Realization of two Fourier-limited solid-state single-photon sources

We demonstrate two solid-state sources of indistinguishable single photons. High resolution laser spectroscopy and optical microscopy were combined at T = 1.4 K to identify individual molecules in two independent microscopes. The Stark effect was exploited to shift the transition frequency of a given molecule and thus obtain single photon sources with perfect spectral overlap. Our experimental arrangement sets the ground for the realization of various quantum interference and information processing experiments.Comment: 6 page

Molecules as Sources for Indistinguishable Single Photons

We report on the triggered generation of indistinguishable photons by solid-state single-photon sources in two separate cryogenic laser scanning microscopes. Organic fluorescent molecules were used as emitters and investigated by means of high resolution laser spectroscopy. Continuous-wave photon correlation measurements on individual molecules proved the isolation of single quantum systems. By using frequency selective pulsed excitation of the molecule and efficient spectral filtering of its emission, we produced triggered Fourier-limited single photons. In a further step, local electric fields were applied to match the emission wavelengths of two different molecules via Stark effect. Identical single photons are indispensible for the realization of various quantum information processing schemes proposed. The solid-state approach presented here prepares the way towards the integration of multiple bright sources of single photons on a single chip.Comment: Accepted for publication in J. Mod. Opt. This is the original submitted versio

Quantum Interference of Tunably Indistinguishable Photons from Remote Organic Molecules

We demonstrate two-photon interference using two remote single molecules as bright solid-state sources of indistinguishable photons. By varying the transition frequency and spectral width of one molecule, we tune and explore the effect of photon distinguishability. We discuss future improvements on the brightness of single-photon beams, their integration by large numbers on chips, and the extension of our experimental scheme to coupling and entanglement of distant molecules

Choosing Dielectric or Magnetic Material to Optimize the Bandwidth of Miniaturized Resonant Antennas

We address the question of the optimal choice of loading material for antenna miniaturization. A new approach to identify the optimal loading material, dielectric or magnetic, is presented for resonant antennas. Instead of equivalent resonance circuits or transmission-line models, we use the analysis of radiation to identify the fields contributing mostly to the stored energy. This helps to determine the beneficial material type. The formulated principle is qualitatively illustrated using three antenna types. Guidelines for different antenna types are presented.Comment: 17 pages, 9 figure

Influence of molecular weight on the phase behavior and structure formation of branched side-chain hairy-rod polyfluorene in bulk phase.

We report on an experimental study of the self-organization and phase behavior of hairy-rod π -conjugated branched side-chain polyfluorene, poly[9,9-bis(2-ethylhexyl)-fluorene-2,7-diyl]—i.e., poly[2,7–(9,9–bis(2–ethylhexyl)fluorene] (PF2∕6) —as a function of molecular weight (Mn) . The results have been compared to those of phenomenological theory. Samples for which Mn=3–147 kg∕mol were used. First, the stiffness of PF2∕6 , the assumption of the theory, has been probed by small-angle neutron scattering in solution. Thermogravimetry has been used to show that PF2∕6 is thermally stable over the conditions studied. Second, the existence of nematic and hexagonal phases has been phenomenologically identified for lower and higher Mn (LMW, Mn<Mn* and HMW, Mn>Mn* ) regimes, respectively, based on free-energy argument of nematic and hexagonal hairy rods and found to correspond to the experimental x-ray diffraction (XRD) results for PF2∕6 . By using the lattice parameters of PF2∕6 as an experimental input, the nematic-hexagonal transition has been predicted in the vicinity of glassification temperature (Tg) of PF2∕6 . Then, by taking the orientation parts of the free energies into account the nematic-hexagonal transition has been calculated as a function of temperature and Mn and a phase diagram has been formed. Below Tg of 80 °C only (frozen) nematic phase is observed for Mn<Mn*=104 g∕mol and crystalline hexagonal phase for Mn>Mn* . The nematic-hexagonal transition upon heating is observed for the HMW regime depending weakly on Mn , being at 140–165 °C for Mn>Mn* . Third, the phase behavior and structure formation as a function of Mn have been probed using powder and fiber XRD and differential scanning calorimetry and reasonable semiquantitative agreement with theory has been found for Mn≥3 kg∕mol . Fourth, structural characteristics are widely discussed. The nematic phase of LMW materials has been observed to be denser than high-temperature nematic phase of HMW compounds. The hexagonal phase has been found to be paracrystalline in the (ab0) plane but a genuine crystal meridionally. We also find that all these materials including the shortest 10-mer possess the formerly observed rigid five-helix hairy-rod molecular structure

Noise of a single electron transistor on a Si3N4 membrane

We have investigated the influence of electron-beam writing on the creation of charge trapping centers which cause 1/f noise in single electron transistors (SET). Two Al/AlOx/Al devices were compared: one where the SET is on a {100} silicon wafer covered by a 120-nm-thick layer of Si3N4, and another one in which the Si was etched away from below the nitride membrane before patterning the SET. The background charge noise was found to be 1×10 exp −3 e/√Hz at 10 Hz in both devices, independent of the substrate thickness.Peer reviewe