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Size-dependent connection between polystyrene nanoplastics on autophagy response throughout individual umbilical abnormal vein endothelial cells.
Inorganic p-type semiconductors have broadly served as hole transport materials (HTLs) in perovskite solar cells (PSCs) in recent years. Among them, NiCo2O4 with its excellent conductivity and hole mobility is the emerging candidate for HTLs and is attracting increasing attention. Here, we employ a simple hydrothermal method to fabricate high-quality mesoporous NiCo2O4 films as HTLs of PSCs. The study finds that the morphology of NiCo2O4 can be regulated from nanosheets (NSs) to nanowires (NWs) as the hydrothermal reaction time increases, and the morphology of NiCo2O4 significantly affects the device performance. Specially, the device with NWs achieves a best efficiency of 11.58%, ascribed to the fact that such a one dimension material could provide a straight path for hole extraction/transport. And benefiting from the mesoporous structures of NiCo2O4 films, all the devices exhibited a very repeatable and desirable long-term stability. Overall, this work develops alternative NiCo2O4 nanostructure-based HTLs and opens up new opportunities in fabricating PSCs.Oxygen-defective ceria, e.g. Gd-doped ceria, shows giant electromechanical properties related to a complex local rearrangement of its lattice. Although they are not entirely identified, the electroactive mechanisms arise from cation and oxygen vacancy (VO) pairs (i.e. Ce-VO), and the local structural elastic distortion in their surroundings. Here, we study the geometry and behaviour of Ce-VO pairs in a grain boundary-free bulk Ce0.9Gd0.1O1.95 single crystal under an AC electric field of ca. 11 kV cm-1. The analysis was carried out through X-ray absorption spectroscopy (XAS) techniques at the Ce L-III edge. Using Density Functional Theory (DFT) calculations, we investigated the effects of the strain on density of states and orbitals at the valence band edge. Our research indicates that electrostriction increases at low temperatures. The electromechanical strain has a structural nature and can rise by one order of magnitude, i.e., from 5 × 10-4 at room temperature to 5 × 10-3 at -193 °C, due to an increase in the population of the electrically active pairs. At a constant VO concentration, the material can thus configure heterogeneous pairs and elastic nanodomains that are either mechanically responsive or not.For the 22 year-old pentanitrogen cation N5+ (01), we surprisingly found that the previously reported transition states (TSs) do not correspond to N2-extrusion. We located the real N2-extrusion TS, which can well reconcile the hitherto remaining inconsistency between the gas-phase and salt-like forms of 01 both in structure and energetics.The reactivity of NOBF4 towards silylene, disilene, germylene, stannylenes has been described. Smooth syntheses of compounds of composition [PhC(NtBu)2E(= O → BF3)N(SiMe3)2, E = Si (3) and Ge (4)] were accomplished from the corresponding tetrylenes. An unusual heterocycle (10) featuring B, Sn, N, P, and O atoms was obtained from the reaction with a stannylene, while a 1,2-vicinal anti addition of fluoride was observed with a disilene (12).Herein, we developed the first Ru(ii) complex-based bioorthogonal two-photon photosensitizers. Through bioorthogonal labelling, they realize effective tumour-specific photodynamic therapy against triple-negative breast cancer cells.Quinazoline skeletons are synthesized by amino acid catabolism/reconstruction combined with the insertion/cyclization of dimethyl sulfoxide for the first time. The amino acid acts as a carbon and nitrogen source through HI-mediated catabolism and is then reconstructed using aromatic amines and dimethyl sulfoxide (DMSO) as a one-carbon synthon. This protocol is of great significance for the further study of the conversion of amino acids.A benzodifuran-based donor-acceptor covalent organic framework was synthesized and employed for efficient simulated sunlight-driven photocatalytic hydrogen evolution from water, which exhibited a superior and steady hydrogen evolution rate of 1390 μmol g-1 h-1 and an outstanding apparent quantum yield (AQY) of 7.8% was obtained at 420 nm.An artificial protocell model mimicking stimuli-triggered extracellular matrix formation is demonstrated based on the self-immobilization of coacervate microdroplets. Endogenous enzyme activity within the microdroplets results in the release of Ca2+ ions that trigger hydrogelation throughout the external environment, which in turn mechanically supports and chemically stabilizes the protocells.A facile and scalable exfoliation approach is developed to prepare large-flake, few-layer MoS2 nanosheets with the assistance of carbon nanotubes (CNTs). CNTs not only facilaite the efficient exfoliation of MoS2 nanosheets, but also benefit their subsequent electrochemical applications for both hydrogen evolution and sodium-ion storage. This CNT-mediated exfoliation approach can be extended to other kinds of 2D materials.A mitochondria-targeted near-infrared fluorescent probe NIR-V with 700 nm emission was designed to monitor cell viscosity changes with high selectivity and sensitivity, which was applied to detect the intracellular viscosity and image pancreatic tissue in a diabetic mouse model. Probe NIR-V provides an effective way to diagnose viscosity related diseases.Ligand-induced activation of CRISPR/Cas9 function is achieved based on a synergic approach through the integration of the theophylline aptamer into protein-unrecognized regions of guide RNA. This design of allosteric regulation opens a new window towards the broad involvement of RNA aptamers for conditional control of CRISPR/Cas9 function.Inspired by the architecture of the macrocycle of heme d1, a series of synthetic mono-, di- and tri-β-oxo-substituted porphyrinoid cobalt(ii) complexes were evaluated as electrocatalytic CO2 reducers, identifying complexes of unusually high efficiencies in generating multi-electron reduction products, including CH4.We demonstrate that lanthanide ions doped in nanometrical silica helices with a chirally arranged siloxane network without any organic mediates show induced chiroptical properties such as circular dichroism and circularly polarized luminescence.In this study, cellulose acetate (CA) and calcium oxide was used to manufacture an CA-CaO separator with high thermal stability and was then coated on polypropylene (PP). learn more The high melting point of CaO and the complexation of CaO and carbonyl groups in CA increased the thermal stability of CA. Because PP is known to have a higher mechanical stability than CA, the CA-CaO separator was coated twice on the PP support, increasing the stability of the entire separator. Adhesion was imparted between the CA film and the PP film without a separate adhesive due to the swelling effect of the solvent and the water pressure treatment, and pores were even formed by the pressure. Water flux data showed that cellulose acetate containing CaO coated on polypropylene (CA-CaO on PP) obtained a relatively high flux value of 71.67 L m-2 h-1 (LMH) at a pressure of 8 bar. Through thermogravimetric analysis and Fourier transform infrared data, it was confirmed that the surfaces of two polymers were bonded and the stability was improved.A photoswitchable near-infrared (NIR) fluorescent nanoparticle (NP) was designed and prepared. The NP showed a characteristic AIE property and high-contrast NIR fluorescence photoswitching with full reversibility. Such efficient NIR fluorescence photoswitching originated from the amplified fluorescence quenching mechanism based on intermolecular energy transfer in a densely packed NP state.A novel, simple, effective and rapid synthetic method to construct the C-2 trifluoromethylated indolinyl ketones via a copper-catalyzed cyclization reaction between N-alkylaniline and β-(trifluoromethyl)-α,β-unsaturated enones was developed. The results of the control experiments show that the reaction may involve a radical mechanism by a single-electron transfer process. Moreover, a broad substrate scope and good functional groups, high diastereoselectivities (dr, up to >20  1) as well as gram-scale synthesis make this approach highly attractive.Electrochemical nitrogen (N2) reduction has been regarded as a promising strategy for artificial ammonia (NH3) production under ambient conditions. Herein, we report the fabrication of molybdenum (Mo) single atoms anchored on activated carbon (Mo-SAs/AC) for the electrochemical N2 reduction to NH3. The surface-rich oxygen functional groups of activated carbon can effectively capture the Mo precursor, and concurrently act as the coordination sites to anchor Mo single atoms by forming Mo-Ox bonds. As a result, the Mo-SAs/AC as an electrocatalyst shows high activity toward the N2 reduction reaction (NRR), affording an NH3 yield rate of 2.55 ± 0.31 mg h-1 mgMo-1 and a faradaic efficiency (FE) of 57.54 ± 6.98% at -0.40 V (vs. RHE) in 0.1 M Na2SO4 electrolyte with good stability and durability. The constructed Mo-Ox sites are responsible for high NRR activity of Mo-SAs/AC.Carbanions serve as key intermediates in a variety of chemical transformations. Particularly, α-borylcarbanions have received considerable attention in recent years because of their peculiar properties, including the ability of boron atom resonance to stabilise the adjacent negatively charged carbon atom. This feature article summarises recent progress in the synthetic utilisation of α-borylcarbanions, including carbon-carbon bond formation with alkyl halides, alkenes, N-heteroarenes, and carbonyls. Carbon-boron bond formation in organohalides mediated by α-borylcarbanions is also summarised.An iron-catalyzed cascade reaction of C(sp3)-Se bond cross-coupling/C-N bond formation was developed. Various 5,13a-dihydro-6H,8H-benzo[5,6][1,3]selenazino[2,3-a]isoquinolin-8-one derivatives were synthesized under mild conditions starting from 1,2,3,4-tetrahydroisoquinolines and 2-hydroselenobenzoic acids. This protocol provides an economical approach for C(sp3)-Se bond formation.Enantioselective nickel-catalyzed reactions of (hetero)arylboronic acids or alkenylboronic acids with substrates containing an alkyne tethered to various acyclic electron-deficient alkenes are described.Correction for 'Micro/nano-net guides M2-pattern macrophage cytoskeleton distribution via Src-ROCK signalling for enhanced angiogenesis' by Yang Yang et al., Biomater. Sci., 2021, DOI 10.1039/d1bm00116g.A photoelectrochemical strategy for the cross-dehydrogenative coupling of unactivated aliphatic hydrogen donors (e.g. alkanes) with benzothiazoles is reported. We used tetrabutylammonium decatungstate as the photocatalyst to activate strong C(sp3)-H bonds in the chosen substrates, while electrochemistry scavenged the extra electrons.This study reports the development of a highly sensitive antibiotic-based discrimination and sensor platform for the detection of Gram-positive bacteria through surface-enhanced Raman spectroscopy (SERS). Herein, a combination of gold nanorod arrays (GNAs) and colloidal gold nanoparticles (AuNPs) was used as a SERS platform. To specifically capture Gram-positive bacteria, both GNAs and AuNPs were functionalized with thiol-modified vancomycin (HS-Van) molecules. Three different strains of bacteria (Bacillus subtilis and Staphylococcus aureus as Gram-positive, and Escherichia coli as Gram-negative) were employed to test the proposed system. HS-Van functionalized GNAs (GNA@Van) captured Gram-positive bacteria with high specificity. Also, the bacteria captured by GNA@Van (GNA@Van@Bct) systems showed high signal-to-noise SERS signals with high reproducibility. Addition of AuNP@Van to GNA@Van@Bct resulted in the emergence of a sandwich system (GNA@Van@Bct@Van@AuNP). This system led to a further enhanced SERS signal.
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