Mixed ionic electronic conductors for improved charge transport in electrotherapeutic devices
This invention addresses the need for efficient dry skin electrodes. Robust, flexible Mixed Ionic Electronic Conductor (MIEC) electrodes were prepared by an aqueous solution route resulting in electrically conductive networks of carbon nanotubes (CNTs) and ionically conductive elastic matrix. The flexible electrode was characterized in terms of conductivity, ionic charge transfer resistance, and water uptake. The flexible electrode maintained low resistance even after multiple cycles of 50% extension and contraction.
1. A method of conducting neuromuscular electrical stimulation (NMES), comprising:
applying an electrode onto a skin of a patient; and
generating a current through the electrode to activate a muscle wherein the electrode comprises:
alternative (a) which includes coalesced elastomer particles, carbon nanotubes (CNTs), and a glycosaminoglycan, wherein the CNTs and glycosaminoglycan are disposed on the exterior of the coalesced elastomer particles; or
alternative (b) which includes elastomer, CNTs, and a glycosaminoglycan and is characterizable by a conductivity of at least 1000 mS/cm that changes by less than 10% after 5 strain cycles of extending the electrode by 50% and allowing the electrode to contract; or
alternative (c) which includes coalesced polymeric particles, electrical conductor, and ionic conductor, wherein the electrical conductor and ionic conductor are disposed on the exterior of the coalesced polymeric particles.
2. The method of claim 1 , wherein the electrode comprises the coalesced elastomer particles of alternative (a), the carbon nanotubes (CNTs) of alternative (a), and the glycosaminoglycan of alternative (a), wherein the CNTs and the glycosaminoglycan are disposed on the exterior of the coalesced elastomer particles.
3. The method of claim 2 , wherein the electrode is characterizable by a conductivity of at least 1000 mS/cm that changes by less than 10% after 5 strain cycles of extending the material by 50% and allowing the material to contract.
4. The method of claim 2 , wherein the electrode comprises 0.1 to 5 wt % glycosaminoglycan.
5. The method of claim 1 , wherein the electrode comprises the elastomer of alternative (b), the CNTs of alternative (b), and the glycosaminoglycan of alternative (b) and is characterizable by a conductivity of at least 1000 mS/cm that changes by less than 10% after 5 strain cycles of extending the material by 50% and allowing the material to contract.
6. The method of claim 5 , wherein the wherein the electrode comprises a mass ratio of glycosaminoglycan to CNT in the range of 0.5 to 5.
7. The method of claim 1 , wherein the electrode comprises the coalesced polymeric particles of alternative (c), the electrical conductor of alternative (c), and the ionic conductor of alternative (c), wherein the electrical conductor and ionic conductor are disposed on the exterior of the coalesced polymeric particles.
8. The method of claim 7 , wherein the coalesced polymeric particles comprise ionically conductive moieties bonded to the coalesced polymeric particles.
9. The method of claim 8 , wherein the ionically conductive moieties are covalently bonded to the coalesced polymeric particles.
10. The method of claim 7 , wherein the polymeric particles are elastomeric.
11. The method of claim 1 , wherein the current is injected as a stimulation pulse.
12. The method of claim 1 , wherein the electrode is configured in the shape of a cuff.
13. The method of claim 1 , wherein the electrode is disposed in an apparatus comprising an array of the electrodes.
14. The method of claim 13 , wherein the apparatus is in the form of a sleeve.
15. The method of claim 1 , wherein the electrode comprises 0.1 to 2 wt % CNTs.
16. The method of claim 1 , wherein the electrode comprises 10 to 60 wt % water.
17. The method of claim 1 , wherein the electrode comprises a mass ratio of glycosaminoglycan to CNT in the range of 0.5 to 5.
18. The method of claim 1 , wherein the electrode comprises 0.01 to 2 wt % Na.
19. The method of claim 1 , wherein the electrode possesses a transference number, ti in the range of 0.10 to about 0.20.
20. The method of claim 1 , wherein the electrode comprises a top and bottom surface, and wherein the bottom surface contacts the skin of the patient.