Electrochemical corrosion behaviors of Ti 3 SiC 2 /Cu composites in a 3.5% NaCl solution
Source abstract
Abstract
Abstract The electrochemical corrosion behaviors of Ti 3 SiC 2 /Cu composite and polycrystalline Ti 3 SiC 2 in a 3.5% NaCl medium were investigated by dynamic potential polarization, potentiostat polarization, and electrochemical impedance spectroscopy. The polycrystalline Ti 3 SiC 2 was tested on the identical condition as a control. The characterizations of XRD, X‐ray photoelectron spectroscopy, scanning electron microscope, and energy‐dispersive spectrometer were used to study the relevant passivation behavior and corrosive mechanism. The self‐corrosion current density of Ti 3 SiC 2 /Cu (6.46 × 10 −6 A/cm 2 ) was slightly higher than that of Ti 3 SiC 2 (1.64 × 10 −7 A/cm 2 ). Under open circuit potential, the corrosion resistance of Ti 3 SiC 2 /Cu was better than that of Ti 3 SiC 2 . Ti 3 SiC 2 /Cu exhibited a typical passivation feature with a narrow passivation interval and a breakdown phenomenon. The better corrosion resistance of Ti 3 SiC 2 was due to the more stable Si layer of the former. In comparison, for Ti 3 SiC 2 /Cu composites, Cu reacted with the reactive Si layers in Ti 3 SiC 2 to form Cu–Si compounds and TiC, destroying the weak interaction between Si layers and Ti–C layers. In the other hand, the as‐formed Cu–Si compounds and TiC dissolved during the corrosion of Ti 3 SiC 2 /Cu in the 3.5% NaCl medium, causing to the destruction of the passivation film on its surface.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: MXene and MAX Phase Materials · Aluminum Alloys Composites Properties · Advanced ceramic materials synthesis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Mechanical Engineering Xinjiang University Urumqi China
State Key Laboratory of Solid Lubrication, Lanzhou Institute of Chemical Physics Chinese Academy of Sciences Lanzhou China
School of Mechanical Engineering Chengdu University Chengdu China
School of Chemical Engineering and Materials Changzhou Institute of Technology Changzhou China
References (35)
Show source-provided references
1. 10.1016/j.ceramint.2022.06.14910.1016/j.ceramint.2022.06.149 ↗
2. 10.1016/j.ceramint.2019.03.14410.1016/j.ceramint.2019.03.144 ↗
3. 10.1111/ijac.1374110.1111/ijac.13741 ↗
4. 10.1016/S0079-6786(00)00006-610.1016/S0079-6786(00)00006-6 ↗
5. 10.1111/jace.1237610.1111/jace.12376 ↗
6. 10.1016/j.matchemphys.2021.12462510.1016/j.matchemphys.2021.124625 ↗
7. MAX phases: bridging the gap between metals and ceramics
8. 10.1111/ijac.1349710.1111/ijac.13497 ↗
9. 10.1016/j.corsci.2006.04.00510.1016/j.corsci.2006.04.005 ↗
10. 10.1016/S0010-938X(02)00227-510.1016/S0010-938X(02)00227-5 ↗
11. 10.1039/C6RA26239B10.1039/C6RA26239B ↗
12. 10.1002/adem.20040007110.1002/adem.200400071 ↗
13. 10.1016/j.ceramint.2015.01.15010.1016/j.ceramint.2015.01.150 ↗
14. 10.1149/MA2005-01/4/22910.1149/MA2005-01/4/229 ↗
15. 10.1016/j.ceramint.2016.03.09910.1016/j.ceramint.2016.03.099 ↗
16. Wettability and wetting process in Cu/Ti3SiC2 system
17. Research progress on strengthening methods and mechanisms of MAX phase ceramics
18. 10.1016/j.ceramint.2022.02.08410.1016/j.ceramint.2022.02.084 ↗
19. 10.1088/2053-1591/ac6a4d10.1088/2053-1591/ac6a4d ↗
20. 10.3390/ma1507251510.3390/ma15072515 ↗
21. 10.3390/met1205086310.3390/met12050863 ↗
22. 10.1016/j.corsci.2005.05.04610.1016/j.corsci.2005.05.046 ↗
23. 10.1016/j.corsci.2008.12.00510.1016/j.corsci.2008.12.005 ↗
24. 10.1351/pac19997106095110.1351/pac199971060951 ↗
25. 10.20964/2017.06.3710.20964/2017.06.37 ↗
26. 10.3390/met1205086310.3390/met12050863 ↗
27. 10.3390/met1203041710.3390/met12030417 ↗
28. 10.1016/j.jallcom.2017.06.19910.1016/j.jallcom.2017.06.199 ↗
29. 10.1016/S0010-938X(99)00003-710.1016/S0010-938X(99)00003-7 ↗
30. 10.1016/S0013-4686(03)00578-410.1016/S0013-4686(03)00578-4 ↗
31. 10.1016/j.corsci.2006.08.01010.1016/j.corsci.2006.08.010 ↗
32. 10.1016/0010-938X(88)90005-410.1016/0010-938X(88)90005-4 ↗
33. 10.1016/S0013-4686(97)00037-610.1016/S0013-4686(97)00037-6 ↗
34. 10.1007/s10008005004110.1007/s100080050041 ↗
35. 10.1016/j.ceramint.2017.01.11110.1016/j.ceramint.2017.01.111 ↗