Thin-film resonators and scanning probe microscopies (SPM) are usually used on low-frequency mechanical systems at the nanoscale or larger. Generally, off-chip approaches are applied to detect mechanical vibrations in these systems, but these methods are not much appropriate for atomic-thin-layer devices with ultrahigh characteristic frequencies and ultrathin thickness. Primarily, those mechanical devices based on atomic-layers provide highly improved properties, which are inapproachable with conventional nanoelectromechanical systems (NEMS). In this report, the assembly and manipulation of single-atomic-layer piezo-resonators as mass sensors with eigen mechanical resonances up to gigahertz are described. The resonators utilize electronic vibration transducers based on piezo-electric polarization charges, allowing direct and optimal atomic-layer sensor exports. This direct detection affords practical applications with the previously inapproachable Q-factor and sensitivity rather than photoelectric conversion. https://www.selleckchem.com/mTOR.html Exploration of a 2406.26 MHz membrane vibration is indicated with a thermo-noise-limited mass resolution of ∼3.0 zg (10-21 g) in room temperature. The fabricated mass sensors are contactless and fast and can afford a method for precision measurements of the ultrasmall mass with two-dimentional materials.Metal halide perovskites have received much attention for their application in light-emitting diodes (LEDs) in the past several years. Rapid progress has been made in efficient green, red, and near-infrared perovskite LEDs. However, the development of blue perovskite LEDs is still lagging far behind. Here, we report efficient sky-blue perovskite LEDs by rearranging low-dimensional phase distribution in quasi-2D perovskites. We incorporated sodium ions into the mixed-Cl/Br quasi-2D perovskites with phenylethylammonium as the organic spacer and cesium lead halide as the inorganic framework. The inclusion of the sodium ion was found to significantly reduce the formation of the n = 1 phase, which was dominated by nonradiative transition, and increase the formation of other small-n phases for efficient exciton energy transfer. By managing the phase distribution, a maximum external quantum efficiency (EQE) of 11.7% was achieved in the sky-blue perovskite LED, with a stable emission peak at 488 nm. Further optimizing the phase distribution and film morphology with Pb content, we demonstrated the sky-blue devices with the average EQE approaching 10%. This strategy of engineering phase distribution of quasi-2D perovskites with a sodium ion could provide a useful way for the fabrication of high-performance blue perovskite LEDs.Chemical modification of cellulose is beneficial to produce highly porous lithium-ion battery (LIB) separators, but introduction of high charge density adversely affects its electrochemical stability in a LiNi1/3Mn1/3Co1/3O2 (NMC)/graphite full cell. In this study, the influence of carboxylate functional groups in 2,2,6,6-tetramethylpiperidine-1-oxyl-mediated oxidized cellulose nanofibers (TOCNs) on the electrochemical performances of the LIB separator was investigated. X-ray photoelectron spectroscopy and in operando mass spectrometry measurements were used to elucidate the cause of failure of the batteries containing TOCN separators in the presence and absence of sodium counterions in the carboxylate groups and additives. For the TOCN separator with sodium carboxylate functional groups, it seems that Na deposition is the dominant reason for poor electrochemical stability of the cell thereof. The poor performance of the protonated TOCN separator, attributed to a high amount of gas evolution, is dramatically also the practical solutions to achieve high electrochemical stability of the materials.Cerium oxide nanoparticles have been shown to mimic oxidoreductase enzymes by catalyzing the decomposition of organic substrates and reactive oxygen species. This mimicry can be found in superoxide radicals and hydrogen peroxides, which are harmful molecules produced in oxidative stress-associated diseases. Despite the fact that nanoparticle functionalization is mandatory in the context of nanomedicine, the influence of polymer coatings on their enzyme-like catalytic activity is poorly understood. In this work, six polymer-coated cerium oxide nanoparticles are prepared by the association of 7.8 nm cerium oxide cores with two poly(sodium acrylate) and four poly(ethylene glycol) (PEG)-grafted copolymers with different terminal or anchoring end groups, such as phosphonic acids. The superoxide dismutase-, catalase-, peroxidase-, and oxidase-like catalytic activities of the coated nanoparticles were systematically studied. It is shown that the polymer coatings do not affect the superoxide dismutase-like, impair the catalase-like and oxidase-like, and surprisingly improves peroxidase-like catalytic activities of cerium oxide nanoparticles. It is also demonstrated that the particles coated with the PEG-grafted copolymers perform better than the poly(acrylic acid)-coated ones as oxidoreductase-like enzymes, a result that confirms the benefit of having phosphonic acids as anchoring groups at the particle surface.Carbon nitride has drawn widespread attention as a low-cost alternative to metal-based materials in the field of photocatalysis. However, the traditionally synthesized carbon nitrides always suffer a bulky architecture, which limits their intrinsic activities. Here, a cycloaddition reaction is proposed to synthesize a triazine-based precursor with implanted sodium and cyano groups, which are mostly retained in the resulting carbon nitride after the following polymerization. Incorporated sodium and cyano defects can not only tune the band structure of the carbon nitride but also provide more additive active sites. The optimized properties enable it an adorable photocatalytic hydrogen evolution rate of 1070 μmol h-1 g-1, varying by almost an order of magnitude from the pristine carbon nitride (79 μmol h-1 g-1). Moreover, a sequential self-assembly strategy has been adopted to further improve its architecture. As a consequence, a three-dimensional (3D) porous carbon nitride microtube cluster is constructed, indicating abundant exposed active sites and the faster separation of charge carriers.