Synthesis of Flower-Like AgI/BiOCOOH p-n Heterojunctions With Enhanced Visible-Light Photocatalytic Performance for the Removal of Toxic Pollutants

In this study, flower-like AgI/BiOCOOH heterojunctions were constructed through a two-step procedure involving the solvothermal synthesis of BiOCOOH microflowers followed by AgI modification using a precipitation method. These novel photocatalysts were systematically examined by XRD, UV–vis DRS, SEM, TEM, EDS, and PL spectroscopy techniques. The AgI/BiOCOOH heterojunction were studied as a decent photocatalyst for the removal of the industrial dye (rhodamine B, and methyl blue) and antibiotic (tetracycline) under visible light. The AgI/BiOCOOH heterojunctions are much more active than bare BiOCOOH, and AgI, which could be ascribed to the improved separation of charge carriers, resulting from the formation of p-n heterojunction between two constituents. The holes (h+) and superoxide radical (•O2-) were detected as the main active species responsible for the pollutant degradation. The results showed that a highly efficient visible-light-driven photocatalytic system was developed for the decomposition of toxic pollutants

A Novel Heterostructure of BiOI Nanosheets Anchored onto MWCNTs with Excellent Visible-Light Photocatalytic Activity

Developing efficient visible-light-driven (VLD) photocatalysts for environmental decontamination has drawn significant attention in recent years. Herein, we have reported a novel heterostructure of multiwalled carbon nanotubes (MWCNTs) coated with BiOI nanosheets as an efficient VLD photocatalyst, which was prepared via a simple solvothermal method. The morphology and structure were characterized by powder X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV-Vis diffuse reflectance spectroscopy (DRS), and specific surface area measurements. The results showed that BiOI nanosheets were well deposited on MWCNTs. The MWCNTs/BiOI composites exhibited remarkably enhanced photocatalytic activity for the degradation of rhodamine B (RhB), methyl orange (MO), and para-chlorophenol (4-CP) under visible-light, compared with pure BiOI. When the MWCNTs content is 3 wt %, the MWCNTs/BiOI composite (3%M-Bi) achieves the highest activity, which is even higher than that of a mechanical mixture (3 wt % MWCNTs + 97 wt % BiOI). The superior photocatalytic activity is predominantly due to the strong coupling interface between MWCNTs and BiOI, which significantly promotes the efficient electron-hole separation. The photo-induced holes (h+) and superoxide radicals (O2−) mainly contribute to the photocatalytic degradation of RhB over 3%M-Bi. Therefore, the MWCNTs/BiOI composite is expected to be an efficient VLD photocatalyst for environmental purification

Hierarchical heterostructures of Bi2MoO6 microflowers decorated with Ag2CO3 nanoparticles for efficient visible-light-driven photocatalytic removal of toxic pollutants

Developing highly active and durable visible-light-driven photocatalysts for the degradation of toxic pollutants is of vital significance. Herein, Ag2CO3 nanoparticles were in situ formed on Bi2MoO6 microflowers to produce Ag2CO3/Bi2MoO6 heterostructures via a facile procedure. The morphologies, phases, chemical compositions, and optical properties of Ag2CO3/Bi2MoO6 were examined by multiple characterization techniques. The Ag2CO3/Bi2MoO6 heterostructures exhibited substantially improved performance in the removal of industrial dyes (rhodamine B (RhB), methyl orange (MO), and methyl blue (MB)), and the antibiotic tetracycline hydrochloride (TC), compared with bare Bi2MoO6 and Ag2CO3 under visible-light irradiation. The enhancement of activity was attributed to the high charge-separation capacity, which results from the matched band alignment of the two components. The cycling experiments showed a good durability of Ag2CO3/Bi2MoO6. Holes were found to be the dominant active species accounting for the pollutant degradation. This compound is a promising candidate for wastewater treatment

Molten Au/Ge alloy migration in Ge nanowires

Herein, we report time-resolved in situ transmission electron microscopy observation of Au particle melting at a Ge nanowire tip, subsequent forming of Au/Ge alloy liquid, and its migrating within the Ge nanowire. The migration direction and position of the Au/Ge liquid can be controlled by the applied voltage and the migration speed shows a linear deceleration in the nanowire. In a migration model proposed, the relevant dynamic mechanisms (electromigration, thermodiffusion, and viscous force, etc.) are discussed in detail. This work associated with the liquid mass transport in the solid nanowires should provide new insights into the crystal growth, interface engineering, and fabrication of the heterogeneous nanostructure-based devices

Antioxidant Phenolic Compounds of Cassava (Manihot esculenta) from Hainan

An activity-directed fractionation and purification process was used to isolate antioxidant components from cassava stems produced in Hainan. The ethyl acetate and n-butanol fractions showed greater DPPH˙and ABTS·+ scavenging activities than other fractions. The ethyl acetate fraction was subjected to column chromatography, to yield ten phenolic compounds: Coniferaldehyde (1), isovanillin (2), 6-deoxyjacareubin (3), scopoletin (4), syringaldehyde (5), pinoresinol (6), p-coumaric acid (7), ficusol (8), balanophonin (9) and ethamivan (10), which possess significant antioxidant activities. The relative order of DPPH· scavenging capacity for these compounds was ascorbic acid (reference) > 6 > 1 > 8 > 10 > 9 > 3 > 4 > 7 > 5 > 2, and that of ABTS·+ scavenging capacity was 5 > 7 > 1 > 10 > 4 > 6 > 8 > 2 > Trolox (reference compound) > 3 > 9. The results showed that these phenolic compounds contributed to the antioxidant activity of cassava