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Raman-Kerr Comb Generation Based on Parametric Wave Mixing in Strongly Driven Raman Molecular Gas Medium
2020, Benoît, Aurélien, Husakou, Anton, Beaudou, Benoît, Debord, Benoît, Gérôme, Frédéric, Benabid, Fetah
We report on experimental and theoretical demonstrations of an optical comb spectrum based on a combination of cascaded stimulated Raman scattering and four-wave mixing mediated by Raman-induced nonresonant Kerr-type nonlinearity. This combination enabled us to transform a conventional quasiperiodic Raman comb into a comb with a single and smaller frequency spacing. This phenomenon is achieved using a hollow-core photonic crystal fiber filled with 40 bars of deuterium and pumped with a high-power picosecond laser. The resultant comb shows more than 100 spectral lines spanning over 220 THz from 800 nm to 1710 nm, with a total output power of 7.1 W. In contrast to a pure Raman comb, a 120 THz wide portion of the spectrum exhibits denser and equally spaced spectral lines with a frequency spacing of around 1.75 THz, which is much smaller than the lowest frequency of the three excited deuterium Raman resonances. A numerical solution of the generalized nonlinear Schrödinger equation in the slowly varying envelope approximation provides very good agreement with the experimental data. The additional sidebands are explained by cascaded four-wave mixing between preexisting spectral lines, mediated by the large Raman-induced optical nonlinearity. The use of such a technique for coherent comb generation is discussed. The results show a route to the generation of optical frequency combs that combine large bandwidth and high power controllable frequency spacing.
Modulating the luminance of organic light-emitting diodes: Via optical stimulation of a photochromic molecular monolayer at transparent oxide electrode
2020, Ligorio, Giovanni, Cotella, Giovanni F., Bonasera, Aurelio, Zorn Morales, Nicolas, Carnicella, Giuseppe, Kobin, Björn, Wang, Qiankun, Koch, Norbert, Hecht, Stefan, List-Kratochvil, Emil J.W., Cacialli, Franco
Self-assembled monolayers (SAMs) deposited on bottom electrodes are commonly used to tune charge carrier injection or blocking in optoelectronic devices. Beside the enhancement of device performance, the fabrication of multifunctional devices in which the output can be modulated by multiple external stimuli remains a challenging target. In this work, we report the functionalization of an indium tin oxide (ITO) electrode with a SAM of a diarylethene derivative designed for optically control the electronic properties. Following the demonstration of dense SAM formation and its photochromic activity, as a proof-of-principle, an organic light-emitting diode (OLED) embedding the light-responsive SAM-covered electrode was fabricated and characterized. Optically addressing the two-terminal device by irradiation with ultraviolet light doubles the electroluminescence. The original value can be restored reversibly by irradiation with visible light. This expanded functionality is based on the photoinduced modulation of the electronic structure of the diarylethene isomers, which impact the charge carriers' confinement within the emissive layer. This approach could be successfully exploited in the field of opto-communication technology, for example to fabricate opto-electronic logic circuits. © 2020 The Royal Society of Chemistry.