13 research outputs found
In situ Free-Surfactant Synthesis and ORR- Electrochemistry of Carbon-Supported Co<sub>3</sub>S<sub>4</sub> and CoSe<sub>2</sub> Nanoparticles
In situ Free-Surfactant Synthesis and ORR- Electrochemistry of Carbon-Supported Co3S4 and CoSe2 Nanoparticle
Co<b>-</b>intercalation of Acid Red 337 and a UV Absorbent into Layered Double Hydroxides: Enhancement of Photostability
Organic–inorganic hybrid pigments
with enhanced thermo-
and photostability have been prepared by co-intercalating C.I. Acid
Red 337 (AR337) and a UV absorbent (BP-4) into the interlayer of ZnAl
layered double hydroxides through a coprecipitation method. The obtained
compounds were characterized by X-ray diffraction, Fourier transform
infrared spectroscopy, scanning electron microscopy, thermogravimetric–differential
thermogravimetric–differential thermal analysis, UV–visible
spectroscopy, and the International Commission on Illumination (CIE)
1976 L*a*b* color scales. The results show the successful co-intercalation
of AR337 and BP-4 into the interlayer region of layered double hydroxides
(LDHs) and reveal the presence of host–guest interactions between
LDH host layers and guest anions of AR337 and BP-4 and guest–guest
interactions between AR337 and BP-4. The intercalation can improve
the thermostability of AR337 due to the protection of LDH layers.
Moreover, the co-intercalation of AR337 and BP-4 not only markedly
enhances the photostability of AR337 but also significantly influences
the color of the hybrid pigment
Synthesis and Gas Sensing Performance of Dandelion-Like ZnO with Hierarchical Porous Structure
It
is of great interest to develop gas-sensing materials with excellent
performance in a facile and mild route. In this work, dandelion-like
hollow ZnO hierarchitectures assembled with ZnO nanoparticles have
been synthesized by annealing a zinc complex precursor, which was
produced from zinc acetate and ammonium bicarbonate at room temperature.
The nanoparticle size in the hierarchitectures enlarges from 10 to
23 nm with the annealing temperature increasing from 350 to 550 °C.
The ZnO hierarchitectures have shown high sensing response (34.5),
fast response (6 s) and recovery (7 s), and low optimal operating
temperature (250 °C) toward 50 ppm ethanol because of large surface
area and rich pore. Also, the obtained ZnO dandelion-like hierarchitectures
exhibits good selectivity toward alcohols. The obtained results suggest
that the dandelion-like ZnO hierarchitectures synthesized herein are
a promising gas sensing material
Template-free Synthesis of Large-Pore-Size Porous Magnesium Silicate Hierarchical Nanostructures for High-Efficiency Removal of Heavy Metal Ions
It
remains a big challenge to develop high-efficiency and low-cost adsorption
materials to remove toxic heavy metal ions in water. Here, we developed
a template-free synthesis method to fabricate high surface area and
large pore size magnesium silicate hierarchical nanostructures in
a mixed solvent of ethanol and water and carefully investigated the
corresponding adsorption behavior for Pb2+, Zn2+, and Cu2+ in aqueous solution. The results reveal that
the ethanol volume fraction in the solvent plays an important role
to optimize the pore structure, which directly determines the adsorption
capacity and the adsorption rate for heavy metal ions. When the ethanol
volume fraction is beyond 50%, the obtained magnesium silicate presents
a flowerlike structure with a hierarchical pore distribution: 0.5–2,
2–30, and 30–200 nm. When the ethanol volume faction
is 90%, for example, the sample exhibits a maximum adsorption capacity
of 436.68, 78.86, and 52.30 mg/g for Pb2+, Zn2+, and Cu2+ ions, which has a BET surface area of 650.50
m2/g and an average pore diameter of 6.89 nm, respectively.
Also, the sample presents excellent repeated adsorption performance
after three elutions. The obtained materials show widely promising
and practical applications in water treatment in a wide pH range from
2.8 to 5.8
Novel Carbon Paper@Magnesium Silicate Composite Porous Films: Design, Fabrication, and Adsorption Behavior for Heavy Metal Ions in Aqueous Solution
It
is of great and increasing interest to explore porous adsorption films
to reduce heavy metal ions in aqueous solution. Here, we for the first
time fabricated carbon paper@magnesium silicate (CP@MS) composite
films for the high-efficiency removal of Zn<sup>2+</sup> and Cu<sup>2+</sup> by a solid-phase transformation from hydromagnesite-coated
CP (CP@MCH) precursor film in a hydrothermal route and detailedly
examined adsorption process for Zn<sup>2+</sup> and Cu<sup>2+</sup> as well as the adsorption mechanism. The suitable initial pH range
is beyond 4.0 for the adsorption of the CP@MS to remove Zn<sup>2+</sup> under the investigated conditions, and the adsorption capacity is
mainly up to the pore size of the porous film. The composite film
exhibits excellent adsorption capacity for both of Zn<sup>2+</sup> and Cu<sup>2+</sup> with the corresponding maximum adsorption quantity
of 198.0 mg g<sup>–1</sup> for Zn<sup>2+</sup> and 113.5 mg
g<sup>–1</sup> for Cu<sup>2+</sup>, which are advantageous
over most of those reported in the literature. Furthermore, the adsorption
behavior of the CP@MS film follows the pseudo-second-order kinetic
model and the Langmuir adsorption equation for Zn<sup>2+</sup> with
the cation-exchange mechanism. Particularly, the CP@MS film shows
promising practical applications for the removal of heavy metal ions
in water by an adsorption–filtration system
An Unlimited Color Palette from Perylene Derivative Molecules Dispersed within Hybrids
Subject to the aggregation-caused quenching mechanism
in the solid
state, perylene and its derivatives turn out to be fascinating organic
fluorophores when separated from each other by their cointercalation
within a layered double hydroxide host structure. Such accommodation
with surfactant spacers limits their stacking usually caused by π–π
interaction between neighboring cores. For each series of fluorophores
having substitution in bay or diimide positions, an optimized composition
is selected based on optical performances and in particular on the
absolute photoluminescence quantum yield. The optimal relative quantity
of phosphor is very low from 0.001 to 0.1% of the total anionic capacity.
When dispersed into a silicone matrix, the loaded films cover from
green (510 nm) to red (625 nm) emission depending on the perylene
derivative molecules. With loaded films overlaid on a blue chip, a
warm white light (color-correlated temperature = 3890 K) with a color-rendering
index as high as 91.1 is reached. In such a light-emitting diode configuration,
the superposition of films for each fluorophore is preferred to the
powder mixture or to the cointercalation of organic phosphors within
the same structure in order to avoid too strong and nonpredictable
reabsorption phenomena between emitting centers
Facile Synthesis and Acetone Sensing Performance of Hierarchical SnO<sub>2</sub> Hollow Microspheres with Controllable Size and Shell Thickness
A facile method to prepare SnO<sub>2</sub> hollow microspheres
has been developed by using SiO<sub>2</sub> microspheres as template
and Na<sub>2</sub>SnO<sub>3</sub> as tin resource. The obtained SnO<sub>2</sub> hollow microspheres were characterized by X-ray diffraction,
scanning electron microscopy, high resolution and transmission electron
microscopy, and Brunauer–Emmett–Teller analysis, and
their sensing performance was also investigated. It was found that
the diameter of SnO<sub>2</sub> hollow microspheres can be easily
controlled in the range of 200–700 nm, and the shell thickness
can be tuned from 7.65 to 30.33 nm. The sensing tests showed that
SnO<sub>2</sub> hollow microspheres not only have high sensing response
and excellent selectivity to acetone, but also exhibit low operating
temperature and rapid response and recovery due to the small crystal
size and thin shell structure of the hollow microspheres, which facilitate
the adsorption, diffusion, and reaction of gases on the surface of
SnO<sub>2</sub> nanoparticles. Therefore, the SnO<sub>2</sub> hollow
microsphere is a promising material for the preparation of high-performance
gas sensors
Doping Metal Elements of WO<sub>3</sub> for Enhancement of NO<sub>2</sub>‑Sensing Performance at Room Temperature
WO<sub>3</sub> nanoparticles doped with Sb, Cd, and Ce were synthesized
by a chemical method to enhance the sensing performance of WO<sub>3</sub> for NO<sub>2</sub> at room temperature. The doping with Sb
element can significantly enhance the NO<sub>2</sub>-sensing properties
of WO<sub>3</sub>. Upon exposure to 10 ppm of NO<sub>2</sub>, particularly
the 2 wt % Sb-doped WO<sub>3</sub> sample exhibits a 6.8-times higher
response and an improved selectivity at room temperature compared
with those of undoped WO<sub>3</sub>. The enhanced NO<sub>2</sub>-sensing
mechanism of WO<sub>3</sub> by doping is discussed in detail, which
is mainly ascribed to the increase of oxygen vacancies in the doped
WO<sub>3</sub> samples as confirmed by Raman, photoluminescence, and
X-ray photoelectron spectroscopy spectra. In addition, the narrower
band gap may also be responsible for the enhancement of response as
observed from the corresponding ultraviolet–visible spectra
Wearable, Washable, and Highly Sensitive Piezoresistive Pressure Sensor Based on a 3D Sponge Network for Real-Time Monitoring Human Body Activities
Wearable
pressure sensors are highly desirable for monitoring human
health and realizing a nice human–machine interaction. Herein,
a chitosan/MXene/polyurethane-sponge/polyvinyl alcohol (CS/MXene/PU
sponge/PVA)-based 3D pressure sensor is developed to simultaneously
achieve wearability, washability, and high sensitivity in a wide region.
In the force-sensitive layer of the sensor, MXene and CS are fully
attached to the PU sponge to ensure that the composite sponge has
remarkable conductivity and washability. Benefiting from the highly
resistive PVA-nanowire spacer, the initial current of the sensor is
reduced significantly so that the sensor exhibits extremely high sensitivity
(84.9 kPa–1 for the less than 5 kPa region and 140.6
kPa–1 for the 5–22 kPa region). Moreover,
the sensor has an excellent fast response time of 200 ms and a short
recovery time of 30 ms, as well as non-attenuating durability over
5000 cycles. With the high sensitivity in a wide range, the sensor
is capable of detecting multiple human and animal activities in real
time, ranging from the large pressure of joint activities to a subtle
pressure of pulse. Furthermore, the sensor also demonstrates the potential
application in measuring pressure distribution. Overall, such a multifunctional
pressure sensor can supply a new platform for the design and development
of wearable health-monitoring equipment and an efficient human–machine
interface