An Approach to Synthesize Thick α‐ and γ‐Al2O3 Coatings by High‐Speed Physical Vapor Deposition
Source abstract
Abstract
Crystalline α‐ and γ‐Al2O3 exhibit in many applications high wear resistance, chemical resistance, and hot hardness, making them interesting materials for production engineering. To synthesize α‐Al2O3 with high coating thickness of s ≥ 10 μm, chemical vapor deposition at temperatures T > 1000 °C is well established. However, there are almost no studies dealing with the synthesis of thick α‐Al2O3 by physical vapor deposition (PVD) at high temperatures T > 700 °C. High‐temperature deposition of thick coatings can be realized by means of the dense hollow cathode plasma, combined with the transport function of the plasma gas in high‐speed (HS) PVD. Herein, crystalline α‐ and γ‐Al2O3 films are deposited on cemented carbides at substrate temperatures T s ≈ 570 °C and T s ≈ 780 °C by HS‐PVD. These coatings exhibit a thickness up to s = 20 μm. Moreover, phase analysis presents α‐phases in coatings synthesized at substrate temperature of T s ≈ 780 °C with significant higher hardness than films by T s ≈ 570 °C. These release the potential of HS‐PVD to synthesize α‐Al2O3 coatings with high thickness. Thereby, a higher thickness of these coatings is beneficial for the wear protection of turning and die casting tools.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Metal and Thin Film Mechanics · Diamond and Carbon-based Materials Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Surface Engineering Institute RWTH Aachen Kackertstraße 15 52072 Aachen Germany
Funding
Deutsche Forschungsgemeinschaft
References (21)
Show source-provided references
1. 10.1016/S0257-8972(02)00482-610.1016/S0257-8972(02)00482-6 ↗
2. 10.1016/j.cirpj.2016.11.00410.1016/j.cirpj.2016.11.004 ↗
3. 10.1016/j.surfcoat.2012.06.08710.1016/j.surfcoat.2012.06.087 ↗
4. 10.1016/j.wear.2017.11.01910.1016/j.wear.2017.11.019 ↗
5. 10.1016/j.surfcoat.2004.08.02110.1016/j.surfcoat.2004.08.021 ↗
6. 10.1002/adem.20090023210.1002/adem.200900232 ↗
7. 10.1016/j.surfcoat.2021.12695910.1016/j.surfcoat.2021.126959 ↗
8. Klocke F. · 2008
9. 10.1016/j.ijrmhm.2019.02.00610.1016/j.ijrmhm.2019.02.006 ↗
10. 10.1002/mawe.20180000810.1002/mawe.201800008 ↗
11. Bobzin K. · Materialwiss. Werkstofftech. · 2013 · 44 · 201300175
12. 10.1016/S0257-8972(97)00341-110.1016/S0257-8972(97)00341-1 ↗
13. 10.1016/0257-8972(95)00270-710.1016/0257-8972(95)00270-7 ↗
14. 10.1016/S0257-8972(96)02992-110.1016/S0257-8972(96)02992-1 ↗
15. 10.1016/S0257-8972(03)00539-510.1016/S0257-8972(03)00539-5 ↗
16. 10.1002/adem.20060004910.1002/adem.200600049 ↗
17. 10.1002/adem.20210102110.1002/adem.202101021 ↗
18. 10.1016/j.surfcoat.2017.09.07110.1016/j.surfcoat.2017.09.071 ↗
19. 10.1016/j.surfcoat.2017.05.03410.1016/j.surfcoat.2017.05.034 ↗
20. 10.1557/S088376940004163410.1557/S0883769400041634 ↗
21. 10.1016/j.surfcoat.2003.10.05810.1016/j.surfcoat.2003.10.058 ↗