Biomedical subjects

Harald Giessen

Publications and source records attributed to Harald Giessen.

4 recordsLinked to original sources

PubMed2006

Metallic photonic crystals based on solution-processible gold nanoparticles.

We demonstrate the fabrication of metallic photonic crystals, in the form of a periodic array of gold nanowires on a waveguide, by spin-coating a colloidal gold suspension onto a photoresist mask and subsequent annealing. The photoresist mask with a period below 500 nm is manufactured by interference lithography on an indium tin oxide (ITO) glass substrate, where the ITO layer has a thickness around 210 nm and acts as the waveguide. The width of the nanowires can be controlled from 100 to 300 nm by changing the duty cycle of the mask. During evaporation of solvent, the gold nanoparticles are drawn to the grooves of the grating with apparently complete dewetting off the photoresist for channels less than 2 microm in width, which therefore form nanowires after the annealing process. Strong coupling between the waveguide mode and the plasmon resonance of the nanowires, which is dependent on the polarization and incidence angle of the light wave, is demonstrated by optical extinction measurements. Continuity of the nanowires is confirmed by conductivity properties. Simplicity, high processing speed, and low cost are the main advantages of this method, which may have a plethora of applications in telecommunication, all-optical switching, sensors, and semiconductor devices.

Crystallization↗

PubMed2005

Transition between different coherent light-matter interaction regimes analyzed by phase-resolved pulse propagation.

We present phase-resolved pulse propagation measurements that allow us to fully describe the transition between several light-matter interaction regimes. The complete range from linear excitation to the breakdown of the photonic bandgap on to self-induced transmission and self-phase modulation is studied on a high-quality multiple-quantum-well Bragg structure. An improved fast-scanning cross-correlation frequency-resolved optical gating setup is applied to retrieve the pulse phase with an excellent signal-to-noise ratio. Calculations using the semiconductor Maxwell-Bloch equations show qualitative agreement with the experimental findings.

Journal Article↗

PubMed2004

Fast profile measurement of micrometer-sized tapered fibers with better than 50-nm accuracy.

The forward scattering of light illuminating a transparent dielectric cylinder, such as a tapered fiber, from the side can be understood as interference of the diffracted, reflected, and transmitted light. Additionally, light can be resonantly coupled into the fiber if a multiple of the wavelength matches the circumference. Using a suitable laser setup with a novel evaluation algorithm allows us to quickly extract the fiber radius from the complex diffraction pattern, obtaining an accuracy of better than 50 nm. We demonstrate experimentally our method, which is noncontact and allows one to simultaneously measure the profile of a several-centimeter-long fiber waist with a diameter near the diffraction limit.

Journal Article↗

PubMedDate not supplied

Excitation beyond the monochromatic laser limit: simultaneous 3-D confocal and multiphoton microscopy with a tapered fiber as white-light laser source.

Confocal and multiphoton microscopy are essential tools in modern life sciences. They allow fast and highly resolved imaging of a steadily growing number of fluorescent markers, ranging from fluorescent proteins to quantum dots and other fluorophores, used for the localization of molecules and the quantitative detection of molecular properties within living cells and organisms. Up to now, only one physical limitation seemed to be unavoidable. Both confocal and multiphoton microscopy rely on lasers as excitation sources, and their monochromatic radiation allows only a limited number of simultaneously usable dyes, which depends on the specific number of laser lines available in the used microscope. We have overcome this limitation by successfully replacing all excitation lasers in a standard confocal microscope with pulsed white light ranging from 430 to 1300 nm generated in a tapered silica fiber. With this easily reproducible method, simultaneous confocal and multiphoton microscopy was demonstrated. By developing a coherent and intense laser source with spectral width comparable to a mercury lamp, we provide the flexibility to excite any desired fluorophore combination.

Animals↗