TY - JOUR
T1 - Mechanisms of oxidation of pure and Si-segregated α-Ti surfaces
AU - Bhattacharya, Somesh Kr
AU - Sahara, Ryoji
AU - Suzuki, Satoshi
AU - Ueda, Kyosuke
AU - Narushima, Takayuki
N1 - Funding Information:
This work was supported by the Council for Science, Technology, and Innovation under the Cross-ministerial Strategic Innovation Promotion Program and the Process Innovation for Super Heat-resistant Metals (PRISM) project funded by Japan Science and Technology Agency . This work was also partially supported by the Japan Society for the Promotion of Science KAKENHI grant (number 15H04117 ). The calculations were performed using the high-performance computing facility at the National Institute for Materials Science.
Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2019/1/1
Y1 - 2019/1/1
N2 - Using first-principles molecular dynamics, we identified the mechanisms of the oxidation of α-Ti surfaces. Si segregation was found to suppress α-case formation in Ti, which was also confirmed experimentally. Charge transfer from the metal atoms to the gas molecules drives the initial stages of oxidation on the pure and Si-segregated α-Ti (0001) surfaces, while during the later stages, oxidation proceeds via oxygen penetration into the slab. Growth of the oxide network was strongly dependent on the oxidation state of the surface Ti atoms. Oxide growth in the Si-segregated material was retarded with the formation of TiO x (0.5 ≤ x ≤ 1) on the surface, which corresponds to the +1.5 oxidation state of the Ti atoms. The simulations and experiments clearly showed that Si reduces the ingress of oxygen into Ti, even at high temperatures. The primary and critical steps of identifying, understanding, and controlling the mechanisms of oxidation of Ti surfaces at high temperatures, as performed here, are expected to aid the design of new alloys with improved oxidation resistance.
AB - Using first-principles molecular dynamics, we identified the mechanisms of the oxidation of α-Ti surfaces. Si segregation was found to suppress α-case formation in Ti, which was also confirmed experimentally. Charge transfer from the metal atoms to the gas molecules drives the initial stages of oxidation on the pure and Si-segregated α-Ti (0001) surfaces, while during the later stages, oxidation proceeds via oxygen penetration into the slab. Growth of the oxide network was strongly dependent on the oxidation state of the surface Ti atoms. Oxide growth in the Si-segregated material was retarded with the formation of TiO x (0.5 ≤ x ≤ 1) on the surface, which corresponds to the +1.5 oxidation state of the Ti atoms. The simulations and experiments clearly showed that Si reduces the ingress of oxygen into Ti, even at high temperatures. The primary and critical steps of identifying, understanding, and controlling the mechanisms of oxidation of Ti surfaces at high temperatures, as performed here, are expected to aid the design of new alloys with improved oxidation resistance.
KW - High temperature
KW - Molecular dynamics
KW - Oxidation
KW - Surface
KW - α-Ti
UR - http://www.scopus.com/inward/record.url?scp=85052892474&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85052892474&partnerID=8YFLogxK
U2 - 10.1016/j.apsusc.2018.08.253
DO - 10.1016/j.apsusc.2018.08.253
M3 - Article
AN - SCOPUS:85052892474
SN - 0169-4332
VL - 463
SP - 686
EP - 692
JO - Applied Surface Science
JF - Applied Surface Science
ER -