29 research outputs found
Bifunctional OER/NRR Catalysts Based on a Thin-Layered Co<sub>3</sub>O<sub>4â<i>x</i></sub>/GO Sandwich Structure
Due to ample low-coordinated surface atoms, a distorted
lattice
endows thin-layered transition metal oxides with a flexible electronic
structure, making them the ideal candidates for overall ammonia synthesis.
This work proposes a novel and facile method for the controllable
synthesis of thin-layered Co3O4 catalysts with
graphene as a conductive matrix to further enhance the overall N2 fixation performance. X-ray photoelectron spectroscopy (XPS)
and synchrotron radiation X-ray absorption spectroscopy (XAS) demonstrate
that the sandwiched Co3O4âx/GO catalysts enable exposure of more coordination unsaturated
active sites, resulting in numerous oxygen vacancies. With a higher
conductivity and distorted crystalline structure, excellent electrochemical
NRR activity is realized with a NH3 production rate of
5.19 mmol gâ1 hâ1 and a Faradaic
efficiency of 10.68% at â0.4 V vs reversible hydrogen electrode
(RHE). The density functional theory (DFT) calculation demonstrates
that introducing oxygen vacancies in thin-layered cobalt oxides could
result in an increased density of states (DOS) near the Fermi level,
which would accelerate the NRR rate-determining step. Charge transfer
could be accelerated through a weak Co 3dâN 2p Ï hybrid
bond with a lower energy level. No obvious performance decay could
be found after six cycles. Furthermore, the sandwiched Co3O4âx/GO catalyst exhibits a low
overpotential of 280 mV@10 mA cmâ2 and an outstanding
durability for the anode OER, even better than those of the benchmark
RuO2. Such an inexpensive sandwiched transition metal oxide
catalyst shows great potential in the field of overall N2 fixation
Low genetic diversity and lack of genetic structure in the giant jellyfish <i>Nemopilema nomurai</i> in Chinese coastal waters
<p>The giant jellyfish <i>Nemopilema nomurai</i> is a scyphozoan species well-known in East Asian Marginal Seas for its damage to fisheries. The genetic diversity and population structure of <i>N. nomurai</i>, collected from five geographic regions in Chinese coastal seas, were examined based on mitochondrial cytochrome <i>c</i> oxidase subunit I (COI) gene and nuclear internal transcribed spacer one (ITS1) sequences. A total of 26 and five unique haplotypes were recovered from the COI and ITS1 genes, respectively. The overall genetic diversity of <i>N. nomurai</i> calculated by the COI and ITS1 sequences was low (haplotype diversity 0.727% and 0.108%, nucleotide diversity 0.212% and 0.039%). The median-joining network analysis revealed a star-like haplotype network. The hierarchical Analysis of Molecular Variance (AMOVA) of COI haplotypes showed that <i>N. nomurai</i> populations form a single population, with a low F<sub>ST</sub> (0.0149, <i>p</i>â=â0.1036). The dispersal ability, together with the biological characteristics, could be important factors for the lack of a geographically structured pattern in <i>N. nomurai</i> in Chinese coastal waters.</p
Enhanced Photoresponse of SnSe-Nanocrystals-Decorated WS<sub>2</sub> Monolayer Phototransistor
Single-layer WS<sub>2</sub> has shown
excellent photoresponse properties, but its promising applications
in high-sensitivity photodetection suffer from the atomic-thickness-limited
adsorption and band-gap-limited spectral selectivity. Here we have
carried out investigations on WS<sub>2</sub> monolayer based phototransistors
with and without decoration of SnSe nanocrystals (NCs) for comparison.
Compared to the solely WS<sub>2</sub> monolayer, SnSe NCs decoration
leads to not only huge enhancement of photoresponse in visible spectrum
but also extension to near-infrared. Under excitation of visible light
in a vacuum, the responsivity at zero gate bias can be enhanced by
more than 45 times to âŒ99 mA/W, and the response time is retained
in millisecond level. Particularly, with extension of photoresponse
to near-infrared (1064 nm), a responsivity of 6.6 mA/W can be still
achieved. The excellent photoresponse from visible to near-infrared
is considered to benefit from synergism of p-type SnSe NCs and n-type
WS<sub>2</sub> monolayer, or in other words, the formed p-n heterojunctions
between p-type SnSe NCs and n-type WS<sub>2</sub> monolayer
Changes in Lipid Profiles of Dried Clams (<i>Mactra chinensis Philippi</i> and <i>Ruditapes philippinarum</i>) during Accelerated Storage and Prediction of Shelf Life
To predict the shelf life through
an Arrhenius model and evaluate
the changes in lipid profiles, two types of dried clams were stored
at 50 and 65 °C and collected periodically for analysis. The
predicted shelf life values of the two dried clam samples were 530
± 14 and 487 ± 24 h (24 °C), and the relative errors
between the actual and predicted values were 5.7 and 6.8%, respectively.
During accelerated storage, the peroxide value, <i>p</i>-anisidine value, thiobarbituric acid-reactive substances value,
total oxidation value, acid value, and free fatty acid content all
increased, while the levels of triacylglycerol, phosphatidylÂcholine,
phosphatidylÂethanolÂamine, major glycerophospholipid molecular
species, and polyunsaturated fatty acid (PUFA) decreased. Moreover,
content of phospholipid containing PUFA decreased significantly than
that of triacylglycerol containing PUFA. Results indicated that the
Arrhenius model was suitable for the shelf life prediction of dried
clams and accelerated storage caused loss in quality of dried clams
in terms of lipids
Ultrahigh-Gain and Fast Photodetectors Built on Atomically Thin Bilayer Tungsten Disulfide Grown by Chemical Vapor Deposition
The
low responsivity observed in photodetectors based on monolayer transition-metal
dichalcogenides has encouraged the pursuit of approaches that can
efficiently enhance the external quantum efficiency, which relies
predominantly on the light absorption, the lifetime of the excess
carriers, and the charge collection efficiency. Here, we demonstrate
that phototransistors fabricated on large-area bilayer tungsten disulfide
(WS<sub>2</sub>) grown by chemical vapor deposition exhibit remarkable
performance with photoresponsivity, photogain, and detectivity of
up to âŒ3 Ă 10<sup>3</sup> A/W, 1.4 Ă 10<sup>4</sup>, and âŒ5 Ă 10<sup>12</sup> Jones, respectively. These
figures of merit of bilayer WS<sub>2</sub> provide a significant
advantage over monolayer WS<sub>2</sub> due to the greatly improved
carrier mobility and significantly reduced contact resistance. The
photoresponsivity of bilayer WS<sub>2</sub> phototransistor can be
further improved to up to 1 Ă 10<sup>4</sup> A/W upon biasing
a gate voltage of 60 V, without evident reduction in detectivity.
Moreover, the bilayer WS<sub>2</sub> phototransistor exhibits a high
response speed of less than 100 ÎŒs, large bandwidth of 4 kHz,
high cycling reliability of over 10<sup>5</sup> cycles, and spatially
homogeneous photoresponse. These outstanding figures of merit make
WS<sub>2</sub> bilayer a highly promising candidate for the design
of high-performance optoelectronics in the visible regime
Electrochemiluminescence Resonance Energy Transfer Based on Ru(phen)<sub>3</sub><sup>2+</sup>-Doped Silica Nanoparticles and Its Application in âTurn-onâ Detection of Ozone
Both the electrochemiluminescence
(ECL) method for sensitive detection
of ozone and the ECL resonance energy transfer (ECRET) using ozone
have been reported for the first time. It is based on the ECRET of
RuÂ(phen)<sub>3</sub><sup>2+</sup>-doped silica nanoparticles (RuSiNPs)
to indigo carmine. In the absence of ozone, the ECL of RuSiNPs is
quenched as a result of the ECRET of RuSiNPs to indigo carmine. In
the presence of ozone, the ECL of the system is âturned onâ
because ozone can oxidize indigo carmine and interrupt the ECRET from
RuSiNPs to indigo carmine. In this way, it provides a simple ECL sensing
of ozone via the proposed RuSiNP-based ECRET strategy with a linear
range from 0.05â3.0 ÎŒM and a limit of detection (LOD)
of 30 nM. The detection takes less than 5 min. This method is also
successfully applied in the analysis of ozone in human serum samples
and atmospheric samples
Stainless Steel Electrode for Sensitive Luminol Electrochemiluminescent Detection of H<sub>2</sub>O<sub>2</sub>, Glucose, and Glucose Oxidase Activity
Electrogenerated
chemiluminescence (ECL) application of stainless
steel, a robust and cost-effective material, has been developed for
the first time. Type 304 stainless steel electrode shows appealing
ECL performance in the luminolâH<sub>2</sub>O<sub>2</sub> system.
It enables the detection of H<sub>2</sub>O<sub>2</sub> with a linear
range from 1 to 1000 nM and a limit of detection of 0.456 nM [signal-to-noise
ratio (S/N) = 3]. The ECL method based on type 304 stainless steel
electrode is more sensitive, more cost-effective, and much simpler
than other ECL methods reported before. Because the stainless steel
electrode has excellent performance for H<sub>2</sub>O<sub>2</sub> detection and H<sub>2</sub>O<sub>2</sub> participates in many important
enzymatic reactions, applications of stainless steel electrode-based
ECL for detection of enzyme activities and enzyme substrates were
further investigated by use of glucose oxidase (GODx) and glucose
as representative enzyme and substrate. The concentrations of glucose
and the activity of GODx were directly proportional to ECL intensities
over a range of 0.1â1000 ÎŒM and 0.001â0.7 units/mL
with limits of detection of 0.076 ÎŒM and 0.00087 unit/mL (S/N
= 3), respectively. This method was successfully used for determining
glucose in honey. Because of their remarkable performance and user-friendly
features, stainless steel electrodes hold great promise in various
electroanalytical applications, such as biosensing, disposable sensors,
and wearable sensors
Purification of the Rv0045c protein by ion exchange chromatography and gel filtration chromatography.
<p>The Rv0045c protein was purified by anion exchange chromatography (A), cation exchange chromatography (B), and gel filtration chromatography (C). The purity was checked by SDS-PAGE analysis after each purification procedure.</p
Electric-Field Control of SpinâOrbit Torques in WS<sub>2</sub>/Permalloy Bilayers
Transition
metal dichalcogenides (TMDs) have drawn great attention owing to their
potential for electronic, optoelectronic, and spintronic applications.
In TMDs/ferromagnetic bilayers, an efficient spin current can be generated
by the TMDs to manipulate the magnetic moments in the ferromagnetic
layer. In this work, we report on the electric-field modulation of
spinâorbit torques (SOTs) in WS<sub>2</sub>/NiFe bilayers by
the spin-torque ferromagnetic resonance technique. It is found that
the radio frequency current can induce a spin accumulation at the
WS<sub>2</sub>/NiFe interface because of the interfacial RashbaâEdelstein
effect. As a consequence, the SOT ratio between the field-like and
antidamping-like torques can be effectively controlled by applying
the back-gate voltage in WS<sub>2</sub>/NiFe bilayers. These results
provide a strategy for controlling the SOT by using semiconducting
TMDs
MALDI-TOF peptide mass fingerprint (PMF) spectrometry of the Rv0045c protein.
<p>The PMF analysis was made from fragments of purified Rv0045c protein derived through trypsin digestion. The expected tryptic masses clearly matched, with 1 Da tolerance, the calculated values. The sequence coverage of these fragments was shown in bold red.</p