Reactive capture and electrochemical conversion of CO2 with ionic liquids and deep eutectic solvents.

Ionic liquids (ILs) and deep eutectic solvents (DESs) have tremendous potential for reactive capture and conversion (RCC) of CO2 due to their wide electrochemical stability window, low volatility, and high CO2 solubility. There is environmental and economic interest in the direct utilization of the captured CO2 using electrified and modular processes that forgo the thermal- or pressure-swing regeneration steps to concentrate CO2, eliminating the need to compress, transport, or store the gas. The conventional electrochemical conversion of CO2 with aqueous electrolytes presents limited CO2 solubility and high energy requirement to achieve industrially relevant products. Additionally, aqueous systems have competitive hydrogen evolution. In the past decade, there has been significant progress toward the design of ILs and DESs, and their composites to separate CO2 from dilute streams. In parallel, but not necessarily in synergy, there have been studies focused on a few select ILs and DESs for electrochemical reduction of CO2, often diluting them with aqueous or non-aqueous solvents. The resulting electrode-electrolyte interfaces present a complex speciation for RCC. In this review, we describe how the ILs and DESs are tuned for RCC and specifically address the CO2 chemisorption and electroreduction mechanisms. Critical bulk and interfacial properties of ILs and DESs are discussed in the context of RCC, and the potential of these electrolytes are presented through a techno-economic evaluation.

From Ln2O2S to Ln10OS14: exploring the sulphur spectrum of trivalent lanthanoid oxysulphides.

While Ln2O2S oxysulphides have increasingly gained attention due to their structural and optoelectronic properties, an expansive compositional space lies beyond as the sulphur-to-oxygen ratio increases. In these oxysulphides, the compounded effect of the 4f states is manifold in the lanthanoid ions and the changing bonding and environment symmetry enables the tuning of their electronic structure and photophysical properties. Their challenging syntheses have made these materials largely unexplored, but recent efforts have been made to bridge the knowledge gap. In this article we present some of the structural characteristics and photophysical properties of the lanthanoid oxysulphide spectrum LnxOySz.

Key Experimental Considerations When Evaluating Functional Ionic Liquids for Combined Capture and Electrochemical Conversion of CO2.

Ionic liquids (ILs) are considered functional electrolytes for the electrocatalytic reduction of CO2 (ECO2R) due to their role in the double-layer structure formation and increased CO2 availability at the electrode surface, which reduces the voltage requirement. However, not all ILs are the same, considering the purity and degree of the functionality of the IL. Further, there are critical experimental factors that impact the evaluation of ILs for ECO2R including the reference electrode, working electrode construction, cosolvent selection, cell geometry, and whether the electrochemical cell is a single compartment or a divided cell. Here, we describe improved synthesis methods of imidazolium cyanopyrrolide IL for electrochemical studies in consideration of precursor composition and reaction time. We explored how IL with cosolvents (i.e. acetonitrile, dimethylformamide, dimethyl sulfoxide, propylene carbonate, and n-methyl-2-pyrrolidone) affects conductivity, CO2 mass transport, and ECO2R activation overpotential together with the effects of electrode materials (Sn, Ag, Au, and glassy carbon). Acetonitrile was found to be the best solvent for lowering the onset potential and increasing the catalytic current density for the production of CO owing to the enhanced ion mobility in combination with the silver electrode. Further, the ECO2R activity of molecular catalysts Ni(cyclam)Cl2 and iron tetraphenylsulfonato porphyrin (FeTPPS) on the carbon cloth electrode maintained high Faradaic efficiencies for CO in the presence of the IL. This study presents best practices for examining nontraditional multifunctional electrolytes amenable to integrated CO2 capture and conversion technologies for homogeneous and heterogeneous ECO2R.

X-ray absorption spectroscopy insights on the structure anisotropy and charge transfer in Chevrel Phase chalcogenides.

The electronic structure and local coordination of binary (Mo6T8) and ternary Chevrel Phases (MxMo6T8) are investigated for a range of metal intercalant and chalcogen compositions. We evaluate differences in the Mo L3-edge and K-edge X-ray absorption near edge structure across the suite of chalcogenides MxMo6T8 (M = Cu, Ni, x = 1-2, T = S, Se, Te), quantifying the effect of compositional and structural modification on electronic structure. Furthermore, we highlight the expansion, contraction, and anisotropy of Mo6 clusters within these Chevrel Phase frameworks through extended X-ray absorption fine structure analysis. Our results show that metal-to-cluster charge transfer upon intercalation is dominated by the chalcogen acceptors, evidenced by significant changes in their respective X-ray absorption spectra in comparison to relatively unaffected Mo cations. These results explain the effects of metal intercalation on the electronic and local structure of Chevrel Phases across various chalcogen compositions, and aid in rationalizing electron distribution within the structure.

Adsorption of perfluorooctanoic acid from water by pH-modulated Brönsted acid and base sites in mesoporous hafnium oxide ceramics.

Per- and polyfluoroalkyl substances (PFAS) are increasingly appearing in drinking water sources globally. Our work focuses specifically on the adsorption of the legacy perfluorooctanoic acid (PFOA) using mesoporous hafnium oxide (MHO) ceramic synthesized via a sol-gel process. Experiments were performed at varying pH to determine the effect of surface charge on adsorption capacity of PFOA by MHO, and to postulate adsorption behavior. At pH 2.3, the adsorption capacity of PFOA on MHO was 20.9 mg/g, whereas at a higher pH of 6.3, it was much lower at 9.2 mg/g. This was due to increased coulombic attractions at lower pH between the positively charged conjugate acid active sites on MHO surface and negatively charged deprotonated PFOA anion in solution. After adsorption, the solid MHO was regenerated via calcination, reducing the amount of toxic solid waste to be disposed since the adsorbent is regenerated, and the PFOA is completely removed.

Multi-dimensional designer catalysts for negative emissions science (NES): bridging the gap between synthesis, simulations, and analysis.

Negative emissions technologies will play a critical role in limiting global warming to sustainable levels. Electrocatalytic and/or photocatalytic CO2 reduction will likely play an important role in this field moving forward, but efficient, selective catalyst materials are needed to enable the widespread adoption of these processes. The rational design of such materials is highly challenging, however, due to the complexity of the reactions involved as well as the large number of structural variables which can influence behavior at heterogeneous interfaces. Currently, there is a significant disconnect between the complexity of materials systems that can be handled experimentally and those that can be modeled theoretically with appropriate rigor and bridging these gaps would greatly accelerate advancements in the field of Negative Emissions Science (NES). Here, we present a perspective on how these gaps between materials design/synthesis, characterization, and theory can be resolved, enabling the rational development of improved materials for CO2 conversion and other NES applications.

Fe(II) Induced Reduction of Incorporated U(VI) to U(V) in Goethite.

Over 60 years of nuclear activities have resulted in a global legacy of radioactive wastes, with uranium considered a key radionuclide in both disposal and contaminated land scenarios. With the understanding that U has been incorporated into a range of iron (oxyhydr)oxides, these minerals may be considered a secondary barrier to the migration of radionuclides in the environment. However, the long-term stability of U-incorporated iron (oxyhydr)oxides is largely unknown, with the end-fate of incorporated species potentially impacted by biogeochemical processes. In particular, studies show that significant electron transfer may occur between stable iron (oxyhydr)oxides such as goethite and adsorbed Fe(II). These interactions can also induce varying degrees of iron (oxyhydr)oxide recrystallization (<4% to >90%). Here, the fate of U(VI)-incorporated goethite during exposure to Fe(II) was investigated using geochemical analysis and X-ray absorption spectroscopy (XAS). Analysis of XAS spectra revealed that incorporated U(VI) was reduced to U(V) as the reaction with Fe(II) progressed, with minimal recrystallization (approximately 2%) of the goethite phase. These results therefore indicate that U may remain incorporated within goethite as U(V) even under iron-reducing conditions. This develops the concept of iron (oxyhydr)oxides acting as a secondary barrier to radionuclide migration in the environment.

Machine Learning Guided Synthesis of Multinary Chevrel Phase Chalcogenides.

The Chevrel phase (CP) is a class of molybdenum chalcogenides that exhibit compelling properties for next-generation battery materials, electrocatalysts, and other energy applications. Despite their promise, CPs are underexplored, with only ∼100 compounds synthesized to date due to the challenge of identifying synthesizable phases. We present an interpretable machine-learned descriptor (Hδ) that rapidly and accurately estimates decomposition enthalpy (ΔHd) to assess CP stability. To develop Hδ, we first used density functional theory to compute ΔHd for 438 CP compositions. We then generated >560 000 descriptors with the new machine learning method SIFT, which provides an easy-to-use approach for developing accurate and interpretable chemical models. From a set of >200 000 compositions, we identified 48 501 CPs that Hδ predicts are synthesizable based on the criterion that ΔHd < 65 meV/atom, which was obtained as a statistical boundary from 67 experimentally synthesized CPs. The set of candidate CPs includes 2307 CP tellurides, an underexplored CP subset with a predicted preference for channel site occupation by cation intercalants that is rare among CPs. We successfully synthesized five of five novel CP tellurides attempted from this set and confirmed their preference for channel site occupation. Our joint computational and experimental approach for developing and validating screening tools that enable the rapid identification of synthesizable materials within a sparse class is likely transferable to other materials families to accelerate their discovery.

Stabilizing Hydrogen Adsorption through Theory-Guided Chalcogen Substitution in Chevrel-Phase Mo6X8 (X=S, Se, Te) Electrocatalysts.

In this work, we implement a facile microwave-assisted synthesis method to yield three binary Chevrel-Phase chalcogenides (Mo6X8; X = S, Se, Te) and investigate the effect of increasing chalcogen electronegativity on hydrogen evolution catalytic activity. Density functional theory predictions indicate that increasing chalcogen electronegativity in these materials will yield a favorable electronic structure for proton reduction. This is confirmed experimentally via X-ray absorption spectroscopy as well as traditional electrochemical analysis. We have identified that increasing the electronegativity of X in Mo6X8 increases the hydrogen adsorption strength owing to a favorable shift in the p-band position as well as an increase in the Lewis basicity of the chalcogen, thereby improving hydrogen evolution reaction energetics. We find that Mo6S8 exhibits the highest hydrogen evolution activity of the Mo6X8 series of catalysts, requiring an overpotential of 321 mV to achieve a current density of 10 mA cm-2ECSA, a Tafel slope of 74 mV per decade, and an exchange current density of 6.01 × 10-4 mA cm-2ECSA. Agreement between theory and experiment in this work indicates that the compositionally tunable Chevrel-Phase chalcogenide family is a promising framework for which electronic structure can be predictably modified to improve catalytic small-molecule reduction reactivity.

Complicaciones no letales en el infarto agudo de miocardio: Análisis en una unidad de cuidados coronarios / Non-lethal complications in the acute myocardial infarction: Analysis in a coronary care unit

RESUMEN Introducción: El infarto agudo de miocardio se define como la presencia de una lesión miocárdica aguda detectada mediante el empleo de biomarcadores cardíacos en el curso demostrado de isquemia miocárdica aguda. Objetivo: Evaluar probables factores asociados a la aparición de complicaciones intrahospitalarias no letales en pacientes con infarto agudo de miocardio con elevación del segmento ST. Método: Se realizó un estudio observacional, analítico, de corte transversal, en la Unidad de Cuidados Coronarios Intensivos del Hospital Clínico-Quirúrgico Manuel Fajardo en 2016 y 2017. Se utilizó el método estadístico descriptivo y las pruebas estadísticas necesarias (χ2 o prueba exacta de Fisher, razón de probabilidades [odds ratio] y t de Student). Resultados: Predominó el sexo masculino (59,0%) y la edad media fue de 62 años. Solo el 41,0% de los pacientes recibió fibrinólisis. La dislipidemia presentó asociación estadísticamente significativa con la aparición de complicaciones (p=0,046). La edad se relacionó con la aparición de complicaciones hemodinámicas (p=0,02). No existieron diferencias estadísticamente significativas entre los pacientes que recibieron trombólisis y los que no, respecto a las complicaciones (OR=1,33;IC 95%: 0,54-3,24), ni entre estas y la topografía del infarto (cara anterior OR=0,57;IC 95%: 0,23-1,43; cara inferior OR=1,73; IC 95%: 0,70-4,27). Conclusiones: La dislipidemia se asoció a la aparición de complicaciones en pacientes con infarto agudo de miocardio; y la edad, con las complicaciones hemodinámicas. La realización de trombólisis y las regiones miocárdicas afectadas no se relacionaron con la aparición de complicaciones intrahospitalarias no letales.

ABSTRACT Introduction: Acute Myocardial Infarction is defined as the presence of acute myocardial injury detected by the use of cardiac biomarkers in the demonstrated evidence of acute myocardial ischemia. Objective: To evaluate possible factors associated with the appearance of non-lethal in-hospital complications in patients presenting with ST-segment elevation acute myocardial infarction. Method: An observational, analytical, cross-sectional study was conducted in the Intensive Coronary Care Unit of the "Hospital Clínico-Quirúrgico Manuel Fajardo" in 2016 and 2017. The descriptive statistical method and the necessary statistical tests (χ2 or Fisher's Exact Test,odds ratio and Student's t-test) were used. Results: The male sex predominated (59.0%) and the average age was 62 years. Only 41.0% of patients received fibrinolysis. Dyslipidemia showed a statistically significant association with the appearance of complications (p=0.046). Age was related to the appearance of hemodynamic complications (p=0.02). There were no statistically significant differences between patients who received thrombolysis and those who did not, regarding complications (OR=1.33; CI 95%: 0.54-3.24), nor between these and the topography of the infarction (anterior wall OR=0.57; CI 95%: 0.23-1.43; inferior wall OR=1.73; CI 95%: 0.70-4.27). Conclusions: Dyslipidemia was associated with the appearance of complications in patients with acute myocardial infarction. Age was associated with hemodynamic complications. Thrombolytic therapy and the affected myocardial walls were not related to the occurrence of non-lethal in-hospital complications.

Microwave near-field imaging of two-dimensional semiconductors.

Optimizing new generations of two-dimensional devices based on van der Waals materials will require techniques capable of measuring variations in electronic properties in situ and with nanometer spatial resolution. We perform scanning microwave microscopy (SMM) imaging of single layers of MoS2 and n- and p-doped WSe2. By controlling the sample charge carrier concentration through the applied tip bias, we are able to reversibly control and optimize the SMM contrast to image variations in electronic structure and the localized effects of surface contaminants. By further performing tip bias-dependent point spectroscopy together with finite element simulations, we distinguish the effects of the quantum capacitance and determine the local dominant charge carrier species and dopant concentration. These results underscore the capability of SMM for the study of 2D materials to image, identify, and study electronic defects.

Improving O2 production of WO3 photoanodes with IrO2 in acidic aqueous electrolyte.

WO3 is a promising candidate for a photoanode material in an acidic electrolyte, in which it is more stable than most metal oxides, but kinetic limitations combined with the large driving force available in the WO3 valence band for water oxidation make competing reactions such as the oxidation of the acid counterion a more favorable reaction. The incorporation of an oxygen evolving catalyst (OEC) on the WO3 surface can improve the kinetics for water oxidation and increase the branching ratio for O2 production. Ir-based OECs were attached to WO3 photoanodes by a variety of methods including sintering from metal salts, sputtering, drop-casting of particles, and electrodeposition to analyze how attachment strategies can affect photoelectrochemical oxygen production at WO3 photoanodes in 1 M H2SO4. High surface coverage of catalyst on the semiconductor was necessary to ensure that most minority-carrier holes contributed to water oxidation through an active catalyst site rather than a side-reaction through the WO3/electrolyte interface. Sputtering of IrO2 layers on WO3 did not detrimentally affect the energy-conversion behavior of the photoanode and improved the O2 yield at 1.2 V vs. RHE from ~0% for bare WO3 to 50-70% for a thin, optically transparent catalyst layer to nearly 100% for thick, opaque catalyst layers. Measurements with a fast one-electron redox couple indicated ohmic behavior at the IrO2/WO3 junction, which provided a shunt pathway for electrocatalytic IrO2 behavior with the WO3 photoanode under reverse bias. Although other OECs were tested, only IrO2 displayed extended stability under the anodic operating conditions in acid as determined by XPS.

A substrate-integrated and scalable templated approach based on rusted steel for the fabrication of polypyrrole nanotube arrays.

We report here a facile, generalizable, and entirely scalable approach for the fabrication of vertically aligned arrays of Fe(2)O(3)/polypyrrole core-shell nanostructures and polypyrrole nanotubes. Our "all electrochemical" approach is based on the fabrication of α-Fe(2)O(3) nanowire arrays by the simple heat treatment of commodity low carbon steel substrates, followed by electropolymerization of conformal polypyrrole sheaths around the nanowires. Subsequently, electrochemical etching of the nanowires yields large-area vertically aligned polypyrrole nanotube arrays on the steel substrate. The developed methodology is generalizable to functionalized pyrrole monomers and represents a significant practical advance of relevance to the technological implementation of conjugated polymer nanostructures in electrochromics, electrochemical energy storage, and sensing.