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At least 559 records · Page 31

Even-even Nd isotopes in an S D -pair shell model

Nucleon pair shell model truncated to SD collective pair subspace (SDPSM) was applied to study the properties of the low-lying states of the even-even 144–156 Nd isotopes. It is found that, within the M scheme, the systems with the number N ν = 7 of neutron pairs (or the number N π = 7 of proton pairs) can be studied in the SDPSM for the first time. The results show that the properties of the low-lying states of the even-even Nd isotopes can be reproduced approximately, and the even-even 144–15 6Nd isotopes may be a good candidate for the first-order shape phase transition.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗

SS-HORSE extension of the no-core shell model: Application to resonances in He 7

Theoretical ab initio studies of resonances in the unbound 7 He nucleus are presented. We perform no-core shell-model calculations with NN interactions Daejeon16 and JISP16 and utilize the SS-HORSE method to calculate the S matrix for two-body channels n + 6 He and n + 6 He* with 6He respectively in the ground and excited 2 + states as well as for the four-body democratic decay channel 4 He + n + n + n. The resonant energies and widths are obtained by numerical location of the S-matrix poles. Here, we describe all experimentally known 7 He resonances and suggest an interpretation of an observed wide resonance of unknown spin-parity.

6 ≤ A ≤ 19↗

Lifetime measurements in 206 Po with a shell-model interpretation

The lifetimes of the first excited 2⁺ and 4⁺ states in 206 Po were measured using the recoil-distance Dopplershift method. The experimental results were compared to large-scale shell-model calculations that describe the deduced transition probabilities well. Those calculations were extended to the neighboring 204,208 Po isotopes giving a good overall description of the yrast states. However, the calculations underpredict the energies of the 6+1 and 8+1 states, which suggests that further improvement of the proton-neutron interaction is required.

190 ≤ A ≤ 219↗

Ab initio leading order effective potential for elastic proton scattering based on the symmetry-adapted no-core shell model

Calculating microscopic optical potentials for elastic scattering at intermediate energies from light nuclei in an ab initio fashion within the Watson expansion has been established within the last few years. Based on the Watson expansion of the multiple scattering series, we employ a nonlocal translationally invariant nuclear density derived within the symmetry-adapted no-core shell model (SA-NCSM) framework from a chiral next-to-next-to-leading order (NNLO) nucleon-nucleon interaction and the very same interaction for a consistent full-folding calculation of the effective (optical) potential for nucleon-nucleus scattering for medium-heavy nuclei. The leading order effective (optical) folding potential is computed by integrating over a translationally invariant SA-NCSM one-body scalar density, spin-projected momentum distribution, and the Wolfenstein amplitudes 𝐴, 𝐶, and 𝑀. The resulting nonlocal potentials serve as input for a momentum space Lippmann-Schwinger equation. In the SA-NCSM, the model space is systematically up-selected using Sp⁡(3,ℝ) symmetry considerations. For the light nucleus of 6 He, we establish a systematic selection scheme in the SA-NCSM for scattering observables. Then, we apply this scheme to calculations of scattering observables, such as differential cross sections, analyzing powers, and spin rotation functions for elastic proton scattering from 20 Ne and 40 Ca in the energy regime between 65 and 200 MeV, and compare to available data. Furthermore, our calculations show that the leading order effective nucleon-nucleus potential in the Watson expansion of multiple scattering theory obtained from an up-selected SA-NCSM model space describes 40 Ca elastic scattering observables reasonably well to about 60 degrees in the center-of-mass frame, which coincides roughly with the validity of the NNLO chiral interaction used to calculate both the nucleon-nucleon amplitudes and the one-body scalar and spin nuclear densities.

Ab initio calculations↗

Non-Markovian Exciton-Phonon Interactions in Core-Shell Colloidal Quantum Dots at Femtosecond Timescales

We perform two-dimensional coherent spectroscopy on CdSe/CdZnS core-shell colloidal quantum dots at cryogenic temperatures. In the two-dimensional spectra, sidebands due to electronic coupling with CdSe lattice LO-phonon modes are observed to have evolutions deviating from the exponential dephasing expected from Markovian spectral diffusion, which is instantaneous and memoryless. Comparison to simulations provides evidence that LO-phonon coupling induces energy-gap fluctuations on the finite timescales of nuclear motion. Furthermore, the femtosecond resolution of our technique probes exciton dynamics directly on the timescales of phonon coupling in nanocrystals.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Relationship Between the Marginal Probability of Failure for a CPP Test and the Recommended Corrosion Control Requirements for Hanford Double Shell Waste Tanks

The Hanford Site in Washington State currently stores millions of gallons of radioactive waste in underground, carbon steel, double shell tanks (DSTs) that were constructed between 1968 and 1986. A chemistry control and monitoring program has been established mitigate corrosion in order to extend the service life for the DSTs. The current waste temperatures in the DSTs are at historical lows (i.e., typically less than 50 °C). The previous chemistry control requirements were determined for conditions at temperatures significantly higher. SRNL undertook a statistically based investigation of the role of nitrate and halide ion (i.e., chloride and fluoride) induced pitting corrosion. The objective was to develop a comprehensive waste chemistry envelope for the simultaneous minimization of the pitting and SCC risks caused by halide and nitrate ions at the lower temperature conditions. On the basis of these tests, new chemistry control requirements were proposed and have since been implemented for pitting corrosion control.

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗

Active Interrogation of the Snyder Shells using a SEA-7 Betatron

The shielded highly enriched uranium (HEU) problem is one that still needs to be addressed. As a first step towards a solution, the Snyder shells (depleted uranium) were actively interrogated with a SEA-7 betatron in various configurations using an MC15 as a detector. These configurations include masses from 0.55 to 5.1 kg, as well as 5.1 kg in a steel container. A strong electromagnetic field (EMF) background was identified in previous work, but the results in this work show all configurations produce a signal well above the background. An initial simulation capability was developed that produces the expected flux profile from the SEA-7 betatron, but further work needs to be done to determine the magnitude of the flux via a combination of experiment and simulation validation. Depleted uranium generally produces more neutrons than HEU, so additional future work will need to include similar measurements of HEU to confirm similar performance of the technique. Additionally the EMF background needs to be better characterized as a function of distance and angle from the SEA-7 source and mitigation techniques explored.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗

Front-End Engineering Design for Carbon Capture from Shell's Deer Park Chemical Complex (Final Scientific/Technical Report)

This is the final scientific/technical report for a Front-End Engineering and Design (FEED) whose objective was to separate and capture over 820,000 tonnes per year (tpy) CO2 emissions from the commercially operated Shell Chemicals Complex located in Deer Park, Texas, USA reducing the overall facility CO2 emissions by 95% while providing energy transition jobs in a commercial area with a high concentration of refinery and chemical facilities producing CO2 emissions. The emission sources at the facility that were in scope were a total of Sixteen Furnaces – 8 OP3 furnaces and 8 OP3/HT2 Furnaces. Other minor sources were out of scope.

01 COAL, LIGNITE, AND PEAT↗

Hydronic Shell: An Affordable Solution for Multifamily Deep Energy Retrofit

Approximately 42% of multi-family buildings in the United States have do not have insulation as required by the building codes. Envelope retrofits of these buildings are needed to improve their thermal performance, provide thermal resilience, and enable a pathway to electrification of space heating systems. Hydronic shell (HS) is a retrofit technique where a stud wall layer is added to a masonry wall along with a convective coil and a fan coil unit fitted in the façade cavity which can provide both heating and cooling to the space. The HS system serves a dual purpose of 1) retrofitting the building envelope and 2) retrofitting the HVAC system and enabling electrification of space heating. The electrification of space heating is possible from the installation of a combination of hydronic system/fan coil unit system which uses a central heat pump as a source of heating water in the cavity between the existing wall and retrofit insulation layer. This study evaluates the performance of the HS system at varying outdoor conditions mimicked by a climate chamber and hot water supply temperature from a water bath. During the ramp-up period, the indoor chamber temperature could be increased from 66 ºF to 69.5 ºF within an hour using heating water at 120 ºF when the outdoor chamber temperature was at 0 ºF. When the indoor chamber temperature was maintained within a deadband, variation in cavity air temperature was mostly influenced by the duration when water was flowing through the cavity convector. It was seen from the testing that the hydronic system alone without use of fan in the system is able to maintain the space temperature at coldest outdoor condition used in the experiment (0 ºF) even at lowest hot water supply temperature chosen (90 ºF). During the ramp-down period, the fastest decline in temperature took 6.4 hours from temperature to drop from 69.6 ºF to 66 ºF which shows tremendous potential of thermal resilience and peak load shifting.

32 ENERGY CONSERVATION, CONSUMPTION, AND UTILIZATI↗

Three-Layer Cylindrical Shell with Nonlinear Deformation

A mathematical model is proposed for the stress–strain state of a three-layer (sandwich) structure, taking account of nonlinear deformation of the supporting layers. Nonlinear deformation of a symmetric three-layer cylindrical shell under the action of transverse loads is considered, for different boundary conditions.

42 ENGINEERING↗

Inner-Shell Photodetachment of Na – Using R-Matrix Methods

Inner-shell photodetachment of Na – near the L-edge threshold was investigated using the R-matrix method. Significant structure was found in the cross section, and this structure is shown to be related to the complicated correlated electron dynamics endemic in negative ions. Comparison with experiment suggests that the absolute values of the measured cross section might be too small by a factor of two.

74 ATOMIC AND MOLECULAR PHYSICS↗

Synthesis and Advanced Characterization of Polymer–Protein Core–Shell Nanoparticles

Enzyme immobilization techniques are widely researched due to their wide range of applications. Polymer–protein core–shell nanoparticles (CSNPs) have emerged as a promising technique for enzyme/protein immobilization via a self-assembly process. Based on the desired application, different sizes and distribution of the polymer–protein CSNPs may be required. This work systematically studies the assembly process of poly(4-vinyl pyridine) and bovine serum albumin CSNPs. Average particle size was controlled by varying the concentrations of each reagent. Particle size and size distributions were monitored by dynamic light scattering, ultra-small-angle X-ray scattering, small-angle X-ray scattering and transmission electron microscopy. Results showed a wide range of CSNPs could be assembled ranging from an average radius as small as 52.3 nm, to particles above 1 µm by adjusting reagent concentrations. In situ X-ray scattering techniques monitored particle assembly as a function of time showing the initial particle growth followed by a decrease in particle size as they reach equilibrium. The results outline a general strategy that can be applied to other CSNP systems to better control particle size and distribution for various applications.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Core-Shell Heterostructures as Solid Oxide Fuel Cell Electrodes

The goals of the project are to synthesize and deploy core-shell heterostructures as solid oxide fuel cell (SOFC) cathodes which exhibit high oxygen reduction rates at lower operating temperatures resulting in high performance at lower operating temperature and simultaneously exhibit longterm resistance to Cr-impurity attack induced performance degradation. An ancillary objective is to eliminate cumbersome, multiple infiltration steps in the cathode to achieve high performance. The expected outcomes are (1) a novel, environmentally benign, and inexpensive synthesis tool for synthesizing complex cathode powders, scalable to high volumes; (2) decrease in energy expenditure during synthesis of cathode powders; (3) up to a factor of 1.5 improvement in maximum power density of single cells at 700ºC; and (4) significant improvements in cell performance degradation rates down to 0.02%/1000 h.

03 NATURAL GAS↗

Core-Shell Heterostructures as Solid Oxide Fuel Cell Electrodes

The goals of the project are to synthesize and deploy core-shell heterostructures as solid oxide fuel cell (SOFC) cathodes which exhibit high oxygen reduction rates at lower operating temperatures resulting in high performance at lower operating temperature and simultaneously exhibit longterm resistance to Cr-impurity attack induced performance degradation. An ancillary objective is to eliminate cumbersome, multiple infiltration steps in the cathode to achieve high performance. The expected outcomes are (1) a novel, environmentally benign, and inexpensive synthesis tool for synthesizing complex cathode powders, scalable to high volumes; (2) decrease in energy expenditure during synthesis of cathode powders; (3) up to a factor of 1.5 improvement in maximum power density of single cells at 700ºC; and (4) significant improvements in cell performance degradation rates down to 0.02%/1000 h.

03 NATURAL GAS↗

Core-Shell Heterostructures as Solid Oxide Fuel Cell Electrodes Quarterly Report

The goals of the project are to synthesize and deploy core-shell heterostructures as solid oxide fuel cell (SOFC) cathodes which exhibit high oxygen reduction rates at lower operating temperatures resulting in high performance at lower operating temperature and simultaneously exhibit longterm resistance to Cr-impurity attack induced performance degradation. An ancillary objective is to eliminate cumbersome, multiple infiltration steps in the cathode to achieve high performance. The expected outcomes are (1) a novel, environmentally benign, and inexpensive synthesis tool for synthesizing complex cathode powders, scalable to high volumes; (2) decrease in energy expenditure during synthesis of cathode powders; (3) up to a factor of 1.5 improvement in maximum power density of single cells at 700ºC; and (4) significant improvements in cell performance degradation rates down to 0.02%/1000 h.

20 FOSSIL-FUELED POWER PLANTS↗

Core-Shell Heterostructures as Solid Oxide Fuel Cell Electrodes Quarterly Report

The goals of the project are to synthesize and deploy core-shell heterostructures as solid oxide fuel cell (SOFC) cathodes which exhibit high oxygen reduction rates at lower operating temperatures resulting in high performance at lower operating temperature and simultaneously exhibit longterm resistance to Cr-impurity attack induced performance degradation. An ancillary objective is to eliminate cumbersome, multiple infiltration steps in the cathode to achieve high performance. The expected outcomes are (1) a novel, environmentally benign, and inexpensive synthesis tool for synthesizing complex cathode powders, scalable to high volumes; (2) decrease in energy expenditure during synthesis of cathode powders; (3) up to a factor of 1.5 improvement in maximum power density of single cells at 700ºC; and (4) significant improvements in cell performance degradation rates down to 0.02%/1000 h.

03 NATURAL GAS↗

Overcoming Barriers Associated with Oral Delivery of Differently Sized Fluorescent Core‐Shell Silica Nanoparticles

Oral delivery, while a highly desirable form of nanoparticle-drug administration, is limited by challenges associated with overcoming several biological barriers. Here, in this study, the authors study how fluorescent and poly(ethylene glycol)-coated (PEGylated) core-shell silica nanoparticles sized 5 to 50 nm interact with major barriers including intestinal mucus, intestinal epithelium, and stomach acid. From imaging fluorescence correlation spectroscopy studies using quasi-total internal reflection fluorescence microscopy, diffusion of nanoparticles through highly scattering mucus is progressively hindered above a critical hydrodynamic size around 20 nm. By studying Caco-2 cell monolayers mimicking the intestinal epithelia, it is observed that ultrasmall nanoparticles below 10 nm diameter (Cornell prime dots, [C’ dots]) show permeabilities correlated with high absorption in humans from primarily enhanced passive passage through tight junctions. Particles above 20 nm diameter exclusively show active transport through cells. After establishing C’ dot stability in artificial gastric juice, in vivo oral gavage experiments in mice demonstrate successful passage through the body followed by renal clearance without protein corona formation. Results suggest C’ dots as viable candidates for oral administration to patients with a proven pathway towards clinical translation and may generate renewed interest in examining silica as a food additive and its effects on nutrition and health.

36 MATERIALS SCIENCE↗

Constructing Highly Durable Fuel Cell Catalysts Through Integrating Graphitic Shell‐Protected Composite Carbon Support with Gaseous Co Deposition‐Driven PtCo Intermetallics

Metal dissolution, nanoparticle agglomeration, and carbon support corrosion cause significant performance degradation of current PtCo catalysts under acidic and oxidative oxygen reduction reaction. Here, in this study, an integrated strategy is presented to design high-performance Pt 3 Co intermetallic catalysts by regulating gaseous Co deposition-driven diffusion into Pt nanoparticles supported on a composite carbon. The composite carbon is derived from ZIF-8/polyaniline, consisting of a high-surface-area (HSC) core and a protective graphitic shell (GS), which is employed to design 40 wt.% Pt/HSC@GS catalyst. The corresponding membrane electrode assemblies (MEAs) can maintain 1.09 A cm −2 at 0.7 V (20. 7% loss) after 10 000 cycles (1.0–1.5 V for carbon stability) and 1.15 A cm −2 (16.1% loss) after 150 000 cycles (0.60–0.95 V for catalyst stability). A ordered Pt 3 Co intermetallic is synthesized via a gaseous Co-deposition process, which yields a homogeneous Co-rich layer onto the Pt nanoparticles on the composite support, thereby facilitating Co diffusion into Pt crystal during subsequent ordering annealing to form the ordered intermetallic structure. This gaseous deposition leads to a thin carbon layer on PtCo nanoparticles, inhibiting particle growth during the annealing and mitigating Co dissolution under dynamic electrochemical conditions. The PtCo catalyst achieves impressive MEA performance and long-term durability (1.45 A cm −2 at 0.7 V after 120 000 cycles) under heavy-duty conditions.

30 DIRECT ENERGY CONVERSION↗