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Monitoring and Controlling of Strain During MOCVD of AlGaN for UV Optoelectronics

Published online by Cambridge University Press:  13 June 2014

Abstract

The grown-in tensile strain, due to a lattice mismatch between AlGaN and GaN, is responsible for the observed cracking that seriously limits the feasibility of nitride-based ultraviolet (UV) emitters. We report in-situ monitoring of strain/stress during MOCVD of AlGaN based on a wafer-curvature measurement technique. The strain/stress measurement confirms the presence of tensile strain during growth of AlGaN pseudomorphically on a thick GaN layer. Further growth leads to the onset of stress relief through crack generation. We find that the growth of AlGaN directly on low-temperature (LT) GaN or AlN buffer layers results in a reduced and possibly controllable strain.

Type
Research Article
Copyright
Copyright © 1999 Materials Research Society

Introduction

Thus far the optoelectronic effort of the III-nitride community has focused primarily on InGaN-based visible light emitting devices for display and data storage applications [Reference Nakamura and Fasol1]. Most of these devices were grown on sapphire substrates with thick GaN layers of 2 to 4 μms inserted for improved structural and morphological quality. (Thick n-GaN layers are also required for low-resistive electrical injection.) The active region typically consists of (higher fraction) InGaN-based quantum wells (QWs) and (lower fraction) InGaN barriers for electrical confinement. Further electrical and optical confinement is attained through the use of wide bandgap AlGaN layers (Figure 1a). Substantial lattice mismatches, however, exist among the III-nitrides; the mismatches (in the in-plane lattice constant) of InN (a ∼ 0.354 nm) and AlN (a = 0.3112 nm) to the thick and presumably relaxed GaN (a = 0.3188 nm) layers are 11% compression and 2.4% tension, respectively [Reference Trampert, Brandt, Ploog, Pankove and Moustakas2]. So far most of the strain-related studies have focused on the optical [Reference Kisielowski, Kruger, Ruvimov, Suski, Ager, Jones, Liliental-Weber, Rubin, Weber, Bremser and Davis3] and structural [Reference Detchprohm, Hiromatsu, Itoh and Akasaki4] properties of thick GaN epilayers on sapphire or SiC substrates.

Figure 1. Schematic diagrams of a blue laser diode (a) and a UV LED (b). The indium-containing layers are labeled in blue and the AlGaN layers are colored in red. (c) Strain-thickness product along the growth direction for the structures of (a) (dashed line) and (b) (solid yellow line). InGaN layers tend to move the curve toward blue (compression) and AlGaN layers to red (tension).

A simple analysis of the state of strain energy, denoted here as strain-thickness product in Figure 1c, reveals the benefit of the alternating AlGaN/InGaN heterolayers (Figure 1a) in balancing the tensile and compressive components to avoid excessive strains and to maintain a pseudomorphic growth (dashed line in Figure 1c). Recently we have reported the growth and device operation of an AlGaN/GaN QW-based UV LED on a thick GaN layer [Reference Han, Crawford, Shul, Figiel, Banas, Zhang, Song, Zhou and Nurmikko5]. The use of various AlGaN confinement layers, in the absence of any InGaN layers (Figure 1b), results in a steep accumulation of grown-in tensile strain (solid line in Figure 1c). Indeed cracking was observed during fabrication of AlGaN/GaN UV LEDs with thick AlGaN barriers (Figure 2a). The presence of cracking causes a significant variation of current-voltage characteristics among the tested devices and contributes to a large leakage current under reverse-bias conditions (Figure 2b). It is worth noting that cracking of AlGaN layers on thick GaN has been reported previously [Reference Gfrorer, Schlusener, Harle, Scholz and Hangleiter6, Reference Perry, Bremser, Zheleva, Linthicum and Davis7].

Figure 2. (a) Top view of an etched circular mesa (100 μm diameter) showing the presence of a high density of cracks. (b) Diode I-V curves taken from various devices across the same cracked sample.

An additional complication arises for AlGaN grown on sapphire, the most common substrate of choice, as the sapphire (linear thermal expansion coefficient α ∼ 7.6×10−6 k−1) exerts a compressive strain to the AlGaN layers (α ∼ 5.6×10−6 k−1) during cool down which tends to mask the grown-in tensile strain due to lattice mismatch. Most of the post-growth ex-situ strain characterizations [Reference Li and Ni8-Reference Vennegues, Beaumont, Vaille and Gilbart13] would in this case measure a combination of a tensile stress due to lattice mismatch and a compressive component due to thermal expansion mismatch. In an attempt to isolate these two competing factors by directly probing the grown-in strain, we have employed an in-situ stress/strain monitor based on wafer-curvature measurement [Reference Hearne, Chason, Han, Floro, Figiel, Hunter, Amano and Tsong14]. In this paper we will report the monitoring and subsequent control of grown-in strain of AlGaN on sapphire using different buffer layer schemes.

Experiment

A high-speed (1200 rpm), inductively heated, rotating disk reactor (RDR) was used to deposit GaN films (nominally 1-3 μm thick) onto 2” diameter, 330 μm thick, (0001) sapphire wafers. Trimethylgallium, trimethylaluminum, and ammonia where used as the precursors, with hydrogen as the carrier gas. A detailed description can be found in Ref. [Reference Han, Ng, Biefeld, Crawford and Follstaedt15]. A two-step deposition process was used. Initially, a LT buffer of GaN (∼550oC) or AlN (∼600oC) was grown. The buffer was then heated to 1050oC and stabilized for 1 minute prior to deposition of the high temperature (HT) layer.

Real time wafer curvature measurements were performed with a multi-beam optical stress sensor (MOSS) [Reference Taylor, Barlett, Chason and Floro16] modified for use on our reactor. To determine the wafer curvature, the divergence of an array of initially parallel laser beams is measured on a CCD camera after reflection of the array from the film/substrate surface. Changes in wafer curvature induce a proportional change in the beam spacing on the camera. This technique provides a direct measurement of the stress during deposition and is described in detail in Ref. [Reference Floro, Chason, Lee, Twesten, Hwang and Freund17].

The relation between film stress (σf), and substrate curvature (κ), is given by Stoney’s equation [Reference Doerner and Nix18],

(1)

hf and hs are the film and substrate thickness, respectively and Ms is the substrate biaxial modulus. Curvature is directly proportional to the product of the film stress and film thickness (σfhf ), both of which vary, in general, during growth. Equation 1 can be derived by balancing the forces and bending moments in the film with those in the substrate, and assuming the film is much thinner then the substrate [Reference Doerner and Nix18]. We also simultaneously obtain information on the surface roughness and film thickness during deposition by monitoring the intensity of one of the reflected laser beams, similar to the method described in Ref. [Reference Ng, Han, Biefeld and Weckwerth19].

Results and Discussion

Figure 3 shows the stress-thickness product (σfhf ) and the reflected beam intensity as functions of growth time (see the following explanation) during growth of an AlGaN (Al∼15%) layer on a 0.6 μm GaN layer grown at 1050°C. We have reported that [Reference Ng, Han, Biefeld and Weckwerth19] in-situ reflectance could provide the information of growth rate from the periodicity of Fabry-Perot interference. Such information in turn enables the conversion of time axis into film thickness (hf ). On a plot of σfhf versus hf , the slope is simply the grown-in stress (σf ). A positive slope on such a plot denotes a tensile stress throughout this paper.

Figure 3 Stress-thickness product and reflectance versus thickness during growth of AlGaN (Al∼0.15) on a 0.6 μm GaN layer

A slight slope of the σfhf curve during GaN growth (in Figure 3) was observed which suggests the presence of a slight tensile stress. The grown-in stress of GaN on sapphire is the subject of another publication [Reference Hearne, Chason, Han, Floro, Figiel, Hunter, Amano and Tsong14]. After a growth transition in adjusting the reactor parameters for the growth of AlGaN (an artifact of an abrupt decrease in the σfhf curve was therefore generated), a steady slope of 1.33 GPa was established which agrees well with the expected value assuming a pseudomorphic growth. After the growth of approximately 0.6 μm of AlGaN, however, a step decrease of the σfhf curve was recorded. Tentatively this feature is designated to be the relief of grown-in tensile stress due to the occurrence of cracking. (Cracking was indeed observed from Nomarski microscopy.) One implication is that the use of a thick GaN bottom layer, a common practice shared by the InGaN-based heterostructures, could lead to a build-up of excessive tensile strain in the case of AlGaN-based heterostructures for UV optoelectronics.

Direct growth of AlGaN on sapphire via LT buffer layers becomes attractive as a means to circumvent and alleviate the mismatch-induced tension imposed inevitably by the two-dimensional growth mode (i.e. AlGaN on a HT GaN layer). In Figures 4 and 5, σfhf and reflectance versus thickness are presented for the growth of AlGaN (Al∼17% in both cases) on LT GaN and AlN buffer layers, respectively, on sapphire substrates. Even though a tensile stress (0.82 GPa) was still measured for AlGaN on LT GaN buffer (Figure 4), it is interesting to note that this value is less than half of the expected stress due to the mismatch between Al0.17Ga0.83N and GaN. One could speculate that the conventional, mismatch-induced strain constraint is somewhat relaxed under a possibly three-dimensional island growth mode.

Figure 4 Stress-thickness product and reflectance versus thickness during growth of AlGaN (Al∼0.17) directly on a LT GaN buffer on sapphire

Figure 5 Stress-thickness product and reflectance versus thickness during growth of AlGaN (Al∼0.17) directly on a LT AlN buffer on sapphire

In the case of direct growth of AlGaN on a LT AlN buffer (Figure 5), the σfhf curve first moves downward, indicative of a compressive stress, before assuming a relatively flat (stress free) growth mode. The origin of the compressive strain during the initial growth of Al0.17Ga0.83N is currently under investigation. A plausible cause is that the AlN nucleation template has a smaller lattice constant than that of AlGaN. The compressive stress was estimated to be around 1.3 GPa, much less than the full mismatch between Al0.17Ga0.83N and AlN (around 9 GPa).

Conclusions

Using a novel in-situ stress monitor, we measured the grown-in strain of AlGaN on various layers. It was found that AlGaN grown on a thick HT GaN layer has a tensile strain well predicated by the pseudomorphic lattice mismatch before strain relaxation occurs. Growth on a LT GaN buffer layer resulted in a relaxation of more than 50% of the coherent tensile strain. The use of a LT AlN buffer caused a compressive strain during the initial (first 0.1 μm) growth of AlGaN. The combination of LT GaN and AlN buffer schemes could lead to the control of strain during AlGaN growth for UV optoelectronics.

The authors gratefully acknowledge valuable interaction with H. Amano (Meijo University, Japan). Technical assistance by T. Kerley and J. Hunter is also acknowledged. Sandia is a multiprogram laboratory, operated by Sandia Corporation, a Lockheed Martin company, for the United States Department of Energy, under contract DE-AC04-94AL85000.

Footnotes

MRS Internet J. Nitride Semicond. Res. 4S1, G7.7 (1999)

References

For a review, see Nakamura, S. and Fasol, G., The Blue Laser Diode, Springer-Verlag, Berlin (1997).CrossRefGoogle Scholar
Trampert, A., Brandt, O., and Ploog, K. H., Gallium Nitride (GaN) I, edited by Pankove, J. I. and Moustakas, T. D., Academic Press, San Diego (1998), p167.Google Scholar
For example, Kisielowski, C., Kruger, J., Ruvimov, S., Suski, T., Ager, J. W. III, Jones, E., Liliental-Weber, Z., Rubin, M., Weber, E. R., Bremser, M. D., and Davis, R. F., Phys. Rev. B 54, 17745 (1996).CrossRefGoogle Scholar
Detchprohm, T., Hiromatsu, K., Itoh, K., and Akasaki, I., Jpn. J. Appl. Phys. 31, L1454 (1992)CrossRefGoogle Scholar
Han, J., Crawford, M. H., Shul, R. J., Figiel, J. J., Banas, M., Zhang, L., Song, Y. K., Zhou, H., and Nurmikko, A. V., Appl. Phys. Lett, 73, 1688 (1998)CrossRefGoogle Scholar
Gfrorer, O., Schlusener, T., Harle, V., Scholz, F., and Hangleiter, A., Mat. Res. Soc. Symp. Proc. 449, 429 (1997)CrossRefGoogle Scholar
Perry, W. G., Bremser, M. B., Zheleva, T., Linthicum, K. J., and Davis, R. F., Thin Solid Films 324, 107 (1998).CrossRefGoogle Scholar
Li, W., Ni, W., Appl. Phys. Lett. 68, 2705 (1996).CrossRefGoogle Scholar
Leszczynski, M., Suski, T., Teisseyre, H., Perlin, P., Grzegory, I., Jun, J., Porowski, S., J. Appl.Phys 76, 4909 (1994).CrossRefGoogle Scholar
Kozawa, T., Kachi, T., Kano, H., Nagase, H., Koide, N., Manabe, K., J. Appl. Phys. 77, 4389, (1995).CrossRefGoogle Scholar
Skromme, B., Zhao, H., Wang, D., Kong, H., Leonard, M., Bulman, G., Molnar, R., Appl. Phys.Lett. 71, 829 (1997)CrossRefGoogle Scholar
Lee, I., Choi, I., Lee, C., Noh, S., Appl. Phys. Lett. 71,1359, (1997)CrossRefGoogle Scholar
Vennegues, P., Beaumont, B., Vaille, M., Gilbart, P., J. of Crystal Growth, 173, 249 (1997).CrossRefGoogle Scholar
Hearne, S., Chason, E. E., Han, J., Floro, J. A., Figiel, J., Hunter, J., Amano, H., Tsong, I., Appl. Phys. Lett. 74, 356 (1999)CrossRefGoogle Scholar
Han, J., Ng, T. B., Biefeld, R. M., Crawford, M. H., Follstaedt, D. M., Appl. Phys. Lett, 71, 3114 (1997)CrossRefGoogle Scholar
Taylor, C., Barlett, D., Chason, E., Floro, J. A., Ind. Physicist 4, 25 (1998)Google Scholar
Floro, J., Chason, E., Lee, S., Twesten, R., Hwang, R., Freund, L., J. Elec. Mat. 26, 969 (1997)CrossRefGoogle Scholar
Doerner, M. and Nix, W., CRC Critical Reviews in Sol. State and Mat. Sci. 14, 224, (1988).Google Scholar
Ng, T. B., Han, J., Biefeld, R. M., and Weckwerth, M. V., J. Electron. Mat. 27, 190 (1998).CrossRefGoogle Scholar
Figure 0

Figure 1. Schematic diagrams of a blue laser diode (a) and a UV LED (b). The indium-containing layers are labeled in blue and the AlGaN layers are colored in red. (c) Strain-thickness product along the growth direction for the structures of (a) (dashed line) and (b) (solid yellow line). InGaN layers tend to move the curve toward blue (compression) and AlGaN layers to red (tension).

Figure 1

Figure 2. (a) Top view of an etched circular mesa (100 μm diameter) showing the presence of a high density of cracks. (b) Diode I-V curves taken from various devices across the same cracked sample.

Figure 2

Figure 3 Stress-thickness product and reflectance versus thickness during growth of AlGaN (Al∼0.15) on a 0.6 μm GaN layer

Figure 3

Figure 4 Stress-thickness product and reflectance versus thickness during growth of AlGaN (Al∼0.17) directly on a LT GaN buffer on sapphire

Figure 4

Figure 5 Stress-thickness product and reflectance versus thickness during growth of AlGaN (Al∼0.17) directly on a LT AlN buffer on sapphire