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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 1,117 records · Page 62
All sourcesNASA NTRSDOE OSTI
DOE OSTI2018

Effect of microstructure on exfoliation corrosion resistance in an Al-Zn-Mg alloy

Highlights: • A quantitative method was proposed to characterize EXCO resistance. • The EXCO product lead to strain in ND and elongation in RD on nearby grains. • Recrystallized grains are more susceptible to EXCO than fibrous grains. • High fraction of high-angle grain boundaries reduces EXCO resistance. • High coverage ratio of η phases on high-angle grain boundaries reduces EXCO resistance. - Abstract: In this work, the effect of microstructure on exfoliation corrosion (EXCO) resistance in an Al-Zn-Mg alloy were investigated using standard EXCO test, together with detailed microstructural examinations mainly by scanning electron microscopy (SEM) and high-angle annular detector dark-field scanning transmission electron microscopy (HAADF-STEM). An EXCO product model was built based on morphologies of EXCO product on longitudinal section and cross section for further measurement and analysis. A quantitative characterization of EXCO resistance by measuring average thickness of EXCO product was conducted, showing average results of 6.94 μm, 10.21 μm and 18.14 μm, which are corresponding to EXCO ratings of P, EA and EB under ASTM G34 standard, respectively. It was concluded that recrystallization, high fraction of high-angle grain boundaries (HAGBs) and high coverage ratio of η phases on HAGBs reduced EXCO resistance.

36 MATERIALS SCIENCE↗
DOE OSTI2015

Converting campus waste into renewable energy – A case study for the University of Cincinnati

Highlights: • A case study to show the benefits of waste-to-energy projects at a university. • Evaluated the technical and economic feasibilities as well as GHG reduction. • A tool for other universities/communities to evaluate waste-to-energy projects. - Abstract: This paper evaluates the implementation of three waste-to-energy projects at the University of Cincinnati: waste cooking oil-to-biodiesel, waste paper-to-fuel pellets and food waste-to-biogas, respectively. The implementation of these waste-to-energy (WTE) projects would lead to the improvement of campus sustainability by minimizing waste management efforts and reducing GHG emissions via the displacement of fossil fuel usage. Technical and economic aspects of their implementation were assessed and the corresponding GHG reduction was estimated. Results showed that on-site implementation of these projects would: (1) divert 3682 L (974 gallons) of waste cooking oil to 3712 L (982 gallons) of biodiesel; (2) produce 138 tonnes of fuel pellets from 133 tonnes of waste paper (with the addition of 20.75 tonnes of plastics) to replace121 tonnes of coal; and (3) produce biogas that would be enough to replace 12,767 m{sup 3} natural gas every year from 146 tonnes of food waste. The economic analysis determined that the payback periods for the three projects would be 16 months for the biodiesel, 155 months for the fuel pellet, and 74 months for the biogas projects. The reduction of GHG emission from the implementation of the three WTE projects was determined to be 9.37 (biodiesel), 260.49 (fuel pellets), and 11.36 (biogas) tonnes of CO{sub 2}-eq per year, respectively.

12 MANAGEMENT OF RADIOACTIVE AND NON-RADIOACTIVE W↗
DOE OSTI2024

Tunable quantum emitters on large-scale foundry silicon photonics

Abstract Controlling large-scale many-body quantum systems at the level of single photons and single atomic systems is a central goal in quantum information science and technology. Intensive research and development has propelled foundry-based silicon-on-insulator photonic integrated circuits to a leading platform for large-scale optical control with individual mode programmability. However, integrating atomic quantum systems with single-emitter tunability remains an open challenge. Here, we overcome this barrier through the hybrid integration of multiple InAs/InP microchiplets containing high-brightness infrared semiconductor quantum dot single photon emitters into advanced silicon-on-insulator photonic integrated circuits fabricated in a 300 mm foundry process. With this platform, we achieve single-photon emission via resonance fluorescence and scalable emission wavelength tunability. The combined control of photonic and quantum systems opens the door to programmable quantum information processors manufactured in leading semiconductor foundries.

Larocque, Hugo (ORCID:000900095849780X)↗
DOE OSTI2022

Removal and recovery of ammonia from simulated wastewater using Ti3C2Tx MXene in flow electrode capacitive deionization

Abstract Flowing electrode capacitive deionization systems (FE-CDI) have recently garnered attention because of their ability to prevent cross contamination and operate in uninterrupted cycles ad infinitum. Typically, FE-CDI electrodes suffer from low conductivity, reducing deionization performance. Utilization of higher mass loadings to combat this leads to poor rheological properties. Herein, Ti 3 C 2 T x MXene was introduced as 1 mg mL −1 slurry electrodes in an FE-CDI system for the removal and recovery of ammonia from simulated agricultural wastewater. The electrode performance was evaluated by operating the FE-CDI system with a feed solution of 500 mg L −1 NH 4 Cl running in batch mode at a constant voltage of 1.20 and −1.20 V in charging and discharging modes, respectively. Despite the low loading, Ti 3 C 2 T x flowing electrodes showed markedly improved performance, achieving 60% ion removal efficiency in a saturation time of 115 min with an adsorption capacity of 460 mg g −1 . To understand the high adsorption performance of the electrodes, physiochemical and structural analysis was done via a variety of characterization techniques such as SEM, TEM, XRD, DLS, and Raman spectroscopy. Cyclic voltammetry and galvanostatic charge/discharge profiles were obtained to evaluate the electrochemical properties of the electrodes. The system proved to be an energy-saving technology by exhibiting a charge efficiency of 58–70% while operating at an energy consumption of 0.45 kWh kg −1 . A 92% regeneration efficiency showed that the electrodes were stable and suitable for long term and scalable usage. The results demonstrate that MXenes have the potential to improve the FE-CDI process for energy-efficient removal and recovery of ammonia.

36 MATERIALS SCIENCE↗
DOE OSTI2021

Characterization and differentiation of aluminum powders used in improvised explosive devices. Part 2: Micromorphometric method refinement and preliminary statistical analysis

Abstract Aluminum (Al) powder is commonly encountered in improvised explosive devices (IEDs) as a metallic fuel due to its availability and low cost. Although available commercially in powder form, amateur bomb‐makers also produce their own Al powder via simple methods found online. In order to provide investigative leads and forensic intelligence, it is important to evaluate not only the composition of homemade devices, but also to distinguish between the various forms of Al powder they contain. To achieve this goal, a method using automated microscopy in combination with statistical techniques has been demonstrated to have the potential to provide source discrimination and investigative leads in source attribution of Al powders in IEDs. The present research refined this method and investigated 59 industrially and amateurly produced Al powder sources with seven subsamples per source using two traditional linear discriminant analyses (LDA), one with a standard data split for training and testing, and another using leave‐one‐out cross‐validation. Averaging the classification accuracies for the two LDA‐based analyses, LDA has the ability to correctly classify 59.26%, 83.35%, and 80.69% of the samples based on their powder source, type, and production method, respectively. This classification accuracy represents a 3407%, 317%, and 61.38% increase in accuracy from random class assignment, respectively. Further, in most instances of incorrect data attribution to a particular source, the subsample has been misidentified with another sample of the same powder type or production method.

Ommen, Danica M.↗
DOE OSTI2023

Solving multiphysics-based inverse problems with learned surrogates and constraints

Abstract Solving multiphysics-based inverse problems for geological carbon storage monitoring can be challenging when multimodal time-lapse data are expensive to collect and costly to simulate numerically. We overcome these challenges by combining computationally cheap learned surrogates with learned constraints. Not only does this combination lead to vastly improved inversions for the important fluid-flow property, permeability, it also provides a natural platform for inverting multimodal data including well measurements and active-source time-lapse seismic data. By adding a learned constraint, we arrive at a computationally feasible inversion approach that remains accurate. This is accomplished by including a trained deep neural network, known as a normalizing flow, which forces the model iterates to remain in-distribution, thereby safeguarding the accuracy of trained Fourier neural operators that act as surrogates for the computationally expensive multiphase flow simulations involving partial differential equation solves. By means of carefully selected experiments, centered around the problem of geological carbon storage, we demonstrate the efficacy of the proposed constrained optimization method on two different data modalities, namely time-lapse well and time-lapse seismic data. While permeability inversions from both these two modalities have their pluses and minuses, their joint inversion benefits from either, yielding valuable superior permeability inversions and CO 2 plume predictions near, and far away, from the monitoring wells.

Yin, Ziyi (ORCID:0000000250248771)↗
NASA NTRS1989

Gradient methods for identification of distributed parameter systems

Parameter-dependence properties are developed in the context of a linear abstract Cauchy problem governed by a parameter-dependent operator. Of particular interest are problems in which the parameter induces an unbounded perturbation of the evolution operator. Conditions are stated under which the derivative of the state with respect to the parameter possesses certain smoothness properties. These properties lead to local convergence results for a gradient-based estimation algorithm based on quasi-linearization. Numerical results concerning a delay-differential equation indicate the effect of a forcing function on parameter sensitivity.

Brewer, Dennis W.↗
DOE OSTI2017

Hotspots of soil N 2 O emission enhanced through water absorption by plant residue

N 2 O is a highly potent greenhouse gas and arable soils represent its major anthropogenic source. Field-scale assessments and predictions of soil N 2 O emission remain uncertain and imprecise due to the episodic and microscale nature of microbial N 2 O production, most of which occurs within very small discrete soil volumes. Such hotspots of N 2 O production are often associated with decomposing plant residue. Here we quantify physical and hydrological soil characteristics that lead to strikingly accelerated N 2 O emissions in plant residue-induced hotspots. Results reveal a mechanism for microscale N 2 O emissions: water absorption by plant residue that creates unique micro-environmental conditions, markedly different from those of the bulk soil. Moisture levels within plant residue exceeded those of bulk soil by 4–10-fold and led to accelerated N 2 O production via microbial denitrification. The presence of large (Ø >35 μm) pores was a prerequisite for maximized hotspot N 2 O production and for subsequent diffusion to the atmosphere. Understanding and modelling hotspot microscale physical and hydrologic characteristics is a promising route to predict N 2 O emissions and thus to develop effective mitigation strategies and estimate global fluxes in a changing environment.

59 BASIC BIOLOGICAL SCIENCES↗
DOE OSTI2023

Interface Coating Design for Dynamic Voltage Stability of Solid‐State Batteries

Abstract Intrinsic or interface thermodynamic voltage windows of solid electrolytes are often narrower than the operational voltage range needed by a full battery, thus various interface decomposition reactions can happen in a practical solid‐state battery. Experimentally, it is found that a proper battery design utilizing the reactions can lead to a dynamic evolution from interface instability to stability, giving the so‐called dynamic voltage stability for advanced battery performance. Here, first the state‐of‐the‐art understanding is articulated about how the dynamic voltage stability should be interpreted in physical picture and treated in computation, emphasizing the potential importance of nonequilibrium reaction pathways. The constrained ensemble computational approach is further applied across most types of solid‐state electrolytes to systematically evaluate and compare their dynamic stability voltage windows in response to the mechanical constriction effect. High‐throughput calculations are used to search for coating materials for different interfaces between sulfide, halide, and oxide electrolytes and typical cathode materials with enhanced dynamic voltage stability. A comparison with experiment is given to highlight the value of these computational predictions.

Wang, Yichao↗
DOE OSTI2018

Tailored Organic Electrode Material Compatible with Sulfide Electrolyte for Stable All‐Solid‐State Sodium Batteries

Abstract All‐solid‐state sodium batteries (ASSSBs) with nonflammable electrolytes and ubiquitous sodium resource are a promising solution to the safety and cost concerns for lithium‐ion batteries. However, the intrinsic mismatch between low anodic decomposition potential of superionic sulfide electrolytes and high operating potentials of sodium‐ion cathodes leads to a volatile cathode–electrolyte interface and undesirable cell performance. Here we report a high‐capacity organic cathode, Na 4 C 6 O 6 , that is chemically and electrochemically compatible with sulfide electrolytes. A bulk‐type ASSSB shows high specific capacity (184 mAh g −1 ) and one of the highest specific energies (395 Wh kg −1 ) among intercalation compound‐based ASSSBs. The capacity retentions of 76 % after 100 cycles at 0.1 C and 70 % after 400 cycles at 0.2 C represent the record stability for ASSSBs. Additionally, Na 4 C 6 O 6 functions as a capable anode material, enabling a symmetric all‐organic ASSSB with Na 4 C 6 O 6 as both cathode and anode materials.

Chi, Xiaowei↗
DOE OSTI2019

Impact of Surface Composition of SrTiO 3 Catalysts for Oxidative Coupling of Methane

Abstract Oxidative coupling of methane (OCM) to C 2 hydrocarbons (C 2 H 6 and C 2 H 4 ) have regained much attention due to the shale gas revolution. Perovskite catalysts have shown promising activity and selectivity to C 2 hydrocarbons. Here, we investigate the effect of surface reconstruction (leading to different surface compositions) of perovskites on the OCM by using SrTiO 3 (STO) as a model catalyst. Different surface densities of Sr (25–96 %) were attained via various treatments of STO. Low energy ion scattering (LEIS) and UV‐Raman results are in good agreement on the surface and subsurface composition of the reconstructed STO. From H 2 ‐TPR, the same H 2 consumption of STO samples allows relating their catalytic performances with surface acid‐base properties (quantified by NH 3 ‐/CO 2 ‐TPD). At 600–800 °C, the surface Sr enrichment was found to enhance CH 4 conversion, C 2 selectivity and the ratio C 2 H 4 /C 2 H 6 up to Sr/(Sr+Ti) of 0.66 and then levels off. Furthermore, the relative concentration of basic sites, base/(base+acid), is found as a better descriptor for STO catalytic performances. This work shows the clear correlation between surface reconstruction, relative basicity/acidity and OCM catalytic performance over perovskite catalysts. The trends here are similar to those for CH 4 combustion over the reconstructed STO in our recent work. Overall, we suggest that tuning surface reconstruction/composition of perovskites can be an effective approach to control CH 4 activation and conversions.

Bai, Lei↗
DOE OSTI2015

Thermal and electrochemical behavior of Cu{sub 4−x}Li{sub x}S{sub 2} (x=1, 2, 3) phases

Several compositions of the Cu{sub 4−x}Li{sub x}S{sub 2} (x=1, 2, 3) series were synthesized via solid-state reaction of the elements. The structural stability at various temperatures and the effect of Li:Cu ratio on the thermal conductivity and the electrochemical performance of Cu{sub 4−x}Li{sub x}S{sub 2}/Li half-cells during charge–discharge process were investigated. Differential scanning calorimetry (DSC) measurements showed a sharp endothermic peak at 140 °C for Cu{sub 4−x}Li{sub x}S{sub 2} samples with x=1 and 2, which is ascribed to a structural phase transition. X-ray diffraction (XRD) measurements on various Cu{sub 4−x}Li{sub x}S{sub 2} samples at temperatures below and above 140 °C indicated a structural phase transition from the room temperature low-symmetry structure to the high temperature cubic structure of Cu{sub 2}S. The thermal conductivity of Cu{sub 4−x}Li{sub x}S{sub 2} samples decreases with decreasing Cu:Li ratio and with increasing temperature. The thermal conductivity of Cu{sub 4−x}Li{sub x}S{sub 2} samples at room temperature decreases from 1.2 W/m K for Cu:Li=3:1 to 0.7 W/m K for Cu:Li=1:3. Cyclic voltammetry of Cu{sub 4−x}Li{sub x}S{sub 2}/Li half-cells showed that high discharge capacity (165 mA h g{sup −1}) and stable reversible charge–discharge process is observed for Cu:Li=2:2, whereas other Cu:Li ratios lead to low discharge capacity and poor reversibility. The electrochemical behavior of Cu{sub 4−x}Li{sub x}S{sub 2}/Li half-cells is rationalized by taking into account the competing reactions of Li{sup +} ions with CuS and Cu{sub 2}S during discharge. - Graphical abstract: Tuning Li content in Cu{sub 4−x}Li{sub x}S{sub 2}/Li half-cells to maintain a Cu/Li ratio equal to unity affords maximum capacity and high stability of the charge–discharge process. - Highlights: • Cu:Li ratio strongly influenced crystal structure and properties of Cu{sub 4-x}Li{sub x}S{sub 2}. • Compositions with x = 1 and 2 undergo structural transformation at above 140 °C. • Thermal conductivity of Cu{sub 4-x}Li{sub x}S{sub 2} phases increases with decreasing Cu:Li ratio. • Stability of Cu{sub 4-x}Li{sub x}S{sub 2}/Li half-cells decreases with Cu:Li ratio. • Initial charge capacity of Cu{sub 4-x}Li{sub x}S{sub 2}/Li half-cells increases with Cu:Li ratio.

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

Hot deformation characterization of duplex low-density steel through 3D processing map development

The high temperature deformation behavior of duplex low-density Fe–18Mn–8Al–0.8C steel was investigated at temperatures in the range of 600–1000 °C. The primary constitutive analysis indicated that the Zener–Hollomon parameter, which represents the coupled effects of temperature and strain rate, significantly varies with the amount of deformation. Accordingly, the 3D processing maps were developed considering the effect of strain and were used to determine the safe and unsafe deformation conditions in association with the microstructural evolution. The deformation at efficiency domain I (900–1100 °C\10{sup −} {sup 2}–10{sup −} {sup 3} s{sup −} {sup 1}) was found to be safe at different strains due to the occurrence of dynamic recrystallization in austenite. The safe efficiency domain II (700–900 °C\1–10{sup −} {sup 1} s{sup −} {sup 1}), which appeared at logarithmic strain of 0.4, was characterized by deformation induced ferrite formation. Scanning electron microscopy revealed that the microband formation and crack initiation at ferrite\austenite interphases were the main causes of deformation instability at 600–800 °C\10{sup −} {sup 2}–10{sup −} {sup 3} s{sup −} {sup 1}. The degree of instability was found to decrease by increasing the strain due to the uniformity of microbanded structure obtained at higher strains. The shear band formation at 900–1100 °C\1–10{sup −} {sup 1} s{sup −} {sup 1} was verified by electron backscattered diffraction. The local dynamic recrystallization of austenite and the deformation induced ferrite formation were observed within shear-banded regions as the results of flow localization. - Graphical abstract: Display Omitted - Highlights: • The 3D processing map is developed for duplex low-density Fe–Mn–Al–C steel. • The efficiency domains shrink, expand or appear with increasing strain. • The occurrence of DRX and DIFF increases the power efficiency. • Crack initiation at α/γ interphase and shear banding lead to failure.

36 MATERIALS SCIENCE↗
DOE OSTI2017

Ultrathin SnS{sub 2} nanosheets as robust polysulfides immobilizers for high performance lithium-sulfur batteries

Highlights: • Ultrathin SnS{sub 2} nanosheets have large surface area and fast charge transfer properties. • Ultrathin SnS{sub 2} nanosheets can greatly improve the electrochemical properties of S/C composites for Li-S batteries. • Superior electrochemical performance of S/C-SnS{sub 2}-10 composites can be ascribed to the optimized synergistic effects between SnS{sub 2} and porous carbon. - Abstract: Ultrathin SnS{sub 2} nanosheets modified sulfur/carbon (S/C-SnS{sub 2}) composites were synthesized through a facile method by mixing sublimed sulfur, Ketjen Black and ultrathin SnS{sub 2} nanosheets. The ultrathin SnS{sub 2} nanosheets can provide remarkable binding strength, large surface area and fast charge transfer, therefore leading to favorable chemical interaction with polysulfides in Li-S batteries. Accompanied with the synergistic effects between physical confinement of porous carbon and chemical interactions of SnS{sub 2}, S/C-SnS{sub 2} composites with different mass ratio of ultrathin SnS{sub 2} nanosheets and C show much improved electrochemical properties. Among them, S/C-SnS{sub 2} composite with 10 wt% of ultrathin SnS{sub 2} nanosheets and 75 wt% of sulfur maintains superior long term cycling capacities of 800 mAh g{sup −1} at 0.5 C after 300 cycles and 540 mAh g{sup −1} at 2 C after 700 cycles.

36 MATERIALS SCIENCE↗
DOE OSTI2017

Magnetic resonance in bilayers of ferrite and functionally graded piezoelectric

Highlights: • Ferromagnetic resonance in a ferrite-piezoelectric laminate is studied. • An electric field induced FMR line broadening results from bending the sample. • Ferrite layer between the two piezoelectric layers shows a large line broadening. - Abstract: The particular purpose of this paper is theoretical modeling of magnetoelectric interactions at the ferromagnetic resonance in a layered structure of a ferrite and a piezoelectric with through-thickness graded polarization. We show that using the functionally graded piezoelectric with through-thickness variation of polarization can lead to an electric field induced broadening of ferromagnetic resonance line. As an example, we consider the laminate based on the yttrium iron garnet layer which is placed between two lead zirconate titanate layers with different poling direction. The maximal ferromagnetic resonance line broadening of 9.3 Oe is obtained for the yttrium iron garnet to lead zirconate titanate layer thickness ratio of 1.7 at 9.3 GHz for E equal to 10 kV/cm.

36 MATERIALS SCIENCE↗