No Arabic abstract
A systematic numerical study of ultrafast nonlinear directional coupler performance based on soliton self-trapping in a novel type of dual-core optical fibre is presented. The considered highly nonlinear fibre structure is composed of a real, intentionally developed soft glass-pair with high refractive index contrast at the level of 0.4 in the near infrared. Nonlinear propagation of picojoule level femtosecond pulses was studied numerically with the aim to identify the best switching performance in input parameter space of 1400 - 1800 nm in terms of excitation wavelengths, and of 75 - 150 fs in terms of pulse width, respectively. For every combination of excitation wavelength and pulse width, the switching energies together with the optimal fibre length were determined and their relation to the input and switching parameters is discussed. The highest switching contrast of 46 dB in the time window of the ultrashort soliton was predicted at combination of 1500 nm excitation wavelength and 75 fs pulse width considering 43 mm fibre length. These results represent significant improvement both from point of view of switching contrast and switching energies, which are only at level of 20 pJ, in comparison to the previously published case of air-glass dual-core photonic crystal fibre. Moreover, the simpler fibre design without cladding microstructure together with the all-solid approach holds promise of improved dual-core symmetry and therefore offers high probability of the successful realization of a low power, compact and simple switching device.
All-optical switching of 77 fs pulses centered at 1560 nm, driven by 270 fs, 1030 nm pulses in a dual-core optical fiber exhibiting high index contrast is presented. The fiber is made of a thermally matched pair of lead silicate and borosilicate glasses used as core and cladding material, respectively. The novel switching approach is based on nonlinear balancing of dual-core asymmetry, by control pulse intensity induced group velocity reduction of the fast fiber channel. Due to the fiber core made of soft glass with high nonlinearity high switching contrast exceeding 20 dB is attained under application of control pulses of only few nanojoule energy. The optimization of the fiber length brought the best results at 14 mm, which is in good correspondence with the calculated coupling length at the signal wavelength. The results express significant progress in comparison to similar studies based on self-switching of solitonic pulses in dual-core fibers and represent high application potential.
We experimentally investigate a nonlinear switching mechanism in a dual-core highly nonlinear optical fiber. We focus the input beam of femtosecond pulses on one core only, to identify transitions between inter-core oscillations, self-trapping in the cross core, and self-trapping of the pulse in the straight core. A model based in the system of coupled nonlinear Schrodinger equations provides surprisingly good agreement with the experimental findings.
We demonstrate ultrafast soliton-based nonlinear balancing of dual-core asymmetry in highly nonlinear photonic crystal fiber at sub-nanojoule pulse energy level. The effect of fiber asymmetry was studied experimentally by selective excitation and monitoring of individual fiber cores at different wavelengths between 1500 nm and 1800 nm. Higher energy transfer rate to non-excited core was observed in the case of fast core excitation due to nonlinear asymmetry balancing of temporal solitons, which was confirmed by the dedicated numerical simulations based on the coupled generalized nonlinear Schrodinger equations. Moreover, the simulation results correspond qualitatively with the experimentally acquired dependences of the output dual-core extinction ratio on excitation energy and wavelength. In the case of 1800 nm fast core excitation, narrow band spectral intensity switching between the output channels was registered with contrast of 23 dB. The switching was achieved by the change of the excitation pulse energy in sub-nanojoule region. The performed detailed analysis of the nonlinear balancing of dual-core asymmetry in solitonic propagation regime opens new perspectives for the development of ultrafast nonlinear all-optical switching devices.
Recently, coherent control of the optical response of thin films of matter in standing waves has attracted considerable attention, ranging from applications in excitation-selective spectroscopy and nonlinear optics to demonstrations of all-optical image processing. Here we show that integration of metamaterial and optical fibre technologies allows the use of coherently controlled absorption in a fully fiberized and packaged switching metadevice. With this metadevice, that controls light with light in a nanoscale plasmonic metamaterial film on an optical fibre tip, we provide proof-of-principle demonstrations of logical functions XOR, NOT and AND that are performed within a coherent fully fiberized network at wavelengths between 1530 nm and 1565 nm. The metadevice performance has been tested with optical signals equivalent to a bitrate of up to 40 Gbit/s and sub-milliwatt power levels. Since coherent absorption can operate at the single photon level and also with 100 THz bandwidth, we argue that the demonstrated all-optical switch concept has potential applications in coherent and quantum information networks.
We present high-resolution spectroscopy of Iodine vapour that is loaded and trapped within the core of a hollow-core photonic crystal fibre (HC-PCF). We compare the observed spectroscopic features to those seen in a conventional iodine cell and show that the saturation characteristics differ significantly. Despite the confined geometry it was still possible to obtain sub-Doppler features with a spectral width of ~6 MHz with very high contrast. We provide a simple theory which closely reproduces all the key observations of the experiment.