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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 1,243 records · Page 69
All sourcesNASA NTRSDOE OSTI
DOE OSTI2013

ANOMALOUS CO{sub 2} ICE TOWARD HOPS-68: A TRACER OF PROTOSTELLAR FEEDBACK

We report the detection of a unique CO{sub 2} ice band toward the deeply embedded, low-mass protostar HOPS-68. Our spectrum, obtained with the Infrared Spectrograph on board the Spitzer Space Telescope, reveals a 15.2 {mu}m CO{sub 2} ice bending mode profile that cannot be modeled with the same ice structure typically found toward other protostars. We develop a modified CO{sub 2} ice profile decomposition, including the addition of new high-quality laboratory spectra of pure, crystalline CO{sub 2} ice. Using this model, we find that 87%-92% of the CO{sub 2} is sequestered as spherical, CO{sub 2}-rich mantles, while typical interstellar ices show evidence of irregularly shaped, hydrogen-rich mantles. We propose that (1) the nearly complete absence of unprocessed ices along the line of sight is due to the flattened envelope structure of HOPS-68, which lacks cold absorbing material in its outer envelope, and possesses an extreme concentration of material within its inner (10 AU) envelope region and (2) an energetic event led to the evaporation of inner envelope ices, followed by cooling and re-condensation, explaining the sequestration of spherical, CO{sub 2} ice mantles in a hydrogen-poor mixture. The mechanism responsible for the sublimation could be either a transient accretion event or shocks in the interaction region between the protostellar outflow and envelope. The proposed scenario is consistent with the rarity of the observed CO{sub 2} ice profile, the formation of nearly pure CO{sub 2} ice, and the production of spherical ice mantles. HOPS-68 may therefore provide a unique window into the protostellar feedback process, as outflows and heating shape the physical and chemical structure of protostellar envelopes and molecular clouds.

79 ASTRONOMY AND ASTROPHYSICS↗
DOE OSTI2014

2π1ν states populated in 135Te from 9Be-induced reactions with a 132Sn beam

γ-ray transitions in 134Te, 135Te, and 136Te were measured from 9Be-induced reactions with a radioactive 132Sn beam at a sub-Coulomb barrier energy of 3 MeV per nucleon using particle-γ coincidence spectroscopy. The transitions were selected by gating on alpha-like particles in a CsI detector following a combination of (9Be,α1n), (9Be,α2n), and (9Be,α3n) incomplete fusion-evaporation reactions. Distorted-wave Born approximation calculations suggest little to no contribution from the (9Be,7He), (9Be,6He), and (9Be,5He) direct reactions.γ-ray transitions from previously known 2+Ⓧν2f7/2 and 4+Ⓧν2f7/2 multiplet members in 135Te are observed. A new γ ray is observed, assigned to the third-excited state in 135Te, and new 2+Ⓧν2f7/2 multiplet members are suggested. In addition, spin assignments are made by using recent one-neutron transfer data. The updated experimental data for 135Te are compared to shell-model calculations for a relatively complete set of states up to the yrast 15/2-,4+Ⓧν2f7/2 multiplet member at 1505 keV.

Allmond, James M.↗
DOE OSTI2012

O{sub 2}(a{sup 1}{Delta}{sub g}) + Mg, Fe, and Ca: Experimental kinetics and formulation of a weak collision, multiwell master equation with spin-hopping

The first excited electronic state of molecular oxygen, O{sub 2}(a{sup 1}{Delta}{sub g}), is formed in the upper atmosphere by the photolysis of O{sub 3}. Its lifetime is over 70 min above 75 km, so that during the day its concentration is about 30 times greater than that of O{sub 3}. In order to explore its potential reactivity with atmospheric constituents produced by meteoric ablation, the reactions of Mg, Fe, and Ca with O{sub 2}(a) were studied in a fast flow tube, where the metal atoms were produced either by thermal evaporation (Ca and Mg) or by pulsed laser ablation of a metal target (Fe), and detected by laser induced fluorescence spectroscopy. O{sub 2}(a) was produced by bubbling a flow of Cl{sub 2} through chilled alkaline H{sub 2}O{sub 2}, and its absolute concentration determined from its optical emission at 1270 nm (O{sub 2}(a{sup 1}{Delta}{sub g}- X{sup 3}{Sigma}{sub g}{sup -}). The following results were obtained at 296 K: k(Mg + O{sub 2}(a) + N{sub 2}{yields} MgO{sub 2}+ N{sub 2}) = (1.8 {+-} 0.2) Multiplication-Sign 10{sup -30} cm{sup 6} molecule{sup -2} s{sup -1}; k(Fe + O{sub 2}(a) {yields} FeO + O) = (1.1 {+-} 0.1) Multiplication-Sign 10{sup -13} cm{sup 3} molecule{sup -1} s{sup -1}; k(Ca + O{sub 2}(a) + N{sub 2}{yields} CaO{sub 2}+ N{sub 2}) = (2.9 {+-} 0.2) Multiplication-Sign 10{sup -28} cm{sup 6} molecule{sup -2} s{sup -1}; and k(Ca + O{sub 2}(a) {yields} CaO + O) = (2.7 {+-} 1.0) Multiplication-Sign 10{sup -12} cm{sup 3} molecule{sup -1} s{sup -1}. The total uncertainty in these rate coefficients, which mostly arises from the systematic uncertainty in the O{sub 2}(a) concentration, is estimated to be {+-}40%. Mg + O{sub 2}(a) occurs exclusively by association on the singlet surface, producing MgO{sub 2}({sup 1}A{sub 1}), with a pressure dependent rate coefficient. Fe + O{sub 2}(a), on the other hand, shows pressure independent kinetics. FeO + O is produced with a probability of only {approx}0.1%. There is no evidence for an association complex, suggesting that this reaction proceeds mostly by near-resonant electronic energy transfer to Fe(a{sup 5}F) + O{sub 2}(X). The reaction of Ca + O{sub 2}(a) occurs in an intermediate regime with two competing pressure dependent channels: (1) a recombination to produce CaO{sub 2}({sup 1}A{sub 1}), and (2) a singlet/triplet non-adiabatic hopping channel leading to CaO + O({sup 3}P). In order to interpret the Ca + O{sub 2}(a) results, we utilized density functional theory along with multireference and explicitly correlated CCSD(T)-F12 electronic structure calculations to examine the lowest lying singlet and triplet surfaces. In addition to mapping stationary points, we used a genetic algorithm to locate minimum energy crossing points between the two surfaces. Simulations of the Ca + O{sub 2}(a) kinetics were then carried out using a combination of both standard and non-adiabatic Rice-Ramsperger-Kassel-Marcus (RRKM) theory implemented within a weak collision, multiwell master equation model. In terms of atmospheric significance, only in the case of Ca does reaction with O{sub 2}(a) compete with O{sub 3} during the daytime between 85 and 110 km.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2015

Analytical model of the effect of misfit dislocation character on the bubble-to-void transition in metals

Here, this paper addresses the role of misfit dislocations in the nucleation and growth of nanoscale He bubbles at interfaces. In a recent work, we studied the nanoscale effects on the capillarity equation and on equilibrium conditions. We proposed an expression for surface energy and for the equation of state, EOS, for He in bubbles, which have a size dependence that captures the role of the interface forces, which become relevant at the nanoscale. Here we determine the EOS for several twist grain boundaries in Fe and Cu and incorporate these results into the rate equation that determines the bubble-to-void transition, focusing on the influence of interface dislocations on the evaporation rate of vacancies. We find a significant effect of the magnitude of the Burgers vector of the dislocations on the critical radius for the transition. In conclusion, these results give a quantitative way to characterize grain boundaries in their ability to capture He and alter the onset of swelling.

36 MATERIALS SCIENCE↗
DOE OSTI2015

Mass variation of a thin liquid film driven by an acoustic wave

In this work, we investigate the dynamics of a thin liquid film subjected to an acoustic field in its bounding vapor space. For large acoustic wavelengths, the field imposes a spatially uniform, temporally periodic temperature and pressure at the vapor side of the film interface, which leads to a periodic driving force for mass exchange with the vapor. Neglecting the dynamics of the vapor space, we adopt the “one-sided” model for evaporation/condensation of thin liquid films. In the interest of determining the effect of oscillatory mass exchange on film stability, we consider films in thermodynamic equilibrium with the mean vapor conditions. The effects of oscillatory phase change on both linear stability and nonlinear dynamics are investigated for slightly inclined ceiling films that are destabilized by gravity and subject to thermocapillary effects. At linear order, this mass exchange is not found to alter the band of unstable wave numbers and only marginally affects the growth rates. Additionally, the mass exchanged during evaporation is balanced by condensation so that the total mass of the liquid film is conserved. However, due to nonlinear effects, we find that traveling waves encouraged by the inclination are subject to net mass loss. It is then found that normal thermocapillary effects enhance this loss, and that anomalous thermocapillarity mitigates or even reverses the loss to a mass gain.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗
DOE OSTI2017

Cross-shell excitations in Si 31

The Si-31 nucleus was produced through the O-18(18O, an) fusion-evaporation reaction at E-lab = 24 MeV. Evaporated a particles from the reaction were detected and identified in the Microball detector array for channel selection. Multiple gamma-ray coincidence events were detected in Gammasphere. The energy and angle information for the alpha particles was used to determine the Si-31 recoil kinematics on an event-by-event basis for a more accurate Doppler correction. A total of 22 new states and 52 new gamma transitions were observed, including 14 from states above the neutron separation energy. The positive-parity states predicted by the shell-model calculations in the sd model space agree well with experiment. The negative-parity states were compared with shell-model calculations in the psdpf model space with some variations in the N = 20 shell gap. The best agreement was found with a shell gap intermediate between that originally used for A approximate to 20 nuclei and that previously adapted for P-32,P-34. This variation suggests the need for a more universal cross-shell interaction.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2016

Nuclear-level densities in the {sup 49}V and {sup 57}Co nuclei on the basis of evaporated-neutron spectra in (p, n) and (d, n) reactions

The spectra of neutrons from the reactions {sup 49}Ti(p, n){sup 49}V and {sup 57}Fe (p, n){sup 57}Co were measured in the range of proton energies between 8 and 11 MeV along with their counterparts from the reactions {sup 48}Ti(d, n){sup 49}V and {sup 56}Fe (d, n){sup 57}Co at the deuteron energies of 2.7 and 3.8 MeV. These measurements were conducted with the aid of a time-of-flight fast-neutron spectrometer on the basis of the EGP-15 pulsed tandem accelerator of the Institute for Physics and Power Engineering (IPPE, Obninsk). An analysis of measured data was performed within the statistical equilibrium and preequilibrium models of nuclear reactions. The respective calculations based on the Hauser–Feshbach formalism of statistical theory were carried out with nuclear-level densities given by the generalized superfluid model of the nucleus, the backshifted Fermi-gas model, and the Gilbert–Cameron composite formula. The nuclear-level densities of {sup 49}V and {sup 57}Co and their energy dependences were determined. The results were discussed together with available experimental data and data recommended by model systematics.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2020

Verification and Validation of MFiX-PIC

This work is aimed at verification and validation (V&V) of particle-in-cell (PIC) approach in the National Energy Technology Laboratory’s (NETL) Multiphase Flow with Interphase eXchanges (MFiX-PIC) which was officially released in April 2019. Under verification, the results from MFiX-PIC are compared with exact or analytical solutions, while experimental results are used for benchmarking under validation. The test suite consists of the following cases: Terminal velocity. Particle advection in time-varying flow field. Particle settling in a dense medium. Evaporation. Rayleigh-Taylor instability. Minimum fluidization. Mini-circulating fluidized bed. The cases reported in a format consistent with the existing Verification and Validation Manual (Musser et al., 2018) explore a wide range of flow velocities and concentration regimes. Only one case considered in this work verifies the implementation of heat and mass transfer routines in MFiX-PIC, while a few other studies are currently underway to further expand the validation space in reacting flows. This study highlights the need for a rigorous analysis to objectively quantify the effect of model parameters. In addition, there is a scarcity of high-quality experimental data in the literature suitable for validating PIC methodology. Future efforts would include performing experiments which provide results for a valuable database. While designing such experiments, particle count should be significant to have sufficient particles per parcel while maintaining an optimal parcel to cell volume ratio. Also, datasets should have objectively assessed experimental uncertainty whereby confidence interval in those measurements become more explicit.

42 ENGINEERING↗
DOE OSTI2020

Dual‐Scale Nanostructures via Evaporative Assembly

Abstract Dual‐scale hierarchical structures with regular microscale patterns and varying degree of nanoscale crystalline order are synthesized on physically and chemically homogeneous substrates by evaporative self‐assembly with a suspension of DNA‐functionalized nanoparticles (NPs) with a charged core shell. For a certain NP concentration range, periodic concentric rings in a stripe‐like micropattern are produced over macroscale surface areas by an NP monolayer with hexagonal lattice structure at the nanoscale. The stripe width, spacing, and nanoparticle ordering can be controlled by varying the NP concentration. The results indicate that the interplay between “stick‐slip” motion of the droplet contact line and coulombic and steric NP interactions control the formation of the observed structures. A simple analytical model is proposed to account for the experimental observations and guide the future design of different nanostructure morphologies. This work demonstrates a simple cost‐effective mask‐free method for fabricating large‐area nanostructured 2D materials and metasurfaces for applications ranging from energy conversion/storage to optoelectronics and nanophotonics.

Srivastava, Sunita↗
DOE OSTI2017

Novel evaporator architecture with entrance-length crossflow-paths for supercritical Organic Rankine Cycles

Here in this article, a novel geometry is proposed for evaporators that are used in Supercritical Organic Rankine Cycles. The proposed geometry consists of successive plenums at several length-scale levels, creating a multi-scale heat exchanger (HX). The channels at the lowest length-scale levels were considered to have their length determined by the thermal entrance-length. Numerical simulations based on turbulent flow correlations for supercritical R134a and water were used to evaluate the performance of heat exchangers. Using the data on pumping power and area of heat exchange, the total present cost was evaluated using a cost model for shell-and-tube heat exchangers. With respect to the shell-and-tube baseline case, the cost per heat load and total costs of new HXs is lowered by approximately 20–26% and 15–30%, respectively. This reduction in present costs of the new HXs were found to be attributed to higher operational costs for the shell-and-tube HXs, as evidenced by the higher pumping power, as well their capital investment costs. The cost savings in the new HX designs compared to those of the shell-and-tube HXs, at similar heat load performance, indicate that the new HX architectures proposed in this paper are valid alternatives to traditional HX designs.

42 ENGINEERING↗
DOE OSTI2020

Molecular understanding of new-particle formation from α-pinene between -50 and +25 °C

Abstract. Highly oxygenated organic molecules (HOMs) contribute substantially to the formation and growth of atmospheric aerosol particles, which affect air quality, human health and Earth's climate. HOMs are formed by rapid, gas-phase autoxidation of volatile organic compounds (VOCs) such as α-pinene, the most abundant monoterpene in the atmosphere. Due to their abundance and low volatility, HOMs can play an important role in new-particle formation (NPF) and the early growth of atmospheric aerosols, even without any further assistance of other low-volatility compounds such as sulfuric acid. Both the autoxidation reaction forming HOMs and their NPF rates are expected to be strongly dependent on temperature. However, experimental data on both effects are limited. Dedicated experiments were performed at the CLOUD (Cosmics Leaving OUtdoor Droplets) chamber at CERN to address this question. In this study, we show that a decrease in temperature (from +25 to -50°C) results in a reduced HOM yield and reduced oxidation state of the products, whereas the NPF rates (J1.7 nm) increase substantially. Measurements with two different chemical ionization mass spectrometers (using nitrate and protonated water as reagent ion, respectively) provide the molecular composition of the gaseous oxidation products, and a two-dimensional volatility basis set (2D VBS) model provides their volatility distribution. The HOM yield decreases with temperature from 6.2 % at 25°C to 0.7 % at -50°C. However, there is a strong reduction of the saturation vapor pressure of each oxidation state as the temperature is reduced. Overall, the reduction in volatility with temperature leads to an increase in the nucleation rates by up to 3 orders of magnitude at -50°C compared with 25°C. In addition, the enhancement of the nucleation rates by ions decreases with decreasing temperature, since the neutral molecular clusters have increased stability against evaporation. The resulting data quantify how the interplay between the temperature-dependent oxidation pathways and the associated vapor pressures affect biogenic NPF at the molecular level. Our measurements, therefore, improve our understanding of pure biogenic NPF for a wide range of tropospheric temperatures and precursor concentrations.

54 ENVIRONMENTAL SCIENCES↗
DOE OSTI2014

Electron-capture supernovae of super-asymptotic giant branch stars and the Crab supernova 1054

An electron-capture supernova (ECSN) is a core-collapse supernova explosion of a super-asymptotic giant branch (SAGB) star with a main-sequence mass M{sub Ms} ∼ 7 - 9.5M{sub ⊙}. The explosion takes place in accordance with core bounce and subsequent neutrino heating and is a unique example successfully produced by first-principle simulations. This allows us to derive a first self-consistent multicolor light curves of a core-collapse supernova. Adopting the explosion properties derived by the first-principle simulation, i.e., the low explosion energy of 1.5 × 10{sup 50} erg and the small {sup 56}Ni mass of 2.5 × 10{sup −3} M{sub ⊙}, we perform a multigroup radiation hydrodynamics calculation of ECSNe and present multicolor light curves of ECSNe of SAGB stars with various envelope mass and hydrogen abundance. We demonstrate that a shock breakout has peak luminosity of L ∼ 2 × 10{sup 44} erg s{sup −1} and can evaporate circumstellar dust up to R ∼ 10{sup 17} cm for a case of carbon dust, that plateau luminosity and plateau duration of ECSNe are L ∼ 10{sup 42} erg s{sup −1} and {sup t} ∼ 60 - 100 days, respectively, and that a plateau is followed by a tail with a luminosity drop by ∼ 4 mag. The ECSN shows a bright and short plateau that is as bright as typical Type II plateau supernovae, and a faint tail that might be influenced by spin-down luminosity of a newborn pulsar. Furthermore, the theoretical models are compared with ECSN candidates: SN 1054 and SN 2008S. We find that SN 1054 shares the characteristics of the ECSNe. For SN 2008S, we find that its faint plateau requires a ECSN model with a significantly low explosion energy of E ∼ 10{sup 48} erg.

79 ASTRONOMY AND ASTROPHYSICS↗
DOE OSTI2014

Systematic study of iodine nuclei in A∼125 mass region

Excited states of {sup 127}I were populated via {sup 124}Sn({sup 7}Li,{sup 4}nγ){sup 127}I fusion-evaporation reaction at beam energy of 33 MeV. Multipolarities of several transitions were determined and spins of corresponding states have been confirmed. The band-head spin and parity of an already reported band at 2901.2 keV has been confirmed. Based on the observed characteristic features and by comparing with the systematics of odd mass iodine nuclei, a πg{sub 7/2}⊗νh{sub 11/2}{sup 2} configuration has been proposed for this band. The experimental B(M1)/B(E2) values for πg{sub 7/2} band were compared with the theoretical results of semi classical model of Frauendorf and Donau and found in well agreement.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗
DOE OSTI2022

A hydrological simulation dataset of the Upper Colorado River Basin from 1983 to 2019

Abstract This article presents a hydrological reconstruction of the Upper Colorado River Basin with an hourly temporal resolution, and 1-km spatial resolution from October 1982 to September 2019. The validated dataset includes a suite of hydrologic variables including streamflow, water table depth, snow water equivalent (SWE) and evapotranspiration (ET) simulated by an integrated hydrological model, ParFlow-CLM. The dataset was validated over the period with a combination of point observations and remotely sensed products. These datasets provide a long-term, natural-flow, simulation for one of the most over-allocated basins in the world.

54 ENVIRONMENTAL SCIENCES↗
DOE OSTI2013

MULTIDIMENSIONAL MODELING OF CORONAL RAIN DYNAMICS

We present the first multidimensional, magnetohydrodynamic simulations that capture the initial formation and long-term sustainment of the enigmatic coronal rain phenomenon. We demonstrate how thermal instability can induce a spectacular display of in situ forming blob-like condensations which then start their intimate ballet on top of initially linear force-free arcades. Our magnetic arcades host a chromospheric, transition region, and coronal plasma. Following coronal rain dynamics for over 80 minutes of physical time, we collect enough statistics to quantify blob widths, lengths, velocity distributions, and other characteristics which directly match modern observational knowledge. Our virtual coronal rain displays the deformation of blobs into V-shaped features, interactions of blobs due to mostly pressure-mediated levitations, and gives the first views of blobs that evaporate in situ or are siphoned over the apex of the background arcade. Our simulations pave the way for systematic surveys of coronal rain showers in true multidimensional settings to connect parameterized heating prescriptions with rain statistics, ultimately allowing us to quantify the coronal heating input.

79 ASTRONOMY AND ASTROPHYSICS↗
DOE OSTI2025

VUV Photoionization Dynamics and Reactivity of Heterogeneous Water Clusters

This feature focuses on bridging isolated water and bulk water studies. It assembles experiments and theory on water clusters, mainly probed by vacuum ultraviolet (VUV) radiation, and summarizes what the effects are of intermolecular interactions on both the spectroscopy and the VUV-induced processes in water. In particular, it highlights studies of heterogeneous water clusters─those incorporating other molecular species such as naphthalene, methane, formic acid, and glycerol─which serve as model systems to investigate the fundamental roles of water in hydrogen bonding networks, proton transfer, and astrochemical processes. These mixed clusters provide a platform to revisit the stability of protonated water clusters and compile observations of ionization-induced structural rearrangements and fragmentation, especially in systems involving hydroxyl-rich cosolvents. This feature then explores energy transfer mechanisms in molecular clusters, following VUV photoexcitation. It concludes with potential future directions. First, we investigate excited-state dynamics in molecular clusters through direct probing, complementing the synchrotron studies discussed here. Second, exploring gas-phase molecule evaporation from confined spaces and interfaces using advanced spectroscopic techniques sheds light on these ubiquitous, yet currently debated, molecular processes.

Cluster chemistry↗
DOE OSTI2017

Isomers and high-spin structures in the N = 81 isotones Xe 135 and Ba 137

In this study, the high-spin structures and isomers of the N=81 isotones 135 Xe and 137 Ba are investigated after multinucleon-transfer (MNT) and fusion-evaporation reactions. Both nuclei are populated (i) in 136 Xe + 238 U and (ii) 136 Xe+ 208 Pb MNT reactions employing the high-resolution Advanced Gamma Tracking Array (AGATA) coupled to the magnetic spectrometer PRISMA, (iii) in the 136 Xe+ 198 Pt MNT reaction employing the γ-ray array GAMMASPHERE in combination with the gas-detector array CHICO, and (iv) via a 11 B+ 130 Te fusion-evaporation reaction with the HORUS γ-ray array at the University of Cologne. The high-spin level schemesof 135 Xe and 137 Ba are considerably extended to higher energies. The 2058-keV (19/2 - ) state in 135 Xe is identified as an isomer, closing a gap in the systematics along the N=81 isotones. Its half-life is measured to be 9.0(9) ns, corresponding to a reduced transition probability of B(E2,19/2 - →15/2 - )=0.52(6) W.u. The experimentally deduced reduced transition probabilities of the isomeric states are compared to shell-model predictions. Finally, latest shell-model calculations reproduce the experimental findings generally well and provide guidance to the interpretation of the new levels.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2017

High-spin structures in Xe 132 and Xe 133 and evidence for isomers along the N = 79 isotones

In this study, the transitional nuclei 132 Xe and 133 Xe are investigated after multinucleon-transfer (MNT) and fusion-evaporation reactions. Both nuclei are populated (i) in 136 Xe + 208 Pb MNT reactions employing the high-resolution Advanced GAmma Tracking Array (AGATA) coupled to the magnetic spectrometer PRISMA, (ii) in the 136 Xe + 198 Pt MNT reaction employing the GAMMASPHERE spectrometer in combination with the gas-detector array CHICO, and (iii) as an evaporation residue after a 130 Te (α,xn) 134-xn Xe fusion-evaporation reaction employing the HORUS γ -ray array at the University of Cologne. The high-spin level schemes are considerably extended above the J π = (7 - ) and (10 + ) isomers in 132 Xe and above the 11/2 - isomer in 133 Xe. The results are compared to the high-spin systematics of the Z = 54 as well as the N = 78 and N = 79 chains. Furthermore, evidence is found for a long-lived (T 1/ 2 » 1 μs) isomer in 133 Xe which closes a gap along the N = 79 isotones. Finally, shell-model calculations employing the SN100PN and PQM130 effective interactions reproduce the experimental findings and provide guidance to the interpretation of the observed high-spin features.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗