1,052 research outputs found

    Wavelength dependent ac-Stark shift of the 1S0 - 3P1 transition at 657 nm in Ca

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    We have measured the ac-Stark shift of the 4s2 1S0 - 4s4p 3P1 line in 40Ca for perturbing laser wavelengths between 780 nm and 1064 nm with a time domain Ramsey-Borde atom interferometer. We found a zero crossing of the shift for the mS = 0 - mP = 0 transition and \sigma polarized perturbation at 800.8(22) nm. The data was analyzed by a model deriving the energy shift from known transition wavelengths and strengths. To fit our data, we adjusted the Einstein A coefficients of the 4s3d 3D - 4s4p 3P and 4s5s 3S - 4s4p 3P fine structure multiplets. With these we can predict vanishing ac-Stark shifts for the 1S0 m = 0 - 3P1 m = 1 transition and \sigma- light at 983(12) nm and at 735.5(20) nm for the transition to the 3P0 level.Comment: 8 pages, 5 figures, 2 table

    Collisional losses, decoherence, and frequency shifts in optical lattice clocks with bosons

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    We have quantified collisional losses, decoherence and the collision shift in a one-dimensional optical lattice clock with bosonic 88Sr. The lattice clock is referenced to the highly forbidden transition 1S0 - 3P0 at 698 nm, which becomes weakly allowed due to state mixing in a homogeneous magnetic field. We were able to quantify three decoherence coefficients, which are due to dephasing collisions, inelastic collisions between atoms in the upper and lower clock state, and atoms in the upper clock state only. Based on the measured coefficients, we determine the operation parameters at which a 1D-lattice clock with 88Sr shows no degradation due to collisions on the relative accuracy level of 10-16.Comment: 4 pages, 3 figure

    Dynamic acoustic field activated cell separation (DAFACS)

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    Advances in diagnostics, cell and stem cell technologies drive the development of application-specific tools for cell and particle separation. Acoustic micro-particle separation offers a promising avenue for highthroughput, label-free, high recovery, cell and particle separation and isolation in regenerative medicine. Here, we demonstrate a novel approach utilizing a dynamic acoustic field that is capable of separating an arbitrary size range of cells. We first demonstrate the method for the separation of particles with different diameters between 6 and 45 μm and secondly particles of different densities in a heterogeneous medium. The dynamic acoustic field is then used to separate dorsal root ganglion cells. The shearless, label-free and low damage characteristics make this method of manipulation particularly suited for biological applications. Advantages of using a dynamic acoustic field for the separation of cells include its inherent safety and biocompatibility, the possibility to operate over large distances (centimetres), high purity (ratio of particle population, up to 100%), and high efficiency (ratio of separated particles over total number of particles to separate, up to 100%)

    Crystalline optical cavity at 4 K with thermal noise limited instability and ultralow drift

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    Crystalline optical cavities are the foundation of today's state-of-the-art ultrastable lasers. Building on our previous silicon cavity effort, we now achieve the fundamental thermal noise-limited stability for a 6 cm long silicon cavity cooled to 4 Kelvin, reaching 6.5×10176.5\times10^{-17} from 0.8 to 80 seconds. We also report for the first time a clear linear dependence of the cavity frequency drift on the incident optical power. The lowest fractional frequency drift of 3×1019-3\times10^{-19}/s is attained at a transmitted power of 40 nW, with an extrapolated drift approaching zero in the absence of optical power. These demonstrations provide a promising direction to reach a new performance domain for stable lasers, with stability better than 1×10171\times10^{-17} and fractional linear drift below 1×10191\times10^{-19}/s

    Transverse laser cooling of a thermal atomic beam of dysprosium

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    A thermal atomic beam of dysprosium (Dy) atoms is cooled using the 4f106s2(J=8)4f106s6p(J=9)4f^{10}6s^2 (J=8) \to 4f^{10}6s6p (J=9) transition at 421 nm. The cooling is done via a standing light wave orthogonal to the atomic beam. Efficient transverse cooling to the Doppler limit is demonstrated for all observable isotopes of dysprosium. Branching ratios to metastable states are demonstrated to be <5×104<5\times10^{-4}. A scheme for enhancement of the nonzero-nuclear-spin-isotope cooling, as well as a method for direct identification of possible trap states, is proposed.Comment: 5 pages, 4 figures v2: 7 pages, 7 figure

    Doppler cooling and trapping on forbidden transitions

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    Ultracold atoms at temperatures close to the recoil limit have been achieved by extending Doppler cooling to forbidden transitions. A cloud of ^40Ca atoms has been cooled and trapped to a temperature as low as 6 \mu K by operating a magneto-optical trap on the spin-forbidden intercombination transition. Quenching the long-lived excited state with an additional laser enhanced the scattering rate by a factor of 15, while a high selectivity in velocity was preserved. With this method more than 10% of pre-cooled atoms from a standard magneto-optical trap have been transferred to the ultracold trap. Monte-Carlo simulations of the cooling process are in good agreement with the experiments

    Molecular basis for the sensitivity of TRP channels to polyunsaturated fatty acids

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    Transient receptor potential (TRP) channels represent a superfamily of unselective cation channels that are subdivided into seven subfamilies based on their sequence homology and differences in gating and functional properties. Little is known about the molecular mechanisms of TRP channel regulation, particularly of the "canonical" TRP (TRPC) subfamily and their activation by polyunsaturated fatty acids (PUFAs). Here, we analyzed the structure-function relationship of Drosophila fruit fly TRPC channels. The primary aim was to uncover the molecular basis of PUFA sensitivity of Drosophila TRP-like (TRPL) and TRPgamma channels. Amino acid (aa) sequence alignment of the three Drosophila TRPC channels revealed 50 aa residues highly conserved in PUFA-sensitive TRPL and TRPgamma channels but not in the PUFA-insensitive TRP channel. Substitution of respective aa in TRPL by corresponding aa of TRP identified 18 residues that are necessary for PUFA-mediated activation of TRPL. Most aa positions are located within a stretch comprising transmembrane domains S2-S4, whereas six aa positions have been assigned to the proximal cytosolic C-terminus. Interestingly, residues I465 and S471 are required for activation by 5,8,11,14-eicosatetraynoic acid (ETYA) but not 5,8,11-eicosatriynoic acid (ETI). As proof of concept, we generated a PUFA-sensitive TRP channel by exchanging the corresponding aa from TRPL to TRP. Our study demonstrates a specific aa pattern in the transmembrane domains S2-S4 and the proximal C-terminus essential for TRP channel activation by PUFAs

    Interrogation laser for a strontium lattice clock

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    We report on the setup and characterization of a 698 nm master-slave diode laser system to probe the 1S0-3P0 clock transition of strontium atoms confined in a one-dimensional optical lattice. A linewidth in the order of around 100 Hz of the laser system has been measured with respect to an ultrastable 657 nm diode laser with 1 Hz linewidth using a femtosecond fiber comb as transfer oscillator. The laser has been used to measure the magnetically induced 1S0-3P0 clock transition in 88Sr where a linewidth of 165 Hz has been observed. The transfer oscillator method provides a virtual beat signal between the two diode lasers that has been used to phase lock the 698 nm laser to the 1 Hz linewidth laser at 657 nm, transferring its stability to the 698 nm laser system.Comment: 5 pages, 7 figures, to be published in "IEEE Transactions on Instrumentation and Measurement, Special Issue CPEM 2008
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