Iron Oxide Nanoparticles Employed as Seeds for the Induction of Microcrystalline Diamond Synthesis
© to the authors 2008
Received: 3 October 2007
Accepted: 9 January 2008
Published: 24 January 2008
Skip to main content
© to the authors 2008
Received: 3 October 2007
Accepted: 9 January 2008
Published: 24 January 2008
Iron nanoparticles were employed to induce the synthesis of diamond on molybdenum, silicon, and quartz substrates. Diamond films were grown using conventional conditions for diamond synthesis by hot filament chemical vapor deposition, except that dispersed iron oxide nanoparticles replaced the seeding. X-ray diffraction, visible, and ultraviolet Raman Spectroscopy, energy-filtered transmission electron microscopy , electron energy-loss spectroscopy, and X-ray photoelectron spectroscopy (XPS) were employed to study the carbon bonding nature of the films and to analyze the carbon clustering around the seed nanoparticles leading to diamond synthesis. The results indicate that iron oxide nanoparticles lose the O atoms, becoming thus active C traps that induce the formation of a dense region of trigonally and tetrahedrally bonded carbon around them with the ensuing precipitation of diamond-type bonds that develop into microcrystalline diamond films under chemical vapor deposition conditions. This approach to diamond induction can be combined with dip pen nanolithography for the selective deposition of diamond and diamond patterning while avoiding surface damage associated to diamond-seeding methods.
Many challenges remain opening regarding the integration of diamond into electronic devices. In particular, seeding processes are typically harsh on the substrate surface, leading to defect creation and lack of reproducibility. Iron-based materials have been used as catalysts in the synthesis of crystalline diamond by high temperature, high-pressure growth [1–3]. Yet, it is difficult to fabricate diamond on iron-based materials by chemical vapor deposition (CVD) due to the rapid diffusion of carbon into the bulk and high carbon solubility . There have been a number of attempts to grow diamond by forming a thin film of iron on silicon substrates [5–7]. Higher diamond nucleation densities with significant amounts of a–C are attained by depositing a thin layer of iron on silicon substrates, thus suggesting that a high carbon concentration resulting in a saturated carbide layer during the initial stage of nucleation is required for producing diamond nucleation sites [8, 9]. Reports by Ahn et al.  and Kohmura et al.  further indicate that there is an optimum iron thickness at which diamond growth prevails.
The above-described developments suggest that the Fe nanoparticles can be employed as diamond nucleation centers: they have a strong affinity for C atoms and yet they are too small to act as C sinks. FeO nanoparticles (nFeO) are ideal candidates for this task because the Fe nanoparticle is passivated by O, which is then removed by the CVD reactions, leaving the active Fe nanoparticle exposed for C trapping and accumulation. The results hereby reported evidence the success of this approach.
Microcrystalline diamond particles and films were synthesized using a custom-built hot filament CVD (HFCVD) apparatus, which is described in detail elsewhere . The films were grown on 14-mm diameter and 0.5-mm thick Mo, Si, and quartz substrates. The substrates were cleaned by sonication in methanol and acetone and dried with inert gas. After cleaning, a suspension of nFeO with nominal particle size distribution in the 7–10 nm range (Integran Technologies Inc.) was applied to the substrates. The surface density of nFeO clusters was estimated to be ∼107 cm−2 by atomic force microscopy and scanning electron microscopy (SEM). However, scattered micron-size patches of unseeded substrate remained. No diamond powder seeding was employed.
A mixture of 2% CH4in H2with a total flow of 100 sccm was directed over the heated rhenium filament kept at 2,700 K and 10 mm above the substrate. The total pressure was kept constant at values between 20 and 50 Torr (2.6–6.6 kPa). The substrates were maintained around 700–730 °C and the deposition time was varied between 30 min and 6 h.
The surface morphology of the films was investigated by SEM using a JEOL JSM 845A Model microscope. Small portions of the diamond samples were placed on Formvar-coated Cu grids and uncoated silicon nitride TEM grids for energy-filtered transmission electron microscopy (EFTEM) and electron energy-loss spectroscopy (EELS) using an energy-filtered LEO 922 OMEGA microscope operating at an accelerating voltage of 200 kV. The structural phases of the films were characterized by micro-Raman spectroscopy (RS) using a triple monochromator (ISA Jobin-Yvon Inc. Model T64000) with 1 cm−1resolution and the 514.5 nm Ar-ion laser line for excitation. The spectra were recorded using an 80× objective that probes an area of about 1–2 μm2. The UV Raman spectra were measured using a double monochormator (ISA Jobin-Yvon Inc.) with a resolution of 3–4 cm−1and the second harmonic generation of 488 nm radiation (244 nm) from an Ar-ion laser.
The X-ray diffraction (XRD) measurements were taken on a Siemens D5000 diffractometer using the Cu Kαline source (λ = 1.5405 Å) inθ–2θ configuration. The X-ray photoelectron spectroscopy (XPS) measurements were taken using a Physical Electronic system (Model PHI5600 ESCA, MN, USA) for elemental analysis at room temperature, which was operated in the constant energy pass mode using monochromatic Al Kα X-rays (hυ = 1,486.6 eV). The resolution of the electron energy analyzer was around 0.25 eV.
The diamond growth rates were around 1.7–1.9 μm/h, which is substantially high for HFCVD (typically 0.1–0.2 μm/h), and the observed nucleation densities were around 107 cm−2, corresponding well to the initial nFeO density and similar to those typically obtained by diamond-seeded diamond deposition . In contrast, previous reports of methods involving some form of Fe seeding, typically thin Fe films, suffered from low growth rates and substantial co-deposition of amorphous carbon (a–C) [6, 7]. Although there might be a slight effect on the nucleation density due to mechanical polishing of the Mo substrates , it does not sufficient to account for the results described above, especially since the quartz and Si substrates were not mechanically polished but nevertheless the growth of a microcrystalline diamond film was also successfully induced on them by nFeO. Another important difference is the diamond quality of the nFeO-induced diamond films according to their Raman spectra.
The bonding structure of the material was determined by RS excited with two radiation energies: visible (2.4 eV) and UV (5.1 eV). The combination of visible and UV Raman is an effective approach for probing both kinds of carbon materials because the Raman scattering cross-section for sp2-bonded carbon in the visible region is 50–230 times higher than that of sp3-bonded carbon . The Stokes-shifted visible and UV Raman spectra of the nFeO-induced diamond films are shown in Fig. 3a. They indicate that there is a relatively small presence of sp2-bonded carbon in the nFeO-induced diamond films. (No plasma etching or any other treatment was performed to enhance the post-deposition diamond quality of the films.)
It has been reported that the formation of a very dense amorphous carbon phase can lead to diamond nucleation [30–32]. In this process, sp3-bonded C clusters start precipitating by consuming the carbon atoms from the dense amorphous carbon phase. Furthermore, there are theoretical studies indicating that diamond nuclei are stable structures when embedded in a–C matrix , and experiments showed that these serve as nucleation centers for subsequent growth . Thus the formation of a dense amorphous carbon phase is a plausible route for nucleating diamond. The iron nanoparticle may act as catalyst in decomposing the hydrocarbon under CVD conditions, after oxygen removal from the initial nFeO, leading to active carbon adsorption [34, 35]. Since there is no room for diffusion into the interior of the Fe nanoparticle and the amount of carbon that the Fe nanoparticle can adsorb is limited, there occurs densification of trigonally and tetrahedrally bonded carbon around the iron nanoparticle and the impending formation of diamond bonds.
From the above analysis, the synthesis of nFeO-induced microcrystalline diamond films can be summarized as follows: (a) iron oxide nanoparticles lose oxygen by chemical vapor reactions that lead to the formation HO and CO radicals, creating active nanoscale iron surfaces for the adsorption and decomposition of the incoming carbon-containing species, and thus for the formation of nanoscale C clusters with trigonal and tetrahedral C bonds; (b) as these carbon clusters densify around the iron nanoparticles, diamond-type bonds start precipitating ; and (c) diamond film deposition continues to occur under conventional diamond growth conditions of high hydrogen dilution which keep the growing surface hydrogenated and preferentially etch away the trigonal carbon bonds.
The iron oxide nanoparticles were employed to induce the formation of diamond nuclei and the synthesis of microcrystalline diamond films. This approach yields relatively high diamond growth rates, low presence of amorphous carbon and can be used for the selective diamond deposition and patterning at the nanoscale through dip pen nanolithography of nFeO followed by chemical vapor deposition. The combined analysis of the various characterization results, indicate that the iron nanoparticles act as nucleation and aggregation sites for carbon and the impending formation of diamond-type bonds. The formation of a dense, mixed C phase around the Fe nanoparticles leading to the precipitation of sp3C bonds is proposed as a plausible explanation for these results.
One of the authors (K.U.) acknowledges the Graduate Research Fellowship granted by the National Science Foundation (Grant No. EPS-0223152). This research project is being carried out under the auspices of the Institute for Functional Nanomaterials (NSF Grant No. 0701525). This research was also supported in parts by NASA Training Grant NNG05GG78H (PR Space Grant), NASA Cooperative Agreement NCC5-595 (PR NASA EPSCoR), and NASA Grant NCC3-1034 (NASA CNM URC). We gratefully acknowledge the use of research facilities of Dr. R. Katiyar, Mr. W. Pérez (micro-Raman spectroscopy), Dr. Antonio Martínez, Mr. Javier Wu (SEM), Dr. Carlos Cabrera (XPS), Ms. Lyda La Torre, and Dr. Vladimir Makarov, Dr. Fabrice Piazza for their discussions.