Formation of composite ternary nitride thin films by magnetron sputtering co-deposition C.S. Sandu , R. Sanjinés, M. Benkahoul, F. Medjani, F. Lévy Institute of Physics of Complex Matter, EPFL, Station 3, CH-1015, Lausanne, Switzerland Available online 12 September 2006 Abstract Thin films of MXN (M stands for early transition metal and X = Si, Ge, Sn) are studied as protective coatings. To extend the knowledge about the formation of nanocomposite films, various MXN systems have been compared. TiSiN, TiGeN, TiSnN, NbSiN, ZrSiN and CrSiN thin films were deposited by reactive magnetron sputtering, from confocal targets in a mixed Ar/N 2 atmosphere. The chemical reactivity of germanium and tin with nitrogen is significantly lower than that of Si and Ti. Therefore, the TiGeN and TiSnN systems are different from TiSiN. Important changes in the morphology and structure of MXN films are induced by X addition. Nanocrystalline composite films are formed in all these investigated ternary systems. As a function of increasing X content (C X ), the size of the crystallites D in the TiSiN, TiGeN, NbSiN and ZrSiN films decreases (from tens of nm to 2 nm) following the relationship C X 1/ D. The segregation of X atoms on the MN crystallite surface is responsible for the limitation of their growth. It results in the formation of a SiN y or TiGe y amorphous phase on the crystallite surfaces. In the case of NbSiN and ZrSiN systems, Si atoms can substitute metal atoms in the cubic MN lattice up to a critical concentration (solubility limit). TiSiN, TiGeN and TiSnN systems are different: no solubility of Si, Ge and Sn in the TiN lattice is observed. For every composite film, the morphology changes result in a maximum hardness value at a typical concentration 2 C X 12 at.%. Resistivity measurements provide experimental mean for determining the limit of Si solubility in MSiN ternary systems and for following the thickness evolution of the SiN y coverage layer in the composite films. © 2006 Elsevier B.V. All rights reserved. Keywords: Ternary nitride; Structural properties; Nanocomposite; Sputtering Contents 1. Introduction .............................................................. 4084 2. Experimental ............................................................. 4084 3. Results ................................................................ 4084 3.1. Chemical composition ..................................................... 4084 3.2. Structure and morphology ................................................... 4085 3.3. Model for the MXN film formation ............................................ 4085 3.4. Mechanical properties ..................................................... 4087 3.5. Electrical resistivity ...................................................... 4087 4. Conclusion .............................................................. 4088 Acknowledgements ............................................................ 4088 Appendix A ................................................................ 4088 References ................................................................. 4089 Surface & Coatings Technology 201 (2006) 4083 4089 www.elsevier.com/locate/surfcoat Corresponding author. Tel.: +41 216935352. E-mail address: sscosmin@gmail.com (C.S. Sandu). 0257-8972/$ - see front matter © 2006 Elsevier B.V. All rights reserved. doi:10.1016/j.surfcoat.2006.08.100