Nondestructive determination of film thickness with laser-induced surface acoustic waves
Xiao Xia, Kong Tao, Qi Hai Yang1, Qing Hui Quan
School of Microelectronic, Tianjin Key Laboratory of Imaging and Sensing Microelectronic Technology, Tianjin University, Tianjin 300072, China

 

† Corresponding author. E-mail: xiaxiao@tju.edu.cn

Project supported by the National Natural Science Foundation of China (Grant No. 61571319).

Abstract

The application of surface acoustic waves (SAWs) for thickness measurement is presented. By studying the impact of film thickness h on the dispersion phenomenon of surface acoustic waves, a method for thickness determination based on theoretical dispersion curve v(fh) and experimental dispersion curve v(f) is developed. The method provides a series of thickness values at different frequencies f, and the mean value is considered as the final result of the measurement. The thicknesses of six interconnect films are determined by SAWs, and the results are compared with the manufacturer’s data. The relative differences are in the range from 0.4% to 2.18%, which indicates that the surface acoustic wave technique is reliable and accurate in the nondestructive thickness determination for films. This method can be generally used for fast and direct determination of film thickness.

1. Introduction

Films are widely applied in aerospace, automotive manufacturing, biomedical engineering, and microelectronic industries.[14] In all such fields, the film thickness is one of the most important parameters for film quality evaluation. Yadav studied the influence of film thickness on structural, optical, and electrical properties of spray deposited antimony doped SnO2 thin films.[5] Ren et al. studied the influence of thickness upon the interfacial water at the solid-liquid interface.[6] Yang et al. analyzed the influence of nanofilm thickness on the elastic properties of B2-NiAl.[7] So the film thickness is not only a parameter that characterizes the geometrical dimensions of the films, but also greatly affects the function and lifetime of the films. Therefore, film thickness determination is an important requirement in many fields of technology.

In order to keep the function of the films after thickness measurement, many nondestructive testing methods have been proposed to measure the film thickness, including eddy current, spectroscopic ellipsometry, and x-ray transmission.[815] These methods work well, but they are all restricted to certain types of materials. The eddy current method is more suitable to measure the thickness of the non-conductive coating on the non-magnetic metal substrate.[810] The spectroscopic ellipsometry is an optical method. The measured material should be transparent.[1113] The x-ray transmission needs the absorption coefficients of the film and substrate to have obvious differences. The limitation for its wide application can be found when the chemical composition of the film is close to that of the substrate.[14,15]

Surface acoustic waves (SAWs) are dispersive during propagating on a layered structure, the surface acoustic waves with different frequencies have different propagation velocities. Due to this feature, the surface acoustic wave method can be applied to film thickness determination. This method is fast, simple, and non-destructive.[1618] In addition, the propagation of SAWs is hardly limited by the material. So this method is suitable to determine the film thicknesses of most materials.

In this paper, the relationship between the geometrical parameter thickness and the dispersion phenomenon of surface acoustic waves is analyzed. Accordingly, a thickness calculation method is developed by using the theoretical dispersion curve v(fh). The thickness calculation of two standard SiO2 films with this method is described in detail. In addition, four low dielectric constant (low-k) samples are also investigated in this study. The results of the six samples are compared with the manufacturer’s data. Comparing the results shows that the thicknesses of the interconnect films can be sensitively detected by the SAWs measurement.

2. Theoretical background

Surface acoustic waves propagate along the surface of a material. The penetration depth of the wave is defined to be equal to the wavelength λ and it reduces with increasing frequency.[16] In a homogeneous and isotropic bulk material, the wave phase velocity v depends on the material parameters: Young’s modulus E, density ρ, and Poisson’s ratio σ, and it is independent of the frequency f of the wave.[19,20]

In the film/substrate structure, the phase velocity v of the waves depends on the film and substrate material parameters and the frequency–thickness product fh.[21,22] The surface acoustic waves are dispersive, and the dispersion phenomenon is resulted from the different SAW phase velocities in the film and substrate materials. Figure 1 illustrates the dispersion phenomenon, it shows the theoretical dispersion curve v(fh) of the SiO2/Si structure. The SAWs propagate along the [110] direction of the silicon. The phase velocities of SAWs in bulk Si and bulk SiO2 are 5081.5 m/s and 3387 m/s, respectively. Because the penetration depth of the wave reduces with the increase of the frequency, lower frequency waves are more affected by the Si substrate. So their propagation velocities are closer to those in bulk Si. In contrast, higher frequency waves are more influenced by the SiO2 film, and their propagation velocities are closer to those in bulk SiO2.

Fig. 1. (color online) The theoretical dispersion curve v(fh) of SiO2/Si structure.

In addition to the frequency, the film thickness has the same effect on the phase velocity of SAWs. The increase of the film thickness can expand the influence of the SiO2 film on SAWs propagation. So the increases of the frequency and the film thickness together result in the change of the wave velocity. According to the physical principles of the elasto-dynamic theory, the phase velocity v of the waves is a function of the frequency–thickness product fh on the condition that the material parameters of the film and substrate are determinate.

For the thickness determination, the SAWs experiment can provide the v (f) curve of the sample. This curve contains information about the film thickness. With the material parameters of the sample, the relationship between the phase velocity v and the frequency–thickness product fh can be calculated. By using the theoretical dispersion curve v(fh) and experimental dispersion curve v(f), the film thickness can be obtained.

3. Experimental procedure

Figure 2 shows the schematic of a surface acoustic wave experimental system. A pulsed laser with a 0.8 ns pulse in width and 337.1 nm in wavelength is used to generate wide-band surface acoustic waves in the test. A cylindrical lens makes the laser beam focus into a line source on the surface of the sample. The surface acoustic waves propagate along the sample and are detected by a piezoelectric detector. A polyvinyllidene fluoride (PVDF) foil is pressed by the wedge-shape knife edge of the detector. It is used to transfer the broad range of vibration signals into electric signals. The electric signals are amplified by an amplifier and recorded by a digital oscilloscope.

Fig. 2. (color online) Schematic of laser-induced surface acoustic wave experimental system.

Two standard SiO2 films with different thicknesses are firstly tested by the SAWs technique to check our method. These films are grown by thermal oxidation on Si substrate. The material parameters of the standard SiO2 film include Young’s modulus E = 72 GPa, density ρ = 2.2 g/cm3, and Poisson’s ratio σ = 0.17. Surface acoustic waves are generated on the sample surface and arranged to propagate in the [110] direction of silicon.

In order to obtain the experimental dispersion curve, the electric signals ui(t) (i indicates different laser position) are detected at two different distances x1 and x2 away from the line-shaped laser source. The SAWs signals of SiO2 I detected at two different positions are shown in Fig 3. The distance between the two detection positions is 3 mm. The two signals have an apparent delay because of the different propagation distances. The electric signals ui(t) are handled by Fourier-transform to obtain the phase angles Φi(f).[23] The phase velocity v(f) can be calculated by the following equation:

where Φ1(f) and Φ2(f) are the phase angles of the SAW signals detected at positions x1 and x2, respectively.

Fig. 3. The SAWs signals detected at different distances (a) x1 and (b) x2 away from the line-shaped laser source on SiO2 I.
4. Determining the thickness

Figure 4 shows the dispersion curves obtained from the above experiments for the two SiO2 samples. In order to reduce the vibration of the curves, two fitting curves of the experimental dispersion curves are calculated by polynomial fitting. The fitting equations of SiO2 I and SiO2 II respectively are

Fig. 4. Experimental dispersion curves and fitting curves of two SiO2 samples.

A method to determine the thickness is developed by combining the theoretical dispersion curve v(fh) and experimental dispersion curve. Because the two SiO2 films employed in this research have the same material parameters, the same theoretical dispersion curve v(fh) is used to calculate the thicknesses of the films. Figure 5 shows this theoretical curve v(fh), which is the initial part of the curve in Fig. 1. The details of this method are given as follows. Select one data point (fhtheoty, v) on the theoretical dispersion curve v(fh). Take the velocity v of this data point into the fitting equation of the experimental dispersion curve, the related frequency fexp can be calculated. It means the same value of velocity v correlates the theoretical dispersion curve v(fh) and the experimental dispersion curve. At last, the thickness h can be easily obtained by comparing the frequency–thickness product fhtheoty of the theoretical dispersion curve and the frequency fexp of the experimental dispersion curve,

Fig. 5. (color online) The theoretical dispersion curve v(fh) used to determine the thicknesses of SiO2 films.

Because theoretical dispersion curve v(fh) contains many data points, a series of thickness values can be calculated from different data points. Table 1 shows the data of the theoretical curve v(fh) in Fig. 5, the frequencies fexp of the two experimental dispersion curves, and the calculation results of the two SiO2 films. The frequencies fexp of the experimental dispersion curves are solved by taking the values of velocity v into Eqs. (2) and (3), respectively. For SiO2 I, because the frequency f of the experimental dispersion curve is in the range from 20 MHz to 120 MHz, six data with fexp = 19.8 MHz to 118.2 MHz are chosen to calculate the thickness. The six calculated results vary only a little, and the mean value 505 nm is considered as the final result. For SiO2 II, the data with fexp = 19.9 MHz to 138.1 MHz are in the range of the experimental dispersion curve. The mean value of the calculated thicknesses is 1004 nm. The manufacturer’s data of these two standard SiO2 films are 500 ± 2 nm and 1000 ± 2 nm, respectively. So the thicknesses determined from the proposed SAWs method agree very well with the manufacturer’s data. The relative differences between the SAWs results and manufacturer’s data for the two films are only 1% and 0.4%, respectively.

Table 1.

The data of the theoretical curve, the frequencies fexp of two experimental dispersion curves, and calculation results of the two SiO2 films.

.
5. Application of the method to low-k samples

Low dielectric constant (low-k) materials are very important to decrease the RC delay in interconnects of integrated circuits.[24,25] The combination of the low-k insulator with lower resistivity metal of Cu is widely used in high speed ultra large-scale integration devices.

The thicknesses of four low-k samples are measured by the proposed SAWs method in this study. Figure 6 shows the experimental dispersion curves and fitting curves of the four samples. These low-k samples are divided into two groups based on the materials of the films. Two films are made of porous black diamond (BD) material, and the other two films are composed of dense black diamond material. The material parameters are listed in Table 2, and they are used to calculate the related theoretical dispersion curves v(fh).

Fig. 6. (color online) Experimental dispersion curves and fitting curves of four low-k samples.
Table 2.

Material parameters of porous and dense black diamond low-k samples.

.

The thicknesses of these samples determined by the SAWs method and the manufacturer’s data are listed in Table 3. As shown in Table 3, there is a good agreement between the SAWs results and the manufacturer’ s data, the largest relative difference between the two sets of data is only 2.18%, which occurs for the dense black diamond II.

Table 3.

Summary of thicknesses obtained from the surface acoustic wave method and manufacturer’s data.

.
6. Conclusion

The surface acoustic wave technique is applied to measure the thicknesses of films of ULSI. A thickness calculation method is developed based on the union of experimental dispersion curve and theoretical dispersion curve v(fh). This calculation method is very simple and fast. A series of thickness values can be calculated at different frequencies f of the experimental dispersion curve. The mean value is considered as the final result of the measurement. So there is another advantage of the method that multiple thickness values can reduce the uncertainty of single data and increase the reliability of the measurement result. Six interconnect films are employed to verify our method. The results of these films are compared with the manufacturer’s data. For these six films, the relative differences between the measurement results and manufacturer’s data are only in the range from 0.4% to 2.18%. The remarkable agreement of the contrast results shows the potential and reliability of the surface acoustic wave technique.

Reference
[1] Fourez S Jenot F Ouaftouh M Duquennoy M Ourak M 2012 Meas. Sci. Technol. 23 085608
[2] Dong G C Baarle D V Frenken J Tang Q W 2016 Chin. Phys. Lett. 33 116101
[3] Zalnezhad E Sarhan A A D 2014 Int. J. Adv. Manuf. Technol. 72 1491
[4] Gu S S Hu X J Huang K 2013 Acta Phys. Sin. 62 118101 in Chinese
[5] Yadav Y Y 2015 Thin Solid Films 591 18
[6] Ren X P Zhou B Li L T Wang C L 2013 Chin. Phys. 22 016801
[7] Yang X Y Zhang J P Wu Y R Liu F S 2015 Acta Phys. Sin. 64 016803 in Chinese
[8] Yin W Peyton A J 2007 NDT E Int. 40 43
[9] Qu Z Zhao Q Meng Y 2014 NDT E Int. 61 53
[10] Chen X L Lei Y Z 2015 Chin. Phys. 24 030301
[11] Franquet A Terryn H Vereecken J 2003 Thin Solid Films 441 76
[12] Gong J B Dong W L Dai R C Wang Z P Zhang Z M Ding Z J 2014 Chin. Phys. 23 087802
[13] Zhao J M Yang P 2012 Microsyst. Technol. 18 1455
[14] Ying A J Murray C E Noyan I C 2009 J. Appl. Crystallogr. 42 401
[15] Kolbe M Beckhoff B Krumrey M Ulm G 2005 Pectroc. Acta Pt. B-Atom. Spectr. 60 505
[16] Schneider D Hofmann R Schwarz T Grosser T Hensel E 2012 Surf. Coat. Technol. 206 2079
[17] Xiao X Qi H Y Tao Y Kikkawa T 2016 Appl. Surf. Sci. 388 448
[18] Xiao X Sun Y Shan X M 2012 Surf. Coat. Technol. 207 240
[19] Schneider D Schulz S E Gessner T 2005 Microelectron. Eng. 82 393
[20] Xiao X Qi H Y Sui X L Kikkawa T 2017 Appl. Surf. Sci. 399 599
[21] Farnell G W Adler E L 1972 Phys. Acoust. 9 New York Academic 35 127 10.1016/B978-0-12-395670-5.50007-6
[22] Xiao X Hata N Yamada K Kikkawa T 2004 Jpn. J. Appl. Phys. 43 508
[23] Xiao X Shan X M Kayaba Y Kohmura K Tanaka H Kikkawa T 2011 Microelectron. Eng. 88 666
[24] Grill A Gates S M Ryan T E Nguyen S V Priyadarshini D 2014 Appl. Phys. Rev. 1 011306
[25] Xiao X Tao Y Sun Y 2014 Chin. Phys. 23 106803