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Biomedical subjects

C Hettich

Publications and source records attributed to C Hettich.

5 recordsLinked to original sources

Generation of a superposition of odd photon number states for quantum information networks.

We report on the experimental observation of quantum-network-compatible light described by a nonpositive Wigner function. The state is generated by photon subtraction from a squeezed vacuum state produced by a continuous wave optical parametric amplifier. Ideally, the state is a coherent superposition of odd photon number states, closely resembling a superposition of weak coherent states |alpha > - |-alpha >. In the limit of low squeezing the state is basically a single photon state. Light is generated with about 10,000 and more events per second in a nearly perfect spatial mode with a Fourier-limited frequency bandwidth which matches well atomic quantum memory requirements. The generated state of light is an excellent input state for testing quantum memories, quantum repeaters, and linear optics quantum computers.

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Measuring the quantum efficiency of the optical emission of single radiating dipoles using a scanning mirror.

Using scanning probe techniques, we show the controlled manipulation of the radiation from single dipoles. In one experiment we study the modification of the fluorescence lifetime of a single molecular dipole in front of a movable silver mirror. A second experiment demonstrates the changing plasmon spectrum of a gold nanoparticle in front of a dielectric mirror. Comparison of our data with theoretical models allows determination of the quantum efficiency of each radiating dipole.

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Nanometer resolution and coherent optical dipole coupling of two individual molecules.

By performing cryogenic laser spectroscopy under a scanning probe electrode that induces a local electric field, we have resolved two individual fluorescent molecules separated by 12 nanometers in an organic crystal. The two molecules undergo a strong coherent dipole-dipole coupling that produces entangled sub- and superradiant states. Under intense laser illumination, both molecules are excited via a two-photon transition, and the fluorescence from this doubly excited system displays photon bunching. Our experimental scheme can be used to optically resolve molecules at the nanometer scale and to manipulate the degree of entanglement among them.

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Diamond colour centres as a nanoscopic light source for scanning near-field optical microscopy.

Recently it was shown that a single molecule at cryogenic temperatures could be used as a local light source for illumination of a sample in the near field. Conventional light-emitting systems such as dye molecules and semiconductor quantum dots could also be used for this purpose, but they suffer from lack of photostability. However, colour centres in diamond have been found to be remarkably stable against bleaching and blinking effects. Here we present the first SNOM images taken with nanoscopic diamond crystals as a light source.

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Optical microscopy using a single-molecule light source

Rapid progress in science on nanoscopic scales has promoted increasing interest in techniques of ultrahigh-resolution optical microscopy. The diffraction limit can be surpassed by illuminating an object in the near field through a sub-wavelength aperture at the end of a sharp metallic probe. Proposed modifications of this technique involve replacing the physical aperture by a nanoscopic active light source. Advances in the spatial and spectral detection of individual fluorescent molecules, using near-field and far-field methods, suggest the possibility of using a single molecule as the illumination source. Here we present optical images taken with a single molecule as a point-like source of illumination, by combining fluorescence excitation spectroscopy with shear-force microscopy. Our single-molecule probe has potential for achieving molecular resolution in optical microscopy; it should also facilitate controlled studies of nanometre-scale phenomena (such as resonant energy transfer) with improved lateral and axial spatial resolution.

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