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Results for “isomer decays”

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28 records · Page 2
All sourcesNASA NTRSDOE OSTI
DOE OSTI2026

Quantum enabled precision measurements of the 229Th nuclear isomer transition (final report)

The existence of the nuclear isomer transition in thorium-229 was first inferred from keV lines in the gamma spectrum of uranium-233 decay more than 40 years ago. Over the years, the value of the transition energy has been refined with indirect measurements using nuclear physics techniques, and the current evidence points to transition energy in the laser-accessible vacuum ultra-violet region of the spectrum. At the start of this project, the two best measurements of the transition energy were 7.8±0.5 eV and 8.28±0.17 eV from high precision gamma ray spectroscopy and kinetic energy of internal conversion electrons, respectively. This project aimed to reduce the uncertainty in the transition energy to 10 meV using direct calorimetric measurements of the decay energy with superconducting nanowire single photon detectors (SNSPDs). Specifically, the method that was pursued was to generate thorium-229 in the excited isomer state by the alpha decay of uranium-233, embed the excited state thorium into an SNSPD, then detect the energy released when the isomer deexcites.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2025

Reaching the prolate-oblate boundary at 𝑁=116 via first fragmentation of a 198 Pt beam: Sharp transition to triaxiality in 189 Ta

High-spin isomers in very-neutron-rich 𝐴≈190 Hf-Ta-W nuclei were populated via the pioneering fragmentation of a 198 Pt primary beam at the National Superconducting Cyclotron Laboratory. The nuclei were implanted in a Si detector stack surrounded by the Gamma-Ray Energy Tracking In-beam Nuclear Array (GRETINA) to detect delayed 𝛾 rays, providing first level schemes using 𝛾−𝛾 coincidence data from isomeric decays in this previously inaccessible region of the nuclear chart. Here, a sudden transition to a strong triaxial shape is observed in the very-neutron-rich 189 Ta (𝑁 = 116) nucleus from axially prolate shapes in lighter Ta isotopes, providing a critical experimental benchmark for competing theoretical predictions of nuclear-shape evolution.

150 ≤ A ≤ 189↗
NASA NTRS1981

Search for effect of longitudinally polarized protons on optically active amino acids

The influence of irradiation by longitudinally polarized protons on the differential decomposition of amino acid is investigated in a test of the Vester Ulbricht hypothesis that L-amino acids were produced in preference to the D isomers on the primitive earth due to the effects of parity violation in beta decay. Samples of DL-leucine were irradiated with protons of both positive and negative longitudinal polarization, then analyzed by gas chromatography. Despite advantages of higher polarization, lower velocity and higher ionization density of protons with respect to electrons, proton irradation is found to lead to no detectable asymmetries in DL-leucine degradation, even at 50% gross degradation.

Lemmon, R. M.↗
DOE OSTI2025

Observation of a new isomer in {sup 185}Au

Delayed γ-ray spectroscopy of 185Au was studied at the Argonne Gas-Filled Analyzer. A new isomer at an excitation energy of 1504.2(4) keV with a half-life of 630(80) ns was identified via γ-γ coincidence analysis, decaying via a 294.8(3) keV transition. Based on Weisskopf estimates, the multipolarity of the 295 keV transition is assigned to be E1, M1, E2, or M2. Possible configurations for this new isomer are discussed based on configuration-constrained potential energy surface calculations.

Fu, X. Y.↗
DOE OSTI2025

Structure of beta-decaying states in the deformed, neutron-rich nucleus 104 Nb

Excited structures in 104 Mo were populated by β decays of the ground and isomeric states in the neutron-rich nucleus 104 Nb. The beams were produced by the CARIBU facility at Argonne National Laboratory, re-accelerated by the ATLAS accelerator and implanted on a moving-tape system in the middle of the GAMMASPHERE array. Separate decay schemes for the two β-decaying states in 104 Nb were constructed for the first time. The structure of the isomers are discussed in the framework of the deformed Nilsson model and systematics of known quasiparticle structures in neighboring nuclei.

Nilsson model↗
NASA NTRS1981

Investigations of electron helicity in optically active molecules using polarized beams of electrons and positrons

A positronium-formation experiment with a high sensitivity to a possible relation between the helicity of beta particles emitted in nuclear beta decay and the optical asymmetry of biological molecules is presented. The experiment is based on a mechanism in which the electrons in optically active molecules possess a helicity of less than 0.001, too weak to detect in radiolysis experiments, the sign of which depends on the chirality of the isomer. A helicity-dependent asymmetry is sought in the formation of the triplet ground state of positronium when a low-energy beam of polarized positrons of reversible helicity interacts with an optically active substance coating a channel electron multiplier. Asymmetries between positronium decays observed at positive and negative helicities for the same substance can thus be determined with a sensitivity of 0.0001, which represents a factor of 100 improvement over previous positronium experiments.

Gidley, D. W.↗
DOE OSTI2025

Active Site Dynamics in Molybdenum-Based Silica-Supported Olefin Metathesis Catalysts: Site Renewal and Decay Beyond the Chauvin Cycle

Heterogeneous olefin metathesis catalysts exhibit low active site densities and unpredictable kinetics due to dynamic active site formation and decay processes. Here, in this study, we establish a quantitative framework that captures active site generation, renewal, and decay in olefin metathesis over silica-supported molybdenum oxide catalysts, enabling a mechanistic explanation of catalytic behavior and strategies to achieve high, stable activity. Steady-state active site titrations reveal that 2,3-dimethyl-butene isomers (4MEs) cofeeding increases active site density by up to 4.3-fold, directly correlating with enhanced metathesis rates. Spectroscopic studies demonstrate that 4MEs facilitate Mo(VI) reduction to Mo(IV) and interact strongly with surface Si–OH groups, generating labile protons that promote active site formation via a 1,2-proton shift mechanism. Kinetic modeling indicates that ethylene acts as a decay promoter, shifting kinetic control away from the Chauvin cycle and suppressing metathesis activity. Comparative studies on catalysts with varying Mo loading reveal that promotion is most effective for dispersed molybdate species, with a decline at higher Mo loadings. These findings provide a unified mechanistic framework for heterogeneous olefin metathesis, offering new strategies to enhance active site accessibility, mitigate deactivation, and optimize catalyst design.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
NASA NTRS1980

Kinetics of the ClO + NO2 + M reaction

The ClO + NO2 + M reaction has been studied with two techniques: Fourier transform infrared spectroscopy of the products, and flash photolysis-ultraviolet absorption to monitor the decay of ClO in excess NO2. The measured third-order rate constant is 1.5 x 10 to the -31st cm to the 6th/molecule-squared per sec at 298 K with M = N2, in good agreement with previous literature values, but the rate constant appears to decrease by up to a factor of three in the presence of increasing amounts of OClO. For the infrared studies a stoichiometric mixture of ClO and NO2 was prepared in a flow system by mixing NO with OClO; at least as much NO2 as ClONO2 was produced under a variety of experimental conditions. These two sets of results are incompatible with the assumption made in previous kinetic studies that ClONO2 is the only recombination product; other isomers such as OClONO or ClOONO are likely to be formed three to four times faster. These results imply that potential stratospheric ozone depletion due to chlorofluoromethanes may be even larger than previously thought.

Molina, M. J.↗
DOE OSTI2025

Yrast structures of 98 Nb and 99 Mo

Neutron-rich nuclei in the A ≈ 100 mass region are interesting due to a rapid shape transition, especially pronounced in the Zr isotopes, and more recently observed in Nb isotopes. 98 Nb, with only one proton and one neutron outside the subshell closure nucleus of 96 Zr, is amenable to shell model calculations. To further examine the rapid shape transition the yrast structure of 98 Nb was established in this work. This was the only yrast structure missing from all immediate neighbors to 96 Zr. The yrast structure of 98 Nb was studied in the fission of the compound systems formed in three heavy-ion induced reactions, 24 Mg (134.5 MeV) + 173 Yb, 23 Na (129 MeV) + 176 Yb, and 18 O (91 MeV) + 208 Pb. Prompt γ-ray spectroscopy was accomplished using the Gammasphere array. Excitation energies up to 3 MeV were observed for the first time in 98 Nb. The yrast structure above the previously known (5) + isomer was established. In the process of studying 98 Nb the yrast structure of positive-parity states in 99 Mo was extended to 3.7 MeV excitation energy, the previously-known 99 Nb level scheme was enriched, and two new levels were added in the level scheme of 97 Zr. The coupling of the odd proton occupying the g 9/2 orbital to the yrast states in the core nucleus of 97 Zr can account for all observed states in 98 Nb. The yrast structure for the positive-parity states of 99 Mo is compared to the deformed ground-state bands of the 101 Ru isotone and of 98,100 Mo.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2026

Shape evolution in neutron-rich Rh isotopes: First measurement of negative-parity isomers in 117,119 Rh

The β-delayed γ-ray spectroscopy of neutron-rich 117,119 Rh isotopes has been investigated at the Radioactive Isotope Beam Factory of RIKEN. The 1/2 − isomers in 117,119 Rh have been identified for the first time. The systematics of energy differences between the 9/2 + and 1/2 − states have been extended up to N = 74, which shows a tendency to first increase with the neutron number N, then reach a maximum at N ≈ 68, and subsequently decrease. Self-consistent triaxial relativistic Hartree-Bogoliubov (TRHB) calculations highlight the crucial role of triaxial deformation, particularly in the positive-parity states, in driving the observed evolution of energy differences. A shape transition from axially symmetric to triaxial and back to symmetric deformation is suggested along the Rh isotopic chain. These findings provide new insights into the structure of neutron-rich nuclei in the A ∼ 110 region and motivate further studies of exotic isotopes in this region to explore the interplay between triaxiality and shell evolution.

72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗