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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 235 records · Page 13
All sourcesNASA NTRSDOE OSTI
DOE OSTI2018

On the Size Effect for Neutron Diffraction by Two-Phase Structures and Applicability of Composite Standards in Analysis of Residual Austenite in Steels

The possibility of using neutron diffraction in quantitative analysis of residual austenite in steels is investigated. According to the obtained results, some properties of neutron diffraction by two-phase structures remain size-independent, which makes it possible to use large composite standards. It is shown that this approach ensures admissible accuracy without using a priori coefficients.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗
DOE OSTI2025

Microstructural and preliminary optical and microwave characterization of erbium-doped CaMoO 4 thin films

This work explores erbium-doped calcium molybdate (Er:CaMoO4) thin films grown on silicon and yttria stabilized zirconia (YSZ) substrates, as a potential solid state system for C-band (utilizing the ∼1.5 μm Er 3+ 4f–4f transition) quantum emitters for quantum network applications. Through molecular beam epitaxial growth experiments and electron microscopy, X-ray diffraction, and reflection electron diffraction studies, we identify an incorporation limited deposition regime that enables a 1:1 Ca:Mo ratio in the growing film leading to single phase CaMoO 4 formation that can be in situ doped with Er (typically 2–100 ppm). We further show that growth on silicon substrates is single phase but polycrystalline in morphology, while growth on YSZ substrates leads to high-quality epitaxial single crystalline CaMoO 4 films. We perform preliminary optical and microwave characterization on the suspected Y 1 –Z 1 transition of 2 ppm, 200 nm epitaxial Er:CaMoO 4 annealed thin films and extract an optical inhomogeneous linewidth of 9.1(1) GHz, an optical excited state lifetime of 6.7(2) ms, a spectral diffusion-limited homogeneous linewidth of 6.7(4) MHz, and an EPR linewidth of 1.10(2) GHz.

Masiulionis, Ignas [Univ. of Chicago, IL (United S↗
DOE OSTI2018

Subwavelength diffraction gratings in the visible spectral range

We report the results of computer calculations and measurements of subwavelength diffraction gratings in the visible range of the radiation spectrum. The influence of various grating parameters (duty cycle, microrelief shape and depth, material, angle of incidence, wavelength, and radiation polarisation) on the diffraction efficiency is studied. A distinctive feature of the subwavelength gratings in question is that the entire diffracted energy of the beam is redistributed into the zero and –1st orders. It is found that the zero order can be suppressed by choosing the depth and shape of the grating relief. The subwavelength gratings with a period of 400 nm are fabricated and measurements are performed using lasers and laser diodes emitting in the visible wavelength range. High diffraction efficiency into the –1st order (more than 70 %) is observed in a wide spectral range of 450 – 650 nm with an increase in the grating relief depth (at a depth of h = 80 nm). It is experimentally demonstrated that under certain conditions, the plasmon resonance effect arises, in which total absorption of incident radiation takes place. The optical elements considered can be used in image processing systems, projection displays, in the development of various sensors, etc. (paper)

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗
DOE OSTI2025

A structural analysis of ordered Cs3Sb films grown on single crystal graphene and silicon carbide substrates

Alkali antimonides are well established as high efficiency, low intrinsic emittance photocathodes for accelerators and photon detectors. However, conventionally grown alkali antimonide films are polycrystalline with surface disorder and roughness that can limit achievable beam brightness. Ordering the crystalline structure of alkali antimonides has the potential to deliver higher brightness electron beams by reducing surface disorder and enabling the engineering of material properties at the level of atomic layers. In this report, we demonstrate the growth of ordered Cs3Sb films on single crystal substrates 3C-SiC and graphene-coated 4H-SiC using pulsed laser deposition and conventional thermal evaporation growth techniques. The crystalline structures of the Cs3Sb films were examined using reflection high energy electron diffraction and x-ray diffraction diagnostics, while film thickness and roughness estimates were made using x-ray reflectivity. With these tools, we observed ordered domains in less than 10 nm thick films with quantum efficiencies greater than 1% at 530 nm. Moreover, we identify structural features such as Laue oscillations indicative of highly ordered films. We found that Cs3Sb films grew with flat, fiber-textured surfaces on 3C-SiC and with multiple ordered domains and sub-nanometer surface roughness on graphene-coated 4H-SiC under our growth conditions. We identify the crystallographic orientations of Cs3Sb grown on graphene-coated 4H-SiC substrates and discuss the significance of examining the crystal structure of these films for growing epitaxial heterostructures in future experiments.

36 MATERIALS SCIENCE↗
DOE OSTI2019

Synthesis of four-, five-, and six-coordinate cobalt(III) bis-o-iminobenzosemiquinone complexes

Cobalt(III) complexes with different 4,6-di-tert-butyl-N-(aryl)-o-iminobenzosemiquinone ligands were synthesized. Four-, five-, or six-coordinate cobalt(III) derivatives can be prepared using various starting metal compounds (CoCl{sub 2}•6H{sub 2}O, (acac){sub 2}Co•2H{sub 2}O) and varying substituents in the N-aryl moiety of the organic ligand. The structures of five synthesized compounds were determined by X-ray diffraction. The electronic and spin states of the five-coordinate cobalt(III) complexes were studied in detail by DFT quantum chemical calculations.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2019

Method for manufacturing a fibre reflection interferometer based on a metal-dielectric diffraction structure

A new method for manufacturing a two-mirror reflection fibre interferometer in a single-mode fibre consisting of an input mirror with an asymmetric reflection coefficients and a highly reflective end mirror is presented and experimentally demonstrated. The input mirror is based on a metal-dielectric diffraction structure in the form of an aperture in an aluminium film and a dielectric multilayer coating, which provides asymmetry of the reflection coefficient. The method includes the calculation of the energy coefficients of the aluminium film with a hole, the determination of the optimal diameter of the hole, as well as making of the hole, the entrance mirror and the resonator with a short fibre base. A sample interferometer is demonstrated that has an increased (at least by two orders of magnitude) radiation resistance compared to variants based on a continuous metal film, namely, at least 100 mW of radiation in a single-mode SMF-28e fibre at a wavelength of 1550 nm. (fibre optics)

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗
DOE OSTI2021

Laser-induced electron diffraction of the ultrafast umbrella motion in ammonia

Visualizing molecular transformations in real-time requires a structural retrieval method with Ångström spatial and femtosecond temporal atomic resolution. Imaging of hydrogen-containing molecules additionally requires an imaging method sensitive to the atomic positions of hydrogen nuclei, with most methods possessing relatively low sensitivity to hydrogen scattering. Laser-induced electron diffraction (LIED) is a table-top technique that can image ultrafast structural changes of gas-phase polyatomic molecules with sub-Ångström and femtosecond spatiotemporal resolution together with relatively high sensitivity to hydrogen scattering. Here, we image the umbrella motion of an isolated ammonia molecule (NH3) following its strong-field ionization. Upon ionization of a neutral ammonia molecule, the ammonia cation (NH3+) undergoes an ultrafast geometrical transformation from a pyramidal (ΦHNH=107°) to planar (ΦHNH=120°) structure in approximately 8 femtoseconds. Using LIED, we retrieve a near-planar (ΦHNH=117 ± 5°) field-dressed NH3+ molecular structure 7.8−9.8 femtoseconds after ionization. Our measured field-dressed NH3+ structure is in excellent agreement with our calculated equilibrium field-dressed structure using quantum chemical ab initio calculations.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗
DOE OSTI2020

X-ray atomic mapping of quantum dots

We report a model-independent atomic-mapping technique for quantum dots (QDs) by combining Bragg reflection x-ray standing wave (XSW) and grazing incidence diffraction (GID) measurements. In this study, we choose GaAs capped InGaAs QDs/GaAs(001) as a model system to show the locations and arrangements of indium atoms within the QDs along various [hkl] directions. This technique directly reveals the actual amount of positional anisotropy and ordering fraction of indium atoms within the QDs by probing the (1¯11), (111), (311), (1¯31), (113), and (1¯13) crystallographic planes. We find that indium atoms are outwardly shifted along the [001] direction by small fractions of the lattice constant, 0.04a GaAs and 0.06a GaAs from Ga sites for 50- and 150-Å GaAs capped InGaAs QDs, respectively. We observe that an improved coherency factor of the indium atoms within the QDs by 45–60% along the [001] and [011] directions reduces the photoluminescence linewidth by 22%, thus making the QDs efficient for QD-laser and optoelectronic device applications. Here, we also find that the position and ordering of In atoms along the (113) and (1¯13) planes are most sensitive to the thickness of the GaAs cap layer. Our XSW-based results are supported by numerical calculations using a QD-macroscopic structural model based on our GID study. We thus show that this atomic-mapping technique will be useful for studying various quantum structures and tuning their properties.

36 MATERIALS SCIENCE↗
DOE OSTI2021

Role of Equilibrium Fluctuations in Light-Induced Order

Engineering novel states of matter with light is at the forefront of materials research. An intensely studied direction is to realize broken-symmetry phases that are “hidden” under equilibrium conditions but can be unleashed by an ultrashort laser pulse. Despite a plethora of experimental discoveries, the nature of these orders and how they transiently appear remain unclear. To this end, we investigate a nonequilibrium charge density wave (CDW) in rare-earth tritellurides, which is suppressed in equilibrium but emerges after photoexcitation. Using a pump-pump-probe protocol implemented in ultrafast electron diffraction, we demonstrate that the light-induced CDW consists solely of order parameter fluctuations, which bear striking similarities to critical fluctuations in equilibrium despite differences in the length scale. By calculating the dynamics of CDW fluctuations in a nonperturbative model, we further show that the strength of the light-induced order is governed by the amplitude of equilibrium fluctuations. Overall, these findings highlight photoinduced fluctuations as an important ingredient for the emergence of transient orders out of equilibrium. Our results further suggest that materials with strong fluctuations in equilibrium are promising platforms to host hidden orders after laser excitation.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗
DOE OSTI2019

Influence of Time-of-Flight Chromatic Aberration on the Dynamics of Propagation of Pulsed Electron Beam in Ultrafast Electron Microscopy: A New Strategy for Better Temporal Resolution

A common strategy aimed at achieving a high temporal resolution in ultrafast electron microscopy and diffraction is based on the use of strong electrostatic fields in the accelerating gap to form fast electron pulses of ultrashort duration. In this work, the dynamics of the propagation of ultrashort photoelectron bunches is studied taking into account the time-of-flight chromatic aberration: the spread-out of electron pulses at the exit from the region of the accelerating electric field. The results of the calculation of the duration of photoelectron pulses taking into account Coulomb repulsion are presented. According to the analysis, the use of strong electrostatic fields in the accelerating gap for the formation of fast electron pulses of ultrashort duration is not a necessary condition for achieving the final high temporal resolution in the method of ultrafast electron microscopy. The modes of operation of ultrafast transmission electron microscope were found for which the temporal resolution increases with the growth of time-of-flight chromatic aberration.

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗
DOE OSTI2019

Use of heavily doped germanosilicate fibres with a small core diameter in stretchers of ultrashort laser pulses at a wavelength of 1.03 μm

The use of a heavily doped germanosilicate fibre with a W-profile refractive index and small core diameter in stretchers of ultrashort laser pulses with their subsequent amplification and compression in all-fibre laser systems is considered. The application of fibres of this type makes it possible to stretch, amplify, and then compress a laser pulse with minimum distortions of its initial shape and width. Due to the dispersion properties of these fibres, which allow the pulse duration to be increased significantly at a small fibre length and the third-order positive dispersion of the diffraction-grating-based output compressor to be compensated for, amplified pulses with an energy of 2 μJ and width of 250 fs, free of a picosecond pedestal, are obtained. Several types of fibres intended for the use in stretchers of ultrashort laser pulses are comparatively analysed from the point of view of their dispersion compatibility with a diffraction-grating-based output compressor. (paper)

71 CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSIC↗
DOE OSTI2026

Noncollinear spin order, field-induced transitions, and short-range correlations in Cu 4 ⁢SO 4 ⁢(OH) 6

We report a comprehensive study of spin-$\frac{1}{2}$ quantum magnet brochantite, Cu 4 ⁢SO 4 ⁢(OH) 6 , combining high-field thermodynamic measurements, polarized neutron diffraction, inelastic neutron scattering, and nuclear magnetic resonance spectroscopy. Using bulk magnetization and specific heat measurements we construct the magnetic 𝐻−𝑇 phase diagram for magnetic fields applied along main crystallographic directions up to 24.1 T. Polarized neutron diffraction reveals a noncollinear magnetic ground state confined to the 𝑎⁢𝑏 plane. A field-induced transition is observed for magnetic fields in the 𝑎⁢𝑏 plane whose critical field and character evolve continuously with field direction in the 𝑎⁢𝑏 plane. While the transition for 𝐻 ∥ 𝑏 might be a spin-flop-like transition, the one for 𝐻 ∥ 𝑎 resembles the short-range correlated state above 𝑇 N , suggesting a magnetic configuration related to the quasi-two-dimensional correlations in the 𝑏⁢𝑐 planes. The experimental results demonstrate that the ground-state and field-induced phases cannot be explained by a simple XXZ model with a single dominant exchange interaction and that weaker interchain and anisotropic interactions have to be taken into account. Our work establishes brochantite as a low-symmetry Cu-based quantum magnet with noncollinear order and complex field-induced behavior.

Prokhnenko, Oleksandr [Helmholtz-Zentrum Berlin (H↗
DOE OSTI2019

Experimental signatures of a three-dimensional quantum spin liquid in effective spin-1/2 Ce 2 Zr 2 O 7 pyrochlore

A quantum spin liquid is a state of matter where unpaired electrons’ spins, although entangled, do not show magnetic order even at the zero temperature. The realization of a quantum spin liquid is a long-sought goal in condensed-matter physics. Although neutron scattering experiments on the two-dimensional spin-1/2 kagome lattice ZnCu 3 (OD) 6 Cl 2 and triangular lattice YbMgGaO 4 have found evidence for the hallmark of a quantum spin liquid at very low temperature (a continuum of magnetic excitations), the presence of magnetic and non-magnetic site chemical disorder complicates the interpretation of the data. Recently, the three-dimensional Ce 3+ pyrochlore lattice Ce 2 Sn 2 O 7 has been suggested as a clean, effective spin-1/2 quantum spin liquid candidate, but evidence of a spin excitation continuum is still missing. Furthermore, we use thermodynamic, muon spin relaxation and neutron scattering experiments on single crystals of Ce 2 Zr 2 O 7 , a compound isostructural to Ce 2 Sn 2 O 7 , to demonstrate the absence of magnetic ordering and the presence of a spin excitation continuum at 35 mK. With no evidence of oxygen deficiency and magnetic/non-magnetic ion disorder seen by neutron diffraction and diffuse scattering measurements, Ce 2 Zr 2 O 7 may be a three-dimensional pyrochlore lattice quantum spin liquid material with minimum magnetic and non-magnetic chemical disorder.

74 ATOMIC AND MOLECULAR PHYSICS↗
DOE OSTI2021

Quantum Plasmonic Sensors

The extraordinary sensitivity of plasmonic sensors is well-known in the optics and photonics community. These sensors exploit simultaneously the enhancement and the localization of electromagnetic fields close to the interface between a metal and a dielectric. This enables, for example, the design of integrated biochemical sensors at scales far below the diffraction limit. Despite their practical realization and successful commercialization, the sensitivity and associated precision of plasmonic sensors are starting to reach their fundamental classical limit given by quantum fluctuations of light—known as the shot-noise limit. To improve the sensing performance of these sensors beyond the classical limit, quantum resources are increasingly being employed. This area of research has become known as “quantum plasmonic sensing”, and it has experienced substantial activity in recent years for applications in chemical and biological sensing. This review aims to cover both plasmonic and quantum techniques for sensing, and it shows how they have been merged to enhance the performance of plasmonic sensors beyond traditional methods. We discuss the general framework developed for quantum plasmonic sensing in recent years, covering the basic theory behind the advancements made, and describe the important works that made these advancements. We also describe several key works in detail, highlighting their motivation, the working principles behind them, and their future impact. The intention of the review is to set a foundation for a burgeoning field of research that is currently being explored out of intellectual curiosity and for a wide range of practical applications in biochemistry, medicine, and pharmaceutical research.

47 OTHER INSTRUMENTATION↗
DOE OSTI2020

Revealing multiple classes of stable quantum emitters in hexagonal boron nitride with correlated optical and electron microscopy

Defects in hexagonal boron nitride (hBN) exhibit high-brightness, room-temperature quantum emission, but their large spectral variability and unknown local structure challenge their technological utility. Here, we directly correlate hBN quantum emission with local strain using a combination of photoluminescence (PL), cathodoluminescence (CL) and nanobeam electron diffraction. Across 40 emitters, we observe zero phonon lines (ZPLs) in PL and CL ranging from 540 to 720 nm. CL mapping reveals that multiple defects and distinct defect species located within an optically diffraction-limited region can each contribute to the observed PL spectra. Local strain maps indicate that strain is not required to activate the emitters and is not solely responsible for the observed ZPL spectral range. Instead, at least four distinct defect classes are responsible for the observed emission range, and all four classes are stable upon both optical and electron illumination. Our findings offer a foundation for future atomic-scale optical characterization of colour centres.

36 MATERIALS SCIENCE↗
DOE OSTI2023

First measurement of the forward rapidity gap distribution in pPb collisions at $\sqrt{s_{NN}}$ = 8.16 TeV

For the first time at LHC energies, the forward rapidity gap spectra from proton-lead collisions for both proton and lead dissociation processes are presented. The analysis is performed over 10.4 units of pseudorapidity at a center-of-mass energy per nucleon pair of $\sqrt{s_{NN}}$ = 8.16 TeV , almost 300 times higher than in previous measurements of diffractive production in proton-nucleus collisions. For lead dissociation processes, which correspond to the pomeron-lead event topology, the EPOS-LHC generator predictions are a factor of 2 below the data, but the model gives a reasonable description of the rapidity gap spectrum shape. For the pomeron-proton topology, the EPOS-LHC , QGSJET II , and HIJING predictions are all at least a factor of 5 lower than the data. The latter effect might be explained by a significant contribution of ultraperipheral photoproduction events mimicking the signature of diffractive processes. These data may be of significant help in understanding the high energy limit of quantum chromodynamics and for modeling cosmic ray air showers.

72 PHYSICS OF ELEMENTARY PARTICLES AND FIELDS↗
DOE OSTI2018

Tunable Synthesis of Hierarchical Superparamagnetic Fe{sub 3}O{sub 4} Nanospheres by a Surfactant-Free Solvothermal Method

Hierarchical Fe{sub 3}O{sub 4} nanospheres with superparamagnetism have been fabricated via a solvothermal method without any surfactants. The effect of reaction parameters like the types of the reagent, the reaction time, and the reagent concentration on the morphology and structure of the resultant samples are investigated. In this method, ferric chloride (FeCl{sub 3} ⋅ 6H{sub 2}O) is used as the iron source, and EG acts as both solvent and reducing agent. The presence of NaHCO{sub 3} or Na{sub 2}CO{sub 3} provides alkine condition and gaseous bubbles in the control over the size of Fe{sub 3}O{sub 4} nanospheres. The formation mechanism for Fe{sub 3}O{sub 4} nanospheres is illustrated by an Ostwald ripening process. The Fe{sub 3}O{sub 4} nanospheres were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), scanning electron microscopy (SEM), and superconducting quantum interference device magnetometer (SQUID-VSM). The Fe{sub 3}O{sub 4} nanospheres exhibited a wider size distribution at the amount of 0.397 mol/L NaHCO{sub 3}, showing a high saturation magnetization close to 84.46 emu/g. The Fe{sub 3}O{sub 4} nanospheres soluble in deionized water is also investigated.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗