Publications by authors named "Chia Min Chang"

Ag nanostructures with surface-enhanced Raman scattering (SERS) activities have been fabricated by applying laser-direct writing (LDW) technique on silver oxide (AgOx) thin films. By controlling the laser powers, multi-level Raman imaging of organic molecules adsorbed on the nanostructures has been observed. This phenomenon is further investigated by atomic-force microscopy and electromagnetic calculation.

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A new fabrication strategy in which Ag plasmonics are embedded in the interface between ZnO nanorods and a conducting substrate is experimentally demonstrated using a femtosecond-laser (fs-laser)-induced plasmonic ZnO/Ag photoelectrodes. This fs-laser fabrication technique can be applied to generate patternable plasmonic nanostructures for improving their effectiveness in hydrogen generation. Plasmonic ZnO/Ag nanostructure photoelectrodes show an increase in the photocurrent of a ZnO nanorod photoelectrodes by higher than 85% at 0.

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We fabricated a three-dimensional five-layered plasmonic resonant cavity by low-cost, efficient and high-throughput femtosecond laser-induced forward transfer (fs-LIFT) technique. The fabricated cavity was characterized by optical measurements, showing two different cavity modes within the measured wavelength region which is in good agreement with numerical simulations. The mode volume corresponding to each resonance is found to be squeezed over 10(4) smaller than the cube of incident wavelength.

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Using femtosecond laser-induced forward transfer techniques we have fabricated gold dots and nanoparticles on glass substrates, as well as nanobumps on gold thin film. The surface morphologies of these structures with different laser fluences and film thicknesses are investigated. We also study the focusing and defocusing properties of the nanofence-an arranged nanobump pattern-by the total-internal reflection microscope.

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Using a femtosecond laser, we have transformed the laser-direct-writing technique into a highly efficient method that can process AgO(x) thin films into Ag nanostructures at a fast scanning rate of 2000 μm(2)/min. The processed AgO(x) thin films exhibit broad-band enhancement of optical absorption and effectively function as active SERS substrates. Probing of the plasmonic hotspots with dyed polymer beads indicates that these hotspots are uniformly distributed over the treated area.

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Femtosecond laser pulses are focused on a thin film of Ge2Sb2Te5 phase-change material, and the transfer of the illuminated material to a nearby substrate is investigated. The size, shape, and phase-state of the fabricated pattern can be effectively controlled by the laser fluence and by the thickness of the Ge2Sb2Te5 film. Results show multi-level electrical and optical reflection states of the fabricated patterns, which may provide a simple and efficient foundation for patterning future phase-change devices.

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Amorphous thin films of Ge(2)Sb(2)Te(5), sputter-deposited on a thin-film gold electrode, are investigated for the purpose of understanding the local electrical conductivity of recorded marks under the influence of focused laser beam. Being amorphous, the as-deposited chalcogenide films have negligible electrical conductivity. With the aid of a focused laser beam, however, we have written on these films micron-sized crystalline marks, ablated holes surrounded by crystalline rings, and other multi-ring structures containing both amorphous and crystalline zones.

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In human motion analysis, in situ calibration of the force plate is necessary to improve the accuracy of the measured ground reaction force (GRF) and center of pressure (COP). Few existing devices are capable of both static and dynamic calibration of the usually non-linear GRF and COP errors, while are also easy to move and/or set up without damaging the building. The current study developed a small device (160 cm × 88 cm × 43 cm) with a mass of 50 kg, equipped with auxiliary wheels and fixing suction pads for rapid deployment and easy set-up.

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A trace analytical method of benzene, toluene, ethylbenzene and xylenes (BTEX) in water has been developed by using headspace solid-phase microextraction (HS-SPME) coupled to cryo-trap gas chromatography-mass spectrometry (GC-MS). The chromatographic peak shape for BTEX was improved by using cryo-trap equipment. The HS-SPME experimental procedures to extract BTEX from water were optimized with a 75 microm carboxen/polydimethylsiloxane (CAR/PDMS)-coated fiber at a sodium chloride concentration of 267 g l(-1), extraction for 15 min at 25 degrees C and desorption at 290 degrees C for 2 min.

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