DocumentCode :
628590
Title :
Corrosion of the Cu/Al interface in Cu-Wire-bonded integrated circuits
Author :
Osenbach, J. ; Wang, B.Q. ; Emerich, S. ; DeLucca, John ; Dongmei Meng
Author_Institution :
LSI Corp. (USA), Allentown, PA, USA
fYear :
2013
fDate :
28-31 May 2013
Firstpage :
1574
Lastpage :
1586
Abstract :
A model for corrosion induced failure in wire bond devices made with either Cu or Au wire was developed. The model is based on detailed analysis of the chemical composition, crystallography, and micro structure of the corrosion induced failure sites. The detailed analysis was enabled by both a scanning electron microscope (SEM) and a transmission electron microscope (TEM) equipped with the appropriate analytical detectors. The combined characterization results were used to develop a detailed failure mechanism model which explains not only the overall chemical reactions but also the resultant two phase microstructures of the corrosion product observed in both metal systems. In addition the model helps to explain why Cu wire bonded devices are more susceptible to corrosion than Au wire bonded devices. In both systems corrosion occurs in the IMC not the end components pure metals. It is proposed this is due to the oxide on the surface of the IMCs being less resistant to pitting corrosion than that for Al. Once IMC passivity is broken down, corrosion of the IMC proceeds via selective oxidation of Al. This leads to the formation of a corroded region which is composed of a two phase microstructure, crystalline γ-Al2O3 with embedded crystalline Au and Cu metal particles. The resulting oxidized interface is highly susceptible to fracture, which is the ultimate reason for device failure. Although similar there are differences in the Cu/Al and Au/Al systems. There is a notable difference in the size and distribution of Cu particles in the aluminum oxide corrosion product of the Cu-Al system as compared to the Au particles in the aluminum oxide corrosion product of the Au-Al system. In particular, the Cu particles appear to be more uniformly distributed as compared to their Au counterparts. This difference is likely related to the crystal structure of the IMC from which the corrosion product was formed. It is proposed that this difference is related to the presence an- probability of Al to Al bonding in the IMC phase/s. Furthermore, the IMC structures are also suspected to be responsible for the better immunity to contamination (specifically Halide) induced corrosion of Au relative to Cu.
Keywords :
aluminium; copper; corrosion; crystallography; fracture; integrated circuit packaging; lead bonding; Al2O3; Cu-Al; Cu-wire-bonded integrated circuit; SEM; TEM; aluminum oxide corrosion product; chemical composition; corrosion induced failure; crystal structure; crystalline γ-Al2O3; crystallography; failure mechanism model; fracture; phase microstructure; pitting corrosion; scanning electron microscope; selective oxidation; transmission electron microscope; wire bond device; Compounds; Corrosion; Diffraction; Gold; Microstructure; Scanning electron microscopy; Wires;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Electronic Components and Technology Conference (ECTC), 2013 IEEE 63rd
Conference_Location :
Las Vegas, NV
ISSN :
0569-5503
Print_ISBN :
978-1-4799-0233-0
Type :
conf
DOI :
10.1109/ECTC.2013.6575782
Filename :
6575782
Link To Document :
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