Engineering Papers⌕ Search

SEARCH · Engineering Papers

Results for “ABERRATION”

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.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,225 records · Page 68
All sourcesNASA NTRSDOE OSTI
DOE OSTI2017

Origin of reduced magnetization and domain formation in small magnetite nanoparticles

We compare the structural, chemical, and magnetic properties of magnetite nanoparticles. Aberration corrected scanning transmission electron microscopy reveals the prevalence of antiphase boundaries in nanoparticles that have significantly reduced magnetization, relative to the bulk. We show that atomistic magnetic modelling of nanoparticles with and without these defects reveal the origin of the reduced moment. Strong antiferromagnetic interactions across antiphase boundaries support multiple magnetic domains even in particles as small as 12–14 nm.

36 MATERIALS SCIENCE↗
DOE OSTI2014

Defocused differential interference contrast microscopy imaging of single plasmonic anisotropic nanoparticles

We present the defocused differential interference contrast (DIC) imaging of gold nanorods. We found that the scattered light and the defocus aberration play an important role in the formation of orientation-dependent DIC image patterns of a gold nanorod. Interestingly, the scattered light from a gold nanorod aligned closer to the polarization directions enables us to directly resolve its spatial orientation under a defocused DIC microscope.

36 MATERIALS SCIENCE↗
DOE OSTI2015

Atomic structure of defects and interfaces in TiO 2 -B and Ca:TiO 2 -B (CaTi 5 O 11 ) films grown on SrTiO 3

The bronze polymorph of titanium dioxide, TiO 2 -B, characterized by a crystal structure with a relatively open layered geometry, is a material of interest for various energy applications, including photovoltaics, catalysts, and high-rate energy storage devices. The related phase, CaTi 5 O 11 , which serves as an effective template layer, when deposited on (100) SrTiO 3 , for the growth of high quality single crystalline films of TiO 2 -B, is also of interest for such applications. For both materials, a detailed understanding of the film growth and defect structure is deemed critical to the successful realization of these applications in thin film devices. Thus, using results obtained with aberration-corrected transmission electron microscopy, we present here an analysis of the defects and interfacial structure in CaTi 5 O 11 films grown on (100) and (110) SrTiO 3 substrates, as well as in the TiO 2 -B film grown on (001) CaTi 5 O 11 .

36 MATERIALS SCIENCE↗
DOE OSTI2015

Antisite Defects in Layered Multiferroic CuCr 0.9 In 0.1 P 2 S 6

The CuCr 1-x In x P 2 S 6 system represents a large family of metal chalcogenophosphates that are unique and promising candidates for 2D materials with functionalities such as ferroelectricity. We carried out detailed microstructural and chemical characterization of these compounds using aberration-corrected STEM, in order to understand the origin of these different ordering phenomena. Quantitative STEM-HAADF imaging and analysis identified the stacking order of an 8-layer thin flake, which leads to the identification of anti-site In 3+ (Cu + ) doping. We believe that these findings will pave the way towards understanding the ferroic coupling phenomena in van der Waals lamellar compounds, as well as the potential applications in 2-D electronics.

36 MATERIALS SCIENCE↗
DOE OSTI2015

Insights into the structure–photoreactivity relationships in well-defined perovskite ferroelectric KNbO 3 nanowires

Structure–function correlations are a central theme in heterogeneous (photo)catalysis. In this study, the geometric and electronic structure of perovskite ferroelectric KNbO 3 nanowires with respective orthorhombic and monoclinic polymorphs have been systematically addressed. By virtue of aberration-corrected scanning transmission electron microscopy, we directly visualize surface photocatalytic active sites, measure local atomic displacements at an accuracy of several picometers, and quantify ferroelectric polarization combined with first-principles calculations. The photoreactivity of the as-prepared KNbO 3 nanowires is assessed toward aqueous rhodamine B degradation under UV light. A synergy between the ferroelectric polarization and electronic structure in photoreactivity enhancement is uncovered, which accounts for the prominent reactivity order: orthorhombic > monoclinic. Additionally, by identifying new photocatalytic products, rhodamine B degradation pathways involving N-deethylation and conjugated structure cleavage are proposed. The findings not only provide new insights into the structure–photoreactivity relationships in perovskite ferroelectric photocatalysts, but also have broad implications in perovskite-based water splitting and photovoltaics, among others.

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

Sequential oligodiacetylene formation for progressive luminescent color conversion via co-micellar strategy

Design and construction of organic systems that can enhance internal quantum efficiency to fully make use of radiative decay during the excitation process is highly desirable for the development of new-generation emissive materials. In practice, to employ those materials with an effective tuning of triplet-state involved multicolor luminescence is quite a considerable issue. This work takes advantage of a diphenyl-diacetylene- based co-micellar nano-ensemble that can undergo a sequential photocrosslinking to form a corresponding trimeric oligodiacetylene and a dimeric oligodiacetylene. Their emissive bands individually cover the visible-light spectral region and such a controllable dual band characteristic can result in a progressive luminescent color conversion from light-green to white and finally to purplish blue. In addition, the oligodiacetylenes possess an ultrafast intersystem crossing characteristic with a small S 1 –T 1 energy gap. The leading thermally activated delayed fluorescence and phosphorescence can be employed to achieve long-life broadband emissions without chromatic aberration in this single organic system, towards the creation of emitting materials with high quantum efficiency. The synthesis of the sub-components is simple and the co-micellar strategy is extremely straightforward. Such a material design and approach may find potential uses in the microfabrication of novel organic light-emitting diodes and sophisticated controllable optoelectronic devices.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2016

Direct-write liquid phase transformations with a scanning transmission electron microscope

The highly energetic electron beam from a scanning transmission electron microscope (STEM) can induce local changes in the state of matter, ranging from local knock-out and atomic movement, to amorphization/crystallization, and chemical/electrochemical reactions occuring at localized liquid-solid and gas-solid interfaces. To date, fundamental studies of e-beam induced phenomena and practical applications have been limited by conventional e-beam rastering modes that allow only for uniform e-beam exposures. Here we develop an automated liquid phase nanolithography method that is capable of directly writing nanometer scaled features within silicon nitride encapsulated liquid cells. An external beam control system, connected to the scan coils of an aberration-corrected STEM, is used to precisely control the position, dwell time, and scan velocity of a sub-nanometer STEM probe. Site-specific locations in a sealed liquid cell containing an aqueous solution of H 2 PdCl 4 are irradiated to controllably deposit palladium onto silicon nitride membranes. We determine the threshold electron dose required for the radiolytic deposition of metallic palladium, explore the influence of electron dose on the feature size and morphology of nanolithographically patterned nanostructures, and propose a feedback-controlled monitoring method for active control of the nanofabricated structures through STEM detector signal monitoring. As a result, this approach enables both fundamental studies of electron beam induced interactions with matter, as well as opens a pathway to fabricate nanostructures with tailored architectures and chemistries via shape-controlled nanolithographic patterning from liquid phase precursors.

43 PARTICLE ACCELERATORS↗
DOE OSTI2016

Revealing the semiconductor–catalyst interface in buried platinum black silicon photocathodes

Nanoporous 'black' silicon semiconductors interfaced with buried platinum nanoparticle catalysts have exhibited stable activity for photoelectrochemical hydrogen evolution even after months of exposure to ambient conditions. The mechanism behind this stability has not been explained in detail, but is thought to involve a Pt/Si interface free from SiOx layer that would adversely affect interfacial charge transfer kinetics. In this paper, we resolve the chemical composition and structure of buried Pt/Si interfaces in black silicon photocathodes from a micron to sub-nanometer level using aberration corrected analytical scanning transmission electron microscopy. Through a controlled electrodeposition of copper on samples aged for one month in ambient conditions, we demonstrate that the main active catalytic sites are the buried Pt nanoparticles located below the 400-800 nm thick nanoporous SiOx layer. Though hydrogen production performance degrades over 100 h under photoelectrochemical operating conditions, this burying strategy preserves an atomically clean catalyst/Si interface free of oxide or other phases under air exposure and provides an example of a potential method for stabilizing silicon photoelectrodes from oxidative degradation in photoelectrochemical applications.

14 SOLAR ENERGY↗
DOE OSTI2018

Rational design and observation of the tight interface between graphene and ligand protected nanocrystals

Heterostructures constructed of graphene and colloidal nanocrystals provide a unique way to exploit the coupled physical properties of the two functional building blocks. Studying the interface structure between the two constituent materials is important to understand the formation mechanism and the resulting physical and chemical properties. Along with ab initio calculations, we elucidate that the bending rigidity and the strong van der Waals interaction of graphene to the metal surface guide the formation of a tight and conformal interface. Using theoretical foundations, we construct colloidal nanocrystal-graphene heterostructures with controlled interfacial structures and directly investigate the cross-sectional structures of them at high resolution by using aberration-corrected transmission electron microscopy. Furthermore the experimental method and observations we present here will link the empirical methods for the formation of nanocrystal-graphene heterostructures to the mechanistic understanding of their properties.

36 MATERIALS SCIENCE↗
DOE OSTI2019

Atomistic manipulation of reversible oxidation and reduction in Ag with an electron beam

Employing electrons for direct control of a nanoscale reaction is highly desirable since it enables fabrication of nanostructures with different properties at atomic resolution and with flexibility of dimensions and location. Here, applying in situ transmission electron microscopy, we show the reversible oxidation and reduction kinetics in Ag, well controlled by changing the dose rate of the electron beam. Aberration-corrected high-resolution transmission electron microscopy observation reveals that O atoms are preferably inserted and extracted along the {111} close-packed planes of Ag, leading to the nucleation and decomposition of nanoscale Ag 2 O islands on the Ag substrate. By controlling the electron beam size and dose rate, we demonstrated the fabrication of an array of 3 nm Ag 2 O nanodots in an Ag matrix. Our results open a new pathway to manipulate an atomistic reaction with an electron beam towards the precise fabrication of nanostructures for device applications.

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

Random anion distribution in MS x Se 2- x (M = Mo, W) crystals and nanosheets

The group VIb dichalcogenides (MX 2 , M = Mo, W; X= S, Se) have a layered molybdenite structure in which M atoms are coordinated by a trigonal prism of X atoms. Ternary solid solutions of MS x Se 2– x were synthesized, microcrystals were grown by chemical vapor transport, and their morphologies and structures were characterized by using synchrotron X-ray diffraction, Rietveld refinement, DIFFaX simulation of structural disorder, scanning electron microscopy, and energy dispersive X-ray spectroscopy. Double aberration corrected scanning transmission electron microscopy was used to determine the anion distributions in single-layer nanosheets exfoliated from the microcrystals. These experiments indicate that the size difference between S and Se atoms does not result in phase separation, consistent with earlier studies of MX 2 monolayer sheets grown by chemical vapor deposition. However, stacking faults occur in microcrystals along the layering axis, particularly in sulfur-rich compositions of MS x Se 2– x solid solutions.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2021

The sol–gel autocombustion as a route towards highly CO 2 -selective, active and long-term stable Cu/ZrO 2 methanol steam reforming catalysts

The adaption of the sol-gel autocombustion method to the Cu/ZrO 2 system opens new pathways for the specific optimisation of the activity, long-term stability and CO 2 selectivity of methanol steam reforming (MSR) catalysts. Calcination of the same post-combustion precursor at 400 °C, 600 °C or 800 °C allows accessing Cu/ZrO 2 interfaces of metallic Cu with either amorphous, tetragonal or monoclinic ZrO 2 , influencing the CO 2 selectivity and the MSR activity distinctly different. While the CO 2 selectivity is less affected, the impact of the post-combustion calcination temperature on the Cu and ZrO 2 catalyst morphology is more pronounced. A porous and largely amorphous ZrO 2 structure in the sample, characteristic for sol-gel autocombustion processes, is obtained at 400 °C. This directly translates into superior activity and long-term stability in MSR compared to Cu/tetragonal ZrO 2 and Cu/monoclinic ZrO 2 obtained by calcination at 600 °C and 800 °C. The morphology of the latter Cu/ZrO 2 catalysts consists of much larger, agglomerated and non-porous crystalline particles. Based on aberration-corrected electron microscopy, we attribute the beneficial catalytic properties of the Cu/amorphous ZrO 2 material partially to the enhanced sintering resistance of copper particles provided by the porous support morphology.

36 MATERIALS SCIENCE↗
DOE OSTI2022

Single atoms and small clusters of atoms may accompany Au and Pd dendrimer-encapsulated nanoparticles

Here we report the presence of small clusters of atoms (<1 nm) (SCs) and single atoms (SAs) in solutions containing 1–2 nm dendrimer-encapsulated nanoparticles (DENs). Au and Pd DENs were imaged using aberration-corrected scanning transmission electron microscopy (ac-STEM), and energy dispersive spectroscopy (EDS) was used to identify and quantify the SAs/SCs. Two main findings have emerged from this work. First, the presence or absence of SAs/SCs depends on both the terminal functional group of the dendrimer (–NH 2 or –OH) and the elemental composition of the DENs (Au or Pd). Second, dialysis can be used to remove the majority of SAs/SCs in cases where a high density of SAs/SCs are present. The foregoing conclusions provide insights into the mechanisms for Au and Pd DEN synthesis and stability. Ultimately, these results demonstrate the need for careful characterization of systems containing nanoparticles to ensure that SAs/SCs, which may be below the detection limit of most analytical methods, are taken into consideration (especially for catalysis experiments).

74 ATOMIC AND MOLECULAR PHYSICS↗
DOE OSTI2025

Building workflows for an interactive human-in-the-loop automated experiment (hAE) in STEM-EELS

Exploring the structural, chemical, and physical properties of matter on the nano- and atomic scales has become possible with the recent advances in aberration-corrected electron energy-loss spectroscopy (EELS) in scanning transmission electron microscopy (STEM). However, the current paradigm of STEM-EELS relies on the classical rectangular grid sampling, in which all surface regions are assumed to be of equal a priori interest. However, this is typically not the case for real-world scenarios, where phenomena of interest are concentrated in a small number of spatial locations, such as interfaces, structural and topological defects, and multi-phase inclusions. One of the foundational problems is the discovery of nanometer- or atomic-scale structures having specific signatures in EELS spectra. Herein, we systematically explore the hyperparameters controlling deep kernel learning (DKL) discovery workflows for STEM-EELS and identify the role of the local structural descriptors and acquisition functions in experiment progression. In agreement with the actual experiment, we observe that for certain parameter combinations the experiment path can be trapped in the local minima. We demonstrate the approaches for monitoring the automated experiment in the real and feature space of the system and knowledge acquisition of the DKL model. Based on these, we construct intervention strategies defining the human-in-the-loop automated experiment (hAE). This approach can be further extended to other techniques including 4D STEM and other forms of spectroscopic imaging. The hAE library is available on Github at https://github.com/utkarshp1161/hAE/tree/main/hAE.

Pratiush, Utkarsh [Univ. of Tennessee, Knoxville, ↗
DOE OSTI2012

Characterization of a one dimensional focusing compound refractive lens using the rotating shearing interferometer technique

A one dimensional (1D) compound refractive lens (CRL) has been characterized using the grating based rotating shearing interferometer technique. The method is based on the calculation of moire fringes orientation to sense wavefront information. The phase shift and the optical aberration introduced by the 1D CRL on an X-ray beam were retrieved from a single moire fringe image. The radius of curvature of the lens at the apex was derived. This physical radius of the CRL, which is also closely related to the focal length of the 1D CRL, was shown to vary with the incident angle of the incoming X-ray beam onto the CRL. The experimental measurement agreed very well with the theoretical expectations.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗
DOE OSTI2012

Heavy-ion transfer reactions at large internuclear distance

The transfer reaction for the {sup 116}Sn+{sup 60}Ni system has been studied using the PRISMA magnetic spectrometer at different bombarding energies from above to well below the Coulomb barrier. The experiment has been done in inverse kinematics and light target-like ions have been detected with PRISMA placed at very forward angles. Good mass, nuclear charge and kinetic energy resolutions have been achieved. Sufficient statistics has been accumulated to extract angular distributions for different bombarding energies have been extracted and the response function of the spectrometer has been studied to correct for the aberration due to the transport of the ions in PRISMA. The comparison between the present case and the previously measured {sup 96}Zr+{sup 40}Ca system, superfluid and near closed shells nuclei, respectively, should significantly improve our understanding of nucleon-nucleon correlation properties in multinucleon transfer processes.

73 NUCLEAR PHYSICS AND RADIATION PHYSICS↗
DOE OSTI2012

Rapid HIFU autofocusing using the entire MR-ARFI image

Phase aberrations and attenuations caused by bone can defocus HIFU in the brain and organs behind the ribcage. To refocus the beam, MR-ARFI can be used to measure tissue displacements created by each element in the transducer, and optimize driving signal delays and amplitudes. We introduce a new MR-ARFI-based autofocusing method that requires many fewer image acquisitions than current methods. The method is validated in simulations of bone and brain HIFU transducers, and compared to a conventional method.

60 APPLIED LIFE SCIENCES↗
DOE OSTI2012

The impact of oxygen on the morphology of gas-phase prepared Au nanoparticles

We present an easy procedure for the synthesis of single crystalline gold nanoparticles with a mean diameter of 4 nm using a DC-sputtering in an argon-oxygen gas mixture. Morphology population statistics have been determined to quantify the influence of oxygen. It is found that the particles undergo a structural transition from predominantly icosahedral to single crystalline particles with increasing amount of oxygen. Aberration-corrected high-resolution transmission electron microscopy investigation proves that likewise prepared single crystalline nanoparticles are defect and oxygen free. In contrast, the icosahedral particles prepared with pure argon show the presence of edge dislocations pointing to an energetic disfavoring already at these relatively small particle sizes. This morphology control of clean and uncovered Au nanoparticles provides a high application potential, e.g., for studying the influence of the particle morphology on plasmonic and catalytic properties.

77 NANOSCIENCE AND NANOTECHNOLOGY↗