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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 1,567 records · Page 87
All sourcesNASA NTRSDOE OSTI
DOE OSTI2025

Measurement of the Drell–Yan forward-backward asymmetry and of the effective leptonic weak mixing angle in proton-proton collisions at $\sqrt{s}$ 13 TeV

The forward-backward asymmetry in Drell-Yan production and the effective leptonic electroweak mixing angle are measured in proton-proton collisions at $\sqrt{s}$ = 13 TeV, collected by the CMS experiment and corresponding to an integrated luminosity of 138 fb$^{-1}$. The measurement uses both dimuon and dielectron events, and is performed as a function of the dilepton mass and rapidity. The unfolded angular coefficient $A_4$ is also extracted, as a function of the dilepton mass and rapidity. Using the CT18Z set of parton distribution functions, we obtain $\sin^{2}\theta^\ell_\text{eff}$ = 0.23152 $\pm$ 0.00031, where the uncertainty includes the experimental and theoretical contributions. The measured value agrees with the standard model fit result to global experimental data. This is the most precise $\sin^{2}\theta^\ell_\text{eff}$ measurement at a hadron collider, with a precision comparable to the results obtained at LEP and SLD.

72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗
DOE OSTI2019

Collisional alpha transport in a weakly non-quasisymmetric stellarator magnetic field</strong

Alpha particle confinement is a serious concern in stellarators and provides strong motivation for optimizing magnetic field configurations. In addition to the collisionless confinement of trapped alphas in stellarators, excessive collisional transport of the trapped alpha particles must be avoided while they tangentially drift due to the magnetic gradient (the ∇B drift).The combination of pitch angle scatter off the background ions and the ∇B drift gives rise to two narrow boundary layers in the trapped region. The first is at the trapped–passing boundary and enables the finite trapped response to be matched to the vanishing passing response of the alphas. The second layer is a region that encompasses the somewhat more deeply trapped alphas with vanishing tangential ∇B drift. Away from (and between) these boundary layers, collisions are ineffective and the alpha ∇B drift simply balances the small radial drift of the trapped alphas. As this balance does not vanish as the trapped–passing boundary is approached, the first collisional boundary layer is necessary and gives rise to $\sqrt{v}$ transport, with v the collision frequency. The vanishing of the tangential drift results in a separate, somewhat wider boundary layer, and significantly stronger superbanana plateau transport that is independent of collisionality. The constraint imposed by the need to avoid significant energy depletion loss in the slowing down tail distribution function sets the allowed departure of a stellarator from an optimal quasisymmetric configuration.

70 PLASMA PHYSICS AND FUSION TECHNOLOGY↗
DOE OSTI2020

Understanding Superionic Conductivity in Lithium and Sodium Salts of Weakly Coordinating Closo -Hexahalocarbaborate Anions

Solid-state ion conductors based on closo-polyborate anions combine high ionic conductivity with a rich array of tunable properties. Cation mobility in these systems is intimately related to the strength of the interaction with the neighboring anionic network and the energy for reorganizing the coordination polyhedra. In this paper, we explore such factors in solid electrolytes with two anions of the weakest coordinating ability, [HCB 11 H 5 Cl 6 ] – and [HCB 11 H 5 Br 6 ] – , and a total of 11 polymorphs are identified for their lithium and sodium salts. Our approach combines ab initio molecular dynamics, synchrotron X-ray powder diffraction, differential scanning calorimetry, and AC impedance measurements to investigate their structures, phase-transition behavior, anion orientational mobilities, and ionic conductivities. We find that M(HCB 11 H 5 X 6 ) (M = Li, Na, X = Cl, Br) compounds exhibit order–disorder polymorphic transitions between 203 and 305 °C and display Li and Na superionic conductivity in the disordered state. Through detailed analysis, we illustrate how cation disordering in these compounds originates from a competitive interplay among the lattice symmetry, the anion reorientational mobility, the geometric and electronic asymmetry of the anion, and the polarizability of the halogen atoms. These factors are compared to other closo-polyborate-based ion conductors to suggest guidelines for optimizing the cation–anion interaction for fast ion mobility. This study expands the known solid-state poly(carba)borate-based materials capable of liquid-like ionic conductivities, unravels the mechanisms responsible for fast ion transport, and provides insights into the development of practical superionic solid electrolytes.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2018

Supercritical Fluid Adsorption to Weakly Attractive Solids: Universal Scaling Laws

In this study, adsorption of light hydrocarbons (C1–C3) confined in the pores of silica aerogel (nominal density 0.2 g/cm 3 ) was studied experimentally and by computer simulation. Five isotherms of ethane (25.0, 32.0, 32.3, 33.0, and 35.0 °C) were obtained over a temperature range including the critical temperature of the bulk fluid (T c = 32.18 °C) to ~220 bar by the vibrating tube densimetry (VTD) method, which yields unique information impossible to obtain by excess sorption measurements. Two isotherms (35 and 50 °C) of methane adsorption in SiO 2 aerogel were measured far above its critical temperature, T c = -82.59 °C, at 0–150 bar using a gravimetric method. The experimental pore fluid properties of methane, ethane, propane, and CO 2 (obtained earlier by VTD for the same SiO 2 aerogel sample) show behavior conforming to the principle of corresponding states over the entire covered reduced temperature ranges from T r = 0.976 to T r = 1.696. The magnitudes of the excess adsorption maxima and the reduced fluid densities where the maxima occur for C1–C3 hydrocarbons and CO 2 are similar functions of the reduced temperature. This behavior indicates that, at least under the conditions covered in this work, the differences in molecular size and shape have only minor impacts on the solid–fluid interactions underlying the adsorption behavior. Lastly, these findings are supported by large-scale GCMC simulations of a lattice gas confined in the pores of a computer representation of the SiO 2 aerogel framework, yielding excess adsorption isotherms in good agreement with experimental measurements, as well as the underlying microstructures of the adsorbed fluids.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗