The Surface-enhanced Raman spectroscopy is the essential tool for various levels of the molecular studies. In order to become widely used as a fast analytical tool, the enhancing structures such as the nanoparticles have to be simple, inexpensive, and offer good flexibility in enhancing properties and the spectral range. In this paper, we investigated the plasmonic properties of the metal nanoparticles, to which the molecules of interest can be adsorbed, forming the bionanocomplexes. Here, for the first time, we provided the collection of the results gathered in one article, which can serve as the basis or guidance for designing the SERS studies on different bionanocomplexes, various nanoparticle structures, sizes, and excitation wavelengths. The presented plasmonic properties describe the spectral position of the plasmonic resonances as results of their size and structure. The electric field enhancement as a key contributor to the SERS effect is given as well. We considered silver and gold nanoparticles and their variations. Gold is one of the best choice, due to its relevant surface properties, however, suffers from the plasmonic activity and rather static spectral position of the plasmonic resonances. Therefore, one of the main purposes was to show the effective resonance tuning using simple and less expensive geometries. We showed the possibility to adjust the plasmonic resonances with the excitation wavelengths from the blue region to the near infrared region of lasers most commonly used for Raman spectroscopy. The presented studies indicated the high potential of the core-shell structures for this kind of applications.
This work presents far-infrared reflectivity spectra collected with synchrotron radiation on specially prepared CdTe monocrystals in the temperature region of 30–300K. The investigated samples were of three different types characterized by the three different levels of hydrogenation—strong, middle, and low ones. In order to interpret the experimental data, the imaginary part of the dielectric function was evaluated by means of Kramers-Kronig transformation. To determine quantitatively the influence of hydrogen atoms on the phonon and vibrational spectra of hydrogenated CdTe crystals we used the special statistical model proposed in this paper. This model takes into account the tetrahedron as the basic structural unit and distinguishes the contribution of the hydrogen-bearing tetrahedra from the contribution of the hydrogen-free ones to the crystal phonon spectra.
Infrared spectroscopy may deliver important information on defects created in CdTe monocrystals grown from Cd and Te components purified in a hydrogen atmosphere before the crystallization process. Reflectivity spectra on different CdTe samples were collected with a FTIR spectrometer using a standard Hg lamp and the IR synchrotron radiation source of the DAFNE synchrotron facility at Frascati. In the 500-2000 cm(-1) frequency region, the characteristic vibrational spectra of oxygen and hydrogen bounded to Cd and Te in the monocrystalline CdTe were observed. Moreover the rich fine structure around the CdTe phonon frequency range has been resolved and the preliminary assignment of several lines has been performed. (c) 2005 WILEY-VCH Verlag GmbH I Co. KGaA, Weinheim
In the HgCdTe (MCT) alloys, a zero-gap state E(g)=Gamma(6)-Gamma(8)=0 may occur as the composition varies from HgTe to CdTe. This singular mechanism of the E(g) variation may be triggered by an external pressure or by a temperature. In this Letter, we present experimental data of the optical reflectivity in the far-infrared (FIR) domain in a wide interval of temperature (from 10 to 290 K) of the Hg1-xCdxTe (x=0.115) samples. Since the intensity of classical IR sources drops abruptly in this spectral region, a brilliant synchrotron radiation FIR source has been used. The results clearly show that frequencies of the optical phonon modes exhibit discontinuity in their temperature dependence when a zero-gap state occurs.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.