Abstract
Na-ion cathode materials operating at high voltage with a stable cycling behavior are needed to develop future high-energy Na-ion cells. However, the irreversible oxygen redox reaction at ...the high-voltage region in sodium layered cathode materials generates structural instability and poor capacity retention upon cycling. Here, we report a doping strategy by incorporating light-weight boron into the cathode active material lattice to decrease the irreversible oxygen oxidation at high voltages (i.e., >4.0 V vs. Na
+
/Na). The presence of covalent B–O bonds and the negative charges of the oxygen atoms ensures a robust ligand framework for the NaLi
1/9
Ni
2/9
Fe
2/9
Mn
4/9
O
2
cathode material while mitigating the excessive oxidation of oxygen for charge compensation and avoiding irreversible structural changes during cell operation. The B-doped cathode material promotes reversible transition metal redox reaction enabling a room-temperature capacity of 160.5 mAh g
−1
at 25 mA g
−1
and capacity retention of 82.8% after 200 cycles at 250 mA g
−1
. A 71.28 mAh single-coated lab-scale Na-ion pouch cell comprising a pre-sodiated hard carbon-based anode and B-doped cathode material is also reported as proof of concept.
Sodium‐ion batteries have gained much attention for their potential application in large‐scale stationary energy storage due to the low cost and abundant sodium sources in the earth. However, the ...electrochemical performance of sodium‐ion full cells (SIFCs) suffers severely from the irreversible consumption of sodium ions of cathode during the solid electrolyte interphase (SEI) formation of hard carbon anode. Here, a high‐efficiency cathode sodiation compensation reagent, sodium oxalate (Na2C2O4), which possesses both a high theoretical capacity of 400 mA h g−1 and a capacity utilization as high as 99%, is proposed. The implementation of Na2C2O4 as sacrificial sodium species is successfully realized by decreasing its oxidation potential from 4.41 to 3.97 V through tuning conductive additives with different physicochemical features, and the corresponding mechanism of oxidation potential manipulation is analyzed. Electrochemical results show that in the full cell based on a hard carbon anode and a P2‐Na2/3Ni1/3Mn1/3Ti1/3O2 cathode with Na2C2O4 as a sodium reservoir to compensate for sodium loss during SEI formation, the capacity retention is increased from 63% to 85% after 200 cycles and the energy density is improved from 129.2 to 172.6 W h kg−1. This work can provide a new avenue for accelerating the development of SIFCs.
The development of sodium‐ion batteries has been hindered so far by the irreversible consumption of sodium ions of the cathode during the solid electrolyte interphase formation. Therefore, in search of a safe, cost‐effective, and highly efficient cathode sodiation reagent, the feasibility of Na2C2O4 as a sodium reservoir source for enhancing the performance of sodium‐ion batteries is investigated.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SBCE, SBMB, UL, UM, UPUK
Covalent organic frameworks (COFs), as a new emerging class of highly crystalline advanced porous materials with fascinating structural tunability and diversity as well as the desired semiconductor ...properties, have gained significant attention as highly promising and efficient photocatalysts or designer platforms for a variety of photocatalytic applications in recent years; thus a comprehensive review is timely to summarize the advances of this field. In this review, a background and brief timeline concerning the developments and key achievements of COFs are provided. Afterwards, a systematic overview of the potential photocatalytic applications realized to date in the fast growing field of COFs is provided with the aim of presenting a full blueprint of COFs for possible photochemical energy conversion and reactions. Finally, the challenges remaining and personal perspectives on further development of this type of material for photocatalysis are presented.
In this review, a comprehensive summary of the potential photocatalytic applications realized to date in the fast-growing field of COFs is provided with the aim to present a full blueprint of COFs for photochemical energy conversion and reactions.
Low‐cost and stable sodium‐layered oxides (such as P2‐ and O3‐phases) are suggested as highly promising cathode materials for Na‐ion batteries (NIBs). Biphasic hybridization, mainly involving P2/O3 ...and P2/P3 biphases, is typically used to boost their electrochemical performances. Herein, a P3/O3 intergrown layered oxide (Na2/3Ni1/3Mn1/3Ti1/3O2) as high‐rate and long‐life cathode for NIBs via tuning the amounts of Ti substitution in Na2/3Ni1/3Mn2/3−xTixO2 (x = 0, 1/6, 1/3, 2/3) is demonstrated. The X‐ray diffraction (XRD) Rietveld refinement and aberration‐corrected scanning transmission electron microscopy show the co‐existence of P3 and O3 phases, and density functional theory calculation corroborates the appearance of the anomalous O3 phase at the Ti substitution amount of 1/3. The P3/O3 biphasic cathode delivers an unexpected rate capability (≈88.7% of the initial capacity at a high rate of 5 C) and cycling stability (≈68.7% capacity retention after 2000 cycles at 1 C), superior to those of the sing phases P3‐Na2/3Ni1/3Mn2/3O2, P3‐Na2/3Ni1/3Mn1/2Ti1/6O2, and O3‐Na2/3Ni1/3Ti2/3O2. The highly reversible structural evolution of the P3/O3 integrated cathode observed by ex situ XRD, ex situ X‐ray absorption spectra, and the rapid Na+ diffusion kinetics, underpin the enhancement. These results show the important role of P3/O3 biphasic hybridization in designing and engineering layered oxide cathodes for NIBs.
P3/O3 biphasic Na2/3Ni1/3Mn1/3Ti1/3O2 cathode material is prepared for Na‐ion batteries by tuning the Ti amounts. This P3/O3 intergrown cathode delivers superior rate capability and cycling stability to those of the pristine P3 and O3 phases, which are underpinned by the observed highly reversible structural transition of P3/O3 biphase and the rapid Na+ diffusion kinetics.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SBCE, SBMB, UL, UM, UPUK
Glioblastoma multiforme (GBM) is the most aggressive primary brain tumor due to the lack of effective therapeutic drugs. Cancer therapy targeting programmed cell death protein 1 (PD-1) or programmed ...death ligand-1 (PD-L1) is of revolutionary. However, the role of intrinsic PD-L1, which determines immune-therapy outcomes, remains largely unclear. Here we demonstrated an oncogenic role of PD-L1 via binding and activating Ras in GBM cells. RNA-sequencing transcriptome data revealed that PD-L1 significantly altered gene expression enriched in cell growth/migration/invasion pathways in human GBM cells. PD-L1 overexpression and knockout or knockdown demonstrated that PD-L1 promoted GBM cell proliferation and migration in vitro and in vivo. Mechanistically, PD-L1 prominently activated epithelial mesenchymal transition (EMT) process in a MEK/Erk- but not PI3K/Akt-dependent manner. Further, we identified intracellular interactions of PD-L1 and H-Ras, which led to Ras/Erk/EMT activation. Finally, we demonstrated that PD-L1 overexpression promoted while knockdown abolished GBM development and invasion in orthotopic GBM models of rodents. Taken together, we found that intracellular PD-L1 confers GBM cell malignancy and aggressiveness via binding Ras and activating the downstream Erk-EMT signaling. Thus, these results shed important insights in improving efficacy of immune therapy for GBM as well as other malignant tumors.
•PD-L1 overexpression promoted while knockdown abolished orthotopic glioma growth.•PD-L1 promoted GBM migration in vivo and in vitro and facilitates epithelial mesenchymal transition.•This facilitation effect is dependent on MEK/Erk but not on PI3K/Akt signaling.•PD-L1 increases Ras activity by Ras binding to activate Ras/Erk/EMT axis.
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GEOZS, IJS, IMTLJ, KILJ, KISLJ, NLZOH, NUK, OILJ, PNG, SAZU, SBCE, SBJE, UILJ, UL, UM, UPCLJ, UPUK, ZAGLJ, ZRSKP
Background Cytoreductive surgery (CRS) plus hyperthermic intraperitoneal chemotherapy (HIPEC) is the standard treatment for pseudomyxoma peritonei (PMP). It can significantly prolong the survival of ...patients, but at the same time may increase the risk of postoperative infection. Method Patients with PMP who underwent CRS + HIPEC at our center were retrospectively analyzed. According to PMP patients, basic clinical data and relevant information of postoperative infection, we analyzed the common sites of postoperative infection, results of microbial culture and the antibiotics sensitivity. Univariate and multivariate analysis were performed to explore infection-related risk factors. Result Among the 482 patients with PMP, 82 (17.0%) patients were infected after CRS + HIPEC. The most common postoperative infection was central venous catheter (CVC) infection (8.1%), followed by abdominal-pelvic infection (5.2%). There were 29 kinds of microbes isolated from the culture (the most common was Staphylococcus epidermidis), including 13 kinds of Gram-positive bacteria, 12 kinds of Gram-negative bacteria, and 4 kinds of funguses. All the antibiotics sensitivity results showed that the most sensitive antibiotics were vancomycin to Gram-positive bacteria (98.4%), levofloxacin to Gram-negative bacteria (68.5%), and fluconazole to fungus (83.3%). Univariate and multivariate analysis revealed the infection independent risk factors as follow: intraoperative blood loss greater than or equal to 350 mL (P = 0.019), ascites volume greater than or equal to 300 mL (P = 0.008). Conclusion PMP patients may have increased infection risk after CRS + HIPEC, especially CVC, abdominal-pelvic and pulmonary infections. The microbial spectrum and antibiotics sensitivity results could help clinicians to take prompt prophylactic and therapeutic approaches against postoperative infection for PMP patients. Keywords: PMP, CRS + HIPEC, postoperative infection, Bacteria, Antibiotic
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DOBA, IZUM, KILJ, NUK, PILJ, PNG, SAZU, SIK, UILJ, UKNU, UL, UM, UPUK
A
bstract
To solve the
μ
problem and generate three tiny neutrino masses in the MSSM, the
μ
from
ν
Supersymmetric Standard Model (
μν
SSM) introduces three singlet right- handed neutrino superfields, ...which lead to the mixing of the Higgs doublets with the sneutrinos. The mixing affects the lightest Higgs boson mass and the Higgs couplings. The present observed 95% CL upper limit on signal strength of the 125 GeV Higgs boson decay
h → Zγ
is 6.6, which still is plenty of space to prove the existence of new physics. In this work, we investigate the signal strength of the 125 GeV Higgs boson decay channel
h → Zγ
in the
μν
SSM. Besides, we consider the two-loop electroweak corrections of muon anomalous magnetic dipole moment (MDM) in the model, which also make important contributions compared with one-loop electroweak corrections.
The structure of hexagonal boron nitride (h-BN) is similar to that of graphite before functionalization and exfoliation. For applications in polymer nanocomposites, chemical exfoliation is a more ...economically attractive route to few-layer h-BN nanosheets. A thermal oxidation process of h-BN powder could achieve large scale exfoliation and hydroxylated functionalization, as described in prior literature. In this report, hydroxylated h-BN (BNO) was prepared by heating h-BN under air, and then covalently incorporated into epoxy resin modified with (3-isocyanatopropyl)triethoxysilane to prepare epoxy resin (EP) nanocomposites by sol-gel process. The structure and morphology of BNO were well characterized. BNO was dispersed in the EP matrix with the form of mainly exfoliated and intercalated structures, and formed strong interfacial interaction with the matrix. Thermogravimetric analysis results revealed that BNO significantly improved thermal stability and thermal oxidative resistance of EP nanocomposites at high temperature. The char yield and the temperature at 50 wt% mass loss were increased and the maximum mass loss rate was remarkably reduced. Moreover, the addition of 3 wt% BNO led to extremely high
T
g
of EP nanocomposite, 42.7 °C higher than that of pure EP, due to improved crosslinking density and confinement effect of BNO sheets on the mobility of polymer networks. Cone calorimeter test results indicated that fire safety properties of EP nanocomposites were also enhanced by the addition of BNO, such as 53.1% reduction in peak heat release rate and 32.6% decrease in total heat release, and decreased release of smoke and toxic gases. The mechanism for enhanced fire retardancy is that thermally stable condensed barrier consisting of h-BN sheets and silicon dioxide for heat and mass transfer protects the matrix from further combustion.
Structure of hexagonal boron nitride (h-BN) is similar to that of graphite before functionalization and exfoliation.
A Cp*‐Rh based D‐shaped binuclear metallacycle and a template‐free molecular Borromean ring (BR) were obtained in high yield using the semi‐rigid thioether dipyridyl ligand ...1,4‐bis(pyridin‐4‐ylthio)methylbenzene (Bptmb). The topological transformation from a binuclear metallacycle and a BR to tetranuclear metallacycles was realized via the controlled oxidation of thioethers. The strategy used in this work can be regarded as a new form of stimuli‐responsive post‐synthesis modification (PSM).
The controlled oxidation from thioether to sulfoxide and sulfone groups is a new post‐synthetic modification to achieve the stimuli‐responsive structural transformation from the molecular Borromean ring to tetranuclear metallacycles.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SBCE, SBMB, UL, UM, UPUK
Condensation of benzene-1,3,5-tricarbohydrazide with benzene-1,4-dicarboxaldehyde generated a new covalent organic framework, COF-ASB (1), in which the organic units are held together via hydrazone ...linkage to form porous frameworks. COF-ASB (1) is highly crystalline and displays good chemical and thermal stability and is permanently porous. In addition, 1 can be an ideal support to load Ru nanoparticles (Ru NPs) to generate Ru@COF-ASB (2). The obtained composite material is able to highly promote one-pot tandem synthesis of imine products from benzyl alcohols and corresponding amines under solvent-free conditions in air.
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IJS, KILJ, NUK, PNG, UL, UM
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