Werner Moritz

Find an error

Name:
Organization: Humboldt-University Berlin , Germany
Department: Walther Nernst Institute of Physical and Theoretical Chemistry
Title: (PhD)
Co-reporter:Werner Moritz, Tatsuo Yoshinobu, Friedhelm Finger, Steffi Krause, Marisa Martin-Fernandez, Michael J. Schöning
Sensors and Actuators B: Chemical 2004 Volume 103(1–2) pp:436-441
Publication Date(Web):29 September 2004
DOI:10.1016/j.snb.2004.04.073
The lateral resolution of photocurrent techniques such as light-addressable potentiometric sensors (LAPS) or scanning photo-induced impedance microscopy (SPIM) is limited by the properties of the semiconductor material used. We investigated metal-insulator-semiconductor (MIS) structures based on amorphous silicon (a-Si) prepared as a thin layer on transparent glass substrates. It was shown that a sub-micrometer resolution can be achieved for this material, which is much better than the results for single crystalline Si. Some limitations caused by light scattering in the structure were observed.
Co-reporter:W Moritz, S Krause, U Roth, D Klimm, A Lippitz
Analytica Chimica Acta 2001 Volume 437(Issue 2) pp:183-190
Publication Date(Web):27 June 2001
DOI:10.1016/S0003-2670(01)00993-X
The silicon based semiconductor structure Si/SiO2/Si3N4/LaF3/Pt can be used as a potentiometric oxygen sensor working at room temperature. A thermal re-activation can be applied to overcome the earlier disadvantage of an increase in response time with continuous use. Using the Pt gate electrode as a resistive heater, very short electrical high-power pulses can be applied. A heating time as short as 300 ns was sufficient for the re-activation of the sensor. This way, only the sensitive thin layer system LaF3/Pt was heated, and the whole sensor was at room temperature immediately after heating. Impedance spectroscopy, X-ray photoelectron spectroscopy (XPS) and quadruple mass spectrometric (QMS)–thermogravimetry (TG) were used to investigate the mechanism of deterioration in dynamic sensor behaviour and re-activation. The formation of hydrated carbonate and the desorption of CO2 and H2O have been shown to be the causes.
2-CHLORO-1,1,1-TRIFLUOROETHANE