Microstructural evolution of Cu-1at% Ti alloy aged in a hydrogen atmosphere and its relation with the electrical conductivity

Ultramicroscopy. 2009 Apr;109(5):593-8. doi: 10.1016/j.ultramic.2008.10.015. Epub 2008 Nov 12.

Abstract

Copper alloys with titanium additions between 1 and 6at% Ti emerge currently as attractive conductive materials for electrical and electronic commercial products, since they exhibit superior mechanical and electrical properties. However, their electrical conductivity is reduced owing to the residual amount of Ti solutes in the Cu solid solution (Cu(ss)) phase. Since Cu shows only poor reactivity with hydrogen (H), while Ti exhibits high affinity to it, we were inspired by the idea that hydrogenation of Cu-Ti alloys would influence their microstructure, resulting in a significant change of their properties. In this contribution, the influence of aging under a deuterium (D(2)) atmosphere of Cu-1at% Ti alloys on their microstructure is investigated to explore the effects on the electrical conductivity. The specimens were investigated by means of transmission electron microscopy (TEM), field ion microscopy (FIM), computer-aided field ion image tomography (cFIIT), and atom probe tomography (APT). At an early aging stage at 623K in a D(2) atmosphere of 0.08MPa, ellipsoidal alpha-Cu(4)Ti precipitates are formed in the alloy, and during subsequent aging, delta-TiD(2) is competitively nucleated instead of growth of alpha-Cu(4)Ti particles. The co-precipitation of alpha-Cu(4)Ti and delta-TiD(2) efficiently reduces the Ti concentration of Cu(ss) matrix, particularly in the later aging stages in comparison to the aging in vacuum conditions. The electrical conductivity of the alloy aged in the D(2) atmosphere increases steeply up to 48% International Annealed Copper Standard (IACS) after 1030h, while it saturates to approximately 20% IACS in the alloy aged in vacuum. The outstanding increase of electrical conductivity during aging in D(2) atmosphere can be basically explained by the reduction of Ti solute concentration in Cu(ss) matrix.

Publication types

  • Research Support, Non-U.S. Gov't