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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 901 records · Page 50
All sourcesNASA NTRSDOE OSTI
DOE OSTI2016

Effect of reactor temperature on direct growth of carbon nanomaterials on stainless steel

Currently, carbon nanomaterials (CNMs) are widely used for various applications due to their extraordinary electrical, thermal and mechanical properties. In this work, CNMs were directly grown on the stainless steel (SS316) via chemical vapor deposition (CVD). Acetone was used as a carbon source and argon was used as carrier gas, to transport the acetone vapor into the reactor when the reaction occurred. Different reactor temperature such as 700, 750, 800, 850 and 900 °C were used to study their effect on CNMs growth. The growth time and argon flow rate were fixed at 30 minutes and 200 ml/min, respectively. Characterization of the morphology of the SS316 surface after CNMs growth using Scanning Electron Microscopy (SEM) showed that the diameter of grown-CNMs increased with the reactor temperature. Energy Dispersive X-ray (EDX) was used to analyze the chemical composition of the SS316 before and after CNMs growth, where the results showed that reduction of catalyst elements such as iron (Fe) and nickel (Ni) at high temperature (700 – 900 °C). Atomic Force Microscopy (AFM) analysis showed that the nano-sized hills were in the range from 21 to 80 nm. The best reactor temperature to produce CNMs was at 800 °C.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2015

Morphological and spectroscopic analysis of cellulose nanocrystals extracted from oil palm empty fruit bunch fiber

This work evaluates the use of oil palm empty fruit bunch (OPEFB) fiber as a source of cellulose to obtain nanocrystalline cellulose (CNC) by acid hydrolysis reaction. The raw OPEFB fibers were pretreated with aqueous Sodium hydroxide at 80°C followed by bleaching treatment and further hydrolyzed with Sulphuric acid at 45°C with limited range of hydrolysis time and acid concentration. The resulting CNC’s were characterized for spectroscopic, crystallographic and morphological properties using Fourier Transform Infrared Spectroscopy (FTIR), X-ray Diffractometer (XRD), Transmission Electron Microscope (TEM) and Atomic Force Microscopy (AFM). Finding of this study shows that the properties of CNC’s are strongly dependent on the hydrolysis time and acid concentration.

36 MATERIALS SCIENCE↗
DOE OSTI2014

Dirac point and transconductance of top-gated graphene field-effect transistors operating at elevated temperature

Top-gated graphene field-effect transistors (GFETs) have been fabricated using bilayer epitaxial graphene grown on the Si-face of 4H-SiC substrates by thermal decomposition of silicon carbide in high vacuum. Graphene films were characterized by Raman spectroscopy, Atomic Force Microscopy, Scanning Tunnelling Microscopy, and Hall measurements to estimate graphene thickness, morphology, and charge transport properties. A 27 nm thick Al₂O₃ gate dielectric was grown by atomic layer deposition with an e-beam evaporated Al seed layer. Electrical characterization of the GFETs has been performed at operating temperatures up to 100 °C limited by deterioration of the gate dielectric performance at higher temperatures. Devices displayed stable operation with the gate oxide dielectric strength exceeding 4.5 MV/cm at 100 °C. Significant shifting of the charge neutrality point and an increase of the peak transconductance were observed in the GFETs as the operating temperature was elevated from room temperature to 100 °C.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2012

Influence of a TiO{sub 2} buffer layer on the magnetic properties of anatase Co:TiO{sub 2} thin films

Our study addresses the influence of a TiO{sub 2} buffer layer on the morphological, structural, and magnetic properties of Co:TiO{sub 2} films grown on (001) SrTiO{sub 3} substrates by RF sputtering. We demonstrate that a direct correlation exist between the morphology, the Co heterogeneity, and the magnetic properties measured in the films. Correlated analysis by cross section transmission electron microscopy, energy dispersive x-ray, and x-ray photoemission spectroscopy reveals that the Co is not uniformly distributed in the film but concentrated in the surface clusters. Atomic force microscopy analysis illustrates that the unbuffered films present a large density of surface clusters. These clusters are not metallic Co but Co rich TiO{sub 2} anatase phase and they are accompanied by structural defects in the film: dislocations, small angle grain boundaries. Magnetometry analysis shows that the unbuffered films have a net ferromagnetic behavior, while in the buffered ones the ferromagnetism is quenched. Therefore, we conclude that the magnetism in unbuffered samples is related to the surface clusters and seems to have an extrinsic nature.

36 MATERIALS SCIENCE↗
DOE OSTI2014

Study of the self-organization processes in lead sulfide quantum dots

A procedure is described for the synthesis of nanoparticles based on lead chalcogenides. The procedure combines the synthesis of colloidal quantum dots (QDs) in aqueous solutions with simultaneous organization of the QDs into ordered arrays. The processes of the self-organization of QDs are analyzed at the nano- and microscopic levels by the photoluminescence method, atomic-force microscopy, and optical microscopy.

36 MATERIALS SCIENCE↗
DOE OSTI2013

Enhanced magnetoelectric sensitivity in Co{sub 0.7}Zn{sub 0.3}Fe{sub 2}O{sub 4}–Bi{sub 0.9}La{sub 0.1}FeO{sub 3} nanocomposites

Graphical abstract: Polycrystalline nanocomposites of xCo{sub 0.7}Zn{sub 0.3}Fe{sub 2}O{sub 4}–(1 − x)Bi{sub 0.9}La{sub 0.1}FeO{sub 3} (x = 0.1, 0.2, 0.3 and 0.4) were prepared by sol–gel method with average crystallite size in the range 70–80 nm as confirmed by AFM image. Magnetization (M) and magnetocapacitance (MC) were found to be enhanced for the nanocomposite. Highlights: ► Co{sub 0.7}Zn{sub 0.3}Fe{sub 2}O{sub 4}–Bi{sub 0.9}La{sub 0.1}FeO{sub 3} nanocomposites (grain size ∼ 90 nm) prepared by sol–gel method. ► Magnetization (M) was found 4.5% more than 0.4CoFe{sub 2}O{sub 4}–0.6BiFeO{sub 3} composite. ► Magnetocapacitance (MC) is observed higher compared to Ba doped BiFeO{sub 3}. ► The value of α{sub E} was found to be 10% more than some reported. - Abstract: We report the magnetoelectric, dielectric and magnetic properties of xCo{sub 0.7}Zn{sub 0.3}Fe{sub 2}O{sub 4}–(1 − x)Bi{sub 0.9}La{sub 0.1}FeO{sub 3} (x = 0.1, 0.2, 0.3 and 0.4) nanocomposites prepared by sol–gel method. The X-ray diffraction patterns of sintered pellets show the formation of composite phases. The average crystallite size obtain by Williamson–Hall plot for different nanocomposites were found to be in the range 70–80 nm, which are in agreement with particle size calculated from atomic force microscopy. Magnetoelectric voltage coefficient (α{sub E} = 315 mV/cm Oe) and the magnetocapacitance (MC = 3.1%) for x = 0.3 were found to be higher than other synthesized nanocomposites.

36 MATERIALS SCIENCE↗
DOE OSTI2014

Effect of Al-mole fraction in Al{sub x}Ga{sub 1−x}N grown by MOCVD

AlGaN/AlN layers were grown by metalorganic chemical vapor deposition (MOCVD) on sapphire substrates. The Al{sub x}Ga{sub 1−x}N layer composition was varied from 15% to 25%. The crystalline quality, thickness and aluminum (Al) composition of AlGaN were determined using high resolution X-ray diffraction (HRXRD). The growth rate decreases on increasing Al composition. Reciprocal space mapping (RSM) was used to estimate the strain and relaxation between AlGaN and AlN. The optical properties of AlGaN layers were investigated by room temperature Photoluminescence (PL). The AlGaN peak shifts towards lower wavelength with Al composition. The surface morphology of AlGaN was studied by atomic force microscopy (AFM). Root mean square (RMS) roughness values were found to be increased in AlGaN layers with composition.

36 MATERIALS SCIENCE↗
DOE OSTI2018

Photocatalytic activity of electrospun MgO nanofibres: Synthesis, characterization and applications

Highlights: • MgO nanofibres with high photocatalytic activity were successfully fabricated. • Electrospinning method via PVA/magnesium precursor based system was used. • Dye degradation of MgO nanofibres was compared with spherical MgO nanoparticles. • MgO nanofibres exhibited excellent photocatalytic activity against Reactive Yellow. • MgO nanofibres show a great potential in efficient treatment of dye effluents. - Abstract: One dimensional MgO nanofibres with high photocatalytic activity were fabricated using the electrospinning method via a polyvinyl alcohol (PVA)/magnesium precursor based system and the dye degradation efficacy of MgO nanofibres was compared with MgO nanospheres. Optimum electrospinning parameters including suitable magnesium precursors were investigated and the formation of MgO nanofibres were confirmed with scanning electron microscopy (SEM) and energy dispersive x-ray (EDX) mapping. Furthermore, the crystalline lattice structure and surface roughness of fabricated nanofibres were evaluated using transmission electron microscopic-electron diffraction mode (TEM-SAED) and atomic force microscopy (AFM), respectively. Fabricated MgO nanofibres exhibited excellent photocatalytic degradation activity against widely used model reactive dye, Reactive Yellow (RY). In contrast to MgO nanospheres, electrospun MgO nanofibres completely degraded the reactive dye under UV irradiation. These photocatalytic MgO nanofibres show a great potential to be used in efficient treatment of industrial dye effluents.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2012

Friction force microscopy study of annealed diamond-like carbon film

In this paper we introduce mechanical and structural characteristics of diamond-like carbon (DLC) films which were prepared on silicon substrates by radio frequency (RF) plasma enhanced chemical vapor deposition (PECVD) method using methane (CH{sub 4}) and hydrogen (H{sub 2}) gas. The films were annealed at various temperatures ranging from 300 to 900 °C in steps of 200 °C using rapid thermal processor (RTP) in nitrogen ambient. Tribological properties of the DLC films were investigated by atomic force microscopy (AFM) in friction force microscopy (FFM) mode. The structural properties of the films were obtained by high resolution transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The wettability of the films was obtained using contact angle measurement. XPS analysis showed that the sp{sup 3} content is decreased from 75.2% to 24.1% while the sp{sup 2} content is increased from 24.8% to 75.9% when the temperature is changed from 300 to 900 °C. The contact angles of DLC films were higher than 70°. The FFM measurement results show that the highest friction coefficient value was achieved at 900 °C annealing temperature.

36 MATERIALS SCIENCE↗
DOE OSTI2019

Solution-derived monolithic thin films with low adhesion surface

Nanostructured thin films were synthesized using a silica-based sol-gel method. The morphology of the films was tailored by controlling the hydrolysis and crosslinking mechanisms of the tetraethyl orthosilicate precursor. Silica nanoparticle self-assembled structures and linear silica chains were crosslinked and formed monolithic nanostructured films. The self-assembly mechanism was investigated using coarse-grained molecular dynamic simulation. Three nanostructured configurations were synthesized and studied to optimize the surface features of the films and minimize the adhesion of sand particles. Surface microscopy imaging and adhesion force measurements using atomic force microscopy with an attached silica particle on the cantilever tip were performed to correlate the adhesion force and the surface structure. The solar specular reflectance of coated solar mirror samples was measured across the solar spectrum before and after the soiling test of the samples. The mechanical properties of the thin films were evaluated using nanoindentation measurements on coated substrates. Here, the solution-derived thin film coatings can provide anti-soiling protection of solar glass in desert environments and increase the efficiency of photovoltaic and concentrated solar power installations.

42 ENGINEERING↗
DOE OSTI2020

H 2 Pc and pentacene on Cu(110)-(2×1)O: A combined STM and nc-AFM study

Scanning tunneling microscopy (STM) and non-contact atomic force microscopy (nc-AFM) with a CuO tip is used to investigate adsorption of metal-free phthalocyanine (H 2 Pc) and pentacene on the Cu(110)-(2×1)O striped-phase reconstructed surface. We show that the combination of STM and nc-AFM is necessary to reveal the detailed adsorption geometry, necessary for interpreting the observed STM contrast. Comparison of the nc-AFM images with simulations shows that some of the H 2 Pc molecules are deformed out-of-plane on this surface, while pentacene retains its molecular geometry regardless of adsorption site. Our research highlights how the stiffness of CuO tips makes it possible to probe the structure of organic semiconductor / metal interfaces.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2026

Evolution of Electronic Properties of Graphene Nanoribbons with Progressive Carving: From Straight to Porous to Chevron Ribbons

Graphene nanoribbons (GNRs) are highly versatile materials due to their unique electronic, magnetic, and optical properties, which can be precisely tuned by controlling their width, edge structure, and topology. Here, we report the on-surface synthesis and characterization of a straight N = 15 armchair GNR with periodic annulene nanopores (15-pGNR). It serves as a structural link between two well-established GNRs: the pristine N = 15 armchair GNR without pores (15-AGNR) and the chevron GNR (cGNR). With the addition of the 15-pGNR reported in this study, these three GNRs form a rare experimentally accessible series of ribbons, in which the evolution of electronic properties can be tracked upon progressive carving of a basic 15-AGNR: first, by creating periodic nanopores to form 15-pGNR and then by extending the pore area and producing meandering cGNR. We have designed a molecular precursor for the 15-pGNR and grown the nanoribbons on single-crystal gold substrates by on-surface synthesis in ultra-high vacuum (UHV) conditions. The atomically precise structure of 15-pGNR was confirmed by scanning tunneling microscopy (STM) and non-contact atomic force microscopy (nc-AFM). The band gap of 15-pGNR was studied by scanning tunneling spectroscopy (STS) and dI/dV mapping, and the occupied electronic levels were investigated by angle-resolved photoemission spectroscopy (ARPES). A theoretical and experimental comparison of 15-pGNRs, 15-AGNRs, and cGNRs demonstrates that the introduction of periodic nanopores into 15-AGNR leads to a more than 2-fold increase in its band gap. In contrast, the band gaps of 15-pGNR and cGNR differ only by about 15%. Such band gap increase can be qualitatively understood to arise from two combined effects, the periodic perforation of the graphene lattice and the confinement effect induced by the GNR width.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2011

Diameter-Dependent Modulus and Melting Behavior in Electrospun Semicrystalline Polymer Fibers

Confinement of the semicrystalline polymers, poly(ethylene-co-vinyl acetate) (PEVA) and low-density polyethylene (LDPE), produced by electrospinning has been observed to produce fibers with large protrusions, which have not been previously observed in fibers of comparable diameters produced by other methods. SAXS spectra confirmed the crystalline structure and determined that the lamellar spacing was almost unchanged from the bulk. Measurement of the mechanical properties of these fibers, by both shear modulation force microscopy (SMFM) and atomic force acoustic microscopy (AFAM), indicates that the modulii of these fibers increases with decreasing diameter, with the onset at {approx}10 {micro}m, which is an order of magnitude larger than previously reported. Melting point measurements indicate a decrease of more than 7% in T{sub m}/T{sub 0} (where T{sub m} is the melting point of semicrystalline polymer fibers and T{sub 0} is the melting point of the bulk polymer) for fibers ranging from 4 to 10 {micro}m in diameter. The functional form of the decrease followed a universal curve for PEVA, when scaled with T{sub 0}.

36 MATERIALS SCIENCE↗
DOE OSTI2017

Electric field directed formation of aligned conjugated polymer fibers

Alternating current (AC) electric fields effectively align poly (3-alkylthiophene) (P3AT) fibers during a one-dimensional crystallization process. Structural, mechanical and electrical properties have been probed using microscopy, small angle neutron scattering (SANS), atomic force microscopy (AFM), x-ray diffraction (XRD), rheology, UV-vis spectroscopy, and dielectric spectroscopy. Optimum frequency and amplitudes were identified for specific P3AT concentrations and for variable solvent quality. Optical microscopy along with SANS and XRD demonstrate alignment persists over both micrometer and nanometer length scales. Small amplitude oscillatory shear rheology also showed that the shear modulus increased for aligned fibers. The structural changes were correlated to improvements in electric conductivity as probed by dielectric spectroscopy. XRD experiments performed with variable sample orientations also showed that the P3HT stacking direction was aligned parallel to the direction of the fiber axis. Electric field alignment was also possible for other alkyl-thiophene polymers and for polymers with simple backbone repeat units.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2024

The effect of low temperature on poly(3-methyl- N -vinylcaprolactam)- b -poly( N -vinylpyrrolidone) diblock copolymer nanovesicles assembled from all-aqueous media

Nanosized polymeric vesicles (polymersomes) self-assembled from double hydrophilic copolymers of poly(3-methyl-N-vinylcaprolactam) n -b-poly(N-vinylpyrrolidone) m (PMVC n -b-PVPON m ) using all aqueous media are a promising platform for biomedical applications, because of their superior stability over liposomes in vivo and high loading capacity. Herein, we explored the temperature-sensitive behavior of PMVC 58 -b-PVPON 65 vesicles using transmission electron microscopy (TEM), dynamic light scattering (DLS), atomic force microscopy (AFM), and small-angle neutron scattering (SANS) in response to lowering the solution temperature from 37 to 25, 20, 14 and 4 °C. The copolymer vesicles with an average size of 350 nm at 37 °C were assembled from the diblock copolymer dissolved in aqueous solution at 4 °C. We show that while the polymersome's size gradually decreases upon the temperature decrease from 37 to 4 °C, the average shell thickness increases from 17 nm to 25 nm, respectively. SANS study revealed that the PMVC 58 -b-PVPON 65 vesicle undergoes a gradual structure evolution from a dense-shell vesicle at 37–25 °C to a highly-hydrated shell vesicle at 20–14 °C to molecular chain aggregates at 4 °C. From SANS contrast matching study, this vesicle behavior is found to be driven by the gradual rehydration of PMVC block at 37–14 °C. The shell hydration at 20–14 °C also correlated with the 4.4-fold decrease in the relative fluorescence intensity from vesicle-encapsulated fluorescent dye, indicating ~80% of the dye release within 12 hours after the vesicle exposure to 14 °C. No significant (<5%) dye release was observed for the vesicle solutions at 37–20 °C, indicating excellent cargo retention inside the vesicles. Our study provides new fundamental insights on temperature-sensitive polymer vesicles and demonstrates that the copolymer assembly into polymersomes can be achieved by decreasing a copolymer aqueous solution temperature below 14 °C followed by solution exposure to ≥20 °C. This type of all-aqueous assembly, instead of nanoprecipitation from organic solvents or solvent exchange, can be highly desirable for encapsulating a wide range of biological molecules, including proteins, peptides, and nucleic acids, into stable polymer vesicles without a need for organic solvents for dissolution of the copolymers that are amphiphilic at physiologically relevant temperatures of 20–37 °C.

36 MATERIALS SCIENCE↗
DOE OSTI2012

Laser Processing of Metals and Polymers

A laser offers a unique set of opportunities for precise delivery of high quality coherent energy. This energy can be tailored to alter the properties of material allowing a very flexible adjustment of the interaction that can lead to melting, vaporization, or just surface modification. Nowadays laser systems can be found in nearly all branches of research and industry for numerous applications. Sufficient evidence exists in the literature to suggest that further advancements in the field of laser material processing will rely significantly on the development of new process schemes. As a result they can be applied in various applications starting from fundamental research on systems, materials and processes performed on a scientific and technical basis for the industrial needs. The interaction of intense laser radiation with solid surfaces has extensively been studied for many years, in part, for development of possible applications. In this thesis, I present several applications of laser processing of metals and polymers including polishing niobium surface, producing a superconducting phase niobium nitride and depositing thin films of niobium nitride and organic material (cyclic olefin copolymer). The treated materials were examined by scanning electron microscopy (SEM), electron probe microanalysis (EPMA), atomic force microscopy (AFM), high resolution optical microscopy, surface profilometry, Fourier transform infrared spectroscopy (FTIR) and x-ray diffraction (XRD). Power spectral density (PSD) spectra computed from AFM data gives further insight into the effect of laser melting on the topography of the treated niobium.

36 MATERIALS SCIENCE↗
DOE OSTI2014

Final technical report for project titled Quantitative Characterization of Cell Aggregation/Adhesion as Predictor for Distribution and Transport of Microorganisms in Subsurface Environment

This project aims to explore and develop enabling methodology and techniques for nano-scale characterization of microbe cell surface contact mechanics, interactions and adhesion quantities that allow for identification and quantification of indicative properties related to microorganism migration and transport behavior in porous media and in subsurface environments. Microbe transport has wide impact and therefore is of great interest in various environmental applications such as in situ or enhanced subsurface bioremediation,filtration processes for water and wastewater treatments and protection of drinking water supplies. Although great progress has been made towards understanding the identities and activities of these microorganisms in the subsurface, to date, little is known of the mechanisms that govern the mobility and transport of microorganisms in DOE’s contaminated sites, making the outcomes of in situ natural attenuation or contaminant stability enhancement unpredictable. Conventionally, movement of microorganisms was believed to follows the rules governing solute (particle) transport. However, recent studies revealed that cell surface properties, especially those pertaining to cell attachment/adhesion and aggregation behavior, can cause the microbe behavior to deviate from non-viable particles and hence greatly influence the mobility and distribution of microorganisms in porous media.This complexity highlights the need to obtain detailed information of cell-cell and cell-surface interactions in order to improve and refine the conceptual and quantitative model development for fate and transport of microorganisms and contaminant in subsurface. Traditional cell surface characterization methods are not sufficient to fully predict the deposition rates and transport behaviors of microorganism observed. A breakthrough of methodology that would allow for quantitative and molecular-level description of intrinsic cell surface properties indicative for cell-surface interactions is essential for the field. To tackle this, we have developed a number of new Bio-nanomechanical techniques, including reflection interference contrast microscopy (RICM) and bio-AFM (Atomic Force Microscopy), for cell adhesion-detachment measurement of the long-range surface interactions, in combination with mathematical modeling, which would allow us to characterize the mechanical behavior from single cell to multi-cell aggregate, critical thresholds for large scale coaggregation and transportation of cells and aggregates in the presence of long range inter-surface forces etc. Although some technical and mathematical challenges remain, the preliminary results promise great breakthrough potential. In this study, we investigated the cellular surface characteristics of representative bio-remediating microorganisms relevant to DOE IFRC (Integrated Field-Scale Subsurface Research Challenges) sites and their transport behaviors in porous media, aiming to draw a groundbreaking correlation between the micro-scale genetic and biological origin-based cell surface properties, the consequent mechanical adhesion and aggregation behaviors, and the macro-scale microbial mobility and retention in porous media, which are unavailable in the literature. The long-term goal is to significantly improve the mechanistic and quantitative understanding of microbial mobility, sorption, and transport within reactive transport models as needed to manipulate subsurface contaminant fate and transport predictions.

54 ENVIRONMENTAL SCIENCES↗
NASA NTRS1999

The Mars Environmental Compatibility Assessment (MECA)

The Mars Environmental Compatibility Assessment (MECA) will evaluate the Martian environment for soil and dust-related hazards to human exploration as part of the Mars Surveyor Program 2001 Lander. Sponsored by the Human Exploration and Development of Space (HEDS) enterprise, MECA's goal is to evaluate potential geochemical and environmental hazards that may confront future martian explorers, and to guide HEDS scientists in the development of high fidelity Mars soil simulants. In addition to objectives related to human exploration, the MECA data set will be rich in information relevant to basic geology, paleoclimate, and exobiology issues. The integrated MECA payload contains a wet-chemistry laboratory, a microscopy station, an electrometer to characterize the electrostatics of the soil and its environment, and arrays of material patches to study the abrasive and adhesive properties of soil grains. MECA is allocated a mass of 10 kg and a peak power usage of 15 W within an enclosure of 35 x 25 x 15 cm (figures I and 2). The Wet Chemistry Laboratory (WCL) consists of four identical cells that will accept samples from surface and subsurface regions accessible to the Lander's robotic arm, mix them with water, and perform extensive analysis of the solution. Using an array of ion-specific electrodes (ISEs), cyclic voltammetry, and electrochemical techniques, the chemistry cells will wet soil samples for measurement of basic soil properties of pH, redox potential, and conductivity. Total dissolved material, as well as targeted ions will be detected to the ppm level, including important exobiological ions such as Na, K+, Ca++, Mg++, NH4+, Cl, S04-, HC03, as well as more toxic ions such as Cu++, Pb++, Cd++, Hg++, and C104-. MECA's microscopy station combines optical and atomic-force microscopy (AFM) to image dust and soil particles from millimeters to nanometers in size. Illumination by red, green, and blue LEDs is augmented by an ultraviolet LED intended to excite fluorescence in the sample. Substrates were chosen to allow experimental study of size distribution, adhesion, abrasion, hardness, color, shape, aggregation, magnetic and other properties. To aid in the detection of potentially dangerous quartz dust, an abrasion tool measures sample hardness relative to quartz and a hard glass (Zerodur).

Meloy, Thomas P.↗