126 research outputs found
Versatile Surfactant/Swelling-Agent Template for Synthesis of Large-Pore Ordered Mesoporous Silicas and Related Hollow Nanoparticles
A surfactant/swelling-agent pair
suitable for templating a variety
of well-defined large-pore nanoporous silicas was identified. The
pair includes a polyÂ(ethylene oxide)-polyÂ(propylene oxide)-polyÂ(ethylene
oxide), PEO-PPO-PEO, block copolymer surfactant (Pluronic F127, EO<sub>106</sub>PO<sub>70</sub>EO<sub>106</sub>) with a large fraction of
long hydrophilic PEO blocks and a swelling agent (toluene) that strongly
solubilizes in micelles of the PEO-PPO-PEO surfactant family. Such
a combination affords micellar templates for both spherical and cylindrical
mesopores with potential to hinder cross-linking of micelle-templated
nanostructures due to stabilization of nanoparticles by long PEO chains.
Under low-temperature conditions (11–12 °C), the Pluronic
F127/toluene pair affords ultralarge-pore FDU-12 (ULP-FDU-12) silica
with face-centered cubic structure of spherical mesopores and related
hollow nanospheres, as well as large-pore SBA-15 (LP-SBA-15) with
two-dimensional hexagonal structure of cylindrical mesopores and related
silica nanotubes. ULP-FDU-12 reaches the unit-cell parameter of 69
nm, which is very large. LP-SBA-15 has a unit-cell parameter up to
26 nm and pore diameter up to ∼20 nm and is exceptionally well
ordered. The hollow nanospheres and nanotubes are attainable through
lowering of the silica-precursor/surfactant ratio. The materials templated
by spherical micelles form when the surfactant/swelling-agent solution
is kept under stirring for extended periods of time before the addition
of the silica precursor. The sizes of entrances to the hollow nanospheres
can be continuously tuned by adjusting the hydrothermal treatment
temperature. The ordered mesoporous silicas can be converted from
open-pore to closed-pore materials through the thermally induced pore
closing. The diversity in morphology, pore size, and pore connectivity
makes the proposed surfactant/swelling-agent templating system unprecedented
in the large mesopore domain
Graphene-Based Membranes for Molecular Separation
In comparison with traditional chemical
separation processes, membrane
separation is much simpler and more efficient. An ideal membrane for
molecular separation should be as thin as possible to maximize its
solvent flux, be mechanically robust to prevent it from fracture,
and have well-defined pore sizes to guarantee its selectivity. Graphene
is an excellent platform for developing size-selective membranes because
of its atomic thickness, high mechanical strength, and chemical inertness.
In this Perspective, we review the recent advancements on the fabrication
of nanoporous graphene membranes and graphene oxide membranes (GOMs)
for molecular separation. The methods of fabricating these membranes
are summarized, and the mechanisms of molecular separation based on
these two types of graphene membranes are compared. The challenges
of synthesizing and transferring large-area nanoporous graphene membranes
and engineering the performances of GOMs are discussed
Ultrasensitive and Selective Nitrogen Dioxide Sensor Based on Self-Assembled Graphene/Polymer Composite Nanofibers
Reduced graphene oxide (rGO) sheets
were self-assembled onto the
surfaces of electrospun polymer nanofibers to form an ultrathin coating.
These rGO/polymer composite nanofibers were used to fabricate nitrogen
dioxide (NO<sub>2</sub>) sensor. This sensor can be performed at room
temperature, and it exhibited a high sensitivity of 1.03 ppm<sup>–1</sup> with excellent selectivity and good reversibility. Furthermore,
the limit of detection was experimentally measured to be as low as
150 ppb, and this value is much lower than the threshold exposure
limit proposed by American Conference of Governmental Industrial Hygienists
(200 ppb)
Biocompatible and Highly Luminescent Near-Infrared CuInS<sub>2</sub>/ZnS Quantum Dots Embedded Silica Beads for Cancer Cell Imaging
Bright and stable CuInS<sub>2</sub>/ZnS@SiO<sub>2</sub> nanoparticles with near-infrared (NIR) emission
were competently prepared by incorporating the as-prepared hydrophobic
CuInS<sub>2</sub>/ZnS quantum dots (QDs) directly into lipophilic
silane micelles and subsequently an exterior silica shell was formed.
The obtained CuInS<sub>2</sub>/ZnS@SiO<sub>2</sub> nanoparticles homogeneously
comprised both single-core and multicore remarkable CuInS<sub>2</sub>/ZnS QDs, while the silica shell thickness could be controlled to
within 5–10 nm and their overall size was 17–25 nm.
Also, the functionalized CuInS<sub>2</sub>/ZnS QDs encapsulated in
the silica spheres, expedited their bioconjugation with holo-Transferrin
(Tf) for further cancer cell imaging. The CuInS<sub>2</sub>/ZnS@SiO<sub>2</sub> nanoparticles not only showed a dominant NIR band-edge luminescence
at 650–720 nm with a quantum yield (QY) between 30 and 50%,
without a recognized photoluminescence (PL) red shift, but also exhibited
excellent PL and colloidal stability in aqueous media. Impressively,
the cytotoxicity studies revealed minor suppression on cell viability
under both CuInS<sub>2</sub>/ZnS@SiO<sub>2</sub> and CuInS<sub>2</sub>/ZnS@SiO<sub>2</sub>@Tf concentrations up to 1 mg/mL. The application
in live-cell imaging revealed that the potential of CuInS<sub>2</sub>/ZnS QDs as biocompatible, robust, cadmium-free, and brilliant NIR
emitters is considered promising for fluorescent labels
One-Pot Synthesis of Fe<sub>3</sub>O<sub>4</sub> Nanoparticle Loaded 3D Porous Graphene Nanocomposites with Enhanced Nanozyme Activity for Glucose Detection
A novel
one-pot strategy is proposed to fabricate 3D porous graphene
(3D GN) decorated with Fe<sub>3</sub>O<sub>4</sub> nanoparticles (Fe<sub>3</sub>O<sub>4</sub> NPs) by using hemin as iron source. During the
process, graphene oxide was simultaneously reduced and self-assembled
to form 3D graphene hydrogel while Fe<sub>3</sub>O<sub>4</sub> NPs
synthesized from hemin distributed uniformly on 3D GN. The preparation
process is simple, facile, economical, and green. The obtained freeze-dried
product (3D GH-5) exhibits outstanding peroxidase-like activity. Compared
to the traditional 2D graphene-based nanocomposites, the introduced
3D porous structure dramatically improved the catalytic activity,
as well as the catalysis velocity and its affinity for substrate.
The high catalytic activity could be ascribed to the formation of
Fe<sub>3</sub>O<sub>4</sub> NPs and 3D porous graphene structures.
Based on its peroxidase-like activity, 3D GH-5 was used for colorimetric
determination of glucose with a low detection limit of 0.8 μM
Additional file 1: Figure S1. of Synthesis of Si-Sb-ZnO Composites as High-Performance Anodes for Lithium-ion Batteries
Cycling performance of ZnO, Si-Sb, Si-Sb-(ZnO)0.3 anode materials
Cost of drugs and hospitalization in the two groups.
<p>Cost of drugs and hospitalization in the two groups.</p
Kaplan-Meier curves for DFS (A) and OS (B) of TNBC patients in the training set according to the prognostic model.
<p>Kaplan-Meier curves for DFS (C) and OS (D) in the validation set.</p
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