342 research outputs found

    Dual and anti-dual modes in dielectric spheres

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    We present how the angular momentum of light can play an important role to induce a dual or anti-dual behaviour on a dielectric particle. Although the material the particle is made of is not dual, i.e. a dielectric does not interact with an electrical field in the same way as it does with a magnetic one, a spherical particle can behave as a dual system when the correct excitation beam is chosen. We study the conditions under which this induced dual or anti-dual behaviour can be induced.Comment: 13 pages, 5 figure

    Measurement and shaping of biphoton spectral wavefunctions

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    In this work we present a simple method to reconstruct the complex spectral wavefunction of a biphoton, and hence gain complete information about the spectral and temporal properties of a photon pair. The technique, which relies on quantum interference, is applicable to biphoton states produced with a monochromatic pump when a shift of the pump frequency produces a shift in the relative frequencies contributing to the biphoton. We demonstrate an example of such a situation in type-II parametric down-conversion (SPDC) allowing arbitrary paraxial spatial pump and detection modes. Moreover, our test cases demonstrate the possibility to shape the spectral wavefunction. This is achieved by choosing the spatial mode of the pump and of the detection modes, and takes advantage of spatiotemporal correlations.Comment: Supplementary information also available. Comments and feedback appreciated. Compared to the previous version, here we have made the following changes: -corrected a typo in the text between Eq. (11) and (12) -corrected a typo in the references -added reference

    Visualizing the emission of a single photon with frequency and time resolved spectroscopy

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    At the dawn of Quantum Physics, Wigner and Weisskopf obtained a full analytical description (a \textit{photon portrait}) of the emission of a single photon by a two-level system, using the basis of frequency modes (Weisskopf and Wigner, "Zeitschrift f\"ur Physik", 63, 1930). A direct experimental reconstruction of this portrait demands an accurate measurement of a time resolved fluorescence spectrum, with high sensitivity to the off-resonant frequencies and ultrafast dynamics describing the photon creation. In this work we demonstrate such an experimental technique in a superconducting waveguide Quantum Electrodynamics (wQED) platform, using single transmon qubit and two coupled transmon qubits as quantum emitters. In both scenarios, the photon portraits agree quantitatively with the predictions of the input-output theory and qualitatively with Wigner-Weisskopf theory. We believe that our technique allows not only for interesting visualization of fundamental principles, but may serve as a tool, e.g. to realize multi-dimensional spectroscopy in waveguide Quantum Electrodynamics.Comment: 18 pages, 10 figures including appendice

    Toward Quantum Superposition of Living Organisms

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    The most striking feature of quantum mechanics is the existence of superposition states, where an object appears to be in different situations at the same time. The existence of such states has been tested with small objects, like atoms, ions, electrons and photons, and even with molecules. More recently, it has been possible to create superpositions of collections of photons, atoms, or Cooper pairs. Current progress in optomechanical systems may soon allow us to create superpositions of even larger objects, like micro-sized mirrors or cantilevers, and thus to test quantum mechanical phenomena at larger scales. Here we propose a method to cool down and create quantum superpositions of the motion of sub-wavelength, arbitrarily shaped dielectric objects trapped inside a high--finesse cavity at a very low pressure. Our method is ideally suited for the smallest living organisms, such as viruses, which survive under low vacuum pressures, and optically behave as dielectric objects. This opens up the possibility of testing the quantum nature of living organisms by creating quantum superposition states in very much the same spirit as the original Schr\"odinger's cat "gedanken" paradigm. We anticipate our essay to be a starting point to experimentally address fundamental questions, such as the role of life and consciousness in quantum mechanics.Comment: 9 pages, 4 figures, published versio

    Symmetry Protection of Photonic Entanglement in the Interaction with a Single Nanoaperture

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    In this work, we experimentally show that quantum entanglement can be symmetry protected in the interaction with a single subwavelength plasmonic nanoaperture, with a total volume of V ∼ 0.2λ^3. In particular, we experimentally demonstrate that two-photon entanglement can be either completely preserved or completely lost after the interaction with the nanoaperture, solely depending on the relative phase between the quantum states. We achieve this effect by using specially engineered two-photon states to match the properties of the nanoaperture. In this way we can access a symmetry protected state, i.e., a state constrained by the geometry of the interaction to retain its entanglement. In spite of the small volume of interaction, we show that the symmetry protected entangled state retains its main properties. This connection between nanophotonics and quantum optics probes the fundamental limits of the phenomenon of quantum interference

    Electromagnetic duality symmetry and helicity conservation for the macroscopic Maxwell's equations (previously "Experimental demonstration of electromagnetic duality symmetry breaking")

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    Modern physics is largely devoted to study conservation laws, such as charge, energy, linear momentum or angular momentum, because they give us information about the symmetries of our universe. Here, we propose to add the relationship between electromagnetic duality and helicity to the toolkit. Generalized electromagnetic duality symmetry, broken in the microscopic Maxwell's equations by the empirical absence of magnetic charges, can be restored for the macroscopic Maxwell's equations. The restoration of this symmetry is shown to be independent of the geometry of the problem. These results provide a simple and powerful tool for the study of light-matter interactions within the framework of symmetries and conservation laws. We apply such framework to the experimental investigation of helicity transformations in cylindrical nanoapertures, and we find that the transformation is significantly enhanced by the coupling to surface modes, where electromagnetic duality is strongly broken.Comment: 26 pages, 4 figure

    Tissue Localization and Extracellular Matrix Degradation by PI, PII and PIII Snake Venom Metalloproteinases: Clues on the Mechanisms of Venom-Induced Hemorrhage

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    20 páginas, 4 figuras, 3 tablas y 7 tablas en material suplementario.Snake venom hemorrhagic metalloproteinases (SVMPs) of the PI, PII and PIII classes were compared in terms of tissue localization and their ability to hydrolyze basement membrane components in vivo, as well as by a proteomics analysis of exudates collected in tissue injected with these enzymes. Immunohistochemical analyses of co-localization of these SVMPs with type IV collagen revealed that PII and PIII enzymes co-localized with type IV collagen in capillaries, arterioles and post-capillary venules to a higher extent than PI SVMP, which showed a more widespread distribution in the tissue. The patterns of hydrolysis by these three SVMPs of laminin, type VI collagen and nidogen in vivo greatly differ, whereas the three enzymes showed a similar pattern of degradation of type IV collagen, supporting the concept that hydrolysis of this component is critical for the destabilization of microvessel structure leading to hemorrhage. Proteomic analysis of wound exudate revealed similarities and differences between the action of the three SVMPs. Higher extent of proteolysis was observed for the PI enzyme regarding several extracellular matrix components and fibrinogen, whereas exudates from mice injected with PII and PIII SVMPs had higher amounts of some intracellular proteins. Our results provide novel clues for understanding the mechanisms by which SVMPs induce damage to the microvasculature and generate hemorrhage.This work was performed in partial fulfillment of the requirements for the PhD degree for Cristina Herrera at Universidad de Costa Rica.Peer reviewe

    Multi‐omics analysis reveals drivers of loss of β‐cell function after newly diagnosed autoimmune type 1 diabetes: An INNODIA multicenter study

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    Aims: Heterogeneity in the rate of beta-cell loss in newly diagnosed type 1 diabetes patients is poorly understood and creates a barrier to designing and interpreting disease-modifying clinical trials. Integrative analyses of baseline multi-omics data obtained after the diagnosis of type 1 diabetes may provide mechanistic insight into the diverse rates of disease progression after type 1 diabetes diagnosis. Methods: We collected samples in a pan-European consortium that enabled the concerted analysis of five different omics modalities in data from 97 newly diagnosed patients. In this study, we used Multi-Omics Factor Analysis to identify molecular signatures correlating with post-diagnosis decline in beta-cell mass measured as fasting C-peptide. Results: Two molecular signatures were significantly correlated with fasting C-peptide levels. One signature showed a correlation to neutrophil degranulation, cytokine signalling, lymphoid and non-lymphoid cell interactions and G-protein coupled receptor signalling events that were inversely associated with a rapid decline in beta-cell function. The second signature was related to translation and viral infection was inversely associated with change in beta-cell function. In addition, the immunomics data revealed a Natural Killer cell signature associated with rapid beta-cell decline. Conclusions: Features that differ between individuals with slow and rapid decline in beta-cell mass could be valuable in staging and prediction of the rate of disease progression and thus enable smarter (shorter and smaller) trial designs for disease modifying therapies as well as offering biomarkers of therapeutic effect
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