Abstract
Using a CO2 laser-equipped electromagnetic levitator, we carried out the containerless crystallization of Si and Ge. From the point of interface morphologies, the relation between growth velocities and undercoolings was classified into three regions. In regions I and II, although the morphologies of growing crystals are different: plate-like needle crystals in region I and facetted dendrite at region II, the growth velocities in these two regions are fundamentally scaled by the thermal diffusivities and the temperature increase caused by the release of the latent heat. This result means that the growth velocity can be expressed by the product of the thermal diffusivity and the growth kinetics. An analysis of the dendrite morphologies revealed that the kinetics of crystal growth in regions I and II represent two-dimensional nucleation at the reentrant corner formed at the edge of the two parallel twins. In region III, thermal diffusion-controlled interface attachment kinetics control as described by a modified Wilson–Frenkel model.
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Introduction
In recent years, with advances in levitation techniques, research on solidification into the undercooled melt1,2 has brought new insight into the formation of metastable structures. Also, with the increase of solar power utilization, industry has shown interest in developing a process to form spherical crystals of Si for solar cell applications.3 In order to manufacture the spherical crystals, drop-tube processing is commonly employed as the mass-production method of choice. Here, the melt is ejected into a drop tube and the stream breaks up into numerous droplets that then solidify during free fall. This process is very simple; however, the yield of high-quality crystals that are suitable for use in solar cells is much lower than that achieved using conventional crystal growth techniques such as Czochraiski (CZ) and Bridgeman methods. The reason for this disadvantage can be simply attributed to the fact that the nucleation and growth of crystals during free fall cannot be monitored. In order to solve this problem, Aoyama, Takamura, and Kuribayashi (hereafter referred to as ATK)4 carried out a series of experiments using an electromagnetic levitation furnace equipped with a high-speed video camera, and they elucidated that the crystallization process is distinguished into three regions: In region I, which is under relatively low undercooling less than 100 K, plate-like needle crystals appear. In region II under medium undercooling, from 100 K to 200 K, facetted dendrites appear. In region III larger than 200 K, the crystal–melt interface macroscopically looks flattened, indicating that the microstructure was significantly refined. In addition, analyzing the relation between undercooling ΔT and the growth velocity V on the basis of a dendrite growth model incorporating linear kinetics,5 ATK reported that the kinetic coefficient μ is 0.4 m/sK. However, Watanabe, Nagayama, and Kuribayashi (WNK),6 based on precise measurement of the crystallization process for levitated droplets, reported that the crystal growth kinetics in regions I and II are not a linear function, but rather they showed an exponential increase, thus implying that the rate-controlling kinetics are not interface attachment but rather two-dimensional (2-D) nucleation. There remain inconsistencies in that the morphology of the crystal-melt interface in region I is quite different from that in region II. Furthermore the relation between ΔT and V, particularly in region II, appears too deviated for the rate-controlling kinetics to be determined. The current investigation unifies the interpretation of containerless crystallization of semiconducting materials by expanding the analysis to include both Ge and Si to resolve remaining inconsistencies.
Experimental Procedure
Containerless crystallization experiments on pure samples of Ge and Si were carried out by using a CO2 laser-equipped electromagnetic levitator (EML) shown schematically in Fig. 1. Except for several samples that unintentionally nucleated spontaneously, nucleation of crystals was forced by application of a trigger-needle of molybdenum at the predetermined undercooling. The growth velocity was measured using a high-speed video camera (HSV) with a maximum sampling rate of 640,000 frames/s; the Si-camera was color video, whereas the Ge-camera was monochrome. The temperature of the levitated samples was measured with a monochromatic pyrometer. Since the emissivity of the solid phase of Si and Ge greatly differs from those of the liquid phase, the emissivity was adjusted so that the temperature of the liquid phase after the recalescence indicated the equilibrium melting temperature (Fig. 2). In order to elucidate the relationship between the microstructure and the rate-determining process, the melt was dropped onto an optically polished silicon plate and then solidified under controlled temperature conditions. The resulting surface morphology was analyzed posttest with a laser-scanning microscope.
Results
Figure 3 shows the selected HSV images of Si taken during recalescence, where ΔT is the bulk undercooling just before the recalescence.6 The dark and bright areas show the undercooled melt and the solidified region, respectively. In Fig. 3a, typical HSV images taken successively at low undercooling, ΔT = 37 K, show the anisotropic line-shaped pattern that forms a circumferential ring on the surface of the sample. Note that this ring is discontinuous suggesting that the line-shaped crystal is not a “line” crystal but rather a plate-like crystalline structure that penetrates the interior of the sample. When the undercooling is larger than 100 K, facetted dendrites appear as seen in Fig. 3b. At an intermediate undercooling, however, not only facetted dendrites but also a mixed-mode of facetted dendrites and line-shaped crystals are observed as shown in Fig. 3c. In these images, the solidification front initially advances massively, and subsequently line-shaped crystals protrude from facetted dendrites showing a mixed mode of both morphologies.
In Ge, the morphological transition with an increase in undercooling is similar to that of Si: that is, at low, medium and intermediate undercoolings, plate-like needle crystals, facetted dendrites and a mixed-mode of facetted dendrites and plate-like needle crystals form, respectively, as seen in Fig. 4.
Figure 5 shows the relations between V and ΔT for both Si and Ge. Although the growth velocities of Si present a curve of near-quadratic shape when plotted as a function of ΔT, in Ge the relation deviates from that of Si at undercoolings larger than 100 K. WNK6 reported that the Si crystal growth kinetics at low and medium undercooling is not due to interface attachment but 2-D nucleation as given by Eq. 1.
where β, ε, and ΔT k are the rate for atoms to be incorporated into interface, the energy barrier for nucleation and growth of a crystal, and the kinetic undercooling at the crystal–melt interface, respectively. In Ge, on the other hand, introducing the threshold undercooling ΔT th, Ishibashi, Nagayama and Kuribayashi (INK)7 reported that at undercoolings larger than 100 K the growth velocities is well expressed by linear kinetics described by Eq. 2.
It is readily apparent that there is an inconsistency in behavior when comparing the V versus ΔT of Ge to that of Si, although both are typical semiconducting material that belong to Group IV. In order to resolve this inconsistency, it is desirable to normalize the data into dimensionless variables. Figure 6 shows the relation between the dimensionless growth velocity \( \tilde{V} \) and dimensionless undercooling \( \Updelta \tilde{T} \) given by Eqs. 3 and 4.
and
where α, a, C P, and ΔH f, which are listed in Table I, are the thermal diffusivity, the interatomic distance, the heat capacity under the constant pressure, and the heat of fusion, respectively. Of particular importance is the observation that in regions I and II for both Si and Ge, crystal growth into undercooled melt can be scaled by the thermal diffusivity and the temperature increase caused by the release of latent heat, although the crystal morphology distinctly changed from the plate-like needle crystals in region I to the facetted dendrites in region II. This result implies that the growth velocities in regions I and II are proportional to the product of the thermal diffusive speed V T and the kinetics term as a function of Gibbs free energy difference between crystal and melt ΔG. Therefore, if the linear approximation for the free energy difference ΔG = ΔH fΔT/T m (T m is the equilibrium melting temperature) is used and the kinetic term is given by a linear function of the undercooling, then the relationship between the growth velocity and the undercooling is readily described by a modified Wilson–Frenkel law8,9 at low undercoolings.
On the morphological characterization of the growing crystal in semiconducting material, Lau and Kui,10 carrying out the quasi-containerless crystallization in Ge, in which the melt was surrounded by oxide flux, reported that the twin-related 〈110〉 and 〈211〉 dendrites appear at low and medium undercoolings, and the twin-free 〈100〉 dendrites are at high undercooling ΔT > 93 K. Furthermore, Leung and Kui,11 extending their containerless technique to Si, reported the similar results: at low and medium undercooling, twin-related 〈110〉 and 〈211〉 dendrites and at high undercooling, twin-free 〈100〉 dendrites. Their conclusion is very clear, but the electron-micrographs that were used as the evidence for their conclusions are obscure. On this point, Nagashio and Kuribayashi,12 on the basis of scanning electron microscopy electron backscatter diffraction pattern analysis, showed that the crystallographic features of Si: 〈110〉 dendrites are grown under the twin-related reentrant corner mechanism, and 〈100〉 dendrites are under the twin-free nucleation and growth mechanism. Thus, the growth directions of primary and secondary arms of the 〈110〉 dendrites are 〈110〉, and those of the 〈100〉 dendrites are 〈100〉 and 〈110〉. On referring to their results, it appears that the plate-like needle crystal corresponds to 〈110〉 dendrites.
Figure 7 shows the typical images of facetted dendrites of Ge: (I) solidified by dropping onto an optically polished silicon plate at ΔT = 151 K showing the 〈100〉 dendrite of four-fold symmetry, and (II) solidified at the equilibrium melting temperatures showing the twin-related 〈110〉 dendrite. Each image was taken by a laser-scanning microscope. In containerless levitation experiments using a drop-quench technique, the 〈211〉 dendrites have not been observed in Ge although Lau and Kui reported that those were formed within the range 60 K < ΔT < 90 K. However, the morphology of the 〈211〉 dendrite that they present is different from that of the Billig’s 〈211〉 dendrite13 and the azimuth relation between triangular etch-pit on the surface and the stem of the dendrite is also different from that of the 〈211〉 dendrite. Furthermore, it was reported that the growth of the 〈211〉 dendrite would be caused by an impurity effect due to the presence of the oxide flux.14 For formation of 〈211〉 dendrites some geometrical restrictions such as unidirectional pulling at very low undercooling are required because multiple interactions among 2-D nuclei on three adjoining reentrant corners are required for the 〈211〉 dendrite to be formed. For the 〈110〉 dendrites only, a single interaction between 2-D nuclei is required on adjacent reentrant corners.15 Finally, in Si and Ge, the direction of the interface stiffness minimum corresponds to that of the interface free energy maximum, that is, 〈100〉,16 and dendrites are known to grow preferentially in the direction of the interface stiffness minimum.8
Discussion
As mentioned above, WNK reported that the rate-controlling kinetics for crystal growth in regions I and II for Si is not linear, which would imply interface attachment kinetics, but rather exponential in character, which would indicate 2-D nucleation and growth is controlling. INK also reported the similar result in Ge. Based on these results, the growth velocities of semiconducting material previously expressed in Eq. 1 can be modified to a new form as seen in Eq. 6.
where β′ is the adhesive probability for atoms that are adhered on the surface to be incorporated into the crystal lattice. In fact, the relation between the growth velocity and the undercooling in Ge, which was presented by Hamilton and Seidensticker,17 implied that the crystal growth kinetics is not due to linear kinetics because if the crystal growth is expressed in this manner, the growth velocity is inversely proportional to the spacing between two parallel twins (see Appendix).
At region III, which corresponds to the undercooling larger than approximately 100 K in Ge and 200 K in Si, the growth kinetics is seen to be the linear in character. Figure 8 shows a micrograph of a section of Si solidified at ΔT = 292 K.18 In this experiment, a small amount of boron was doped to accentuate the contrast of the interface of the initially formed dendrite. In this figure, cross-like morphologies show the fragments broken up from the initially formed dendrite due to the capillary force that acts on the interface. The fourfold axial symmetry of the fragments indicates that the initial growth direction indicates formation of 〈100〉 dendrites. Nagashio et al.18 reported that in Si when the undercooling exceeds 100 K, fragmentation of dendrites occurs resulting in significant grain refinement with increase of undercooling until ΔT > 200 K when grain size becomes relatively constant. This effect is due to the cross-like fragments acting as a “seed” for new grains. If the surfaces of the primary and secondary dendrite arms are assumed to consist of {111} planes, then the interfacial energy of which is minimum, the surface morphology of the 〈100〉 dendrite arms should appear as a wavy pattern that consists of paired chevron and groove couples, whereas that of 〈110〉 dendrite is flat and parallel to the dendrite axis. Therefore, in 〈100〉 dendrites, the arms characterized by the wavy pattern are easily broken. At undercoolings higher than this, dendrite breakup will occur and observed growth velocities would deviate downward from the prediction using the dendrite growth model, due to the interference caused by the overlapping diffusion fields built up around the fragmented dendrites. Thus, the apparent diffusion length d d = α/V is elongated. Furthermore, electro-magnetic stirring facilitates dendrite fragmentation.19 On the other hand, Devaud and Turnbull,20 and Lau and Kui reported that in Ge the grain refinement occurred at ΔT > 300 K and ΔT ~ 230 K. This is because for Ge the value of \( \tilde{V} \) at \( \Updelta \tilde{T} > 0.15 \) differs from that of Si.
In the previous section, we showed that the crystal growth velocities at regions I and II in both Si and Ge are expressed by the thermal diffusion-controlled growth model. It is common to evaluate growth of other nonsemiconductor pure materials using the “Collision-limited growth model.”21 The reason for this is that in the atomic diffusion-controlled growth model, a diffusive velocity given by V D = D/a (D is the self-diffusion coefficient) is at most 10–20 m/s, which is much less than the growth velocities measured in pure Ni samples.22 However, the growth velocity predicted by the collision-limited growth model is much larger than that simulated by molecular dynamics and density-functional theory.23 We must use the diffusion-controlled growth model because for semiconductors, the larger entropy difference between the melt and the crystal requires a massive scale of the thermal diffusion from the interface to the undercooled melt.
Conclusion
Using Si and Ge as the model material, we carried out the undercooled solidification of the semiconducting material. From the point of the interface morphologies, the relation between growth velocities and undercoolings was classified into three regions. The morphologies of the growing crystals at regions I, II, and III are plate-like needle crystals, facetted dendrites, and massive dendrites, respectively. Normalization of the relation between growth velocities and undercoolings into dimensionless quantities revealed that the growth velocities in regions I and II can be scaled by the thermal diffusivity and the temperature increase caused by the release of the latent heat, indicating that the growth velocities are proportional to the product of the thermal diffusive speed and the kinetics term as a function of Gibbs free energy difference. Analyzing the growth velocities on the basis of this dendrite growth model, it was found that at low undercooling, the rate-controlling process is two-dimensional nucleation kinetics, and at high undercooling thermal diffusion-controlled interface attachment kinetics.
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Appendix
Appendix
If the tip of a growing crystal can be assumed to be hemispherical in shape, then the diffusion equation at the steady state for heat conduction into undercooled melt is expressed by
where T(r) is the temperature at r, the distance from the centroid of the tip. If the boundary condition is given by T = T ∞ at r = ∞, then T(r) is expressed by
If the growth velocity is assumed to be proportional to the temperature gradient and also undercooling at the crystal-melt interface, r = r i , then the growth velocity is given by
Therefore the constant of integration A is expressed by
where l k is a kinetics length given by \( l_{k} = {{C_{\text{P}} \alpha } \mathord{\left/ {\vphantom {{C_{\text{P}} \alpha } {\mu \Updelta H_{\text{f}} }}} \right. \kern-\nulldelimiterspace} {\mu \Updelta H_{\text{f}} }} \) and Γ is Gibbs-Thomson coefficient \( \Upgamma = {\gamma \mathord{\left/ {\vphantom {\gamma {\Updelta S_{\text{f}} }}} \right. \kern-\nulldelimiterspace} {\Updelta S_{\text{f}} }} \). Then the thermal diffusion-controlled crystal growth velocity into the undercooled melt is given by
where r i , l k , and \( r_{n}^{*} \) are the tip radius, kinetic length given by \( r_{n}^{ * } = {{2\gamma } \mathord{\left/ {\vphantom {{2\gamma } {\Updelta S_{\text{f}} \Updelta T_{k} }}} \right. \kern-\nulldelimiterspace} {\Updelta S_{\text{f}} \Updelta T_{k} }} \).
In the case of the crystal growth based on the twin-related reentrant corner growth model, r i can be assumed to be less than the spacing between two parallel twins. Therefore, Eq. A5 can be approximated by
because r i ≫ l k and r i ≫ \( r_{n}^{*} \). Thus, the growth velocity is inversely proportional to the spacing between two parallel twins.
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Ishibashi, Y., Kuribayashi, K. & Nagayama, K. Rapid Crystallization of Levitated and Undercooled Semiconducting Material Melts. JOM 64, 1102–1108 (2012). https://doi.org/10.1007/s11837-012-0423-0
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DOI: https://doi.org/10.1007/s11837-012-0423-0