Methods of making silver/silver chloride electrodes by vapor deposition techniques
A method for forming an Ag/AgCl coated electrode includes providing a polymeric electrode substrate made of Acrylonitrile Butadiene Styrene (ABS). A layer of silver (Ag) is deposited on the polymeric electrode substrate using physical vapor deposition (PVD) to form an Ag coated electrode. The layer of Ag is deposited to a first thickness by sputtering an Ag target onto the polymeric electrode substrate. The Ag coated electrode is then converted to a layer of silver/silver chloride (Ag/AgCl) by dipping it into a conversion solution. The resulting Ag/AgCl coated surface electrode provides improved performance and stability for various applications.
1 . A method for forming an Ag/AgCl coated electrode, comprising:
providing a polymeric electrode substrate, the polymeric electrode substrate comprising Acrylonitrile Butadiene Styrene (ABS), wherein the polymeric electrode substrate is configured as a neuromonitoring electrode;
depositing a layer of silver (Ag) on the polymeric electrode substrate by physical vapor deposition (PVD) to form an Ag coated electrode, the layer of Ag being deposited to a first thickness, and the depositing comprising sputtering an Ag target onto the polymeric electrode substrate, wherein a deposition rate is determined at least in part on the material and the shape of the electrode substrate; and
converting the layer of Ag to a layer of silver/silver chloride (Ag/AgCl) to form a Ag/AgCl coated surface electrode, the converting comprising dipping the Ag coated electrode into a conversion solution, wherein the conversion solution consists essentially of 1.0 M ferric chloride (FeCl 3 ), and wherein the conversion solution is not heated.
2 . The method of claim 1 , the polymeric electrode substrate comprising 20% glass-filled ABS.
3 . The method of claim 1 , the polymeric electrode substrate being injection molded.
4 . The method of claim 1 , the first thickness being about 0.74 μm.
5 . The method of claim 4 , the sputtering being carried out for up to about 300 seconds.
6 . The method of claim 1 , the first thickness being about 1.2-1.25 μm.
7 . The method of claim 6 , the sputtering being carried out for up to about 500 seconds.
8 . The method of claim 1 , the depositing further comprising at least one of:
roughing a surface of the polymeric electrode substrate;
generating a high vacuum environment; and
etching the surface of the polymeric electrode substrate.
9 . The method of claim 1 , the depositing being carried out in the presence of a heat sink.
10 . The method of claim 1 , the dipping being carried out for a time period of about 30-60 seconds.
11 . The method of claim 1 , the converting further comprising a rinsing step.
12 . The method of claim 1 , the converting further comprising a stabilizing step.
13 . The method of claim 12 , the stabilizing step comprising placing the Ag/AgCl coated surface electrode in a stabilizing solution.
14 . The method of claim 13 , the stabilizing solution comprising one or more of water, NaCl, and glycerin, and the Ag/AgCl coated surface electrode is placed in the stabilizing solution for a stabilization time period.
15 . The method of claim 1 , the converting further comprising a drying step.
16 . The method of claim 15 , the drying step comprising baking the Ag/AgCl coated surface electrode for a drying time period.
17 . The method of claim 1 , the polymeric electrode substrate configured such that a plurality of surfaces of the polymeric electrode substrate can be coated while being turned in a sputtering chamber during the depositing.
18 . The method of claim 17 , wherein the electrode substrate is substantially free of 90° angles and/or undercuts along a longitudinal axis of the electrode substrate.
19 . The method of claim 1 , wherein the deposition rate versus a cycle time is tuned based on a predetermined thickness of the deposition layer.