35 research outputs found
High Areal Capacity Hybrid MagnesiumāLithium-Ion Battery with 99.9% Coulombic Efficiency for Large-Scale Energy Storage
Hybrid magnesiumālithium-ion
batteries (MLIBs) featuring dendrite-free deposition of Mg anode and
Li-intercalation cathode are safe alternatives to Li-ion batteries
for large-scale energy storage. Here we report for the first time
the excellent stability of a high areal capacity MLIB cell and dendrite-free
deposition behavior of Mg under high current density (2 mA cm<sup>ā2</sup>). The hybrid cell showed no capacity loss for 100
cycles with Coulombic efficiency as high as 99.9%, whereas the control
cell with a Li-metal anode only retained 30% of its original capacity
with Coulombic efficiency well below 90%. The use of TiS<sub>2</sub> as a cathode enabled the highest specific capacity and one of the
best rate performances among reported MLIBs. Postmortem analysis of
the cycled cells revealed dendrite-free Mg deposition on a Mg anode
surface, while mossy Li dendrites were observed covering the Li surface
and penetrated into separators in the Li cell. The energy density
of a MLIB could be further improved by developing electrolytes with
higher salt concentration and wider electrochemical window, leading
to new opportunities for its application in large-scale energy storage
Responses of osteoblasts under varied tensile stress types induced by stretching basement materials
Osteoblasts are mechanosensitive cells. Tensile stress with different conditions, including loading time, frequency, magnitude, etc. would cause varied responses in osteoblasts. However, it was not clarified that the effect of the loading types on the osteoblasts. In this study, we focused on the effect of varied tensile stress types on osteoblasts, including isotropic stretch, biaxial stretch, and uniaxial stretch with the negative ratio of transverse strain to axial strain (NR) ā1, 0, and 0.2 respectively. Cell proliferation was determined to be most efficient when stimulated by 6% strain at a frequency of 1āHz and a negative value of 0 for 1āh/day. The varied strain resulted in a thickening of the F-actin cytoskeleton and a thinning of the nucleus. Nuclear flattening caused Yes-associated protein (YAP) to be transported to the nucleus. It was suggested that the influence of loading types on the mechanobiology responses must be noticed. The mechanism of cell mechanical sensitivity under varied loading types was explored, which would provide good suggestions for designing microstructures to control deformation patterns in bone tissue engineering.</p
Heavily nāDopable ĻāConjugated Redox Polymers with Ultrafast Energy Storage Capability
We
report here the first successful demonstration of a āĻ-conjugated
redox polymerā simultaneously featuring a Ļ-conjugated
backbone and integrated redox sites, which can be stably and reversibly
n-doped to a high doping level of 2.0 with significantly enhanced
electronic conductivity. The properties of such a heavily n-dopable
polymer, polyĀ{[<i>N</i>,<i>N</i>ā²-bisĀ(2-octyldodecyl)-1,4,5,8-naphthalenedicarboximide-2,6-diyl]-<i>alt</i>-5,5ā²-(2,2ā²-bithiophene)} (PĀ(NDI2OD-T2)),
were compared <i>vis-aĢ-vis</i> to those of the corresponding
backbone-insulated polyĀ{[<i>N</i>,<i>N</i>ā²-bisĀ(2-octyldodecyl)-1,4,5,8-naphthalenedicarboximide-2,6-diyl]-<i>alt</i>-5,5ā²-[2,2ā²-(1,2-ethanediyl)Ābithiophene]}
(PĀ(NDI2OD-TET)). When evaluated as a charge storage material for rechargeable
Li batteries, PĀ(NDI2OD-T2) delivers 95% of its theoretical capacity
at a high rate of 100C (72 s per chargeādischarge cycle) under
practical measurement conditions as well as 96% capacity retention
after 3000 cycles of deep dischargeācharge. Electrochemical,
impedance, and charge-transport measurements unambiguously demonstrate
that the ultrafast electrode kinetics of PĀ(NDI2OD-T2) are attributed
to the high electronic conductivity of the polymer in the heavily
n-doped state
Additional file 1 of Clinical courses and outcomes of COVID-19 associated pulmonary aspergillosis in 168 patients with the SARS-CoV-2 omicron variant
Supplementary Material 1: Supplementary Table 1. Comparison of laboratory results of CAPA group and non-fungal infection group. Supplementary Table 2. Differences between survival group and death group in patients with CAP
A Yolk-Shell Design for Stabilized and Scalable Li-Ion Battery Alloy Anodes
Silicon is regarded as one of the most promising anode
materials
for next generation lithium-ion batteries. For use in practical applications,
a Si electrode must have high capacity, long cycle life, high efficiency,
and the fabrication must be industrially scalable. Here, we design
and fabricate a yolk-shell structure to meet all these needs. The
fabrication is carried out without special equipment and mostly at
room temperature. Commercially available Si nanoparticles are completely
sealed inside conformal, thin, self-supporting carbon shells, with
rationally designed void space in between the particles and the shell.
The well-defined void space allows the Si particles to expand freely
without breaking the outer carbon shell, therefore stabilizing the
solid-electrolyte interphase on the shell surface. High capacity (ā¼2800
mAh/g at C/10), long cycle life (1000 cycles with 74% capacity retention),
and high Coulombic efficiency (99.84%) have been realized in this
yolk-shell structured Si electrode
Scalable Green Method to Fabricate Magnetically Separable NiFe<sub>2</sub>O<sub>4</sub>āReduced Graphene Oxide Nanocomposites with Enhanced Photocatalytic Performance Driven by Visible Light
A reduced graphene oxide (RGO)-supported
nickel ferrite (NiFe<sub>2</sub>O<sub>4</sub>) photocatalyst was prepared
by a simple mechanical
ball-milling method. No additional solvents, toxic chemical reductants,
or ultrasonic or high-temperature heat treatments were needed. The
exfoliation and reduction of graphite oxide (GO) and the <i>in
situ</i> anchoring of NiFe<sub>2</sub>O<sub>4</sub> nanoparticles
on graphene sheets were fulfilled simultaneously under the strong
shear force. The structure characterization shows that the NiFe<sub>2</sub>O<sub>4</sub> nanoparticles were uniformly dispersed on RGO
sheets. Amazingly, after coupling with an appropriate amount of RGO,
the photocatalytically inert NiFe<sub>2</sub>O<sub>4</sub> exhibited
superior photodegradation performance and recycling stability for
the degradation of organic pollutant under visible-light irradiation
at room temperature. It suggested that the synergistic effect between
RGO and NiFe<sub>2</sub>O<sub>4</sub> improved the photocatalytic
performance of the composite. Moreover, the NiFe<sub>2</sub>O<sub>4</sub>-RGO is magnetically separable for recycling. Hopefully, this
work could shed light on the environment-friendly large-scale production
of graphene-based composites through the efficient ball-milling method
ONSD measurement.
<p>The ONSD measurement was assessed 3 mm posterior to the orbit. The ONSDs of the patient with increased ICPs were significantly enlarged.</p
Time-Resolved Fluoroimmunoassay as an Advantageous Analytical Method for Assessing the Total Concentration and Environmental Risk of Fluoroquinolones in Surface Waters
Due to the widespread occurrence in the environment and
potential risk toward organisms of fluoroquinolones (FQs), it is of
importance to develop high efficient methods for assessing their occurrence
and environmental risk. A monoclonal antibody (Mab) with broad cross-reactivity
to FQs was produced by immunizing BALB/c mice with a synthesized immunogen
prepared by conjugating ciprofloxacin with bovine serum albumin. This
developed Mab (C2F3C2) showed broad and high cross-reactivity (40.3ā116%)
to 12 out of the 13 studied FQs. Using this Mab and norfloxacin conjugated
with carrier protein ovalbumin as coating antigen, a time-resolved
fluoroimmunoassay (TRFIA) method was developed for determining the
total concentration of at least 12 FQs in environmental waters. The
respective detection limit (LOD) and IC<sub>50</sub> calculated from
the standard curve were 0.053 Ī¼g/L and 1.83 Ī¼g/L for enrofloxacin
(ENR). The LODs of the other FQs, estimated based on the corresponding
cross-reactivity and the LOD of ENR, were in the range of 0.051ā0.10
Ī¼g/L. The developed TRFIA method showed good tolerance to various
interfering substances present in environmental matrix at relevant
levels, such as humic acids (0ā10 mg/L DOC), water hardness
(0ā2% Ca<sup>2+</sup> and Mg<sup>2+</sup>, w/v), and heavy
metals (0ā1 mg/L). The spiked recoveries estimated by spiking
0.5, 1, and 2 Ī¼g/L of five representative FQs into various water
samples including paddy water, tap water, pond water, and river water
were in the range of 63ā120%. The measured total FQ concentration
by TRFIA agreed well with that of liquid chromatographyātandem
mass spectrometry and was applied to directly evaluate the occurrence
and environmental risk of FQs in the surface water of a case area.
TRFIA showed high efficiency and great potential in environmental
risk assessment as it measures directly the total concentration of
a class of pollutants
Solubility Phase Diagram of the Quaternary System Li<sup>+</sup>, Mg<sup>2+</sup>//Cl<sup>ā</sup>, SO<sub>4</sub><sup>2ā</sup>āH<sub>2</sub>O at 298.15 K: Experimental Redetermination and Model Simulation
Solubility isotherms for the ternary
system MgCl<sub>2</sub>āMgSO<sub>4</sub>āH<sub>2</sub>O and the quaternary reciprocal system
Li<sup>+</sup>, Mg<sup>2+</sup>//Cl<sup>ā</sup>, SO<sub>4</sub><sup>2ā</sup>āH<sub>2</sub>O were determined at 298.15
K by an isothermal dissolution method. In the ternary phase diagram,
there are six solubility branches corresponding to the solid phases
MgSO<sub>4</sub>Ā·<i>n</i>H<sub>2</sub>O<sub>(s)</sub> (<i>n</i> = 7, 6, 5, 4, 1) and MgCl<sub>2</sub>Ā·6H<sub>2</sub>O<sub>(s)</sub>. In the quaternary equilibrium phase diagram,
there are 16 solubility co-saturated lines corresponding to the solid
phases MgSO<sub>4</sub>Ā·<i>n</i>H<sub>2</sub>O<sub>(s)</sub> (<i>n</i> = 7, 6, 5, 4, 1), MgCl<sub>2</sub>Ā·6H<sub>2</sub>O<sub>(s)</sub>, Li<sub>2</sub>SO<sub>4</sub>Ā·H<sub>2</sub>O<sub>(s)</sub>, LiClĀ·MgCl<sub>2</sub>Ā·7H<sub>2</sub>O<sub>(s)</sub>, and LiClĀ·H<sub>2</sub>O<sub>(s)</sub>. This report
describes for the first time that the equilibrium solid phases MgSO<sub>4</sub>Ā·H<sub>2</sub>O<sub>(s)</sub> and MgSO<sub>4</sub>Ā·4H<sub>2</sub>O<sub>(s)</sub> have been found to exist in this quaternary
system. However, the phase field of MgSO<sub>4</sub>Ā·H<sub>2</sub>O<sub>(s)</sub> overlaps with the phase fields of MgSO<sub>4</sub>Ā·4H<sub>2</sub>O<sub>(s)</sub> and MgSO<sub>4</sub>Ā·5H<sub>2</sub>O<sub>(s)</sub>, which indicates that MgSO<sub>4</sub>Ā·4H<sub>2</sub>O<sub>(s)</sub> and MgSO<sub>4</sub>Ā·5H<sub>2</sub>O<sub>(s)</sub> are metastable phases; MgSO<sub>4</sub>Ā·H<sub>2</sub>O<sub>(s)</sub> is a relatively more stable phase in both the ternary
and quaternary systems. A PitzerāSimonsonāClegg thermodynamic
model was used to simulate the properties of the sub-binary and subternary
systems and to predict the solubility phase diagram of the quaternary
system. The results of the modeling are in reasonable agreement with
the experimental data