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Results for “synthesis (scalable processing)”

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 181 records · Page 10
All sourcesNASA NTRSDOE OSTI
DOE OSTI2017

(-)ESI/CAD MS n Procedure for Sequencing Lignin Oligomers Based on a Study of Synthetic Model Compounds with β-O-4 and 5-5 Linkages

Here, seven synthesized G-lignin oligomer model compounds (ranging in size from dimers to an octamer) with 5-5 and/or β-O-4 linkages, and three synthesized S-lignin model compounds (a dimer, trimer, and tetramer) with β-O-4 linkages, were evaporated and deprotonated using negative-ion mode ESI in a linear quadrupole ion trap/Fourier transform ion cyclotron resonance mass spectrometer. The collision-activated dissociation (CAD) fragmentation patterns (obtained in MS 2 and MS 3 experiments, respectively) for the negative ions were studied to develop a procedure for sequencing unknown lignin oligomers. On the basis of the observed fragmentation patterns, the measured elemental compositions of the most abundant fragment ions, and quantum chemical calculations, the most important reaction pathways and likely mechanisms were delineated. Many of these reactions occur via charge-remote fragmentation mechanisms. Deprotonated compounds with only β-O-4 linkages, or both 5-5 and β-O-4 linkages, showed major 1,2-eliminations of neutral compounds containing one, two, or three aromatic rings. The most likely mechanisms for these reactions are charge-remote Maccoll and retro-ene eliminations resulting in the cleavage of a β-O-4 linkage. Finally, facile losses of H 2 O and CH 2 O were also observed for all deprotonated model compounds, which involve a previously published charge-driven mechanism. Characteristic “ion groups” and “key ions” were identified that, when combined with their CAD products (MS 3 experiments), can be used to sequence unknown oligomers.

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

Chemoresponsive Nanofluidic Pump That Turns Off in the Presence of Lead Ion

There are many applications that require the integration of a pump and a chemical sensor so that the solution being pumped can be analyzed in real time for a specific chemical species and the flow adjusted according to the measured concentration of that species. In this paper, we describe an alternative strategy: a chemoresponsive pump where a single device acts as both the sensor and pump simultaneously. We demonstrate this concept with a nanofluidic Pb 2+ -responsive pump that uses electroosmotic flow as the pumping technology, and a Pb 2+ -binding ionophore that allows the device to selectively respond to Pb 2+ . The pump yields high flow rates at low Pb 2+ concentrations (<1 μM), but flow rate decreases with concentrations above this threshold and ultimately goes to zero at concentrations above 100 μM.

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

ZnSb Polymorphs with Improved Thermoelectric Properties

Zn$_x$Sb$_{1–x}$ systems are one of the most promising materials for thermoelectric applications due to their low cost, low toxicity, and high thermoelectric figure of merit. We report the discovery and characterization of novel ZnSb polymorphs with improved thermoelectric properties from a systematic $ab initio$ structural search. The putative ground state at low temperature is a structure with $Pbca$ symmetry. Corresponding electron and phonon transport properties are computed, where the lattice thermal conductivity was accurately obtained through third-order interatomic force constants. At 500 K, both the reduced figure of merit $S^2/L$ as well as the lattice thermal conductivity are superior to any previously reported numbers on ZnSb polymorphs, rendering the $Pbca$ phase a promising candidate for an exceptionally good thermoelectric material.

36 MATERIALS SCIENCE↗
DOE OSTI2016

Pillar[5]arene Based Conjugated Microporous Polymers for Propane/Methane Separation through Host–Guest Complexation

We present an efficient strategy for the preparation of conjugated microporous polymers incorporating pillar[5]arenes (P5-CMPs) with surface areas up to 400 m 2 g –1 via Pd-catalyzed Sonogashira–Hagihara cross-coupling reaction of triflate functionalized pillar[5]arene with 1,4-diethynylbenzene and 4,4'-diethynyl-1,1'-biphenyl linkers. In an effort to transfer intrinsic properties of pillar[5]arene, that is its ability to form strong host–guest complexes with linear hydrocarbons in solution, into the solid-state, we investigated the affinity of P5-CMPs toward propane gas. Unlike previously reported porous solids, which showed isosteric heats of adsorption ($Q$ st ) for propane in the range of 32.9–36.9 kJ mol–1 at zero coverage and increasing $Q$ st with rising loading due to intermolecular interactions between propane molecules, we observed very high $Q$ st values up to 53 kJ mol –1 at zero coverage, which gradually decreased to ~35 kJ mol –1 with increasing loadings. This observation indicates strong supramolecular host–guest complexation between propane and pillar[5]arene via multiple C–H/$π$ interactions, i.e., “macrocyclic effect” arising from the ideal size match of kinetic diameter of propane to the cavity of pillar[5]arene. This approach also allowed us to introduce thermodynamic selectivity for the separation of saturated hydrocarbons with low polarizability. High affinity of P5-CMPs for propane facilitated its efficient breakthrough separation from a simulated natural gas mixture (methane:propane, 9:1) at 298 K.

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

Facet-Specific Stability of ZIF-8 in the Presence of Acid Gases Dissolved in Aqueous Solutions

ZIF-8 is a crystalline microporous material that has been widely studied because of its thermal and chemical stability relative to other metal–organic frameworks (MOFs) and its potential for use in a number of gas adsorption, separation, and catalysis applications. However, most studies focus on characterization of the bulk structure of ZIF-8, ignoring the potential effect of the particle shape and the external surface on these applications. This report describes studies that examined the stability of the {110} and {100} crystallographic facets of ZIF-8 under mildly acidic conditions. Though the {110} facet is more thermodynamically stable than the {100} facet, it is found to be more susceptible to degradation by acid exposure. It is hypothesized that the mechanism of particle degradation follows a shrinking-core model, with surface imidazolates being replaced by hydroxyls, as suggested by complementary X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy characterization. Computational investigations support this hypothesis and suggest that the reaction energy for insertion of water into the Zn–MeIm bond is more favorable on the {110} facet than on the {100} facet because of steric constraints. Additionally, the reaction energies are more favorable on both surfaces in the presence of SO 2 . These findings have implications for the formation of surface barriers that can affect mass transfer into or out of the ZIF crystals. This study represents the first comprehensive investigation of differences between exposed surface facets of a MOF.

36 MATERIALS SCIENCE↗
DOE OSTI2017

A Chemical Understanding of the Band Convergence in Thermoelectric CoSb 3 Skutterudites: Influence of Electron Population, Local Thermal Expansion, and Bonding Interactions

N-Type skutterudites, such as Yb x Co 4 Sb 12 , have recently been shown to exhibit high valley degeneracy with possible band convergence, explaining the excellent thermoelectric efficiency of these materials. Using a combined theoretical and experimental approach involving temperature-dependent synchrotron diffraction, molecular orbital diagrams, and computational studies, the chemical nature of critical features in the band structure is highlighted. We identify how n-type doping on the filler site induces structural changes that are observed in both the diffraction data and computational results. Additionally, we show how chemical n-type doping slightly alters the electronic band structure, moving the high-valley degeneracy secondary conduction band closer to the primary conduction band and thus inducing band convergence.

36 MATERIALS SCIENCE↗
DOE OSTI2017

Using the 18-Electron Rule To Understand the Nominal 19-Electron Half-Heusler NbCoSb with Nb Vacancies

The 18-electron rule is a widely used criterion in the search for new half-Heusler thermoelectric materials. However, several 19-electron compounds such as NbCoSb have been found to be stable and exhibit thermoelectric properties rivaling state-of-the art materials. Using synchrotron X-ray diffraction and density functional theory calculations, we show that samples with nominal (19-electron) composition NbCoSb actually contain a half-Heusler phase with composition Nb0.84CoSb. The large amount of stable Nb vacancies reduces the overall electron count, which brings the stoichiometry of the compound close to an 18-electron count, and stabilizes the material. Excess electrons beyond 18 electrons provide heavy doping needed to make these good thermoelectric materials. This work demonstrates that considering possible defect chemistry and allowing small variation of electron counting leads to extra degrees of freedom for tailoring thermoelectric properties and exploring new compounds. Here we discuss the 18-electron rule as a guide to find defect-free half-Heusler semiconductors. Other electron counts such as 19-electron NbCoSb can also be expected to be stable as n-type metals, perhaps with cation vacancy defects to reduce the electron count.

36 MATERIALS SCIENCE↗
DOE OSTI2017

Thermoelectric Properties of n-type ZrNiPb-Based Half-Heuslers

Here we investigate the half-Heusler ZrNiPb as a n-type thermoelectric material. Our results show that the n-type ZrNiPb-based materials can achieve high peak power factors, ~50 μW cm –1 K –2 , by optimally tuning the carrier concentration via Bi doping. By further Sn-alloying in Pb site, we achieve a significant reduction of lattice thermal conductivity while maintaining the power factor almost unchanged and hence noticeably improve the ZT. Our work demonstrates that n-type ZrNiPb-based half-Heuslers are promising thermoelectric materials.

36 MATERIALS SCIENCE↗
DOE OSTI2017

Solvent-Engineering Method to Deposit Compact Bismuth-Based Thin Films: Mechanism and Application to Photovoltaics

Bismuth-based materials have been studied as alternatives to lead-based perovskite materials for photovoltaic applications. However, poor film quality has limited device performance. Here, we developed a solvent-engineering method and show that it is applicable to several bismuth-based compounds. Through this method, we obtained compact films of methylammonium bismuth iodide (MBI), cesium bismuth iodide (CBI), and formamidinium bismuth iodide (FBI). On the basis of film growth theory and experimental analyses, we propose a possible mechanism of film formation. Additionally, we demonstrate that the resultant compact MBI film is more suitable to fabricate efficient and stable photovoltaic devices compared to baseline MBI films with pinholes. We further employed a new hole-transporting material to reduce the valence-band offset with the MBI. The best-performing photovoltaic device exhibits an open-circuit voltage of 0.85 V, fill factor of 73%, and a power conversion efficiency of 0.71%, the highest reported values for MBI-based photovoltaic devices.

14 SOLAR ENERGY↗
DOE OSTI2018

Impact of Size Dispersity, Ligand Coverage, and Ligand Length on the Structure of PbS Nanocrystal Superlattices

Understanding self-assembly is a critical step toward controlling structure at the nanometer length scale. Furthermore, small changes in nanoscale morphology can have large impacts on the performance of nanomaterial devices. In this work, we experimentally explore how the physical properties of lead sulfide (PbS) nanocrystals, such as the surface ligands and core size dispersity, affect the ability of these nanocrystals to self-assemble. Here, we quantified the self-assembly quality by monitoring grain size and the percentage of nanocrystals with coherent alignment of their atomic planes. We found that the ensemble size dispersity plays a large role in superlattice formation and that even small improvements in size distribution led to shorter neighbor-to-neighbor distances in superlattices (more efficient packing), larger grain sizes, and increased nanocrystal alignment. Additionally, the ligand coverage on nanocrystal surfaces had a significant influence on the self-assembly, and excess precipitation steps were highly detrimental to the formation of ordered solids. We show that surface ligand length is a more flexible parameter and that high-quality superlattices can still be achieved with compact surface ligands, so long as the nanocrystal size dispersity and ligand coverage are sufficient. Lastly, we investigated several different colloidal solvents, finding toluene to provide the best ordering, and show that nanocrystal self-assembly is largely unhindered by nanocrystal age. Overall, these results guide our understanding of the underlying factors influencing nanocrystal self-assembly and provide strategies for forming well-engineered superlattices.

36 MATERIALS SCIENCE↗
DOE OSTI2017

Formation Mechanisms and Defect Engineering of Imine-Based Porous Organic Cages

The syntheses of porous organic cages (POCs) represent an important synthetic puzzle in dynamic covalent chemistry based self-sorting. Improved understanding of the formation mechanisms of POCs can lead to control and rational design of cages with desired functionality. Herein, we explore the formation mechanisms of imine-based POCs using time-resolved electrospray mass spectrometry, and electronic structure calculations at the density functional theory and correlated molecular orbital theory levels. We find that the synthesis of the [4+6] cycloimine cage CC3-R and the [2+3] cycloimine cage CC-pentane both proceed through similar intermediates via a series of consecutive reactions. The proposed reaction mechanisms are supported by electronic structure calculations. Based on our observations from both experiments and calculations, we propose a comprehensive method for designing and predicting new POC species. In addition, the observation of stable incomplete cages during CC3-R synthesis inspired us to design intentionally defective cages. These “missing-linker” type molecular defects are installed into CC3-R via non-solvent induced crystallization. The defective CC3-R materials are found to have enhanced CO2 interaction and improved CO 2 uptake capacity due to the additional functional groups present within the CC3 crystals.

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

U 8 Al 19 Si 6 , A Uranium Aluminide Silicide with a Stuffed Supercell Grown from Aluminum Flux

In this work, U 8 Al 19 Si 6 is formed from the reaction of uranium oxide and silicon in aluminum flux. Growth of this material is dependent on the presence of surface hydroxyl groups on alumina in the crucible. The compound forms as large cuboid crystals with a complex new structure that is a cubic stuffed supercell of UAl 3 (AuCu 3 parent structure type). It features a 4-fold expansion of the unit cell axis and the addition of atoms on two extra positions resulting in Pm$\bar{3n}$ symmetry. The ordered distribution of aluminum and silicon was determined using single crystal neutron diffraction. The magnetic susceptibility shows temperature independent paramagnetic behavior, while heat capacity measurements are consistent with Fermi liquid characteristics at low temperatures where the Sommerfeld constant is enhanced in comparison to that of a conventional metal. Lastly, these bulk thermodynamic properties indicate that U 8 Al 19 Si 6 is an itinerant electron Pauli paramagnet with moderately enhanced mass charge carrier quasiparticles.

36 MATERIALS SCIENCE↗
DOE OSTI2018

Selective Transfer of Rotationally Commensurate MoS 2 from an Epitaxially Grown van der Waals Heterostructure

We report that large-scale synthesis of high-quality two-dimensional (2D) semiconductors is critical for their incorporation in emerging electronic and optoelectronic technologies. In particular, chemical vapor deposition (CVD) of transition-metal dichalcogenides (TMDs) via van der Waals epitaxy on epitaxial graphene (EG) leads to rotationally commensurate TMDs in contrast to randomly aligned TMDs grown on amorphous oxide substrates. However, the interlayer coupling between TMDs and EG hinders the investigation and utilization of the intrinsic electronic properties of the resulting TMDs, thus requiring their isolation from the EG growth substrate. To address this issue, we report here a technique for selectively transferring monolayer molybdenum disulfide (MoS 2 ) from CVD-grown MoS 2 -EG van der Waals heterojunctions using copper (Cu) adhesion layers. The choice of Cu as the adhesion layer is motivated by density functional theory calculations that predict the preferential binding of monolayer MoS 2 to Cu in contrast to graphene. Atomic force microscopy and optical spectroscopy confirm the large-scale transfer of rotationally commensurate MoS 2 onto SiO 2 /Si substrates without cracks, wrinkles, or residues. Furthermore, the transferred MoS 2 shows high performance in field-effect transistors with mobilities of up to 30 cm 2 /V s and on/off ratios of up to 10 6 at room temperature. Lastly, this transfer technique can likely be generalized to other TMDs and related 2D materials grown on EG, thus offering a broad range of benefits in nanoelectronic, optoelectronic, and photonic applications.

36 MATERIALS SCIENCE↗
DOE OSTI2019

Tuning Anionic Chemistry To Improve Kinetics of Mg Intercalation

Rechargeable Mg batteries (RMBs) hold great promise for high energy density in consumer electronics because of the high theoretical volumetric capacity and dendrite-free stripping/plating of Mg. Their development, however, is severely limited by the sluggish diffusion of Mg 2+ in inorganic cathodes, mainly induced by strong interaction between Mg 2+ and host anions. In this paper, for the first time, we systematically investigate how anionic chemistry (O, S, and Se) affects Mg 2+ migration in layered MX 2 (M = Ti and V; X = O, S, and Se), by combining theoretical density functional theory (DFT) calculations with electrochemical characterizations. At room temperature, TiSe 2 and VSe 2 achieve much better electrochemical performance than TiS 2 and VS 2 , due to the faster migration of Mg 2+ in selenide than in sulfide and oxide, as demonstrated by electrochemical kinetic characterizations and DFT calculations. The improved kinetics of selenide can be attributed to three criteria: (i) larger diffusion channel, (ii) weaker interaction between Mg 2+ and anion lattice, and (iii) higher electronic conductivity. Finally, the three criteria might not only be applicable to layered materials but also be generalizable to materials with other structures, like Chevrel phase, spinel, olivine, etc., which paves the way for the future design and modification of intercalation materials for RMBs.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2017

Single-Molecule Fluorescence Spectroscopy of Photosynthetic Systems

Photosynthesis begins when a network of pigment–protein complexes captures solar energy and transports it to the reaction center, where charge separation occurs. When necessary (under low light conditions), photosynthetic organisms perform this energy transport and charge separation with near unity quantum efficiency. Remarkably, this high efficiency is maintained under physiological conditions, which include thermal fluctuations of the pigment–protein complexes and changing local environments. These conditions introduce multiple types of heterogeneity in the pigment–protein complexes, including structural heterogeneity, energetic heterogeneity, and functional heterogeneity. Understanding how photosynthetic light-harvesting functions in the face of these fluctuations requires understanding this heterogeneity, which, in turn, requires characterization of individual pigment–protein complexes. Single-molecule spectroscopy has the power to probe individual complexes. In this review, we present an overview of the common techniques for single-molecule fluorescence spectroscopy applied to photosynthetic systems and describe selected experiments on these systems. We discuss how these experiments provide a new understanding of the impact of heterogeneity on light harvesting and thus how these systems are optimized to capture sunlight under physiological conditions.

14 SOLAR ENERGY↗
DOE OSTI2016

Enhanced Acid-Catalyzed Biomass Conversion to Hydroxymethylfurfural Following Cellulose Solvent- and Organic Solvent-Based Lignocellulosic Fractionation Pretreatment

Cellulose is a promising, sustainable source of reduced carbon for producing fuels and chemicals to displace petroleumderived products. One hurdle to realizing this potential is the recalcitrance of cellulose to enzymatic and acid catalytic depolymerization. Numerous pretreatments to enhance the reactivity of cellulose prior to enzymatic hydrolysis have been developed for the production of fermentatively derived biofuels. However, little work has been published on the effects of pretreatment on acid-catalyzed hydrolysis of cellulose combined with the catalytic conversion of the resultant glucose to products [e.g., 5-hydroxymethylfurfural (HMF), $γ$-valerolactone (GVL), etc.].

09 BIOMASS FUELS↗
DOE OSTI2018

Role of Amine Structure on Hydrogen Sulfide Capture from Dilute Gas Streams Using Solid Adsorbents

The hydrogen sulfide composition in biogas ranges from 0 to 5% depending on the feed source to the biogas digester. To meet renewable natural gas specifications of 0–4 ppm of H 2 S content, technologies that remove H 2 S from raw biogas feeds are needed. This contribution assesses three adsorbents with similar textural and physical properties but with different amines grafted to the surface. Specifically, materials containing primary, secondary, and tertiary amines at the end of a propyl surface linker grafted on a silica support are explored. H 2 S adsorption isotherms and cyclic studies are presented for these materials, and it is shown that secondary amines have the best amine efficiency while tertiary amines are the most stable for H 2 S capture, of the materials studied. The results suggest the consideration of secondary and tertiary amines for the design of amine adsorbents suitable for H 2 S removal in dilute gas streams over multiple cycles.

09 BIOMASS FUELS↗