Exploration of low‐cost and earth‐abundant photocatalysts for highly efficient solar photocatalytic water splitting is of great importance. Although transition‐metal dichalcogenides (TMDs) showed ...outstanding performance as co‐catalysts for the hydrogen evolution reaction (HER), designing TMD‐hybridized photocatalysts with abundant active sites for the HER still remains challenge. Here, a facile one‐pot wet‐chemical method is developed to prepare MS2–CdS (M=W or Mo) nanohybrids. Surprisedly, in the obtained nanohybrids, single‐layer MS2 nanosheets with lateral size of 4–10 nm selectively grow on the Cd‐rich (0001) surface of wurtzite CdS nanocrystals. These MS2–CdS nanohybrids possess a large number of edge sites in the MS2 layers, which are active sites for the HER. The photocatalytic performances of WS2–CdS and MoS2–CdS nanohybrids towards the HER under visible light irradiation (>420 nm) are about 16 and 12 times that of pure CdS, respectively. Importantly, the MS2–CdS nanohybrids showed enhanced stability after a long‐time test (16 h), and 70 % of catalytic activity still remained.
A single layer makes the difference: MS2–CdS (M=W or Mo) nanohybrids with single‐layer MS2 nanosheets selectively grown on the Cd‐rich (0001) surface of wurtzite CdS nanocrystals (see picture) are synthesized by a facile one‐pot wet‐chemical method. The MS2–CdS nanohybrids showed excellent photocatalytic activity towards the hydrogen evolution reaction and good stability.
Understanding the molecular mechanisms regulating the maintenance and destruction of intervertebral disc may lead to the development of new therapies for intervertebral disc degeneration (IDD). Here ...we present evidence from miRNA microarray analyses of clinical data sets along with in vitro and in vivo experiments that miR-141 is a key regulator of IDD. Gain- and loss-of-function studies show that miR-141 drives IDD by inducing nucleus pulposus (NP) apoptosis. Furthermore, miR-141 KO in mice attenuated spontaneous and surgically induced IDD. Mechanistically, miR-141 promotes IDD development by targeting and depleting SIRT1, a negative regulator of NF-κB pathway. Therapeutically, upregulation or downregulation of miR-141 by nanoparticle delivery in IDD model aggravated or alleviated experimental IDD, respectively. Our findings reveal a novel mechanism by which miR-141, in part, promotes IDD progression by interacting with SIRT1/NF-κB pathway. Blockade of miR-141 in vivo may serve as a potential therapeutic approach in the treatment of IDD.
Phase control plays an important role in the precise synthesis of inorganic materials, as the phase structure has a profound influence on properties such as conductivity and chemical stability. ...Phase-controlled preparation has been challenging for the metallic-phase group-VI transition metal dichalcogenides (the transition metals are Mo and W, and the chalcogens are S, Se and Te), which show better performance in electrocatalysis than their semiconducting counterparts. Here, we report the large-scale preparation of micrometre-sized metallic-phase 1T′-MoX2 (X = S, Se)-layered bulk crystals in high purity. We reveal that 1T′-MoS2 crystals feature a distorted octahedral coordination structure and are convertible to 2H-MoS2 following thermal annealing or laser irradiation. Electrochemical measurements show that the basal plane of 1T′-MoS2 is much more active than that of 2H-MoS2 for the electrocatalytic hydrogen evolution reaction in an acidic medium.
Yolk/shell particles possess a unique structure that is composed of hollow shells that encapsulate other particles but with an interstitial space between them. These structures are different from ...core/shell particles in that the core particles are freely movable in the shell. Yolk/shell particles combine the properties of each component, and can find potential applications in catalysis, lithium ion batteries, and biosensors. In this Research News article, a soft‐template‐assisted method for the preparation of yolk/silica shell particles is presented. The demonstrated method is simple and general, and can produce hollow silica spheres incorporated with different particles independent of their diameters, geometry, and composition. Furthermore, yolk/mesoporous silica shell particles and multishelled particles are also prepared through optimization of the experimental conditions. Finally, potential applications of these particles are discussed.
A mixture of anionic and zwitterionic surfactants was used as soft templates for the preparation of yolk/silica shell particles. Moreover, it is demonstrated that yolk/mesoporous silica shell particles and multishelled particles can be synthesized by this strategy (see figure).
We report acute antibody responses to SARS-CoV-2 in 285 patients with COVID-19. Within 19 days after symptom onset, 100% of patients tested positive for antiviral immunoglobulin-G (IgG). ...Seroconversion for IgG and IgM occurred simultaneously or sequentially. Both IgG and IgM titers plateaued within 6 days after seroconversion. Serological testing may be helpful for the diagnosis of suspected patients with negative RT-PCR results and for the identification of asymptomatic infections.
Nanostructured transition metal dichalcogenides (TMDs) are proven to be efficient and robust earth‐abundant electrocatalysts to potentially replace precious platinum‐based catalysts for the hydrogen ...evolution reaction (HER). However, the catalytic efficiency of reported TMD catalysts is still limited by their low‐density active sites, low conductivity, and/or uncleaned surface. Herein, a general and facile method is reported for high‐yield, large‐scale production of water‐dispersed, ultrasmall‐sized, high‐percentage 1T‐phase, single‐layer TMD nanodots with high‐density active edge sites and clean surface, including MoS2, WS2, MoSe2, Mo0.5W0.5S2, and MoSSe, which exhibit much enhanced electrochemical HER performances as compared to their corresponding nanosheets. Impressively, the obtained MoSSe nanodots achieve a low overpotential of −140 mV at current density of 10 mA cm−2, a Tafel slope of 40 mV dec−1, and excellent long‐term durability. The experimental and theoretical results suggest that the excellent catalytic activity of MoSSe nanodots is attributed to the high‐density active edge sites, high‐percentage metallic 1T phase, alloying effect and basal‐plane Se‐vacancy. This work provides a universal and effective way toward the synthesis of TMD nanostructures with abundant active sites for electrocatalysis, which can also be used for other applications such as batteries, sensors, and bioimaging.
A general and facile method is developed for high‐yield, large‐scale production of water‐dispersed, ultrasmall, high‐percentage 1T‐phase, single‐layer transition metal dichalcogenide nanodots with high‐density active edge sites and clean surface, including MoS2, WS2, MoSe2, Mo0.5W0.5S2, and MoSSe, which exhibit much enhanced electrochemical hydrogen evolution reaction performances as compared to their corresponding nanosheets.
This paper investigates adaptive fuzzy tracking control for high-order nonlinear time-delay systems with full-state constraints and input saturation. By adopting fuzzy approximation technique, ...frequently used growth assumptions imposed on unknown system nonlinearities are removed. High-order barrier Lyapunov functions are employed to prevent the transgression of full-state constraints. The auxiliary subsystem and the Nussbaum gain technique are utilized to analyze the effect of input saturation. Appropriate Lyapunov-Krasovskii functionals are constructed to compensate the adverse effect caused by the unknown time-delay. Novel feasibility conditions are formulated as sufficient conditions for the existence of proposed control. It is rigorously proved that all the closed-loop signals are bounded in the semi-global sense, error signals converge to small bounded compact sets, full-state constraints, and input saturation are not violated, and the arguments of unknown nonlinearities are constrained within a compact set, on which fuzzy approximation is valid. Eventually, the theoretical result is confirmed by two simulation examples.
Crystal-phase engineering offers opportunities for the rational design and synthesis of noble metal nanomaterials with unusual crystal phases that normally do not exist in bulk materials. However, it ...remains a challenge to use these materials as seeds to construct heterometallic nanostructures with desired crystal phases and morphologies for promising applications such as catalysis. Here, we report a strategy for the synthesis of binary and ternary hybrid noble metal nanostructures. Our synthesized crystal-phase heterostructured 4H/fcc Au nanowires enable the epitaxial growth of Ru nanorods on the 4H phase and fcc-twin boundary in Au nanowires, resulting in hybrid Au-Ru nanowires. Moreover, the method can be extended to the epitaxial growth of Rh, Ru-Rh and Ru-Pt nanorods on the 4H/fcc Au nanowires to form unique hybrid nanowires. Importantly, the Au-Ru hybrid nanowires with tunable compositions exhibit excellent electrocatalytic performance towards the hydrogen evolution reaction in alkaline media.
Semiconducting nanosheets with microscale lateral size are attractive building blocks for the fabrication of electronic and optoelectronic devices. The phase‐controlled chemical synthesis of ...semiconducting nanosheets is of particular interest, because their intriguing properties are not only related to their size and shape, but also phase‐dependent. Herein, a facile method for the synthesis of phase‐pure, microsized, two‐dimensional (2D) CuSe nanosheets with an average thickness of approximately 5 nm is demonstrated. These hexagonal‐phased CuSe nanosheets were transformed into cubic‐phased Cu2−xSe nanosheets with the same morphology simply by treatment with heat in the presence of CuI cations. The phase transformation, proposed to be a template‐assisted process, can be extended to other systems, such as CuS and Cu1.97S nanoplates. Our study offers a new method for the phase‐controlled preparation of 2D nanomaterials, which are not readily accessible by conventional wet‐chemical methods.
Not fazed by change: A facile solution‐based strategy was used for the preparation of microsized CuSe nanosheets. As‐prepared CuSe with a hexagonal phase was transformed into Cu2−xSe with a cubic phase through simple treatment with heat without damaging the shape of the original 2D nanosheets (see picture). The two kinds of nanosheets show different optical properties and are both promising building blocks for the construction of various devices.
Phase engineering of nanomaterials (PEN) offers a promising route to rationally tune the physicochemical properties of nanomaterials and further enhance their performance in various applications. ...However, it remains a great challenge to construct well‐defined crystalline@amorphous core–shell heterostructured nanomaterials with the same chemical components. Herein, the synthesis of binary (Pd‐P) crystalline@amorphous heterostructured nanoplates using Cu3−χP nanoplates as templates, via cation exchange, is reported. The obtained nanoplate possesses a crystalline core and an amorphous shell with the same elemental components, referred to as c‐Pd‐P@a‐Pd‐P. Moreover, the obtained c‐Pd‐P@a‐Pd‐P nanoplates can serve as templates to be further alloyed with Ni, forming ternary (Pd‐Ni‐P) crystalline@amorphous heterostructured nanoplates, referred to as c‐Pd‐Ni‐P@a‐Pd‐Ni‐P. The atomic content of Ni in the c‐Pd‐Ni‐P@a‐Pd‐Ni‐P nanoplates can be tuned in the range from 9.47 to 38.61 at%. When used as a catalyst, the c‐Pd‐Ni‐P@a‐Pd‐Ni‐P nanoplates with 9.47 at% Ni exhibit excellent electrocatalytic activity toward ethanol oxidation, showing a high mass current density up to 3.05 A mgPd−1, which is 4.5 times that of the commercial Pd/C catalyst (0.68 A mgPd−1).
Binary (Pd‐P) and ternary (Pd‐Ni‐P) nanoplates, both with crystalline@amorphous core–shell nanostructures, are synthesized using Cu3−χP nanoplates as templates. The obtained c‐Pd‐Ni‐P@a‐Pd‐Ni‐P heterostructured nanoplates exhibit superior electrocatalytic performance toward the ethanol oxidation reaction in alkaline media compared to c‐Pd‐P@a‐Pd‐P heterostructured nanoplates and commercial Pd/C catalysts.
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