Conductive Polymer Electrodes for Neural Prosthetic Applications

1985 ◽  
Vol 55 ◽  
Author(s):  
J. S. Foos ◽  
S. M. Erker

ABSTRACTA variety of materials have been evaluated for use as electrodes for neural stimulation. In an effort to maximize the charge density on the electrode surface, faradaic stimulation electrodes have been investigated. Electrodes consisting of thin films of polypyrrole on Pt have been studied in phosphate buffered saline using cyclic voltammetry at 100 mV/s. The electrode capacity diminishes initially but stabilizes after ˜500 cycles. The electrodes were further evaluated in pulsing experiments using constant current, biphasic pulses. In these experiments, significant charge storage was observed only when using pulse widths greater than 5 ms. A modified polypyrrole was prepared using anthraquinone containing electrolyte. This new material is an apparent improvement over the polypyrrole previously studied.

1987 ◽  
Vol 110 ◽  
Author(s):  
Ellen M. Kelliher ◽  
Timothy L. Rose

AbstractThe charge injection limits of a variety of thin film redox materials considered for use as neural stimulation electrodes were evaluated under standardized conditions. Materials tested included the oxides of Ni, Ir, Rh, Ru, and Mn as well as conductive polypyrrole films. Electrodes with geometric areas of, ∼10–4 cm2were tested in bicarbonate buffered saline of pH 7.3. An electrochemically “safe” potential window was determined for each material by cyclic voltammetry. Charge injection capabilities within that window are evaluated with constant current 0.2 msec pulses. Pulse modes include anodic first and cathodic first biphasic pulses and monophasic cathodal pulses applied to electrodes held at an anodic bias. Pulsing from the anodic bias increased the charge limits for all the materials, but the most dramatic improvement was for Rh oxide. The highest charge injection values were obtained with oxides of iridium and rhodium and were of comparable value for the anodic bias mode of pulsing. Where the effect of film thickness was examined, the charge injection limit leveled off at 2–4 mC/cm2geometric as the film thickness increased.


2018 ◽  
Author(s):  
Hakeem K. Henry ◽  
Sang Bok Lee

The PMo<sub>12</sub>-PPy heterogeneous cathode was synthesized electrochemically. In doing so, the PMo<sub>12</sub> redox-active material was impregnated throughout the conductive polymer matrix of the poly(pyrrole) nanowires. All chemicals and reagents used were purchased from Sigma-Aldrich. Anodized aluminum oxide (AAO) purchased from Whatman served as the porous hard template for nanowire deposition. A thin layer of gold of approximately 200nm was sputtered onto the disordered side of the AAO membrane to serve as the current collector. Copper tape was connected to the sputtered gold for contact and the device was sealed in parafilm with heat with an exposed area of 0.32 cm<sup>2</sup> to serve as the electroactive area for deposition. All electrochemical synthesis and experiments were conducted using a Bio-Logic MPG2 potentiostat. The deposition was carried out using a 3-electrode beaker cell setup with a solution of acetonitrile containing 5mM and 14mM of the phosphomolybdic acid and pyrrole monomer, respectively. The synthesis was achieved using chronoamperometry to apply a constant voltage of 0.8V vs. Ag/AgCl (BASi) to oxidatively polymerize the pyrrole monomer to poly(pyrrole). To prevent the POM from chemically polymerizing the pyrrole, an injection method was used in which the pyrrole monomer was added to the POM solution only after the deposition voltage had already been applied. The deposition was well controlled by limiting the amount of charge transferred to 300mC. Following deposition, the AAO template was removed by soaking in 3M sodium hydroxide (NaOH) for 20 minutes and rinsed several times with water. After synthesis, all cathodes underwent electrochemical testing to determine their performance using cyclic voltammetry and constant current charge-discharge cycling in 0.1 M Mg(ClO<sub>4</sub>)<sub>2</sub>/PC electrolyte. The cathodes were further characterized using scanning electron microscopy (SEM), transmission electron microscopy (TEM), scanning transmission electron microscopy (STEM), and x-ray photoelectron spectroscopy (XPS).


2018 ◽  
Author(s):  
Nicholas Marshall

A set of experiments in surface-initiated ring-opening metathesis polymerization, including end-functionalization of growing brushes and contact angle/cyclic voltammetry measurements. We report preparation and CV of two different conjugated polymer films, and several endgroup and sidechain functionalization experiments using cross-metathesis and active ester substitution.<br>


2012 ◽  
Vol 2012 ◽  
pp. 1-5 ◽  
Author(s):  
Rakefet Ofek Almog ◽  
Hadar Ben-Yoav ◽  
Yelena Sverdlov ◽  
Tsvi Shmilovich ◽  
Slava Krylov ◽  
...  

Integrated polypyrrole, a conductive polymer, interconnects on polymeric substrates were microfabricated for flexible sensors and actuators applications. It allows manufacturing of moving polymeric microcomponents suitable, for example, for micro-optical-electromechanical (MOEMS) systems or implanted sensors. This generic technology allows producing “all polymer” components where the polymers serve as both the structural and the actuating materials. In this paper we present two possible novel architectures that integrate polypyrrole conductors with other structural polymers: (a) polypyrrole embedded into flexible polydimethylsiloxane (PDMS) matrix forming high aspect ratio electrodes and (b) polypyrrole deposited on planar structures. Self-aligned polypyrrole electropolymerization was developed and demonstrated for conducting polymer lines on either gold or copper seed layers. The electropolymerization process, using cyclic voltammetry from an electrolyte containing the monomer, is described, as well as the devices’ characteristics. Finally, we discuss the effect of integrating conducting polymers with metal seed layer, thus enhancing the device durability and reliability.


Author(s):  
Sharmila Patil ◽  
M. A. More ◽  
P. P. Patil

2021 ◽  
Author(s):  
Xiangjun Pu ◽  
Dong Zhao ◽  
Chenglong Fu ◽  
Zhongxue Chen ◽  
Shunan Cao ◽  
...  

2001 ◽  
Vol 80-81 ◽  
pp. 243-248 ◽  
Author(s):  
O. González-Varona ◽  
B. Garrido ◽  
A. Pérez-Rodríguez ◽  
Caroline Bonafos ◽  
Josep Montserrat ◽  
...  

2020 ◽  
Author(s):  
Mohammad Hossein Mazaheri Kouhani ◽  
Alexander Istomin ◽  
Proyag Datta ◽  
Neil H. Talbot

Advances in neural prosthetic technologies demand ever increasing novelty in material composition to enhance the mechanical and electrochemical properties of existing microelectrode arrays. Conductive polymers present advantages such as mechanical flexibility, outstanding biocompatibility, remarkable electrical properties and, most of all, cellular agreement. However, for long-term chronic applications, they fall short in their electrochemical endurance and mechanical adhesion to their substrate materials. Multiple electrochemical approaches have been investigated to improve the adherence of Poly(3,4-ethylenedioxythiophene) (PEDOT) to underlying metallic thin films. In this work, an electrochemical treatment of diazonium salt on platinum microelectrodes is incorporated as an electrochemical adhesion promoter for PEDOT and it is further combined with using the highly microporous geometry of Platinum Grey (Pt-Grey); a technology developed by Second Sight Medical Products Inc (SSMP). The intertwined mechanical integration of Pt-Grey and PEDOT molecules together with the covalent binding agency of diazonium salt demostrate a composite coating technology with long-term stability of more than 452 days while providing >70× enhancement to the interfacial capacitive impedance.


2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Anis Allagui ◽  
Todd J. Freeborn ◽  
Ahmed S. Elwakil ◽  
Brent J. Maundy

Abstract The electric characteristics of electric-double layer capacitors (EDLCs) are determined by their capacitance which is usually measured in the time domain from constant-current charging/discharging and cyclic voltammetry tests, and from the frequency domain using nonlinear least-squares fitting of spectral impedance. The time-voltage and current-voltage profiles from the first two techniques are commonly treated by assuming ideal S s C behavior in spite of the nonlinear response of the device, which in turn provides inaccurate values for its characteristic metrics. In this paper we revisit the calculation of capacitance, power and energy of EDLCs from the time domain constant-current step response and linear voltage waveform, under the assumption that the device behaves as an equivalent fractional-order circuit consisting of a resistance R s in series with a constant phase element (CPE(Q, α), with Q being a pseudocapacitance and α a dispersion coefficient). In particular, we show with the derived (R s , Q, α)-based expressions, that the corresponding nonlinear effects in voltage-time and current-voltage can be encompassed through nonlinear terms function of the coefficient α, which is not possible with the classical R s C model. We validate our formulae with the experimental measurements of different EDLCs.


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