Abstract

Pulsed reactive magnetron sputtering was used to deposit Zr–B–C–N films as a function of the N2/Ar ratio in the plasma. The microstructure evolution of the films was studied by high-resolution transmission electron microscopy, X-ray photoelectron spectroscopy and nanoindentation. Zr–B–C–N films with a chemical composition (in at.% without 1–2 at.% H and<1 at.% O and Ar) of Zr61B27C6N3, Zr41B30C8N20, Zr26B26C5N42 and Zr24B19C6N49 were produced using a nitrogen fraction of 0%, 5%, 10% and 15%. The Zr61B27C6N3 film consists of fcc B-rich Zr(B,C,N) nano-columnar structures concealed by an amorphous matrix. The fcc B-rich Zr(B,C,N) columns exhibit a preferred orientation with their [111] parallel to the film growth direction. The Zr41B30C8N20 film possesses the highest hardness and consists of nano-needle structures (∼40nm long and ∼10nm wide) separated by amorphous boundaries. The nano-needles have a face-centered cubic (fcc) structure and are composed of ZrN and/or Zr(B,C,N) nano-domain structures (∼2nm) that are semi-coherently joined via Zr–N monolayer interfaces. The Zr26B26C5N42 film is composed mainly of refined crystalline ZrN nano-needle structures (∼2nm) embedded in an amorphous structure, and the Zr24B19C6N49 film has an amorphous-like structure. In the Zr41B30C8N20 film, the formation of ZrN and/or Zr(B,C,N) nano-domain structures, semi-coherently joined via Zr–N monolayer interfaces within the nano-needle structures, play a critical role in achieving high hardness and modulus. The annihilation of such a structure and the introduction of additional amorphous structure into the films by changing the N/Zr ratio via varying the N2 fraction in the gas mixture result in a significant decrease in the mechanical properties.

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