13 research outputs found
Amorphous Nickel-Based Thin Film As a Janus Electrocatalyst for Water Splitting
Hydrogen generated by water splitting
provides a renewable energy source, but development of materials with
efficient electrocatalytic water splitting capability is challenging.
Thin-film electrocatalytic material (H<sub>2</sub>–NiCat) with
robust water reduction properties, which can be readily prepared by
a reduction-induced electrodeposition method from nickel salts in
a borate-buffered electrolyte (pH 9.2), is reported. The material
consists of nanoparticles with nickel oxide or hydroxide species located
at the surface and metallic nickel in the bulk. The catalyst mediates
H<sub>2</sub> evolution in a near-neutral aqueous buffer at low overpotential.
The catalyst requires a subsequent oxidative pretreatment in order
to attain a well-defined hydrogen evolution reaction (HER) activity,
and the 1.5 h anodized catalyst film exhibits a HER current density
of about 1.50 mA cm<sup>–2</sup> at 0.452 V overpotential over
a period of 24 h with no observable corrosion. In addition, it can
be converted by anodic equilibration into an amorphous Ni-based oxide
film (O<sub>2</sub>–NiCat) to catalyze O<sub>2</sub> evolution,
and the switch between the two catalytic forms is fully reversible.
The robust, bifunctional, switchable, and noble-metal-free catalytic
material has immense potential in artificial solar water-splitting
devices
Synthesis of Crystalline Pyramidal ε‑FeSi and Morphology- and Size-Dependent Ferromagnetism
Crystalline pyramidal ε-FeSi
particles smaller than 1 μm
in size with {111} lateral facets are synthesized by a spontaneous
chemical vapor deposition method. The nanocrystals initially nucleate
from the amorphous film via self-clustering forming a rectangular
ε-FeSi (001) terrace as a result of the cubic crystalline structure
and subsequent anisotropic accumulation on the terrace produces the
pyramidal morphology. Room-temperature ferromagnetism is observed
from ε-FeSi particles larger than 250 nm and having the {111}
facets. A model is postulated to explain the morphology- and size-dependent
ferromagnetism based on the nonuniform Fe atomic arrangement that
forms atomic-scale islands on the surface and dipole interaction among
these islands in the large enough particles. The morphology- and size-dependent
ferromagnetism allows control of the magnetic moments of mesostructures
and is important to spintronics and other applications
Absorption Properties and Spectroscopic Studies of Dilute Sulfur Dioxide in Aqueous Glycerol Solutions
Isothermal gas–liquid equilibrium (GLE) data were
reported
at 298.15 K and 123.15 kPa for the absorption of dilute SO<sub>2</sub> in aqueous glycerol solutions, in which SO<sub>2</sub> partial pressures
are calculated in the range of (0 to 140) Pa. The GLE data were obtained
with uncertainties within ±0.02 K for temperatures, ± 0.133
kPa for total pressures, ± 3.5% for SO<sub>2</sub> concentration
in the gas phase, and ±5% for SO<sub>2</sub> concentration in
the liquid phase. The measurements showed that the solubility of dilute
SO<sub>2</sub> in the system of glycerol (1) + water (2) increases
with the increasing glycerol concentrations in the whole composition,
and the solubility of SO<sub>2</sub> in the system of glycerol (1)
+ water (2) presents an extreme minimum of 60.1 mg·L<sup>–1</sup> at the mass fraction of <i>w</i><sub><i>1</i></sub> = 1.00 when SO<sub>2</sub> in the gas phase is designed at <i>y</i><sub>SO2</sub> = 5 × 10<sup>–4</sup>. In addition,
UV, FTIR (Fourier transform infrared), <sup>1</sup>H NMR, and fluorescence
spectra in the absorption processes of SO<sub>2</sub> in the system
of glycerol (1) + water (2) were investigated to present important
absorption mechanism. Based on the spectral results obtained, the
possibility of intermolecular hydrogen bond formation by hydroxyl
oxygen atoms in the glycerol molecule with hydrogen atom in the H<sub>2</sub>O molecule and S···O interaction formation
by hydroxyl oxygen atom in the glycerol molecule with sulfur atom
in the SO<sub>2</sub> molecule are discussed
Table_1_Transcriptomics-based investigation of molecular mechanisms underlying synergistic antimicrobial effects of AgNPs and Domiphen on the human fungal pathogen Aspergillus fumigatus.XLSX
Critically ill patients have higher risk of serious fungal infections, such as invasive aspergillosis (IA) which is mainly caused by the human fungal pathogen Aspergillus fumigatus. Triazole drugs are the primary therapeutic agents for the first-line treatment of IA, which could easily cause drug resistance problems. Here, we assess the potential of AgNPs synthesized with Artemisia argyi leaf extract and domiphen as new antifungal agents to produce synergistic antimicrobial effects on Aspergillus fumigatus, and dissect possible molecular mechanisms of action. Plate inoculation assays combined with drug susceptibility test and cytotoxicity test showed that the combination of AgNPs and domiphen has synergistic antimicrobial effects on A. fumigatus with low cytotoxicity. Gene Ontology (GO) enrichment analysis showed that AgNPs and domiphen inhibit the growth of A. fumigatus by suppressing nitrate assimilation, and purine nucleobase metabolic process and amino acid transmembrane transport, respectively. When the two drugs are combined, AgNPs has epistatic effects on domiphen. Moreover, the combination of AgNPs and domiphen primarily influence secondary metabolites biosynthesis, steroid biosynthesis and nucleotide sugar metabolism of A. fumigatus via Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis. Furthermore, protein–protein interactions (PPI) analysis combined with validation experiments showed that the combination of AgNPs and domiphen could enhance the expression of copper transporter and inhibit nitrogen source metabolism. In addition, the synergistic antimicrobial effects could be enhanced or eliminated depending on exogenous addition of copper and nitrogen source, respectively. Taken together, the results of this study provide a theoretical basis and a new strategy for the treatment of IA.</p
Data_Sheet_1_Transcriptomics-based investigation of molecular mechanisms underlying synergistic antimicrobial effects of AgNPs and Domiphen on the human fungal pathogen Aspergillus fumigatus.PDF
Critically ill patients have higher risk of serious fungal infections, such as invasive aspergillosis (IA) which is mainly caused by the human fungal pathogen Aspergillus fumigatus. Triazole drugs are the primary therapeutic agents for the first-line treatment of IA, which could easily cause drug resistance problems. Here, we assess the potential of AgNPs synthesized with Artemisia argyi leaf extract and domiphen as new antifungal agents to produce synergistic antimicrobial effects on Aspergillus fumigatus, and dissect possible molecular mechanisms of action. Plate inoculation assays combined with drug susceptibility test and cytotoxicity test showed that the combination of AgNPs and domiphen has synergistic antimicrobial effects on A. fumigatus with low cytotoxicity. Gene Ontology (GO) enrichment analysis showed that AgNPs and domiphen inhibit the growth of A. fumigatus by suppressing nitrate assimilation, and purine nucleobase metabolic process and amino acid transmembrane transport, respectively. When the two drugs are combined, AgNPs has epistatic effects on domiphen. Moreover, the combination of AgNPs and domiphen primarily influence secondary metabolites biosynthesis, steroid biosynthesis and nucleotide sugar metabolism of A. fumigatus via Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis. Furthermore, protein–protein interactions (PPI) analysis combined with validation experiments showed that the combination of AgNPs and domiphen could enhance the expression of copper transporter and inhibit nitrogen source metabolism. In addition, the synergistic antimicrobial effects could be enhanced or eliminated depending on exogenous addition of copper and nitrogen source, respectively. Taken together, the results of this study provide a theoretical basis and a new strategy for the treatment of IA.</p
Strong Facet-Induced and Light-Controlled Room-Temperature Ferromagnetism in Semiconducting β‑FeSi<sub>2</sub> Nanocubes
Crystalline
β-FeSi<sub>2</sub> nanocubes with two {100} facets
and four {011} lateral facets synthesized by spontaneous one-step
chemical vapor deposition exhibit strong room-temperature ferromagnetism
with saturation magnetization of 15 emu/g. The room-temperature ferromagnetism
is observed from the β-FeSi<sub>2</sub> nanocubes larger than
150 nm with both the {100} and {011} facets. The ferromagnetism is
tentatively explained with a simplified model including both the itinerant
electrons in surface states and the local moments on Fe atoms near
the surfaces. The work demonstrates the transformation from a nonmagnetic
semiconductor to a magnetic one by exposing specific facets and the
room-temperature ferromagnetism can be manipulated under light irradiation.
The semiconducting β-FeSi<sub>2</sub> nanocubes may have large
potential in silicon-based spintronic applications
Inverted U-Shaped Relationship between Central Venous Pressure and Intra-Abdominal Pressure in the Early Phase of Severe Acute Pancreatitis: A Retrospective Study
<div><p>Objective</p><p>Many studies have indicated that intra-abdominal pressure (IAP) is positively correlated with central venous pressure (CVP) in severe cases. However, although elevated IAP is common in patients with severe acute pancreatitis (SAP), its relationship with CVP remains unclear. Our study aimed to investigate the association of IAP with CVP in early-phase SAP patients.</p><p>Methods</p><p>In total, 116 SAP patients were included in this retrospective study. On the first day of hospitalization, blood samples were collected for biochemical examination and cytokine concentration monitoring. Additionally, a urinary catheter and right subclavian vein catheter were inserted for IAP and CVP measurement, respectively. Other routine clinical data were also recorded.</p><p>Results</p><p>Within 24 hours after hospitalization, CVP fluctuated and increased with increasing IAP up to 15.7 mmHg (<i>P</i> = 0.054) but decreased with increasing IAP when the IAP was > 15.7 mmHg (<i>P</i> < 0.001). After adjusting for abdominal perfusion pressure (APP) and mean arterial pressure (MAP), a similar distribution was observed. An inverted U-shaped trend between IAP and CVP was also present in the groups classified according to the patient’s sex, local complications, ascites, and serum amylase levels.</p><p>Conclusions</p><p>CVP and IAP have an inverted U-shaped relationship, with a peak at an IAP of 15.7 mmHg in the early phase of SAP. After this peak, CVP decreases as IAP increases. These results have crucial implications for clinical fluid resuscitation in SAP patients. In particular, because one CVP value might be correlated with different IAP values in patients with the same CVP, the volume of fluid needed might be different.</p></div
Smoothing curve of CVP (cmH<sub>2</sub>O) by IAP (mmHg) in different groups considering.
<p>A: patients' gender; B: local complication; C: ascites; D: serum amylase.</p
Adjusted Effect of IAP on CVP [β (95%CI) <i>P</i> value].
<p>Outcome variance: CVP (cmH<sub>2</sub>O); risk factor: IAP (mmHg).</p><p>Model I: Multiple regression model (no adjusted related risk factors);</p><p>Model II: Multiple regression model adjusted APP level;</p><p>Model III: Multiple regression model adjusted MAP level.</p><p>CVP: central venous pressure; IAP: intra abdominal pressure; MAP: mean arterial pressure; APP: abdominal perfusion pressure.</p><p>Adjusted Effect of IAP on CVP [β (95%CI) <i>P</i> value].</p
Characteristics of the study population by intra-abdomnal pressure quartiles.
<p>Q1: the patients with IAP≤15.7mmHg; Q2: the patients with IAP>15.7 mmHg.</p><p><i>P</i>: value from Kruskal Test (rank sum test);</p><p>*<i>P</i>: value from ANOVA.</p><p>RBC: count of red blood cell; APACHE II score: Acute Physiology and Chronic Health Evaluation II score; APP: abdominal perfusion pressure; MAP: mean arterial pressure.</p><p>[mean±SD or n(%)]</p><p>Characteristics of the study population by intra-abdomnal pressure quartiles.</p