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Results for “AM Powder Characterization”

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

Dispersion and properties of zirconia suspensions for stereolithography

Abstract Stereolithography is an attractive technique for the fabrication of complex‐shaped ceramic components with high dimensional accuracy. One of the challenges in this technology is the development of high solid loading, low viscosity photosensitive ceramic suspension. In this study, the dispersion of zirconia in photocurable resin and the slurry properties were intensively investigated. Rheological measurements showed that DISPERBYK‐103 proved to be an effective dispersant. 42 vol% ZrO 2 suspension was successfully prepared using 3.5 wt% DISPERBYK‐103 as the dispersant, with a suitable viscosity (4.88 Pa·s) below the maximum allowable viscosity value (5 Pa·s) for stereolithography applications. The adsorption behavior of DISPERBYK‐103 on the surface of zirconia powders was characterized by TG and FT‐IR, confirming the dispersion effect of dispersant. Contact angle measurements were also conducted to show that the adsorption of DISPERBYK‐103 could help to improve the wettability between powder and photocurable resin. Results showed that DISPERBYK‐103 was effective for the preparation of suitable slurries for the development of ZrO 2 ceramics through stereolithography.

Li, Xingbang↗
DOE OSTI2024

Compatibility of LaFe13−x−yMnxSiyH1.6 and Eutectic Liquid GaInSn Alloy

The heat transfer rate of magnetocaloric regenerators is a topic of extensive research and the cyclability of these regenerators is critical to the operation of systems with a high coefficient of performance (e.g., potentially >22, significantly higher than typical vapor compression cooling technologies). To enable a high operating frequency that will result in a high specific cooling power, the heat transfer fluid should have high thermal conductivity and lower specific heat, i.e., higher thermal diffusivity. Eutectic metal alloys possess these qualities, such as gallium–indium–tin (Galinstan), whose thermal diffusivity has been found to be approximately an order of magnitude higher than water. For this study, the effects of eutectic liquid Galinstan exposure on the phase stability of LaFe13−x−yMnxSiyH1.6 magnetocaloric powders in an active magnetic regenerator device were investigated. The powders were characterized before and after exposure to Galinstan using X-ray diffraction, in which the phases were determined using the Rietveld refinement technique and X-ray fluorescence. It was found that after Galinstan exposure, hydrogen containing phases were present in the powder, suggesting that the hydrogen was lost from the magnetocaloric phase. The magnetocaloric phase degradation indicates that the powder was incompatible with the Galinstan metal in an environment with moisture.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2025

Solving the “Coloring Problem” in InPd 3– x Ag x ( x = 0–0.7) by Phase Diagrams Modeling and Diffraction Experiments

Here, a series of InPd 3–x Ag x (x = 0–1) compositions were synthesized by conventional high-temperature synthesis, and as-synthesized samples were characterized by powder X-ray diffraction experiments. Up to x = 0.7, InPd 3–x Ag x adopts the ternary substitutional variant of the InPd 3 structure (TiAl 3 -type), when x > 0.7, elemental Ag starts to segregate along with the main phase. Accurate structural characterization in InPd 3–x Ag x faces a critical challenge due to the narrow X-ray scattering contrast among constituents In, Pd, and Ag and nearly identical neutron scattering lengths of Pd and Ag. To overcome this “coloring problem”, a combination of calculation of phase diagrams modeling (CALPHAD) and diffraction techniques (X-ray and neutron) was employed. In the compositional range 0 ≤ x ≤ 0.7, InPd 3–x Ag x presents a ternary variant of the TiAl 3 -type structure, where Ag atoms selectively substitute one (the 2b Wyckoff site) of the two Pd sites in InPd 3 . Notably, in contrast to the isologous InPd 3–x Cu x (x = 0–1) system, Ag substitution does not form an ordered VRh 2 Sn-type structure at the limiting composition. The distinct site preference in InPd 3–x Ag x is elucidated by charge population analysis, electronic structure calculations, and orbital-resolved chemical bonding investigations, and the extent of substitution is supported by formation free energy calculations.

36 MATERIALS SCIENCE↗
DOE OSTI2019

Solution Combustion Synthesis of Fe{sub 3}O{sub 4} Powders Using Mixture of CTAB and Citric Acid Fuels

Magnetite (Fe{sub 3}O{sub 4}) powders were synthesized by solution combustion method using a mixture of cetyltrimethylammonium bromide (CTAB) and citric acid fuels at various fuel to oxidant ratios (ϕ = 0.5, 1, 1.5, and 2). Phase evolution investigated by x-ray diffraction method showed single-phase Fe{sub 3}O{sub 4} powders were only formed at ϕ = 1 using mixture of fuels, while impurity α-Fe{sub 2}O{sub 3} phase together with magnetite phase was completely disappeared at ϕ = 2 for CTAB fuel alone. The specific surface area and porous structures of the as-combusted Fe{sub 3}O{sub 4} powders were characterized by N{sub 2} adsorption-desorption isotherms and scanning electron microscopy techniques, respectively. The specific surface area using the mixture of fuels (37 m{sup 2}/g) was higher than that of CTAB fuel alone (32 m{sup 2}/g). Magnetic properties of the as-combusted powders were studied by vibration sample magnetometry method. The highest saturation magnetization of 83 emu/g was achieved by mixture of fuels at ϕ = 1, due to the high purity and large particle size.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2023

A multimodal flow reactor for photocatalysis under atmospheric conditions

Photocatalysis is a promising concept for the direct conversion of solar energy into fuels and chemicals. The design, experimental protocol, and performance of a multimodal and versatile flow reactor for the characterization of powdered and immobilized photocatalysts are presented in this report. Ultimately, this instrument enables rigorous evaluation of photocatalysis performance metrics. The apparatus quantifies transient gas-phase reaction products via online real-time gas analyzer mass spectrometry (RTGA-MS). For H 2 , the most challenging gas, the photocatalytic system’s RTGA-MS gas detection sensitivity spans over three orders of magnitude and can detect down to tens of parts per million under atmospheric conditions. Using Pt nanoparticles supported on anatase TiO 2 photocatalyst via wet impregnation, the instrument’s capability for the characterization of photocatalytic H 2 evolution is demonstrated, resulting in an apparent quantum yield (AQY) of 48.1% ± 0.9% at 320 nm, 45.7% ± 0.3% at 340 nm and 31% ± 1% at 360 nm. The photodeposition of Pt on anatase TiO 2 was employed to demonstrate the instrument’s capability to track the transient behavior of photocatalysts, resulting in an improved 55% ± 2% AQY for H 2 evolution at 340 nm from aqueous methanol. This photocatalytic instrument enables systematic study of a wide variety of photocatalytic reactions such as water splitting and CO 2 reduction to valuable C2+ fuels and chemicals.

14 SOLAR ENERGY↗
DOE OSTI2019

Structural and Magnetic Behavior of BaAl{sub x}Cr{sub y}Fe{sub 11}O{sub 19} (x + y = 1) Hexagonal Ferrites

The present study aims to analyze barium hexagonal ferrite and its derivation behavior using sol-gel auto-combustion co-doped with Al{sup 3+}/Cr{sup 3+}ions. Also, the effects of dopants on structural and magnetic properties of prepared samples were investigated. To this purpose, the finest powders were preheated at 500 °C for 1 h and calcinated at 900 °C about 2 h. Then, the magnetic powders were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), field emission scanning electron microscope (FESEM), and vibrating sample magnetometer (VSM). The XRD patterns show the magnetoplumbite phase. According to the Scherrer equation applied, inserting ions led to a decrease in lattice parameters (a and c) and crystallite size. The morphology of synthesized samples was observed by FESEM and proved the hexagonal shapes of the prepared samples. The nanoparticles sizes were recorded between 59 and 79 nm. Moreover, the magnetic properties of prepared samples were specified by VSM. The saturation magnetization (M{sub s}) and remnant magnetization (M{sub r}) of the synthesized magnetic powders were decreased by inserting Al{sup 3+}/Cr{sup 3+} ions, while coercivity (H{sub c}) increased from 5215 to 7178 Oe. .

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2025

An innovative radial gradient material design using hot isostatic pressing for applications in extreme environments

Functionally graded materials (FGMs) are highly advanced continuous or discontinuous structures whose structural and material properties vary along a singular geometric dimension either in the axial or radial direction. Here, the radial gradient FGM design makes for an optimal structural design to incorporate a bi-metallic structure with a copper-based high entropy alloy (Cu-HEA) with good mechanical properties and high irradiation resistance, and Chromium (Cr) with great corrosion resistance. This study focuses on the experimental design of a metal powder loading mechanism to fabricate a bi-metallic radial gradient structure using Cu-HEA and 99.9 % pure Cr metal powders. The powder loading strategy uses custom-designed concentric cylindrical dividers to separate the individual compositions. Two benchtop trial runs were performed for design optimization. The optimized design was then implemented to eventually load the HEA and Cr powders for consolidation via powder metallurgy hot isostatic pressing (PM-HIP). The electron microscopy analysis reveals the successful fabrication of the radial gradient structure with the chemical mapping analysis, demonstrating the gradual composition shift from the HEA at the center to the pure-Cr at the periphery via a three-step gradient.

High Entropy Alloys (HEAs)↗
DOE OSTI2021

Tandem Catalytic Antioxidant Nanoparticles Comprising Cerium Carbonate and Photoactive Metal Oxides

While photoactive metal oxides such as TiO 2 find widespread use in paints and coatings as well as cosmetics and suncare products, they also generate reactive oxygen species (ROS), which degrade materials and are associated with human-health pathologies. Here, we demonstrate a robust and potent catalytic antioxidant consisting of earth-abundant cerium carbonate nanoparticles and micron-size Ce 2 (CO 3 ) 3 . 8H 2 O, which are characterized by powder X-ray diffraction and scanning nanobeam electron diffraction. When dispersed with photoactive metal oxides, these cerium carbonate catalysts decrease the photodecomposition rate of organic dyes and commercial pigment colorants in aqueous media by up to 820-fold, as well as in acrylic coatings. X-ray photoelectron spectroscopy and kinetic experiments support the same tandem catalysis mechanism of photoprotection when using both micron-size Ce 2 (CO 3 ) 3 . 8H 2 O and cerium carbonate nanoparticles. This mechanism involves ROS disproportionation (catalyzed by cerium carbonate) and H 2 O 2 decomposition (partially catalyzed by TiO 2 ) pathways, both of which cerium carbonate also catalyzes on its own, crudely mimicking the function of the cascade system of superoxide dismutase and catalase enzymes. When cerium carbonate nanoparticles were dispersed at 2 wt % in polymethylmethacrylate, the transparency of the polymer film was preserved and the photo-oxidative degradation of the polymer was prevented following UV irradiation at 254 nm, which otherwise resulted in the loss of optical properties and hydroxylation as characterized by ATR-FTIR spectroscopy, in the control polymer lacking cerium carbonate. Similar observations were made regarding color preservation in paint films comprising dye and insoluble commercial colorant pigments. The material chemistry associated with this photoprotection catalysis is subtle and emphasizes the importance of both Ce(III) and carbonate together, as both CePO 4 and Na 2 CO 3 are inactive. In conclusion, this emphasis is also apparent in comparisons of photoprotection catalysis with previously reported cerium oxide nanoparticles, which are significantly less active compared with Ce 2 (CO 3 ) 3 . 8H 2 O under the same conditions.

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

Preparation, structure and down-shifting luminescence of Yb3+ doped KLa5O5(VO4)2

Highlights: • The host of the studied phosphor KLa{sub 5}O{sub 5}(VO{sub 4}){sub 2} is new. • The down-shifting luminescence of Yb{sup 3+} single-doped KLa{sub 5}O{sub 5}(VO{sub 4}){sub 2} is firstly reported. • The crystal structure and luminescence of KLa{sub 5}O{sub 5}(VO{sub 4}){sub 2} were clearly investigated. • The NIR emission of Yb{sup 3+} is effectively sensitized by ultraviolet photon due to ET. - Abstract: Yb{sup 3+} doped KLa{sub 5}O{sub 5}(VO{sub 4}){sub 2} phosphors were successfully synthesized by traditional high temperature solid-state reaction. The crystal structure of the prepared powders were characterized by X-ray diffraction. The band gap of the samples were evaluated by diffuse reflectance spectroscopy. The down-shifting luminescence properties of the phosphors were investigated by steady-state photoluminescence (PL) and excitation spectra. The results show that Yb{sup 3+} near infrared emission can be sensitized by the broad VO charge-transfer band in UV range. The studied Yb{sup 3+} doped KLa{sub 5}O{sub 5}(VO{sub 4}){sub 2} phosphors can potentially improve the efficiency of solar cells.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2023

Evidence of a Uranium‐Paddlewheel Node in a Catecholate‐Based Metal–Organic Framework

Abstract The interactions between uranium and non‐innocent organic species are an essential component of fundamental uranium redox chemistry. However, they have seldom been explored in the context of multidimensional, porous materials. Uranium‐based metal–organic frameworks (MOFs) offer a new angle to study these interactions, as these self‐assembled species stabilize uranium species through immobilization by organic linkers within a crystalline framework, while potentially providing a method for adjusting metal oxidation state through coordination of non‐innocent linkers. We report the synthesis of the MOF NU‐1700 , assembled from U 4+ ‐paddlewheel nodes and catecholate‐based linkers. We propose this highly unusual structure, which contains two U 4+ ions in a paddlewheel built from four linkers—a first among uranium materials—as a result of extensive characterization via powder X‐ray diffraction (PXRD), sorption, transmission electron microscopy (TEM), and thermogravimetric analysis (TGA), in addition to density functional theory (DFT) calculations.

Knapp, Julia G.↗
DOE OSTI2023

Evidence of a Uranium‐Paddlewheel Node in a Catecholate‐Based Metal–Organic Framework

Abstract The interactions between uranium and non‐innocent organic species are an essential component of fundamental uranium redox chemistry. However, they have seldom been explored in the context of multidimensional, porous materials. Uranium‐based metal–organic frameworks (MOFs) offer a new angle to study these interactions, as these self‐assembled species stabilize uranium species through immobilization by organic linkers within a crystalline framework, while potentially providing a method for adjusting metal oxidation state through coordination of non‐innocent linkers. We report the synthesis of the MOF NU‐1700 , assembled from U 4+ ‐paddlewheel nodes and catecholate‐based linkers. We propose this highly unusual structure, which contains two U 4+ ions in a paddlewheel built from four linkers—a first among uranium materials—as a result of extensive characterization via powder X‐ray diffraction (PXRD), sorption, transmission electron microscopy (TEM), and thermogravimetric analysis (TGA), in addition to density functional theory (DFT) calculations.

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

Effects of Nd, Er Doping on the Structure and Magnetic Properties of YFeO{sub 3}

Nd, Er co-doped YFeO{sub 3} compounds were synthesized by sol-gel method. The prepared compounds were characterized by powder x-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), energy-dispersive x-ray (EDX), and vibrating sample magnetometer (VSM) integrated in a physical property measurement system (PPMS-9), respectively. The results show that the compounds possess orthorhombic perovskite structure. The Y{sub 0.5}Er{sub 0.1}Nd{sub 0.4}FeO{sub 3} compound mainly consists of five elements (Er, Nd, Y, Fe, and O) and atom ratio matched well with the formula. With the increase of Nd{sup 3+} doping content in Y{sub 0.5}Er{sub 0.5−x}Nd{sub x}FeO{sub 3} (x = 0, 0.1, 0.2, 0.3, and 0.4), the coercivity increases gradually while the saturation magnetization and remanent magnetization decrease at the same time. Introducing Nd{sup 3+} and Er{sup 3+} ions into YFeO{sub 3} will make a change on a structure distortion, resulting in the decrease of the Fe–O–Fe angle and the consequent reduction of superexchange effect. From our research results, the relationship between the r (R{sup 3+}) and the superexchange bond angle is different from pure-phase orthoferrites R FeO{sub 3}.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
DOE OSTI2019

Enhanced Magneto-optical and Antibacterial Studies of Bi{sub 1−x}Mg{sub x}FeO{sub 3} (0.0 ≤ x ≤ 0.15)) Nanoparticles

Mg-doped BiFeO{sub 3} (Bi{sub 1−x}Mg{sub x}FeO{sub 3} (0.00 ≤ x ≤ 0.15)) nanoparticles (NPs) have been successfully prepared by simple solution combustion method using urea as fuel. The obtained product was sintered at 550 °C for 2 h to get pure-phase formation. The as-prepared samples were characterized by powder X-ray diffraction (XRD), Fourier transform infrared (FT-IR), field emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDX), transmission electron microscope (TEM), ultraviolet–visible (UV-Vis) absorption, photoluminescence (PL) spectra, and vibrating sample magnetometer (VSM) analysis. Powder XRD study revealed that all products exhibit rhombohedral structure with pure-phase formation. The average crystallite size of the samples decreased from 56.25 to 46.15 nm with increasing the concentration of Mg (x = 0.00, 0.05, 0.10, and 0.15). Surface morphology of the samples were analyzed by FE-SEM and TEM micrograph techniques, and the grain distribution was not quite homogeneous and observed agglomeration of the particles, which is mainly due to the magnetic interaction among them. EDX analysis confirmed the presence of Bi, Fe, O, and Mg elements without any form of impurity peak in all products. PL spectra shows a high intense peak at 464 nm, which is attributed to blue emission. The saturation magnetization is enhanced with increasing Mg doping level at RT. Antibacterial activity of Bi{sub 1−x}Mg{sub x}FeO{sub 3} NPs was found to be enhanced with increase in Mg doping concentration as it causes a reduction in the grain size of the samples.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2018

Nonlinear Resonance Response of Porous Beam-Type Implants Corresponding to Various Morphology Shapes for Bone Tissue Engineering Applications

Having excellent biocompatibility and apatite mineralization as well as efficient mechanical properties makes bredigite as one of the most attractive bioceramics. A beam-type porous biological implant in a 3D-printed architecture is designed with micron pore size. The surface properties, morphology, and size of the composed powders are evaluated using Scherrer and Williamson-Hall equation. The effect of MNPs deposition into the bredigite bioceramics and correlation with temperature effect on roughness of the prepared bio-nanocomposite are also investigated for hyperthermia application potential. The composed powders are characterized by x-ray diffraction, and then scanning electron microscopy (SEM), differential scanning calorimetry, thermogravimetric analysis (weight change, TGA), and atomic force microscopy are utilized to evaluate the surface topography. The resonance response is the tendency of a bone scaffold to respond at prominent amplitude while the frequency of its oscillations is equal to the structure’s natural frequency of vibration. Therefore, based on the obtained mechanical properties via the experimental approach for the bio-nanocomposite material, an analytical solution based upon the multiple-timescale method is carried out to analyze the nonlinear primary resonance of a 3D-printed porous beam-type biological implant under uniform-distributed load. According to SEM observations, there are hard agglomerates in the bredigite-magnetite nanoparticles (Br-MNPs) bio-nanocomposite material with low weight fraction of MNPs. However, they are broken down by increasing the amount of MNPs. Also, it is displayed that for lower MNPs weight fraction, the height of jump phenomenon related to the nonlinear resonance response is maximum and minimum for, respectively, irregular and mesoporous shapes of morphology, but their associated forcing amplitudes related to the bifurcation points are minimum and maximum, respectively.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2018

Photocatalytic inactivation of Vibrio fischeri using Fe2O3-TiO2-based nanoparticles

Highlights: • A marine bacterium (Vibrio fisheri) was examined as biofilm forming microorganism. • The inactivation of bacteria was performed in saline and nutrient growth media. • The performance of five TiO{sub 2} based photocatalysts was investigated. • Effective inactivation of bacteria was achieved by visible light driven photocatalysts. Biofouling is a major problem in water membrane processes, especially in seawater reverse osmosis plants. Inactivation of Vibrio fischeri (a well-known marine bacterium forming biofilm) through photocatalysis via visible light was investigated in this work using active Fe{sub 2}O{sub 3}-TiO{sub 2} nanoparticles. Five Fe{sub 2}O{sub 3}-TiO{sub 2} photocatalysts with different weight percentage of Fe{sub 2}O{sub 3} (0–5 wt%) were synthesized using an ultrasonic-assisted co-precipitation method. The photocatalysts were characterized by powder X-ray diffraction (XRD), BET surface area, transmission electron Æ (TEM) plus selected area electron diffraction (SAED) patterns, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX) and diffuse-reflectance spectroscopy (DRS). Based on the design of experiments, the synthesized photocatalysts were tested for inactivation of V. fischeri under visible light irradiation at different temperatures (25–35 °C) and different photocatalyst dosage (0.1–2 g/L). The photocatalytic microbial inactivation experiments were performed in artificial seawater appropriate for growth of the marine bacterium. The results revealed that the highest inactivation efficiency of V. fischeri was achieved when 1 g/L of 2.5 wt% Fe{sub 2}O{sub 3}-TiO{sub 2} were used, at 35 °C. Photocatalytic inactivation of microorganisms using visible light-driven Fe{sub 2}O{sub 3}-TiO{sub 2} photocatalysts, could introduce an innovative green method in pretreatment units of reverse osmosis plants to control the membrane biofouling.

54 ENVIRONMENTAL SCIENCES↗
DOE OSTI2021

Catalytic degradation of waste rubbers and plastics over zeolites to produce aromatic hydrocarbons

Catalytic conversion of waste rubbers and plastics into aromatic hydrocarbons is a promising approach to waste management and energy recovery. In the present study, acidic HY zeolites were supported by cobalt, iron, and zirconium, and the catalysts were characterized by powder X-ray diffraction, nitrogen adsorption-desorption, ammonia temperature programmed desorption, X-ray photoelectron spectroscopy, and pyridine-Fourier transform infrared spectroscopy. Here, the catalytic degradation of waste polybutadiene rubbers (BR) was conducted to investigate the degradation mechanism and evaluate the catalytic activity of supported zeolites. Experimental results indicated that HY loaded by zirconium and iron led to a higher content of Lewis acid sites as opposed to cobalt supported one. Compared with the non-catalytic pyrolysis of BR, the zirconium supported HY (Zr/HY) led to a 10-fold increase in aromatic hydrocarbons production with a distinctively high selectivity of 97.9%. A series of waste polymers including waste tires (WT), polyethylene (PE), polycarbonate (PC), and BR, were subjected to catalytic pyrolysis to explore the effects of polymer type on aromatic hydrocarbons generation, and BR was the most effective substrate, with yield enhancement reaching 2.4 over Zr/HY. Catalytic co-pyrolysis of waste rubbers and plastics was conducted to probe the effect of polymer structure on aromatic hydrocarbons formation, where a significant synergistic effect was observed in the PE co-fed with PC run.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2023

Synthesis, structure and canted antiferromagnetism of layered cobalt hydroxide sorbate

Layered hybrid organic–inorganic compounds of the transition metal hydroxides, in which part of the hydroxide ions are exchanged for organic ligands that act as spacers of the 2-dimensional inorganic layers, elicit new or enhanced properties. The interlayer ligands enable fine-tuning of the physicochemical properties of the metal hydroxide layers, including their magnetism. Specifically, within the Co(OH) 2 family of transition ion hydroxides, this approach has been leveraged to stabilize antiferromagnetic and ferrimagnetic ground states for pillared and layered complexes, respectively. Here, in this work, we further investigate the effects of changing dimensionality, local Co coordination, and interlayer spacing on the magnetic ground state of brucite-like β-Co(OH) layered complexes. We report the hydrothermal synthesis of a new crystalline material, Co(OH)(sorb), where the inorganic layers are spaced by monotopic, doubly unsaturated sorbate ligands (sorb = [C 6 H 7 O 2 ] – ). The material was structurally characterized using powder X-ray and neutron diffraction measurements and the crystal structure was solved ab initio from powder diffraction data and refined using the Rietveld method. The magnetic susceptibility and magnetization measurements reveal canted antiferromagnetic ordering with T N = 41.7 K. This report augments our understanding of tuning magnetism through dimensionality in layered complexes and represents a step forward in the design of new 2D layered hybrid compounds.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗