Synthesis of highly transparent ultrananocrystalline diamond films from a low-pressure, low-temperature focused microwave plasma jet
© Liao et al; licensee Springer. 2012
Received: 25 August 2011
Accepted: 19 January 2012
Published: 19 January 2012
This paper describes a new low-temperature process underlying the synthesis of highly transparent ultrananocrystalline diamond [UNCD] films by low-pressure and unheated microwave plasma jet-enhanced chemical vapor deposition with Ar-1%CH4-10%H2 gas chemistry. The unique low-pressure/low-temperature [LPLT] plasma jet-enhanced growth even with added H2 and unheated substrates yields UNCD films similar to those prepared by plasma-enhanced growth without addition of H2 and heating procedure. This is due to the focused plasma jet which effectively compensated for the sluggish kinetics associated with LPLT growth. The effects of pressure on UNCD film synthesis from the microwave plasma jet were systematically investigated. The results indicated that the substrate temperature, grain size, surface roughness, and sp 3 carbon content in the films decreased with decreasing pressure. The reason is due to the great reduction of Hα emission to lower the etching of sp 2 carbon phase, resulting from the increase of mean free path with decreasing pressure. We have demonstrated that the transition from nanocrystalline (80 nm) to ultrananocrystalline (3 to 5 nm) diamond films grown via microwave Ar-1%CH4-10%H2 plasma jets could be controlled by changing the pressure from 100 to 30 Torr. The 250-nm-thick UNCD film was synthesized on glass substrates (glass transition temperature [Tg] 557°C) using the unique LPLT (30 Torr/460°C) microwave plasma jet, which produced UNCD films with a high sp 3 carbon content (95.65%) and offered high optical transmittance (approximately 86% at 700 nm).
Keywordsultrananocrystalline diamond films focused microwave plasma jet low-pressure/low-temperature synthesis transmittance
The ultrananocrystalline diamond [UNCD] films are outstanding material candidates for multifunctional device applications and attracting strong scientific and technological interests due to their unique properties stemming from their ultrafine (< 10 nm) grains and a pure diamond phase, such as high wear resistance , optical transparency from deep UV to far infrared [2, 3], chemical stability, excellent electron field emission [4, 5], and superior capacity to incorporate n-type dopants in addition to a smooth surface [6–9]. However, improving the syntheses and applications of UNCD films for functional devices and components highly requires the development of a new low-temperature and low-pressure process for wider uses in substrates and an effective growth with low consumption of source gases, besides optimizing the performance of UNCD films by controlling the pre-growth seeding and growth parameters .
Microwave plasma chemical vapor deposition [MPCVD] from Ar-1%CH4 gas chemistry was typically used to synthesize UNCD films in order to greatly enhance plasma species activity and diamond secondary nucleation [10–12]. The normal growth temperature and pressure of UNCD films synthesized by microwave Ar-1%CH4 plasma without addition of H2 were 800°C and above 100 Torr, respectively [10–12]. The growth temperature depended on the substrate and plasma heating during synthesis. Commonly, the plasma heating cannot be avoided during UNCD growth; thus, minimizing the plasma heating is crucial to realize a low-temperature synthesis. Therefore, argon-rich (hydrogen-poor) microwave plasma is popularly adopted for low-temperature preparation of UNCD films due to the much lower thermal conductivity of argon and much less power levels required for argon plasma formation compared with hydrogen .
The microwave plasma jet-enhanced chemical vapor deposition [MPJCVD] for UNCD film synthesis developed in our lab takes several advantages compared with the regular MPCVD process, namely which can improve the density and activity of plasma species through excitation of the focused plasma jet [13, 14], enabling it to achieve high-efficiency and high-quality deposition at low-pressure/low-temperature [LPLT] conditions (without substrate heating). The MPJCVD-enhanced growth [MEG] is particularly critical in LPLT deposition to compensate for the insufficient density and kinetics of growth species associated with LPLT synthesis. Therefore, we describe here a unique plasma jet technique to successfully grow UNCD films at LPLT (30 Torr/460°C) that yields films with smooth surface, pure diamond nanograins (3 to 8 nm), and high optical transmittance in the visible light region using relatively low pressure, low power (700 W), and even with addition of H2 (Ar-1%CH4-10%H2) compared with the typical plasma processes [10–12]. The highly transparent UNCD films were grown directly on glass substrates with a low glass transition temperature (Tg 557°C). The process opens further feasibility for the LPLT synthesis of UNCD films, providing a promising platform fabrication for diamond-based multifunctional devices and coating on low-melting point materials with low cost. The synthesis and characteristics of UNCD films produced by the MEG technique at various growth pressures (5 to 100 Torr) and temperatures (400°C to 700°C) were systematically studied by in situ optical emission spectroscopy [OES], visible Raman spectroscopy, synchrotron-based X-ray absorption near-edge structure [XANES] spectroscopy, atomic force microscopy [AFM], field-emission scanning electron microscopy [FESEM], and field-emission transmission electron microscopy [FETEM].
The diamond films were synthesized using the homemade MPJCVD system. The plasma jet was induced in Ar-1%CH4-10%H2 gas chemistry at a microwave power of 700 W. The total pressure of reactant gas was varied from 5 to 100 Torr (5, 15, 30, 60, 80, and 100 Torr) in the synthesis of diamond films. The deposition process was carried out without heating the substrates. The substrate temperature was influenced only by plasma jet heating at various pressures from 5 to 100 Torr, which increased from approximately 400°C to 700°C with increasing pressure. The growth rate of the diamond films using plasma jet was gradually increased with increasing pressure, approximately 0.25 μm/h at 30 Torr and approximately 0.97 μm/h at 100 Torr. The thickness of the diamond films was confirmed by a FESEM image of the cross section. N-type Si wafers with a (100) orientation were initially used as substrates for the deposition of diamond films at various pressures. The glass substrates with Tg of 557°C were applied to support LPLT UNCD films for the fabrication of highly transparent coatings and further confirmed the successful synthesis of UNCD films at a LPLT condition without any damage to the substrates. Pretreatment on the substrates was performed by the spin coating of a diamond nanoparticle solution to enhance nucleation at low temperature .
The as-grown films were characterized by FESEM (S-4800, Hitachi, Chiyoda-ku, Tokyo, Japan), visible Raman spectroscopy (micro-Raman, Renishaw Inc, Taichung, Taiwan), synchrotron-based XANES spectroscopy (Carbon K-edge spectra with a resolution of 0.1 eV, total electron yield mold, at the Dragon BL11A beamline of the National Synchrotron Radiation Research Center in Taiwan), FETEM (Tecnai F30, Philips, Best, The Netherlands), and AFM (NS3a, Digital Instruments, Santa Barbara, CA, USA) for obtaining comprehensive information on the surface morphology, roughness, atomic bonding nature, and detailed nanostructural characterizations. Optical transmission spectrum of the as-grown UNCD films ranging from 350 to 950 nm was characterized with a UV-A/Visible/near-IR spectrophotometer (MP100-M, Mission Peak Optics, Fremont, CA, USA). The focused microwave plasma jet was analyzed during synthesis by in situ OES (BTC112E, B&W TEK, Newark, DE, USA) to explore the species composition at different growth processes.
Results and discussion
Two trans-polyacetylene [t-PA] bands were observed in the spectra at approximately 1, 140 and 1, 480 cm-1 while the films were grown at above 60 Torr, which represented the NCD structures that existed at the GBs in the films [15, 19, 20]. Interestingly, the spectra were found to show a peak centered at approximately 1, 190 cm-1 as the synthesis was at a pressure from 15 to 80 Torr. The decrease in this peak with increasing pressure is opposite to the t-PA bands in the spectra. This phenomenon likely originated from the difference in the crystal size between UNCD and NCD films. Moreover, the concurrent absence or weakening of the peaks located at 1, 190 and 1, 140 cm-1 (t-PA) for the sample grown at 100 Torr suggested that the content of C-H bonds (t-PA) in the films would be decreased with increasing pressure (5 to 100 Torr) and temperature (400°C to 700°C). A decrease in the relative GB fraction for t-PA bands existed, and the increase in the substrate temperature was to promote hydrogen desorption from the films [10, 18]. The decrease of hydrogen trapping during synthesis is expectably caused by high-temperature growth (high-pressure) due to the hydrogen desorption temperature which is between 600°C and 1, 000°C . The above features of visible Raman spectra are similar to those of the UNCD films deposited by microwave Ar-1%CH4 plasma at various substrate heating , but the bonding structure and quality of the films are controlled by pressure via the MEG process, suggesting that the MEG process could improve the synthesis of the UNCD films at LPLT without substrate heating.
The transmittance spectrum of the UNCD film with a thickness around 250 nm grown from the LPLT MEG process on the glass substrate was measured in the range of 350 to 950 nm (Figure 5a). The scheme of the measurement is illustrated in the bottom left inset of Figure 5. The optical transmittance of the as-grown UNCD film is oscillated due to the interference effect during the photon transmission in the film, resulting in the variation of transmittance from 60% at 450 nm to 86% at 700 nm. The transmittance of the diamond films is dominated by the surface smoothness and diamond (sp 3 bonding) content in the films . The film grown at 30 Torr/460°C consisted of pure diamond nanocrystallites (3 to 8 nm) without any thermal damage to the substrate, which retained a high degree of diamond purity (95.65%) but revealed a far smoother surface (12.8 nm root-mean-square [rms]) to minimize light scattering from the surface of the diamond films (Figure 5b), resulting in the outstanding optical transparency obtained from the LPLT synthesis. The transmission analysis complemented the SEM, TEM, AFM, XANES, visible Raman, and OES analyses to constitute convincing evidence of successful fabrication of highly transparent UNCD films at LPLT condition and completed investigation of the relationships between the growth conditions, nanostructures, and material properties of the diamond films synthesized from the focused microwave Ar-1%CH4-10%H2 plasma jet at different growth processes.
A no-heating LPLT MEG technique has been developed successfully to synthesize UNCD films on glass substrates with high transparency (approximately 86% at 700 nm), smooth surface (approximately 12.8 nm rms), uniform diamond nanocrystallites (3 to 8 nm), and very high sp 3 content (95.65%) using relatively low-output power (700 W), low Ar gas chemistry (Ar-1%CH4-10%H2), low pressure (30 Torr), and even low temperature (460°C) compared with the typical microwave Ar-1%CH4 plasma with heating procedures. The synthesis of UNCD films using the uniquely focused plasma jet was confirmed to efficiently compensate for the sluggish kinetics and insufficient density of plasma species during the LPLT synthesis. A new and effective way to control the crystal size, surface morphology, and growth mechanism of diamond films by regulating the growth pressure in a systematic study was reported. Based on the TEM images of all films, it has been demonstrated that the transition of grain size from NCD (80 nm) to UNCD (3 to 8 nm) films controlled by the pressure ranged from 100 to 30 Torr. The reason is due to the increase of the mean free path for the excitation of plasma with decreasing pressure, resulting in a decreased amount of atomic hydrogen emission to greatly lower the etching of the sp 2 carbon phase during synthesis. The NBD and XANES characterizations further demonstrated the ultrananocrystalline diamond nature of the films grown from the focused microwave Ar-1%CH4-10%H2 plasma jet at LPLT condition.
The authors would like to thank Dr. Chung-Li Dong and Dr. Chi-Liang Chen for the XANES investigations at the Dragon BL11A beamline of the National Synchrotron Radiation Research Center (NSRRC). This work was financially supported by the main research projects of the National Science Council of the Republic of China under grant numbers NSC 100-2221-E-027-047 and NSC 100-2221-E-027-015.
- Kim K-H, Moldovan N, Ke C, Espinosa HD, Xiao X, Carlisle JA, Auciello O: Novel ultrananocrystalline diamond probes for high-resolution low-wear nanolithographic techniques. Small 2005, 1: 866–874. 10.1002/smll.200500028View Article
- Kriele A, Williams OA, Wolfer M, Brink D, Müller-Sebert W, Nebel CE: Tuneable optical lenses from diamond thin films. Appl Phys Lett 2009, 95: 031905–1-031905–3.View Article
- Joseph PT, Tai NH, Chen YC, Cheng HF, Lin IN: Transparent ultrananocrystalline diamond films on quartz substrate. Diamond Relat Mater 2008, 17: 476–480. 10.1016/j.diamond.2007.10.013View Article
- Zhu W, Kochanski GP, Jin S: Low-field electron emission from undoped nanostructured diamond. Science 1998, 282: 1471–1473.View Article
- Garguilo JM, Koeck FAM, Nemanich RJ, Xiao XC, Carlisle JA, Auciello O: Thermionic field emission from nanocrystalline diamond-coated silicon tip arrays. Phys Rev B 2005, 72: 165404–1-165404–6.View Article
- Bhattacharyya S, Auciello O, Birrell J, Carlisle JA, Curtiss LA, Goyette AN, Gruen DM, Krauss AR, Schlueter J, Sumant A, Zapol P: Synthesis and characterization of highly-conducting nitrogen-doped ultrananocrystalline diamond films. Appl Phys Lett 2001, 79: 1441–1443. 10.1063/1.1400761View Article
- Williams OA, Curat S, Gerbi JE, Gruen DM, Jackman RB: n-Type conductivity in ultrananocrystalline diamond films. Appl Phys Lett 2004, 85: 1680–1682. 10.1063/1.1785288View Article
- Zapol P, Sternberg M, Curtis LA, Frauenheim T, Gruen DM: Tight-binding molecular dynamics simulation of impurities in ultrananocrystalline diamond grain boundaries. Phys Rev B 2002, 65: 0454031–4540311.
- Zhou D, McCauley TG, Qin LC, Krauss AR, Gruen DM: Synthesis of nanocrystalline diamond thin films from an Ar-CH4 microwave plasma. J Appl Phys 1998, 83: 540–543. 10.1063/1.366668View Article
- Xiao X, Birrell J, Gerbi JE, Auciello O, Carlisle JA: Low temperature growth of ultrananocrystalline diamond. J Appl Phys 2004, 96: 2232–2239. 10.1063/1.1769609View Article
- Zhou D, Gruen DM, Qin LC, McCauley TG, Krauss AR: Control of diamond film microstructure by Ar additions to CH4/H2 microwave plasmas. J Appl Phys 1998, 84: 1981–1989. 10.1063/1.368331View Article
- Sumant AV, Grierson DS, Gerbi JE, Carlisle JA, Auciello O, Carpick RW: Surface chemistry and bonding configuration of ultrananocrystalline diamond surfaces and their effects on nanotribological properties. Phys Rev B 2007, 76: 235429–1-235429–11.View Article
- Lin CR, Liao WH, Wei DH, Tsai JS, Chang CK, Fang WC: Formation of ultrananocrystalline diamond films with nitrogen addition. Diamond Relat Mater 2011, 20: 380–384. 10.1016/j.diamond.2010.12.015View Article
- Lin CR, Liao WH, Wei DH, Chang CK, Fang WC, Chen CL, Dong CL, Chen JL, Guo JH: Improvement on the synthesis technique of ultrananocrystalline diamond films by using microwave plasma jet chemical vapor deposition. J Cryst Growth 2011, 326: 212–217. 10.1016/j.jcrysgro.2011.01.100View Article
- Veres M, Tóth S, Koós M: Grain boundary fine structure of ultrananocrystalline diamond thin films measured by Raman scattering. Appl Phys Lett 2007, 91: 031913–1-031913–3.View Article
- Wang CS, Chen HC, Shih WC, Cheng HF, Lin IN: Effect of H2/Ar plasma on growth behavior of ultra-nanocrystalline diamond films: the TEM study. Diamond Relat Mater 2010, 19: 138–142. 10.1016/j.diamond.2009.10.023View Article
- Yang Q, Yang S, Li YS, Lu X, Hirose A: NEXAFS characterization of nanocrystalline diamond thin films synthesized with high methane concentrations. Diamond Relat Mater 2007, 16: 730–734. 10.1016/j.diamond.2007.01.033View Article
- Xiao X, Wang J, Liu C, Carlisle JA, Mech B, Greenberg R, Guven D, Freda R, Humayun MS, Weiland J, Auciello O: In vitro and in vivo evaluation of ultrananocrystalline diamond for coating of implantable retinal microchips. J Biomed Mater Res B 2006, 77: 273–281.View Article
- Ferrari AC, Robertson J: Interpretation of Raman spectra of disordered and amorphous carbon. Phys Rev B 2000, 61: 14095–14107. 10.1103/PhysRevB.61.14095View Article
- Ferrari AC, Robertson J: Origin of the 1150-cm-1Raman mode in nanocrystalline diamond. Phys Rev B 2001, 63: 1214051–1214054.View Article
- Schulberg MT, Fox CA, Kubiak GD, Stulen RH: Hydrogen desorption from chemical vapor deposited diamond films. J Appl Phys 1995, 77: 3484–3490. 10.1063/1.358642View Article
- Lifshitz Y, Meng XM, Lee ST, Akhveldiany R, Hoffman A: Visualization of diamond nucleation and growth from energetic species. Phys Rev Lett 2004, 93: 056101–1-056101–4.View Article
- Laikhtman A, Gouzman I, Hoffman A, Comtet G, Hellner L, Dujardin G: Sensitivity of near-edge x-ray absorption fine structure spectroscopy to ion beam damage in diamond films. J Appl Phys 1999, 86: 4192–4198. 10.1063/1.371346View Article
- Dong CL, Chen SS, Chiou JW, Chen YY, Guo JH, Cheng HF, Lin IN, Chang CL: Effect of surface treatments on the electronic properties of ultra-nanocrystalline diamond films. Diamond Relat Mater 2008, 17: 1150–1153. 10.1016/j.diamond.2007.12.001View Article
- Ma KL, Tang JX, Zou YS, Ye Q, Zhang WJ, Lee ST: Photoemission spectroscopic study of nitrogen-incorporated nanocrystalline diamond films. Appl Phys Lett 2007, 90: 092105–1-092105–3.
- You MS, Hong FCN, Jeng YR, Huang SM: Low temperature growth of highly transparent nanocrystalline diamond films on quartz glass by hot filament chemical vapor deposition. Diamond Relat Mater 2009, 18: 155–159. 10.1016/j.diamond.2008.07.015View Article
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