Mechanism of Carbon Diffusion and Phase‐Transition‐Induced FCC‐TiC Formation via Hot Pressing
Titanium carbide (TiC), which typically forms at the solid-state diffusion interface in steel-titanium (Ti) composite structures, significantly influences steel-Ti interface bonding. However, the atomic-level formation mechanism of this carbide remains unclear. Herein, the TiC crystal structure and formation mechanism are investigated through experiments involving TA2 pure Ti and 45# carbon steel under solid-state diffusion conditions. Analysis of the solid-state diffusion behavior between the steel and Ti, based on selected area electron diffraction, reveals the formation of a continuous micro-nano TiC layer with a balanced (FCC) crystal structure on the substrate near the Ti side of the interface. Using the integrated differential phase contrast technique, occupation of the octahedral interstices in the FCC-TiC lattice by carbon (C) atoms is confirmed for the first time. Additionally, it is suggested that C diffusion and phase transformation jointly induce the FCC-TiC crystal phase transformation under hot-pressing conditions. Finally, the atomic-scale TiC formation mechanism is elucidated. The findings of this study may guide the design and development of high-performance materials with unique properties for aerospace equipment manufacturing.
Authors
- Cheng Gu (ORCID: https://orcid.org/0000-0002-2244-6551)
- Yuefeng Ying (ORCID: https://orcid.org/0000-0002-5415-8730)
- Sheng Zeng (ORCID: https://orcid.org/0000-0002-9283-6598)
- Linhong Deng (ORCID: https://orcid.org/0000-0003-1970-8239)
- Guoqiang You (ORCID: https://orcid.org/0000-0001-7562-107X)
- Bin Jiang (ORCID: https://orcid.org/0000-0003-3798-1159)
Institutions
- Chongqing University (CN)
- Chongqing Academy of Science and Technology (CN)
- Chongqing University of Technology (CN)
Publication Details
- Journal
- Advanced Science
- Published
- 2025-10-07
- DOI
- https://doi.org/10.1002/advs.202511724
- Primary Topic
- Advanced materials and composites
- Type
- article
- Field-Weighted Citation Impact
- 0.00