Point-Contact Spectroscopy of Iron-Based Layered Superconductor LaO0.9_{0.9}F0.1−δ_{0.1-\delta}FeAs

We present point-contact spectroscopy data for junctions between a normal metal and the newly discovered F-doped superconductor LaO$_{0.9}$F$_{0.1-\delta}$FeAs (F-LaOFeAs). A zero-bias conductance peak was observed and its shape and magnitude suggests the presence of Andreev bound states at the surface of F-LaOFeAs, which provides a possible evidence of an unconventional pairing symmetry with a nodal gap function. The maximum gap value $\Delta_0\approx3.9\pm0.7$meV was determined from the measured spectra, in good agreement with the recent experiments on specific heat and lower critical field.Comment: 5 pages, 4 figure

Integrating localization and energy-awareness: A novel geographic routing protocol for underwater wireless sensor networks

Underwater wireless sensor networks (UWSNs) are the enabling technology for a new era of underwater monitoring and actuation applications. While an efficient routing protocol for data packet delivery is crucial to UWSNs, design of such a protocol faces many challenges due to the characteristics of the acoustic channel used for communication. One of the challenges is high energy consumption by sensors in routing, which critically shortens the lifespan of the sensors involved in packet delivery. In this paper, we present a novel energy-efficient localization-based geographic routing protocol EEL, which uses location information and residual energy of sensor nodes to greedily forward data packets to sink nodes. EEL periodically updates the location information of nodes in an UWSN and effectively adapt to the dynamic topological changes of the network. EEL iterates through a list of candidate forwarding nodes by considering the NADV (Normalized Advancement) of these nodes that determines their transmission priority levels. Simulation results show that EEL can effectively locate sensor nodes while significantly improving the packet delivery ratio and reducing the energy consumption in a routing process as compared to other routing protocols used by UWSNs

Construction of highly enantioenriched spirocyclopentaneoxindoles containing four consecutive stereocenters via thiourea-catalyzed asymmetric Michael–Henry cascade reactions

The thiourea-catalyzed asymmetric synthesis of highly enantioenriched spirocyclopentaneoxindoles containing chiral amide functional groups using simple 3-substituted oxindoles and nitrovinylacetamide as starting materials was achieved successfully. This protocol features operational simplicity, high atom economy, and high catalytic asymmetry, thus representing a versatile approach to the synthesis of highly enantioenriched spirocyclopentaneoxindoles

Carcinoma-associated fibroblasts derived exosomes modulate breast cancer cell stemness through exonic circHIF1A by miR-580-5p in hypoxic stress

Abstract Hypoxia is a common phenomenon in solid tumors. The roles of exosomes from hypoxic breast cancer stroma are less studied. So, the study was aimed to investigate the role of exosomes from hypoxic cancer-associated fibroblasts (CAFs) cells in breast cancer. The circRNA array analysis was performed to screen differential expressed circRNAs between hypoxic and normoxic CAFs exosomes. Candidate circHIF1A (circ_0032138) was screened out and it was confirmed that circHIF1A was up-regulated in the exosomes from hypoxic CAFs and their exosomes. Through investigating cellular functions including cell proliferation and stem cell features, it was demonstrated that hypoxic CAFs exosomes transferred circHIF1A into breast cancer cells, which played an important role in cancer stem cell properties sponging miR-580-5p by regulating CD44 expression. In a summary, circHIF1A from hypoxic CAFs exosomes played an important role in stem cell properties of breast cancer. CircHIF1A may act as a target molecule of breast cancer therapy

State-of-the-art in carbides/carbon composites for electromagnetic wave absorption

Summary: Electromagnetic wave absorbing materials (EWAMs) have made great progress in the past decades, and are playing an increasingly important role in radiation prevention and antiradar detection due to their essential attenuation toward incident EM wave. With the flourish of nanotechnology, the design of high-performance EWAMs is not just dependent on the intrinsic characteristics of single-component medium, but pays more attention to the synergistic effects from different components to generate rich loss mechanisms. Among various candidates, carbides and carbon materials are usually labeled with the features of chemical stability, low density, tunable dielectric property, and diversified morphology/microstructure, and thus the combination of carbides and carbon materials will be a promising way to acquire new EWAMs with good practical application prospects. In this review, we introduce EM loss mechanisms related to dielectric composites, and then highlight the state-of-the-art progress in carbides/carbon composites as high-performance EWAMs, including silicon carbide/carbon, MXene/carbon, molybdenum carbide/carbon, as well as some uncommon carbides/carbon composites and multicomponent composites. The critical information regarding composition optimization, structural engineering, performance reinforcement, and structure-function relationship are discussed in detail. In addition, some challenges and perspectives for the development of carbides/carbon composites are also proposed after comparing the performance of some representative composites

Ag2O and NiO Decorated CuFe2O4 with Enhanced Photocatalytic Performance to Improve the Degradation Efficiency of Methylene Blue

Dye wastewater is a serious threat to human health and life. It is an important task for researchers to treat it efficiently. Among many treatment methods, the photo-Fenton method can rapidly degrade organic pollutants. In this study, a ternary photocatalyst, Ag2O-NiO/CuFe2O4, was prepared and applied for a photo-Fenton reaction to degrade methylene blue (MB). MB had the best degradation effect when 10 mg of the catalyst were used in an 80 mL reaction system for measurement. The degradation rate of MB was up to 96.67% in 60 min with a high degradation rate constant k=5.67×10−2min−1. The total organic carbon (TOC) degradation rate was 78.64% with a TOC degradation rate constant of k=2.57×10−2min−1. Therefore, this study fully proves that Ag2O-NiO/CuFe2O4 can catalyze the photo-Fenton reaction and effectively degrade MB

A low-nuclear Ag4 nanocluster as a customized catalyst for the cyclization of propargylamine with CO2

Abstract The preparation of 2-Oxazolidinones using CO2 offers opportunities for green chemistry, but multi-site activation is difficult for most catalysts. Here, A low-nuclear Ag4 catalytic system is successfully customized, which solves the simultaneous activation of acetylene (-C≡C) and amino (-NH-) and realizes the cyclization of propargylamine with CO2 under mild conditions. As expected, the Turnover Number (TON) and Turnover Frequency (TOF) values of the Ag4 nanocluster (NC) are higher than most of reported catalysts. The Ag4* NC intermediates are isolated and confirmed their structures by Electrospray ionization (ESI) and 1H Nuclear Magnetic Resonance (1H NMR). Additionally, the key role of multiple Ag atoms revealed the feasibility and importance of low-nuclear catalysts at the atomic level, confirming the reaction pathways that are inaccessible to the Ag single-atom catalyst and Ag2 NC. Importantly, the nanocomposite achieves multiple recoveries and gram scale product acquisition. These results provide guidance for the design of more efficient and targeted catalytic materials

Enantioselective Assembly of Spirolactones through NHC-Catalyzed Remote γ‑Carbon Addition of Enals with Isatins

A chiral <i>N</i>-heterocyclic carbene (NHC)-catalyzed formal [4 + 2] annulation of β-methyl substituted enals with isatins was developed to construct six-membered spirolactones bearing highly congested quaternary carbon stereocentersin good yields and high enantioselectivities. The strategy realized a challenging remote γ-carbon addition of enals and chiral control of β-methyl substituted enals in the presence of the NHC catalyst only