RT Journal Article T1 Bonding structure and hydrogen content in silicon nitride thin films deposited by the electron cyclotron resonance plasma method A1 Mártil de la Plaza, Ignacio A1 González Díaz, Germán A1 Prado Millán, Álvaro del A1 San Andrés Serrano, Enrique AB The bonding structure and hydrogen content of amorphous hydrogenated silicon nitride (a-SiNx:H) thin films have been investigated by infrared spectroscopy and ion beam techniques. Electron cyclotron resonance plasma enhanced chemical vapor deposition was used to produce these films under different values of gas flow ratio, deposition temperature, and microwave power. The amount of bonded hydrogen was calculated from the N-H and Si-H infrared absorption bands. An increase of the SiH4 partial pressure during deposition was found to have the same effect on the H content as an increase of the substrate temperature: both cause a decrease of the N-H bond density and an increase in the number of Si-H bonds. This is explained by a competitive process in the formation of N-H and Si-H bonds during the growth of the film, whereby Si-H bonds are favored at the expense of N-H bonds when either the SiH4 flow or the substrate temperature are increased. Such tendency to chemical order is compared with previous results in which the same behavior was induced by thermal annealing or ion beam bombardment. PB Elsevier Science SA SN 0040-6090 YR 2004 FD 2004-07-01 LK https://hdl.handle.net/20.500.14352/51119 UL https://hdl.handle.net/20.500.14352/51119 LA eng NO [1] D.A. Buchanan, IBM J. Res. Dev., 43, (1999), 245.[2] I.A. Ross, Proc. IEEE, 86, (1998), 7.[3] T.P. Ma, IEEE Trans.Electron Devices, 45, (1998), 680.[4] S.S. He, M.J. Williams, D.J. Stephens, G. Lucovsky , J. Non-Cryst. Solids, 164–166, (1993), 731.[5] S. Summers, H.S. Reehal, G.H. Shirkoochi, J. Phys. D, 34, (2001), 2782.[6] W.A. Lanford, M.J. Rand, J. Appl. Phys., 49, (1978), 2473.[7] W.Bohne, W. Fuhs, J. Röhrich, B. Selle, G. González-Díaz, I. Mártil, F.L. Martínez, Á. del Prado, Surf. Interface Anal., 30, (2000), 534.[8] L. Wang, H.S. Reehal, F.L. Martínez, E. San Andrés, Á. del Prado, Semicond. Sci. Technol., 18, (2003), 633.[9] F.L. Martínez, Á. del Prado, I. Mártil, G. González-Díaz, W. Bohne, W. Fuhs, J. Röhrich, B. Selle, I. Sieber, Phys. Rev. B, 63, (2001), 245320.[10] Z. Yin, F.W. Smith, Phys. Rev. B, 43, (1991), 4507.[11] I.N. Levine, Physical Chemistry, McGraw-Hill, New York, 1988.[12] F.W. Smith, Z. Yin, J. Non-Cryst. Solids, 137–138(1991), 871.[13] G. Lucovsky, Z. Zing, D.R. Lee, J. Vac. Sci. Technol. B, 14, (1996), 2832.[14] Z. Jing, G. Lucovsky ,J.L. Whitten, J. Vac. Sci. Technol. B, 13, (1995), 1613.[15] N.N. Greenwood, A. Earnshaw, Chemistry of the Elements, Pergamon, Oxford, 1984. NO European Vacuum Congress (EVC-8)(8. 2003, Berlin, Alemania) / Annual Conference of the German-Vacuum-Society (DVG) (2. 2003, Berlin, Alemania). © 2003 Elsevier B.V. All rights reserved. This work was partially supported by the Ministry of Science and Technology (Spain) under contract TIC2001 y 1253. NO Ministry of Science and Technology (Spain) DS Docta Complutense RD 6 may 2024