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Dive into the research topics where Gerald Urban is active.

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Featured researches published by Gerald Urban.


Journal of Chemical Physics | 2003

Determination of quantum confinement in CdSe nanocrystals by cyclic voltammetry

Erol Kucur; Jürgen Riegler; Gerald Urban; Thomas Nann

Ionization potentials Ip, electron affinities E.A., and the quantum confinement in CdSe nanocrystals were determined by means of cyclic voltammetry. The results were compared to values obtained from spectroscopic measurements, especially UV/vis absorption and photoluminescence emission spectra. Absolute band gap positions were obtained from the electrochemical measurements and discussed with regard to vacuum level values. The results are in good agreement with theoretical expectations and spectroscopic data.


Biosensors and Bioelectronics | 1991

Miniaturized thin-film biosensors using covalently immobilized glucose oxidase☆

Gerald Urban; Gerhard Jobst; F. Kohl; A. Jachimowicz; F. Olcaytug; O. Tilado; P. Goiser; Gerhard E. Nauer; Fritz Pittner; Thomas Schalkhammer; Eva Mann-Buxbaum

Abstract The production of a miniaturized glucose sensor by means of thin-film technology is reported. Two main problems related to miniaturization and device integration were solved: (1) the microminiaturization of a suitable electrochemical cell; (2) localized enzyme immobilization with a technology well suited for device integration. The well-known glucose oxidase/H 2 O 2 system was used to determine the glucose concentration. A miniaturized four-electrode arrangement was introduced to measure H 2 O 2 produced by the enzyme. A double working electrode array for reproducibility tests or differential measurements to suppress interferences is easily produced and can be placed on glass or flexible polymer substrates by means of thin-film technology. The enzyme was covalently coupled to a derivatized platinum thin-film working electrode by means of 1,2-arenequinones, which yield highly reproducible, fast and stable sensors. Measurement of a drop (5 μl) of physiological glucose solution is easily performed, giving a stable response after 40 s.


Applied Physics Letters | 2010

Improved efficiency of hybrid solar cells based on non-ligand-exchanged CdSe quantum dots and poly(3-hexylthiophene)

Yunfei Zhou; Frank S. Riehle; Ying Yuan; Hans-Frieder Schleiermacher; Michael Niggemann; Gerald Urban; Michael Krüger

We report on bulk-heterojunction hybrid solar cells based on blends of non-ligand-exchanged CdSe quantum dots (QDs) and the conjugated polymer poly(3-hexylthiophene) with improved power conversion efficiencies of about 2% under AM1.5G illumination after spectral mismatch correction. This is the highest reported value for a spherical CdSe QD based photovoltaic device. After synthesis, the CdSe QDs are treated by a simple and fast acid-assisted washing procedure, which has been identified as a crucial factor in enhancing the device performance. A simple model of a reduced ligand sphere is proposed explaining the power conversion efficiency improvement.


Biosensors and Bioelectronics | 1992

Miniaturized multi-enzyme biosensors integrated with pH sensors on flexible polymer carriers for in vivo applications

Gerald Urban; Gerhard Jobst; Franz Keplinger; E. Aschauer; O. Tilado; R. Fasching; F. Kohl

Abstract An electrochemical glucose sensor has been integrated, together with a pH sensor, on a flexible polyimide substrate for in vivo applications. The glucose sensor is based on the measurement of H 2 O 2 produced by the membrane-entrapped enzyme glucose oxidase (GOD). To minimize electrochemical interference, an electrode configuration was designed to perform differential measurements. The solid-state pH sensor employs a PVC-based neutral carrier membrane. The enzymes GOD and catalase were immobilized into two layers of photolithographically patterned hydrogels. The intended use of this device is the short-term monitoring of glucose and pH in intensive care units and operating theatres, especially for neurosurgical applications. The developed immobilization technique can also be used to create integrated multi-sensor chips for clinical analysers. The glucose and pH sensor exhibited excellent performance during tests in buffer solutions, serum and whole blood.


Biosensors and Bioelectronics | 2002

Biosensor arrays for simultaneous measurement of glucose, lactate, glutamate, and glutamine

Isabella Moser; Gerhard Jobst; Gerald Urban

For simultaneous measurement of glucose, lactate, glutamine, and glutamate a biosensor array is implemented in a micro flow-system thus giving a microsystem. The microsystem consists of a glass chip with the integrated biosensor array and a bottom part, which comprises a gold counter electrode, a 300 microm thick seal, and electrical interconnection lines. The flow device has a total internal volume of 2.1 or 6 microl when integrated with a mixer on chip. The biosensors with no crosstalking and high long term stability were produced by modifying the electrochemical transducers and utilizing photopatternable enzyme membranes. The use of appropriate miniaturization technology leads to mass producable devices for in vivo and ex vivo applications in whole blood and fermentation broth. Due to a novel glutaminase with an activity optimum in the neutral pH range direct and simultaneous monitoring of glutamine together with glucose, lactate, and glutamate could be performed.


Analytica Chimica Acta | 1997

Design and development of a miniaturised total chemical analysis system for on-line lactate and glucose monitoring in biological samples

Eithne Dempsey; Dermot Diamond; Malcolm R. Smyth; Gerald Urban; Gerhard Jobst; Isabella Moser; Elisabeth Verpoorte; Andreas Manz; H. Michael Widmer; Kai Rabenstein; R. Freaney

A miniaturised Total chemical Analysis System (μTAS) for glucose and lactate measurement in biological samples constructed based on an integrated microdialysis sampling and detection system. The complete system incorporates a microdialysis probe for intravascular monitoring in an ex vivo mini-shunt arrangement, and a silicon micromachined stack with incorporated miniaturised flow cell/sensor array. The prototype device has been developed based on state-of-the-art membrane and printed circuit board technology. The flow-through detection system is based on a three-dimensional flow circuit incorporating silicon chips with stacked micromachined channels. An integrated biosensor array (comprising enzyme sensors specific for glucose and lactate) is placed at the base of the stack allowing the detector to be incorporated within the μTAS assembly. These glucose and lactate biosensors are prepared using photolithographic techniques, with measurement based on the detection of hydrogen peroxide at glucose oxidase and lactate oxidase modified platinum electrodes. The resulting amperometric current (at 500 mV vs, Ag/AgCl) is proportional to the concentration of analyte in the sample. All instrumentation is under computer control and the complete unit allows continuous on-line monitoring of glucose and lactate, with fast stable signals over the relevant physiological range for both analytes. The microdialysis system provides 100% sampling efficiency. Sensor performance studies undertaken include optimisation of sensitivity, linearity, operational stability, background current, storage stability and hydration time. The total system (sampling and detection) response time is of the order of 4 min, with sensor sensitivity 1-5 nA mM-1 for glucose and lactate over the range 0.1-33 and 0.05-15 mM, respectively.


Sensors and Actuators A-physical | 2000

Wide range semiconductor flow sensors

A. Glaninger; A Jachimowicz; F. Kohl; R. Chabicovsky; Gerald Urban

Abstract Micromachined flow sensors based on thin film germanium thermistors offer high flow sensitivities and short response times. Using the controlled overtemperature scheme, the measurable air flow velocity ranges from ±0.01 to ±200 m/s and the response time to large step changes of the air velocity is less than 20 ms. In the constant power mode, a signal rise time of 1.6 ms has been demonstrated by the application of shock waves. An air flow measuring range from 0.6 ml/h to at least 150 l/h has been achieved, e.g. with a rectangular flow channel of 0.54 mm 2 cross-sectional area. Using a lookup table transformation, a linearized output signal can be obtained within 25 μs.


Analytical Chemistry | 2013

Microfluidic Chip with Integrated Electrical Cell-Impedance Sensing for Monitoring Single Cancer Cell Migration in Three-Dimensional Matrixes

Tien Anh Nguyen; Tsung-I Yin; Diego Reyes; Gerald Urban

Cell migration has been recognized as one hallmark of malignant tumor progression. By integrating the method of electrical cell-substrate impedance sensing (ECIS) with the Boyden chamber design, the state-of-the-art techniques provide kinetic information about cell migration and invasion processes in three-dimensional (3D) extracellular matrixes. However, the information related to the initial stage of cell migration with single-cell resolution, which plays a unique role in the metastasis-invasion cascade of cancer, is not yet available. In this paper, we present a microfluidic device integrated with ECIS for investigating single cancer cell migration in 3D matrixes. Using microfluidics techniques without the requirement of physical connections to off-chip pneumatics, the proposed sensor chip can efficiently capture single cells on microelectrode arrays for sequential on-chip 2D or 3D cell culture and impedance measurement. An on-chip single-cell migration assay was successfully demonstrated within several minutes. Migration of single metastatic MDA-MB-231 cells in their initial stage can be monitored in real time; it shows a rapid change in impedance magnitude of approximately 10 Ω/s, whereas no prominent impedance change is observed for less-metastasis MCF-7 cells. The proposed sensor chip, allowing for a rapid and selective detection of the migratory properties of cancer cells at the single-cell level, could be applied as a new tool for cancer research.


Biosensors and Bioelectronics | 2011

A highly efficient buckypaper-based electrode material for mediatorless laccase-catalyzed dioxygen reduction

L. Hussein; Stefanie Rubenwolf; F. von Stetten; Gerald Urban; Roland Zengerle; Michael Krueger; Sven Kerzenmacher

The redox enzyme laccase from Trametes versicolor efficiently catalyzes the oxygen reduction reaction (ORR) in mediatorless biofuel cell cathodes when adsorbed onto multi-walled carbon nanotubes (MWCNTs). In this work we demonstrate that the fabrication of MWCNTs in form of buckypaper (BP) results in an excellent electrode material for laccase-catalyzed cathodes. BPs are mechanically stable, self-entangling mats with high dispersion of MWCNTs resulting in easy to handle homogeneous layers with highly mesoporous structures and excellent electrical conductivities. All biocathodes have been electrochemically investigated in oxygen-saturated buffer at pH 5 by galvanostatic polarization and potentiodynamic linear sweep voltammetry. Both methods confirm an efficient direct interaction of laccase with BP with a high open circuit potential of 0.882 V vs. normal hydrogen electrode (NHE). The high oxygen reduction performance leads to high current densities of 422±71 μA cm(-2) at a typical cathode potential of 0.744 V vs. NHE. When the current density is normalized to the mass of the electrode material (mass activity), the BP-based film electrodes exhibit a 68-fold higher current density at 0.744 V vs. NHE than electrodes fabricated from the same MWCNTs in a non-dispersed agglomerated form as packed electrodes. This clearly shows that MWCNTs can act more efficiently as cathode when prepared in form of BP. This can be attributed to reduced diffusional mass transfer limitations and enhanced electrical conductivity. BP is thus a very promising material for the construction of mediatorless laccase cathodes for ORR in biofuel cells. In addition we demonstrated that these electrodes exhibit a high tolerance towards glucose, the most common bioanode fuel.


Physical Chemistry Chemical Physics | 2011

Fabrication and characterization of buckypaper-based nanostructured electrodes as a novel material for biofuel cell applications

L. Hussein; Gerald Urban; Michael Krüger

The fabrication process of buckypapers (BPs) made from stable suspensions of as-received or functionalized multi-walled carbon nanotubes (MWCNTs) with high purity (97.5 wt%, Baytubes), their characterization and their utilization towards novel biofuel cell electrode applications are reported. The BPs can vary in thickness between 1 μm and 200 μm, are mechanically robust, flexible, stable in solvents, possess high meso-porosities as well as high apparent electrical conductivities of up to 2500 S m(-1). Potentiodynamic measurements of biocathodes based on bilirubin oxidase (BOD)-decorated BPs for the oxygen reduction reaction (ORR) in neutral media (phosphate buffer solution) containing glucose indicate that BP electrodes based on functionalized MWCNTs (fBPs) perform better than BP electrodes of as-received MWCNTs and have high potential as an effective electrode material in biofuel cells and biosensors.

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Can Dincer

University of Freiburg

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F. Kohl

Danube University Krems

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A. Jachimowicz

Vienna University of Technology

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F. Olcaytug

University of Freiburg

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