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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 307 records · Page 17
All sourcesNASA NTRSDOE OSTI
DOE OSTI2018

Chemical Sensor Development and Antibacterial Activities Based on Polyaniline/Gemini Surfactants for Environmental Safety

The polyaniline doped novel anionic gemini surfactant (PANI/GS) was chemically synthesized by a micellar polymerization process and then characterized in details by X-ray powder diffractometry, scanning electron microscopy, and FTIR spectroscopy. The results show the presence of polyaniline in the emeraldine base was formed by doping with gemini surfactant. The thermal properties of the composites were studied by carrying out thermal gravimetric analysis. The PANI/GS were found to be soluble in common organic solvents such as chloroform as well as DMSO. The antibacterial activity of the obtained PANI/GS was also evaluated against Gram positive bacteria Bacillus subtilis, Gram negative bacteria Escherichia coli and antibiotics (Amoxicillin) using the agar plate. The antibacterial study showed that the PANI/GS was found to be most effective against both B. subtilis and E. coli respectively which was significant compared to the amoxicillin. Beside that thin-layer of PANI/GS onto glassy carbon electrode (GCE) was fabricated with conducting 5% nafion coating agents to fabricate a sensitive and selective Cd{sup 2+} ionsic sensor in short response time into the phosphate buffer phase. The fabricated cationic-sensor was exhibited higher sensitivity, large-dynamic concentration ranges, long-term stability, and improved electrochemical performances towards Cd{sup 2+} ions. The calibration plot is linear (r{sup 2}, 0.9799) over the large Cd{sup 2+} concentration ranges (10.0 nM–1.0 mM). The sensitivity and detection limit is calculated as 2.324 µA µM{sup −1}cm{sup −2} and 6.85 nM (signal-to-noise ratio, at a SNR of 3) respectively. These novel efforts are intiated a well-known method for significant cationic sensor development with directly fabricated nanocomposite onto GCE for the detection of hazardous toxins in ecological and environmental fields in huge scales. Graphical Abstract: .

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2019

Physicochemical, Microstructural and Thermal Characterization of Chitosan from Blue Crab Shell Waste and Its Bioactivity Characteristics

The aim of the present study was to characterize the chitosan synthesized from blue crab (Callinectes sapidus, Rathbun, 1986) shell waste and to investigate its physicochemical and microstructural analyses as well as its antioxidant and antibacterial potentials. Microstructural and elemental characterization of the synthesized and commercial chitosan powders were performed using fourier transform infra-red spectroscopy, scanning electron microscopy and energy dispersive X-ray spectroscopy. Thermal analysis were done using thermogravimetric analysis. Antioxidant and antimicrobial analysis were done using by DPPH (1,1-diphenyl-2-picrylhydrazyl) free radical scavenging assay and agar well diffusion assay, respectively. The yield of the synthesized chitosan was calculated as 7.47% with moisture and ash contents of 0.151 ± 0.0025% and 0.19 ± 0.01%, respectively. Synthesized chitosan demonstrated the values of degree of deacetylation (71%), water (620.029 ± 52.59%) and fat (437.93 ± 15.92%) binding capacities, solubility (94.15 ± 2.84%), viscosity (463.25 ± 13.10 cPs) and whiteness (90.23 ± 0.27%). Antioxidant activity of synthesized chitosan was found to be moderate (55.30 ± 5.05%) when compared to ascorbic acid standard (87.61 ± 1.34). Chitosan obtained from blue crab shell also showed moderate antibacterial activity against Staphylococcus aureus and Escherichia coli. The findings of the study indicated that blue crab shell waste might be a potentially effective biopolymer source for commercial applications especially in food industry.

36 MATERIALS SCIENCE↗
DOE OSTI2021

Evolution of global and local deformation in additively manufactured octet truss lattice structures

Additively manufactured lattice truss structures, often referred to as architected cellular materials, present significant advantages over conventional structures due to their unique characteristics such as high strength-to-weight ratios and surface area-to-volume ratios. These geometrically complex structures, however, come with concomitant challenges for qualification and inspection. In this study, compression testing interrupted with micro-computed tomography inspection was conducted to monitor the evolution of global and local deformation throughout the loading process of 304L stainless steel octet truss lattice structures. Both two- and three-dimensional image analysis techniques were leveraged to characterize geometric heterogeneities resulting from the laser powder bed fusion manufacturing process as well as track the structure throughout deformation. Variations from model-predicted behavior resulting from these heterogeneities are considered relative to the predicted and actual responses of the structures during compression to better understand, model, and predict the octet truss lattice structure compression response.

36 MATERIALS SCIENCE↗
DOE OSTI2017

Tb{sup 3+} induced orange persistent luminescence in Cs{sub 2}CaP{sub 2}O{sub 7}:Eu{sup 2+}: The role of the auxiliary codopant

Highlights: • The orange persistent luminescence of Cs{sub 2}CaP{sub 2}O{sub 7}:Eu{sup 2+},Tb{sup 3+} was first reported. • The role of Tb{sup 3+} was discussed. • The TL curve reveals there are two traps responsible for the persistent luminescence. - Abstract: This study reports an orange emitting persistent phosphor Cs{sub 2}CaP{sub 2}O{sub 7}:Eu{sup 2+},Tb{sup 3+}. The material was synthesized by solid state reaction method in a reducing atmosphere. The persistent phosphor was characterized in detail by X-ray powder diffraction, photoluminescence, persistent luminescence and thermoluminescence spectra. After UV irradiation, Cs{sub 2}CaP{sub 2}O{sub 7}:Eu{sup 2+},Tb{sup 3+} phosphor shows an orange persistent luminescence (∼590 nm) at room temperature, whereas only photoluminescence is observed in Eu{sup 2+} singly doped samples. Both of the photoluminescence and persistent luminescence is due to the 4f{sup 6}5d{sup 1} → 4f{sup 7} transition of Eu{sup 2+} and the emission lines of Tb{sup 3+} are totally absent. The deconvolution of the thermoluminescence curve reveals there are two kinds of traps responsible for the persistent luminescence. The depth of the dominating trap is 0.61 eV. Based on experimental results, the role of Tb{sup 3+} and the trapping/detrapping processes of charge carriers were discussed. An energy level scheme was proposed to explain the mechanisms of persistent luminescence as well as photoluminescence.

36 MATERIALS SCIENCE↗
DOE OSTI2018

An Ultrahigh CO 2 -Loaded Silicalite-1 Zeolite: Structural Stability and Physical Properties at High Pressures and Temperatures

We report the formation of an ultrahigh CO 2 -loaded pure-SiO 2 silicalite-1 structure at high pressure (0.7 GPa) from the interaction of empty zeolite and fluid CO 2 medium. The CO 2 -filled structure was characterized in situ by means of synchrotron powder X-ray diffraction. Rietveld refinements and Fourier recycling allowed the location of 16 guest carbon dioxide molecules per unit cell within the straight and sinusoidal channels of the porous framework to be analyzed. The complete filling of pores by CO 2 molecules favors structural stability under compression, avoiding pressure-induced amorphization below 20 GPa, and significantly reduces the compressibility of the system compared to that of the parental empty one. Additionally, the structure of CO 2 -loaded silicalite-1 was monitored at high pressures and temperatures, and its thermal expansivity was estimated.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2019

Metallopolymerization as a Strategy to Translate Ligand-Modulated Chemoselectivity to Porous Catalysts

Porous catalysts have garnered substantial interest as potential platforms for group-transfer catalysis due to the ability to noncovalently colocalize substrates in proximity to site-isolated reactive intermediates. In contrast to soluble molecular catalysts, the limited synthetic toolbox available to prepare porous catalysts presents a formidable challenge to controlling the primary coordination sphere of lattice-confined catalysts and thus modulating the electronic structures of reactive catalyst intermediates. Here, we utilize Sonogashira cross-coupling chemistry to prepare a family of porous metallopolymers in the primary coordination sphere of Ru 2 sites. The newly synthesized materials are characterized by IR, elemental analysis, gas sorption, powder X-ray diffraction, thermogravimetric analysis, X-ray absorption spectroscopy, and diffuse-reflectance UV–vis-NIR spectroscopy. The resulting porous materials are catalysts for nitrene-transfer chemistry, and the chemoselectivity for allylic amination versus olefin aziridination can be tuned by modulating the primary coordination sphere of the catalyst sites. Furthermore, the demonstration of metallopolymerization as a rational synthetic strategy enables ligand-modulated chemoselectivity to be achieved with porous catalysts and represents a new opportunity to tailor the functionality of heterogeneous catalyst materials.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2020

Mesoporous Crystalline Niobium Oxide with a High Surface Area: A Solid Acid Catalyst for Alkyne Hydration

A mesoporous crystalline niobium oxide with tunable pore sizes was synthesized via the sol–gel-based inverse micelle method. The material shows a surface area of 127 m 2 /g, which is the highest surface area reported so far for crystalline niobium oxide synthesized by soft template methods. The material also has a monomodal pore size distribution with an average pore diameter of 5.6 nm. A comprehensive characterization of niobium oxide was performed using powder X-ray diffraction, Brunauer–Emmett–Teller, thermogravimetric analysis, scanning electron microscopy, transmission electron microscopy, UV–vis, and X-ray photoelectron spectroscopy. The material acts as an environmentally friendly, solid acid catalyst toward hydration of alkynes under with excellent catalytic activity (99% conversion, 99% selectivity, and 4.39 h –1 TOF). Brønsted acid sites present in the catalyst were found to be responsible for the high catalytic activity. Lastly, the catalyst was reusable up to five cycles without a significant loss of the activity.

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

Ambient-Temperature Hydrogen Storage via Vanadium(II)-Dihydrogen Complexation in a Metal-Organic Framework

In this report, the widespread implementation of H 2 as a fuel is currently hindered by the high pressures or cryogenic temperatures required to achieve reasonable storage densities. In contrast, the realization of materials that strongly and reversibly adsorb hydrogen at ambient temperatures and moderate pressures could transform the transportation sector and expand adoption of fuel cells in other applications. To date, however, no adsorbent has been identified that exhibits a binding enthalpy within the optimal range of -15 to -25 kJ/mol for ambient-temperature hydrogen storage. Here, we report the hydrogen adsorption properties of the metal-organic framework (MOF) V 2 Cl 2.8 (btdd) (H 2 btdd, bis(1 H -1,2,3-triazolo[4,5- b ],[4',5'- i ])dibenzo[1,4]dioxin), which features exposed vanadium(II) sites capable of backbonding with weak π acids. Significantly, gas adsorption data reveal that this material binds H 2 with an enthalpy of -21 kJ/mol. This binding energy enables usable hydrogen capacities that exceed that of compressed storage under the same operating conditions. The Kubas-type vanadium(II)-dihydrogen complexation is characterized by a combination of techniques. From powder neutron diffraction data, a V-D 2 (centroid) distance of 1.966(8) Å is obtained, the shortest yet reported for a MOF. Using in situ infrared spectroscopy, the H-H stretch was identified, and it displays a red shift of 242 cm -1 . Electronic structure calculations show that a main contribution to bonding stems from the interaction between the vanadium d π and H 2 σ* orbital. Ultimately, the pursuit of MOFs containing high densities of weakly π-basic metal sites may enable storage capacities under ambient conditions that far surpass those accessible with compressed gas storage.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2026

In Situ Insights into Enhanced Cooperative Ligand Exchange Kinetics via Solvent-Induced Restacking in a 2D Metal–Organic Framework

Understanding the reaction kinetics at catalytically active sites is crucial for integrating catalytic two-dimensional (2D) materials into industrial processes. This study focuses on in situ observation of ligand exchange kinetics and solvent-assisted structural restacking transition in the 2D paddle wheel-based MOF [Cu 2 (dttc) 2 ] n (DUT-134(Cu), dttc = dithieno[3,2-b:2′,3′- d]thiophene-2,6-dicarboxylate). The ligand exchange process, involving the replacement of dimethylformamide (DMF) with nitriles such as acetonitrile (ACN), pentanenitrile, and heptanenitrile, was investigated using advanced in situ characterization techniques with high temporal resolution, including powder X-ray diffraction and Raman spectroscopy. The larger analytes exhibited reduced exchange rates, consistent with enhanced steric hindrance and greater diffusion constraints. Interestingly, the study revealed that the exchange of DMF with ACN induces a structural transition to higher symmetry within few seconds, a transition from AB to AA stacking mode of the layers, and a widening of the interlayer distance. Crucially, this structural transition dramatically accelerates the solvent exchange process through cooperative effects, offering critical advantages for catalytic applications. Notably, the reverse exchange from ACN to DMF proceeds more slowly and does not reverse the structural changes, but a new phase is formed with preserved AA stacking. By isotope labeling of linker molecules in combination with two complementary theoretical vibrational simulation methods, the precise assignment of Raman bands and the vibrational modes associated with the ligand exchange process could be achieved. These pioneering insights into the dynamic behavior of 2D MOFs, coupled with ligand exchange, establish a highly promising and transformative approach to achieving enhanced tunability and responsiveness in future catalytic applications.

Layers↗
DOE OSTI2017

Magnetic ground state of the Ising-like antiferromagnet DyScO 3

Here, we report on the low-temperature magnetic properties of the DyScO 3 perovskite, which were characterized by means of single crystal and powder neutron scattering, and by magnetization measurements. Below T N = 3.15 K, Dy 3+ moments form an antiferromagnetic structure with an easy axis of magnetization lying in the ab plane. The magnetic moments are inclined at an angle of ~ ±28° to the b axis. We show that the ground-state Kramers doublet of Dy 3+ is made up of primarily |±15/2> eigenvectors and well separated by a crystal field from the first excited state at E 1 = 24.9 meV. This leads to an extreme Ising single-ion anisotropy, M ⊥ /M ∥ ~0.05. The transverse magnetic fluctuations, which are proportional to M 2 ⊥ /M 2 ∥ , are suppressed, and only moment fluctuations along the local Ising direction are allowed. We also found that the Dy-Dy dipolar interactions along the crystallographic c axis are two to four times larger than in-plane interactions.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2018

Spin freezing into a disordered state in CaFeT i 2 O 6 synthesized under high pressure

Double perovskites exhibit a variety of interesting phenomena due to numerous combinations of cation orderings and distortions. CaMnTi 2 O 6 and CaFeTi 2 O 6 are the only two discovered double perovskites that have the columnar type A-site ordering associated with the a + a + c – titling system. The former perovskite, synthesized recently, has a polar structure below T c and shows an unusual ferroelectricity. The latter, while synthesized decades ago, received less investigation. Here, we have synthesized CaFeTi 2 O 6 under high pressure and carried out thorough characterizations through measurements of x-ray powder diffraction (XRD), second harmonic generation (SHG), dc and ac magnetization, Mössbauer spectra, resistivity, thermoelectric power, and specific heat. Although the structural refinement of the XRD pattern cannot distinguish two possible tetragonal phases, SHG measurements help to rule out the possibility of a polar structure observed in CaMnTi 2 O 6 . Fitting the paramagnetic susceptibility to a Curie-Weiss law gives a negligible Weiss constant. The weak exchange interaction gives way to a dipole-dipole interaction and single-ion anisotropy. An anomaly at 1.2 K in the specific heat is too broad for a magnetic transition, but suggestive of a spin-ice-like state as in the pyrochlores. Mössbauer spectroscopy shows two distinct iron sites, as expected for the crystal structure. Both sites are occupied by high-spin Fe 2+ as indicated by the isomer shift. The sharply different temperature dependence of the quadrupole splitting at the two iron sites can be well explained based on the local structural distortions from the refinement of XRD patterns. In conclusion, the line broadening associated with long spin-relaxation times is observed at 6 K as the spin freezing transition is approached from high temperatures.

36 MATERIALS SCIENCE↗
DOE OSTI2022

Magnetic order and spin liquid behavior in [Mo 3 ] 11+ molecular magnets

Molecular magnets based on [Mo 3 ] 11+ units with one unpaired electron per trimer have attracted recent interest due to the identification of quantum spin liquid candidacy in some family members. Here, we present comprehensive measurements on polycrystalline samples of ZnScMo 3 O 8 , MgScMo 3 O 8 , and Na 3 Sc 2 Mo 5 O 16 with the same Mo 3 O 13 magnetic building blocks. In this work, the crystal structures are characterized with x-ray or neutron powder diffraction and the magnetic ground states are determined by performing ac and dc susceptibility, specific heat, neutron powder diffraction, and muon spin relaxation measurements. Our work indicates that ZnScMo 3 O 8 and MgScMo 3 O 8 have ferromagnetic Curie-Weiss temperatures of 18.5 and 11.9 K, ordered ground states with net moments (low-moment ferromagnetism or canted antiferromagnetism), and zero field ordering temperatures of $T_c$ = 6 K and $T_c$ < 2 K, respectively. On the other hand, Na 3 Sc 2 Mo 5 O 16 hosts a dynamical magnetic ground state with no evidence for magnetic ordering or spin freezing down to 20 mK despite an antiferromagnetic Curie-Weiss temperature of –36.2 K, and therefore is a candidate for quantum spin liquid behavior. By comparing the present results to past work on the same family of materials, we construct a phase diagram which illustrates that the magnetic ground states of these Mo-based molecular magnets are very sensitive to small changes in the nearest-neighbor Mo-Mo distance.

36 MATERIALS SCIENCE↗
DOE OSTI2018

In situ measurements of reactions in a glass-forming batch by X-ray and neutron diffraction

We report the batch materials used in glass production are often too coarse to allow phase evolution measurements by in situ high-temperature x-ray diffraction (HTXRD). Reducing the particle sizes to accommodate these measurements changes the reaction kinetics and can alter the reaction pathway. Unlike conventional laboratory XRD, which operates in reflection mode and analyzes the surface region of finely ground powder, neutron diffraction can be used to characterize as-received batch materials by means of an intense beam which penetrates through a bulk sample. In this study, the phase evolution in a glass-forming batch made with fine batch materials was probed in situ by both HTXRD and time-of-flight neutron diffraction to determine the similarities and differences between measurements by the two techniques. Therefore, the same composition, prepared using the coarser, as-received size distributions of the same batch materials, was studied by both techniques, demonstrating the unique capability of neutron diffraction to analyze material which is too coarse for the HTXRD, and to reveal the effect of the particle size distribution on the reaction kinetics.

36 MATERIALS SCIENCE↗
DOE OSTI2018

New compositional data on ancient mortars and plasters from Pompeii (Campania – Southern Italy): Archaeometric results and considerations about their time evolution

Highlights: • Mortar samples from Pompeii, with different constructive functions, were studied. • Characterization of the materials can be used for preparing compatible mortars. • Analogies and differences were highlighted to identify the constructive phases. • Preliminary statistic models were proposed to discriminate materials and constructive phases. Twenty-six samples of mortar used for various construction applications (joint mortars, floor mortars, filling mortars and plasters) were collected from different areas of the archaeological site of Pompeii (Campania - Sothern Italy). The mortar samples belong to various historical periods covering approximately 2000 years, from the 2nd century BC to the post excavation period (18–19th century). The samples were characterized employing Optical Microscopy (OM), X-ray Powder Diffraction (XRPD), X-ray Fluorescence (XRF), Electron Probe Micro Analysis (EPMA) and Raman Spectroscopy. Moreover, image analysis was carried out using JMicroVision software in order to determine the percentages of binder, macropores and aggregate, in terms of crushed ceramic fragments (cocciopesto), rock fragments and monocrystals. The application of these techniques allowed obtaining a complete chemical and minero-petrographic characterization of the samples, which may prove useful for preparing compatible repair mortars for future restoration works. The archaeometric study provided new data on the production technology of the mortars and the analogies and differences observed among the samples, enabled us to distinguish different constructive phases, thus confirming or rebutting the archaeological hypothesis on the dating of some samples. By combining compositional variables through the discriminant analysis, it was also possible to analyse the time evolution of the materials and to construct preliminary multivariate statistical models, helpful to identify the various typologies of mortars used in the different historical periods.

36 MATERIALS SCIENCE↗
DOE OSTI2018

Direct Production of Ferrochrome by Segregation Reduction of Chromite in the Presence of Calcium Chloride

A solid reduction process is described whereby chromite is reduced with the help of calcium chloride to produce ferrochrome alloy powders with high metal recovery. The process involves segregation reduction of chromite using graphite as the reductant and calcium chloride as the segregation catalyst. Experiments were performed in the temperature range of 1200–1400 °C to evaluate the influences of various design parameters using both a thermogravimetric analyzer and an electric tube furnace with continuous off-gas analysis. The reduced products were characterized by scanning electron microscopy, X-ray powder diffraction, synchrotron X-ray absorption spectroscopy, and were subjected to wet chemical analysis. It was concluded that the addition of calcium chloride not only accelerated the carbothermic reduction of chromite but also promoted the formation and growth of individual ferrochrome alloy particles. The alloy formation within chromite particles was minimized, enabling the effective separation of ferrochrome alloy particles from the unwanted gangue without the need for fine grinding. Majority of the calcium chloride remained in a recoverable form, with a small percentage (<10 wt %) consumed by reacting with the siliceous gangue forming wadalite. Pure ferrochrome alloy powders were successfully produced with high metal recovery using elutriating separation.

36 MATERIALS SCIENCE↗
DOE OSTI2018

Preliminary Characterization and Mechanical Performance of Additively Manufactured HT9

Laser-blown powder deposition of HT9 was performed to evaluate the feasibility of using advanced manufacturing to fabricate creep strength enhanced ferritic steels. The as-printed materials were tensile tested at room temperature, 330°C, and 550°C to provide a baseline value for the strength levels. The as-fabricated strengths are then compared with wrought materials in the published literature. The strength parameters for the as-fabricated HT9 was found to be significantly higher than that of wrought HT9 without sacrifice in ductility. Two different heat treatment cycles, deemed ACO3 and FCRD, involving two different austentizing temperatures (1065°C and 1040°C) and tempering temperatures (750°C and 760°C) were then evaluated. The heat-treated samples were also tensile tested and were found to show strength and ductility parameters which closely mimicked that of the wrought HT9 literature data. Detailed multi-scale characterization was performed at various length scales. The as-fabricated structure showed a refined martensitic structure with a significant fraction of δ-ferrite present. Closer examination using TEM showed a refined distribution of carbides (predominantly M 23 C 6 and MX or M2X), which would have precipitated during the deposition process. Upon heat treatment, it was seen that the precipitates were more homogenous and refined in the case of the specimens heat treated according to the ACO 3 cycle although there was no significant difference in the strength or the hardness results. However, the specimens heat-treated per the FCRD cycle showed significantly smaller prior austenite grains (measure and give quantitative numbers), which could result in better Charpy toughness. However, the toughness was not evaluated and will be performed in the future. In addition, possible thermos-mechanical treatments (TMT) to refine the grain structure and improve the toughness without compromising the ductility will also be evaluated in the future.

36 MATERIALS SCIENCE↗
DOE OSTI2024

In-situ and ex-situ characterization of irradiated AM materials

This study investigates the irradiation performance of laser powder bed fusion (LPBF) 316L and 316H stainless steels (SS), and their wrought counterparts. While LPBF 316L has been more studied, LPBF 316H is relatively new, with little prior data on its irradiation behavior. The research involved fabricating, preparing, irradiating, and characterizing six materials: LPBF 316L (two variants), LPBF 316H (two variants), and wrought 316L and 316H. LPBF materials were subjected to various heat treatments, including solution annealing and stress relief, and were irradiated using in-situ and ex-situ ion techniques at temperatures of 300°C and 600°C, with doses ranging from 0.2 dpa to 25 dpa. Under ex-situ irradiation with 4 MeV Ni 2+ ions at 600°C, the dislocation cell structures in LPBF316L-1 and LPBF316H-1 gradually evolved into a uniform dislocation network. At a low irradiation dose (0.2 dpa), the cell structures were still partially visible. At 2 dpa, a uniform dislocation network formed, though remnants of the original cell structure were still discernible as contrast domains. At 5 dpa and 10 dpa, even the contrast domains vanished. For irradiation at 300°C, the cell structure was still clearly visible at 0.2 dpa for LPBF316L-1. For LPBF316H-1, the dislocation cell structure was less apparent at the same dose but was still recognizable. With further increase in dose at 300°C, the dislocation cell walls were completely replaced by irradiation-induced defects and no longer visible. Void formation was observed for irradiation at 600°C. At 2 dpa, no evident voids were observed in either LPBF316L-1 or LPBF316H-1.

36 MATERIALS SCIENCE↗
DOE OSTI2019

Improved Oxygen Reduction Reaction Activity of Nanostructured CoS 2 through Electrochemical Tuning

Searching for efficient Pt-free oxygen reduction reaction (ORR) electrocatalysts has been actively pursued among the current electrocatalyst research community. The family of transition-metal chalcogenides, especially cobalt disulfide (CoS 2 ), has been reported as competitive ORR catalysts. In this work, we perform a detailed analysis of the intrinsic activity in terms of onset potentials and selectivity toward hydrogen peroxide of CoS 2 in both acid and alkaline medium. Our detailed characterizations of this system via X-ray powder diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and calculated bulk and surface thermodynamics and ORR mechanism reveal pH-dependent electrochemical evolution of the CoS 2 surfaces. Using XPS results before and after ORR in combination with density functional theory (DFT) calculations for individual surfaces reveals sulfur to oxygen substitution, and partial dissolution occurs in acidic media, while thin cobalt oxide films supported by CoS 2 are formed in alkaline media. The comprehensive DFT calculations of the ORR activities on these systems reveal that sulfur is an unlikely ORR active site, while undercoordinated Co metal site in the CoS 2 is less active than very active undercoordinated Co metal site in the Co oxide film. Using these guiding principles, we then demonstrate that electrochemical lithium (Li) tuning of CoS 2 in organic electrolyte increases its ORR performance in both acid and alkaline medium. Detailed characterizations demonstrate that the grain size of CoS 2 particle is considerably reduced and has a much richer surface oxygen content after electrochemical Li tuning (LiET-CoS 2 ) as the direct consequence of the Li galvanostatic cycling. The general efficacy of this method toward transition-metal chalcogenides (T-M-X) is further demonstrated by enhanced ORR activities of CoS and Ni 3 S 2 in alkaline and neutral medium, respectively. This work opens up an opportunity for probing more advanced T-M-X-based catalysts.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗