Mg-doped SrTiO₃ photocatalyst with Ag-Co cocatalyst for enhanced selective conversion of CO₂ to CO using H₂O as the electron donor

Photocatalytic conversion of CO₂ by H₂O is a promising method for solving energy and environmental problems. In this context, efficient photocatalysts that facilitate the selective conversion of CO₂ to the value-added chemical CO are essential. In this study, for the first time in the literature, we used an Mg-doped SrTiO₃ photocatalyst (Mg–SrTiO₃) for the photocatalytic conversion of CO₂ to CO using H₂O as the electron donor under monochromatic UV-light irradiation at 365 nm. Compared to pristine SrTiO₃, Mg–SrTiO₃, which was prepared via a flux method, exhibited dramatically enhanced conversion of CO₂ to CO in the presence of an Ag–Co cocatalyst. Moreover, the selectivity toward CO evolution was >99%, which indicates suppression of the unnecessary and competitive H₂ evolution. Scanning electron microscopy of Mg–SrTiO₃ revealed edge-shaved cubic particles, which were correlated to the anisotropic distribution of photogenerated electrons and holes and the consequent enhancement of photocatalytic activity. Furthermore, the Mg-doping temperature and amount used to prepare Mg–SrTiO₃ influenced the substitution of Ti⁴⁺ sites by Mg²⁺ in the bulk of SrTiO₃, thereby affecting the CO evolution. The apparent quantum efficiency of optimal Mg–SrTiO₃ in the photocatalytic conversion of CO₂ was determined to be 0.05%

Daptomycin-related Musculoskeletal Adverse Events and Statin Use

Background. There is a growing concern about the association between the combined use of daptomycin (DAP) and statins and the occurrence of musculoskeletal adverse events (MAEs), but this remains controversial. This study aimed to clarify the association between statin use and DAP-related MAEs. Methods. We used a mixed approach that combines 2 methodologies. First, we conducted a meta-analysis to examine the effects of statin use on DAP-related MAEs. Second, we conducted a disproportionality analysis using the US Food and Drug Administration Adverse Events Reporting System (FAERS) to further confirm the results of the meta-analysis and to examine the effect of each type of statin on DAP-related MAEs in a large population. Results. In the meta-analysis, statin use significantly increased the incidence of DAP-related rhabdomyolysis (odds ratio [OR]: 3.83; 95% confidence interval [CI]: 1.43–10.26) but not DAP-related myopathy (OR: 1.72; 95% CI: .95–3.12). In the disproportionality analysis using the FAERS, the use of statin significantly increased the reporting OR (ROR) for DAP-related myopathy (ROR: 5.69; 95% CI: 4.31–7.51) and rhabdomyolysis (ROR: 5.77; 95% CI: 4.33–7.68). Atorvastatin, rosuvastatin, and simvastatin all increased the incidence of DAP-related myopathy and rhabdomyolysis. Conclusion. The mixed approach combining a meta-analysis and disproportionality analysis showed that statin use was associated with the occurrence of DAP-related rhabdomyolysis. The appropriate use of statins and DAP should be performed with careful consideration of its safety

Mg-doped SrTiO3 Photocatalyst with Ag-Co Cocatalyst for Enhanced Selective Conversion of CO2 to CO Using H2O as the Electron Donor

Photocatalytic conversion of CO2 by H2O is a promising method for solving energy and environmental problems. In this context, efficient photocatalysts that facilitate the selective conversion of CO2 to the value-added chemical CO are essential. In this study, for the first time in the literature, we used an Mg-doped SrTiO3 photocatalyst (Mg-SrTiO3) for the photocatalytic conversion of CO2 to CO using H2O as the electron donor under monochromatic UV-light irradiation at 365 nm. Compared to pristine SrTiO3, Mg-SrTiO3, which is prepared via a flux method, exhibited dramatically enhanced conversion of CO2 to CO in the presence of Ag-Co cocatalyst. Moreover, the selectivity toward CO evolution was greater than 99%, indicating suppression of the unnecessary and competitive H2 evolution. Scanning electron microscopy of Mg-SrTiO3 revealed edge-shaved cubic particles, which were correlated to the anisotropic distribution of photogenerated electrons and holes and the consequent enhancement of photocatalytic activity. Furthermore, the Mg-doping temperature and amount used to prepare Mg-SrTiO3 influenced the substitution of Ti4+ sites in the bulk of SrTiO3 by Mg2+, thereby affecting the CO evolution. The apparent quantum efficiency of optimal Mg-SrTiO3 in the photocatalytic conversion of CO2 was determined to be 0.05%

Low-Polarization Lithium–Oxygen Battery Using [DEME][TFSI] Ionic Liquid Electrolyte

The room-temperature molten salt mixture of N,N-diethyl-N-(2-methoxyethyl)-N-methylammonium bis(trifluoromethanesulfonyl) imide ([DEME][TFSI]) and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) salt is herein reported as electrolyte for application in Liâ\u80\u93O2batteries. The [DEME][TFSI]â\u80\u93LiTFSI solution is studied in terms of ionic conductivity, viscosity, electrochemical stability, and compatibility with lithium metal at 30 °C, 40 °C, and 60 °C. The electrolyte shows suitable properties for application in Liâ\u80\u93O2battery, allowing a reversible, low-polarization dischargeâ\u80\u93charge performance with a capacity of about 13 Ah g-1carbonin the positive electrode and coulombic efficiency approaching 100 %. The reversibility of the oxygen reduction reaction (ORR)/oxygen evolution reaction (OER) is demonstrated by ex situ XRD and SEM studies. Furthermore, the study of the cycling behavior of the Liâ\u80\u93O2cell using the [DEME][TFSI]-LiTFSI electrolyte at increasing temperatures (from 30 to 60 °C) evidences enhanced energy efficiency together with morphology changes of the deposited species at the working electrode. In addition, the use of carbon-coated Zn0.9Fe0.1O (TMO-C) lithium-conversion anode in an ionic-liquid-based Li-ion/oxygen configuration is preliminarily demonstrated

New Electrode and Electrolyte Configurations for Lithium-Oxygen Battery

Cathode configurations reported herein are alternative to the most diffused ones for application in lithium-oxygen batteries, using an ionic liquid-based electrolyte. The electrodes employ high surface area conductive carbon as the reaction host, and polytetrafluoroethylene as the binding agent to enhance the oxygen reduction reaction (ORR)/oxygen evolution reaction (OER) reversibility. Roll-pressed, self-standing electrodes (SSEs) and thinner, spray deposited electrodes (SDEs) are characterized in lithium-oxygen cells using an ionic liquid (IL) based electrolyte formed by mixing lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) salt and N,N-diethyl-N-(2-methoxyethyl)-N-methylammonium bis(trifluoromethanesulfonyl)imide (DEMETFSI). The electrochemical results reveal reversible reactions for both electrode configurations, but improved electrochemical performance for the self-standing electrodes in lithium-oxygen cells. These electrodes show charge/discharge polarizations at 60 °C limited to 0.4 V, with capacity up to 1 mAh cmâ\u88\u922and energy efficiency of about 88 %, while the spray deposited electrodes reveal, under the same conditions, a polarization of 0.6 V and energy efficiency of 80 %. The roll pressed electrode combined with the DEMETFSI-LiTFSI electrolyte and a composite LixSn-C alloy anode forms a full Li-ion oxygen cell showing extremely limited polarization, and remarkable energy efficiency