We realize simultaneous quantum degeneracy in mixtures consisting of the alkali and alkaline-earth-like atoms Li and Yb. This is accomplished within an optical trap by sympathetic cooling of the fermionic isotope ⁶Li with evaporatively cooled bosonic ¹⁷⁴Yb and, separately, fermionic ¹⁷³Yb. Using cross-thermalization studies, we also measure the elastic s-wave scattering lengths of both Li-Yb combinations, |a(⁶Li-¹⁷⁴Yb)| = 1.0 ± 0.2 nm and |a(⁶Li-¹⁷³Yb)| = 0.9 ± 0.2 nm. The equality of these lengths is found to be consistent with mass-scaling analysis. The quantum degenerate mixtures of Li and Yb, as realized here, can be the basis for creation of ultracold molecules with electron spin degrees of freedom, studies of novel Efimov trimers, and impurity probes of superfluid systems.
Thorium-229 is a unique case in nuclear physics: it presents a metastable first excited state 229m Th, just a few electronvolts above the nuclear ground state. This so-called isomer is accessible by VUV lasers, which allows transferring the amazing precision of atomic laser spectroscopy to nuclear physics. Being able to manipulate the 229 Th nuclear states at will opens up a multitude of prospects, from studies of the fundamental interactions in physics to applications as a compact and robust nuclear clock. However, direct optical excitation of the isomer or its radiative decay back to the ground state has not yet been observed, and a series of key nuclear structure parameters such as the exact energies and half-lives of the low-lying nuclear levels of 229 Th are yet unknown. Here we present the first active optical pumping into 229m Th. Our scheme employs narrow-band 29 keV synchrotron radiation to resonantly excite the second excited state, which then predominantly decays into the isomer. We determine the resonance energy with 0.07 eV accuracy, measure a half-life of 82.2 ps, an excitation linewidth of 1.70 neV, and extract the branching ratio of the second excited state into the ground and isomeric state respectively. These measurements allow us to re-evaluate gamma spectroscopy data that have been collected over 40 years.
The microphase structure of noncrystalline poly(ethylene-co-13.3 mol % methacrylic acid) (E-0.133MAA) ionomers was investigated by using infrared (IR) spectroscopic, X-ray scattering, differential scanning calorimetric (DSC), and dielectric measurements. The noncrystallinity was confirmed by small-angle X-ray scattering (SAXS) and DSC studies, which has enabled a quantitative analysis of the SAXS ionic peak associated with ionic aggregates without being perturbed by the polyethylene lamellae peak. In 60% neutralized Na ionomer, it was revealed that almost 100% of MAA side groups including unneutralized COOH are incorporated into the ionic aggregates with an average ionic core radius (R 1) of ∼6 Å. The dielectric relaxation studies showed that the ionic aggregates form a microphase-separated ionic cluster. Analysis of dielectric strengths indicated the most (∼90%) of the COONa groups are present in the ionic cluster. On the other hand, in the 60% neutralized Zn ionomer, both SAXS and dielectric studies indicated that the ionic aggregates with R 1 ∼ 4 Å are almost isolated and dispersed in the matrix; the formation of ionic cluster was not recognized. Similarly to partly crystalline E-MAA ionomers, all noncrystalline E-0.133MAA ionomers exhibited an endothermic peak at 320−330 K (labeled T i) on the first heating, depending on the aging time at room temperature. Several factors that would be critical for the DSC T i peak were discussed. It was concluded that the DSC T i peak is certainly associated with changes of the state of ionic aggregate region.
The nitroxide spin probe ESR method was applied to the study of chain aggregation in aqueous solutions of poly(ethylene-co-methacrylic acid) (EMAA) ionomers. The probes selected differed in their hydrophilicity and in the position of the nitroxide group with respect to the head group. Two spectral sites were detected for the more hydrophilic probes and were assigned respectively to probes with restricted mobility incorporated in large aggregates and to probes with high mobility dispersed in the water phase and/or in the proximity of single-chain micelles (unimers); only the site with restricted mobility was detected in the more hydrophobic probes. The spectral parameters for the site associated with the aggregates suggest that the probes are located in different regions of the aggregates and are faithful reporters on the local hydration and polarity. On the basis of analysis of ESR spectra for six spin probes, we suggest that the aggregates present in aqueous solutions consist of three main regions: a hydrophobic core, an intermediate layer that contains both ionomer chains and some ions, and a hydrophilic region where most of the ions are located. The results for the solutions were compared with results obtained for ionomer membranes equilibrated with water. This study has revealed important structural differences between the aggregates in EMAA ionomers, and in the perfluorinated ionomers (PFI) that were studied previously by the method used in this study. The most important difference is the gradual increase in hydration of the EMAA aggregates from the hydrophobic core to the solvent−ionomer interface, compared to the complete phase separation into ionic and nonpolar domains in the PFI.
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