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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 55 records · Page 3
All sourcesNASA NTRSDOE OSTI
DOE OSTI2019

Na 4 MnV(PO 4 ) 3 -rGO as Advanced cathode for aqueous and non-aqueous sodium ion batteries

NASICON-type Na 4 MnV(PO 4 ) 3 with reduced graphene oxide (rGO) has been synthesized by the simple sol-gel reaction and characterized by different analytical techniques. The resulted material has been explored as a cathode material for rechargeable non-aqueous and aqueous sodium-ion batteries. In non-aqueous electrolytes, the as-synthesized Na 4 MnV(PO 4 ) 3 -rGO composite shows stable discharge capacity of 86 mAh g -1 at 0.1 C and 68 mAh g -1 at 0.2 C after 100 cycles in half-cell and full-cell configurations, respectively. In aqueous electrolytes, it delivers an initial discharge capacity of 92 mAh g -1 at 1 C rate in half-cells and 97 mAh g -1 at 10 C rate in full-cells having NaTi 2 (PO 4 ) 3 -MWCNT as the anode. Stable cycleability and high rate capabilities of Na 4 MnV(PO 4 ) 3 -rGO composite can be attributed to the very strong and sustainable conductive percolation networks for both electrons and Na + ions. The obtained results reveal that the aqueous electrolyte cell has a huge scope for gird level energy storage applications.

25 ENERGY STORAGE↗
DOE OSTI2019

Molecular thermodynamic modeling of aqueous Na + -K + -Mg 2+ -Ca 2+ -SO 4 2- quinary system

As part of the effort to develop a comprehensive molecular thermodynamic model for high salinity produced water based on the electrolyte nonrandom two-liquid theory, this work presents the model results for the aqueous Na + -K + -Mg 2+ -Ca 2+ -SO 4 2- quinary system. With the binary interaction parameters fully parameterized for the water-electrolyte pairs and the electrolyte-electrolyte pairs, the model satisfactorily describes the thermodynamic properties for the aqueous quinary system and its binary, ternary, and quaternary subsystems for the temperature range 273.15–473.15 K and the salt concentrations up to saturation. The model results are compared with the salt solubility and thermodynamic data available for the subsystems with special attention to systems involving (Ca 2+ SO 4 2- ).

Chemistry↗
DOE OSTI2020

An Open-Cell Environmental Transmission Electron Microscopy Technique for In Situ Characterization of Samples in Aqueous Liquid Solutions

The desire to image specimens in liquids has led to the development of open-cell and closed-cell techniques in transmission electron microscopy (TEM). The closed-cell approach is currently more common in TEM and has yielded new insights into a number of biological and materials processes in liquid environments. The open-cell approach, which requires an environmental TEM (ETEM), is technically challenging but may be advantageous in certain circumstances due to fewer restrictions on specimen and detector geometry. Here, we demonstrate a novel approach to open-cell liquid TEM, in which we use salt particles to facilitate the in situ formation of droplets of aqueous solution that envelope specimen particles coloaded with the salt. This is achieved by controlling sample temperature between 1 and 10°C and introducing water vapor to the ETEM chamber above the critical pressure for the formation of liquid water on the salt particles. Our use of in situ hydration enables specimens to be loaded into a microscope in a dry state using standard 3 mm TEM grids, allowing specimens to be prepared using trivial sample preparation techniques. Furthermore, our future aim will be to combine this technique with an in situ light source to study photocorrosion in aqueous environments.

47 OTHER INSTRUMENTATION↗
DOE OSTI2024

Spectroelectrochemical determination of thiolate self-assembled monolayer adsorptive stability in aqueous and non-aqueous electrolytes

Self-assembled monolayers (SAM) are ubiquitous in studies of modified electrodes for sensing, electrocatalysis, and environmental and energy applications. However, determining their adsorptive stability is crucial to ensure robust experiments. Here, in this work, the stable potential window (SPW) in which a SAM-covered electrode can function without inducing SAM desorption was determined for aromatic SAMs on gold electrodes in aqueous and non-aqueous solvents. The SPWs were determined by employing cyclic voltammetry, attenuated total reflectance surface-enhanced infrared absorption spectroscopy (ATR-SEIRAS), and surface plasmon resonance (SPR). The electrochemical and spectroscopic findings concluded that all the aromatic SAMs used displayed similar trends and SPWs. In aqueous systems, the SPW lies between the reductive desorption and oxidative desorption, with pH being the decisive factor affecting the range of the SPW, with the widest SPW observed at pH 1. In the non-aqueous electrolytes, the desorption of SAMs was observed to be slow and progressive. The polarity of the solvent was the main factor in determining the SPW. The lower the polarity of the solvent, the larger the SPW, with 1-butanol displaying the widest SPW. This work showcases the power of spectroelectrochemical analysis and provides ample future directions for the use of non-polar solvents to increase SAM stability in electrochemical applications.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2011

Control Of Screening Of A Charged Particle In Electrolytic Aqueous Paul Trap

Individual charged particles could be trapped and confined by the combined radio-frequency and DC quadrupole electric field of an aqueous Paul trap. Viscosity of water improves confinement and extends the range of the trap parameters which characterize the stability of the trap. Electrolyte, if present in aqueous solution, may screen the charged particle and thus partially or fully suppress electrophoretic interaction with the applied filed, possibly reducing it to a generally much weaker dielectrophoretic interaction with an induced dipole. Applying molecular dynamics simulation we show that the quadrupole field has a different effect at the electrolyte ions and at much heavier charged particle, effectively eliminating the screening by electrolyte ions and reinstating the electrophoretic confinement.

74 ATOMIC AND MOLECULAR PHYSICS↗
DOE OSTI2018

Water-lubricated intercalation in V2O5·nH2O for high-capacity and high-rate aqueous rechargeable zinc batteries

Co-intercalation is an effective approach to tune the diffusion coefficient with which cations insert into the electrodes for energy storage devices. By applying this concept in aqueous Zn batteries, a prospective system for stationary energy storage, we demonstrate the critical role of structural H2O on Zn2+ intercalation into bilayer V2O5·nH2O. The H2O solvation of Zn2+ largely reduces its effective charge and thus electrostatic interaction with the V2O5 framework, evidently promoting the diffusion of solvated Zn2+. Benefited from the ‘lubricating’ effect, the aqueous Zn battery shows a specific energy of ~ 305 Wh kg-1 (based on cathode), comparable to those of LiCoO2//Graphite batteries. Meanwhile, it can maintain an energy density of 199 Wh kg-1 at a high power density of 24 kW kg-1 with a capacity retention of 88% after 900 cycles, making it a promising candidate for high-performance, low-cost, safe and environmentally friendly energy storage device.

Yan, Mengyu↗
DOE OSTI2018

Ion-Sieving Carbon Nanoshells for Deeply Rechargeable Zn-Based Aqueous Batteries

As an alternative to lithium-ion batteries, Zn-based aqueous batteries feature nonflammable electrolytes, high theoretical energy density, and abundant materials. However, a deeply rechargeable Zn anode in lean electrolyte configuration is still lacking. Different from the solid-to-solid reaction mechanism in lithium-ion batteries, Zn anodes in alkaline electrolytes go through a solid-solute-solid mechanism (Zn-Zn(OH) 4 2- -ZnO), which introduces two problems. First, discharge product ZnO on the surface prevents further reaction of Zn underneath, which leads to low utilization of active material and poor rechargeability. Second, soluble intermediates change Zn anode morphology over cycling. In this work, an ion-sieving carbon nanoshell coated ZnO nanoparticle anode is reported, synthesized in a scalable way with controllable shell thickness, to solve the problems of passivation and dissolution simultaneously. The nanosized ZnO prevents passivation, while microporous carbon shell slows down Zn species dissolution. Under extremely harsh testing conditions (closed cell, lean electrolyte, no ZnO saturation), this Zn anode shows significantly improved performance compared to Zn foil and bare ZnO nanoparticles. The deeply rechargeable Zn anode reported is an important step toward practical high-energy rechargeable aqueous batteries (e.g., Zn-air batteries). And the ion-sieving nanoshell concept demonstrated is potentially beneficial to other electrodes such as sulfur cathode for Li-S batteries.

catalysis (heterogeneous), defects, membrane, carb↗
DOE OSTI2016

Methanogenesis-induced pH–Eh shifts drives aqueous metal(loid) mobility in sulfide mineral systems under CO2 enriched conditions

Accounting for microbially-mediated CO2 transformation is pivotal to assessing geochemical implications for elevated CO2 in subsurface environments. A series of batch-reactor experiments were conducted to decipher links between autotrophic methanogenesis, CO2 dynamics and aqueous Fe, As and Pb concentrations in the presence of sulfide minerals. Microbially-mediated solubility-trapping followed by pseudo-first order reduction of HCO3- to CH4 (k’ = 0.28-0.59 d-1) accounted for 95% of the CO2 loss from methanogenic experiments. Bicarbonate-to-methane reduction was pivotal in the mitigation of CO2-induced acidity (~1 pH unit) and enhancement of reducing conditions (Eh change from -0.215 to -0.332V ). Methanogenesis-associated shifts in pH-Eh values showed no significant effect on aqueous Pb but favored, 1) increased aqueous As as a result of microbially-mediated dissolution of arsenopyrite and 2) decreased aqueous Fe due to mineral-trapping of CO2-mobilized Fe as Fe-carbonate. Its order of occurrence (and magnitude), relative to solubility- and mineral-trapping, highlighted the potential for autotrophic methanogenesis to modulate both carbon sequestration and contaminant mobility in CO2-impacted subsurface environments.

Microbial CO2 transformation, CO2 sequestration, m↗
DOE OSTI2017

Enhanced Hydrothermal Stability and Catalytic Activity of LaxZryOz Mixed Oxides for the Ketonization of Acetic Acid in the Aqueous Condensed Phase

Common ketonization catalysts such as ZrO2, CeO2, and TiO2-based catalysts have been reported to lose surface area, undergo phase transformation, and lose catalytic activity when utilized in the condensed aqueous phase. In this work, we synthesized a series of LaxZryOz mixed-metal oxides with different La:Zr atomic ratios with the goal of enhancing the catalytic activity and stability for the ketonization of acetic acid in condensed aqueous media at 568 K. We synthesized a hydrothermally stable LaxZryOz mixed-metal oxide catalyst with ketonization activity360 and 40 times more active than La2O3 and ZrO2, respectively. Catalyst characterization techniques suggest that the enhanced stability of the LaxZryOz catalysts is observed with the formation of a phase isomorphic with tetragonal ZrO2. DRIFT spectroscopy measurements indicated the enhanced catalytic activity of LaxZryOz catalysts correlated with greater acetic acid surface population in the presence of H2O versus pure ZrO2.

ketonization, deoxygenation, carboxylic acid, acet↗
DOE OSTI2015

Direct Aqueous-Phase Synthesis of Sub-10 nm “Luminous Pearls” with Enhanced in vivo Renewable Near-Infrared persistent luminescence

Near-infrared persistent luminescence nanoparticles (PLNPs) possess unique near-infrared persistent luminescence properties. They have recently been emerging as important materials for a wide variety of applications in chemistry and biology. Yet, they must endure high-temperature solid-state annealing reactions and subsequent complicated physical post-treatments. Herein, we report on a first direct aqueous-phase chemical synthesis route of NIR PLNPs and present their enhanced in vivo renewable near-infrared persistent luminescence. Our method leads to monodisperse PL nanoparticles as small as ca. 8 nm. More importantly, such sub-10 nm nanocrystals are readily dispersed, functionalized as well as form stable colloidal solutions in aqueous solution and cell culture medium for biological applications. Under bio-tissue penetrable red-light excitation, we found that such nanocrystals possess superior renewable PL photoluminescence in vitro and in vivo than current larger counterparts made by existing methods. We believe that this solid-state-reaction-free chemical approach overcomes the current key roadblock in regard to PLNP development, and thus will pave the way to broad use of these advanced miniature “luminous pearls” in photonics and biophotonics.

Luminous Pearls, Near-Infrared persistent luminesc↗
DOE OSTI2011

In situ imaging of orthoclase-aqueous solution interfaces with x-ray reflection interface microscopy

The use of x-ray reflection interface microscopy (XRIM) to image molecular-scale topography at the aqueous-solid interface, in situ, is described. Specifically, we image interfacial topography of the orthoclase-(001)-aqueous solution interface at room temperature and describe the challenges associated with in situ XRIM imaging. The measurements show that the reflectivity signal for in situ XRIM measurements is substantially smaller than that for ex situ measurements, because of both intrinsic and extrinsic factors. There is also a systematic temporal reduction in the image intensity with increasing x-ray dose, revealing that interaction of the focused x-ray beam with the orthoclase interfaces leads to interfacial perturbations, presumably in the form of surface roughening. This image fading is localized to the x-ray beam footprint, suggesting that the primary damage mechanism is initiated by photoelectrons produced by x-ray beam absorption near the substrate-electrolyte interface. Finally, the role of aqueous solution composition in controlling the sensitivity of the orthoclase surface to x-ray beam-induced effects is explored. A substantial increase in the orthoclase (001) surface stability was observed in solutions having elevated ionic strength, apparently as a result of the reduced lifetime of radiation chemistry products at these conditions.

36 MATERIALS SCIENCE↗