Unveiling Enhanced PEC Water Oxidation: Morphology Tuning and Interfacial Phase Change in α-Fe2O3@K-OMS-2 Branched Core-Shell Nanoarrays.

A simple fabrication method that involves two steps of hydrothermal reaction has been demonstrated for the growth of α-Fe2O3@K-OMS-2 branched core-shell nanoarrays. Different reactant concentrations in the shell-forming step led to different morphologies in the resultant composites, denoted as 0.25 OC, 0.5 OC, and 1.0 OC. Both 0.25 OC and 0.5 OC formed perfect branched core-shell structures, with 0.5 OC possessing longer branches, which were observed by SEM and TEM. The core K-OMS-2 and shell α-Fe2O3 were confirmed by grazing incidence X-ray diffraction (GIXRD), EDS mapping, and atomic alignment from high-resolution STEM images. Further investigation with high-resolution HAADF-STEM, EELS, and XPS indicated the existence of an ultrathin layer of Mn3O4 sandwiched at the interface. All composite materials offered greatly enhanced photocurrent density at 1.23 VRHE, compared to the pristine Fe2O3 photoanode (0.33 mA/cm2), and sample 0.5 OC showed the highest photocurrent density of 2.81 mA/cm2. Photoelectrochemical (PEC) performance was evaluated for the samples by conducting linear sweep voltammetry (LSV), applied bias photo-to-current efficiency (ABPE), electrochemical impedance spectroscopy (EIS), incident-photo-to-current efficiency (IPCE), transient photocurrent responses, and stability tests. The charge separation and transfer efficiencies, together with the electrochemically active surface area, were also investigated. The significant enhancement in sample 0.5 OC is ascribed to the synergetic effect brought by the longer branches in the core-shell structure, the conductive K-OMS-2 core, and the formation of the Mn3O4 thin layer formed between the core and shell.

Multiple interface coupling on natural tourmaline enables high-efficiency removal of antibiotic: Superior property and mechanism.

Reasonably designing highly active, environmentally friendly, and cost-effective catalysts for efficient elimination of pollutants from water is desirable but challenging. Herein, an efficient heterogeneous photo-Fenton catalyst tourmaline (TM)/tungsten oxide (WO3-x) (named TW10) containing tungsten/boron/iron (W/B/Fe) synergistic active centers and 90% of cheap natural tourmaline (TM) mineral rich in Fe and B elements. The TW10 catalyst can quickly activate peroxymonosulfate (PMS) to generate massive active free radicals, which may induce the rapid and efficient degradation of tetracycline (TC). The TW10/PMS/Visible light system can effectively degrade up to 98.7% of tetracycline (TC) in actual waters (i.e. seawater, Yellow River, and Yangtze River water), and the catalytic degradation rates reach 1.65, 5.569, and 2.38 times higher than those of TM, WO3-x, and commercial P25 (Degussa, Germany), respectively. In addition, the catalyst can be recycled and reused multiple times. Electron spin resonance spectroscopy (EPR), X-ray photoelectron spectroscopy (XPS), and liquid chromatograph-mass spectrometer (LC-MS) analyses confirm that the synergistic catalytic effect of W/B/Fe sites on the TW10 catalyst accelerates the electron transfer between Fe(II) and Fe(III), as well as between W(V) and W(VI), and thus promotes the rapid degradation of TC. The catalytic reaction mechanism and degradation pathway of TC were explored. This work provides a feasible route for the design and development of new eco-friendly and efficient catalyst.

Arsenate Anion-π Interactions on Amine-Modified Polydivinylbenzene in Aqueous Systems: Experimental and Theoretical Investigation.

Anion-π interactions aiding in the adsorption of anions in the solution phase, though challenging to quantify, have attracted a lot of attention in supramolecular chemistry. We present the design of a polymer adsorbent that quantifies the adsorption of arsenate ions experimentally by optimizing anion-π interactions in a purely aqueous system and use density functional theory to compare these results with theoretical data. Arsenate anions are removed from water by amine-functionalized polydivinylbenzene using the comonomer 1-vinyl-1,2,4-triazole, which was cross-linked with divinylbenzene via radical polymerization in a hydrothermal procedure. The amine-functionalized polydivinylbenzene successfully removed arsenate anions from water with a capacity of 46 mg g-1, a 70% increase compared to the nonfunctionalized polydivinylbenzene (27 mg g-1) capacity under the same conditions. Adsorption is best described by the Sips isotherm model with a correlation coefficient R2 factor of 0.99, indicating that adsorption sites are homogeneous, and adsorption occurred by forming a monolayer. Kinetic studies indicated that adsorption is second order in the amine-functionalized polydivinylbenzene. Computational studies using density functional theory showed that the 1-vinyl-1,2,4-triazole comonomer improved the thermodynamic stability of the anionic-π interactions of polydivinylbenzene with arsenate anions. Electrostatic interactions dominate the mechanism of adsorption in polydivinylbenzene compared to the anion-induced interactions that dominate adsorption in amine-functionalized polydivinylbenzene.

Cycling-Induced Capacity Increase of Bulk and Artificially Layered LiTaO3 Anodes in Lithium-Ion Batteries.

Tantalum-based oxide electrodes have recently drawn much attention as promising anode materials owing to their hybrid Li+ storage mechanism. However, the utilization of LiTaO3 electrode materials that can deliver a high theoretical capacity of 568 mAh g-1 has been neglected. Herein, we prepare a layered LiTaO3 electrode formed artificially by restacking LiTaO3 nanosheets using a facile synthesis method and investigate the Li+ storage performance of this electrode compared with its bulk counterpart. The designed artificially layered anode reaches specific capacities of 474, 290, and 201 mAh g-1, respectively, at 56 (>500 cycles), 280 (>1000 cycles), and 1120 mAg-1 (>2000 cycles) current densities. We also determine that the Li+ storage capacity of the layered LiTaO3 demonstrates a cycling-induced capacity increase after a certain number of cycles. Adopting various characterization techniques on LiTaO3 electrodes before and after electrochemical cycling, we attribute the origin of the cycling-induced improvement of the Li+ storage capacity in these electrodes to the amorphization of the electrode after cycling, formation of metallic tantalum during the partially irreversible conversion mechanism, lower activation overpotential of electrodes due to the formation of Li-rich species by the lithium insertion mechanism, and finally the intrinsic piezoelectric behavior of LiTaO3 that can regulate Li+ diffusion kinetics.

Why surface hydrophobicity promotes CO2 electroreduction: a case study of hydrophobic polymer N-heterocyclic carbenes.

We report the use of polymer N-heterocyclic carbenes (NHCs) to control the microenvironment surrounding metal nanocatalysts, thereby enhancing their catalytic performance in CO2 electroreduction. Three polymer NHC ligands were designed with different hydrophobicity: hydrophilic poly(ethylene oxide) (PEO-NHC), hydrophobic polystyrene (PS-NHC), and amphiphilic block copolymer (BCP) (PEO-b-PS-NHC). All three polymer NHCs exhibited enhanced reactivity of gold nanoparticles (AuNPs) during CO2 electroreduction by suppressing proton reduction. Notably, the incorporation of hydrophobic PS segments in both PS-NHC and PEO-b-PS-NHC led to a twofold increase in the partial current density for CO formation, as compared to the hydrophilic PEO-NHC. While polymer ligands did not hinder ion diffusion, their hydrophobicity altered the localized hydrogen bonding structures of water. This was confirmed experimentally and theoretically through attenuated total reflectance surface-enhanced infrared absorption spectroscopy and molecular dynamics simulation, demonstrating improved CO2 diffusion and subsequent reduction in the presence of hydrophobic polymers. Furthermore, NHCs exhibited reasonable stability under reductive conditions, preserving the structural integrity of AuNPs, unlike thiol-ended polymers. The combination of NHC binding motifs with hydrophobic polymers provides valuable insights into controlling the microenvironment of metal nanocatalysts, offering a bioinspired strategy for the design of artificial metalloenzymes.

Ca substitution improves the catalytic activity of perovskite LaCoO3 toward toluene: comprehension of electronic structure alteration.

For perovskite La1-xCaxCoO3 (Ca-x, x = 0-0.3), Ca-0.2 with the closest O p band center to the Fermi level, displays the best catalytic activity for toluene oxidation. The O p band center determines the reducibility and active oxygen content. This finding is beneficial for the design of highly active perovskite catalysts.

COVID-19 Detection Using a 3D-Printed Micropipette Tip and a Smartphone.

The COVID-19 pandemic has caused over 7 million deaths worldwide and over 1 million deaths in the US as of October 15, 2022. Virus testing lags behind the level or availability necessary for pandemic events like COVID-19, especially in resource-limited settings. Here, we report a low cost, mix-and-read COVID-19 assay using a synthetic SARS-CoV-2 sensor, imaged and processed using a smartphone. The assay was optimized for saliva and employs 3D-printed micropipette tips with a layer of monoclonal anti-SARS-CoV-2 inside the tip. A polymeric sensor for SARS-CoV-2 spike (S) protein (COVRs) synthesized as a thin film on silica nanoparticles provides 3,3',5-5'-tetramethylbenzidine responsive color detection using streptavidin-poly-horseradish peroxidase (ST-poly-HRP) with 400 HRP labels per molecule. COVRs were engineered with an NHS-PEG4-biotin coating to reduce nonspecific binding and provide affinity for ST-poly-HRP labels. COVRs binds to S-proteins with binding strengths and capacities much larger than salivary proteins in 10% artificial saliva-0.01%-Triton X-100 (as virus deactivator). A limit of detection (LOD) of 200 TCID50/mL (TCID50 = tissue culture infectious dose 50%) in artificial saliva was obtained using the Color Grab smartphone app and verified using ImageJ. Viral load values obtained in 10% pooled human saliva spiked with inactivated SARS-COV-2 virus gave excellent correlation with viral loads obtained from qPCR (p = 0.0003, r = 0.99).

Recent Advances in Tetra- (Ti, Sn, Zr, Hf) and Pentavalent (Nb, V, Ta) Metal-Substituted Molecular Sieve Catalysis.

Metal substitution of molecular sieve systems is a major driving force in developing novel catalytic processes to meet current demands of green chemistry concepts and to achieve sustainability in the chemical industry and in other aspects of our everyday life. The advantages of metal-substituted molecular sieves include high surface areas, molecular sieving effects, confinement effects, and active site and morphology variability and stability. The present review aims to comprehensively and critically assess recent advances in the area of tetra- (Ti, Sn, Zr, Hf) and pentavalent (V, Nb, Ta) metal-substituted molecular sieves, which are mainly characterized for their Lewis acidic active sites. Metal oxide molecular sieve materials with properties similar to those of zeolites and siliceous molecular sieve systems are also discussed, in addition to relevant studies on metal-organic frameworks (MOFs) and some composite MOF systems. In particular, this review focuses on (i) synthesis aspects determining active site accessibility and local environment; (ii) advances in active site characterization and, importantly, quantification; (iii) selective redox and isomerization reaction applications; and (iv) photoelectrocatalytic applications.

Rapid photooxidation and removal of As(III) from drinking water using Fe-Mn composite oxide.

Fe-Mn composite oxide (FMO) is widely applied to the oxidation and removal of As(III) from water. However, As(III) can directly reduce manganese oxides, decreasing the oxidation capacity or reusability and thereby greatly limiting the applicability of FMO. Here, the oxidation capacity and reusability of FMO for As(III) were efficiently improved by light radiation, and the effect of typical coexisting ions (SO42- and Ca2+) on the removal of As(III) was also studied. O2•- produced from excited manganese oxide and ligand-to-metal charge transfer in iron oxide-As(III) complex enhanced As(III) oxidation and removal under light radiation. At an initial As(III) concentration of 1000 µg L-1, the total As concentration was respectively decreased to 11.5, 1.5 and 4.4 µg L-1 under darkness, UV light and sunlight at 180 min, and could be reduced to below the guideline limitation of drinking water (10 µg L-1) within 40 and 60 min under UV light and sunlight, respectively. SO42- exhibited negligible effect on As removal efficiency because FMO had obviously lower adsorption capacity and selectivity for SO42- than for As(V). The adsorption of coexisting Ca2+ on manganese oxide decreased the negative charge on the FMO surface, thereby improving As(III) adsorption and oxidation. FMO exhibited excellent reusability, and a total As removal efficiency of 99.1% was still maintained after five cycles of an adsorption-desorption process under UV light. This work elucidates the photochemical oxidation and removal mechanism of FMO for As(III), and proposes a low-cost and efficient method for the detoxification of As(III)-contaminated drinking water.

Highly Mesoporous MoO3 Catalysts for Electrophilic Aromatic Substitution.

Herein, a straightforward synthesis method for highly mesoporous molybdenum oxide has been demonstrated via use of inverse micelles and molybdenum-oxo cluster formation. The synthesized catalyst is stable, crystalline, and MoO3 phase pure, as confirmed through thermogravimetric analysis, X-ray diffraction, and X-ray photoelectron spectroscopy. Further results from electron paramagnetic resonance, Raman spectroscopy, and UV-vis spectroscopy confirm the MoO3 phase purity. Chemisorption studies reveal that the synthesized material is 65 times more active than its commercial parts. The quantitative value of ammonia chemisorption for the synthesized catalyst is 1270 µmol/g, whereas the commercial catalyst only gives 22 µmol/g. These materials were tested for electrophilic substitution reactions since they are excellent solid acid. Electrophilic substitution of benzyl alcohol with toluene gives a >99% conversion with ∼80% of selectivity toward the methyl diphenylmethane product. The turnover number and turnover frequency values were calculated to be as high as 115 and 38, respectively. A substrate scope study shows that the reaction has preference toward electron-donating groups, whereas electron-withdrawing groups block the reaction. Based on the obtained results, a mechanism has been proposed.

Ultrathin MnO2-Coated FeOOH Catalyst for Indoor Formaldehyde Oxidation at Ambient Temperature: New Insight into Surface Reactive Oxygen Species and In-Field Testing in an Air Cleaner.

Herein, we tailored a series of ultrathin MnO2 nanolayers coated on the surface of commercial goethite (α-FeOOH) by a facile in situ chemical precipitation method. α-FeOOH inhibited the MnO2 crystal growth via the incorporation of K+ ions between MnO2 and α-FeOOH interfaces during the synthesis process. The hybrid design of MnO2 with an ultrathin nanolayer structure could reduce the electron transfer resistance and bring abundant oxygen vacancies, accelerating the activation of molecular O2 to generate more oxygen-free radical species and favoring the thermodynamic HCHO oxidation. The ROS quenching in gas/aqueous systems and DRIFTS results demonstrated that •O2- was responsible for HCHO oxidization, which assisted the preliminary intermediate dioxymethylene dehydrogenation into formate species. The 25%MnO2@FeOOH(25wt% of MnO2) catalyst was subsequently loaded into the filter substrates of a commercial air cleaner and tested in an indoor room with actual application conditions. As a result, the composite filter could eliminate different initial concentrations of HCHO (150-450 ppb) to the WHO guideline value (≈81 ppb) within 60 min. Furthermore, the 25%MnO2@FeOOH sample was also effective against the representative bacteria and mold in indoor air. This study provides new insight into the role of the chemisorbed ROS for HCHO oxidation at ambient temperature.

Magnetically Doped Molybdenum Disulfide Layers for Enhanced Carbon Dioxide Capture.

Carbon capture and storage (CCS) technologies have the potential for reducing greenhouse gas emissions and creating clean energy solutions. One of the major aspects of the CCS technology is designing energy-efficient adsorbent materials for carbon dioxide capture. In this research, using a combination of first-principles theory, synthesis, and property measurements, we explore the CO2 gas adsorption capacity of MoS2 sheets via doping with iron, cobalt, and nickel. We show that substitutional dopants act as active sites for CO2 adsorption. The adsorption performance is determined to be dependent on the type of dopant species as well as its concentration. Nickel-doped MoS2 is found to be the best adsorbent for carbon capture with a relatively high gas adsorption capacity compared to pure MoS2 and iron- and cobalt-doped MoS2. Specifically, Brunauer-Emmett-Teller (BET) measurements show that 8 atom % Ni-MoS2 has the highest surface area (51 m2/g), indicating the highest CO2 uptake relative to the other concentrations and other dopants. Furthermore, we report that doping could lead to different magnetic solutions with changing electronic structures where narrow band gaps and the semimetallic tendency of the substrate are observed and can have an influence on the CO2 adsorption ability of MoS2. Our results provide a key strategy to the characteristic tendencies for designing highly active and optimized MoS2-based adsorbent materials utilizing the least volume of catalysts for CO2 capture and conversion.

Effect of iron substitution in cryptomelane on the heterogeneous reaction with isoprene.

Biogenic isoprene is an important pollutant for regional air quality. Being ubiquitously distributed on the earth surface, manganese (hydr)oxides should play a vital role in the transformation of isoprene. Cryptomelane is a typical manganese oxide with isomorphous substitution of Fe for Mn, but less attention has been paid to its heterogeneous reaction with isoprene. When Fe3+ replaces Mn3+, K+ is depleted and Mn3+ is oxidized to Mn4+. In contrast, oxygen vacancies are formed when Fe3+ substitutes Mn4+. Fe substitution creates weak crystallites and abundant mesopores, resulting in the increase of isoprene adsorption. As found by theoretical calculations, the Mn4+-O2- bonds at the cross sections of the tunnels is more active than that on the outer wall of the tunnels. After the adsorption of isoprene, bridging carboxylate species and hydrogen-bonding water are produced and the surface octahedra are distorted, i.e., Mn4+O6 → Mn3+O6-δ. As the heat facilitates the breakage of Mn4+-O2-, the increase of environmental temperature enhances the oxidation of isoprene. The above findings shed light on the effect of Fe substitution in cryptomelane to enhance the oxidation of isoprene, and illustrates that heterogeneous reaction with isoprene impairs the transformation of other environmental substances on cryptomelane.

Partial oxidation of methane to methanol on boron nitride at near critical acetonitrile.

Direct catalytic conversion of methane to methanol with O2 has been a fundamental challenge in unlocking abundant natural gas supplies. Metal-free methane conversion with 17% methanol yield based on the limiting reagent O2 at 275 °C was achieved with near supercritical acetonitrile in the presence of boron nitride. Reaction temperature, catalyst loading, dwell time, methane-oxygen molar ratio, and solvent-oxygen molar ratios were identified as critical factors controlling methane activation and the methanol yield. Extension of the study to ethane (C2) showed moderate yields of methanol (3.6%) and ethanol (4.5%).

In Situ Studies of Single-Nanoparticle-Level Nickel Thermal Oxidation: From Early Oxide Nucleation to Diffusion-Balanced Oxide Thickening.

High-temperature oxidation mechanisms of metallic nanoparticles have been extensively investigated; however, it is challenging to determine whether the kinetic modeling is applicable at the nanoscale and how the differences in nanoparticle size influence the oxidation mechanisms. In this work, we study thermal oxidation of pristine Ni nanoparticles ranging from 4 to 50 nm in 1 bar 1%O2/N2 at 600 °C using in situ gas-cell environmental transmission electron microscopy. Real-space in situ oxidation videos revealed an unexpected nanoparticle surface refacetting before oxidation and a strong Ni nanoparticle size dependence, leading to distinct structural development during the oxidation and different final NiO morphology. By quantifying the NiO thickness/volume change in real space, individual nanoparticle-level oxidation kinetics was established and directly correlated with nanoparticle microstructural evolution with specified fast and slow oxidation directions. Thus, for the size-dependent Ni nanoparticle oxidation, we propose a unified oxidation theory with a two-stage oxidation process: stage 1: dominated by the early NiO nucleation (Avrami-Erofeev model) and stage 2: the Wagner diffusion-balanced NiO shell thickening (Wanger model). In particular, to what extent the oxidation would proceed into stage 2 dictates the final NiO morphology, which depends on the Ni starting radius with respect to the critical thickness under given oxidation conditions. The overall oxidation duration is controlled by both the diffusivity of Ni2+ in NiO and the Ni in Ni self-diffusion. We also compare the single-particle kinetic curve with the collective one and discuss the effects of nanoparticle size differences on kinetic model analysis.

Removal of As(V) from wastewaters using magnetic iron oxides formed by zero-valent iron electrocoagulation.

Electrocoagulation of zero-valent iron has been widely applied to the removal of dissolved arsenic, but the solid-liquid separation of arsenic-containing precipitates remains technically challenging. In this work, zero-valent iron was electrochemically oxidized to magnetic iron oxides for the removal of As(Ⅴ) from simulated and actual mining wastewaters. The results indicated that lepidocrocite was formed when zero-valent iron was oxidized by dissolved oxygen, but ferrihydrite and green rust were first formed and then transformed to magnetic iron oxides (mainly magnetite and maghemite) in the electrochemical oxidation from 0 to 0.9 V (vs. SCE), which facilitates the adsorption of As(V) and subsequent solid-liquid separation under a magnetic field. In simulated As(V)-containing solution with initial pH 7.0, zero-valent iron was electrochemically oxidized to magnetite and maghemite at 0.6 V (vs. SCE) for 2 h. The As(V) concentration first decreased from 5127.5 to 26.8 µg L-1 with a removal ratio of 99.5%. In actual mining wastewaters, zero-valent iron was electrochemically oxidized to maghemite at 0.6 V (vs. SCE) for 24 h, and the As(V) concentration decreased from 5486.4 to 3.6 µg L-1 with a removal ratio of 99.9%. The removal ratio of As(V) increased slightly with increasing potential, and increased first and then decreased with increasing initial pH. Compared with that of SO42- and NO3-, the presence of Cl- significantly enhanced the removal of As(V). This work provides a highly efficient, facile and low-cost technique for the treatment of arsenic-containing wastewaters.

Role of catalytic nitrile decomposition in tricopper complex mediated direct partial oxidation of methane to methanol.

Synthetic homogeneous system known to date performing methane to methanol conversion using O2 as terminal oxidant is unique and based on copper complex with piperazine-based ligand (Cu3L in Fig. 1) in a medium of acetonitrile. Prior work have shown that in order to achieve catalytic turnover, hydrogen peroxide is needed to regenerate the active site. We show in this paper that reaction solvent based on organic nitrile decompose concurrently with methane activation and that in the absence of either acetonitrile, Cu complex or hydrogen peroxide, the catalytic turnover does not happen. We show in this manuscript that the direct methane oxidation to methanol might have been mediated by catalytic Radziszewski oxidation between acetonitrile and H2O2. Additionally we have discovered that in the absence of methane, peroxide mediated acetonitrile decomposition also makes methanol via a background reaction which was hitherto unknown.

Structure-property correlations and scaling in the magnetic and magnetocaloric properties of GdCrO3particles.

The structure, magnetic, and magnetocaloric (MC) properties of orthorhombic nanocrystalline GdCrO3with six particle sizes: ⟨d⟩ = 87, 103, 145, 224, 318, and 352 nm are reported. The particle size was tailored by annealing under different temperatures and estimated by scanning electron microscopy. With increase in ⟨d⟩, Goldschmidt tolerance factort, orthorhombic strains, and out-of-plane Cr-O1-Cr bond angle first decrease, reaching minimum values for ⟨d⟩ = 224 nm, and then increase for sample with ⟨d⟩ = 318 nm and 352 nm, thus showing a V-shaped variation. Temperature dependence of the magnetization (M) reveals an antiferromagnetic transition atTNCr∼168K for ⟨d⟩ ⩾ 224 nm andTNCr∼167K for ⟨d⟩ < 224 nm and an essentiallyd-independent spin-reorientation atTSR= 9 K.Mmeasured at 5 K and 7 T first increases with increase in ⟨d⟩, reaching maximum value for sample with ⟨d⟩ = 224 nm, and then decreases for samples with ⟨d⟩ = 318 nm and 352 nm, showing an inverted-V variation with ⟨d⟩. Similar ⟨d⟩-dependence is observed for the magnetic entropy change (MEC) and relative cooling power (RCP) showing a close relationship between the structural and magnetic properties of GdCrO3nanoparticles investigated here. The 224 nm sample with the minimum values oft,s, and Cr-O1-Cr bond angle exhibits the maximum value of MEC (-ΔS) = 37.8 J kg-1 K-1at 5 K under a field variation (ΔH) of 7 T and its large estimated RCP of 623.6 J Kg-1is comparable with those of typical MC materials. Both (-ΔS) and RCP are shown to scale with the saturation magnetizationMS, suggesting thatMSis the crucial factor controlling their magnitudes. Assuming (-ΔS) ∼ (ΔH)n, the temperature dependence ofnfor the six samples are determined,nvarying between 1.3 at 5 K ton= 2.2 at 130 K in line with its expected magnitudes based on mean-field theory. These results on structure-property correlations and scaling in GdCrO3suggest that its MC properties are tunable for potential low-temperature magnetic refrigeration applications.

Focused Ion Beam-Prepared Transmission Electron Microscopy Examination of Atmospheric Chemical Vapor-Infiltrated Silicon Carbide Morphology.

Silicon carbide (SiC)-based ceramic matrix composites (CMCs) are utilized for their refractory properties in the aerospace industry. The composition and structure of these materials are crucial to maintaining the strength, toughness, oxidation, and creep resistances that are desired of silicon carbide. This work analyzes the chemical composition of the matrix in batches of SiC/SiC (silicon carbide fiber-reinforced silicon carbide matrix) minicomposites that are processed by chemical vapor infiltration of the BN interphase and SiC matrix on single Hi-Nicalon Type S fiber tows using a range of processing parameters. The analysis was performed here to investigate the potential causes of variation in matrix tensile strength in the various batches of minicomposites. Six different morphologies present in the silicon carbide matrix were observed: smooth, nodular, rough nodular, bumpy, nucleated, and plate-like. It was found that high-matrix tensile strength minicomposite batches contained solely the smooth morphology, while low-matrix tensile strength minicomposite batches contained a variety of other morphologies. FIB/TEM was used to study the atomic and crystal character of each individual morphology. Smooth SiC is oriented by the (111) planes and is primarily SiC, while the other morphologies are randomly oriented and contain significant oxygen. These results match the tensile strength tests, which pointed to smooth SiC as the strongest matrix material.