First Measurement of Collectivity of Coexisting Shapes based on Type II Shell Evolution: The Case of 96^{96}Zr

Background: Type II shell evolution has recently been identified as a microscopic cause for nuclear shape coexistence. Purpose: Establish a low-lying rotational band in 96-Zr. Methods: High-resolution inelastic electron scattering and a relative analysis of transition strengths are used. Results: The B(E2; 0_1^+ -> 2_2^+) value is measured and electromagnetic decay strengths of the secdond 2^+ state are deduced. Conclusions: Shape coexistence is established for 96-Zr. Type II shell evolution provides a systematic and quantitative mechanism to understand deformation at low excitation energies.Comment: 5 pages, 4 figure

Dipole Strength Distributions from HIGS Experiments

A series of photon scattering experiments has been performed on the double-beta decay partners 76Ge and 76Se, in order to investigate their dipole response up to the neutron separation threshold. Gamma-ray beams from bremsstrahlung at the S-DALINAC and from Compton-backscattering at HIGS have been used to measure absolute cross sections and parities of dipole excited states, respectively. The HIGS data allows for indirect measurement of averaged branching ratios, which leads to significant corrections in the observed excitation cross sections. Results are compared to statistical calculations, to test photon strength functions and the Axel-Brink hypothesi

Energy separation of the 1⁺/1⁻ parity doublet in ²⁰Ne

The parity doublet of 1⁺/1⁻ states of Ne⁻²⁰ at 11.26 MeV excitation energy is one of the best known test cases to study the weak part of the nuclear Hamiltonian. The feasibility of parity violation experiments depend on the effective nuclear enhancement factor (RN/|E(1⁺) − E(l⁻)|) which amplifies the impact of the matrix element of the weak interaction on observables indicating parity mixing. An extreme large value of Rn/|E(1⁺) − E(l⁻)| = (670 ± 7000) MeV⁻¹ was reported for the doublet in ²⁰Ne. The large uncertainty depends amongst others on the large uncertainty of |E(1⁺) − E(l⁻)| = 7.7±5.5 keV of the parity doublet. Nuclear resonance fluorescence (NRF) experiments with linearly and circularly polarized photon beams were performed at the High Intensity Gamma-Ray Source at Duke University, Durham, NC, USA, to determine the energy difference of the parity doublet with higher precision. The different angular distributions for 0⁺ → 1⁻ → 0⁺ and 0⁺ → 1⁺ → 0⁺ NRF cascades in polarized γ-ray beams were used to determine the energy difference of the parity doublet to 2.9(13) keV

Structure of high-lying levels populated in the Y-96 -> Zr-96 beta decay

The nature of $J^{\pi}=1^-$ levels of $^{96}$Zr below the $\beta$-decay $Q_{\beta}$ value of $^{96}$Y has been investigated in high-resolution $\gamma$-ray spectroscopy following the $\beta$ decay as well as in a campaign of inelastic photon scattering experiments. Branching ratios extracted from $\beta$ decay allow the absolute $E1$ excitation strength to be determined for levels populated in both reactions. The combined data represents a comprehensive approach to the wavefunction of $1^-$ levels below the $Q_{\beta}$ value, which are investigated in the theoretical approach of the Quasiparticle Phonon Model. This study clarifies the nuclear structure properties associated with the enhanced population of high-lying levels in the $^{96}$Y$_{gs}$ $\beta$ decay, one of the three most important contributors to the high-energy reactor antineutrino spectrum

Hydrogen-Promoted Chlorination of RuO2(110)

High-resolution core-level photoemission spectroscopy and temperature-programmed reaction experiments together with density functional theory calculations were used to elucidate on the atomic scale the chlorination mechanism of ruthenium dioxide RuO2(110) by hydrogen chloride exposure. The surface-selective chlorination accounts for the extraordinary stability of the RuO2 catalyst in the Sumitomo process ? the heterogeneously catalyzed oxidation of hydrogen chloride by oxygen. The selective replacement of bridging oxygen atoms by chlorine atoms depends on the formation of water molecules serving as leaving groups. Water is produced by the chlorine-assisted recombination of two neighboring surface hydroxyl groups at around 450 K, a temperature where water instantaneously leaves the surface. Finally, the bridging vacancy is rapidly filled in by chlorine atoms, thereby forming bridging chlorine atoms. Preadsorbed hydrogen has shown to facilitate the chlorination process for stoichiometry reasons. The general strategy of transforming bridging O atoms into a good leaving group has been corroborated by the chlorination of RuO2(110) via CO pretreatment with CO2 as the leaving group and subsequent Cl2 exposure

Structure of high-lying levels populated in the 96Y →96Zr β decay

WOS:000713124400027The nature of the high-lying final levels of the 96Ygs β decay, one of the three most important contributors to the high-energy reactor antineutrino spectrum, has been investigated in high-resolution γ-ray spectroscopy following the β decay as well as in a campaign of inelastic photon scattering experiments. The comprehensive approach establishes 1− levels associated with the Pygmy Dipole Resonance as high-lying final levels in the β decay. Branching ratios extracted from β decay complement photon scattering and allow the absolute E1 excitation strength to be determined for levels populated in both reactions. The combined data represents a comprehensive approach to the wavefunction of the 1− levels below the Qβ value, which are investigated in the Quasiparticle Phonon Model. The calculations reveal that the components populated in β decay contribute only with small amplitudes to the complex wavefunction of these 1− levels. A comparison of the β decay results to data from total absorption γ-ray spectroscopy demonstrates a good agreement between both measurements