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K. Yokota

Publications and source records attributed to K. Yokota.

7 recordsLinked to original sources

Spectroscopy of $A=9$ hyperlithium by the $(e,e^{\prime}K^{+})$ reaction

Missing mass spectroscopy with the $(e,e^{\prime}K^{+})$ reaction was performed at Jefferson Laboratory's Hall C for the neutron rich $Λ$ hypernucleus $^{9}_Λ{\rm Li}$. The ground state energy was obtained to be $B_Λ^{\rm g.s.}=8.84\pm0.17^{\rm stat.}\pm0.15^{\rm sys.}~{\rm MeV}$ by using shell model calculations of a cross section ratio and an energy separation of the spin doublet states ($3/2^{+}_1$ and $5/2^{+}_1$). In addition, peaks that are considered to be states of [$^{8}{\rm Li}(3^{+})\otimes s_Λ=3/2^{+}_{2}, 1/2^{+}$] and [$^{8}{\rm Li}(1^{+})\otimes s_Λ=5/2^{+}_{2}, 7/2^{+}$] were observed at $E_Λ({\rm no.~2})=1.74\pm0.27^{\rm stat.}\pm0.11^{\rm sys.}~{\rm MeV}$ and $E_Λ({\rm no.~3})=3.30\pm0.24^{\rm stat.}\pm0.11^{\rm sys.}~{\rm MeV}$, respectively. The $E_Λ({\rm no.~3})$ is larger than shell model predictions by a few hundred keV, and the difference would indicate that a ${\rm ^{5}He}+t$ structure is more developed for the $3^{+}$ state than those for the $2^{+}$ and $1^{+}$ states in a core nucleus $^{8}{\rm Li}$ as a cluster model calculation suggests.

nucl-ex

Spectroscopy of the neutron-rich hypernucleus $^{7}_Λ$He from electron scattering

The missing mass spectroscopy of the $^{7}_Λ$He hypernucleus was performed, using the $^{7}$Li$(e,e^{\prime}K^{+})^{7}_Λ$He reaction at the Thomas Jefferson National Accelerator Facility Hall C. The $Λ$ binding energy of the ground state (1/2$^{+}$) was determined with a smaller error than that of the previous measurement, being $B_Λ$ = 5.55 $\pm$ 0.10(stat.) $\pm$ 0.11(sys.) MeV. The experiment also provided new insight into charge symmetry breaking in p-shell hypernuclear systems. Finally, a peak at $B_Λ$ = 3.65 $\pm$ 0.20(stat.) $\pm$ 0.11(sys.) MeV was observed and assigned as a mixture of 3/2$^{+}$ and 5/2$^{+}$ states, confirming the "gluelike" behavior of $Λ$, which makes an unstable state in $^{6}$He stable against neutron emission.

nucl-ex

High Resolution Spectroscopic Study of $^{10}_Λ$Be

Spectroscopy of a $^{10}_Λ$Be hypernucleus was carried out at JLab Hall C using the $(e,e^{\prime}K^{+})$ reaction. A new magnetic spectrometer system (SPL+HES+HKS), specifically designed for high resolution hypernuclear spectroscopy, was used to obtain an energy spectrum with a resolution of 0.78 MeV (FWHM). The well-calibrated spectrometer system of the present experiment using the $p(e,e^{\prime}K^{+})Λ,Σ^{0}$ reactions allowed us to determine the energy levels, and the binding energy of the ground state peak (mixture of 1$^{-}$ and 2$^{-}$ states) was obtained to be B$_Λ$=8.55$\pm$0.07(stat.)$\pm$0.11(sys.) MeV. The result indicates that the ground state energy is shallower than that of an emulsion study by about 0.5 MeV which provides valuable experimental information on charge symmetry breaking effect in the $ΛN$ interaction.

nucl-ex

Direct Measurements of the Lifetime of Heavy Hypernuclei

The lifetime of a Lambda particle embedded in a nucleus (hypernucleus) decreases from that of free Lambda decay due to the opening of the Lambda N to NN weak decay channel. However, it is generally believed that the lifetime of a hypernucleus attains a constant value (saturation) for medium to heavy hypernuclear masses, yet this hypothesis has been difficult to verify. The present paper reports a direct measurement of the lifetime of medium-heavy hypernuclei produced with a photon-beam from Fe, Cu, Ag, and Bi targets. The recoiling hypernuclei were detected by a fission fragment detector using low-pressure multi-wire proportional chambers. The experiment agrees remarkably well with the only previously-measured single-species heavy-hypernucleus lifetime, that of Fe56_Lambda at KEK, and has significantly higher precision. The experiment disagrees with the measured lifetime of an unknown combination of heavy hypernuclei with 180<A<225 and, with a small statistical and systematic uncertainty, strongly favors the expected saturation of the lifetime decrease.

nucl-ex

Electrostatic Self-assembly : A New Route Towards Nanostructures

During the last 3 years, our group has investigated extensively the complexation mechanism between neutral-polyelectrolyte block copolymers with oppositely charged species. These species are surfactant micelles, multivalent counterions and inorganic nanoparticles. In the three cases, we have established the thermodynamical phase diagram of these systems, and found broad regions where supramolecular aggregates spontaneously form via electrostatic self-assembly. From earlier works, it was suspected that these mixed colloids exhibit a core-shell structure. However, their inner structure was unveiled by us only recently, using a combination of light, neutron and x-ray scattering experiments.

cond-mat.soft

Interactions between Polymers and Nanoparticles : Formation of Supermicellar Hybrid Aggregates

When polyelectrolyte-neutral block copolymers are mixed in solutions to oppositely charged species (e.g. surfactant micelles, macromolecules, proteins etc), there is the formation of stable supermicellar aggregates combining both components. The resulting colloidal complexes exhibit a core-shell structure and the mechanism yielding to their formation is electrostatic self-assembly. In this contribution, we report on the structural properties of supermicellar aggregates made from yttrium-based inorganic nanoparticles (radius 2 nm) and polyelectrolyte-neutral block copolymers in aqueous solutions. The yttrium hydroxyacetate particles were chosen as a model system for inorganic colloids, and also for their use in industrial applications as precursors for ceramic and opto-electronic materials. The copolymers placed under scrutiny are the water soluble and asymmetric poly(sodium acrylate)poly(acrylamide) diblocks. Using static and dynamical light scattering experiments, we demonstrate the analogy between surfactant micelles and nanoparticles in the complexation phenomenon with oppositely charged polymers. We also determine the sizes and the aggregation numbers of the hybrid organic-inorganic complexes. Several additional properties are discussed, such as the remarkable stability of the hybrid aggregates and the dependence of their sizes on the mixing conditions.

cond-mat.soft

Stabilization and Controlled Association of Inorganic Nanoparticles using Block Copolymers

We report on the structural properties of mixed aggregates made from rare-earth inorganic nanoparticles (radius 20 Angstroms) and polyelectrolyte-neutral block copolymers in aqueous solutions. Using scattering experiments and Monte Carlo simulations, we show that these mixed aggregates have a hierarchical core-shell microstructure. The core is made of densely packed nanoparticles and it is surrounded by a corona of neutral chains. This microstructure results from a process of controlled association and confers to the hybrid aggregates a remarkable colloidal stability.

cond-mat.soft