Thermodynamics and Kinetics of Ti2N Formation by N Atom Intercalation in Ti

TL;DR

This study explores the thermodynamics and kinetics of Ti2N formation through N atom intercalation in titanium, revealing a diffusionless growth process and providing detailed energetic and diffusion pathway insights.

Contribution

It demonstrates that N intercalation can lead to Ti2N formation via a diffusionless process, supported by DFT calculations of energetics and diffusion pathways.

Findings

N intercalation is thermodynamically favored at each nitridation step.

Ti2N forms via a diffusionless displacement of Ti atoms.

Diffusion coefficients of N from surface to bulk were calculated.

Abstract

Although Ti2N and Ti belong to different crystal systems and Bravais lattices, we show that N intercalation in Hexagonal Close-Packed (HCP) Ti can lead to the formation of Ti2N by diffusionless displacement of Ti atoms, which is a nucleation-free growth process. This is due to the structural similarity of Ti atoms in Ti and Ti2N. For N intercalation in Ti, the first N2 molecule should adsorb on the surface of Ti {0001} and dissociate into N atoms, and then enough of the adsorbed N atoms should diffuse into Ti to form Ti2N. We calculated the enthalpy of formation for each step during N intercalation using density functional theory (DFT). We found that N intercalation was thermodynamically favored at each step of nitridation till the formation of Ti2N. We identified the transition network for each diffusion path and calculated the diffusion coefficient of N from surface to sub-surface to bulk.