Weimann C.,Karlsruhe Institute of Technology |
Fratz M.,Fraunhofer Institute for Physical Measurement Techniques |
Wolfelschneider H.,Fraunhofer Institute for Physical Measurement Techniques |
Freude W.,Karlsruhe Institute of Technology |
And 4 more authors.
We improve the accuracy of distance measurements with synthetic-wavelength interferometry by referencing the spectral spacing of the free-running light sources to a high-precision radio-frequency oscillator. In addition, we increase the unambiguity range with a time-of-flight technique. Distances to scattering technical surfaces can be measured with micrometer accuracy and an unambiguity range of 1.17 m. The measurement rate amounts to 300 Hz. © 2015 Optical Society of America. Source
Waldbaur A.,Institute of Microstructure Technology IMT |
Kittelmann J.,Karlsruhe Institute of Technology |
Radtke C.P.,Karlsruhe Institute of Technology |
Hubbuch J.,Karlsruhe Institute of Technology |
Rapp B.E.,Institute of Microstructure Technology IMT
Lab on a Chip - Miniaturisation for Chemistry and Biology
We describe a generic microfluidic interface design that allows the connection of microfluidic chips to established industrial liquid handling stations (LHS). A molding tool has been designed that allows fabrication of low-cost disposable polydimethylsiloxane (PDMS) chips with interfaces that provide convenient and reversible connection of the microfluidic chip to industrial LHS. The concept allows complete freedom of design for the microfluidic chip itself. In this setup all peripheral fluidic components (such as valves and pumps) usually required for microfluidic experiments are provided by the LHS. Experiments (including readout) can be carried out fully automated using the hardware and software provided by LHS manufacturer. Our approach uses a chip interface that is compatible with widely used and industrially established LHS which is a significant advancement towards near-industrial experimental design in microfluidics and will greatly facilitate the acceptance and translation of microfluidics technology in industry. © 2013 The Royal Society of Chemistry. Source
Schindler P.C.,Karlsruhe Institute of Technology |
Schmogrow R.,Karlsruhe Institute of Technology |
Dreschmann M.,Karlsruhe Institute of Technology |
Meyer J.,Karlsruhe Institute of Technology |
And 16 more authors.
Journal of Optical Communications and Networking
We demonstrate a remotely seeded flexible passive optical network (PON) with multiple low-speed subscribers but only a single optical line terminal transceiver operating at a data rate of 31.25 Gbits/s. The scheme is based on a colorless frequency division multiplexing (FDM)-PON with centralized wavelength control. Multiplexing and demultiplexing in the optical network unit (ONU) is performed in the electronic domain and relies either on FDM with Nyquist sinc-pulse shaping or on orthogonal frequency division multiplexing (OFDM). This way the ONU can perform processing at low speed in the baseband. Further, the ONU is colorless by means of a remote seed for upstream transmission and a remote local oscillator for heterodyne reception, all of which helps in keeping maintenance and costs for an ONU potentially low and will simplify wavelength allocation in a future software defined network architecture. To extend the reach, semiconductor optical amplifiers are used for optical amplification in the downstream and upstream. © 2009-2012 OSA. Source
Liu X.,Light Technology |
Liu X.,Institute of Microstructure Technology IMT |
Lebedkin S.,Institute of Nanotechnology INT |
Besser H.,Karlsruhe Institute of Technology |
And 13 more authors.
Organic semiconductor distributed feedback (DFB) lasers are of interest as external or chip-integrated excitation sources in the visible spectral range for miniaturized Raman-on-chip biomolecular detection systems. However, the inherently limited excitation power of such lasers as well as oftentimes low analyte concentrations requires efficient Raman detection schemes. We present an approach using surface-enhanced Raman scattering (SERS) substrates, which has the potential to significantly improve the sensitivity of on-chip Raman detection systems. Instead of lithographically fabricated Au/Ag-coated periodic nanostructures on Si/SiO2 wafers, which can provide large SERS enhancements but are expensive and time-consuming to fabricate, we use low-cost and large-area SERS substrates made via laser-assisted nanoreplication. These substrates comprise gold-coated cyclic olefin copolymer (COC) nanopillar arrays, which show an estimated SERS enhancement factor of up to ∼107. The effect of the nanopillar diameter (60-260 nm) and interpillar spacing (10-190 nm) on the local electromagnetic field enhancement is studied by finite-difference-time-domain (FDTD) modeling. The favorable SERS detection capability of this setup is verified by using rhodamine 6G and adenosine as analytes and an organic semiconductor DFB laser with an emission wavelength of 631.4 nm as the external fiber-coupled excitation source. © 2014 American Chemical Society. Source
Waldbaur A.,Institute of Microstructure Technology IMT |
Waterkotte B.,Fritz Haber Institute |
Waterkotte B.,Institute of Functional Interfaces IFG |
Schmitz K.,Fritz Haber Institute |
And 3 more authors.
Protein patterns of different shapes and densities are useful tools for studies of cell behavior and to create biomaterials that induce specific cellular responses. Up to now the dominant techniques for creating protein patterns are mostly based on serial writing processes or require templates such as photomasks or elastomer stamps. Only a few of these techniques permit the creation of grayscale patterns. Herein, the development of a lithography system using a digital mirror device which allows fast patterning of proteins by immobilizing fluorescently labeled molecules via photobleaching is reported. Grayscale patterns of biotin with pixel sizes in the range of 2.5 μm are generated within 10 s of exposure on an area of about 5 mm2. This maskless projection lithography method permits the rapid and inexpensive generation of protein patterns definable by any user-defined grayscale digital image on substrate areas in the mm2 to cm2 range. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. Source