Stable structure and fast ion diffusion: N-doped VO2 3D porous nanoflowers for applications in ultrafast rechargeable aqueous zinc-ion batteries.

Aqueous rechargeable zinc-ion batteries (ARZIBs) are promising candidates for fast-charging energy-storage systems. The issues of stronger interactions between Zn2+ and the cathode for ultrafast ARZIBs can be partially addressed by enhancing mass transfer and ion diffusion of the cathode. Herein, via thermal oxidation for the first time, N-doped VO2 porous nanoflowers with short ion diffusion paths and improved electrical conductivity were synthesized as ARZIBs cathode materials. The introduction of nitrogen derived from the vanadium-based-zeolite imidazolyl framework (V-ZIF) contributes to enhanced electrical conductivity and faster ion diffusion, while the thermal oxidation of the VS2 precursor assists the final product in exhibiting a more stable three-dimensional nanoflower structure. In particular, the N-doped VO2 cathode shows excellent cycle stability and superior rate capability with the delivered capacities of 165.02 mAh g-1 and 85 mAh g-1, at 10 A g-1 and 30 A g-1, and the capacity retention of 91.4% after 2200 cycles and 99% after 9000 cycles, respectively. Remarkably, the battery takes less than 10 s to be fully charged at 30 A g-1. Hence, this work provides a new avenue for designing unique nanostructured vanadium oxides and developing electrode materials suitable for ultrafast charging.

Nitrogen-Doped Metallic MoS2 Derived from a Metal-Organic Framework for Aqueous Rechargeable Zinc-Ion Batteries.

Molybdenum disulfide (MoS2) has been extensively studied as a potential storage material for batteries. However, the electrochemical performance of MoS2 is far from ideal, and it exhibits severe activity fading resulting from its low electronic conductivity. The present work synthesizes nitrogen (N)-doped 1T MoS2 nanoflowers made of ultrathin nanosheets via the one-step hydrothermal sulfurization of a molybdenum-based metal-organic framework precursor. The resulting metallic phase shows improved conductivity and hydrophilicity, and characterization demonstrates that N doping effectively expands the interlayer spacing and increases the concentration of sulfur vacancies serving as defects. This material demonstrates high rate performance and good cycling stability when used as the cathode in an aqueous rechargeable zinc-ion battery (ARZIB). Its performance is superior to those of pure 1T MoS2 and 2H MoS2 synthesized with MoO3 as the molybdenum source. Ex situ X-ray photoelectron spectroscopy and X-ray diffraction analyses are performed to explore the reaction mechanism during charging and discharging of the N-doped 1T MoS2. A three-cell series ARZIB system containing this material is used to power five light-emitting diodes to confirm the possible practical applications of this technology.

High stability of photovoltaic cells with phenethylammonium iodide-passivated perovskite layers and printable copper phthalocyanine-modified carbon electrodes.

Defects caused by the structural disorder of perovskites and voltage loss resulting from mismatched band structure are important issues to address to improve the performance of carbon-based perovskite solar cells. Different from the conventional approaches of additive-based passivation of perovskite precursors and introducing a hole-transport layer between the perovskite layer and carbon electrode, herein we report a defect-healing method using phenethyl ammonium iodide (PEAI) treatment and band-structure modification using high-work-function inorganic copper phthalocyanine (CuPc). Because of its relatively smoother surfaces and lower defect content, the optimized device after PEAI-based passivation of the perovskite achieves a power conversion efficiency (PCE) of 11.74%. The PCE is further raised to 13.41% through the auxiliary energy-level matching and high hole extraction abilities of the CuPc-modified carbon electrode. The best-performing device exhibits excellent moisture tolerance and thermal stability with minor current density-voltage hysteresis.

Improved photovoltage of printable perovskite solar cells via Nb5+ doped SnO2 compact layer.

The state-of-the-art perovskite solar cells (PSCs) with SnO2 electron transporting material (ETL) layer displays the probability of conquering the low electron mobility and serious leakage current loss of the TiO2 ETL layer in photoelectronic devices. The rapid development of SnO2 ETL layer has brought perovskite efficiencies >20%. However, high density of defect states and voltage loss of high temperature SnO2 are still latent impediment for the long-term stability and hysteresis effect of photovoltaics. Herein, Nb5+ doped SnO2 with deeper energy level is utilized as a compact ETL for printable mesoscopic PSCs. It promotes carrier concentration increase caused by n-type doping, assists Fermi energy level and conduction band minimum to move the deeper energy level, and significantly reduces interface carrier recombination, thus increasing the photovoltage of the device. As a result, the use of Nb5+ doped SnO2 brings high photovoltage of 0.92 V, which is 40 mV higher than that of 0.88 V for device based on SnO2 compact layer. The resulting PSCs displays outstanding efficiency of 13.53%, which contains an ∼10% improvements compared to those without Nb5+ doping. Our study emphasizes the significance of element doping for compact layer and lays the groundwork for high efficiency PSCs.

A UHPLC-QTOF-MS/MS method for the simultaneous determination of eight triterpene compounds from Poria cocos (Schw.) Wolf extract in rat plasma: Application to a comparative pharmacokinetic study.

Poria cum Radix Pini (PRP), White Poria (WP), Rubra Poria (RP), and Poriae Cutis (PC), different parts of the dried sclerotium of Poria cocos (Schw.) Wolf (PCW), have possessed various pharmacological effects and clinical application. In the present study, a novel ultra-high performance liquid chromatography/quadrupole time-of-flight mass spectrometry (UHPLC-QTOF-MS/MS) method was developed and validated for the simultaneous determination of eight triterpene compounds in rat plasma and then was applied in the comparison of pharmacokinetic characteristics of PRP, WP, RP, and PC extracts. Chromatographic separation was performed on an ACQUITY UPLC® BEH C18 (2.1 × 100 mm, 5 µm) with a mobile phase composed of aqueous solution (containing 0.5‰ formic acid and 0.5 mmol/L ammonium acetate) and acetonitrile in gradient elution. Mass spectrometric of the analytes and internal standard (IS) were conducted in negative electrospray ionization with high-resolution multiple reaction monitoring (MRMHR) mode. The lower limit of quantification (LLOQ) for the eight analytes were in the range of 2.00-20.16 ng/mL. All calibration curves showed good linearity (r > 0.993). The inter- and intra-batch precision and accuracy for the eight triterpene compounds were acceptable. The results indicated that the eight triterpene compounds displayed different pharmacokinetic characteristics in PRP, WP, RP, and PC, and that poricoic acid B, poricoic acid A, pachymic acid, dehydrotrametenolic acid, dehydrotumulosic acid, polyporenic acid C and dehydropachymic acid may be the major bioactive compounds of PCW contributing to the diuretic effect.

The increasing prevalence of myopia in junior high school students in the Haidian District of Beijing, China: a 10-year population-based survey.

BACKGROUND: Myopia is a leading cause of preventable blindness. Although, multiple cross-sectional epidemiological studies have confirmed that there is a high prevalence of myopia in high school-aged students in China. However, few longitudinal studies have been performed to assess junior high school students. In the present study, we investigate changes in the prevalence of myopia in third year junior high school (grade 9) students in the Haidian District of Beijing, China, from 2006 to 2015. METHODS: A retrospective, longitudinal cohort study was performed over 10 years. A total of 37,424 third-year middle school (grade 9) students from 8 junior high schools in Haidian district, Beijing, were included. Participants underwent a comprehensive ophthalmic examination in which they were evaluated using autorefraction under cycloplegia and submitted to retinoscopy to assess accuracy. According to the spherical equivalent refraction (SER) of the right eye, subjects were separated into the following groups: non-myopia, -0.5 ≤ SER diopters (D); low myopia, -3.0 ≤ SER < -0.5 D; moderate myopia, -6.0 ≤ SER < -3.0 D; and high myopia, SER > -6.0 D. The following characteristics were measured: refractive error; the proportion of subjects with non- myopia, low myopia, moderate myopia and high myopia; and the difference in the prevalence of myopia between male and female subjects. RESULTS: From 2006 to 2015, the prevalence of non-myopia (from 44.05% to 34.52%) and low myopia (from 32.27% to 20.73%) decreased, while the prevalence of moderate myopia (from 19.72% to 38.06%) and high myopia (from 3.96% to 6.69%) significantly increased. For refractive error, the worse eye was -2.23 ± 2.42 D (median, -1.75; range - 12.75 to +8.50) in 2006 and -3.13 ± 2.66 D (median, -2.75; range - 12.75 to +8.50) in 2015. When the entire population was considered, the overall prevalence of myopia increased from 55.95% in 2005 to 65.48% in 2015. There was a significant positive relationship between the year and the prevalence of myopia in both girls and boys. Girls were more likely than boys to have myopia (odds ratio, 1.43 [95% CI, 1.14-1.96]), especially moderate myopia, and the prevalence of moderate and high myopia were higher in girls than in boys. CONCLUSIONS: During the last 10 years, the prevalence of myopia significantly increased on an annual basis among third-year junior high school students in the Haidian District of Beijing, China. The total prevalence of myopia was significantly higher in girl than in boy participants. The refractive status of this age group deserves particular attention.

A pre-classification strategy based on UPLC-Triple-TOF/MS for metabolic screening and identification of Radix glehniae in rats.

Traditional Chinese Medicines (TCMs) have gained increasing popularity in modern society. However, the profiles of TCMs in vivo are still unclear owing to their complexity and low level in vivo. In this study, UPLC-Triple-TOF techniques were employed for data acquiring, and a novel pre-classification strategy was developed to rapidly and systematically screen and identify the absorbed constituents and metabolites of TCMs in vivo using Radix glehniae as the research object. In this strategy, pre-classification for absorbed constituents was first performed according to the similarity of their structures. Then representative constituents were elected from every class and analyzed separately to screen non-target absorbed constituents and metabolites in biosamples. This pre-classification strategy is basing on target (known) constituents to screen non-target (unknown) constituents from the massive data acquired by mass spectrometry. Finally, the screened candidate compounds were interpreted and identified based on a predicted metabolic pathway, well - studied fragmentation rules, a predicted metabolic pathway, polarity and retention time of the compounds, and some related literature. With this method, a total of 111 absorbed constituents and metabolites of Radix glehniae in rats' urine, plasma, and bile samples were screened and identified or tentatively characterized successfully. This strategy provides an idea for the screening and identification of the metabolites of other TCMs.