AVS 62nd International Symposium & Exhibition
    Thin Film Wednesday Sessions
       Session TF+AS+BI-WeA

Paper TF+AS+BI-WeA9
Improving the Long-Term Stability of Thin-Film Contact and Electrode Metallizations for Implantable Silicon Neural Interfaces

Wednesday, October 21, 2015, 5:00 pm, Room 114

Session: Thin Films for Biological and Biomedical Applications
Presenter: Brian Baker, University of Utah
Authors: B. Baker, University of Utah
R. Caldwell, University of Utah
H. Mandal, Blackrock Microsystems
R. Sharma, University of Utah
P. Tathireddy, University of Utah
L.W. Rieth, University of Utah
Correspondent: Click to Email

The Utah Electrode Array (UEA) is a penetrating multi-electrode interface designed to be implanted and communicate directly with the brain and peripheral nerves through recording and stimulation. These devices are used for treating neural disorders and controlling prosthetics.

The UEA is micromachined out of single crystal silicon and uses a Pt/Ir/IrOx thin film metallization stack as an electrical interface on the electrode tip and a Pt/Ir/Pt stack on the backside contacts. Delamination of these thin metal layers has been observed during fabrication processes, soak testing, and in vivo operation, and is the critical failure mode examined in this study.

Db-FIB and Cross-sectional STEM analysis were used to identify Kirkendall voids as the root cause of the adhesion failures. This investigation showed that these voids form during the platinum silicide annealing process at the interface between the PtSi and the Ir layers.

Typical thicknesses of the UEA metallization are 200 nm/500 nm/520 nm Pt/Ir/IrOx, and 200 nm/200 nm/325 nm Pt/Ir/Pt. We report the results of replacing the 200 nm base layer with 1) a 25 nm Pt base layer or 2) a 50 nm co-sputtered PtSi base layer. These layers were subjected to typical UEA annealing conditions of 375 °C in forming gas for 45 minutes, followed by a 475 °C, 30 minute oxygen anneal.

Cross-sectional STEM elemental mapping of each film stack showed complete transformation of the platinum layer to PtSi, with a 40 nm layer of iridium silicide formed at the PtSi/Ir interface. In addition, a a reduction in the nanogaps caused by Kirkendall voiding was demonstrated by STEM analysis in the two new film stacks.

Both the 25 nm Pt base layer stack and the 50 nm co-sputtered PtSi base layer stack demonstrate low-resistance Ohmic contacts and wire bondability after annealing. Further electrical characterization of these thinner base layer stacks used on tip metal demonstrated impedances of 5-10 kOhms and charge injection capacities of 1-2 mC/cm2 for typical electrode tip surface areas. Cross-sectional STEM analysis of the reactively sputtered iridium oxide film reveals a three dimensional morphology whose nanostructures provide a large augmentation of electrode surface area and a corresponding increase in charge injection capacity. In vitro stimulation and accelerated lifetime tests are ongoing and electrical measurements and thin film adhesion stability will be reported.