Most common colors in our world as we see them, for example, in crystals, pigments, metals and salt solutions are the result from light scattering properties of electrons in atoms and molecules. Nevertheless, colors can also result from light interference effects, which are of great importance in the life of organisms. The structural colors of living organisms, e.g., the wings of some birds, insects and butteries, are often more intense and almost angle-independent. Understanding this specific color formation is of great interest for biology and for engineered materials with a broad range of biomimetic real world applications due to forgoing of toxic dyes and pigments. Therefore, the generation of artificial color formation with lithographic methods offers many advantages not available in coated multilayer systems because it avoids multiple complex fabrication steps. <p> </p>In the present work, we report an effortless fabrication method to generate structural coloration based on microand nano-structures using 3d-laser writing technique. The uniform micro- and nano-structures were produced in a thin polymer film with an refractive index of 1.51. The single structures are aligned in an array to create a blue color field. The identification of the influence of the structures on the artificial color formation was performed using scanning electron microscopy. The optical properties of the blue color was analyzed via an angle-resolved spectrometer.
To respond to current demands of nano- and microtechnologies, e.g., miniaturization and integration, different bottom-up strategies have been developed. These strategies are based on picking, placing, and assembly of multiple components to produce microsystems with desired features. This paper covers the fabrication of arbitrary-shaped microcomponents by two-photon polymerization and the trapping, moving, and aligning of these structures by the use of a holographic optical tweezer. The main focus is on the assembly technique based on a cantilever microsnap-fit. More precisely, mechanical properties are characterized by optical forces and a suitable geometry of the snap-fit is designed. As a result of these investigations, a fast and simple assembly technique is developed. Furthermore, disassembly is provided by an optimized design. These findings suggest that the microsnap-fit is suitable for the assembly of miniaturized systems and could broaden the application opportunities of bottom-up strategies.
A promising fabrication method for graphene is the reduction of graphene oxide (GO), this can be achieved photochemically by laser irradiation. In this study, we examine the results of latter method by a femtosecond fiber laser (1030 nm, 280 fs). The chemical properties of the irradiated areas were analyzed by Raman and X-ray photoelectron spectroscopy (XPS) and electrical properties were evaluated using sheet resistance measurements. We found that, within a wide range of fluences (8.5 mJ/cm<sup>2 </sup>to 57.8 mJ/cm<sup>2</sup>) at high overlapping rates (>99.45 %), photochemical oxygen reduction can be achieved. However, hybridization transition of sp<sup>3</sup> to sp<sup>2</sup> graphene-like structures only takes place at upper fluences of the mentioned range.
Ultrashort pulse laser ablation has become an important tool for material processing. Adding liquids to the process can be beneficial for a reduced debris and heat affected zone width. Another application is the production of ligand-free nanoparticles. By measuring the ablation rate of iron for femtosecond pulsed laser ablation in different solvents and solvent-mixtures, the influence of the solvent properties on the ablation process is studied. The ablation efficiency is quantified by measuring the ablation rate in dependency of the fluence from 0.05 J/cm<sup>2</sup> up to 5 J/cm<sup>2</sup> in water-ethanol and water-acetone mixtures which are varied in 25 % steps. The ablation rate is significantly influenced by the solvent-mixtures.
Laser pulses in the picosecond and femtosecond regime enable nearly non-thermal material processing where heat effects like molten pools and thermal tensions are often significantly reduced. However, a residual amount of laser energy transforms into heat. As a consequence cumulative multiple shot processing leads to heat accumulation and subsequently lower manufacturing accuracy. To increase the processing throughput without losing quality, it is important to optimize the laser pulse properties and the ablation strategy to further reduce thermal effects. Due to a low heat capacity in small structures, it is necessary to consider the substrate dimensions while performing micro- and nanoprocessing. In contrast to bulk material ablation, the heat dissipation is confined by the small heat capacity of microstructures. Especially for complex structures, it is time-consuming to find efficient processing parameters manually. For this reason, an in-situ evaluation system based on electrical resistivity measurements for on-line control of the ablation process was developed to optimize the laser parameters. In the work presented, the efficiency of 35 femtosecond pulsed laser ablation was evaluated on copper structures in the micrometer range. Furthermore, these results have been compared and evaluated with surface profiles measured by white-light interferometry.
This paper reports ex-situ preparation of conductive polymer/single-walled carbon nanotubes (SWNTs) nanocomposites by adding high conductive SWNTs to the polymer matrix. Sonication methods were used to disperse the SWNTs in the polymer. The conductivity of the nanocomposites is tuned by increasing the concentration of SWNTs. Furthermore, we present two-photon polymerization (2PP) method to fabricate structures on the basis of conductive photosensitive composites. The conductive structures were successfully generated by means of 2PP effect induced by a femtosecond laser.
Pumping and mixing of small volumes of liquid samples are basic processes in microfluidic applications. Among the number of different principles for active transportation of the fluids microrotors have been investigated from the beginning. The main challenge in microrotors, however, has been the driving principle. In this work a new approach for a very simple magnetic driving principle has been realized. More precisely, we take advantage of optical grippers to fabricate various microrotors and introduce an optical force method to characterize the fluid flow generated by rotating the structures through magnetic actuation. The microrotors are built of silica and magnetic microspheres which are initially coated with Streptavidin or Biotin molecules. Holographic optical tweezers (HOT) are used to trap, to position, and to assemble the microspheres with the chemical interaction of the biomolecules leading to a stable binding. Using this technique, complex designs of microrotors can be realized. The magnetic response of the magnetic microspheres enables the rotation and control of the structures through an external magnetic field. The generated fluid flow around the microrotor is measured optically by inserting a probe particle next to the rotor. While the probe particle is trapped by optical forces the flow force leads to a displacement of the particle from the trapping position. This displacement is directly related to the flow velocity and can be measured and calibrated. Variations of the microrotor design and rotating speed lead to characteristic flow fields.
The present work reveals the structural and magnetic properties of iron oxide (Fe<sub>x</sub>O<sub>y</sub>) nanoparticles (NPs) prepared by femtosecond laser ablation. The Fe<sub>x</sub>O<sub>y</sub>-NPs were produced in solutions consisting of different ratios of water and acetone. Laser ablation in water yields agglomerates and that in acetone yields chain structures whereas that in water/acetone show a mixture of both. We observe significant fabrication dependent properties such as different crystallinities and magnetic behaviors. The structural characterization shows a change from iron (Fe) to a Fe<sub>x</sub>O<sub>y</sub> state of the NPs which depends on the solution composition. Furthermore, transmission electron microscopy measurements exhibit a broad particle size distribution in all samples but with significant differences in the mean sizes. Using magnetic measurements we show that nanoparticles fabricated in pure acetone have lower coercive fields which come along with a smaller mean particle size and therefore increasing superparamagnetic behavior.