MXene-Derived Na+ -Pillared Vanadate Cathodes for Dendrite-Free Potassium Metal Batteries.

Cation-intercalated vanadates, which have considerable promise as the cathode for high-performance potassium metal batteries (PMBs), suffer from structural collapse upon K+ insertion and desertion. Exotic cations in the vanadate cathode may ease the collapse, yet their effect on the intrinsic cation remains speculative. Herein, a stable and dendrite-free PMB, composed of a Na+ and K+ co-intercalated vanadate (NKVO) cathode and a liquid NaK alloy anode, is presented. A series of NKVO with tuneable Na/K ratios are facilely prepared using MXene precursors, in which Na+ is testified to be immobilized upon cycling, functioning as a structural pillar. Due to stronger ionic bonding and lower Fermi level of Na+ compared to K+ , moderate Na+ intercalation could reduce K+ binding to the solvation sheath and favor K+ diffusion kinetics. As a result, the MXene-derived Na+ -pillared NKVO exhibits markedly improved specific capacities, rate performance, and cycle stability than the Na+ -free counterpart. Moreover, thermally-treated carbon paper, which imitates the microscopic structure of Chinese Xuan paper, allows high surface tension liquid NaK alloy to adhere readily, enabling dendrite-free metal anodes. By clarifying the role of foreign intercalating cations, this study may lead to a more rational design of stable and high-performance electrode materials.

Nb2 CTx MXene Derived Polymorphic Nb2 O5.

Previously, heat treatment was the only feasible route for tuning the crystal phases of niobium pentoxide (Nb2 O5 ). With the use of Nb2 CTx MXene precursors, the first case of phase tuning of Nb2 O5 in the low-temperature hydrothermal synthesis using sulfuric acid regulating agents is presented. By varying the amount of the agent, four pure-phase Nb2 O5 crystals and mixed phases in-between are obtained. The required amount is found to be related to the H-covered surface energy calculated based on density functional theory. Overall, MXene-derived B-phase Nb2 O5 is of particular interest due to its exceptionally high capacities as lithium-ion battery anodes, which are three times higher than the routine synthesized one. Oxygen vacancies induced by crystallographic shear would be responsible for the extraordinary performance. The proposed phase tuning strategy encourages the prudent synthesis of difficult-to-obtain crystal phases.

MXene-Derived Metal-Organic Framework@MXene Heterostructures toward Electrochemical NO Sensing.

The electrochemical sensing of nitric oxide (NO) molecules by metal-organic framework (MOF) catalysts has been impeded, to a large extent, owing to their poor electrical conductivity and weak NO adsorption. In this work, incomplete in situ conversion of V2 CTx (T = terminal atoms) MXene to MOF is adopted, forming MOF@MXene heterostructures, which outperform MXene and MOF monocomponents toward electrochemical NO sensing. Density functional theory (DFT) calculation results indicate metal-like electronic characters for the heterostructure benefiting from the dominating contribution of the V 3d orbitals of the metallic MXene. Moreover, plane-averaged charge density difference shows substantial charge redistribution occurs at the heterointerfaces, producing a built-in field, which facilitates charge transfer. Besides, molecular mechanics-based simulated annealing calculation reveals greatly enhanced adsorption energies of NO molecules on the heterointerfaces than that on separate MOFs and MXenes. Hence, the facilitated charge transfer and preferential NO adsorption are responsible for the dramatically promoted performance toward NO sensing. The prudent design of MOF@MXene heterostructure may spur advanced electrocatalysts for electrochemical sensing.

Compositional and drug-resistance profiling of pathogens in patients with severe acute pancreatitis: a retrospective study.

BACKGROUND: Infection is one of the important causes of death in patients with severe acute pancreatitis (SAP), but the bacterial spectrum and antibiotic resistance are constantly changing. Making good use of antibiotics and controlling multi-drug-resistant (MDR) bacterial infections are of vital importance in improving the cure rate of SAP. We conducted a retrospective study in the hope of providing references for antibiotic selection and control of drug-resistant bacteria. METHODS: Retrospective analysis was performed on the data of patients hospitalized in our hospital due to acute pancreatitis (AP) in the past 5 years. General data were classified and statistically analyzed. Subsequently, the bacterial spectrum characteristics and the data related to drug-resistant bacterial infection of 569 AP patients were analyzed. Finally, unconditional logistic regression analysis was conducted to analyze the risk factors of MDR infection. RESULTS: A total of 398 patients were enrolled in this study and the hospitalization data and associated results were analyzed. A total of 461 strains of pathogenic bacteria were detected, including 223 (48.4%) gram-negative bacterial strains, 190 (41.2%) gram-positive bacterial strains and 48 (10.4%) fungal strains. The detection rates of resistance in gram-negative and gram-positive bacterial strains were 48.0% (107/223) and 25.3% (48/190), respectively. There were significant differences between the MDR group and the non-MDR group for the factors of precautionary antibiotic use, kinds of antibiotics used, receipt of carbapenem, tracheal intubation, hemofiltration and number of hospitalization days in the intensive care unit. Unconditional logistic regression revealed 2 risk factors for MDR bacterial infection. CONCLUSIONS: Our results illustrate that gram-negative bacteria were the most common pathogens in SAP infection, and the proportion of gram-positive bacteria increased notably. The rate of antibiotic resistance was higher than previously reported. Unconditional logistic regression analysis showed that using more types of antibiotics and the number of hospitalization days in the ICU were the risk factors associated with MDR bacterial infection.

Bio-derived yellow porous TiO2: the lithiation induced activation of an oxygen-vacancy dominated TiO2 lattice evoking a large boost in lithium storage performance.

Oxygen deficient TiO2 has attracted extensive attention owning to its narrow bandgap and high electrical conductivity. In this work, novel yellow TiO2 with hierarchically porous architecture is fabricated by a facile pyrolysis method in air via a biomass template. The obtained yellow TiO2 exhibits interesting lithiation induced activation during cycling, which gives rise to a phase change from poorly crystallized TiO2 to an amorphous phase, accompanied by a colour change from yellow to black. In contrast to the intercalation mechanism reported in most of the literature on the TiO2 anode of LIBs, notably, the reversible redox reaction between Ti3+ and metal Ti can be verified in this case, demonstrating the novel conversion reaction mechanism of the TiO2 electrode. Based on this, the yellow porous TiO2 delivers enhanced electrochemical performance as an anode for LIBs with a superior capacity of 480 mA h g-1 at 5 A g-1 and a high capacity of 206 mA h g-1 at 10 A g-1 after 8000 cycles.

Marine-Biomass-Derived Porous Carbon Sheets with a Tunable N-Doping Content for Superior Sodium-Ion Storage.

Synthesis of the electrode materials of sodium-ion storage devices from sustainable precursors via green methods is highly desirable. In this work, we fabricated a unique N, O dual-doped biocarbon nanosheet with hierarchical porosity by direct pyrolysis of low-cost cuttlebones and simple air oxidation activation (AOA) technique. With prolonging AOA time, thickness of the carbon sheets could be reduced controllably (from 35 to 5 nm), which may lead to tunable preparation of carbon nanosheets with a certain thickness. Besides, an unexpected increase in N-doping amount from 7.5 to 13.9 atom % was observed after AOA, demonstrating the unique role of AOA in tuning the doped heteroatoms of carbon matrix. This was also the first example of increasing N-doping content in carbons by treatment in air. More importantly, by optimizing the thickness of carbon sheets and heteroatom doping via AOA, superior sodium capacity-cycling retention-rate capability combinations were achieved. Specifically, a current state-of-the-art Na+ storage capacity of 640 mAh g-1 was obtained, which was comparable with the lithium-ion storage in carbon materials. Even after charging/discharging at large current densities (2 and 10 A g-1) for 10 000 cycles, the as-obtained samples still retained the capacities of 270 and 138 mAh g-1, respectively, with more than 90% retention. The assembled sodium-ion capacitors also delivered a high integrated energy-power density (36 kW h kg-1 at an ultrahigh power density of 53 000 W kg-1) and good cycling stability (90.5% of capacitance retention after 8000 cycles at 5 A g-1).

Preparation of adsorbents for the removal of endotoxin.

By using the agar beads as the support, L-lysine as the ligand, three kinds of absorbents with different spacers for removal of endotoxin were prepared. The adsorption capacity of three adsorbents was compared. Among them, Ag3, with L-lysine ligand and hexamethylendiamine as the spacer, was the best in adsorption capacity and was selected for hemoperfusion on rabbits. The results showed the level of endotoxin in endotoxemia rabbit after hemoperfusion was near normal level. The clearance percentage of endotoxin was 73.6%

Maternal lineages of Pinus densata, a diploid hybrid.

Previous morphological, allozyme and chloroplast DNA data have suggested that Pinus densata originated through hybridization between P. tabuliformis and P. yunnanensis. In the present study, sequence and restriction site analyses of maternally inherited mitochondrial nad1 intron were used to detect variation patterns in 19 populations of P. tabuliformis, P. yunnanensis and P. densata. A total of three mitotypes (A, B, C) were detected. All but one of the populations of P. yunnanensis possessed mitotype B while all populations of P. tabuliformis had mitotype A. Pinus densata populations, on the other hand, harboured both mitotypes A and B, which are characteristic of P. tabuliformis and P. yunnanensis, respectively. This result gives strong additional evidence supporting the hybrid origin of this diploid pine. The distribution of mitotypes indicated very different mating compositions and evolutionary history among P. densata populations. It seems that local founder populations and backcrosses may have played important roles in the early establishment of P. densata populations. The uplift of the Tibetan Plateau had a significant impact on the distribution of maternal lineages of P. densata populations.