Fine Structural and Carbon Source Analysis for Diamond Crystal Growth using an Fe-Ni-C System at High Pressure and High Temperature
FAN Xiao-Hong1,2,XU Bin2**,NIU Zhen2,ZHAI Tong-Guang3,TIAN Bin2
1School of Material Science and Engineering, Shandong University, Ji'nan 250101 2School of Materials Science and Engineering, Shandong Jianzhu University, Ji'nan 250101 3Department of Chemical and Materials Engineering, University of Kentucky, Lexington, USA
Fine Structural and Carbon Source Analysis for Diamond Crystal Growth using an Fe-Ni-C System at High Pressure and High Temperature
FAN Xiao-Hong1,2,XU Bin2**,NIU Zhen2,ZHAI Tong-Guang3,TIAN Bin2
1School of Material Science and Engineering, Shandong University, Ji'nan 250101 2School of Materials Science and Engineering, Shandong Jianzhu University, Ji'nan 250101 3Department of Chemical and Materials Engineering, University of Kentucky, Lexington, USA
摘要Diamond is synthesized in an Fe-Ni-C system at high pressure and high temperature, the C sp3 content profile through different thicknesses of interface between diamond and the catalyst film is measured by using electron energy loss spectroscopy. It is found that the C sp3 content varies from 87.33% to 78.15% when the measured position is located at the inner face near the diamond and then changes to 6 µm further away. Transmission electron microscope examinations show that there are different phases in the interface, such as Fe3C, γ−(Fe,Ni), and graphite, but the graphite phase diminishes gradually towards the inner face of the interface. These results profoundly indicate that the carbon atoms, required for diamond growth, could only come from the carbon-rich phase, Fe3C, but not directly from the graphite. It is possible that carbon atoms from the graphite in the interface first react with Fe atoms to produce carbide Fe3C during diamond synthesis at high pressure and high temperature. The Fe3C finally decomposes into carbon atoms with the sp3 electron state at the interface to form the diamond.
Abstract:Diamond is synthesized in an Fe-Ni-C system at high pressure and high temperature, the C sp3 content profile through different thicknesses of interface between diamond and the catalyst film is measured by using electron energy loss spectroscopy. It is found that the C sp3 content varies from 87.33% to 78.15% when the measured position is located at the inner face near the diamond and then changes to 6 µm further away. Transmission electron microscope examinations show that there are different phases in the interface, such as Fe3C, γ−(Fe,Ni), and graphite, but the graphite phase diminishes gradually towards the inner face of the interface. These results profoundly indicate that the carbon atoms, required for diamond growth, could only come from the carbon-rich phase, Fe3C, but not directly from the graphite. It is possible that carbon atoms from the graphite in the interface first react with Fe atoms to produce carbide Fe3C during diamond synthesis at high pressure and high temperature. The Fe3C finally decomposes into carbon atoms with the sp3 electron state at the interface to form the diamond.
FAN Xiao-Hong,XU Bin**,NIU Zhen,ZHAI Tong-Guang,TIAN Bin. Fine Structural and Carbon Source Analysis for Diamond Crystal Growth using an Fe-Ni-C System at High Pressure and High Temperature[J]. 中国物理快报, 2012, 29(4): 48102-048102.
FAN Xiao-Hong,XU Bin**,NIU Zhen,ZHAI Tong-Guang,TIAN Bin. Fine Structural and Carbon Source Analysis for Diamond Crystal Growth using an Fe-Ni-C System at High Pressure and High Temperature. Chin. Phys. Lett., 2012, 29(4): 48102-048102.
[1] Bundy F P, Hall H T, Strong H M, Wentorf R H 1955 Nature 176 51[2] Liu X B, Jia X P, Guo X K et al 2010 Cryst. Growth Design 10 2895[3] Liu. X B, Ma H A, Zhao Z F et al 2011 Diamond Relat. Mater. 20 468[4] Palafnik L S, Gladkikh L I 1979 The Properties of Diamond (New York: Academic)[5] Sung J 2000 J. Mate. Sci. 35 6041[6] Xu B, Li M S, Li L et al 2007 Mater. Sci. Eng. A 454 293[7] Strong H M and Hanneman R E 1967 J. Chem. Phys. 46 3668[8] Pate B B 1986 Surf. Sci. 165 83[9] Giardini A A, Kohn J A, Eckart D W and Tydings J E 1961 Am. Miner. 46 976[10] Wentorf R H 1971 J. Phys. Chem. 75 1833[11] Yan X, Kanda H, Ohsawa T et al 1990 J. Mater. Sci. 25 1585[12] Yin L W, Li M S, Cui J J et al 2002 J. Cryst. Growth 234 1[13] Solozhenko V L, Turkevich V Z, Kurakevych O O et al 2002 J. Phys. Chem. B 106 6634[14] Li Y and Hao Z Y 2005 Diam. Abrasives Eng. 5 55[15] Egerton R F 2009 Rep. Prog. Phys. 72 2[16] Yoshikawa M, Mori Y, Obata H et al 1995 Appl. Phys. Lett. 67 694[17] Li L, Xu B and Li M S 2008 Chin. Sci. Bull. 53 937[18] Caveney R J 1992 Mater. Sci. Eng. B 11 197[19] Hao Z Y, Chen Y F and Zou G T 1996 Synthetic Diamond (Changchun: Jilin University Press) (in Chinese)[20] Zhang K C and Zhang L H 1997 Science and Technology for Crystal Growth (Beijing: Science Press) (in Chinese)[21] Liu Z L, Li Z L and Liu W D 2002 Interface Electronic Structure and Interfacial Properties (Beijing: Science Press) (in Chinese)