Publications by authors named "Yuyang Qin"

Photoelectrochemical photodetectors (PEC PDs) are promising in underwater optoelectronic devices because of their low cost, good sensitivity, and self-powered characteristics. However, achieving high-performance omnidirectional visible PEC PDs using seawater as the electrolyte is still challenging, hindering their practical application. This work successfully synthesized CuO nanobelt arrays (NAs) on a linear copper wire via a low-temperature solution method with an annealing process.

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The field of photoelectrochemical-type (PEC) ultraviolet (UV) photodetectors has witnessed swift progression due to their facile fabrication processes and self-powered function. The realization of high-performance and self-powered PEC UV photodetectors is attractive and challenging. In this study, the application of ZnAl mixed metal oxide (MMO) heterojunctions in self-powered PEC UV photodetectors is introduced for the first time.

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Unlabelled: Background: Rising global temperatures have been linked to an increased incidence of heat stress (HS)-induced myocardial damage.

Methods: This study aimed to investigate the therapeutic potential of shikimic acid (SA) on HS-induced myocardial damage using network pharmacology, molecular docking, molecular dynamics (MD) simulations, and in vitro experiments.

Results: Network pharmacology analysis indicated that SA significantly attenuates the inflammatory response to HS by modulating 60 targets, including TNF, IL-6, and STAT3, which are enriched in the PI3K/AKT signaling pathway.

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In recent years, mRNA vaccine has achieved increasing interest owing to its high potency, safety, ease of production, and low-cost manufacturing. Currently approved mRNA vaccines are administered intramuscularly to transfect local antigen-presenting cells (APCs) to initiate low to moderate immune responses. Spleen, the largest secondary lymphoid organ in the body which contains a large number of APCs close to B and T lymphocytes, could be the ideal site for effective initiation of an enhanced immune response.

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Hexagonal boron nitride nanosheets (BNNSs) possess remarkable potential for various applications due to their unprecedented properties. However, the scalable production of BNNSs with both expansive surface and high solubility continues to present a significant challenge. Herein, we propose an innovative and efficient two-step method for manufacturing hydroxyl-functionalized BNNSs (OH-BNNSs).

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In the past decade, adoptive cell therapy with chimeric antigen receptor-T (CAR-T) cells has revolutionized cancer treatment. However, the complexity and high costs involved in manufacturing current adoptive cell therapy greatly inhibit its widespread availability and access. To address this, in situ cell therapy, which directly reprograms immune cells inside the body, has recently been developed as a promising alternative.

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The increasing number of approved nucleic acid therapeutics demonstrates the potential for the prevention and treatment of a broad spectrum of diseases. This trend underscores the significant impact and promise of nucleic acid-based treatments in the field of medicine. Nevertheless, employing nucleic acids as therapeutics is challenging due to their susceptibility to degradation by nucleases and their unfavorable physicochemical characteristics that hinder delivery into cells.

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The BiOClI/g-CN nanosheet (BCI-CN) was successfully immobilized on polyolefin polyester fiber (PPF) through the hydrothermal method. The novel immobilized BiOClI/g-CN nanocomposites (BCI-CN-PPF) were characterized by scanning electron microscope (SEM), energy dispersive spectroscopy EDS, X-ray powder diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and UV-vis diffuse reflectance spectroscopy (UV-vis DRS) to confirm that BCI-CN was successfully immobilized on PPF with abundant oxygen vacancies reserved. Under simulated solar light irradiation, 100 % of bisphenol A (BPA) with an initial concentration of 10 mg·L was degraded by BCI-CN-PPF (0.

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Calcium-dependent synaptic vesicle exocytosis is mediated by SNARE complex formation. The transition from the Munc18-1/syntaxin-1 complex to the SNARE complex is catalyzed by the Munc13-1 MUN domain and involves at least two conformational changes: opening of the syntaxin-1 linker region and extension of Munc18-1 domain 3a. However, the relationship and the action order of the two conformational changes remain not fully understood.

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A novel strain FDN-02 was isolated from a sequencing batch biofilm reactor. FDN-02 was identified as Paracoccus sp., and the Genbank Sequence_ID was MW652628.

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We report that lightweight, anisotropic, mechanically flexible, and high performance thermally insulating materials are fabricated by the assembly of graphene oxide (GO) and polyimide (PI). With an appropriate ratio between GO and PI building blocks, the rGO/PI thermally insulating material exhibits hierarchically aligned microstructures with high porosity. These microstructures endow the rGO/PI nanocomposite with low mass density and super-insulating property (extremely low thermal conductivity of 0.

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Graphene-enhanced polymer matrix nanocomposites are attracting ever increasing attention in the electromagnetic (EM) interference (EMI) shielding field because of their improved electrical property. Normally, the graphene is introduced into the matrix by chemical functionalization strategy. Unfortunately, the electrical conductivity of the nanocomposite is weak because the graphene nanosheets are not interconnected.

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Lightweight, high-performance, thermally insulating, and antifrosting porous materials are in increasing demand to improve energy efficiency in many fields, such as aerospace and wearable devices. However, traditional thermally insulating materials (porous ceramics, polymer-based sponges) could not simultaneously meet these demands. Here, we propose a hierarchical assembly strategy for producing nanocomposite foams with lightweight, mechanically flexible, superinsulating, and antifrosting properties.

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Electrical stimulation of shape-memory polymers (SMPs) has many advantages over thermal methods; creating an efficient conductive path through the bulk polymers is essential for developing high performance electroactive systems. Here, we show that a three-dimensional (3D) porous carbon nanotube sponge can serve as a built-in integral conductive network to provide internal, homogeneous, in situ Joule heating for shape-memory polymers, thus significantly improving the mechanical and thermal behavior of SMPs. As a result, the 3D nanocomposites show a fast response and produce large exerting forces (with a maximum flexural stress of 14.

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The creation of stiff yet multifunctional three-dimensional porous carbon architecture at very low cost is still challenging. In this work, lightweight and stiff carbon foam (CF) with adjustable pore structure was prepared by using flour as the basic element via a simple fermentation and carbonization process. The compressive strength of CF exhibits a high value of 3.

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The creation of superelastic, flexible three-dimensional (3D) graphene-based architectures is still a great challenge due to structure collapse or significant plastic deformation. Herein, we report a facile approach of transforming the mechanically fragile reduced graphene oxide (rGO) aerogel into superflexible 3D architectures by introducing water-soluble polyimide (PI). The rGO/PI nanocomposites are fabricated using strategies of freeze casting and thermal annealing.

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