Preparing of Diamond in the presence of CH4-H2 in a cold plasma produced by a magnetron. Habibi,Maryam 1 ;Ghoranneviss,Mahmood 1 ;Naranji,Reza 2 1.Plasma Physics Research Center, Science & Research Branch, I.A.University, P.O.Box 14665-678, Tehran, Iran. 2.I.A.University, Ardabil Branch, Ardabil, Iran. Abstract In this paper we have prepared diamond by depositing the mixture of CH4 and H2 (%98 H2 and %2 CH4) on silicon substrate in a cold plasma produced by a DC magnetron. The percentage of the mixture is %98 H2 and %2 CH4 at the pressure of 5*10^-3 Torr. Different pressures and different exposure times have been examined and different analyser such as SEM,Raman Spectrum and XRD have been used to investigate the results. 1.Introduction Diamond thin films have been formed by DC plasma chemical vapor deposition from a gaseous mixture of methan 2% and Hydrogen 98% . It has been confirmed that diamond can be grow from the vapor phase at low pressure where graphite in the stable modification of carbon.The main growth methods used are hot filament chemical vapor deposition and plasma with the deposition of above gas mixture. It is said that the active species for diamond synthesis at low pressure are methyl radicals and hydrogen atom in the gas temperature region(<2500 K). In this paper , the growth of diamond thin films by the DC plasma CVD method will be described. The characteristics of DC plasma measured by the Langmuir double probe method and were characterized using X-ray diffraction, scanning electron microscopy. The plasma plays an important role during deposition of diamond films by electron assisted chemical vapor deposition. 2.Experimental The fig.1 shows the schematic diagram of electron assisted CVD apparatus. In this apparatus,the voltage applied on negative and positive plates of cathode and anode , emits the electrons from cathode to anode , that anode and cathode used are made of AL. The reaction gases which are CH4 and H2 are fed to the vacuum chamber through the thermal mass flow controller. The pressure of the reaction gas in measured using a diaphragm gauge. A substrate is silicon is set on the anode. The vacuum chamber is evacuated to 10^-4 Torr and H2, CH4 introduced in to the chamber , In this case we adjust pressure to 10^-2 Torr then DC voltage is applied to start discharge. Then the gas mixture of 2% CH4 in H2 is applied continuously at the gas flow. 3.Results The diamond films have been prepared an silicon with discharge voltage 2 kv , discharge current 50-200(mA), temperature of filament 2000 0 C.The structure of prepared films is analyzed by means of X-ray diffraction scanning electron microscopy. The X-ray diffraction,SEM and Raman Spectrum are shown in fig.2-4. Fig.5 shows that continuous polycrystalline diamond film is formed and has good crystal habit.. 4.Conclusion Diamond films can be formed by the DC plasma CVD method. The polycrystalline diamond films can be prepared in the wide range of technology parameters. By knowing diagnostics of the plasma parameters is useful for providing essential information of PCVD and controlling preparation of high quality diamond. 5.References [1]. S.Matsumoto,Y.Sato,M.Kamo and N.Setaka:J.Appl.Phys.21(1982)483. [2]. M.Kamo, Y.Sato,S.Matsumoto and N.Setaka:J.Cryst.Growth 62(1983)642. [3]. S.Matsumoto:J.Mater.Sei.Lett. 4(1985)600. [4]. A.Sawabe and T.Inuzuka:Appl.Phys.Lett. 46(1985)146. [5]. K.Suzuki, A.sawabe, H.Yasuda and T.Inuzuka:Appl.Phys.Lett. 50(1987)728. [6]. R. C. Devries, Annu. Rev. Mater. Sci. 17, 167 (1987). [7]. R. Messier, A. R. Badzian, T. Badzian, K. E. Spear, P. Bachmann, and R. Roy, Thin Solid Films 153, 1 (1987). [8]. R. Roy, Nature (London) 325, 17 (1987). [9]. J. C. Angus and C. C. Hayman, Science 241, 913 (1988). [10]. K. Suzuki, A. Sawabe and T.Inuzuka:Appl.Phys. Lett. 53(1988)1818. [11]. F. G. Celi, P. E. Pehrsson, H.-t. Wang and J. E. Butler:Appl. Phys. Lett. 52(1988)2043. [12]. F. G. Celii and J. E. Butler:Appl. Phys. Lett. 54(1989)1013. [13]. K. E. Spear, J. Am. Ceram. Soc. 72, 171 (1989). [14]. J. C. Angus, F. A. Buck, M. Sunkara, T. F. Groth, C. C. Hayman, and R. Gat, MRS Bull. October, 38 (1989). [15]. W. A. Yarbrough and R. Messier, Science 247, 688 (1990). [16]. J. C. Angus, “History and Current Status of Diamond Growth at Metastable Conditions, “ Proc. Of the 1st Int. Symp. On Diamond and Diamond-Like Films, The Electrochem. Soc., Pennington, New Jersey, 1989, J. P. Dismukes, A. J. Purdes, K. E. Spear, B. S. Meyerson, K. V. Ravi, T. D. Moustakas, and M. Yoder, eds. (1989), P. 1. [17]. B. V. Spitsyn, L. L. Bouilov, and B. V. Derjaguin, J. Crystal Growth 52, 219 (1981). [18]. M. Cowperthwaite and S. H. Bauer: J. Chem. Phys. 36(1962) 1743. [19]. R. E. Duff and S. H. Bauer: J. Chem. Phys. 36(1962) 1754. [20]. Matsumoto , Sato , Tsutsumi , Setaka “Growth of Diamond Particles from Methane Hydrogen Gas” , Journal of materials science. 17 , (1982) , 3106-3112. Fig.1 – Schematic diagram of electron assisted CVD apparatus. Fig.2.2 – Shows the X-ray diffraction pattern of prepared film. Fig.3 – SEM picture of Diamond film Fig.4 – Raman Spectrum obtion from coating DLC on silicon substrate.
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