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Transfer-matrix formalism for the calculation of optical response in multilayer systems: from coherent to incoherent interference

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Abstract

We present a novel way to account for partially coherent interference in multilayer systems via the transfer-matrix method. The novel feature is that there is no need to use modified Fresnel coefficients or the square of their amplitudes to work in the incoherent limit. The transition from coherent to incoherent interference is achieved by introducing a random phase of increasing intensity in the propagating media. This random phase can simulate the effect of defects or impurities. This method provides a general way of dealing with optical multilayer systems, in which coherent and incoherent interference are treated on equal footing.

©2010 Optical Society of America

The study of multilayer films has gained increasing interest in recent years due to their many potential uses as optical coatings and as transparent conductive electrodes in optoelectronic devices such as flat displays, thin film transistors and solar cells [14]. In particular, the unique optical properties of multilayer films play a vital role in the construction of thin-film solar cells [5,6], where an important challenge is to increase the absorption of the near-bandgap light, which would allow a reduction in the thickness of the cell. Consequently, the ability to predict and tune the optical properties at the semiconductor interface can greatly contribute to reducing the cost of thin-film solar cells. In addition, multilayer systems have been used to study photon localization [7], model ion-implanted materials [8,9], and to determine the thicknesses, densities and roughness of films in combination with X-ray reflectivity measurements [10]. Therefore, developing a general method that allows the study of the optical response of multilayer systems is of fundamental importance for designing and tuning more efficient optoelectronic devices.

The reflectance and transmittance of a multilayer structure can be calculated by using the transfer matrix method [1113]. However, the form of the conventional transfer matrix assumes coherent light propagation, which may lead to narrow oscillations in the calculated reflectance and transmittance spectra of the system. In practice, due to interference-destroying effects these oscillations may not be observable. Consequently, in order to have a realistic description of the optical properties of multilayer systems these interference-destroying effects should be introduced. There have been previous attempts to modify the transfer matrix in order to take into account incoherent interference [14,15], as well as partial coherence [1618]. However, in the proposed methods the square of the amplitude of the electric field, or Fresnel coefficients, are used to study the incoherent case. The case of partial coherence simulates macroscopic surface or interface roughness, and is introduced by multiplying the Fresnel coefficients by correction factors.

In this article, we present a modified transfer matrix method to calculate the optical properties of multilayer systems that includes coherent, partially coherent, and incoherent interference. The modeling of the partially coherent and incoherent cases is done by adding a random phase that simulates the effects of impurities or defects in the layer. The value of the random phase can be gradually varied in order to go from coherence to incoherence. The capabilities of the method are illustrated by presenting calculations of the optical properties of Si and ZnO films. The physical meaning of the random phase as well as potential methods for modeling materials with varying impurity profiles and interface roughness are discussed. An additional advantage of this method is that the partial coherence or incoherence can be separately/individually introduced for each layer, without having to calculate the intensity matrix for all the layers as it has been previously implemented.

The transfer matrix method is used to solve Maxwell’s equations in a multilayer system subject to a uniform incident field E. The field in the medium is divided into two components, the forward (transmitted) component E + and the backward (reflected) component E - (see Fig. 1 ).

 figure: Fig. 1

Fig. 1 Multilayer system composed of N layers with complex refractive indices, ni, and N + 1 interfaces. The sign + and - on the electric field amplitudes, Ei, indicate left- and right-going waves, respectively. The prime is used for waves at the right hand side of an interface.

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The amplitudes of the field at the left- and right-hand side of an interface are related by:

(Em1+Em1)=Im1,m(Em+Em)
where,
Im1,m=1tm1,m(1rm1,mrm1,m1)
and tm-1,m and rm-1,m are the transmission and reflection Fresnel coefficients respectively.

The field amplitudes at the left- and right-hand side of the mth layer are related by:

(Em'+Em')=Pm(Em+Em),
where,
Pm=(eiδm00eiδm).
δ is the phase shift due to the wave passing through the film m, and is defined by
δm=2πσnmdmcosφm,
where σ is the wave number, nm is the complex refractive index of the mth layer, dm is the thickness of the mth layer, and φ m is the complex propagation angle following Snell’s law (n0 sinφ 0 = n 1 sinφ 1 = … = nN +1 sinφ N +1). The above matrix transformations can be applied for the N layers and N + 1 interfaces resulting in:
(E0+E0)=I01P1I12P2I23PNIN(N+1)(EN+1+EN+1)=(T11T12T21T22)(EN+1+EN+1).
T 0,( N +1), defined by
T0,(N+1)=I01P1I12P2I23PNIN(N+1),
is the system transfer matrix.

The reflection and transmission coefficients of the multilayer system can be calculated from the elements of the transfer matrix as follows:

r=E0E0+=T21T11,
t=EN+1'+E0+=1T11.

Since the transmission and reflection coefficients are related to the elements of the transfer matrix, the matrix can be written as follows:

T0,(N+1)=1t0,N+1[1rN+1,0r0,N+1t0,N+1tN+1,0r0,N+1rN+1,0].

In previous work [18,15], the incoherence was treated by replacing the reflection and transmission vectors by the squares of their amplitudes. In this way the conventional (coherent) transfer matrix was replaced by an intensity matrix, as:

T0,(N+1)=1|t0,N+1|2[1|rN+1,0|2|r0,N+1|2(|t0,N+1tN+1,0|2|r0,N+1rN+1,0|2)].

The way in which the partial coherence and incoherence are introduced in our method is as follows. A random phase is added to the phase shift in the selected layer. Therefore, Eq. (5) is re-written as follows:

δm=2πσnmdmcosφm+βRand,
where β takes values between 0 and π, and Rand is a randomly generated number between −1 and 1. The randomly generated numbers are uniformly distributed. The final transmittance is obtained by averaging the calculated transmittances with different sequences of random numbers.

The physical meaning of this random phase is to simulate impurities or defects in the layer, which would introduce a dephasing or loss of coherence such as the one we are introducing by adding the termβRand. If the concentration of defects is large then the loss of coherence would be complete and the system would be in the completely incoherent case as it has been dealt with before in Refs. 15 and 18. In our method, the total incoherence is represented by introducing a random phase with β = π, while in the partial coherence cases 0<β< π.

The calculation of the optical response in the incoherent limit is illustrated in Fig. 2 . The figure shows the calculated transmittance vs. wavelength for a crystalline Si film of 150 nm thickness in air. The curves corresponding to the coherent case, β = 0, and the incoherent limit, β = π, are displayed. Also, as a reference, the curve for the incoherent limit calculated from the intensity matrix method is shown. It can be observed that the curve corresponding to the coherent limit presents oscillations while these oscillations have vanished in the incoherent limit. In addition, the agreement between this method and the intensity matrix method can be clearly observed from the superposition of the two curves representing the incoherent limit.

 figure: Fig. 2

Fig. 2 Transmittance vs. wavelength for a crystalline Si film of 150 nm thickness in the coherent and incoherent limits. The solid red line corresponds to the coherent limit; the solid green line corresponds to the incoherent limit calculated using the squares of the amplitudes of the transmission coefficients; and the dashed blue line corresponds to the incoherent limit calculated using the added random phase with β = π. A filter of 10 moving averages was used to smooth the blue curve.

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In our calculations of the incoherent limit using the random phase method, a random phase with β = π was used. The calculations of the transmittance vs. the wavelength were repeated 30 times, with 30 sequences of randomly generated numbers, and the results of the 30 runs were averaged to obtain the incoherent curve. The calculated curve (β = π) displayed in Fig. 2 was further smoothed by using a filter of 10 moving averages. The application of this filter did not distort the original results and it was only applied to reduce the noise. This noise is due to the limited number of runs we averaged to obtain the incoherent curve. It can be clearly observed from Fig. 2 that with only 30 runs the transmittance curve calculated using the random phase method has converged to the curve calculated using the intensity matrix. This figure clearly displays that by introducing a random phase one can successfully simulate the coherence-destroying effects that lead to complete incoherence.

The partial coherence cases can be simulated by introducing a random phase of smaller magnitude. In these cases a certain loss of coherence is introduced; the partial coherence cases represent an intermediate situation between the coherent limit and the complete incoherence. Figure 3 shows the transmittance for a 150 nm film of crystalline Si as a function of the wavelength. The coherent limit and the complete incoherent limit are shown as a reference. It can be observed from this plot two intermediate cases of partial coherence, one with β = π/3 and one with β = π/4. It can be seen that as the magnitude of β decreases the curves approach that of the complete coherent limit. Therefore, by changing β from π to 0 one can calculate the transmittance from the complete incoherent case to the coherent limit.

 figure: Fig. 3

Fig. 3 Transmittance vs. wavelength for a crystalline Si film of 150 nm thickness in the coherent and partially coherent regimes. The dash-dotted red curve corresponds to the coherent limit. The solid blue and green curves, which correspond to the partially coherent regime, were calculated using the random phase method with β = π/4 and β = π/3 respectively. As a reference the incoherent limit is also plotted (dashed green curve). The curves corresponding to the partial coherence limit were smoothed using a filter of 5 moving averages.

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Another interesting feature of this method is the capability of gradually varying the incoherence degree independently on individual layers. The loss of coherence is introduced in each layer by introducing a random phase to each phase shift as shown in Eq. (12). In this case δ1 and δ2, the phase shifts of layer 1 and layer 2 respectively, are written as:

δ1=2πσn1d1cosφ1+β1Rand1,
δ2=2πσn2d2cosφ2+β2Rand2.

The capability of introducing different incoherence degrees in each layer is displayed in Fig. 4 , where the transmittance of a two layer system is presented. This figure shows the transmittance of a 150 nm ZnO film on a 150 nm Si film vs. wavelength. It shows the complete incoherent limit, where β1 = β2 = π, the coherent limit where β1 = β2 = 0, and two intermediate cases. For the first case, β1 = 0 and β2 = π, which means that the ZnO layer is treated as coherent, and in the second case β1 = 0 and β2 = π/2. It can be seen from this last case that the transmittance is rapidly approaching the coherent limit.

 figure: Fig. 4

Fig. 4 Transmittance vs. wavelength for a two layer system consisting of a ZnO film of 150 nm thickness and a crystalline Si film of 150 nm thickness. The black curve represents the complete incoherent limit; the (dash-dotted) green curve represents a coherent ZnO layer on an incoherent Si layer; the (dashed) blue curve represents a coherent ZnO layer on a partially coherent Si layer; and the solid red curve represents the complete coherent limit. The curves corresponding to the partial coherence and incoherent limit were smoothed using a filter of 5 moving averages (for wavenumbers > 0.6 μm).

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This method presents a unique way to study the optical response of multilayer systems since the transition from coherence to incoherence can be easily achieved. For instance, this method provides the potential to simulate layered films with impurities or scattering center defects. Moreover, as the degree of incoherence can be modified in each layer independently, it can be very useful to study systems with varying profiles of impurity concentrations by varying the value of β in each film. Also, this method could present an alternative route to study multilayered nanoporous films with different degrees of nanoporosity [19].

In addition, the introduction of partial coherence is expected to be very useful for simulating the effects of interface roughness on the scale of the wavelength. For instance, the interface morphology can be a key variable for optimizing the performance of thin film solar cells since the reflectivity of the semiconductor interface can critically affect the performance of the cell [20]. The surface roughness in a multilayer system can, if large enough, cause phase differences between the reflected and transmitted beams. This effect can also be simulated by the inclusion of a random phase of varying intensity.

In summary, we have developed a method for calculating the optical response of multilayer systems, which can deal with coherent, partially coherent, and incoherent interference on equal footing. This method is based on the transfer matrix method employed in its usual way via Fresnel coefficients in a 2x2 matrix configuration. The novel feature is that there is no need to use modified Fresnel coefficients or the square of their amplitudes to work in the incoherent limit. The transition from coherent, to partially coherent, to incoherent interference is achieved by introducing a random phase of increasing intensity in the propagating media. This random phase can account for the effect of defects or impurities in the layer. The capabilities of the method were presented by calculating the optical properties of Si and ZnO films from the coherent to the incoherent limit.

Acknowledgments

This work was supported in part by NSF (Grant No. DMR-0906025), DOE (the Division of Material Sciences and Engineering, Office of Basic Sciences, and BES-CMSN), and DOE (Office of Energy Efficiency and Renewable Energy, Industrial Technologies Program) under contract DE-AC05-00OR22725.

References and links

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4. H. Cho, C. Yun, and S. Yoo, “Multilayer transparent electrode for organic light-emitting diodes: tuning its optical characteristics,” Opt. Express 18(4), 3404–3414 (2010). [CrossRef]   [PubMed]  

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8. C. C. Katsidis, D. I. Siapkas, D. Panknin, N. Hatzopoulos, and W. Skorupa, “General transfer-matrix method for optical multilayer systems with coherent, partially coherent,and incoherent interference,” Microelectron. Eng. 28, 439 (1995). [CrossRef]  

9. X. L. Ruan and M. Kaviany, “Enhanced nonradiative relaxation and photoluminescence quenching in random, doped nanocrystalline powders,” J. Appl. Phys. 97(10), 104331 (2005). [CrossRef]  

10. S. Logothetidis and G. Stergioudis, “Studies of density and surface roughness of ultrathin amorphous carbon films with regards to thickness with x-ray reflectometry and spectroscopic ellipsometry,” Appl. Phys. Lett. 71(17), 2463 (1997). [CrossRef]  

11. P. Yeh, Optical Waves in Layered Media (Wiley, New York, 1988).

12. Z. Knittl, Optics of Thin Films: An Optical Multilayer Theory (Wiley, London, 1976).

13. O. S. Heavens, Optical Properties of Thin Films (Dover, New York, 1965).

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16. C. L. Mitsas and D. I. Siapkas, “Generalized matrix method for analysis of coherent and incoherent reflectance and transmittance of multilayer structures with rough surfaces, interfaces, and finite substrates,” Appl. Opt. 34(10), 1678 (1995). [CrossRef]   [PubMed]  

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Figures (4)

Fig. 1
Fig. 1 Multilayer system composed of N layers with complex refractive indices, ni, and N + 1 interfaces. The sign + and - on the electric field amplitudes, Ei, indicate left- and right-going waves, respectively. The prime is used for waves at the right hand side of an interface.
Fig. 2
Fig. 2 Transmittance vs. wavelength for a crystalline Si film of 150 nm thickness in the coherent and incoherent limits. The solid red line corresponds to the coherent limit; the solid green line corresponds to the incoherent limit calculated using the squares of the amplitudes of the transmission coefficients; and the dashed blue line corresponds to the incoherent limit calculated using the added random phase with β = π. A filter of 10 moving averages was used to smooth the blue curve.
Fig. 3
Fig. 3 Transmittance vs. wavelength for a crystalline Si film of 150 nm thickness in the coherent and partially coherent regimes. The dash-dotted red curve corresponds to the coherent limit. The solid blue and green curves, which correspond to the partially coherent regime, were calculated using the random phase method with β = π/4 and β = π/3 respectively. As a reference the incoherent limit is also plotted (dashed green curve). The curves corresponding to the partial coherence limit were smoothed using a filter of 5 moving averages.
Fig. 4
Fig. 4 Transmittance vs. wavelength for a two layer system consisting of a ZnO film of 150 nm thickness and a crystalline Si film of 150 nm thickness. The black curve represents the complete incoherent limit; the (dash-dotted) green curve represents a coherent ZnO layer on an incoherent Si layer; the (dashed) blue curve represents a coherent ZnO layer on a partially coherent Si layer; and the solid red curve represents the complete coherent limit. The curves corresponding to the partial coherence and incoherent limit were smoothed using a filter of 5 moving averages (for wavenumbers > 0.6 μm).

Equations (14)

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( E m 1 + E m 1 ) = I m 1 , m ( E m + E m )
I m 1 , m = 1 t m 1 , m ( 1 r m 1 , m r m 1 , m 1 )
( E m ' + E m ' ) = P m ( E m + E m ) ,
P m = ( e i δ m 0 0 e i δ m ) .
δ m = 2 π σ n m d m cos φ m ,
( E 0 + E 0 ) = I 01 P 1 I 12 P 2 I 23 P N I N ( N + 1 ) ( E N + 1 + E N + 1 ) = ( T 11 T 12 T 21 T 22 ) ( E N + 1 + E N + 1 ) .
T 0 , ( N + 1 ) = I 01 P 1 I 12 P 2 I 23 P N I N ( N + 1 ) ,
r = E 0 E 0 + = T 21 T 11 ,
t = E N + 1 ' + E 0 + = 1 T 11 .
T 0 , ( N + 1 ) = 1 t 0 , N + 1 [ 1 r N + 1 , 0 r 0 , N + 1 t 0 , N + 1 t N + 1 , 0 r 0 , N + 1 r N + 1 , 0 ] .
T 0 , ( N + 1 ) = 1 | t 0 , N + 1 | 2 [ 1 | r N + 1 , 0 | 2 | r 0 , N + 1 | 2 ( | t 0 , N + 1 t N + 1 , 0 | 2 | r 0 , N + 1 r N + 1 , 0 | 2 ) ] .
δ m = 2 π σ n m d m cos φ m + β R a n d ,
δ 1 = 2 π σ n 1 d 1 cos φ 1 + β 1 R a n d 1 ,
δ 2 = 2 π σ n 2 d 2 cos φ 2 + β 2 R a n d 2 .
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