47 research outputs found

    Femtosecond-scale switching based on excited free-carriers

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    We describe novel optical switching schemes operating at femtosecond time scales by employing free carrier (FC) excitation. Such unprecedented switching times are made possible by spatially patterning the density of the excited FCs. In the first realization, we rely on diffusion, i.e., on the nonlocality of the FC nonlinear response of the semiconductor, to erase the initial FC pattern and, thereby, eliminate the reflectivity of the system. In the second realization, we erase the FC pattern by launching a second pump pulse at a controlled delay. We discuss the advantages and limitations of the proposed approaches and demonstrate their potential applicability for switching ultrashort pulses propagating in silicon waveguides. We show switching efficiencies of up to 50% for 100 fs pump pulses, which is an unusually high level of efficiency for such a short interaction time, a result of the use of the strong FC nonlinearity. Due to limitations of saturation and pattern effects, these schemes can be employed for switching applications that require femtosecond features but standard repetition rates. Such applications include switching of ultrashort pulses, femtosecond spectroscopy (gating), time-reversal of short pulses for aberration compensation, and many more. This approach is also the starting point for ultrafast amplitude modulations and a new route toward the spatio-temporal shaping of short optical pulse

    Identifying the role of the local density of optical states in frequency conversion of light in confined media

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    We have reversibly switched the resonance of a GaAs-AlAs microcavity in the near-infrared near λ=1300 nm within 300 fs by the electronic Kerr effect. We reveal by pump-probe spectroscopy a remarkable red shift or blue shift of the light confined inside the cavity for small pulse delays, depending on their temporal ordering. The color-converted light is efficiently generated in a broad frequency continuum that differs markedly from the instantaneous cavity resonance in terms of the central frequency and bandwidth. From observations on cavities with different quality factors, we identify the role of the local density of optical states (LDOS) available to the newly generated light frequencies. In particular, we distinguish the effect of the LDOS related to the cavity resonance itself, and the LDOS continuum that leaks in from the vacuum surrounding the cavity. Our new insights provide a unified picture for seemingly disparate results in traditional and nanophotonic nonlinear optics

    Controlling the quality factor of a tuning-fork resonance between 9 K and 300 K for scanning-probe microscopy

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    We study the dynamic response of a mechanical quartz tuning fork in the temperature range from 9 K to 300 K. Since the quality factor Q of the resonance strongly depends on temperature, we implement a procedure to control the quality factor of the resonance. We show that we are able to dynamically change the quality factor and keep it constant over the whole temperature range. This procedure is suitable for applications in scanning probe microscopy.Comment: 5 pages, 6 figure

    Extraction of optical Bloch modes in a photonic-crystal waveguide

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    We perform phase-sensitive near-field scanning optical microscopy on photonic-crystal waveguides. The observed intricate field patterns are analyzed by spatial Fourier transformations, revealing several guided TE- and TM-like modes. Using the reconstruction algorithm proposed by Ha, et al. (Opt. Lett. 34 (2009)), we decompose the measured two-dimensional field pattern in a superposition of propagating Bloch modes. This opens new possibilities to study specific modes in near-field measurements. We apply the method to study the transverse behavior of a guided TE-like mode, where the mode extends deeper in the surrounding photonic crystal when the band edge is approached

    Quantitative measurement of combustion gases in harsh environments using NDIR spectroscopy

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    The global climate change calls for more environmentally friendly use of energy and has led to stricter limits and regulations for the emissions of various greenhouse gases. Consequently, there is nowadays an increasing need for the detection of exhaust and natural gases. This need leads to an ever-growing market for gas sensors, which, at the moment, is dominated by chemical sensors. Yet, the increasing demands to also measure under harsh environmental conditions pave the way for non-invasive measurements and thus optical detection techniques. Here, we present the development of two optical detection systems using non-dispersive infrared absorption spectroscopy (NDIR). One system is intended for civilian use, capable of detecting both CO as well as CO2 in the range of 4–5&thinsp;µm. Furthermore, restrictions regarding size and economic viability are put on this sensor so it can compete with existing sensors. For CO2, an estimated resolution of 444&thinsp;ppm is achieved, which is competitive with established sensors on the market. For CO an estimated resolution of 1401&thinsp;ppm was achieved, rendering it necessary to improve this sensor to be competitive with other available sensors. The second system is used in an exhaust system and is capable of detecting CO2 at 3.2&thinsp;µm facing cross-sensitivity with H2O. A data analysis method is described to separate the CO2 and H2O signals, revealing a time resolution of 33&thinsp;µs.</p

    Magnetoplasmonic design rules for active magneto-optics

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    Light polarization rotators and non-reciprocal optical isolators are essential building blocks in photonics technology. These macroscopic passive devices are commonly based on magneto-optical Faraday and Kerr polarization rotation. Magnetoplasmonics - the combination of magnetism and plasmonics - is a promising route to bring these devices to the nanoscale. We introduce design rules for highly tunable active magnetoplasmonic elements in which we can tailor the amplitude and sign of the Kerr response over a broad spectral range

    Designer Magnetoplasmonics with Nickel Nanoferromagnets

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    We introduce a new perspective on magnetoplasmonics in nickel nanoferromagnets by exploiting the phase tunability of the optical polarizability due to localized surface plasmons and simultaneous magneto-optical activity. We demonstrate how the concerted action of nanoplasmonics and magnetization can manipulate the sign of rotation of the reflected light’s polarization (i.e., to produce Kerr rotation reversal) in ferromagnetic nanomaterials and, further, how this effect can be dynamically controlled and employed to devise conceptually new schemes for biochemosensing. © 2011 American Chemical Society.A.D. and Z.P. acknowledge support from the Swedish Research Council and Swedish Foundation for Strategic Research (Framework program Functional Electromagnetic Metamaterials, project RMA08). J.Å. acknowledges support from the Swedish Research Council, the Swedish Foundation for Strategic Research (Future Research Leader Programme), and the G€oran Gustafsson Foundation. J.Å. is a Royal Swedish Academy of Sciences Research Fellow supported by a grant from the Knut and Alice Wallenberg Foundation. V.B. acknowledges the G€oran Gustafsson Foundation and the Blanceflor Boncompagni-Ludovisi Foundation. P.V. acknowledges funding from the Basque Government through the ETORGAI Program, Project No. ER- 2010/00032 and Program No. PI2009-17, the Spanish Ministry of Science and Education under Projects No. CSD2006-53 and No. MAT2009-07980. J.N. acknowledges funding for the Generalitat de Catalunya and the Spanish Ministry of Science and Education through No. 2009-SGR-1292 and No. MAT2010-20616-C02 projects.Peer Reviewe

    PCDDs, PCDFs, and PCBs co-occurrence in TiO2 nanoparticles

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    In the present study, we report on the co-occurrence of persistent organic pollutants (POPs) adsorbed on nanoparticular titanium dioxide (TiO2). We report on the finding of polychlorinated dibenzodioxins (PCDDs), polychlorinated dibenzofurans (PCDFs), and polychlorinated biphenyls (PCBs) on the surface of commercially available TiO2 nanoparticles, being formed during the fabrication process of the TiO2. Thereby, the samples comprise PCBs with higher congener numbers or, in the absence of PCBs, a high concentration of PCDDs and PCDFs. This new class of POPs on an active catalytic surface and the great range of applications of nanoparticular TiO2, such as in color pigments, cosmetics, and inks, give rise to great concern due to their potential toxicity
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