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Recent experimental data shown a promising direction in employing nano-plasmonics for increasing efficiencies of the solar cells. The effect is due to metallic nanoparticles’ plasmons mediating energy transfer from the incoming e-m wave to the semiconductor in a regime violating limits in energy transitions imposed by the momentum conservation, due to translational invariance departure in surface nano-modified system. The chapter presents analysis of material dependence of near-field coupling to band electrons of surface plazmons in metallic nanoparticles deposited on the top of semiconductor substrate in nano-modified solar cells. Various materials for metal and substrate are comparatively studied upon the quantum Fermi Golden Rule approach in theoretical quantitative modeling of the plasmon-electron coupling that enhances ordinary PV effect. The material dependence of the plasmon-mediated efficiency growth in two types of solar cells, multi-crystalline Si and CIGS (copper-indium-gallium-diselenide), modified by various surface-deposited metallic nanoparticles is additionally illustrated by the experimental data.
Department of Quantum Technology, Wrocław University of Science and Technology, Poland
Witold A. Jacak*
Department of Quantum Technology, Wrocław University of Science and Technology, Poland
*Address all correspondence to: witold.aleksander.jacak@pwr.wroc.pl
1. Introduction
The plasmon-mediated sunlight energy harvesting in metal-nano-modified solar cells is caused by three effects: the strong concentration of electric field of plasmon oscillations close to metallic components with local large curvature, the large amplitude of plasmon oscillations in metallic nanoparticles and the enhancement of the probability of interband excitations in semiconductor substrate caused by breaking of the translational symmetry for a nanoparticle and the dipole near-field coupling of surface plasmons with semiconductor band electrons [1, 2, 3, 4, 5, 6, 7]. The transition probability for transfer of electrons from the valence band to the conduction band in a semiconductor, essential for efficiency of the photovoltaic effect, grows due to the electric field amplitude enhancement and due to admission of all oblique transitions not here prohibited by the momentum conservation [4]. In the ordinary photo effect Kiriejew [8], the interband transitions are confined to only vertical ones between states with almost the same momentum due to the momentum conservation and the fact that the sunlight photons have very small momentum (owing to large light velocity, c) which almost does not change electron momentum at scattering: for excitation energy ħω beyond the forbidden gap, Eg, in the substrate semiconductor, ħω=cq gives q≪p, where p∼πħl is the semiconductor band quasi-momentum scale in the Brillouin zone (l denotes here the elementary cell linear size). Thus the change of the band electron momentum p1=p2+q is negligible on the scale of the Brillouin zone and p1≃p2 (because c=108 m/s) and only the vertical, conserving momentum, interband transitions contribute to the ordinary photo effect, i.e., when the transition is caused by free photons with momentum q and energy ħω=cq.
However, for interaction of band electrons with surface plasmon from the metallic nanoparticle deposited on the semiconductor surface, the situation changes significantly. In the near-field regime [9], the potential of the plasmon dipole on the nanosphere is proportional to 1R2 (R is a distance from the sphere center), which has the infinite decomposition in Fourier picture and thus overlaps with all quasi-momenta in the substrate semiconductor Brillouin zone. This is in contrary to the potential of the free photon which contributes via only single eiq⋅r−ħωt/ħ plane-wave Fourier component.
The resulted effect of oblique interband transitions can be accounted for via the Fermi Golden Rule (FGR). According the FGR scheme [10], the probability of interband transitions is proportional to matrix element of the perturbation potential between initial and final states and summed up over all initial states in the valence band and over all final states in the conduction band assuming only the energy conservation, Epp1+ħω=Enp2, where Epnp is the valence-p (conduction-n) band dispersion and ħω is the excitation energy related to damped and forced by sunlight surface plasmon oscillations with the bare self-energy value ħω1=ħωp3 (i.e., the Mie energy [11, 12], ħωp=ħnee2m∗ε0 is the bulk-plasmon energy in metal [13], ne is the density of collective electrons in metal, m∗ is the effective mass of electron in metal, e is the electron charge and ε0 is the dielectric constant) with not-defined momentum, however. The initial momentum, p1, and the final one, p2, can be arbitrary because the momentum conservation is rule out by the matrix element of the local dipole interaction.
The chapter is organized as follows. In Section 2, we present the quantum calculation of the efficiency of photo effect mediated by plasmons in metallic nanoparticles deposited on the top of a semiconductor photodiode. This efficiency has been accounted by application of the Fermi golden rule to the near-field coupling of dipole-plasmons with band electrons in the semiconductor substrate. The resulted transition probability is next utilized to the derivation of the plasmon damping rate due to coupling with band electrons which we present in Section 3. Section 4 addressed to analysis of the by-plasmon enhanced photo effect efficiency in various materials, including various metals for nanoparticles with plasmons and various semiconductor substrates. Section 5 contains also comparison with experiment both for laboratory Si photodiode covered with metallic nanoparticles as well as for standard solar cells, Si-multi-crystal and CIGS.
2. Plasmon-mediated photo effect: Fermi Golden Rule calculus of probability of electron interband excitation due to plasmons
The perturbation of electron band system in the substrate semiconductor due to the presence of dipole surface plasmon oscillations in metallic nanosphere (with a radius a) deposited on the semiconductor surface, has the form of the potential of the e-m field of an oscillating dipole. The Fourier components of the electric Eω and magnetic Bω fields produced in the distance R from the center of considered nanosphere with the dipole of surface plasmon with the frequency ω, have the form [9],
Eω=1εD0k2R+ikR2−1R3+n̂n̂⋅D0−k2R−3ikR2+3R3eikRE1
and
Bω=ikεD0×n̂ikR−1R2eikR,E2
(ε is the dielectric permittivity). In the case of the spherical symmetry, the dipole of plasmon is considered as pinned to the center of the nanosphere (the origin of the reference frame system), D=D0e−iωt. In Eqs. (1) and (2), we used the notation for the retarded argument, iωt−Rc=iωt−ikR, n̂=RR, ω=ck, momentum p=ħk. The terms with denominators R3, R2 and R are referred to near-, medium- and far-field zones of the dipole radiation, correspondingly. Because we consider the interaction with a closely adjacent layer of the substrate semiconductor, all terms with denominators R2 and R we neglect as small in comparison to the term with R3 denominator—this is the near-field zone approximation (the magnetic field disappears and the electric field is of the form of a static dipole field [9]). Therefore the related perturbation potential added to the system Hamiltonian attains the form,
w=eψRt=eεR2n̂⋅D0sinωt+α=w+eiωt+w−e−iωt.E3
The term w+=w−∗=eεR2eiα2in̂⋅D0 describes emission, i.e., the case of our interest.
According to the FGR [10], the interband transition probability is proportional to
wk1k2=2πħ<k1w+k2>2δEpk1−Enk2+ħω,E4
where the Bloch states in the conduction and valence bands are assumed as planar waves (for simplicity), Ψk=12π3/2eik⋅R−iEnpkt/ħ, Epk=−ħ2k22mp∗−Eg,Enk=ħ2k22mn∗ (indices n,p refer to electrons from the conduction and valence bands, respectively, Eg is the forbidden gap).
The matrix element,
<k1∣w+∣k2>=12π3∫d3Reε2ieiαn̂⋅D01R2e−ik1−k2⋅R.E5
can be found analytically by a direct integration, which gives the formula (q=k1−k2),
Next, we must sum up overall initial and final states in both bands. Thus, for the total interband transition probability we have,
δw=∫d3k1∫d3k2f11−f2w(k1k2)−f21−f1w(k2k1),E7
where f1,f2 assign the temperature dependent distribution functions (Fermi-Dirac distribution functions) for initial and final states, respectively. For room temperatures, f2≃0 and f1≃1, which leads to,
δw=∫d3k1∫d3k2⋅wk1k2.E8
After some also analytical integration in the above formula, we arrive at the expression,
according to assumed band dispersions, mn∗ and mp∗ denote the effective masses of electrons and holes, μ=mn∗mp∗mn∗+mp∗ is the reduced mass, the parameter ξ=2ħω−Egmn∗+mp∗ħ. In limiting cases for a nanoparticle radius a, we finally obtain,
With regard to two limiting cases, aξ≪1 or aξ≫1, ξ=2ħω−Egmn∗+mp∗ħ, we see that a≃1/ξ≃>2×10−9mforħω−EgEg<0.02<2×10−9mforħω−EgEg>0.02, and this range weakly depends on effective masses and Eg. Thus for nanoparticles with radii a>2 nm, the first regime holds only close to Eg (less than the 2% distance to limiting Eg), whereas the second regime holds in the rest of the ω domain. For comparison, a≃1/ξ≃>0.5×10−9mforħω−EgEg<0.5<0.5×10−9mforħω−EgEg>0.5, the first region widens considerably (to ca. 50% relative distance to Eg), but holds only for ultrasmall size of nanoparticles (a<0.5 nm). For larger nanospheres, e.g., with a>10 nm, the second regime is thus dominating.
One can notice that the above formula, Eq. (9) and its explicit form in limiting situations given by Eq. (10), is the generalization of to the ordinary photo effect, for which the transition probability is different [8],
δw0=423μ5/2e2mp∗2ωεħ3εE02V8πħωħω−Eg3/2.E11
The number of photons of the ω e-m wave with electric field component amplitude E0 in the volume V equals to, εE02V8πħω, hence the probability of single photon absorption by the semiconductor per time unit, attains the form in the ordinary photo effect [8],
q0=δw0εE02V8πħω−1=4423μ5/2e2mp∗2ωεħ3ħω−Eg3/2,E12
(factor (4) corresponds here to spin degeneration of band electrons).
In the case of mediation by plasmons, all oblique interband transitions contribute, not only vertical ones (as it was for the interaction with the planar wave in the ordinary photo effect). This results in an enhancement of the transition probability for the near-field coupling in comparison to the photon (planar wave) absorption rate in a semiconductor in the ordinary photo effect. The enhancement of the probability of transition due to hopping not conserving momentum, is, however, gradually quenched with the radius a growth, as expressed by Eq. (10).
The probability of energy absorption in the semiconductor via mediation of surface plasmons per single photon incident on the metallic nanospheres, qm, equals to the product of δw (given by Eq. (10)) and the number, Nm, of metallic nanoparticles divided by photon density with additional phenomenological factor β responsible for all effects not directly accounted for (as deposition separation and surface properties reducing the coupling strength, as well as energy losses due to electron scattering and irradiation to far-field zone (Lorentz friction [9]) into upper hemisphere, if the metallic nanoparticle is not completely embedded in the substrate semiconductor medium),
3. Damping rate for plasmons in a metallic nanoparticle deposited on a top of a semicoductor
Assuming that the energy acquired by the semiconductor band system, A, is equal to the output of plasmon oscillation energy (resulting in plasmon damping), one can estimate the corresponding damping rate of plasmon oscillations. Namely, at the damped (lowering in time) plasmon amplitude D0t=D0e−t/τ′, one finds for a total transmitted energy,
where τ′ is the damping time-rate and β accounts for losses (not included in the model). Comparing the value of A given by the formula (14) with the energy loss of damping plasmon estimated in Ref. [4] (the initial energy of the plasmon oscillations which has been transferred step-by-step to the semiconductor, A=D022εa3), one can find
By τ′, we denote here a large damping of plasmons due to energy transfer to the semiconductor substrate highly exceeding the internal damping, characterized by τ, due to scattering of electrons inside the metallic nanoparticle [4] (1τ≪1τ′). We neglect also the irradiation to far-field upper hemisphere zone of plasmon energy due to the Lorentz friction, which is also smaller than near-field zone energy transfer to the substrate [4].
For example, for nanospheres of Au deposited on the Si layer, we obtain for Mie self-frequency ω=ω1,
for light(heavy) carriers in Si, mn∗=0.190.98m, mp∗=0.160.52m, m is the bare electron mass, μ=mn∗mp∗mn∗+mp∗ and Eg=1.14 eV, ħω1=2.72 eV. For these parameters and nanospheres with the radius a in the range of 5−50 nm, the lower case of Eq. (16) applies (at ω=ω1). The parameter β fitted from the experimental data [4, 14] equals to ca 0.001.
In another scenario when the output of the plasmon energy is recovered by continuous income from the sunlight, one can consider the energy-balanced state. In an idealized case, whole incoming energy of the monochromatic ω e-m wave is transferred to the semiconductor via plasmons, and we deal with the stationary behavior of a driven and damped oscillator for plasmons. Even though the free undamped plasmon has the Mie self-resonance frequency, ω1=ωp3, the frequency of plasma oscillation equals to the driven electric field frequency, ω, of the incident e-m wave of photons. Because of an instant leakage of the plasmon energy in near-field to semiconductor substrate, this large damping of plasmon causes a red-shift and widening of the resonance, as for every damped and driven oscillator. The widened resonance enables the energy transfer from plasmons to electrons to embrace also frequencies lower or larger than Mie frequency but limited from below by the semiconductor gap Eg/ħ.
The incident sunlight dispersion covers the visible spectrum and also some UV and infra-red tails. The total efficiency of the plasmon channel corresponds to a sum (integration) overall Fourier components ω>Eg/ħ of light interfered with intensity distribution of sunlight spectrum. To model this behavior, it is necessary to consider separately each single monochromatic e-m mode, i.e., a Fourier component ω. Its electric field excites plasmon with this frequency and this plasmon is damping with the rate 1τ′(15). This damping causes a red shift of a resonance and reduces the resonance amplitude, which in turn allows for the accommodation to the balance of energy transfer to the semiconductor with incident sunlight e-m wave energy intensity (defined by it electric field amplitude E0) at the frequency ω. Within this damped and driven oscillator model, the amplitude of plasmon oscillations D0ω is constant in time and shaped by fω=1ω12−ω22+4ω2/τ′2. The extremum of red-shifted resonance is attained at ωm=ω11−2ω1τ′−2 with corresponding amplitude ∼τ′/2ω12−τ′−2. The red shift is proportional to 1/ω1τ′2. In the case of the described energy transfer balance, one obtains according to Eq. (10),
where fω=1ω12−ω22+4ω2/τ′2 corresponds to amplitude factor for driven damped oscillator and D0=e2neE04πa33mfω (in Eq. (10)); the amplitude of the electric field, E0, in the incident e-m wave is next ruled out from Eq. (17) due to normalization per single photon as in Eq. (13); C0=Nm4/3πa3V, V is the volume of the semiconductor, Nm is the number of metallic nanospheres.
The ratio, qmq0, revealing the advantage of the plasmon-mediated photo effect over the ordinary photo effect can be expressed as follows
This ratio turns out to be of order of 104β40Hnm for the surface density of nanoparticles (as in experiment in Ref. [14]), ns∼108/cm2; note that C0=ns4πa3/3H, H is a thickness of the semiconductor layer, which including the phenomenological factor β, and the thickness H (we have confirmed experimentally that the range of the near-field zone exceeds the Mie wave-length), is sufficient to explain the scale of the experimentally observed strong enhancement of absorption rate in semiconductors due to plasmons. The strong enhancement of this transition probability is linked with the allowance of momentum-non-conserved transitions, which is, however, reduced with the radius a growth. The strengthening of the near-field induced interband transitions, in the case of large nanospheres, is, however, still significant as the quenching of oblique interband transitions is partly compensated by ∼a3 growth of the amplitude of dipole plasmon oscillations. The trade-off between these two competing size-dependent factors is responsible for the observed experimental enhancement of light absorption and emission in diode systems mediated by surface plasmons in nanoparticle surface coverings [7, 14, 15, 16, 17, 18].
4. Efficiency of the light absorption channel via plasmon for various materials
Nanoparticles of gold and silver (sometimes also of copper) are mostly used in plasmon photovoltaics because their surface plasmon resonances are located within the visible light spectrum. These nanoparticles can be deposited on various semiconductor substrates with different material parameters. We list here the appropriate parameters usable for comparison with experiment for various configurations of the plasmon solar cell systems. In order to compare with the experiment, we can estimate the photocurrent in the case of a semiconductor photodiode with the metallically modified photoactive surface. This photocurrent is given by I′=∣e∣Nq0+qmA, where N is the number of incident photons and q0 and qm are the probabilities of single photon absorption in the ordinary photo effect [8] and of single photon absorption mediated by the presence of metallic nanospheres, respectively, as derived in the previous paragraph; A=τfntn+τfptp is the amplification factor (τfnp is the annihilation time of both sign carriers, tnp is the drive time for carriers [the time of traversing the distance between electrodes]). From the above formulae, it follows that (here I=I′qm=0, i.e., the photocurrent without metallic modifications),
In Tables 1, 2, 3, we list parameters for several semiconductor substrates and for a metallic nanoparticle few materials, which allow for comparison of the ratio qm/q0 for various material configurations by formula (18).
Substrate material parameters to formula (18) (m=9.1×10−31kg, the mass of bare electron; lh–light holes, hh–heavy holes, L–longitudinal, T–transverse).
Formula (18) is exemplified in Figure 1 for Au nanoparticles deposited on Si semiconductor (continuous line)–this reproduces well the experimental behavior (red dashed/dotted) [14]. Both channels of photon absorption resulting in photocurrent in the semiconductor sample are included, the direct ordinary photo effect absorption with probability of transitions given by q0 and the plasmon-mediated absorption with probability qm, respectively. Note also that some additional effects like reflection of the incident photons or destructive interference on metallic net would contribute and it was phenomenologically accounted in the plasmon-mediated channel by an experiment-fitted factor β. The collective interference type corrections are rather not strong for the considered low densities of metallic coverings of order of 108/cm2, and nanosphere sizes well lower than the resonant wavelength, though for larger concentrations and larger nanosphere sizes, would play a stronger reducing role (reflecting photons) [6, 19]. The resonance threshold was accounted for the damped resonance envelope function in Eq. (19) including also semiconductor band-gap limit. The relatively high value of qmq0∼104β40Hnm enables a significant growth of the efficiency of the photoenergy transfer to the semiconductor, mediated by surface plasmons in nanoparticles deposited on the active layer, by increasing β or reducing H (at constant ns). However, because of the fact that an enhancement of β easily induces the overdamped regime of plasmon oscillations, the more prospective would be lowering of H especially convenient in thin film solar cells. The overall behavior of I′/Iω=1+qm/q0 calculated according to the relation (19), and depicted in Figure 1, agrees quite well with the experimental observations [14], in the position, height and shape of the photocurrent curves for distinct samples (the strongest enhancement is achieved for a=40nm, for Au and Si substrate).
In Figure 2, we present the spectral dependence of the plasmonic efficiency enhancement with respect to substrate change (Si, CIGS and GaAs) for the same Au nanoparticles with radius a=50nm and the same nanoparticle concentration ns=108/cm2. One can note that for the CIGS substrate (copper-indium-gallium-diselenide) the spectral characteristics is narrower and blue shifted in comparison to Si and GaAs. Figure 2 reveals an increase in efficiency of the plasmon effect with growth of the value of forbidden gap Eg conserving other parameters not changed. Especially significantly influential material parameter occurs, however, a mass of holes, cf. Figure 3, which is also noticeable from Eq. (18). The mass of holes, mp∗2, enters the denominator in the formula (12) for the ordinary photo effect and next the numerator in Eq. (18). The higher mass mp∗ the lower efficiency q0 of the ordinary photo effect is and higher the ratio qmq0. In Figure 4, the material comparison of metal material of nanoparticles (Au, Ag and Cu) is presented for two their sizes (a=50,25nm). The blue shift of spectral characteristics for Ag and Cu in comparison to Au is noticeable (cf. also Figure 5) and even more visible for lower radii of nanoparticles due to narrowing of spectral curves (cf. Figure 6). From the comparison in Figures 5 and 6, for Si and CIGS substrates with Au, Ag and Cu nanoparticles of size a=50,25nm (at the nanoparticle concentration ns=108/cm2), one can notice that Au nanoparticles utilize the visible spectrum in the better manner than Ag or Cu ones. The advantage of Au nanoparticles is greater in the case of Si substrate and is reduced for CIGS substrate because the blue shift of Eg in CIGS with respect to Si. In the case of CIGS (especially for large nanoparticles, a=50nm), the advantage of Au beyond Ag in overall utilization of sunlight spectrum disappears, whereas is pronounced in the case of Si substrate. Later, we describe an experimental confirmation of this behavior of Si and CIGS substrates, at laboratory sunlight-type illumination by Yamashita DensoYSS-50Aunder AM1.5 [19].
For nanoparticles of gold (Au) and silver (Ag) of size, a=50nm, optimized due to formula (18), deposited on the multi-crystalline silicon (mc-Si) and on the copper-indium-gallium-diselenide (CIGS) solar cells, the measured [19] overall increase of cell efficiency attains the level of even 5%. The application of suitable concentration of Au and Ag nanoparticles onto mc-Si solar cells increases their efficiency by 5.6 and 4.8%, respectively [19]. Application of Au and Ag nanoparticles onto surface of CIGS solar cells improves their efficiency by 1.2 and 1.4%, respectively [19]. This is visualized in Figures 7 and 8, where it is compared an increase in solar cell overall efficiency (the ratio of the field beneath the I-V curve for the metallically improved solar cell and the clean solar cell; the same size (50 nm for radius) and the same concentration (from the 5% colloidal solution sputtering over the surface) has been applied to different samples)—for more detail cf. Ref. [19].
Worth noting is an agreement of experimentally observed difference in the increase of the efficiency due to the plasmon effect in both cases, of mc-Si and CIGS cells, if one compares the results of application of Au and Ag particles (at the same size of metallic nanoparticles and the same their surface concentration). This behavior agrees with the theoretical study of the material dependence of the plasmon effect, as shown above. From Figures 2, 3, 4, 5, we see that for Si substrate Au nanoparticles with radii 50 nm better utilize the solar light spectrum than Ag or Cu particles (cf. Figure 5), and indeed in the experiment (cf. Figure 8) for Au nanoparticles the efficiency growth is ca. 10% larger than for Ag nanoparticles of the same size and concentration on the substrate m-Si solar cell. Interestingly, for the substrate CIGS cell, the effect is weaker and inverted, cf. Figure 9. This also is noticeable from the theoretical modeling—due to different Eg and effective masses of carriers for CIGS with respect to mc-Si. The maxima for efficiency enhancement for Au and Ag mutually shift in such a way that for CIGS Ag nanoparticles a bit better suit to solar light spectrum than Au nanoparticles. However, to analyze these effects in more detail, a measurement of spectral characteristics of all considered structures at varying but monochromatic illumination uniformly calibrated should be performed.
We have demonstrated by application of the Fermi Golden Rule scheme, that the efficiency of the energy transfer channel between the surface plasmon oscillations in a metallic nanoparticles and a substrate semiconductor depends on parameters of both deposited metallic particles (its radius and material) as well as on semiconductor parameters (energy gap, and effective masses of electron and holes). Found by us formula which generalizes the ordinary photo effect onto the plasmon-mediated one, agrees well with the experimental measurements in laboratory photodiode configuration. The measured ratio of photocurrent in the setup with and without metallic nano-components is compared with the theoretically predicted scenario. The quantitative consistence is obtained both in the shape of the spectral characteristics and in the particle size dependence (as illustrated for Si diode with deposited Au nanoparticles with radii 25, 40 and 50 nm). The qualitative agreement has been achieved also for complete solar cells where the plasmon effect is obscured by other elements of the long series of effects resulting in overall solar cell efficiency beyond only efficiency of the absorption of photons. We have compared the experimental data for multi-crystalline Si solar cell and CIGS (copper-indium-gallium-diselenide) solar cell covered or not with gold and silver nanoparticles with radii of order of 50 nm. The increase of the overall photovoltaic efficiency for metallically modified cells varies between 1.5 (CIGS) and 6% (Si), depending on nanoparticle concentration (for too dense concentration the efficiency drops down). A bit better increase (ca. 10% difference) causes Au nanoparticles for Si cell in comparison to Ag nanoparticles, whereas for CIGS cell, the difference between effect of Ag nanoparticles and Au ones is inverted and strongly reduced. This also agrees qualitatively with theory predictions taken into account differences in Mie frequency in Au and Ag and also different semiconductor parameters for Si and CIGS.
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Written By
Janusz E. Jacak and Witold A. Jacak
Submitted: March 7th, 2018Reviewed: May 25th, 2018Published: November 21st, 2018