Localized Surface Plasmon Resonances : Noble Metal Nanoparticle Interaction with Rare-Earth Ions

© 2012 Rivera et al., licensee InTech. This is an open access chapter distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Localized Surface Plasmon Resonances: Noble Metal Nanoparticle Interaction with Rare-Earth Ions


Introduction
Particles of sizes between 1 and 100 nm show fascinating properties with unusual characteristics that lead to the formation of unique properties in nanosystems, which are not observed in ordinary materials.These are considered hereby as nanoparticles (NPs).Additionally, metallic NPs with sizes smaller than the wavelength of light show strong dipolar excitations in the form of localized surface plasmon resonances (LSPR).LSPRs are nonpropagating excitations of the conduction electrons of metallic NPs coupled to the electromagnetic field [1].This effect has been the subject of extensive research, both fundamental and with a view to applications [2,3].The resonance frequency of the oscillation, i.e., the surface plasmon (SP) energy, it is essentially determined by the dielectric properties of the metal and the surrounding medium, and by the particle size and shape.The collective charge oscillation causes a large resonant enhancement of the local field inside aand near the NP.This field enhancement is used in surface-enhanced Raman scattering (SERS) [4] and is currently discussed for potential applications in nonlinear optical devices [5], in optical tweezers [6], and generally for the manipulation of the local photonic density of states.
Rare-earth (RE) elements are a group of chemical elements known as Lanthanides that occur together in the periodic table.These elements are used in common consumer goods such as: computer memory, DVD's, rechargeable batteries, cell phones, car catalytic converters, magnets, fluorescent lighting and much more.Furthermore, play an essential role in modern national defense, e.g.: lanthanum in night-vision goggles, neodymium in laser range-finders, guidance systems, communications; europium in fluorescents and phosphors in lamps and monitors; erbium amplifiers in fiber-optics data transmission; samarium in permanent magnets stable at high temperatures and, others technological applications.We center our attention in the RE ions and their optical properties that are widely employed in photonic.Devices of general interest span RE ions concentrations of tens to several thousand parts per million (ppm), resulting in devices of one to tens of meters long such as channel waveguides and optical fiber, respectively.In optical devices, the RE should ideally be confined as a delta function in the center of the core for maximum gain per unit pump power.Thereby, there is a necessary tradeoff between the confinement and the RE ions concentration, such that the more confined structures require a higher rare-earth ions concentration.An important feature that distinguishes them from other optically active ions: they emit and absorb over narrow wavelength ranges, the wavelengths of the emission and absorption transitions depend the host material, the intensities of these transitions are weak, the lifetimes of metastable states are long, and the quantum efficiencies tend to be high, except in aqueous solutions.These properties lead to excellent performance of RE ions in many optical applications.Devices that provide gain (e.g.lasers and amplifiers), must have low scattering losses, and one is restricted to using single-crystal or glass hosts.Whereas in many applications crystalline materials are preferred for reasons that include higher peak cross sections or better thermal conductivities, the versatility of glasses and the broader emission and absorption spectra they provide have led to the use of RE doped glasses in many applications, eventually running into the clustering limit for the particular host glass composition [7].
Most of existing and potential future applications of NPs suffer from damping caused by metal absorption.Sudarkin and Demkovich [8] suggested increasing the propagation length of the surface plasmon polariton 1 (SPP) by creating the population inversion in the dielectric medium adjacent to the metallic surface (film).Recently, gain-assisted propagation of the SPPs at the interface between a metal and a dielectric with optical gain has been analyzed theoretically [9,10].Thus, NPs embedded in a gain media represent a field enhancement sustained that resonant excitation can lead to a reduction in the threshold for achieving inversion in the optically active surrounding medium, and the presence of gain can counteract the inherent absorption losses in the NP [1].While this enhancement of plasmon resonances in gain medium not is experimentally confirmed, amplification of fluorescence due to field enhancement in gain medium with metal NPs has been observed [11,12,13,14].
In the present chapter, we explore the physics of localized surface plasmons by first considering the interaction of metal NPs with an electromagnetic wave in order to arrive at the resonance condition (LSPR).After, we show studies of plasmon resonances in particles with different shapes and sizes, and the effects of interactions between particles in the ensemble.Then we will focus on the RE ions, discussing the optical properties of the trivalent ions through the principles of quantum mechanics (in terms of oscillator strengths) with special interest in the interactions between the 4f electrons themselves.Since all the other electronic shells are spherically symmetric.Finally we present diverse experimental results of the interaction of RE ions interaction with NPs, resulting in an enhancement of the intensity emission of the RE ions due to long-range electromagnetic interaction between LSPR and the RE ions.
In this context, it is worth mentioning that the main purpose of this chapter is to show some of concrete concept of noble metallic nanoparticle interaction with rare-earth ions exhibiting a field enhancement in transparent medium with noble metal NPs embedded via a localized surface plasmon resonance.

Localized surface plasmon resonance and metallic nanoparticles
First, we know that a surface plasmon resonance (SPR) can be described as the resonance collective oscillation of valence electrons in a solid stimulated by beam of light incident (electromagnetic field -see Figure 1).The resonance condition is established when the frequency of light matches the natural frequency of valence electrons oscillating against from this restoring force.SPR in nanometer-sized structures is called LSPR.For gold and silver NPs, the resonance falls into the visible region of the electromagnetic spectrum.A striking consequence of this is the bright colors exhibited by particles both in transmitted and reflected light, due to resonantly enhanced absorption and scattering.This effect has found applications for many hundreds of years, for example in the staining of glass for windows or ornamental cups 2 .The corresponding electric field strength pattern for a 100 nm silver sphere, irradiated at a wavelength of 514 nm, this is reproduced from X. Lu et al. [15].

Noble metal nanoparticles in an electric field
For spherical NPs smaller than compared to local variations of the involved electromagnetic fields (d<<λ) in the surrounding medium, the quasi-static approximation [16], we lead to a 2 Localized surface plasmons have been observed since the Romans who used gold and silver nanoparticles to create colored glass objects such as the Lycurgus Cup (4th Century A.D.).A gold sol in the British museum, created by Michael Faraday in 1857, is still exhibiting its red color due to the plasmon resonance at ,530 nm [L.M. Liz-Marzan, Mater.Today 7, 26 (2004).].
good agreement between theory and experiment.So, one can calculate the spatial field distribution (assuming as a problem of a particle in an electrostatic field), from the Laplace equation for the potential 2 0 ∇Φ= , therefore the electric field E =−∇Φ.Besides, the harmonic time dependence can then be added to the solution once the field distributions are well known.The solution this problem was obtained by Jackson [17]: E0 is the amplitude of the electric field, NP ε and m ε are the dielectric permittivity of the NP and of the surrounding medium respectively, both are function the excitation frequency ω , r is the module of the position vector.Here out Φ describes the superposition of the applied field and that of a dipole located at the NP center, i.e., an applied field induces dipole moment inside the sphere proportional to 0 E .Additionally, we can arrive at ( ) With 2/ k πλ = and n is the unit vector in the direction of the point P of interest.For kr<<1 (near zone) we have the electrostatic result of (5).The magnetic field present has the form ( ) . Hence, in the near field the fields are predominantly electric and for static field ( ) 0 kr → , the magnetic field vanishes.For kr>>1, the dipole fields have spherical-wave form: ( ) From the viewpoint of optics, it is much interesting to note that another consequence of the enhanced polarization α in which a NP scatters and absorbs light [18].For a sphere of volume V and dielectric function  9 2

Mie theory
For particles with larger dimensions, where the quasi-static approximation is not justified due to significant phase-changes of the driving field over the particle volume, a rigorous electrodynamics approach is required.This way, Gustav Mie solved Maxwell's equations for the case of an incoming plane interacting with a spherical particle [19].In essence, the electromagnetic fields are expanded in multipole contributions and the expansion coefficients are found by applying the correct boundary conditions for electromagnetic fields at the interface between the metallic NP and its surrounding.
The extinction cross section of a spherical NP is given by the following expression: Here the parameters an and bn are defined as: The size parameter β is defined as We will focus our attention in silver and gold, since the localized plasmon resonance condition mentioned above is satisfied at visible light frequencies.Additional advantages of these metal NPs include simple preparation methods for a wide range of sizes and shapes and easy surface conjugation to a variety of ligands.
We now evaluate the extinction cross section using the Mie theory from equation ( 9), Figure 2, we take dielectric constants for silver and gold from Palik [20], and the medium dielectric constant is assumed to be 1.0 (i.e., a particle in a vacuum) and 2.0 for NPs with sizes different.
We can see from Figure 2 the dependence of resonance frequency with size of NPs (silver and gold) and the refraction index (surrounding medium).K. Lance Kelly et al. (2003), show that for spherical NPs clear differences between the quasistatic and the Mie theory results.However, the important features are retained, e.g. the frequency resonance.Although Mie theory is not a very expensive calculation, the quasistatic expressions are convenient to use when only qualitative information is needed [21].Now, Figure 3 shows clearly the dependence of resonance frequency embedded in a glass (with refraction index of: 1.99 for 400 nm, 1.88 for 630 nm, 1.75 for 900 nm and 1.70 for 1000 nm) and in a bulk with refraction index 2, in both cases with 20 nm size and a size distribution of 20 % STD, this simulation was extracted from program MiePlot v4.2.11 of Philip Laven.Also, it is possible to observe an increment of bandwidth and the intensity of peak for NPs embedded in the glass when compared with the material bulk.Therefore, LSPR results in enhanced local electromagnetic fields near the surface of the NP (Novotny & Hecht, 2006) [22], see Figure 1.Hideki Nabika and Shigehito Deki [23], show an experimental evidence of this dependence above mentioned for silver NPs of different sizes were synthesized by reducing AgNO3 with N,N-dimethylformamide (DMF), Poly(vinylpyrrolidone) (PVP) aqueous solution (10 mL, 10 wt %) was added to DMF (80 mL), followed by an addition of AgNO3 aqueous solution (10 mL).They obtained three sets of spherical silver NPs with a particle diameter varying from 9.7 to 27.1 nm and rod-shaped silver NPs with an aspect ratio of 1.79, its results are show Figure 4.
Thereby, the LSPR properties are sensitive to its environment in the order of its shape and size [24], the dielectric function of the glass host containing the NPs, changes the LSPR bandwidth and resonance frequency, see Figure 2-4.
We can be written as the sum of the bound and quasi-free (conduction) electron contributions [25]:  , γ is the damping the resonance, ω the excitation frequency, ωp the plasma frequency.The bound electron contribution ib ε remains unchanged [26].A similar expression can be used for the contribution of conduction electrons [27]: Where the first term, 0 1/τ is associated to bulklike electron scattering process in the particle and the second term is a consequence of quasi-electron-free interaction with the surface and, for a sphere, VF is the Fermi velocity, and gs is the surface factor [25].Nevertheless, the LSPR dependence on the matrix refractive index (n λ ) also can be calculated by [12]: , where n′ is the electrons density, e the electron charge, () ( ) the dielectric permittivity, and m * the electron mass.On the other hand, in the Gans theory, the LSPR is only a function of the aspect ratio and refractive index.Thus, in certain conditions, a linear relationship between them can be resulted [28].Nevertheless, numerical results suggest that, even when the aspect ratio is fixed and the retardation effect is weak, the position of longitudinal resonance can still depend strongly with the aspect ratio [29,30] .Using the model of Cheng -ping Huang et al [31], we can write: ( ) Where κ = l/2r is the aspect ratio of the NPs (with the inner radius r and in a cylindrical region with the length l), and δ is the skin depth.Cheng -ping Huang considered the problem as using an LC circuit model without solving the Laplace or Maxwell equations, and show that its results overcomes the deficiency of Gans theory and provides a new insight into the phenomenon.This way, we can observe resonance wavelength change with the aspect ratio of NP, Figure 5.This means a breakdown of the linear behavior presenting oscillations electrons originating from the amorphous geometry of the NPs associated with the inertia of electrons, see inset Figure 2 as well.Figure 6 illustrates this further, via experiments of X. Lu et al. [15] and Mock et al. [32].Panel (a) the nanobar Ag NPs and the corresponding dark-field light scattering spectra, in broad agreement with the simulated results shown in [15].Panel (b) shows the dipolar plasmon lineshapes of colloidal silver NPs of different shapes [32].

Coupling between metallic nanoparticles
We can say that the localized plasmon resonance frequency of a single metallic NP can be shifted through of alterations in shape, size and surrounding medium from the Frohlich condition, section 2.1.Nevertheless, in a NP ensembles we can obtain additional shifts due to electromagnetic interactions between the localized modes, see Figure 3 and 4 (c).These interactions are basically of a dipolar nature (when d<<λ).So, the NP ensemble can be treated as an ensemble of interacting dipoles (in a first approximation).Those NPs can be embedded into a host matrix ordered or random, in one-, two-or three-dimensional arrays with interparticle spacing D. Electromagnetic coupling of those arrays shows interesting localization effects for closely spaced particles such as, enhancement process due to field localization in NP junctions.Assuming a dipolar approximation the NPs can be treated as point dipoles.In this sense, two regimes have to be distinguished (i) For D<<λ, near-field interactions with a distance dependence of D -3 dominate, equation ( 5), and the NP array is described as an array of point dipoles coupling via their near-field, see section 2.1 and Figure 7.These arrays can serve as hot-spots for field enhancement, e.g. in a context of surface-enhanced Raman scattering (SERS).(ii) For larger NP separations, far-field dipolar coupling with a distance dependence of D -1 dominates, see section 2.1.
Therefore, the maximum field enhancement is determined by the shortest distance between two equipotential particles.Today, there are several theoretical methodologies available to describe the interaction among the metallic NPs with electromagnetic radiation [33,34,35,36,37,38,39,40].

Rare-earths
Rare earths ions in solids are either divalent or trivalent.Their electronic configuration is 4f N 5s 2 5p 6 or 4f N-1 5s 2 5p 6 , respectively.By far the most common valence state of the RE ions in solids is the trivalent one.Those ions have a long history in optical and magnetic applications.We have special interest in the devices luminescent using crystal, powders, and glasses.On the other hand, divalent RE ions have also been used in laser devices, but only in relatively exotic ones for cryogenic operation [41,42].The 4f electrons are not the outermost ones.They are shielded from external fields by two electronic shells with larger radial extension (5s 2 5p 6 ), which explains the atomic nature of their spectra absorption/emission, Figure 8. Thus the 4f electrons are only weakly perturbed by the charges of the surrounding atoms.Important characteristics that distinguish them from other optically active ions are: (i) the wavelengths of the emission and absorption transitions are relatively insensitive to host material, (ii) the intensities of these transitions are weak, (iii) the lifetimes of metastable states are long and, (iv) the quantum efficiencies tend to be high.This is why the RE ions are such a useful probe in a solid; the crystal environment constitutes only a small perturbation on the atomic energy levels, and many of the solid state, and hence spectroscopic, properties can be understood from a consideration of the free ions.In turn, the wavefunctions of the free ions constitute a good zero order approximation for a description of solid-state properties, Figure 8.
The solutions to this problem can then befactored into a product of a radial and angular function.Whereas the radial function depends on the details of the potential the spherical symmetry ensures that the angular component is identicalwith that of a hydrogen atom and can be expressed as spherical harmonics.Except for Ce 3+ and Yb 3+, which have only one electron, the solutions of the central-field problem are products of one-electron states that are antisymmetric under the interchange of a pair of electrons, as required by the Pauli exclusion principle.
In describing the state of a multielectron atom, the orbital angular momenta and the spin angular momenta are added separately.The sum of the orbital angular momenta is designated by the letter L, and the total spin is characterized by S. The total angular momentum J of the atom may then be obtained by vector addition of L and S. The collection of energy states with common values of J, L, and S is called a term.Here, the Russell-Saunders notation for the energy levels (terms) is used, 2S+1 LJ, this takes into account the spin-spin coupling, orbit-orbit coupling and spin-orbit coupling.The energy levels of a free RE ion are usually interpreted by considering only interactions between the 4f electrons themselves.Since all the other electronic shells are spherically symmetric, Figure 8, their effect on all the terms of a configuration is the same in first order, and therefore do not contribute significantly to the relative positions of the 4f energy levels, we can write: () () Where () i Ur is the potential in which the electron i is moving.The first two terms of the Hamiltonian (equation ( 13)) are spherically symmetric and therefore do not remove any of the degeneracies within the configuration of the 4f electrons, therefore we can neglect.The next two terms, which represent the mutual Coulomb interaction of the 4f electrons (HC) and their spin-orbit interaction (HSO) are responsible for the energy level structure of the 4f electrons.Details of the matrix element calculations of HC and HSO can be found in ref. [44,45].
Figure 8 shows the radial distribution functions 4f, 5s, 5p, and 6s electrons for Gd + as obtained from Harteww-Fock calculation by Freeman and Watson [46].We can see that the 4f electrons are inner electrons with relatively small <r n > values.As we shall see, the crystal field interaction will be small in REs.It is also evident that the 4f wavefunctions do not extend very far beyond the 5s and 5p shells.Thus, all quantities of a solid depend on an overlap of the 4f wavefunctions with those of a neighboring ion have to be small in RE compounds.

Trivalent ions in a static crystal field
The 4f shell of the RE ions are an unfilled shell and therefore have a spherical charge distribution.If the ion is introduced into a crystal, the ion experiences an inhomogeneous electrostatic field, the so-called crystal field, which is produced by the charge distribution into the crystal.This crystal field distorts the closed shells of the RE ion.Producing an effect on the energy level 4f, i.e., removes to a certain degree the degeneracy of the free ion 4f levels, thus producing a major modification of the energy levels (but this depends on the crystal symmetry).In the luminescence spectrum are observed additional transitions, which originate from the excited crystal field levels of the ground term is evident, and the spectra look more complicated.On the other hand, these spectrums can be used to determine the crystal field energies of the ground term.
We shall now try to understand the behavior of these additional transitions.To do so we draw on our treatment of the Coulomb interaction of the 4f electrons.The crystal field interaction comes by the interaction of the 4f electrons with all the charges of the crystal with all charges of the crystal, except for trivial factors, it is therefore given by one over the radius vector between the 4f electrons and the crystal charges.This function is given, apart from radial factors, of two spherical harmonics kq Y , one containing the coordinates of the 4f electrons, the other containing coordinates of the crystal charge.The latter has to be integrated over the whole crystal, whereupon it gives the strength of the crystal potential at the site of the RE ion.Finally, this shows the existence of the splitting telling us that the development of the crystal potential into spherical harmonics contains a second order term.

Crystal field splitting
Crystal field splitting has two aspects: (i) symmetry, namely, the number of the levels into which an ion is free the J term are split in a crystal field of a given symmetry; (ii) the actual size of the crystal field splitting.This way, the point charge model can be used for illustrative purposes but not for a quantitative description of the crystal field interaction.A realistic description of this interaction must take into account that the crystal field is built up of the spatially extended charge clouds of the individual ions.Thus, these charge clouds can penetrate each other and thereby interact.Hence, we can considered the following elements: 1.The ions are considered static in the crystal, i.e., we can neglected the lattice vibrations and their effect on the energy levels.2. We regard the 4f electrons of one RE ion, as representative of those of all the RE ions in the crystal and, thus the interaction of 4f electrons of adjacent ions is neglected.3. The crystal consists of the extended charge distributions.This produces an overlap of the charge distributions of the neighboring ions and the 4f electrons.Aditionally, a charge transfer between 4f electrons and the electrons of the ligands can take place.Both contribute to the crystal field interaction.4. The 4f electrons of one ion are considered to be independent of each other, that is correlation effects play no significant role.
Therewith, we can calculate the crystal potential ( ) iii r ϕ θ Φ at the site of the 4f electrons and the potential energy of the 4f electrons in this potential.If the crystal has charge density () R ρ and the 4f electrons have radius ri, we have: Where r< and r> are, respectively, the smaller and larger value of r and ri.Here Pk(cos[x]) are the Legendre polynomials.Also, the equation ( 15) can be re-write as: Where the crystal field parameter Bk,q (k ≤ 6 for f electrons) and the summation i is carried out over all the 4f electrons of the ions.Bk,q have the form: Here Ck,q is called a tensor operator and is defined as: 0.5 , , 4 21 In early treatments of the crystal fiel interaction it was assumed that in RE compounds the point charge contribution would be the dominant part of the crystal field interaction.Then, in equation ( 16) the integral over the lattice can be replaced by a sum over all lattice points and k r < can be replaced by k i r .The latter replacement can be performed as long as the charge distribution of the crystal does not enter that of the 4f electrons (as long as ri < R), which implies that the potential acting on the 4f electrons obeys the Laplace equation Figure 9 further illustrates the effect of spin-orbit and crystal field interactions on the energy levels of the Er 3+ ion.This figure were extracted from A.J. Kenyon [47].A further splitting of the energy levels comes about when the ion is placed in a silica host.The 4f N configuration is composed for a number of states where the quantum numbers (L, S, J, and another arbitrary one) define the terms of the configuration, all of which are degenerate in the central-field approximation, as illustrated in Figure 9. Next in the hierarchy is spin-orbit, the strongest of the magnetic interactions.Spin-orbit lifts the degeneracy in total angular momentum and splits the LS terms into J levels, Figure 9.
We can see that the environment provided by silica hosts destroys the spherically symmetric environment that Er 3+ ions enjoy in the vapor phase.Thus the degeneracy of the 4f atomic states will be lifted to some degree.This splitting is also referred to as stark splitting, and the resulting states are called Stark components (of the parent manifold).The even-k terms in the expansion split the free ion J multiplets into Stark components generally separated by 10-100 cm -1 (see Figure 9).The ion-lattice interaction can mix multiplets with different J values (J mixing), although it usually remains a good quantum number.The odd-k terms admix higher lying states of opposite parity [e.g., 4f N 15d 1 ] into the 4f N configuration.This admixture does not affect the positions of the energy levels, but it has a very important effect on the strengths of the optical transitions between levels.

Optical properties
In recent years most of the interest in luminescent RE ions has concentrated on the trivalent erbium (Er 3+ ), and in particular its emission band around 1550 nm.This emission is within the telecommunication windows, and fortuitously coincides with the 1550 nm intra-4f 4 I13/2→ 4 I15/2 transition of the Er 3+ ion.
For this reason exists today a great interest in utilizing erbium-doped materials for gain elements and sources in telecommunications systems [48,49,50].The development of the erbium-doped fiber amplifier (EDFA) in the late 1980s [51,52] exploited the 4 I13/2→ 4 I15/2 transition and allowed the transmission and amplification of signals in the 1530-1560 nm region without the necessity for expensive optical to electrical conversion [53].Hence, it is originated a driving force for research in RE doped fibers and integrated optics waveguides has been their use for amplifying weak signals in optical communications systems at 1300 and 1600 nm.This may be achieved by simply splicing a section of RE-doped fiber into the transmission one and injecting pump light through a fiber coupler.The signal generated within the RE emission band stimulates emission of radiation at the same frequency, amplifying the optical communication signal with high gain, high efficiency and low noise, which is highly advantageous for optical communications [54].There are five main RE candidates for use as dopants in fiber or waveguide amplifiers for optical communications systems: Er 3+ , Tm 3+ , Nd 3+ , Pr 3+ and Dy 3+ .The Er 3+ and Tm 3+ ions are the choice for the 1400-1600 nm window centered at 1550 nm, based on the 4 I13/2→ 4 I15/2 transition of Er 3+ ion and the 3 H4→ 3 F4 transition of Tm 3+ ion.The 4 F3/2→ 4 I13/2 emission of Nd 3+ ion, the 1 G4→ 3 H5 transition of Pr 3+ ion and the 6 F11/2( 6 H9/2)→ 6 H15/2 transition of Dy 3+ ion are all potentially useful for the 1300 nm telecommunication window.
Further, the 3+ ions all exhibit intense narrow-band intra-4f luminescence in a wide variety of hosts, and the shielding provided by the 5s 2 and 5p 6 electrons (see Figure 8), which means that rare-earth radiative transitions in solid hosts resemble those of the free ions and electron-phonon coupling is weak.Although some of the divalent species also exhibit luminescence (e.g., samarium and europium), it is the trivalent ions that are of most interest.As mentioned previously, the intra-4f transitions are parity forbidden and are made partially allowed by crystal field interactions mixing opposite parity wavefunctions, resulting in luminescence lifetimes long (often in the millisecond range), and linewidths narrow.The selection of an appropriate ion with intense and narrow-band emission can be obtained across much of the visible region and into the near-infrared.Figure 10 shows energy level diagrams for the isolated 3+ ions of each of the 13 lanthanides with partially filled 4f orbitals.
Almost all the RE ions their emission is due to optical transitions within the f-manifold (e.g.Tb 3+ (4f 8 ), Gd 3+ (4f 7 ) and Eu 3+ (4f 7 ).The 4f-electrons are well shielded from the chemical environment and therefore have almost retained their atomic character.Nevertheless, for a number of RE ions, also broad emission bands are known.Prominent examples are Eu 2+ and Ce 3+ .Here, the emission is from to 5d-4f optical transitions.As electrons participate in the chemical bonding, the d-f emission spectra consist of broad bands.These transition types are allowed and are consequently very fast (a few µs or less).Some line emission is not a specific property of RE ions and in addition to that, in the case of RE ions, broad emission spectra can be obtained as well, depending on the optical transitions involved.In this respect, RE ions are not unique.The unique properties of the RE ions originate from the fact that the spectral position of the emission lines is almost independent of the host lattice, in contrast to line emission generate by the emission of metal ions.

Radiative transitions: Intensities of optical transitions
The terms shown in equation ( 13) are time-dependent; thereby, they do not lead to stationary states of the system.This way, they are treated using time-dependent perturbation theory resulting in transitions between the states established by the static interactions.In luminescent devices the most important term is VEF which gives rise to the emission and absorption of photons from decay radiative of the RE ions.This involves the interaction between the electron charge and the electric field and, the interaction between the electron spin and the magnetic field.
The experimental data on spectra of RE ions show that the radiation is mostly electric dipole (ED) nature, though some cases of the magnetic dipole radiation are also observed.Since the optical transitions take place between levels of a particular 4f N configuration, the electric dipole radiation is forbidden in first order, because the electric dipole operator has uneven parity and the transition matrix element must have even parity (Laporte selection rules).
Van Vleck [55] pointed out the dipole electric radiation can only occur because the 4f N states have admixtures of 4f N-1 nl configuration (nl will be mostly 5d), thus the 4f N-1 nl has to be chosen such that it has opposite parity from 4f N .The admixture is produced via interactios that have odd parity and this depend of the host matrix of the RE ions.However, we can have four dominant sources of optical radiation in RE ions spectra: i. Forced electric dipole induced by odd terms of the crystal field.
ii. Forced electric dipole radiation induiced by lattices radiation.
iii.Allowed magnetic dipole transition.iv.Allowed electric quadrupole radiation.
In free atoms, magnetic dipole is about six orders of magnitude weaker than the electric dipole radiation.This latter occurs only as a consequence of a perturbation, both kinds of radiation shows up in the RE spectra with about intensity.Then, quadrupole radiation are less probable still in comparison with the magnetic dipole.
There are different types of transitions between levels (called electric dipole, electric quadrupole, and magnetic dipole) and therefore the transitions are divided into allowed ones (with a high probability) and so-called forbidden transitions (for transitions where the electric dipole transition is quantum mechanically forbidden).
For the first order allowed magnetic dipole radiation the free atom selection rules are still quite valid: ( ) In the electric dipole case we have: Δ , 2 J l Δ≤ .However, since ED transitions is induced by the crystal field, the free atom selection rules break down almost completely, i.e., the selection rules with regard to the L, S and J quantum numbers are now essential governed by the crystal field interaction yielding 6 J Δ≤ (approximately).For the electric quadrupole case the rules selection is: 0, , 2 SL J Δ= Δ Δ≤ .
We now outline the Judd-Ofelt theory for the determination of the intensities in RE crystal spectra [56,57].It is in essence a quantification of the ideas formulated by van Vleck [55] under optical radiation sources.Intensities are often expressed in terms of oscillator strengths, where the total oscillator strength for a transition from an energy level a to an energy level b is given: Here h is the Planck constant, υ the frequency of the transition a→b, n the refraction index of host.Sed and Smd are the electric dipole and magnetic dipole intensities respectively and are defined as: U ( λ ) is a tensor operator of rank λ, and the sum runs over the three terms values 2, 4 and 6 of λ.With: ( ) 21 21 The λ Ω parameters have so far been assumed to arise solely from crystal field; however, they also contain contributions from admixtures by the lattice vibrations.The asterisk means that for * , kq B the radial integral is to be taken between states 4f and nl instead of 4f and 4f.Also, it is interesting to determine the coefficient for spontaneous light from state a ( ) Here c velocity of light in vacuum.The Judd-Ofelt formalism has been applied to the analysis of a number of systems.In most of these analyses the crystal field splitting of the terms is neglected; therefore, the total absorption intensities between the ground term and the excited terms are analyzed with only three empirical parameters ( ) 2,4 and 6 If b is an excited state that decays only by the emission of photons, its observed that relaxation rate is the sum of the probabilities for transitions to all possible final states.The total rate is the reciprocal of the excited-state lifetime τa ( ) The branching ratio a,b, for the transition b → a is the fraction of all spontaneous decay processes that occur through that channel and is defined as follows: ( The branching ratio, which has an important influence on the performance of a device based on a particular transition, appears often in the discussion of specific ions.It has a significant effect on the threshold of a laser and the efficiency of an amplifier.

Metallic nanoparticle embedded in a gain media: LSPR interaction radiative transitions
The RE-doped laser crystals and glasses are among the most popular solid-state gain media.In order of maintaining the efficiency of these materials in which the RE dopant is uniformily dispersed, as in multi-component glasses.In this sense, glasses have good optical, mechanical, and thermal properties to withstand the severe operating conditions of optical amplifier.Desirable properties include hardness, chemical inertness, absence of internal strain and refractive index variations, resistance to radiation-induced color centers, and ease of fabrication.Furthermore, the matrix host composition affects the solubility of the RE dopant, this affect the lifetime, absorption, emission, and excited state absorption cross sections of the dopant transitions [47].This competing absorption phenomenon can seriously diminish the efficiency of an optical device.For example, a decrease in the excited-state absorption for Er 3+doped fibers going from a germane-silicate host to an alumina-silicate host has been verified [58], demonstrating the importance of host selection for a given RE ion or laser transition.Host glasses compatible with this relatively high concentration of RE without clustering require the open, chain-like structure of phosphate glasses or the addition of modifier ions (Ca, Na, K, Li, or other) to open the silicate structure and increase solubility [48].The limitation owing to clustering in a predominantly silica host without modifier ions has been well documented [19].
The maximum erbium concentration in silica for optimum amplifier performance has been suggested to be lesser to 100 ppm [59].However a 14.4-dB gain, 900-ppm erbium-doped silica fiber amplifier has been reported, indicating that higher concentrations can produce useful devices [48].Nevertheless, the interactions between host and RE ions, it is necessary to consider background losses from impurity absorption and scattering mechanisms that decrease the efficiency of the optical device.For example, depending on the phonon energies of the host matrix, some of the level lifetimes can be strongly quenched by multi-phonon transitions.Such effects are minimized in low-phonon-energy host media such as fluoride fibers.The effect of internal loss is most dramatic in distributed amplifiers, where pump light must travel long distances in the process of distributing gain.
Additionally, into the glass matrix can happen diverse kinds of interactions, in particular dipole-dipole interactions between the RE ions similar or of different species, allow energy transfer between those.This is exploited e.g. in Er 3+ -Yb 3+ -codoped fibers, where the pump radiation is dominantly absorbed by Yb 3+ ions and mostly transferred to Er 3+ ions [48].
In this way, RE-doped glasses shown are excellent materials that provide gain media.This makes them ideal candidates for embedding metallic NPs, resulting in new materials for the fabrication of devices optical with large enhancements even when the gain is saturated due light localization effects.It has been shown theoretically and experimentally that homogeneous aggregates of structures supporting LSPR can lead to extremely large enhancement of local field amplitudes exceeding those of single structures [60,61].Besides, inorganic glasses are the host matrix for metallic NPs formation.The wide temperature range of glass viscosity growth provides the possibility to control over the NPs size within the wide range by means of modifying the temperature and duration of thermal processing.
In fact, only such kind of matrix makes it possible to control and investigate all the stages of NPs formation, including the starting stage [14,62].
The LSPR in metallic NPs is predicted to exhibit a singularity when the surrounding dielectric medium has a critical value of optical gain [63].This singularity is obtained from the equation (4), for ()

Re 2
NP m εω ε  ≈−  , the NP absorption presents a maximum.This is socalled the Frohlich condition is associated with dipole mode [1].
Therefore, the strong local electric field induced by the NP (LSPR) can enhance the total electric field, and can also improve the quantum yield of the luminenescence of the RE ions from the NP (this strong enhancement of electromagnetic fields is essential in nonlinear optics effects) [64,65].Thus, the enhancement obtained with these NPs is due to the formation of EDs which generates a polarization given by ' , where x  is the distance between each NP , 3 6 qd π = is the NP specific volume, ' N is the conduction electrons density, and e is the electronic charge [12].Therefore, we obtained a modification in the local electric field by these dipoles (local field correction).Using the results obtained by O.L. Malta et al [66], the effective electric field can be written as: Where 0 ε is the dielectric constant in the presence of an external electromagnetic field of amplitude E0.In the presence of an electromagnetic wave we have LSPR which forms EDs separated by different distance r  , some of which will contribute to the luminescence enhancement.
Assuming that the RE ions may occupy different sites in the host, a direct coupling between the excited states of the RE ions and the NPs modifies the Stark levels energies [12,13,67].As the NPs just give a contribution to the local field when the light is present, the oscillator strength of a spectral line, corresponding to transition from the ion ground level i to the component f of the excited level can be re-write as: The second term into parenthesis is added to the equation from the Judd-Ofelt theory [56,57], and represents the ED transition due to LSPR of NP.To obtain non vanishing matrix elements of the components (1)   NP D λ it is necessary to admix into i and f other states of opposite parity.
Thus, the initial and final states are: ( ) ( ) Where V is the crystalline field, equation ( 16), responsible for the Stark levels and treated as a perturbation, φi and φf have the same parity, φ β has opposite parity in relation of φi and φf, P  is the ED from the light interaction.For example, Er 3+ ions presented an electronic configuration [Xe]4f 11 , with J =15/2 been the spin-orbit ground state because the f shell is more than half-filled.The order of these Stark levels depends on the strength of the crystal field and the influence of NP P  .
This can be observed experimentally in the luminescence spectra of different RE ions shown in Figure 11 interaction with silver or gold NPs in different host matrix, as a blue-or redshift (see equation 26) and a pronounced increase in luminescence (see equation 25).
In this scenario, the influence of NP P  appeared in the luminescence spectra as a blue or a red -shift of the peaks, e.g. a transfer energy from the NPs dipoles to RE ions, thus modifying the Stark energy level's bandwidth, see Figure 11.This energy transfer is obtained from the second term added in equation (25) and can be understood through the following definition: ( ) Frequency UC spectra for excitation at 980 nm, (for composition see Ref. [68].After the cooling the samples were annealed for different durations (24, 48, and 72 h) in order to nucleate silver NPs [68].(c).Upconversion spectra extracted from [69] under excitation wavelength at λex=798 nm (for composition and for amplification ratio see Ref.The enhancement of luminescence was found to be reproducible for all ours samples.These pictures was extracted and modified from Ref. [12].These spectrums are of Er 3+ -doped tellurite glass, more details see [12].(i).Luminescence spectra of Er 3+ :Au-doped tellurite glass for several annealing times, pumped at 980 nm.Picture on the left; Upconversion, for the range 400<λ< 900 nm.Picture on the right; Energy-levels diagram of Er 3+ for the luminescence spectra.ET stands for energy transfer, CET for cooperative energy transfer, Q for quenching, GSA for ground state absorption, NR for non-radiative decay, and ESA for excited state absorption.For more details see Ref. [13].
Nevertheless, an interesting question arises: how these NPs are excited?
As explained above, those NPs can be excited by a predefined incident radiation through a direct coupling between the excited states of the both RE ions and NPs, resulting in: (i) a local field increase (Frohlich condition), at ωp, (ii) a nonradiatively decay (heat generation by Joule effect) or (iii) a radiative energy release which depends on the albedo of the NPs.Thereby, the exact response of LSPR will depend on the details of the physical system (e.g.arrangement, shape, host matrix), and usually not strictly symmetric about the resonant frequency.A schematic representation of the interaction process within the RE:NP system is depicted in Figure 12 (a).
Also we can elucidate the enhancement (quenching) from the process of energy transfer as following: Er 3+ emission promotes energy transfers into a plasmonic mode, which can decay nonradiatively by heat generation (Joule effect) or radiatively by releasing energy that depends on the albedo of the NPs.We consider two types of emission from a system of identical dipoles [74]: Where () Ray scatt Q is the Rayleigh scattering [67,68] and, y = ωD/c, with c the speed of light.
Therefore the total intensity IT, can be written as [62]: We consider I1 as the contribution from the emitter dipole (RE ions) uncoupled to the metal and I2 the plasmon enhanced emission from coupled dipoles, see Figure 12 (b).
Finally, we can obtain the following conditions:  .Thus, the maximum field enhancement is determined by the shortest distance between two equipotential particles.It corroborates well with the demonstration in the references [12,13,67,75].
Another possible mechanism for the energy transfer is due to that part of silver or gold (small silver or gold aggregates) probably remained under the form of ions, atoms, charged or neutral dimmers and multimers.Consequently, the contribution of the latter species to the RE luminescence enhancement and band shape features cannot be excluded [14], Figure 11.Moreover, the insertion of silver or gold in the samples leads to strong modification of the glassy network and consequently on the RE local environment, this is verified in reference [62].

Conclusion
This chapter present results where it was demonstrated the simultaneous exploitation of the enhanced local field due to NPs and energy transfer processes in order to enhance the luminescence spectra of a glassy composite material, and others.Besides, from these nanoparticles it is possible to modulate the down/up-conversion emission of the REs with applicability in areas such as optical telecommunication, including biomedical imaging and energy conversion.On the other hand, this significant enhanced fluorescence has high potential for application in photonics, optical displays, lasers and optical memory devices, amongst others.However, the success of new applications of nanoparticles depends on improvement in the understanding of the properties of LSPR and the environment around them.Further efforts and systematic studies must be realized in order to offer new developments to extend the analytical applications field of metallic nanoparticle interaction with rare-earth ions.
We hope that this chapter stimulated our readers for the development of theoretical and experimental work on plasmonics and rare-earths.

Figure 1 .
Figure 1.Left: Schematic of the electron charge displacement (valence electrons) in a metallic NP (LSPR) interacting with an incident plane wave, with electric field polarized E into a host matrix.Right:The corresponding electric field strength pattern for a 100 nm silver sphere, irradiated at a wavelength of 514 nm, this is reproduced from X. Lu et al.[15].
Here α is the (complex) polarizability of the NP in the electrostatic approximation.Under the condition that 2NP m εε + is a minimum, the polarizability shows a resonant enhancement.Thus, we can also write the Frohlich condition dipole surface plasmon of the NP (in an oscillating field).Nevertheless, the distribution of the electric field in E inside and out E outside the sphere can be written as: moment.Therefore, a resonance in α implies a resonant improvement of both the internal and dipolar fields, resulting in prominent applications of NPs in optical devices.Now consider a plane wave incident with ( ) e., we have a scattering of the plane wave by the NP.In this sense, the electromagnetic fields associated with an electric dipole in the near, intermediate and radiation zones are[17]: λ0 is the incident wavelength with respect to vacuum, and m0 represents the refractive index of the surrounding medium.The Ricatti-Bessel functions Ψ and ξ are defined in terms of the half-integer-order Bessel function of the first kind (Jn+1/2(z)), the half-integer-order Hankel function of the second kind.

Figure 2 .
Figure 2. Extinction cross section from Mie theory for (a) silver and (b) gold NPs.Both in function of size with refraction index 1 (line curves) and 2 (dot lines).Inset figure shows a red-shift with the increment of size NPs and refraction index.

Figure 3 .
Figure 3. Extinction cross section from Mie theory via the program MiePlot v4.2.11 of Philip Laven, for silver and gold NPs with a size distribution of 20 % STD of 20 nm size embedded in a glass with refraction index in function of the wavelength and a bulk with refraction index 2 constant.In both cases, we observed a red-shift (see arrow).Inset figure shows the size distribution of NPs for 50 NPs in both cases.

Figure 5 .
Figure 5. Resonance wavelength with aspect ratio from Cheng -ping Huang prediction for radius different and embedded in a bulk with refraction index 1.0 , 1.5 and 2.0.

Figure 6 .
Figure 6.Panel (a) scattering spectra.In the insets are SEM images of the individual Ag nanobars.X. Lu et al.[15].For simple, highly symmetric shapes (sphere, cube and triangular plate), the spectra are dominated by a single peak, but with the peak position sensitive to the shape, and ranging from 400 to up 800 nm.Panel (b) Scattering spectra of single silver nanoparticles of different shapes obtained in dark-field configuration.Mock et al.[32].

Figure 7
Figure 7 shows the near field coupling between NPs.Here, the restoring force acting on the oscillating electrons of each NP in the chain is either increased or decreased by the charge distribution of neighboring particles.Depending on the polarization direction of the exciting light, this leads to a blue-shift of the plasmon resonance for the excitation of transverse modes, Figure 7 (a), and a red-shift for longitudinal modes, Figure 7 (b).

Figure 7 .
Figure 7. Schematic of near-field coupling between metallic NPs for two different polarizations.

Figure 8 .Where
Figure 8. Square of the radial wavefunctions for the 4f, 5s, 5p and 6s energy levels from Hartree-Fock.It was a calculation for Gd + by Freeman e Watson (1962)[46].Picture inset schematically shows that the 4f orbital is within the 6s, 5p and 5s levels.
of the 4f electrons.

Figure 9 .
Figure 9.The effect of spin-orbit and crystal field splitting on the energy levels of the Er 3+ ion in silica matrix.The energy diagram shows the hierarchy of splitting resulting from electron-electron and electron-host interactions.Figure extracted from A.J. Kenyon [47].

Figure 10 .
Figure 10.Energy levels of the triply charged lanthanide ions.Besides, the most technologically important radiative transitions are labeled.Figure adapted from A.J. Kenyon [47].

Figure 11 .
Figure 11.(a).Fluorescence spectra of the Eu 3+ ions in the presence (a) and in the absence (b) of AgNPs.The silver concentration is 7.5 in weight percent.The matrix glass composition can be found in[66].(b).Frequency UC spectra for excitation at 980 nm, (for composition see Ref.[68].After the cooling the samples were annealed for different durations (24, 48, and 72 h) in order to nucleate silver NPs[68].(c).Upconversion spectra extracted from[69] under excitation wavelength at λex=798 nm (for composition and for amplification ratio see Ref.[69].The bases of the emission curves (c), (d), and (e) have been uplifted for better visibility.(d).PL spectra extracted from[70] (i) Eu(III)EDTA, 3H2O complex, (ii) Eu complex with Au nanoparticles and (iii) Eu complex with Au-ZnO nanoparticles.(e).Upconversion spectra of Tm 3+ /Yb 3+ codoped PbO-GeO2 samples containing silver NPs obtained by pumping the samples with a diode laser operating at 980 nm.For more details see[71].(f).PL spectra (λexc≈337 nm) of sy-activated with 0.037 mol% Ag containing glasses co-doped with 0.19 mol% Sm (black curve), Dy (red), and Tb (blue), respectively, and of non-activated and non-annealed (n.a.) 0.037 mol% Ag containing samples co-doped with 0.19 mol% Sm (grey), Dy (magenta), and Tb (light blue)[72].(g).Picture on the left, Integrated PL enhancement in periodic (circle) and Fibonacci (square) nanoparticle arrays of various interparticle separations.The top inset shows the representative PL spectrum of periodic (bottom), Fibonacci (top) nanoparticle arrays with Δmin= 50 nm and unpatterned area (middle),and the inset bottom shown the SEM micrograph of (left) periodic, (right) Fibonacci array Au nanocylinders.Picture on the right, PL lifetime of periodic (circle), Fibonacci (square), unpatterned Figure 11.(a).Fluorescence spectra of the Eu 3+ ions in the presence (a) and in the absence (b) of AgNPs.The silver concentration is 7.5 in weight percent.The matrix glass composition can be found in[66].(b).Frequency UC spectra for excitation at 980 nm, (for composition see Ref.[68].After the cooling the samples were annealed for different durations (24, 48, and 72 h) in order to nucleate silver NPs[68].(c).Upconversion spectra extracted from[69] under excitation wavelength at λex=798 nm (for composition and for amplification ratio see Ref.[69].The bases of the emission curves (c), (d), and (e) have been uplifted for better visibility.(d).PL spectra extracted from[70] (i) Eu(III)EDTA, 3H2O complex, (ii) Eu complex with Au nanoparticles and (iii) Eu complex with Au-ZnO nanoparticles.(e).Upconversion spectra of Tm 3+ /Yb 3+ codoped PbO-GeO2 samples containing silver NPs obtained by pumping the samples with a diode laser operating at 980 nm.For more details see[71].(f).PL spectra (λexc≈337 nm) of sy-activated with 0.037 mol% Ag containing glasses co-doped with 0.19 mol% Sm (black curve), Dy (red), and Tb (blue), respectively, and of non-activated and non-annealed (n.a.) 0.037 mol% Ag containing samples co-doped with 0.19 mol% Sm (grey), Dy (magenta), and Tb (light blue)[72].(g).Picture on the left, Integrated PL enhancement in periodic (circle) and Fibonacci (square) nanoparticle arrays of various interparticle separations.The top inset shows the representative PL spectrum of periodic (bottom), Fibonacci (top) nanoparticle arrays with Δmin= 50 nm and unpatterned area (middle),and the inset bottom shown the SEM micrograph of (left) periodic, (right) Fibonacci array Au nanocylinders.Picture on the right, PL lifetime of periodic (circle), Fibonacci (square), unpatterned I1 is the intensity emission for a single emitter, I2 is the intensity emission of the NP, Ip the pump intensity, p η is the pump efficiency, 0 η is the internal quantum efficiency of the energy transfer, LSPR η is the efficiency of the energy transfer (nonradiative) to LSPR modes and the scattering efficiency of the plasmon at the emission wavelength scatt Q is: e. the luminescence enhancement depends on the incident radiation frequency and the NP size.But, as were mentioned, the incident radiation for the NP activation comes from the emitter dipole ( )1 LSPR I ηand not from the pump radiation (Ip), i.e., from transition radiative from RE.The coupling efficiency LSPR η is defined by: ΓLSPR is the energy transfer rate to the LSPR mode[73,74].

Figure 12 .
Figure 12.(a) Energy level scheme for a resonant and RE ion absorption.The dot line indicates the energy transfer between RE→NP or NP→ RE, and the vertical dot line shows the transition radiative under consideration.The curved arrows indicate non-radiative transitions.(b) Schematic representation of the system RE:NP.A monochromatic plane wave with pump intensity (Ip) which is proportional to the pump wavelength λpump, induces the following processes: (i) absorption of RE ion, Ip, (ii) activation of NPs, due the coupling RE:NP (transitions levels), 1 LSPR I η (iii) NP transmitter, via electric dipole.Such coupling depends on the coupling efficiency LSPR η

Table 1 .
The most frequently used laser-active RE ions and host media together with typical emission wavelength ranges are shown in the table 1: Common laser-active rare earth ions and host media and important emission wavelengths.