The vibrational spectroscopies have been largely employed in the determination of the molecular structure and played a central role in many areas, from fundamental chemistry to materials engineering. Among these techniques, the Raman spectroscopy is essential today in the study of nanostructured materials and biological systems in
2. Raman scattering
The Raman spectra have a different origin compared to infrared absorption (IR); an inelastic scattering process is responsible for the appearance of the vibrational bands. In IR spectroscopy, the radiation is absorbed by available vibrational states (, , ,… ), it means that photon energy must be coincident with the energy difference between two available states. Thus, , being
Hence, this scattering process can be visualized as a perturbation of the molecule by incident photon, which
A vibration (vibration coordinate is Raman active when the polarizability (or induced dipolar momentum) of the molecule is changed; being described as: . Hence, as the nature of the Raman effect is physically different from the infrared, the selection rules are also different, which lead to different spectra. In fact, these two techniques are complementary, being used in many cases combined for structural elucidation.
Nowadays, the Raman spectra can be collected in instruments having microscope (see Figure 2). The laser line is introduced to the sample on the microscope stage. In fact, more sophisticated microscopes can be attached in the Raman spectrograph, as STM or AFM microscopes and also electron microscopes [9, 10]. The scattered light is collected at 180°, and a high efficiency notch filter must be used to cutoff the incident radiation and also the elastic scattering because the Raman signal is very small (typically a cross section factor of 10−6 to 10−12 of the incident radiation). Raman microscopy is a nondestructive technique and usually has no requirement for sample preparation, and the measurements can be done in aqueous solution (not possible in conventional IR spectroscopy). The main advantage here is the ability to focus the laser on a very small part of the sample (1 μm approximately or smaller). The high lateral resolution and depth of field (the order of a few micrometers) are very useful, for instance, in the study of nanostructured materials and
3. Resonance Raman
In the off-resonance or normal Raman spectroscopy, the intensities are linearly proportional to the intensity of the incident light (Io, see Figure 3), proportional to the fourth power of the wavelength of the scattered light (λs4 or νs in wavenumber units), and proportional to the square of the polarizability tensor ([α]2) [6, 7, 8, 16]. However, when the laser line has similar energy to a permitted electronic transition, the Raman signal is amplified for about 105 magnitude orders; this is what characterizes the resonance Raman effect. The theoretical formalism developed by Albrecht et al. is commonly employed in the interpretation of the resonance Raman [6, 7, 8, 16].
Generally, the tensor of polarizability is described as shown in Figure 3. The equation is formed in the numerator part by transition dipole moment integrals between the electronic ground state (g, for the vibrational m or n states) and an excited electronic state (e, for any vibrational v states). The sum is done over all possible (e,v) states. In the denominator part is the difference or sum of the scattered and incident light, added by the dumping factor (i Γev) that contents information about the lifetime of the transition states. This enormous intensification makes, in principle, the Raman spectrum easy to be acquired. But, in a state of resonance, a lot of radiation is absorbed, leading to a local heating and frequently can be observed a decomposition of the sample. Despite this problem, the RR spectroscopy has been largely used in the study of the different chromophore units present in many compounds varying from conducting polymers, nanocomposites, carbon allotropes to DNA [17, 18, 19, 20, 21].
4. Surface-enhanced Raman spectroscopy
The Raman signal can also be amplified by the adsorption of molecules in certain metallic surfaces. This behavior was discovered in 1974 by Fleishmann, Hendra and McQuillan . Initially, the phenomena was associated to the increase of metallic surface area during oxidation–reduction cycles, but soon, it was evident that the strong increase of the Raman signal cannot be explained only considering the changes in metallic surface [23, 24, 25]. Finally, this new intensification process is known as surface enhanced Raman spectroscopy (SERS), evidently this process can be combined to RR effect and the acronym for this behavior is SERRS.
There are two main mechanisms to explain the SERS effect: (1) the electromagnetic model and (2) the charge transfer or chemical model. In the electromagnetic model, the interactions among the incident electromagnetic radiations (laser lines) with the surfaces are the main concerns. In this model, the form, size, alignment and type of metallic substrate are the main characteristics to shape the absorption of the surface plasmon resonance. The enhancement of the local electromagnetic field promoted by surface plasmon resonances is more efficient in metallic regions named hot-spots (nanoscale gaps or nanoholes), and as a consequence, the SERS signal from molecules adsorbed in hot-spots dominates the overall detected intensity [26, 27].
In the charge-transfer or chemical model, the interactions between the adsorbed molecules (mainly molecular orientation) with the metallic atoms involved in adsorption (atoms organization) are considered. The adsorption increases the polarizability of the molecule, which can be further increased by charge transfer between the adsorbed molecule and the metallic surface induced by the incident radiation [28, 29]. The applied electrical potential can also be considered in cases where the molecules are adsorbed in an electrode. The SERS technique permits the study of surface interactions, adsorption process, electrode reactions, biological systems, single molecule detection, and so on [30, 31, 32, 33].
Hence, this introduction tries to summarize the principles of main mechanisms of intensification of the Raman signal. These two effects (Resonance Raman and SERS) can be used separately or combined in the structural studies. In addition, the attachment of powerful microscopes with atomic/molecular resolution can also amplify the Raman signal, and this is the case of Tip-enhanced Raman spectroscopy (TERS). As a consequence, this combination opens the opportunity to study the Raman signal at unparalleled spatial resolution. In the present book, some examples of the state-of-the-art applications of Raman spectroscopy in characterization of materials and biomaterials, mainly through resonance Raman (RR) and surface-enhanced Raman spectroscopy (SERS) are deeply discussed.
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