Mechanical properties of VMoNO as a function of oxygen concentration: Toward development of hard and tough refractory oxynitridesShow others and affiliations
2019 (English)In: Journal of Vacuum Science & Technology. A. Vacuum, Surfaces, and Films, ISSN 0734-2101, E-ISSN 1520-8559, Vol. 37, no 6, article id 061508Article in journal (Refereed) Published
Abstract [en]
Improved toughness is a central goal in the development of wear-resistant refractory ceramic coatings. Extensive theoretical and experimental research has revealed that NaCl-structure VMoN alloys exhibit surprisingly high ductility combined with high hardness and toughness. However, during operation, protective coatings inevitably oxidize, a problem that may compromise material properties and performance. Here, the authors explore the role of oxidation in altering VMoN properties. Density functional theory and theoretical intrinsic hardness models are used to investigate the mechanical behavior of cubic V0.5Mo0.5N1-xOx solid solutions as a function of the oxygen concentration x. Elastic constant and intrinsic hardness calculations show that oxidation does not degrade the mechanical properties of V0.5Mo0.5N. Electronic structure analyses indicate that the presence of oxygen reduces the covalent bond character, which slightly lowers the alloy strength and intrinsic hardness. Nevertheless, the character of metallic d-d states, which are crucial for allowing plastic deformation and enhancing toughness, remains unaffected. Overall, the authors' results suggest that VMoNO oxynitrides, with oxygen concentrations as high as 50%, possess high intrinsic hardness, while still being ductile. Published by the AVS.
Place, publisher, year, edition, pages
American Institute of Physics (AIP), 2019. Vol. 37, no 6, article id 061508
National Category
Inorganic Chemistry
Identifiers
URN: urn:nbn:se:oru:diva-79130DOI: 10.1116/1.5125302ISI: 000504231200029Scopus ID: 2-s2.0-85074096790OAI: oai:DiVA.org:oru-79130DiVA, id: diva2:1385401
Funder
Vinnova, 2016-05156
Note
The authors acknowledge financial support from the Swedish Government Strategic Research Area Grant in Materials Science on Advanced Functional Materials at Linköping University (Faculty Grant SFO-Mat-LiU No. 2009 00971). Calculations were performed using the resources provided by the Swedish National Infrastructure for Computing (SNIC), on the Triolith and Tetralith Clusters located at the National Supercomputer Centre (NSC) in Linköping and on the Kebnekaise cluster located at the High Performance Computing Center North (HPC2 N) in Umeå. D.G.S. gratefully acknowledges financial support from the Olle Engkvist Foundation and the competence center FunMat-II supported by the Swedish Agency for Innovation Systems (Vinnova, Grant No. 2016-05156).
2020-01-142020-01-142025-04-25Bibliographically approved