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Recently developed solid-state catalysts can mediate carbon dioxide (CO 2 ) electroreduction to valuable products at high rates and selectivities. However, under commercially relevant current densities of > 200 milliamperes per square centimeter (mA cm −2 ), catalysts often undergo particle agglomeration, active-phase change, and/or element dissolution, making the long-term operational stability a considerable challenge. Here we report an indium sulfide catalyst that is stabilized by adding zinc in the structure and shows dramatically improved stability. The obtained ZnIn 2 S 4 catalyst can reduce CO 2 to formate with 99.3% Faradaic efficiency at 300 mA cm −2 over 60 h of continuous operation without decay. By contrast, similarly synthesized indium sulfide without zinc participation deteriorates quickly under the same conditions. Combining experimental and theoretical studies, we unveil that the introduction of zinc largely enhances the covalency of In-S bonds, which “locks” sulfur—a catalytic site that can activate H 2 O to react with CO 2 , yielding HCOO* intermediates—from being dissolved during high-rate electrolysis. Developing durable catalysts for carbon dioxide reduction to formate at commercial-scale current densities is challenging. This work reports that indium sulfide stabilized through zinc incorporation can produce formate efficiently and quickly at high current densities over long timescales.

Seawater electrolysis using renewable electricity offers an attractive route to sustainable hydrogen production, but the sluggish electrode kinetics and poor durability are two major challenges. We report a molybdenum nitride (Mo 2 N) catalyst for the hydrogen evolution reaction with activity comparable to commercial platinum on carbon (Pt/C) catalyst in natural seawater. The catalyst operates more than 1000 hours of continuous testing at 100 mA cm −2 without degradation, whereas massive precipitate (mainly magnesium hydroxide) forms on the Pt/C counterpart after 36 hours of operation at 10 mA cm −2 . Our investigation reveals that ammonium groups generate in situ at the catalyst surface, which not only improve the connectivity of hydrogen-bond networks but also suppress the local pH increase, enabling the enhanced performances. Moreover, a zero-gap membrane flow electrolyser assembled by this catalyst exhibits a current density of 1 A cm −2 at 1.87 V and 60 o C in simulated seawater and runs steadily over 900 hours. Efficient catalysts for seawater electrolysis are crucial for sustainable hydrogen production but struggle with slow kinetics and low durability. Here, the authors report a molybdenum nitride catalyst that in situ generates ammonium groups, enhancing both performance and stability in natural seawater.

Thermal and dielectric properties of rigid-rod bifunctional epoxy resin 4,4-bis(2,3-epoxypropoxy) biphenyl epoxy (BP) and commercial epoxy resin diglycidyl ether of bisphenol A (DGEBA) were studied using differential scanning calorimeter (DSC), thermogravimetric analyzer (TGA), dynamic mechanical analyzer (DMA), thermal mechanical analyzer (TMA) and dielectric analyzer (DEA). These two epoxies were cured with cyanate ester hardener 2,2’-bis(4-cyanatophenyl) propane (AroCy B10). The BP/B10 system consisting of a rigid-rod structure exhibited better thermal properties than the DGEBA/B10 system with a flexible structure. Anisotropic BP/B10 (2:1) had the highest 5% weight loss temperature, the highest amount of residue and a smaller thermal expansion coefficient than the commercial DGEBA/B10 system. The BP/B10 system, which cured at the LC phase temperature, had higher Tg than the commercial DGEBA/B10 system, as found from dynamic mechanical analysis. The BP/B10 system also demonstrated better dielectric properties than the commercial DGEBA/B10 system when enough curing agent was provided.

The electrochemical CO2 reduction reaction (CO2RR) on Cu catalyst holds great promise for converting CO2 into valuable multicarbon (C2+) compounds, but still suffers poor selectivity due to the sluggish kinetics of forming carbon–carbon (C–C) bonds. Here we reported a perovskite oxide-derived Cu catalyst with abundant grain boundaries for efficient C–C coupling. These grain boundaries are readily created from the structural reconstruction induced by CO2-assisted La leaching. Using this defective catalyst, we achieved a maximum C2+ Faradaic efficiency of 80.3% with partial current density over 400 mA cm−2 in neutral electrolyte in a flow-cell electrolyzer. By combining the structural and spectroscopic investigations, we uncovered that the in-situ generated defective sites trapped by grain boundaries enable favorable CO adsorption and thus promote C–C coupling kinetics for C2+ products formation. This work showcases the great potential of perovskite materials for efficient production of valuable multicarbon compounds via CO2RR electrochemistry.

Chenopodium formosanum (CF), rich in nutrients and antioxidants, is a native plant in Taiwan. During the harvest, the seeds are collected, while the roots, stems, and leaves remain on the field as agricultural waste. In this study, di(phenyl)-(2,4,6-trinitrophenyl)iminoazanium (DPPH) radical scavenging ability and 2,2′-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) radical scavenging ability experiments of seeds, leaves, stems, and roots were designed using the Taguchi method (TM) under three conditions: Ethanol concentration (0–100%), temperature (25–65 °C), and extraction time (30–150 min). The result demonstrates that seeds and leaves have higher radical scavenging ability than stems and roots. Many studies focused on CF seeds. Therefore, this study selected CF leaves and optimized DPPH, ABTS, total phenol content (TPC), total flavonoid content (TFC), and reducing power (RP) through TM, showing that the predicted value of the leaf is close to the actual value. The optimized results of CF leaves were DPPH 85.22%, ABTS 46.51%, TPC 116.54 µg GAE/mL, TFC 143.46 µg QE/mL, and RP 23.29 µg VCE (vitamin C equivalent)/mL. The DPPH and ABTS of CF leaves were second only to the results of CF seeds. It can be seen that CF leaves have the potential as a source of antioxidants and help in waste reduction.

In this study, a new monitoring method was developed, titled infrared thermal imaging technology, which can effectively evaluate the thermal effect of the charge-discharge test in the vanadium/iodine redox flow battery (V/I RFB). The results show that the all-vanadium redox flow battery (all-V RFB) has a greater molar reaction Gibbs free energy change than that of the V/I RFB, representing a large thermal effect of the all-V RFB than the V/I RFB. The charge-discharge parameters, flow rate and current density, are important factors for inducing the thermal effect, because of the concentration polarization and the ohmic resistor. The new membrane (HS-SO3H) shows a high ion exchange capacity and a good ions crossover inhibitory for the V/I RFB system, and has a high coulomb efficiency that reaches 96%. The voltage efficiency was enhanced from 61% to 86% using the C-TiO2-Pd composite electrode as a cathode with the serpentine-type flow field for the V/I RFB. By adopting the high-resolution images of an infrared thermal imaging technology with the function of the temperature profile data, it is useful to evaluate the key components’ performance of the V/I RFB, and is a favorable candidate in the developing of the redox flow battery system.

pH responsive chitosan and 3-Glycidyloxypropyl trimethoxysilane (GPTMS) hydrogels were synthesized by the sol-gel crosslinking reaction. GPTMS was introduced to influence several behaviors of the chitosan hydrogels, such as the swelling ratio, mechanical properties, swelling thermodynamics, kinetics, and expansion mechanism. The functional groups of Chitosan/GPTMS hybrid hydrogels were verified by FT-IR spectrometer. Differential scanning calorimetry (DSC) and the thermogravimetric analysis (TGA) were used to analyzed the thermal behavior of water molecules, the expansion of thermodynamics, and the content of water molecules in the hydrogel. The results show that hydrogel consists of 50 wt.% GPTMS (CG50) and has good mechanical properties and sensitivity to pH response characteristics in the acidic/alkaline buffer solution. The increase of GPTMS content leads to the increase of hydrophobic groups in the hydrogel and causes the decrease of the overall water content and the freezing bond water content. When the hydrogels were immersed in acid solution, the interaction force parameter was smaller than that of DI-water and alkaline. It means that the interaction forces between hydrogel and water molecules are relatively strong. The swelling kinetics of hybrid hydrogels were investigated to inspect the swelling mechanism. The result is consistent with the Fisk’s diffusion mechanism, meaning that the rate of water penetration is adjustable. The biodegradable hydrogel (CG50) in this study has good environmental sensitivity and mechanical properties. It is suitable to be applied in the fields of drug release or biomedical technology.

This study is aimed to investigate the clinical significance and the short-term prognostic value of frag- mented QRS （fQRS） for patients with acute myocardial infarction （AMI）. Three hundred patients with AMI were tested with retrospective analysis on the patients＇ clinical information, hospitalized treatment, fQRS onset time, location of lesions, and other relevant data, in order to assess the relationship between the presence of fQRS and its prognosis. The rates of malignant cardiac arrhythmia, left ventricular systolic dysfunction （LVSD）, and mortality in the positive fQRS group were 13.6%, 29.2%, and 23.7%, respectively, with all showing a p value 〈0.05. For the ST segment elevation myocardial infarction （STEMI） subgroup, all the rates showed significant differences with a p value 〈0.01, while for the non-STEMI （NSTEMI） subgroup showed no significant differences. In patients with a positive fQRS, there were no differences in malignant cardiac arrhythmia between patients with and without percutaneous coronary in- tervention （PCI） （p〉0.05）. As for the LVSD and mortality, the p values between patients with and without PCI were 0.031 and 0.000, respectively, suggesting statistical significance. The results imply that AMI patients with positive fQRS especially for the patients with STEMI had higher rates of malignant cardiac arrhythmia, LVSD, and mortality than the non-fQRS group. Patients of AMI with positive fQRS, who underwent early revascularization, could lower the incidence of the cardiovascular event. In addition, the presence of fQRS could be used as an indication of early in- tervention treatment for patients.

Carbon dioxide corrosion behavior of low-alloy pipeline steel with 1% Cr exposed to CO2-saturated solution was investigated by immersion experiment. SEM, EDX, TEM, EPMA and XRD were utilized to investigate the microstructure, corrosion morphologies, corrosion phases and elements distribution of corrosion scale. The results demon strate that the microstructure of tested steel consists of ferrite and carbides. During the corrosion process, ferrite dissolves preferentially, leaving carbide particles behind. The residual carbide particles may promote the nucleation of FeCO3 crystal. The phase comprising of the inner layer is Cr compound, and the one of the outer layer is FeCO3. The formation process of corrosion scale can be illustrated as follows： Firstly, a thin scale consisting of thin inner layer and outer layer is formed, which represents poor corrosion resistance; then, the inner layer changes little, once it has been formed, and the outer layer becomes thick and compact, which demonstrates that a fine corrosion resistance is obtained. The chemical elements of chromium and molybdenum accumulate in the inner layer of corrosion scale. The corrosion behavior of low- alloy steel based on microstructure and morphology characterization is also discussed.