SiC Nanowires Synthesized by Rapidly Heating a Mixture of SiO and Arc-Discharge Plasma Pretreated Carbon Black

  • Feng-Lei Wang1,

    Affiliated with

    • Li-Ying Zhang1 and

      Affiliated with

      • Ya-Fei Zhang1Email author

        Affiliated with

        Nanoscale Research Letters20084:153

        DOI: 10.1007/s11671-008-9216-3

        Received: 17 September 2008

        Accepted: 11 November 2008

        Published: 22 November 2008

        Abstract

        SiC nanowires have been synthesized at 1,600 °C by using a simple and low-cost method in a high-frequency induction furnace. The commercial SiO powder and the arc-discharge plasma pretreated carbon black were mixed and used as the source materials. The heating-up and reaction time is less than half an hour. It was found that most of the nanowires have core-shell SiC/SiO2nanostructures. The nucleation, precipitation, and growth processes were discussed in terms of the oxide-assisted cluster-solid mechanism.

        Keywords

        Silicon carbide Nanowires Induction heating

        Introduction

        Silicon carbide (SiC) has been widely used in the fields of electronic and optic devices due to its unique properties, such as a wide band gap of 2.3–3.3 eV, high strength, and Young’s modulus, good resistance to oxidation and corrosion, excellent thermal conductivity, and electron mobility [14]. One-dimensional (1D) SiC materials, i.e., nanowires, nanofibers, nanorods, and nanocables have recently attracted much attention because they have been thought suitable for the fabrication of high temperature, high frequency, and high power nanoscaled electronic devices [59].

        The first successfully synthesis of 1D SiC nanowires was in 1995 by using carbon nanotube as a template [10]. Up to now, lots of approaches have been developed, for example, arc-discharge [11], laser ablation [12], sol–gel method [13], carbon thermal reduction [14], and chemical vapor deposition [15]. Recently, metal catalyst assisted synthesis of 1D SiC nanostructures had also been reported [16, 17]. In most of these methods, expensive raw materials, catalysts, and sophisticated techniques were used. These drawbacks may limit the massive fabrication and application of SiC nanowires. It is still a challenge for scientists and industrials to synthesize large-scale SiC nanowires by using a simple and rapid method.

        In this paper, we report a novel method to fabricate β-SiC nanowires by using a high-frequency induction furnace with a graphite tube. A mixture of commercial SiO and the carbon black powder with loose structures pretreated by an arc-discharge plasma method was used as the starting materials. After heating the source materials in graphite tube in argon atmosphere, bright blue powders can be observed in the tube, which were characterized as β-SiC nanowires with core-shell structures. The total heating-up and reaction time is less than 1 h, and more than 200 g products can obtain per day. The modified oxide-assisted cluster-solid growth mechanism was used to explain the formation of core-shell SiC/SiO2nanowires.

        Experimental

        The fabrication of β-SiC nanowires was carried out in a high-frequency introduction furnace. First, commercial carbon black was pretreated in order to form porous and loose structures, which can make the reaction much easier. The carbon black was pressed to a carbon rod and put into an arc-discharge plasma instrument. After treating for about 1 h, a black powder with loose structures was obtained.

        The as-prepared carbon black was mixed with the commercial SiO powder (mass ratio of 1:1) and ball-milled for several hours. Then, the precursor was loaded in a graphite boat and located in a high-purity graphite tube. As a heating crucible, the graphite tube was placed in a horizontal quartz tube and heated in a high-frequency induction furnace. The furnace was first evacuated to 50 Pa, and then the argon gas was introduced until the furnace pressure reached about 4 × 104 Pa, which was maintained throughout the whole experimental process. The powder was rapidly heated to 1,600 °C within 3 min and kept for 40 min. A bright blue-colored powder was found in the graphite boat. The schematic diagram of the apparatus is shown in Fig. 1.
        http://static-content.springer.com/image/art%3A10.1007%2Fs11671-008-9216-3/MediaObjects/11671_2008_Article_9216_Fig1_HTML.jpg
        Figure 1

        Schematic diagram of the apparatus for synthesis of SiC nanowires

        An energy-dispersive X-ray (EDX, INCA OXFORD) spectroscopy and an X-ray diffraction (XRD, D/MAX-RA) were used to characterize the composition and crystal structure of samples. A field-emission scanning electron microscopy (SEM, FEI SIRION 200) and a transmission electron microscopy (TEM, JEM-2010) were employed to observe the morphology and the detail structure of the nanowires.

        Results and Discussion

        Figure 2shows the typical SEM image of the carbon black, which was treated in an arc-discharge plasma instrument. The loose and porous nanostructures were formed, which have more surface areas compared with original materials. This provides more chance for the reaction with SiO vapor. The inset in Fig. 2displays the corresponding EDX spectrum, indicating only two elements (carbon and oxide) existed in the pretreated carbon black.
        http://static-content.springer.com/image/art%3A10.1007%2Fs11671-008-9216-3/MediaObjects/11671_2008_Article_9216_Fig2_HTML.jpg
        Figure 2

        SEM image and EDX pattern of carbon black after arc-discharge plasma treatment

        The characteristic XRD pattern of the products is showed in Fig. 3. The major diffraction peaks can be indexed as the (1 1 1), (2 0 0), (2 2 0), (3 1 1), and (2 2 2) reflections of cubic β-SiC (unit cell parametera = 0.4370 nm). These values are almost identical to the known values for standard β-SiC (JCPDS Card No. 29–1129). Moreover, there is amorphous background in the XRD pattern, which is similar to amorphous SiO2. Furthermore, the diffraction peaks are broadened, which may be related to the inner thinner β-SiC nanowire and the outer amorphous silicon oxide wrapping layer.
        http://static-content.springer.com/image/art%3A10.1007%2Fs11671-008-9216-3/MediaObjects/11671_2008_Article_9216_Fig3_HTML.jpg
        Figure 3

        XRD pattern of the SiC nanowires

        Figure 4 shows the SEM and TEM images of the as-synthesized nanowires without any other treatments. In Fig. 4a and b, it can be seen that the nanowires have almost uniform diameters and smooth surfaces. The diameter of nanowires can be roughly estimated in the range of 60–100 nm and the length are several microns. The observed impurities in SEM images were the intermediate product of SiO2 and the residual carbon. To validate the existing of impurities, high-temperature oxidation and hydrofluoric acid (5%) treatment were used to get rid of the residual carbon and SiO2, respectively. In the high-temperature oxidation processing, about 72% of the as-synthesized sample remained as well as 28% of carbon was oxidized. After dipping in hydrofluoric acid (5%) for 2 h, about 74% of the residual sample remained when SiO2 was corroded. Therefore, it can be concluded that the yield of SiC nanowires was about 53%. The inset in Fig. 4a displays the corresponding EDX spectrum, indicating three elements (silicon, carbon, and oxide) exist in the nanowires. The TEM image in Fig. 4c shows detailed structure of the nanowire. One can find that the nanowire has a core-shell nanocabled structure. According to the component ratio obtained by EDX results, the core ought to be crystallized SiC and the shell is amorphous SiO2. In fact, the unique core-shell SiC/SiO2 structure has also been observed by other researchers [1820].
        http://static-content.springer.com/image/art%3A10.1007%2Fs11671-008-9216-3/MediaObjects/11671_2008_Article_9216_Fig4_HTML.jpg
        Figure 4

        a The SEM image of SiC nanowires;b the magnified SEM image of SiC nanowires; andc the TEM image of SiC nanwires with a core-shell SiC/SiO2structure. The inset ina shows the EDX pattern of SiC nanowires

        Vapor–liquid–solid (VLS) mechanism has usually been used to explain the growth process of 1D nanomaterials [21]. However, it seems unsuitable to interpret our experiments and results because there is no catalyst liquid droplet available during the high-frequency induction heating procedure. The oxide-assisted cluster-solid mechanism proposed by Zhang et al. [22], which was established to interpret the growth process of Si/SiO2 nanowires, may be used to understand the growth process of core-shell SiC/SiO2 nanowires. In terms of this mechanism, there exist three processes, that is, nucleation, precipitation, and growth. Figure 5 illustrates the schematic diagram of growing process. As the temperature is up to 1,600 °C, SiO powder will vaporize and react with the carbon source as follows:
        http://static-content.springer.com/image/art%3A10.1007%2Fs11671-008-9216-3/MediaObjects/11671_2008_Article_9216_Equ1_HTML.gif
        (1)
        where v and s refer to vapor and solid states of the material, respectively. It will generate SiC and SiO2 nanoparticles in this process, which provide crystalline nucleus for growth of nanowires. Actually, three different atoms (silicon, carbon, and oxygen) contained in the nanoparticles. The superfluous of any element will lead to the occurrence of precipitation (separate out) process. Reaction 2 can occur under a supersaturated condition of CO [23]:
        http://static-content.springer.com/image/art%3A10.1007%2Fs11671-008-9216-3/MediaObjects/11671_2008_Article_9216_Equ2_HTML.gif
        (2)
        http://static-content.springer.com/image/art%3A10.1007%2Fs11671-008-9216-3/MediaObjects/11671_2008_Article_9216_Fig5_HTML.jpg
        Figure 5

        Schematic diagram of growing process of SiC nanowire

        When SiO vapor is prevail, the following reaction will occur:
        http://static-content.springer.com/image/art%3A10.1007%2Fs11671-008-9216-3/MediaObjects/11671_2008_Article_9216_Equ3_HTML.gif
        (3)

        No matter what reaction is in the ascendant, SiC can generate and provide to the nanoparticles. Since there exist sufficient silica and carbon atoms in the reaction atmosphere, the precipitation (separate out) of SiC is possible. When the reaction 3is dominant, SiO2is then the main resultant and can separate out accompanying with the growth of SiC nanocrystals. This is why SiC nanowires are wrapped by SiO2layers.

        At the same time, the CO2gas generated from reaction 2may react with the carbon source as follows:
        http://static-content.springer.com/image/art%3A10.1007%2Fs11671-008-9216-3/MediaObjects/11671_2008_Article_9216_Equ4_HTML.gif
        (4)

        The partial supersaturation of CO gas can lead to a diameter distribution of the as-synthesized SiC nanowires [24, 25]. The CO gas is hard to be got rid of from graphite crucible in our experiment, and therefore, leads to the distribution of the diameter in as-synthesized SiC/SiO2 nanowires.

        Conclusion

        We present a simple, rapid, and low-cost method to synthesize massive β-SiC nanowires by a high-frequency induction heating procedure. A ball-milled mixture of SiO and carbon black was used as source materials. The carbon black were pretreated in an arc-discharge plasma instrument in order to form loose and porous structures. The heating-up and the reaction time is less than 1 h. The nanowires have core-shell SiC/SiO2structures in which the core of SiC crystallizes very well, whereas the SiO2has amorphous structure. The diameter of nanowires is ranged from 60 to 100 nm and the length is up to several microns. This method provides a promising candidate for industrial fabrication of β-SiC nanowires.

        Declarations

        Acknowledgments

        This work is supported by the National Basic Research Program of China (No. 2006CB300406) and the Shanghai Science and Technology Grant (No: 0752nm015) as well as the National Natural Science Foundation of China (No. 50730008). The authors also thank the Instrumental Analysis Center of Shanghai Jiao Tong University for the Materials Characterization.

        Authors’ Affiliations

        (1)
        National Key Laboratory of Nano/Micro Fabrication Technology, Key Laboratory for Thin Film and Microfabrication of the Ministry of Education, Research Institute of Micro/Nano Science and Technology, Shanghai Jiao Tong University

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        © to the authors 2008