Effect of pre-deformation on hydrogen diffusion and hydrogen induced damage in commercially pure titanium

Abstract

This work aims to elucidate the interaction between hydrogen atoms and pre-introduced dislocations in commercially pure titanium (CP-Ti). Positron annihilation spectroscopy supplemented by the first-principle calculations was utilized to reveal the effects of dislocation densities on the formation of hydride types and the concentration of hydrogen-induced defects in CP-Ti. Results show that, in the hydrogen-charged sample with 40 % deformation, hydrogen-induced damage gradually decreases when the hydrogen enters the sample at a depth of about 350 nm. This finding suggests that the high-density dislocations present in deformed specimens effectively trap hydrogen atoms and inhibit their diffusion, which ultimately mitigate damage within the samples. γ-TiH and δ-TiH2 hydrides are observed in the hydrogen-charged sample. The thermal desorption spectroscopy results show that the desorption amount of deuterium decreases from 1.14 × 1018 D/cm2 to 5.10 × 1017 D/cm2 with an increase in dislocation density because dislocations inhibit the diffusion of deuterium. In samples with higher deformation, the high dislocation density inhibits the formation of δ-TiH2 hydrides and promotes the formation of γ-TiH hydrides, which significantly reduce the hardening of samples. These results provide insight into the interaction of hydrogen with pre-introduced defects and provide strong theoretical support for the development and improvement of more damage-resistant materials.