Quinolinones Alkaloids with AChE Inhibitory Activity from Mangrove Endophytic Fungus Penicillium citrinum YX-002.

Acetylcholinesterase (AChE) inhibitory activity-guided studies on the mangrove-derived endophytic fungus Penicillium citrinum YX-002 led to the isolation of nine secondary metabolites, including one new quinolinone derivative, quinolactone A (1), a pair of epimers quinolactacin C1 (2) and 3-epi-quinolactacin C1 (3), together with six known analogs (4-9). Their structures were elucidated based on extensive mass spectrometry (MS) and 1D/2D nuclear magnetic resonance (NMR) spectroscopic analyses, and compared with data in the literature. The absolute configurations of compounds 1-3 was determined by combination of electronic circular dichroism (ECD) calculations and X-Ray single crystal diffraction technique using CuKα radiation. In bioassays, compounds 1, 4 and 7 showed moderate AChE inhibitory activities with IC50 values of 27.6, 19.4 and 11.2 µmol/L, respectively. The structure-activity relationships (SARs) analysis suggested that the existence of carbonyl group on C-3 and the oxygen atom on the five-membered ring were beneficial to the activity. Molecular docking results showed that compound 7 had a lower affinity interaction energy (-9.3 kcal/mol) with stronger interactions with different sites in AChE activities, which explained its higher activities.

Chemical Sensors using Single-Molecule Electrical Measurements.

Driven by the digitization and informatization of contemporary society, electrical sensors are developing toward minimal structure, intelligent function, and high detection resolution. Single-molecule electrical measurement techniques have been proven to be capable of label-free molecular recognition and detection, which opens a new strategy for the design of efficient single-molecule detection sensors. In this review, we outline the main advances and potentials of single-molecule electronics for qualitative identification and recognition assays at the single-molecule level. Strategies for single-molecule electro-sensing and its main applications are reviewed, mainly in the detection of ions, small molecules, oligomers, genetic materials, and proteins. This review summarizes the remaining challenges in the current development of single-molecule electrical sensing and presents some potential perspectives for this field.

Bi2 Te3 /Bi2 Se3 /Bi2 S3 Cascade Heterostructure for Fast-Response and High-Photoresponsivity Photodetector and High-Efficiency Water Splitting with a Small Bias Voltage.

Large-scale multi-heterostructure and optimal band alignment are significantly challenging but vital for photoelectrochemical (PEC)-type photodetector and water splitting. Herein, the centimeter-scale bismuth chalcogenides-based cascade heterostructure is successfully synthesized by a sequential vapor phase deposition method. The multi-staggered band alignment of Bi2 Te3 /Bi2 Se3 /Bi2 S3 is optimized and verified by X-ray photoelectron spectroscopy. The PEC photodetectors based on these cascade heterostructures demonstrate the highest photoresponsivity (103 mA W-1 at -0.1 V and 3.5 mAW-1 at 0 V under 475 nm light excitation) among the previous reports based on two-dimensional materials and related heterostructures. Furthermore, the photodetectors display a fast response (≈8 ms), a high detectivity (8.96 × 109 Jones), a high external quantum efficiency (26.17%), and a high incident photon-to-current efficiency (27.04%) at 475 nm. Due to the rapid charge transport and efficient light absorption, the Bi2 Te3 /Bi2 Se3 /Bi2 S3 cascade heterostructure demonstrates a highly efficient hydrogen production rate (≈0.416 mmol cm-2  h-1 and ≈14.320 µmol cm-2  h-1 with or without sacrificial agent, respectively), which is far superior to those of pure bismuth chalcogenides and its type-II heterostructures. The large-scale cascade heterostructure offers an innovative method to improve the performance of optoelectronic devices in the future.

Vertically oriented SnS2 on MoS2 nanosheets for high-photoresponsivity and fast-response self-powered photoelectrochemical photodetectors.

Van der Waals heterostructures have great potential for the emerging self-powered photoelectrochemical photodetectors due to their outstanding photoelectric conversion capability and efficient interfacial carrier transportation. By considering the band alignment, structural design, and growth optimization, the heterostructures of vertically oriented SnS2 with different densities on MoS2 nanosheets are designed and fabricated using a two-step epitaxial growth method. Compared with SnS2, MoS2, and low density-vertical SnS2/MoS2 heterostructure, the high density-vertical SnS2/MoS2 heterostructure exhibits largely enhanced self-powered photodetection performances, such as a giant photocurrent density (∼932.8 µA cm-2), an excellent photoresponsivity (4.66 mA W-1), and an ultrafast response/recovery time (3.6/6.4 ms) in the ultraviolet-visible range. This impressive enhancement of high density-vertical SnS2/MoS2 photodetectors is mainly ascribed to the essentially improved charge transfer and carrier transport of type-II band alignment heterostructures and the efficient light absorption from the unique light-trapping structure. In addition, the photoelectrocatalytic water splitting performance of the high density-vertical SnS2/MoS2 heterostructure also benefits from the type-II band alignment and the light-trapping structure. This work provides valuable inspiration for the design of two-dimensional optoelectronic and photoelectrochemical devices with improved performance by the morphology and heterostructure design.

Sb2S3/Sb2Se3 heterojunction for high-performance photodetection and hydrogen production.

Photoelectrochemical (PEC)-type devices provide promising ways for harvesting solar energy and converting it to electric and chemical energy with a low-cost and simple manufacturing process. However, the high light absorption, fast carrier separation, and low carrier recombination are still great challenges in reaching high performance for PEC devices. As emergent two-dimensional (2D) materials, Sb2Se3 and Sb2S3 exhibit desirable photoelectric properties due to the narrow bandgap, large optical absorption, and high carrier mobility. Herein, Sb2S3/Sb2Se3 heterojunction is synthesized by a two-step physical vapor deposition method. The type-II Sb2S3/Sb2Se3 heterojunction displays excellentphotoelectric properties such as a high photocurrent density (Iph âˆ¼ 162 µA cm-2), a high photoresponsivity (Rph âˆ¼ 3700 µA W-1), and a fast time response speed (rising time ∼ 2 ms and falling time ∼ 4.5 ms) even in harsh environment (H2SO4 electrolyte). Especially, the Sb2S3/Sb2Se3 shows an excellent self-powered photoresponse (Iph âˆ¼ 40 µA cm-2, Rph âˆ¼ 850 µA W-1). This increment is attributed to the improvement in light absorption, charge separation, and charge transfer efficiency. Taking these advantages, the Sb2S3/Sb2Se3 heterojunction also exhibits higher PEC water splitting synergically, which is approximately 3 times larger than that of Sb2Se3 and Sb2S3. These results pave the way for high-performance PEC devices by integrating 2D narrow bandgap semiconductors.

Enhanced UV-Vis photodetector performance by optimizing interfacial charge transportation in the heterostructure by SnS and SnSe2.

Optimizing interfacial charge transfer in type-II heterostructures, is one promising solution to improve efficiency of the solar energy conversion in photodetectors and solar cells. Herein, the SnS/SnSe2/ITO and SnSe2/SnS/ITO heterostructures are prepared by two-step physical vapor epitaxial growth. X-ray photoelectron spectroscopy confirms the SnS/SnSe2 heterostructure belongs to type-II band-alignment. The SnS/SnSe2 based photodetector shows higher photoresponsivity, which is approximately 2, 9, and 14 times larger than that of SnSe2/SnS, SnSe2, and SnS, respectively. The improvement of SnS/SnSe2 in photoelectric response mainly comes from high light harvesting and efficient charge transportation than individual SnSe2 and SnS, which is verified by UV-Vis absorption spectra. Electrochemical impedance spectroscopy, open circuit potentials, and Mott-Schottky characterization results further confirm that the better photodetection performance of SnS/SnSe2/ITO than that of SnSe2/SnS/ITO heterostructure is from the appropriate energy level cascade facilitating electron transport. These results provide an effective way to further improve the performance of heterostructure-based optoelectronic devices by an appropriate interface design.

Effect of anisotropic conductivity of Ag2S-modified Zn m In2S3+m (m = 1, 5) on the photocatalytic properties in solar hydrogen evolution.

3 wt% Ag2S/Zn5In2S8 (3A/Z5) and 3 wt% Ag2S/ZnIn2S4 (3A/Z1) were prepared by a two-step synthesis method. The first-principles calculations revealed that the anisotropic carrier transport property of Zn5In2S8 (Z5) is much stronger than that of ZnIn2S4 (Z1). Furthermore, unsynchronized electron and hole transport leads to higher bulk carrier separation efficiency in Z5. After accelerating the surface photocatalytic reaction rate by Ag2S modification, the differences between 3A/Z5 and 3A/Z1 in the bulk carrier separation were further enlarged. Photoelectrochemical tests confirmed that the bulk charge separation efficiency of 3A/Z5 is 13.70%, which is 7.4 times higher than 3A/Z1 (1.84%). Because of the high bulk carrier separation efficiency, the 3A/Z5 exhibits a promising photocatalytic hydrogen production rate, reaching 3189 µmol h-1 g-1. Through intuitive evidence, this work proves that material with stronger anisotropic conductivity has higher bulk carrier separation efficiency, thus has the potential to exhibit high photocatalytic hydrogen production performance.