Fe doping mechanism of Na0.44MnO2 tunnel phase cathode electrode in sodium-ion batteries.

Due to its stability and low cost, the tunnel-style sodium-manganese oxide (Na0.44MnO2) material is deemed a popular cathode choice for sodium-ion rechargeable batteries. However, the Jahn-Teller effect caused by Mn3+ in the material results in poor capacity and cycling stability. The purpose of this experimental study is to partially replace Mn3+ with Fe3+, in order to reduce the Jahn-Teller effect of the material during charging and discharging process. The results of Raman spectroscopy and X-ray photoelectron spectroscopy confirmed that the content of Mn3+ decreased after Fe3+ doping. Electrochemical studies show that the Na0.44Mn0.994Fe0.006O2 cathode has better rate performance (exhibits a reversible capacity of 87.9 mAh/g at 2 C) and cycle stability in sodium-ion batteries. The diffusion coefficient of sodium ions increases by Fe3+ doping. The excellent rate performance and capacity improvement are verified by density functional theory (DFT) calculation. After doping, the band gap decreases significantly, and the results show that the state density of O 2p increases near the Fermi level, which promotes the oxidation-reduction of oxygen. This work provides a straightforward approach to enhance the performance of Na0.44MnO2 nanorods, and this performance improvement has guiding significance for the design of other materials in the energy storage domain.

Preparation of Li3V2(PO4)3 as cathode material for aqueous zinc ion batteries by a hydrothermal assisted sol-gel method and its properties.

To alleviate the depletion of lithium resources and improve battery capacity and rate capacity, the development of aqueous zinc-ion batteries (AZIBs) is crucial. The open channels monoclinic structure Li3V2(PO4)3 is conducive to the transfer and diffusion of guest ions, making it a promising cathode material for AZIBs. Therefore, in this study, nanoneedles and particles Li3V2(PO4)3 cathode materials for AZIBs were prepared by a hydrothermal assisted sol-gel method, and the effect of synthesized pH values was studied. XRD results show that all samples had the monoclinic structure, and the Li3V2(PO4)3 sample prepared at pH = 7 exhibits (LVP-pH7) the highest peak tips and narrowest peak widths. SEM images demonstrate that all samples have the morphology character of randomly oriented needles and irregular particles, with the LVP-pH7 sample having more needle-like particles that contribute to ion diffusion. EDS results show uniform distribution of P, V, and O elements in the LVP-pH7 sample, and no obvious aggregation phenomenon is observed. Electrochemical tests have shown that the LVP-pH7 sample exhibits excellent cycling performance (97.37% after 50 cycles at 200 mA g-1) and rate ability compared to other samples. The CV test results showed that compared with other samples, the LVP-pH7 sample had the most excellent ionic diffusion coefficient (2.44 × 10-12 cm2 s-1). Additionally, the Rct of LVP-pH7 is the lowest (319.83 Ω) according to the findings of EIS and Nyquist plot fitting, showing a decreased charge transfer resistance and raising the kinetics of the reaction.

GABAergic Neuromuscular Junction Suppresses Intestinal Defense of Caenorhabditis elegans by Attenuating Muscular Oxidative Phosphorylation.

Innate immunity is an ancient and evolutionarily conserved system that constitutes the first line of host defense against invading microbes. We previously determined that the GABAergic neuromuscular junction (NMJ) suppresses intestinal innate immunity via muscular insulin signaling. Here, we found that a muscular mitochondrial oxidative phosphorylation pathway of Caenorhabditis elegans is involved in GABAergic NMJs-mediated intestinal defense. Deficiency in GABAergic neurotransmission increases reactive oxygen species (ROS) abundance and inhibits the nuclear translocation of SKN-1, whereas exogenous GABA administration represses it. SKN-1 is an important transcription factor involved in oxidative stress and the innate immune response. Moreover, deficiency in GABAergic postsynaptic UNC-49/GABAAR robustly promotes the mitochondrial function of GABAergic postsynaptic muscle cells, which may contribute to the muscular ROS decrease and intestinal SKN-1 suppression, ultimately inhibiting the intestinal defense of C. elegans. Our findings reveal a potential role of muscle mitochondrial ROS in intestinal defense in vivo and expand our understanding of mechanisms of intestinal innate immunity.

Initiating a high-temperature zinc ion battery through a triazolium-based ionic liquid.

Triazolium-based ionic liquids (T1, T2 and T3) with or without terminal hydroxyl groups were prepared via Cu(i) catalysed azide-alkyne click chemistry and their properties were investigated using various technologies. The hydroxyl groups obviously affected their physicochemical properties, where with a decrease in the number of hydroxyl groups, their stability and conductivity were enhanced. T1, T2 and T3 showed relatively high thermal stability, and their electrochemical stability windows (ESWs) were 4.76, 4.11 and 3.52 V, respectively. T1S-20 was obtained via the addition of zinc trifluoromethanesulfonic acid (Zn(CF3SO3)2) and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) to T1, displaying conductivity and ESW values of 1.55 × 10-3 S cm-1 and 6.36 V at 30 °C, respectively. Subsequently, a Zn/Li3V2(PO4)3 battery was assembled using T1S-20 as the electrolyte and its performances at 30 °C and 80 °C were investigated. The battery showed a capacity of 81 mA h g-1 at 30 °C, and its capacity retention rate was 89% after 50 cycles. After increasing the temperature to 80 °C, its initial capacity increased to 111 mA h g-1 with a capacity retention rate of 93.6% after 100 cycles, which was much higher than that of the aqueous electrolyte (WS-20)-based zinc ion battery (71.8%). Simultaneously, the T1S-20 electrolyte-based battery exhibited a good charge/discharge efficiency, and its Coulomb efficiency was 99%. Consequently, the T1S-20 electrolyte displayed a better performance in the Zn/Li3V2(PO4)3 battery than that with the aqueous electrolyte, especially at high temperature.

Current progress on plastic/microplastic degradation: Fact influences and mechanism.

Plastic pollution, particularly non-degradable residual plastic films and microplastics (MPs), is a serious environmental problem that continues to worsen each year. Numerous studies have characterized the degradation of plastic fragments; however, there is known a lack of about the state of current physicochemical biodegradation methods used for plastics treatment and their degradation efficiency. Therefore, this review explores the effects of different physicochemical factors on plastics/MPs degradation, including mechanical comminution, ultraviolet radiation, high temperature, and pH value. Further, this review discusses different mechanisms of physicochemical degradation and summarizes the degradation efficiency of these factors under various conditions. Additionally, the important role of enzymes in the biodegradation mechanism of plastics/MPs is also discussed. Collectively, the topics discussed in this review provide a solid basis for future research on plastics/MPs degradation methods and their effects.

Improved Electrochemical Performance of 0.5Li2MnO3·0.5LiNi0.5Mn0.5O2 Cathode Materials for Lithium Ion Batteries Synthesized by Ionic-Liquid-Assisted Hydrothermal Method.

Well-dispersed Li-rich Mn-based 0.5Li2MnO3·0.5LiNi0.5Mn0.5O2 nanoparticles with diameter ranging from 50 to 100 nm are synthesized by a hydrothermal method in the presence of N-hexyl pyridinium tetrafluoroborate ionic liquid ([HPy][BF4]). The microstructures and electrochemical performance of the prepared cathode materials are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and electrochemical measurements. The XRD results show that the sample prepared by ionic-liquid-assisted hydrothermal method exhibits a typical Li-rich Mn-based pure phase and lower cation mixing. SEM and TEM images indicate that the extent of particle agglomeration of the ionic-liquid-assisted sample is lower compared to the traditional hydrothermal sample. Electrochemical test results indicate that the materials synthesized by ionic-liquid-assisted hydrothermal method exhibit better rate capability and cyclability. Besides, electrochemical impedance spectroscopy (EIS) results suggest that the charge transfer resistance of 0.5Li2MnO3· 0.5LiNi0.5Mn0.5O2 synthesized by ionic-liquid-assisted hydrothermal method is much lower, which enhances the reaction kinetics.

[Determination of artemisinic acid in Artemisia annua at different growth stages based on spot area].

OBJECTIVE: Based on the important medicinal applications of artemisinic acid and the superiority of Thin Layer Chromagraphy (TLC), the spot area method of TLC was presented to determine the content changes of artemisinic acid of Artemisia annua at different growing stages. METHODS: The separation conditions including chromatographic solutions and chromogenic agent were optimized. The detection limit and the linear concentration range were analyzed. And the content changes of artemisinic acid of Artemisia annua at different growing stages were detected. RESULTS: The results showed that artemisinic acid extracted from Artemisia annua could be separated completely by the chromatographic solutions composed by petroleum ether,acetone and ethyl acetate (80: 19: 1). The artemisinic acid was clearly colored using the chromogenic agent consisting by ethanol, bromophenol blue and sulfuric acid. The detection limit of TLC was 0.05 mg/mL. The spot area of TLC had a good linear relationship within the range of 0.05-0.6 mg/mL, accorded with regression equation of y = 11.162 x + 0.0823. The results showed that the content of artemisinic acid at 0.041 mg/g in April which below the detection limit of TLC had no color spot. Contrarily, the spots of artemisinic acid were obvious in materials growing from May to September, and content was about 0.7, 1.2, 2.1, 2.4 and 2.7 mg/g, respectively corresponding to results by HPLC. CONCLUSION: The method can be applied to the quantitative analysis of artemisinic acid in Artemisia annua.

[Optimization on ultrasonic extraction technology of total coumarines in cortex fraxini].

OBJECTIVE: To optimize the ultrasonic extraction technology of total coumarins in Cortex Fraxini. METHODS: The effects of ethanol concentration, ratio of solid to liquid, extraction temperature, ultrasonic frequency and extraction time in extraction procedure on the extraction rate of total coumarins in Cortex Fraxini was researched by single factor experiment, the optimal extraction technology was determined by orthogonal experiment. RESULTS: The optimal extraction technology of total coumarins in Cortex Fraxini was:mixing the material with 60% ethanol according to ratio of solid to liquid 1:10 (W/V), ultrasonic frequency 175 W and extracting 40 min at 50 degrees C. The extraction rate of total coumarins reached 6.283% with the optimal extraction technology. CONCLUSION: Compares with the classic Soxhlet extraction, ultrasound is a less time-comsuming, low energy and great efficiency tool for the fast extraction of coumarins from Cortex Fraxini.

[Variation of content of artemisic acid in different growth stages of Artemisia annua].

OBJECTIVE: To study the variation of content of Artemisic acid of Artemisia annua from eight areas of four provinces around Wuling Mountain. METHODS: Artemisic acid of plants were extracted by organic solvent method. Qualitative and quantitative analysis of Artemisic acid were measured by thin layer chromatography (TLC) and high performance thin layer chromatography (HPLC), respectively. RESULTS: The results showed the average levels of Artemisic acid in May and August changed from 0.964 to 2.288 mg/g and from 1.837 to 3.737 mg/g, respectively. The average level in August was 1.5 times as that in May. The Artemisic acid in cultured plants was higher than the levels in wild plants, and Artemisic acid in plant collected below 300 m altitude was higher than that of the plant collected above 300 m altitude. CONCLUSION: The biosynthesis of Artemisic acid depends on the plant growth stage,which is mainly accumulated in plant at the mature stage.