UC process for green emission occurs, due to cross relaxation processes of two Er3+ ions only within nanoparticles with core-shell architecture. Moreover, the energy difference between the 2H11/2 and 4S3/2 levels and associated constant of NaYF4@NaYF4 host lattice were determined and they reached ~ 813 cm-1 and 14.27 (r2 = 0.998), respectively. In order to investigate the suitability of nanoparticles for optical temperature sensing, the emission spectra were measured in a wide temperature range from 158 to 298 K. An exceptionally high value of relative sensitivity was obtained at 158 K and it amounted to 4.25% K-1. Further temperature increase resulted in gradual decrease of relative sensitivity, however, it maintained a high value > 1% K-1 in the entire analyzed temperature range.
RESUMEN
High quality opal photonic crystals (PhCs) were successfully fabricated by self-assembling of monodisperse Eu(3+)/SiO(2) core/shell nanospheres. Angular resolved photoluminescence (PL) spectra of a PhC sample were measured with different pumping powers, and its PL emission strongly depended on spectroscopic position of the photonic stop band and the optical pumping power. Suppression of the PL occurred in the directions where the emission lines aligned with the center of the photonic stop band. Suppression and enhancement of the PL were observed at low- and high-pumping powers, respectively, in the directions where the emission lines were located at the edges of the photonic stop band. When pumping power exceeded 6 µJ/pulse, a super-linear dependence was found between the pumping power and PL intensity. The dramatic enhancement of PL was attributed to the amplification of spontaneous emission resulted from the creation of large population inversion and the slow group velocity of the emitted light inside the PhC. The opal PhC provided highly angular-selective quasi-monochromatic PL output, which can be useful for a variety of optical applications.
RESUMEN
We present a novel type of surface-enhanced Raman scattering (SERS) substrate constituted of a 3-dimensinal polymeric inverse opal (IO) photonic crystal frame with gold nanorods (Au-NRs) decorating on the top layer. This substrate employs resonant excitation as well as constructive backward scattering of Raman signals to produce large enhancement of SERS output. For the incoming excitation, Au-NRs with appropriate aspect ratio were adopted to align their longitudinal localized surface plasmon band with the excitation laser wavelength. For the outgoing SERS signal, the spectral position of the photonic band gap was tuned to reflect Raman-scattered light constructively. This SERS substrate produces not only strong but also uniform SERS output due to the well control of Au-NRs distribution by the periodic IO structure, readily suitable for sensing applications.
RESUMEN
A novel hybrid surface-enhanced Raman scattering (SERS) substrate based on Au nanoparticles decorated inverse opal (IO) photonic crystal (PhC) is presented. In addition to the enhancement contributed from Au nanoparticles, a desired Raman signal can be selectively further enhanced by appropriately overlapping the center of photonic bandgap of the IO PhC with the wavelength of the Raman signal. Furthermore, the lattice structure of the IO PhC provides excellent control of the distribution of Au nanoparticles to produce SERS spectra with high uniformity. The new design of SERS substrate provides extra maneuverability for ultra-high sensitivity sensor applications.