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Electrode Interface (electrode + interface)

Distribution by Scientific Domains

Medical Sciences	40%

Selected Abstracts

Nanoparticle-Structured Ligand Framework as Electrode Interfaces

ELECTROANALYSIS, Issue 1-2 2004
Nancy
Abstract Nanostructured thin film assemblies derived from metal or oxide nanocrystal cores and functionalized molecular shells provide large surface-to-volume ratio and three-dimensional ligand frameworks. In this article, we report results of an investigation of the nanostructured materials for electroanalysis. Monolayer-capped gold nanoparticles of 2-nm core diameter and carboxylic acid-functionalized alkyl thiols were assembled on electrode surfaces via an exchange-crosslinking-precipitation reaction route, and were studied as a model system. The network assemblies exhibit open frameworks in which the void space forms channels with the nanometer sized cores defining its size and the shell structures defining its chemical specificity. Such nanostructures were exploited to demonstrate the viability of responsive materials for interfacial incorporation and fluxes of ionic species. The nanomaterials were characterized by an array of techniques, including cyclic voltammetry, electrochemical quartz-crystal nanobalance, flow injection analysis, and surface infrared reflection spectroscopy. The current responses and mass loading as a result of the incorporation of ionic species into the nanostructure have been analyzed. The potential application of the nanostructured thin films for electrochemical detection in microfluidic systems is also discussed. [source]

Electrochemical Nanotransistor from Mixed-Polymer Brushes

ADVANCED MATERIALS, Issue 16 2010
Tsz Kin Tam
Reversible switching of the electrode interface between OFF/ON states is achieved by electrochemically triggered reorganization of a nanostructured polymer brush associated with the interface. The switching process is accomplished by local interfacial pH changes allowing operation in buffered biological environments (see figure). The fabricated device mimics the performance of switching electronic devices such as transistors. [source]

Gold-Tip Electrodes,A New "Deep Lesion" Technology for Catheter Ablation?

JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, Issue 7 2005
In Vitro Comparison of a Gold Alloy Versus Platinum, Iridium Tip Electrode Ablation Catheter
Radiofrequency (RF) catheter ablation is widely used to induce focal myocardial necrosis using the effect of resistive heating through high-frequency current delivery. It is current standard to limit the target tissue,electrode interface temperature to a maximum of 60,70°C to avoid char formation. Gold (Au) exhibits a thermal conductivity of nearly four times greater than platinum (Pt,Ir) (3.17 W/cm Kelvin vs 0.716 W/cm Kelvin), it was therefore hypothesized that RF ablation using a gold electrode would create broader and deeper lesions as a result of a better heat conduction from the tissue,electrode interface and additional cooling of the gold electrode by "heat loss" to the intracardiac blood. Both mechanisms would allow applying more RF power to the tissue before the electrode,tissue interface temperature limit is reached. To test this hypothesis, we performed in vitro isolated liver and pig heart investigations comparing lesion depths of a new Au-alloy-tip electrode to standard Pt,Ir electrode material. Mean lesion depth in liver tissue for Pt,Ir was 4.33 ± 0.45 mm (n = 60) whereas Au electrode was able to achieve significantly deeper lesions (5.86 ± 0.37 mm [n = 60; P < 0.001]). The mean power delivered using Pt,Ir was 6.95 ± 2.41 W whereas Au tip electrode delivered 9.64 ± 3.78 W indicating a statistically significant difference (P < 0.05). In vitro pig heart tissue Au ablation (n = 20) increased significantly the lesion depth (Au: 4.85 ± 1.01 mm, Pt,Ir: 2.96 ± 0.81 mm, n = 20; P < 0.001). Au tip electrode again applied significantly more power (P < 0.001). Gold-tip electrode catheters were able to induce deeper lesions using RF ablation in vitro as compared to Pt,Ir tip electrode material. In liver and in pig heart tissue, the increase in lesion depth was associated with a significant increase in the average power applied with the gold electrode at the same level of electrode,tissue temperature as compared to platinum material. [source]

Intraoperative Study of Polarization and Evoked Response Signals in Different Endocardial Electrode Designs

PACING AND CLINICAL ELECTROPHYSIOLOGY, Issue 7 2001
CHING LAU
LAU, C., et al.: Intraoperative Study of Polarization and Evoked Response Signals in Different Endocardial Electrode Designs. Some new generation pacemakers use an algorithm based on evoked response (ER) detection to verify beat-to-beat capture and to enable automatic adjustment of output. This is a prospective acute study of polarization signal (PS) and ER in nine currently available electrodes. Intraoperative testing of ventricular bipolar electrodes used the Autocapture (AC) algorithm. The intrinsic R wave, PS, ER, acceptance of AC function, and stimulation thresholds (STs) were obtained. Ventricular electrodes were categorized as follows: titanium nitride (TiN)-coated passive and active fixation, high impedance (HI), passive fixation (VP), iridium oxide-coated titanium (IROX) (VI), and platinum helix (PH) active fixation. Acute testing was performed in 217 patients with an average age of 74.26 years, 59.6% were men with primary pacing indication-SSS (46.3%). There were no significant differences found with respect to R wave and threshold between the various electrodes. PH active-fixation electrodes had significantly higher ER and PS than other groups including the TiN-coated active-fixation electrodes. TiNcoated electrodes (active and passive fixation) had significantly lower PS than other electrodes. As a result, TiN electrodes had a significantly higher functional rate of AC (91.7%), whereas PH had the lowest rate (0%). In conclusion, (1) polarization characteristics are significantly different for commercially available ventricular electrodes, (2) certain physical features at the tissue to electrode interface like TiN coating appears to be more important in determining PS than electrode tip size and fixation method, and (3) the current algorithm for AC requires electrodes that provide low polarization for satisfactory performance. [source]

Molecules on Si: Electronics with Chemistry

ADVANCED MATERIALS, Issue 2 2010
Ayelet Vilan
Abstract Basic scientific interest in using a semiconducting electrode in molecule-based electronics arises from the rich electrostatic landscape presented by semiconductor interfaces. Technological interest rests on the promise that combining existing semiconductor (primarily Si) electronics with (mostly organic) molecules will result in a whole that is larger than the sum of its parts. Such a hybrid approach appears presently particularly relevant for sensors and photovoltaics. Semiconductors, especially Si, present an important experimental test-bed for assessing electronic transport behavior of molecules, because they allow varying the critical interface energetics without, to a first approximation, altering the interfacial chemistry. To investigate semiconductor-molecule electronics we need reproducible, high-yield preparations of samples that allow reliable and reproducible data collection. Only in that way can we explore how the molecule/electrode interfaces affect or even dictate charge transport, which may then provide a basis for models with predictive power. To consider these issues and questions we will, in this Progress Report, review junctions based on direct bonding of molecules to oxide-free Si. describe the possible charge transport mechanisms across such interfaces and evaluate in how far they can be quantified. investigate to what extent imperfections in the monolayer are important for transport across the monolayer. revisit the concept of energy levels in such hybrid systems. [source]