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Volume 3, Article 13
Raj Singh , RJ Barrett, JJ Gomes, Ferdynand P. Dabkowski
Laser Diode Manufacturing and Development, Polaroid Corporation
T.D. Moustakas
Department of Electrical and Computing Engineering and Center for Photonics Research, Boston University
C-plane sapphire substrates were coated with PECVD SiO2 and
photolithographically patterned with different size and shape openings.
Subsequently, these patterned substrates were introduced in a horizontal,
hot-wall quartz reactor for the GaN growth. It was observed that single crystal
GaN growth was preferentially initiated in the openings in the oxide layer.
This selective area growth was followed by epitaxial lateral overgrowth (ELO),
leading to the formation of hexagonal GaN prisms terminated in smooth, vertical
(100) facets. We have been successful in shearing these pyramid structures from
the sapphire substrates as individual devices, which do not require any
post-growth etching for feature definition. This procedure allows for the
dramatic reduction of the process complexity and the duration and expense for
GaN growth for device applications. Stimulated emission results on these
self-formed optical cavities are also presented.
In this paper, we report the selective area growth (SAG) of GaN directly on patterned (0001) sapphire substrates by the HVPE technique, thus eliminating an entire GaN growth sequence. The selective area growth leads to epitaxial lateral overgrowth (ELO) of the GaN on the patterned substrate. Bare sapphire substrates were coated with a silicon dioxide layer. The SiO2 was photolithographically patterned and etched to make selective area patterns on the sapphire substrate. These substrates were used for the ELO-GaN growth. The pattern was chosen in such a manner that coalescence between the individual GaN islands nucleated in the openings was not possible in the growth times employed for these samples. This allowed for the growth of segregated GaN structures, in the form of hexagonal pyramids, on these patterned substrates. These structures were studied by optical and scanning electron microscopy. Photoluminescence and optical pumping studies were also performed to characterize the ELO-GaN layers.
ELO-growth of GaN was carried out on patterned sapphire substrates. C-plane sapphire wafers were coated with 5000 Å of PECVD deposited SiO2. Subsequently, photolithography and wet etching were used to pattern the SiO2/sapphire wafers. A schematic of one of the mask patterns used in this study is shown in Figure 2. It consisted of 100 µm diameter circles centered on grid spacing of 500 µm. The oxide layer was etched to reveal the surface of sapphire under the circles. After chemical degreasing, the patterned substrates were mounted on a quartz holder and introduced in the growth chamber. They were thermally degassed at the growth temperature of 1050-1070 °C in a nitrogen ambient. After half an hour of degassing, ammonia was introduced for surface nitridation for 15 minutes. Subsequently, hydrogen chloride gas flow was started to initiate the growth of GaN. The duration of the growths was typically between 15 to 60 min. No intentional doping was used during the growth of the GaN layers reported in this study. The growth parameters were first optimized for GaN deposited on bare sapphire (unpatterned) substrates. Under these conditions, uniform coverage of the entire substrate by highly transparent GaN was obtained. The growth rate was controlled by the HCl flow rate and was typically between 15-25 µm/hr on unpatterned sapphire substrates.
After the growth, the samples were cooled to room temperature in a nitrogen stream. Visual inspection of the samples revealed that GaN had preferentially nucleated in the openings in the oxide layer. Polycrystalline deposits of GaN on the remaining portion of the masking dielectric layer were also observed. These samples were subsequently etched in a buffered oxide etch solution, resulting in the removal of the SiO2 masking layer as well as the polycrstalline GaN deposits.
Figure 4 shows the edge and top view of one of these hexagonal GaN islands. The mask pattern used for this particular sample consisted of 25 µm square openings on 500 µm centers. In plan view, two surface morphologies were observed on the top of the GaN pyramid. In the center region directly above the opening in the silicon dioxide layer, the surface morphology was rough and showed signs of coalescence of individual nuclei, which initiated on the sapphire surface. On the other hand, the laterally over grown material had a much more smoother morphology. However, the edge view revealed that the top of the epitaxial overgrowth region was not completely flat. The differences in the surface morphologies between the laterally overgrown and directly grown GaN were expected due to the difference in the defect structure. The edge view showed that the walls of the hexagonal structure were very smooth and perpendicular. No features were observable on the wall surfaces at higher (>100,000) magnification of the SEM.
Room temperature photoluminescence for a GaN pyramid structure is shown in Figure 5. The sample was excited with a 10mW He-Cd laser incident normally to the substrate surface. The emission was dispersed through a 0.5m spectrometer to obtain the wavelength scan. The room temperature PL spectrum showed the near band edge emission at 361 nm with a FWHM of 12.5 nm. No yellow luminescence was observed under these excitation conditions, attesting to the good material quality of the pyramid structure. The background electron concentration, for thick GaN films grown under similar conditions was determined by Hall effect measurements to be between 1017 to 1018 cm-3.
Room temperature optical pumping studies on these GaN hexagon structures were carried out using a focussed nitrogen laser pump at 337 nm with a peak power of 40 kW (10 ns pulse). Stimulated emission, as indicated by linewidth narrowing and red shift of the luminescence, was observed. The threshold of stimulated emission was at an incident power density of 3.4 MW/cm2. This value of threshold is significantly lower than that previously reported (30 MW/cm2) for similar structures prepared by the MOVPE method [5]. The peak of the stimulated emission was observed at 377.8nm with a FWHM of 1.2 nm, at twice the threshold pump intensity. Line width narrowing and the output emission power intensity as a function of incident power density are shown in Figure 6. The slope of the peak intensity versus power density increased by a factor of 172 above threshold. We expected to observe longitudinal lasing modes for these structures with smooth and parallel walls. However, the hexagonal structure does not have simple Fabry-Perot cavity modes and the power density of the pump varied greatly ( > 10%) over spectral collection time. Thus no longitudinal modes were observed.
Further improvements in the growth of ternary alloys and p-type doping of GaN
by the HVPE growth technique, coupled with the ELO-GaN growth will make it
possible to fabricate complete device structures without post-growth etching.
This will make it possible to fabricate atomically smooth laser mirror facets
in-situ, resulting in improved device performance. Specifically, the growth of
a-plane GaN (110) on r-plane sapphire (011
) will result in rectangular
features. This may be more suitable for the definition of in-situ rectangular
laser cavities.
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[5]T. Akasaka, Y. Kobayashi, S. Ando, N. Kobayashi, M. Kumagai, "Selective MOVPE of GaN and AlxGa1-xN with smooth vertical facets", Proc. Second Int. Conf. Nitride Semicond., Tokushima, Japan 490 (1997)
Figure 1. Schematic of the HVPE growth system for GaN selective area growth |
| Figure 3. SEM image of the selective area grown GaN pyramid structures. |
| Figure 5. Room temperature PL from a GaN film (unintentionally doped) grown by HVPE |
| Figure 6. Stimulated emission from the GaN hexagonal pyramid structure. Peak intensity and emission linewidth as a function of incident power density. |
© 1998 The Materials Research Society
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