Properties of electrochemical double-layer capacitors with carbon-nanotubes-on-carbon-fiber-felt electrodes

Carbon nanotube (CNT) layers deposited on carbon fiber cloth (CFC) materials have been studied as electrodes of electrochemical double layer capacitors (EDLCs), in particular, the electrochemical performance and cycle stability of symmetric EDLCs in an organic electrolyte (tetraethyl-ammonium-fluoroborate in acetonitrile). Due to the large surface area of carbon-fibers, the CNT mass loading can be as high as 18 mg/cm2 which is magnitudes larger than that of what can be deposited on aluminum or nickel metal sheets. The area normalized double layer capacitance of CNT/CFC electrodes in the above organic electrolytes were found to be in the range of 100 – 400 mF/cm2, and the specific capacitances were 18 to 48 F/g. These latter values are below the achievable values of single-wall CNT of 80 F/g; the lower values can be attributed to the presence of multi-walled CNTs of some quantities, having lower accessible surface area. The energy density of CNT/CFC supercapacitors is 0.8 – 1.5 Wh/kg, while the power density varies between 5-20 kW/kg calculated on electrode level. Excellent cycling stability of EDLCs built with CNT-on carbon felt electrodes has been demonstrated up to 1 million cycles, which is due to the inert nature of substrate causing the absence of corrosion process and high mass load of CNT

Compact binary waveform recovery from the cross-correlated data of two detectors by matched filtering with spinning templates

We investigate whether the recovery chances of highly spinning waveforms by matched filtering with randomly chosen spinning waveforms generated with the LAL package are improved by a cross-correlation of the simulated output of the L1 and H1 LIGO detectors. We find that a properly defined correlated overlap improves the mass estimates and enhaces the recovery of spin angles

A compact multifunctional microfluidic platform for exploring cellular dynamics in real-time using electrochemical detection

Downscaling of microfluidic cell culture and detection devices for electrochemical monitoring has mostly focused on miniaturization of the microfluidic chips which are often designed for specific applications and therefore lack functional flexibility. We present a compact microfluidic cell culture and electrochemical analysis platform with in-built fluid handling and detection, enabling complete cell based assays comprising on-line electrode cleaning, sterilization, surface functionalization, cell seeding, cultivation and electrochemical real-time monitoring of cellular dynamics. To demonstrate the versatility and multifunctionality of the platform, we explored amperometric monitoring of intracellular redox activity in yeast (Saccharomyces cerevisiae) and detection of exocytotically released dopamine from rat pheochromocytoma cells (PC12). Electrochemical impedance spectroscopy was used in both applications for monitoring cell sedimentation and adhesion as well as proliferation in the case of PC12 cells. The influence of flow rate on the signal amplitude in the detection of redox metabolism as well as the effect of mechanical stimulation on dopamine release were demonstrated using the programmable fluid handling capability. The here presented platform is aimed at applications utilizing cell based assays, ranging from e.g. monitoring of drug effects in pharmacological studies, characterization of neural stem cell differentiation, and screening of genetically modified microorganisms to environmental monitoring

Real-time monitoring of cellular dynamics using a microfluidic cell culture system with integrated electrode array and potentiostat

A versatile microfluidic, multichamber cell culture and analysis system with an integrated electrode array and potentiostat suitable for electrochemical detection and microscopic imaging is presented in this paper. The system, which allows on-line electrode cleaning and modification, was developed for real-time monitoring of cellular dynamics, exemplified in this work by monitoring of redox metabolism inside living yeast cells and dopamine release from PC12 cell