Microstructure and Mechanical Properties of ZrN, ZrCN and ZrC Coatings Grown by Chemical Vapor Deposition

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Microstructure and Mechanical Properties of ZrN, ZrCN and ZrC Coatings Grown by Chemical Vapor Deposition. / Frank, Florian; Tkadletz, Michael; Czettl, Christoph et al.
In: Coatings, Vol. 11.2021, No. 5, 491, 22.04.2021, p. 1-13.

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@article{65ea4ded802e44fca440d7d3fc3815f3,
title = "Microstructure and Mechanical Properties of ZrN, ZrCN and ZrC Coatings Grown by Chemical Vapor Deposition",
abstract = "As the demands for wear-resistant coatings in the cutting industry are constantly rising, new materials that have the potential to exhibit enhanced coating properties are continuously explored. Chemical vapor deposited (CVD) Zr(N,C) is a promising alternative to the well-established and thoroughly investigated Ti(C,N) coating system, owing to its advantageous mechanical and thermal properties. Thus, within this work, CVD ZrN, ZrCN and ZrC coatings were deposited at 1000 ◦ C, and subsequently their microstructure and mechanical properties were investigated in detail. Scanning electron microscopy, electron backscatter diffraction and X-ray diffraction experiments revealed that all coatings exhibited a columnar structure and a fiber texture, where ZrN and ZrCN displayed a <100> preferred orientation in growth direction and ZrC showed a <110> texture. Tensile residual stresses that arise due to a mismatch in the coefficient of thermal expansion between the cemented carbide substrate and the coating material decreased with the addition of C to the coatings. No stress relaxation through thermal crack formation was observed in the coatings. The highest hardness was determined for the ZrC coating with 28.1 ± 1.0 GPa and the lowest for the ZrN coating with 22.1 ± 0.9 GPa. Addition of C to the ZrN coating increased the hardness to 26.1 ± 1.6 GPa, which can be explained by a more covalent bonding character, as well as by solid solution strengthening. The ZrCN coating exhibited the highest Young{\textquoteright}s modulus, followed by the ZrC and ZrN coatings, which can be attributed to differences in their electronic band structure. ",
author = "Florian Frank and Michael Tkadletz and Christoph Czettl and Nina Schalk",
note = "Publisher Copyright: {\textcopyright} 2021 by the authors. Licensee MDPI, Basel, Switzerland.",
year = "2021",
month = apr,
day = "22",
doi = "10.3390/coatings11050491",
language = "English",
volume = "11.2021",
pages = "1--13",
journal = "Coatings",
issn = "2079-6412",
publisher = "Multidisciplinary Digital Publishing Institute (MDPI)",
number = "5",

}

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TY - JOUR

T1 - Microstructure and Mechanical Properties of ZrN, ZrCN and ZrC Coatings Grown by Chemical Vapor Deposition

AU - Frank, Florian

AU - Tkadletz, Michael

AU - Czettl, Christoph

AU - Schalk, Nina

N1 - Publisher Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland.

PY - 2021/4/22

Y1 - 2021/4/22

N2 - As the demands for wear-resistant coatings in the cutting industry are constantly rising, new materials that have the potential to exhibit enhanced coating properties are continuously explored. Chemical vapor deposited (CVD) Zr(N,C) is a promising alternative to the well-established and thoroughly investigated Ti(C,N) coating system, owing to its advantageous mechanical and thermal properties. Thus, within this work, CVD ZrN, ZrCN and ZrC coatings were deposited at 1000 ◦ C, and subsequently their microstructure and mechanical properties were investigated in detail. Scanning electron microscopy, electron backscatter diffraction and X-ray diffraction experiments revealed that all coatings exhibited a columnar structure and a fiber texture, where ZrN and ZrCN displayed a <100> preferred orientation in growth direction and ZrC showed a <110> texture. Tensile residual stresses that arise due to a mismatch in the coefficient of thermal expansion between the cemented carbide substrate and the coating material decreased with the addition of C to the coatings. No stress relaxation through thermal crack formation was observed in the coatings. The highest hardness was determined for the ZrC coating with 28.1 ± 1.0 GPa and the lowest for the ZrN coating with 22.1 ± 0.9 GPa. Addition of C to the ZrN coating increased the hardness to 26.1 ± 1.6 GPa, which can be explained by a more covalent bonding character, as well as by solid solution strengthening. The ZrCN coating exhibited the highest Young’s modulus, followed by the ZrC and ZrN coatings, which can be attributed to differences in their electronic band structure.

AB - As the demands for wear-resistant coatings in the cutting industry are constantly rising, new materials that have the potential to exhibit enhanced coating properties are continuously explored. Chemical vapor deposited (CVD) Zr(N,C) is a promising alternative to the well-established and thoroughly investigated Ti(C,N) coating system, owing to its advantageous mechanical and thermal properties. Thus, within this work, CVD ZrN, ZrCN and ZrC coatings were deposited at 1000 ◦ C, and subsequently their microstructure and mechanical properties were investigated in detail. Scanning electron microscopy, electron backscatter diffraction and X-ray diffraction experiments revealed that all coatings exhibited a columnar structure and a fiber texture, where ZrN and ZrCN displayed a <100> preferred orientation in growth direction and ZrC showed a <110> texture. Tensile residual stresses that arise due to a mismatch in the coefficient of thermal expansion between the cemented carbide substrate and the coating material decreased with the addition of C to the coatings. No stress relaxation through thermal crack formation was observed in the coatings. The highest hardness was determined for the ZrC coating with 28.1 ± 1.0 GPa and the lowest for the ZrN coating with 22.1 ± 0.9 GPa. Addition of C to the ZrN coating increased the hardness to 26.1 ± 1.6 GPa, which can be explained by a more covalent bonding character, as well as by solid solution strengthening. The ZrCN coating exhibited the highest Young’s modulus, followed by the ZrC and ZrN coatings, which can be attributed to differences in their electronic band structure.

UR - http://www.scopus.com/inward/record.url?scp=85105462194&partnerID=8YFLogxK

U2 - 10.3390/coatings11050491

DO - 10.3390/coatings11050491

M3 - Article

VL - 11.2021

SP - 1

EP - 13

JO - Coatings

JF - Coatings

SN - 2079-6412

IS - 5

M1 - 491

ER -