28 research outputs found
MagneĢli-Phase Ti<sub>4</sub>O<sub>7</sub> Nanosphere Electrocatalyst Support for Carbon-Free Oxygen Electrodes in LithiumāOxygen Batteries
Lithiumāoxygen
batteries have been considerably researched
due to their potential for high energy density compared to some rechargeable
batteries. However, it is known that the stability of a carbon-based
oxygen electrode is insufficient owing to the promotion of carbonate
formation, which results in capacity fading and large overpotential
in lithiumāoxygen batteries. To improve the chemical stability
in organic-based electrolytes, alternative electrocatalyst support
materials are required. The TiāO crystal system appears to
provide a good compromise between electrochemical performance and
cost and is thus an interesting material for further investigation.
Here, we investigate a carbon-free electrode with the goal of identifying
routes for its successful optimization. To replace carbon materials
as an electrocatalyst support, MagneĢli Ti<sub>4</sub>O<sub>7</sub> nanospheres were synthesized from anatase TiO<sub>2</sub> nanospheres via a controlled thermochemical reduction. The MagneĢli
Ti<sub>4</sub>O<sub>7</sub> nanospheres demonstrated effective overpotential
characteristics (1.53 V) compared to the anatase TiO<sub>2</sub> nanospheres
(1.91 V) during chargeādischarge cycling at a current rate
of 100 mA g<sup>ā1</sup>. Additionally, RuO<sub>2</sub>@MagneĢli-Ti<sub>4</sub>O<sub>7</sub> nanospheres were prepared as a bifunctional
catalyst-containing oxygen electrode for lithiumāoxygen batteries,
providing a remarkably reduced overpotential (0.9 V)
Highly Reversible Li Storage in Hybrid NiO/Ni/Graphene Nanocomposites Prepared by an Electrical Wire Explosion Process
NiO/Ni/graphene
nanocomposites were prepared using a simple and environmentally friendly
method comprising an electrical wire pulse technique in oleic acid
containing graphenes and subsequent annealing to form anodes for Li
ion batteries. The control product of NiO/Ni nanocomposite was prepared
under the same conditions and characterized by structural and electrochemical
analysis. The obtained NiO/Ni/graphene nanocomposite particles had
sizes of 5ā12 nm and a high surface area of 137 m<sup>2</sup> g<sup>ā1</sup>. In comparison to NiO/Ni, NiO/Ni/graphene
exhibited improved cycling performance and good rate capability. Reversible
capacity was maintained at over 600 mA h g<sup>ā1</sup> at
0.2 C and was attributed to the alleviation in volume change and improved
electrical conductivity of NiO/Ni/graphene nanocomposites
Heteroepitaxy-Induced Rutile VO<sub>2</sub> with Abundantly Exposed (002) Facets for High Lithium Electroactivity
Research on VO<sub>2</sub> cathodes
for lithium ion batteries has
been mainly focused on the VO<sub>2</sub> (B) phase. However, rutile
VO<sub>2</sub> (M/R) has rarely been studied because of the intrinsically
low lithium activity resulting from the highly anisotropic nature
of lithium accommodation. Here, we demonstrate that heteroepitaxial
engineering can be an effective strategy for activating the anisotropic
electrode and developing kinetically superior electrodes. Appropriate
lattice mismatch between the active material (VO<sub>2</sub>) and
conductive support (Sb:SnO<sub>2</sub>) yields a coherent interface,
where tensile strain aids preferential growth along the rutile <i>c</i>-axis as well as expansion in the <i>ab</i> plane
and thereby the exposure of reactive (002) facets. The VO<sub>2</sub>āSb:SnO<sub>2</sub> electrode exhibits high reversible capacity
(350 mA h g<sup>ā1</sup> at 100 mA g<sup>ā1</sup>) and
ultrafast rate capability (196 mA h g<sup>ā1</sup> at 2000
mA g<sup>ā1</sup>) with structural stability, which represents
record-high performance compared with previous VO<sub>2</sub> reports,
including those on other polymorphs such as VO<sub>2</sub> (A) and
VO<sub>2</sub> (B)
The prognostic value of CT radiomic features for patients with pulmonary adenocarcinoma treated with EGFR tyrosine kinase inhibitors
<div><p>Purpose</p><p>To determine if the radiomic features on CT can predict progression-free survival (PFS) in epidermal growth factor receptor (<i>EGFR</i>) mutant adenocarcinoma patients treated with first-line EGFR tyrosine kinase inhibitors (TKIs) and to identify the incremental value of radiomic features over conventional clinical factors in PFS prediction.</p><p>Methods</p><p>In this institutional review boardāapproved retrospective study, pretreatment contrast-enhanced CT and first follow-up CT after initiation of TKIs were analyzed in 48 patients (M:F = 23:25; median age: 61 years). Radiomic features at baseline, at 1<sup>st</sup> first follow-up, and the percentage change between the two were determined. A Cox regression model was used to predict PFS with nonredundant radiomic features and clinical factors, respectively. The incremental value of radiomic features over the clinical factors in PFS prediction was also assessed by way of a concordance index.</p><p>Results</p><p>Roundness (HR: 3.91; 95% CI: 1.72, 8.90; P = 0.001) and grey-level nonuniformity (HR: 3.60; 95% CI: 1.80, 7.18; P<0.001) were independent predictors of PFS. For clinical factors, patient age (HR: 2.11; 95% CI: 1.01, 4.39; P = 0.046), baseline tumor diameter (HR: 1.03; 95% CI: 1.01, 1.05; P = 0.002), and treatment response (HR: 0.46; 95% CI: 0.24, 0.87; P = 0.017) were independent predictors. The addition of radiomic features to clinical factors significantly improved predictive performance (concordance index; combined model = 0.77, clinical-only model = 0.69, P<0.001).</p><p>Conclusions</p><p>Radiomic features enable PFS estimation in <i>EGFR</i> mutant adenocarcinoma patients treated with first-line EGFR TKIs. Radiomic features combined with clinical factors provide significant improvement in prognostic performance compared with using only clinical factors.</p></div
Kaplan-Meier plots demonstrating the performance of each estimation model.
<p>Patients were divided in to low- and high-probability groups for progression-free survival according to the median value of output from (A) the radiomic model (HR: 5.34, 95% CI: 2.42, 11.76; P<0.001, (B) the clinical-factor model (HR: 2.51, 95% CI: 1.37, 4.59; P = 0.003), and (C) the combined model (HR: 5.49, 95% CI: 2.77, 10.89; P<0.001). CI, confidence interval; HR, hazard ratio.</p
Spearmanās rank correlation coefficients of textural parameters compared to the value of co-occurrence entropy.
<p>Abbreviations are listed in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0189766#pone.0189766.s002" target="_blank">S1 Table</a>.</p
Patient characteristics, clinical factors, and TKI treatment.
<p>Patient characteristics, clinical factors, and TKI treatment.</p
Cox proportional regression analysis of the optimal cutoff value calculated from the exploratory dataset.
<p>Cox proportional regression analysis of the optimal cutoff value calculated from the exploratory dataset.</p
Schematic flow of textural analysis.
<p><b>(A) FDG-PET/CT scan acquisition. (B) Placement of a volume of interest on the primary tumor. (C) Tumor segmentation by isocontour with SUV of 3.5 (D) Gray scale resampling and texture feature extraction in global, local, and regional scales.</b> Abbreviations: Co = Co-occurrence, NID = Neighborhood intensity difference, VA = Voxel alignment, ISZ = intensity size zone.</p