Theoretical analysis of diamond mechanosynthesis. Part II. C2 mediated growth of diamond C(110) surface via Si/Ge-triadamantane dimer placement tools

Journal of Computational and Theoretical Nanoscience

Volumn 1, Issue 1, 2004, Pages 71-80

  Mann, David J ^a   Peng, Jingping ^a   Freitas Jr , Robert A ^a   Merkle, Ralph C ^a  

^a ZYVEX CORPORATION   (United States)

Author keywords

Adamantane; Carbon; Density Functional Theory; Diamond; Dicarbon; Dimer Placement; Mechanosynthesis; Nanotechnology; Positional Control; VASP

Indexed keywords

CARBON; COMPUTER SIMULATION; DIMERS; GERMANIUM; MOLECULAR DYNAMICS; NANOTECHNOLOGY; POSITION CONTROL; POTENTIAL ENERGY; PROBABILITY DENSITY FUNCTION; SILICON; SYNTHESIS (CHEMICAL);

ADAMANTANE; DENSITY CONTROL FUNCTION; DICARBON; DIMER PLACEMENT; MECHANOSYNTHESIS; POSITIONAL CONTROL; VASP;

DIAMONDS;

EID: 20444381454     PISSN: 15461955     EISSN: None     Source Type: Journal    
DOI: 10.1166/jctn.2004.008     Document Type: Article

References (22)

1. J. Peng, R. A. Freitas Jr., and R. C. Merkle, J. Comput. Theor. Nanosci. 1, 63 (2004).
2. R. C. Merkle and R. A. Freitas Jr., J. Nanosci. Nanotechnol. 3, 319 (2003).
3. C. B. Musgrave, J. K. Perry, R. C. Merkle, and W. A. Goddard III, Nanotechnology 2, 187 (1991).
4. M. Page and D. W. Brenner, J. Am. Chem. Soc. 113, 3270 (1991).
5. X. Y. Chang, M. Perry, J. Peploski, D. L. Thompson, and L. M. Raff, J. Chem. Phys. 99, 4748 (1993).
6. S. B. Sinnott, R. J. Colton, C. T. White, and D. W. Brenner, Surf. Sci. 316, L1055 (1994).
7. D. W. Brenner, S. B. Sinnott, J. A. Harrison, and O. A. Shenderova, Nanotechnology 7, 161 (1996).
8. A. Ricca, C. W. Bauschlicher Jr., J. K. Kang, and C. B. Musgrave, Surf. Sci. 429, 199 (1999).
9. G. Kresse and J. Furthmuller, Vienna Ab-initio Simulation Package (VASP): The Guide, VASP Group, Institut fur Materialphysik, Universität Wien, Sensengasse 8, A-1130 Wien, Vienna, Austria (2003).
10. S. Landa, Chem. Listy. 27, 415 (1933).
11. A. P. Marchand, Science 299, 52 (2003).
12. J. E. Dahl, S. G. Liu, R. M. K. Carlson, Science 299, 96 (2003).
13. P. von R. Schleyer, J. Ain. Chem. Soc. 79, 3292 (1957).
14. E. Boelema, J. Strating, and Hans Wynberg, Tetrahedron Lett. 12, 1175 (1972).
15. W. David Graham, P. von R. Schleyer, E. W. Hagaman, and E. Wenkert, J. Am. Chem. Soc. 95, 5785 (1973).
16. C. A. Cupas, P. von R. Schleyer, and D. J. Trecker, J. Am. Chem. Soc. 87, 917 (1965).
17. Van Zandt Williams, Jr., P. von R. Schleyer, G. J. Gleicher, and L. B. Rodewald, J. Am. Chem. Soc. 88, 3862 (1966).
18. W. Burns, T. R. B. Mitchell, M. Anthony McKervey, J. J. Rooney, G. Ferguson, and P. Roberts, J. Chem. Soc. Chem. Commun. 1976, 893 (1976).
19. M. Shen, H. F. Schaefer III, C. Liang, J.-H. Lii, N. L. Allinger, and P. von Rague Schleyer, J. Am. Chem. Soc. 114, 497 (1992).
20. N. Auner, J. Weis, eds., Organosilicon Chemistry: From Molecules to Materials, VCH and John Wiley, New York; Vols. I (1994), II (1995), III (1998), IV (2000), V (2003).
21. J. Drake, Organogennanium Compounds, Springer-Verlag, New York (1994).
22. T. F. Rutledge, Acetylenic Compounds: Preparation and Substitution Reactions, Reinhold Book Corp., New York (1968).