Study on the nitridation of β-Ga2O3 films
Cheng Fei1, Li Yue-Wen1, Zhao Hong1, †, Xiu Xiang-Qian1, 2, ‡, Jia Zhi-Tai2, Liu Duo2, Hua Xue-Mei1, Xie Zi-Li1, Tao Tao1, Chen Peng1, Liu Bin1, Zhang Rong1, §, Zheng You-Dou1
Key Laboratory of Advanced Photonic and Electronic Materials, School of Electronic Science and Engineering, Nanjing University, Nanjing 210093, China
State Key Laboratory of Crystal Materials, Shandong University, Jinan 250100, China

 

† Corresponding author. E-mail: zhaohong@nju.edu.cn xqxiu@nju.edu.cn rzhang@nju.edu.cn

Abstract

Single-crystal GaN layers have been obtained by nitriding β-Ga2O3 films in NH3 atmosphere. The effect of the temperature and time on the nitridation and conversion of Ga2O3 films have been investigated. The nitridation process results in lots of holes in the surface of films. The higher nitridation temperature and longer time can promote the nitridation and improve the crystal quality of GaN films. The converted GaN porous films show the single-crystal structures and low-stress, which can be used as templates for the epitaxial growth of high-quality GaN.

1. Introduction

GaN-based nitrides have been widely used in optical devices and high power or high temperature microelectronic devices.[13] However, one of the main problems for high quality GaN growth is lack of a suitable lattice-match substrate. Foreign substrates, such as sapphire and Si, bring about a large number of defects in GaN epilayers, although they are the most popular substrates.[4,5] The ideal substrate would be GaN for the homoepitaxy.

β-Ga2O3 is an ultra-wide band gap semiconductor and has excellent properties, such as high transparency in the region from visible to UV regions, high electrical conductivity and thermal stability at high temperature.[68] The lattice mismatch between GaN and β-Ga2O3 is relatively small, as low as 2.6%.[9] So, β-Ga2O3 can also be applied as a substrate for GaN epitaxial growth.[10,11] It has been reported that the (100) cleavage plane of β-Ga2O3 undergoes a surface reconstruction under nitridation at high temperature and NH3 gas, which causes the surface to match GaN naturally.[12] The surface of β-Ga2O3 film can be nitridated to acquire good lattice-matching of GaN for the direct growth of GaN. And, GaN films converted from β-Ga2O3 by nitridation with NH3 can be also used as a substrate or template for GaN homogeneous epitaxial growth. In this work, we report the influences of temperature and time on the nitridation to better understand the process.

2. Experimental details

The 2-inch (1 inch = 2.54 cm) β-Ga2O3 films have been grown by self-made halide vapor phase epitaxy (HVPE) system.[13] The as-grown β-Ga2O3 is transparent and smooth, the surface roughness is about 6.2 nm obtained by the analysis of atomic force microscope. The as-grown β-Ga2O3 films have been cut into 1 cm for the nitridation process. The nitridation of β-Ga2O3 films has been carried out in a quartz tube furnace with the NH3 flow rate of 200 sccm at different temperatures and times, respectively. After nitridation, all the samples exhibit yellowish and translucent. The surface morphologies were studied by scanning electron microscopy (SEM, JSM-700 F). The structural properties were measured by means of high-resolution x-ray diffraction (XRD, BRUKER-D8) and Raman spectroscopy (Raman, OLYMPUS-BX41).

3. Results and discussion
3.1. Analysis of nitridation temperature

Figure 1 shows the surface morphologies of β-Ga2O3 film and as-nitridated films at different temperatures for 0.5 h. The scanning electron microscopy images randomly observed at different areas indicate that the surface morphology of as-nitridated film is similar and uniform. It can be seen that lots of holes appear in the surface after nitridation. In the higher magnification, the surface consists of lots of hillock pits, showing a stratified or sheet structure. The rough surface may be due to the nitridation of β-Ga2O3 at NH3 atmosphere, and the β-Ga2O3 decomposed into GaO, Ga2O, and Ga, releasing O2 simultaneously.[14] More tiny hillock pits appear obviously in the surface of sample with increasing the temperature. When the nitridation temperature is up to 1000 °C and above, the β-Ga2O3 film is nitridated heavily and show a porous network structure. The decomposition and nitridation of β-Ga2O3 at high temperature may results in the porous layer.[15] The density and diameter of the hillock pits increased as the nitridation temperature was increased from a temperature range of 850 °C–1050 °C due to the enhancement of the β-Ga2O3 decomposition rate.[16]

Fig. 1. The SEM images of β-Ga2O3 film and the samples after nitridation at different temperatures for 0.5 h. The insets are SEM images in the higher magnification.

The XRD patterns ( scan) of β-Ga2O3 film and as-nitridated films at different temperatures for 0.5 h are exhibited in Fig. 2. The XRD peaks at 18.84°, 38.3°, 58.98° correspond to diffractions from the (-201), (-402), (-603) planes of β-Ga2O3, respectively.[17] When the nitridation temperature is 850 °C, the peaks of β-Ga2O3 are dominant and a weak peak for the GaN (002) reflection occurs at 34.4°.[18] It indicates that β-Ga2O3 have been converted partly to GaN at 850 °C. The intensity of GaN (002) diffraction peak gradually increases and the full width at half maximum (FWHM) decreases with the increasing nitridation temperature. Conversely, the intensity of peaks belonging to β-Ga2O3 gradually decreases. After a further increase of the nitridation temperature to 1000 °C, the diffraction peaks belonging to β-Ga2O3 entirely disappear and only a high intense single sharp XRD peak corresponding to GaN (002) plane dominates. XRD results reveal that the crystalline quality of the formed GaN increases with increasing nitridation temperature and the GaN films have a preferential orientation along (002) direction.

Fig. 2. XRD patterns of β-Ga2O3 film and the samples after nitridation at different temperatures for 0.5 h.

Raman spectra has been measured at room temperature by using an argon ion laser (** nm). Figure 3(a) illustrates the Raman spectra of β-Ga2O3 film and as-nitridated films at different temperatures for 0.5 h. For β-Ga2O3, eight Raman peaks were observed with no blue shift as compared to the bulk Raman peaks.[19] After nitridation at 850 °C, the Raman spectra shows no obvious changes, expect a slight reduction of the peak intensity. For β-Ga2O3 films nitridated at 950 °C and 1000 °C, the phonon modes related to β-Ga2O3 are diminished and the Raman peaks corresponding to GaN at 142 cm−1, 422 cm−1, 568.8 cm−1, and 734 cm−1 evolved. The Raman peak at 568.8 cm−1 for the E2 (high) phonon mode of GaN shows a slight blue-shift as compared to the standard Raman spectra of bulk GaN crystal,[2022] which may results from lattice strain by the conversion from β-Ga2O3 to GaN. During the nitridation process, the N atoms decomposing from NH3 would replace the O atoms in Ga–O6 or Ga–O4 bond configurations to form Ga–N4 or Ga–N6 bond configurations. And the Ga–N6 bond configuration is unstable and will spontaneously convert to more stable Ga–N4 bond configuration.[23] So the strain may be caused by the incomplete conversion with the short nitridation time, and enough nitridation time would promote the complete transformation which is verified by the effect of the nitridation time below. And the intensity of the Raman peak corresponding to GaN gradually increases with the increase of nitridation temperature. Raman analyses further confirm that the surface of β-Ga2O3 films has converted to GaN. Figure 3(b) shows the change in Raman peak intensity of the A3g phonon mode of β-Ga2O3 and the E2 (high) phonon mode of GaN, respectively. The slope of the fold lines at 950 °C–1050 °C indicates that high temperature accelerates the conversion from β-Ga2O3 to GaN. The efficient conversion of the β-Ga2O3 to GaN can be achieved at nitridation temperature of 1050 °C.

Fig. 3. Raman spectra of β-Ga2O3 film and the samples after nitridation at different temperatures for 0.5 h (a) and the curve of Raman peak intensity of the Ga2O3-A3g mode and the GaN-E2 (high) mode with the nitridation temperature (b).
3.2. Analysis of nitridation time

Figure 4 shows the SEM images of as-nitridated β-Ga2O3 films at 1050 °C for different times. As the nitridation time is increased from 0.5 h to 3 h, the density and diameter of the hillock pits in the surface increase due to the enhancement of the β-Ga2O3 decomposition. And a porous network layers forms obviously in the surface of sample after the nitridation. The above may result from that the β-Ga2O3 film is dissociated and converted to GaN under NH3 atmosphere.

Fig. 4. The SEM images of β-Ga2O3 films after nitridation at 1050 °C for different times. The insets are SEM images in the higher magnification.

Figure 5(a) shows the XRD patterns of as-nitridated β-Ga2O3 films at 1050 °C for different times. As is shown in Fig. 5(a), the XRD patterns contain strong diffraction peaks corresponding to GaN (002). And there are two weak peaks corresponding to β-Ga2O3 in the sample nitridated at 1050 °C for 1 h and 2 h. The appearance of β-Ga2O3 peaks possibly be ascribed to the emerging non-surface layer of the β-Ga2O3 film by nitridation. The XRD results reveal that the converted GaN films have a preferential orientation along (002) direction.

Fig. 5. XRD patterns of β-Ga2O3 films after nitridation at 1050 °C for different times (a). The XRC patterns of GaN (002) and (102) formed at 1050 °C for different times (b).

In order to characterize the crystal quality, the x-ray rocking curves (XRC) of the GaN (002) and (102) planes were obtained from as-nitridated β-Ga2O3 films at 1050 °C for different times. As shown in Fig. 5(b), the FWHM value of the GaN (002) and (102) plane remarkably decreases. The change of FWHM value indicates that the crystal quality of the GaN films becomes better with the increase of nitridation time because of the atom reconstruction during the nitridation process. The discrete FWHM value of GaN (102) may be attributed to the lack of N under a low NH3 flow rate. The XRC results indicate that the converted GaN films show the single-crystal structure and the nitridation time can improve the crystal quality of GaN films.

Figure 6 illustrates the Raman spectra of as-nitridated β-Ga2O3 films at 1050 °C for different times. In addition to the phonon modes of GaN, the A3g phonon mode of β-Ga2O3 is also observed in the spectra of as-nitridated films. And the peak intensity of the A3g phonon mode of β-Ga2O3 gradually decreases until it disappears as the nitridation process proceeds. It should be noted that while the A3g phonon mode of β-Ga2O3 is still observed, the E2 (high) phonon mode of GaN shows a blue-shift, which indicates the existence of compressive stress in GaN. And the blue-shift offset of the E2 (high) phonon mode is decreasing with the increase of nitridation time. As discussed earlier, the stress results from the incomplete conversion from β-Ga2O3 to GaN. When the nitridation time increases to 3 h, the E2 (high) peak is located at 567.7 cm−1 with no blue-shift compared with that of bulk GaN, which means that there is no significant stress in GaN film nitridated at 1050 °C for 3 h. So, it can be concluded that the enough nitridation time significantly improves the quality of GaN converted from β-Ga2O3, which is in accordance with the XRC analysis.

Fig. 6. Raman spectra of β-Ga2O3 films after nitridation at 1050 °C for different times.
4. Conclusion and perspectives

In summary, GaN films have been obtained from the β-Ga2O3 films by the nitridation under the NH3 atmosphere. The nitridated films show a porous network surface morphology. The structural analysis indicates that the nitridated surface layer is single-crystal GaN layer. After full nitridation at 1050 °C for 3 h, GaN layers show no significant stress. The nitridation temperature and time can promote and improve the crystal quality of GaN films. The porous GaN films obtained by the nitridation of β-Ga2O3 can be used as templates for the epitaxial growth of GaN instead of the expensive bulk GaN substrates.

Reference
[1] Denault K A Cantore M Nakamura S DenBaars S P Seshadri R 2013 AIP Adv. 3 072107 https://doi.org/10.1063/1.4813837
[2] Nakamura S Senoh M Nagahama S Iwasa N Yamada T Matsushita T Kiyoku H Sugimoto Y Kozaki T Umemoto H Sano M Chocho K 1997 Jpn. J. Appl. Phys. 36 L1568 https://doi.org/10.1143/JJAP.36.L1568
[3] Pearton S J Ren F 2000 Adv. Mater. 12 1571 https://doi.org/10.1002/1521-4095(200011)12:21<1571::AID-ADMA1571>3.0.CO;2-T
[4] Ohta J Fujioka H Oshima M Fujiwara K Ishii A 2003 Appl. Phys. Lett. 83 3075 https://doi.org/10.1063/1.1618379
[5] Zhao D G Xu S J Xie M H Tong S Y Yang H 2003 Appl. Phys. Lett. 83 677 https://doi.org/10.1063/1.1592306
[6] Tippins H H 1965 Phys. Rev. 140 A316 https://doi.org/10.1103/PhysRev.140.A316
[7] Ueda N Hosono H Waseda R Kawazoe H 1997 Appl. Phys. Lett. 70 3561 https://doi.org/10.1063/1.119233
[8] Miyata T Nakatani T Minami T 2000 Thin Solid Films 373 145 https://doi.org/10.1016/S0040-6090(00)01123-8
[9] Víllora E G Shimamura K Kitamura K Aoki K Ujiie T 2007 Appl. Phys. Lett. 90 234102 https://doi.org/10.1063/1.2745645
[10] Shimamura K Víllora E G Domen K Yui K Aoki K Ichinose N 2005 Jpn. J. Appl. Phys. 44 L7 https://doi.org/10.1143/JJAP.44.L7
[11] Tsai T Y Ou S L Hung M T Wuu D S Horng R H 2011 J. Electrochem. Soc. 158 H1172 https://doi.org/10.1149/2.073111jes
[12] Víllora E G Shimamura K Aoki K Ichinose N 2004 J. Cryst. Growth 270 462 https://doi.org/10.1016/j.jcrysgro.2004.06.045
[13] Xiong Z N Xiu X Q Li Y W Hua X M Xie Z L Chen P Liu B Han P Zhang R Zheng Y D 2018 Chin. Phys. Lett. 35 58101 https://doi.org/10.1088/0256-307X/35/5/058101
[14] Li X Xia C He X L Pei G Q Zhang J G Xu J 2008 Chin. Opt. Lett. 6 282 https://doi.org/10.3788/COL20080604.0282
[15] Tomm Y Reiche P Klimm D Fukuda T 2000 J. Crystal Growth 220 510 https://doi.org/10.1016/S0022-0248(00)00851-4
[16] Kumar M Sarau G Heilmann M Christiansen S Kumar V Singh R 2017 J. Phys. D: Appl. Phys. 50 035302 https://doi.org/10.1088/1361-6463/50/3/035302
[17] Fantner E B Ryan T Schurman M Ferguson I T 2000 Mater Sci. Forum. 321–324 1056 https://doi.org/10.4028/www.scientific.net/MSF.321-324.1056
[18] Kumar M S Kumar J 2003 Mater. Chem. Phys. 77 341 https://doi.org/10.1016/S0254-0584(02)00012-3
[19] Onuma T Fujioka S Yamaguchi T Itoh Y Higashiwaki M Sasaki K Masui T Honda T 2014 J. Crystal Growth 401 330 https://doi.org/10.1016/j.jcrysgro.2013.12.061
[20] Filippidis L Siegle H Hoffmann A Thomsen C Karch K Bechstedt F 1996 Phys. Status Solidi B 198 621 https://doi.org/10.1002/pssb.2221980207
[21] Davydov V Y Kitaev Y E Goncharuk I N Smirnov A N Graul J Semchinova O Uffmann D Smirnov M B Mirgorodsky A P Evarestov R A 1998 Phys. Rev. B 58 12899 https://doi.org/10.1103/PhysRevB.58.12899
[22] Bao K Y Guo G Zhang L F Liu R Y Sun H X Zhong Z G 2011 J. Phys. Chem. C 115 13200 https://doi.org/10.1021/jp202624a
[23] Li Y W Xiu X Q Jia Z T Liu D Hua X M Xie Z L Tao T Chen P Liu B Tao X T Zhang R Zheng Y D 2019 Superlattices Microstruct 126 98 https://doi.org/10.1016/j.spmi.2018.12.024