117 research outputs found
Investigation on Upconversion Luminescence and Optical Temperature Sensing Behavior for Ba<sub>2</sub>Gd<sub>2</sub>Si<sub>4</sub>O<sub>13</sub>:Yb<sup>3+</sup>-Er<sup>3+</sup>/Ho<sup>3+</sup>/Tm<sup>3+</sup> Phosphors
To
explore new phosphors for temperature sensing with high detection
sensitivity, the Yb<sup>3+</sup>-Er<sup>3+</sup>/Ho<sup>3+</sup>/Tm<sup>3+</sup> doped Ba<sub>2</sub>Gd<sub>2</sub>Si<sub>4</sub>O<sub>13</sub> (BGS) was designed. Different strategies were introduced based on
the upconversion (UC) luminescence. For BGS:0.2Yb<sup>3+</sup>,0.02Er<sup>3+</sup>, the fluorescence intensity ratio (FIR) of two green emissions
of Er<sup>3+</sup> shows a gradual enhancement with increasing temperature
due to the thermally coupled levels. The piecewise expression of sensitivity
was proposed in the temperature range of 293–553 K based on
the Boltzmann distribution. For BGS:0.2Yb<sup>3+</sup>,0.01Ho<sup>3+</sup>, the FIR of the red to green emissions of Ho<sup>3+</sup> changes with temperature, showing a linear relationship from 293
to 453 K. The absolute sensitivity was gained to be 0.0452 K<sup>–1</sup>. For BGS:0.2Yb<sup>3+</sup>,0.02Tm<sup>3+</sup>, the high absolute
and relative sensitivities were both achieved by employing the thermally
coupled (<sup>3</sup>F<sub>2</sub>,<sup>3</sup>F<sub>3</sub>) and <sup>3</sup>H<sub>4</sub> levels of Tm<sup>3+</sup>. The above study could
have special reference to the development of new luminescent materials
with high sensitivity
Utilization of Li-Rich Phases in Aluminum Anodes for Improved Cycling Performance through Strategic Thermal Control
Lithium-ion batteries with aluminum anodes had appeared
to resolve
critical dendrite issues of lithium metal cells in the 1970s. However,
the poor cycling performance attributed to aluminum anodes would lead
to their obsolescence. In this work, we demonstrate how strategic
thermal control in cycling aluminum anodes circumvents the problematic
α/β phase transformations that yield poor cycling life.
Instead, electrochemical formation of the Li3Al2 and Li2–xAl phases necessitates
temperatures slightly above ambient, as the Li3Al2 and Li2–xAl phases are key enablers
for high capacity and stable cycling. While delivering a competitive
capacity level (ca. 1 Ah kg–1-Al), cycling among
those higher-order phases is found to be significantly improved, from
several cycles to 100 cycles with ca. 67% capacity retention. Importantly,
because modern battery charging is likely to occur above room temperature
due to ohmic heating, the thermal conditions explored here are expected
to be realized in a variety of applications. Furthermore, we show
that elevated temperature is not necessary for aluminum anode delithiation,
thus creating additional synergies with many practical scenarios
A Combination of Guanidyl and Phenyl Groups on a Dendrimer Enables Efficient siRNA and DNA Delivery
Gene
therapy has received considerable attention due to its great
potential in the treatment of various diseases; however, the design
of efficient and biocompatible carriers for the delivery of siRNA
as well as DNA still remains a major challenge. In this study, we
developed an efficient carrier for gene delivery by modification of
a compound containing both guanidyl and phenyl groups on the surface
of a cationic dendrimer. The guanidyl group on the dendrimer facilitates
nucleic acid condensation via specific guanidinium–phosphate
interactions, whereas the phenyl group on the polymer is critical
for efficient endosomal escape. The combination of guanidyl and phenyl
shows a synergistic effect in facilitated endocytosis. The designed
material is much more efficient in siRNA and DNA delivery than control
materials such as dendrimers engineered with a guanidyl or phenyl
group only, as well as intact dendrimers, and shows comparable efficacy
to commercial transfection reagent Lipofectamine 2000. In addition,
the material and its complex with nucleic acid show minimal toxicity
on the transfected cells. This study provides a new strategy to develop
multifunctional polymers for efficient siRNA and DNA delivery
High-Spin Iron(II) Alkynyl Complexes with N‑Heterocyclic Carbene Ligation: Synthesis, Characterization, and Reactivity Study
High-spin
ironÂ(II) alkynyl complexes [(IPr<sub>2</sub>Me<sub>2</sub>)<sub>2</sub>ÂFeÂ(Cî—¼CBu<sup><i>t</i></sup>)<sub>2</sub>]
(<b>1</b>) and [(IPr<sub>2</sub>Me<sub>2</sub>)<sub>2</sub>FeÂ(Cî—¼CR)Â(NHMes)]
(R = Bu<sup><i>t</i></sup> <b>2</b>, SiMe<sub>3</sub> <b>3</b>) bearing a monodentate N-heterocyclic carbene ligand
IPr<sub>2</sub>Me<sub>2</sub> (1,3-diisopropyl-4,5-dimethylimidazol-2-ylidene)
have been prepared by salt metathesis and/or amine elimination methods
and characterized by various spectroscopic methods. Complex <b>1</b> reacts with PMe<sub>3</sub> (4 equiv) and Bu<sup><i>t</i></sup>NC (4 equiv) to form <i>trans</i>-[(PMe<sub>3</sub>)<sub>4</sub>ÂFeÂ(Cî—¼CBu<sup><i>t</i></sup>)<sub>2</sub>] (<b>4</b>) and [η<sup>3</sup>-{(Bu<sup><i>t</i></sup>Cî—¼C)Â(Bu<sup><i>t</i></sup>)ÂCCÂ(IPr<sub>2</sub>Me<sub>2</sub>)ÂCÂ(NBu<sup><i>t</i></sup>)}ÂFeÂ(NCBu<sup><i>t</i></sup>)<sub>3</sub>]
(<b>5</b>), respectively. In contrast, the reactions of <b>1</b> with 4-Pr<sup><i>i</i></sup>-C<sub>6</sub>H<sub>4</sub>NCO and Pr<sup><i>i</i></sup>NCNPr<sup><i>i</i></sup> lead to the formation of the zwitterionic salts 4-Pr<sup><i>i</i></sup>-C<sub>6</sub>H<sub>4</sub>NCÂ(O)Â(IPr<sub>2</sub>Me<sub>2</sub>) and (Pr<sup><i>i</i></sup>N)<sub>2</sub>CÂ(IPr<sub>2</sub>Me<sub>2</sub>), respectively. The interaction of <b>1</b> with I<sub>2</sub> gives Bu<sup><i>t</i></sup>Cî—¼CCî—¼CBu<sup><i>t</i></sup> and (IPr<sub>2</sub>Me<sub>2</sub>)<sub>2</sub>FeI<sub>2</sub>. The CÂ(sp)–CÂ(sp<sup>3</sup>) cross-coupling products <i>n</i>-C<sub>8</sub>H<sub>17</sub>Cî—¼CBu<sup><i>t</i></sup> and <i>c</i>-C<sub>6</sub>H<sub>11</sub>Cî—¼CBu<sup><i>t</i></sup> are formed in high yields when <b>1</b> is treated with
the corresponding alkyl halides <i>n</i>-C<sub>8</sub>H<sub>17</sub>X and <i>c</i>-C<sub>6</sub>H<sub>11</sub>X (X
= Br, Cl). The formation of the ring-opening product 7,7-dimethyloct-1-en-5-yne
in the reaction of <b>1</b> with cyclopropylmethyl bromide supports
the radical character of the cross-coupling reaction
Upconversion Luminescence and Discussion of Sensitivity Improvement for Optical Temperature Sensing Application
Upconversion (UC)
based luminescent materials have promising applications in noncontact
temperature sensors. How to improve the sensitivity is one main object
at present. This work presented several strategies for optical temperature
sensing based on UC spectra of the Y<sub>2</sub>WO<sub>6</sub>:Yb<sup>3+</sup>-Er<sup>3+</sup>/Ho<sup>3+</sup>/Tm<sup>3+</sup> phosphors.
The improvement for the relative (<i>S</i><sub>R</sub>)
and absolute (<i>S</i><sub>A</sub>) sensitivities were discussed
by using a fluorescence intensity ratio technique. It includes thermally
coupled levels (TCLs) and non-TCLs. It was proposed that a piecewise
expression could be employed to achieve high <i>S</i><sub>A</sub> value for TCLs. However, improving the <i>S</i><sub>R</sub> value is limited for TCLs. With regard to the non-TCLs, <i>S</i><sub>R</sub> and <i>S</i><sub>A</sub> are not
restricted, but not easy to be improved synchronously. On the other
hand, the morphology and UC spectra of the samples were also studied.
The above investigation could be instructive to develop new luminescent
materials with high sensitivity
Anion Intercalation into Graphite Electrode from Ethylene Carbonate Solutions Dissolving both Lithium Hexafluorophosphate and Lithium Bis(trifluoromethanesulfonyl)imide
The
diluted solutions of lithium bis(trifluoromethanesulfonimide)
(LiTFSI) dissolving in organic solvents (ca. ethylene carbonate (EC))
are not compatible with dual-ion batteries (DIBs) mainly by virtue
of the drastic decomposition of electrolyte solutions before the reversible
storage of TFSI– in graphite positive electrodes.
In this work, lithium hexafluorophosphate (LiPF6) is introduced
into 1 M LiTFSI-EC solution to strengthen the oxidative endurance.
The EC solutions with mixed salts demonstrate a synergistic effect
in terms of anion storage in graphite electrode. The anion storage
behavior of graphite electrode in the solutions of 1 M LiTFSI+LiPF6-EC is systematically investigated by conventional electrochemical
tests of Li/graphite cells, in combination with ex situ/in situ X–ray diffraction measurements of
graphite positive electrode and energy-dispersive spectroscopic analyses
of the surface of graphite electrodes
The Value of Routine Biopsy during Percutaneous Kyphoplasty for Vertebral Compression Fractures
<div><p>Objective</p><p>Percutaneous kyphoplasty (PKP) is now widely performed to treat VCF, which is usually caused by osteoporosis. Previous researches have reported unsuspected malignancies found by biopsy. However, the safety and cost-effective profiles of routine biopsy during PKP are unclear. The purpose of this study was to evaluate the feasibility of routine biopsy during PKP in treatment of VCF.</p><p>Methods</p><p>Ninety-three patients (September 2007–November 2010) undergoing PKP without biopsy were reviewed as the control group. One hundred and three consecutive patients (November 2010–September 2013) undergoing PKP with biopsy of every operated vertebral level were prospectively enrolled as the biopsy group. The rate of unsuspected lesions was reported, and the severe adverse events, surgical duration, cement leakage rate and pain control were compared between the two groups.</p><p>Results</p><p>No statistically significant differences were found between the two groups, regarding the severe adverse events, surgical duration, cement leakage rate and pain control. Four unsuspected lesions were found in the biopsy group, three of which were malignancies with a 2.9% (3/103) unsuspected malignancy rate. The economic analysis showed that routine biopsy was cost-effective in finding new malignancies comparing with a routine cancer screening campaign.</p><p>Conclusions</p><p>Routine biopsy during PKP was safe and cost-effective in finding unsuspected malignancies. We advocate routine biopsy in every operated vertebral level during PKP for VCF patients.</p></div
Comparison of demographics, surgical duration, cement leakage rate and pain control between the biopsy and control groups.
<p>Comparison of demographics, surgical duration, cement leakage rate and pain control between the biopsy and control groups.</p
Electrostatic Assembly Preparation of High-Toughness Zirconium Diboride-Based Ceramic Composites with Enhanced Thermal Shock Resistance Performance
The
central problem of using ceramic as a structural material is
its brittleness, which associated with rigid covalent or ionic bonds.
Whiskers or fibers of strong ceramics such as silicon carbide (SiC)
or silicon nitride (Si<sub>3</sub>N<sub>4</sub>) are widely embedded
in a ceramic matrix to improve the strength and toughness. The incorporation
of these insulating fillers can impede the thermal flow in ceramic
matrix, thus decrease its thermal shock resistance that is required
in some practical applications. Here we demonstrate that the toughness
and thermal shock resistance of zirconium diboride (ZrB<sub>2</sub>)/SiC composites can be improved simultaneously by introducing graphene
into composites via electrostatic assembly and subsequent sintering
treatment. The incorporated graphene creates weak interfaces of grain
boundaries (GBs) and optimal thermal conductance paths inside composites.
In comparison to pristine ZrB<sub>2</sub>–SiC composites, the
toughness of (2.0%) ZrB<sub>2</sub>–SiC/graphene composites
exhibited a 61% increasing (from 4.3 to 6.93 MPa·m<sup>1/2</sup>) after spark plasma sintering (SPS); the retained strength after
thermal shock increased as high as 74.8% at 400 °C and 304.4%
at 500 °C. Present work presents an important guideline for producing
high-toughness ceramic-based composites with enhanced thermal shock
properties
Characterization of the Translationally Controlled Tumor Protein (TCTP) Interactome Reveals Novel Binding Partners in Human Cancer Cells
Translationally
controlled tumor protein (TCTP) is a highly conserved
housekeeping protein present in eukaryotic organisms. It is involved
in regulating many fundamental processes and plays a critical role
in tumor reversion and tumorigenesis. Increasing evidence suggests
that TCTP plays a role in the regulation of cell fate determination
and is a promising therapeutic target for cancer. To decipher the
exact mechanisms by which TCTP functions and how all these functions
are integrated, we analyzed the interactome of TCTP in HeLa cells
by coimmunoÂprecipitation (IP) and mass spectrometry (MS). A
total of 98 proteins were identified. We confirmed the in vitro and
in vivo association of TCTP with six of the identified binding proteins
using reciprocal IP and bimolecular fluorescence complementation (BiFC)
analysis, respectively. Moreover, TCTP interacted with Y-box-binding
protein 1 (YBX1), and their interaction was localized to the N-terminal
region of TCTP and the 1–129 amino acid (aa) residues of YBX1.
The YBX1 protein plays an important role in cell proliferation, RNA
splicing, DNA repair, drug resistance, and stress response to extracellular
signals. These data suggest that the interaction of TCTP with YBX1
might cooperate or coordinate their functions in the control of diverse
regulatory pathways in cancer cells. Taken together, our results not
only reveal a large number of TCTP-associated proteins that possess
pleiotropic functions, but also provide novel insights into the molecular
mechanisms of TCTP in tumorigenesis
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