RESUMO
A new, simple, technique is demonstrated to laterally access the cladding holes of solid-core photonic crystal fibers (PCFs) or the central hole of hollow-core PCFs by blowing a hole through the fiber wall (using a fusion splicer and the application of pressure). For both fiber types material was subsequently and successfully inserted into the holes. The proposed method compares favorably with other reported selective filling techniques in terms of simplicity and reproducibility. Also, since the holes are laterally filled, simultaneous optical access to the PCFs is possible, which can prove useful for practical sensing applications. As a proof-of-concept experiment, Rhodamine fluorescence measurements are shown.
RESUMO
The development of microstructured fibres offers the prospect of improved fibre sensing for low refractive index materials such as liquids and gases. A number of approaches are possible. Here we present a new approach to evanescent field sensing, in which both core and cladding are microstructured. The fibre was fabricated and tested, and simulations and experimental results are shown in the visible region to demonstrate the utility of this approach for sensing.
RESUMO
Femtosecond optical measurement techniques have been used to study the primary photoprocesses in the light-driven transmembrane proton pump bacteriorhodopsin. Light-adapted bacteriorhodopsin was excited with a 60-femtosecond pump pulse at 618 nanometers, and the transient absorption spectra from 560 to 710 nanometers were recorded from -50 to 1000 femtoseconds by means of 6-femtosecond probe pulses. By 60 femtoseconds, a broad transient hole appeared in the absorption spectrum whose amplitude remained constant for about 200 femtoseconds. Stimulated emission in the 660- to 710-nanometer region and excited-state absorption in the 560- to 580-nanometer region appeared promptly and then shifted and decayed from 0 to approximately 150 femtoseconds. These spectral features provide a direct observation of the 13-trans to 13-cis torsional isomerization of the retinal chromophore on the excited-state potential surface. Absorption due to the primary ground-state photoproduct J appears with a time constant of approximately 500 femtoseconds.
