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Influencing the Crystallization of Glass-Ceramics by Ultrashort Pulsed Laser Irradiation after Nucleation

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DOI: 10.4236/njgc.2018.81001    412 Downloads   660 Views   Citations

ABSTRACT

An ultra-fast laser with central wavelength at 1064 nm and 10 ps pulse duration was used to tightly focus laser radiation with a microscope objective inside the volume of nucleated Lithium Aluminosilicate (LAS) glass-ceramic. The nonlinear absorption of the LAS glass-ceramic was measured for different laser parameters and a thermal simulation was performed to determine the temperature field inside the laser-modified area. After laser processing, the samples were crystallized in a furnace and the effect of the laser-induced modifications on the microstructure was analyzed with SEM. The SEM analysis shows an increase in the length and size of whisker-shaped β-spodumene crystals in the laser-modified area. By increasing the dimension of these whisker-shaped crystals, the flexural strength of LAS can be improved locally. First four-point bending flexural tests were performed to examine the influence on the mechanical properties.

1. Introduction

One advantage of laser radiation is the possibility to deposit energy on a very small and well defined area. This effect was used in [1] to show the feasibility of gradual and partial crystallization of glass-ceramics using continuous wave (CW) laser radiation. Due to the use of CW laser radiation, the crystallization process could only be started from the body surface.

Tight focusing of ultrashort-pulsed (USP) laser radiation enables the deposition of energy inside the volume of transparent dielectrics. Thereby it is possible to generate local material modifications on the micro and nanometer scale in the bulk material. If the intensity I of the laser radiation is sufficiently high, energy can be absorbed due to the effects of nonlinear absorption (NLA). Heat transfer from the electrons to the lattice then results in material modifications [2] . Depending on the laser parameters like pulse width τPulse, pulse repetition frequency (PRF) fPulse, pulse energy EPulse and the optical and thermal properties of the dielectric, different temperatures emerge in the focal area. This leads to various effects like void formation, change of the birefringent index or the production of micro cracks.

Since the development of industrial femto second lasers, many interesting applications have evolved based on the effect of NLA. Examples which involve the change of the birefringent index are writing of waveguides [3] or data storage with 3D Bit Arrays [4] . Another application of NLA is the production of microfluidic devices. By treating photosensitive glass with laser radiation, complex 3D structures can be produced inside the bulk material and microfluidic channels can be etched in a second step [5] . Finally, NLA is used in the micro machining field for laser welding of two overlapping glass plates at their interface through the first plate [6] .

In this paper, NLA induced thermal treatment by picosecond laser irradiation at 1064 nm wavelength of Lithium Aluminosilicate (LAS) glass-ceramic in the nucleated state is discussed. By destroying the crystallization seeds or changing their distribution, the microstructure after the crystallization in the furnace can be modified locally. The modification of the material is related to calculated temperature distributions. Finally, the impact of the treatment on the flexural strength of the LAS glass-ceramic is discussed.

2. Experimental Setup

2.1. Laser System

The setup for the irradiation experiments is illustrated in Figure 1. A picosecond laser with central wavelength at 1064 nm, 10 ps pulse duration and a variable pulse repetition rate from 50 kHz to 8.2 MHz was used. A pulse on demand module enabled the pulse picking. The beam expander with a magnification of two was necessary to reduce the power density on the mirrors and in the objective. The beam was focused with a microscope objective with a NA of 0.4. The theoretical radius in the focal plane of the beam ω0 in air was calculated [7] :

ω 0 = M 2 λ π N A . (1)

where M2 is the beam quality factor, λ is the wavelength and NA is the numerical aperture. Calculated for this laser system with a M2 < 1.1, the focal radius is approximately 0.9 μm.

The sample was moved by a CNC controlled axis system in all three dimensions. A power meter was mounted on the backside of the sample to measure the power transmitted through the sample.

2.2. Lithium Aluminosilicate Glass-Ceramic Samples

The glass-ceramic examined in this paper belongs to the Li2O-Al2O3-SiO2 (LAS) System and is described in [8] . The experiments presented in this work were all performed in the nucleated state, reached after a 30 minutes long treatment in the furnace at 660˚C. The measured material properties of the examined LAS glass-ceramic samples can be found in Table 1 for all three states.

To prevent surface absorption related to physical imperfections like grooves, scratches, cracks or pores [9] , the samples were polished. For the NLA characterization, plates with a size of 3 × 30 × 83 mm were used. The samples for the four-point bending flexural test had a dimension of 3 × 4 × 43 mm.

3. Nonlinear Absorption

Because of the high band gap energy EG of multiple eV, absorption in LAS glass-ceramic of 1064 nm laser irradiation (EPhoton ≈ 1 eV) cannot be explained by linear electron-photon interaction. A single photon with 1064 nm wavelength

Figure 1. Experimental setup for the production of laser-induced modifications inside LAS.

Table 1. Properties of the examined Lithium Aluminosilicate glass-ceramic in all three states.

has not enough energy to lift an electron from the valence band to the conduction band.

To enable a modification in LAS glass-ceramic, the density of electrons in the conduction band must reach 1019 cm−3 [10] . To reach these intensities the USP laser light was focused tightly by a microscope objective with high NA. The high intensity of the laser light enables a process where multiple photons stimulate the same electron simultaneously and lift it to the conduction band (multiphoton ionization). Consequently, electron plasma is formed in the conduction band, which absorbs the laser energy very effectively (avalanche mechanism) and transfers it to the lattice, heating it up. This process is described in [11] .

3.1. Absorption Curves of LAS

To measure the absorption curves of LAS a sample was moved with constant speed of 20 mm/s through the focus of the laser beam. The transmitted pulse energy Qt on the backside was measured with the power meter (Figure 1) and compared to the pulse energy Q0 with no sample in between. The nonlinear absorption Aexp was calculated with [12]

A exp = 1 Q t Q 0 1 ( 1 R 2 ) . (2)

The parameter R is the Fresnel reflectivity, which is calculated for the special case of perpendicular irradiation using

R = ( n 1 n 2 n 1 + n 2 ) 2 , (3)

where n1 is the refractive index of air and n2 is the refractive index of nucleated LAS. The calculated value for R with n1 = 1 and n2 = 1.54 is 0.045. This means that 4.5% of the laser light will be reflected. Figure 2 shows the measured absorption curve for the LAS glass-ceramic in the nucleated state for different laser pulse energy and PRF values.

The maximum absorption is in the range of 40%. If the PRF increases, the rate of NLA increases as well. The threshold intensity for visible laser-induced modifications was determined with 2.6 × 1017 W/m2 by using a light microscope. The smallest measured width of the modifications ω0 was determined with 0.35 µm, which is much less then theoretically calculated. This results in a threshold pulse energy of 2.1 µJ.

3.2. Absorbed Laser Power

The laser-modified area SMod has been measured by a light microscope on the polished surface in direction of axis movement. In Figure 3 SMod is plotted versus the overall absorbed laser power given by WAb

W A b = A exp f P u l s e Q 0 = A exp P A v g , (4)

where PAvg is the measured laser power. A good correlation between the

Figure 2. Experimental measurement of the nonlinear absorption of LAS.

Figure 3. Laser-modified area SMod vs. absorbed laser power WAB for the LAS glass-ceramic@20 mm/s sample speed.

laser-modified area SMod and the absorbed laser power WAb can be found by fitting the data points using a polynomial function.

4. Thermal Simulation

4.1. Model

Thermal simulations of the irradiated region were performed to compare the material modifications with the calculated temperature profile. The laser induced modifications were simulated by a line heat source with a continuous heat delivery of w(z) at x = y = 0 over a defined length of 0 < z < l in an infinite solid, which moves with a constant speed of vAxis along the x axis. The temperature distribution T(x, y, z) in a steady state with an initial temperature T0 can be written using [13]

T ( x , y , z ) = 1 4 π K 0 l w ( z ) s exp { v A x i s 2 α ( x + s ) } d z + T 0 , (5)

where s2 = x2 + y2 + (z − z')2, K is the thermal conductivity and α the thermal diffusivity, which can be calculated by K/(ρ∙c) where ρ is the mass density and c is the specific heat of the LAS glass-ceramic. The model used for the thermal simulation is illustrated in Figure 4.

The maximum temperature in the y − z plane can be found where dT/dx equals zero by solving

0 l w ( z ) s exp { v 2 α ( x + s ) } { x r 3 v 2 α ( x r 1 ) } d z = 0 . (6)

According to [14] w(z) can be written as a simple function of z given by

w ( z ) = a z m + b , (7)

where a, b and m are positive constants. By rearranging Equation (4) the calculated absorption ACalc can be written as follows:

A C a l c = W A b f Q 0 . (8)

Replacing WAb with the integral over w(z):

A C a l c = 1 f Q 0 0 l w ( z ) d z . (9)

Solving Equation (9) analytically with the defined function of w(z) in Equation (7) ACalc becomes

A C a l c = 1 f Q 0 ( a m + 1 l m + 1 + b l ) . (10)

Now it is possible to fit a, b and m. The length l of the laser modified area was measured.

Figure 4. Model of a moving line heat source with heat delivery w(z).

4.2. Results

For a modification with a fPulse of 50 kHz and a speed of vAxis of 20 mm/s an experimental absorption AEx of 40.4% was calculated. The pulse energy Q0 was 41.2 µJ and the length of the laser absorbed region was 151.8 µm. The values for m = 1, a = 4.9 × 107 W/m2 and b = 1825 W/m were taken and adapted from [14] . The absorption ACalc became 40.7%.

Because no thermal data of nucleated LAS glass-ceramic were available, the values for conductivity and diffusivity were taken from soda-lime glass (SLG) [15] with K = 1.005 W/(m∙K) and α = 4.365 × 10−7 m2/s. The comparison of the calculated temperature distribution in the yz-plane and the polished cross-section of a modified region is shown in Figure 5 for T0 = 25˚C. The direction of the laser is along the z-axis in negative direction and the movement of the axis is perpendicular to the plane of the image.

By overlapping the isothermal line for the melting point of SLG (viscosity η = 101 Pa∙s) at 1400˚C [16] on a picture of the cross-section of the laser-induced modification, the model shows a good convergence. The material inside the drop shaped area was exposed to temperatures higher than the melting point of LAS glass-ceramic. This could lead to a destruction or a displacement of the crystal seeds.

5. Experiments

5.1. Laser-Induced Modifications

Thirty flexural bending samples have been structured with five different parameter sets according to Figure 6. The exact values for every parameter set can be found in Table 2. The samples were mounted in a small vice and then moved through the laser focus by the CNC axis system.

Figure 5. Simulation of the maximum cycle temperature with isothermal lines.

Figure 6. Laser-induced continuous modifications inside LAS glass-ceramic bending samples.

Table 2. Parameter settings for the laser treatment of the LAS samples.

The feedrate vAxis and the pulse repetition frequency fPulse have not been changed to analyze the influence of the pulse energy Q0 and the density of the induced modifications. 13 samples have not been treated by laser but were crystallized with the same temperature profile to get a reference value.

5.2. SEM Analysis after Crystallization

Figure 7 shows a scanning electron microscopy (SEM) image of the polished and with hydrofluoric acid (HF) etched surface of the x − y plane after the crystallization of the samples for 90 minutes at 820˚C. The microstructure reveals a network of needle-like (whisker-shaped) interlocked crystals embedded in the glassy matrix. A cross-section through a laser-induced modification is clearly visible in the middle of the image (between the dashed lines).

In the area of the laser-induced modification, the needle-like crystals are much longer and thicker. This effect could be caused either by destruction or displacement of the crystal seeds in the molten state. Both approaches would

Figure 7. Laser-induced continuous modification inside LAS glass-ceramic - vAxis = 20 mm/s, fPulse = 50 kHz, Q0 = 30 μJ.

explain a reduced density of crystal seeds inside the laser treated area, which results in the growth of these longer and thicker crystals. The orientation of the crystals inside the laser treated area is more or less parallel to the y-axis. This leads to the hypothesis that the crystals grow from the interface between treated and untreated area.

Anmin et al. [17] have observed that an increase of the flexural strength depends on the size of these interlocked whisker-shaped β-spodumene crystals. By locally increasing the length and size of this β-spodumene crystal through laser radiation, an effect on the flexural strength is expected to be visible.

5.3. Four-Point Bending Flexural Strength

Figure 8 shows the single results of the four-point bending flexural strength tests according to DIN EN ISO 6872. For each parameter set the standard deviation around the mean value is indicated through error bars.

The results of the four-point bending flexural tests showed so far, that a laser treatment of nucleated samples is not increasing the average value significantly. A single sample of the group A1 reached a flexural strength of 295.2 Mpa. This effect suggests that a higher density of laser-induced modifications could increase the flexural strength.

6. Conclusions

It was possible to show that the treatment of nucleated LAS samples with USP laser radiation leads to a change in the microstructure after the crystallization process. A thermal simulation enabled an estimation of the temperature

Figure 8. Bending flexural strength of laser treated LAS glass-ceramic samples compared to reference samples without laser treatment.

distribution inside the laser-induced area. The correlation between the isothermal lines for the melting point of LAS and the cross-section of the laser-modified area indicate that the crystal seeds are destroyed or displaced during the laser treatment.

The destruction or displacement of the crystal seeds inside the laser-modified area leads to the growth of longer and thicker β-spodumene crystals. The orientation of the crystals seems to be perpendicular to movement direction of the laser focus. A dependency of the size of these β-spodumene crystals and the bending flexural strength was proven in previous papers, but first four-point bending flexural tests showed that it was not possible to increase the flexural strength significantly, even if some samples reached good values.

Conflicts of Interest

The authors declare no conflicts of interest.

Cite this paper

Senn, F. , Holtz, R. , Gross-Barsnick, S. and Reisgen, U. (2018) Influencing the Crystallization of Glass-Ceramics by Ultrashort Pulsed Laser Irradiation after Nucleation. New Journal of Glass and Ceramics, 8, 1-11. doi: 10.4236/njgc.2018.81001.

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