A Bondable Metallization Stack That Prevents Diffusion of Oxygen and Gold into Monolithically Integrated Circuits Operating Above 500 degree C

We investigate use of tantalum silicide (TaSi sub(2), 400 nm)/platinum (Pt, 200 nm)/iridium (Ir, 200 nm)/platinum (Pt, 200 nm) as both a bond metal and a diffusion barrier to prevent oxygen (from air) and gold (from the wire bond) from infiltrating silicon carbide (SiC) monolithically integrated cir...

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Bibliographic Details
Published inJournal of electronic materials Vol. 41; no. 5; pp. 915 - 920
Main Authors Spry, D J, Lukco, D
Format Journal Article
LanguageEnglish
Published 01.05.2012
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Summary:We investigate use of tantalum silicide (TaSi sub(2), 400 nm)/platinum (Pt, 200 nm)/iridium (Ir, 200 nm)/platinum (Pt, 200 nm) as both a bond metal and a diffusion barrier to prevent oxygen (from air) and gold (from the wire bond) from infiltrating silicon carbide (SiC) monolithically integrated circuits operating above 500 degree C for over 1000 h in air. The TaSi sub(2)/Pt/Ir/Pt metallization is easily bonded for electrical connection to off-chip circuitry and does not require extra anneals or masking steps. It can be used directly on ohmic contact metals, dielectric insulating layers, or interconnect metal, because it adheres to silicon dioxide (SiO sub(2)), silicon nitride (Si sub(3)N sub(4)), and titanium (Ti). In this study, we investigate use of the new metallization of TaSi sub(2)/Pt/Lr/Pt (in deposition order) with TaSi sub(2) resting on top of a Ti-SiC contact annealed at 600 degree C for 30 min in nitrogen, which allows the TaSi sub(2) layer to react with the bottom platinum layer to form the Pt sub(2)Si diffusion barrier at the Pt-Ir interface. Since the iridium layer does not readily form a silicide, it prevents the silicon from migrating into the topmost platinum layer during further annealing or high-temperature integrated circuit operation. This leaves a pure platinum layer at the surface, ideal for gold wire bonding. We discuss the characteristics of the TaSi sub(2)/Pt/Ir/Pt metallization at 500 degree C after 10 h, 100 h, and 1000 h in air ambient and N2 ambient. Auger electron spectroscopy (AES) depth profiles of the metallization and field-emission scanning electron microscopy-focused ion beam (FESEM-FIB) cross-sections are also discussed.
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ISSN:0361-5235