Carbonized Bark by Laser Treatment for Efficient Solar-Driven Interface Evaporation.

Interfacial localization of solar thermal energy conversion to drive evaporation is a promising water treatment technology, especially for gaining pure water in freshwater-deficient areas. Phoenix tree bark is chosen as the raw material mainly because of its low cost and renewability. The carbonized bark with broadened pore sizes possess efficient steam escape channels and light absorption structure. The film with a double-layer structure is constructed through converting the surface of the bark into the carbonized structure under controllable laser treatment. The evaporation efficiency is calculated to be 74% under 1 sun by enhancing the photothermal conversion ability and efficiently opening the surface water transport channels simultaneously. The distillation water exhibits large resistance values (9.65 MΩ) and low concentrations of four primary ions (Na+, K+, Mg2+, and Ca2+), which achieves international standard for drinking water. In addition, the carbonized bark also exhibits all-right purified performance toward water evaporation from dye wastewater. The low cost and clean technology provides new inspiration for the future development of applicable solar thermal energy-driven water treatment systems.

In-situ synthesized and pattern Ag/Bi2Se3 composite structure by LDW and photothermal conversion.

Bi2Se3 nanofilm has exhibited many promising potentials application in the field of photo-to-heat conversion. A highly-efficient photo-to-heat conversion system of Ag/Bi2Se3 composite nanofilm is successfully fabricated through laser direct writing (LDW) technique. The localized heat induced by laser simultaneously achieve Ag particles synthesis, transfer and patterning in a single processing step. The thermal reaction process includes the forming of nanoparticles based on the process of the thermal reduction, laser ablation, sputtering deposition and so on. The thermal storage capability and photothermal conversion stability have been greatly improved through preventing the heat from loss and efficient LSPR enhancing. The photothermal conversion mechanism of composition film is discussed in detail. This work suggests that the laser-assisted transfer technique give rise to a new expectation of functional composite nanofilm application for energy conversion.

Surface Plasmon-Enhanced Luminescence of CdSe/CdS Quantum Dots Film Based on Au Nanoshell Arrays.

In this paper, Au nanoshell arrays, serving as a photo-activated material, are fabricated via the combination of self-assembled nanosphere lithography and the thermal decomposing polymer method. The intensity and position of surface plasmonic resonance can be tuned from the visible region to the near-infrared region by changing the size of Au nanoshell arrays. When resonance absorption peaks of metal nanoparticles are matched with emission wavelengths of core-shell CdSe/CdS quantum dots, fluorescent intensity of CdSe/CdS quantum dots can be strongly enhanced. The physical mechanism of fluorescent enhancement is explained.

Morphological evolution of self-deposition Bi2Se3 nanosheets by oxygen plasma treatment.

Bi2Se3 nanosheets were successfully synthesized by a microwave-assisted approach in the presence of polyvinylpyrroli done at a temperature of 180 °C for 2 h. The thin film was prepared on a silicon wafer via a self-deposition process in a Bi2Se3 nanosheet ink solution using the evaporation-induced self-assembly method. The structure and morphology of the obtained products were characterized by X-ray diffraction, scanning electron microscopy (SEM), x-ray photoelectron spectroscopy, and Raman spectroscopy. The highly uniform Bi2Se3 particles could be formed by controlling the oxygen plasma treatment time. After the plasma pretreatment from 10 to 20 s, the surface of Bi2Se3 film evolved from the worm-like structure to particles. The highly uniform thin film was formed on further increasing the plasma treatment time, which is consistent with the observed SEM results. Several important processes can result in the morphological evolution of Bi2Se3 nanosheets: (1) formation of Bi2Se3 oxide layer; (2) self-assembly of oxide nanoparticles under the action of high-energy oxygen plasma; and (3) electrostatic interaction and etching mechanism.

Design and preparation of quantum dots fluorescent probes for in situ identification of Microthrix parvicella in bulking sludge.

A series of quantum dots (QDs) fluorescent probes for the in situ identification of Microthrix parvicella (M. parvicella) in bulking sludge were designed and prepared. In the preparation of CdTe/CdS QDs, the 11-mercaptoundecanoic acid (11-acid) and 16-mercaptohexadecanoic acid (16-acid) were used as the stabilizer. The prepared QDs probes were characterized by Fourier transform infrared (FT-IR), X-ray diffraction (XRD), and transmission electron microscopy (TEM), and the results showed that the CdTe/CdS QDs formed a core-shell structure and the long carbon chain was successfully grafted onto its surface. And the three QDs probes had different crystallinity and particle size, which was due to the inhibition effect of long carbon chain. The optical properties test results showed that although the formed core-shell structure and long carbon chain affected the fluorescent intensity, adsorption, and emission spectra of the QDs probes, the probes B and C had a large stokes-shift of 82 and 101 nm, which was a benefit for their fluorescent labeling property. In the fluorescent identification of M. parvicella, the probes B and C effectively adsorbed onto the surface of M. parvicella through a hydrophobic bond, and then identified M. parvicella by their unique fluorescence. In addition, it was found that a better hydrophobic property resulted in better identification efficiency.

The fluorescent interactions between amphiphilic chitosan derivatives and water-soluble quantum dots.

The LCC-CdTe quantum dots (QDs) hybrid was fabricated by mixing the N-lauryl-N, O-carboxymethyl chitosan (LCC) micelle with water-soluble CdTe QDs in an aqueous solution via hydrophobic forces and the electronic attraction. The structures of LCC and LCC-CdTe QDs hybrid were determined by differential scanning calorimetry (DSC), Fourier transform infrared (FT-IR) spectroscopy and transmission electron microscopy (TEM). The results showed that the lauryl and carboxymethyl were successfully grafted to chitosan oligosaccharide (CSO), and a number of CdTe QDs were encapsulated by LCC micelle to form a core/shell structure. The tested results of the fluorescent characteristics of LCC, CdTe QDs and LCC-CdTe QDs hybrid showed that there were some obvious fluorescent interactions between LCC and CdTe QDs. Meanwhile, with the change in LCC space structure, the fluorescent interactions between LCC and QDs showed different fluorescent characteristics. The QDs fluorescent (FL) intensity increased first and then decreased to almost quenching, while LCC FL intensity decreased continually.

A Novel Separation Method of Microthrix parvicella Filaments from Activated Sludge by a Hydrophobic Plate.

The aim of this paper is to develop a novel method to separate Microthrix parvicella (M. parvicella) filaments from activated sludge easily and quickly, as there are a few difficulties in the isolation of M. parvicella filaments, such as complicated isolation process, time consuming, etc. In this work, a series of hydrophobic plate with and without microchannels have been prepared for the separation of M. parvicella filaments. The results showed that the presence of microchannels and hydrophobic property of the hydrophobic plates affected the separation efficiency of M. parvicella significantly. The scanning electron microscope and Keyence Digital Microscope analysis results showed that the diameter of microchannels was similar to the width of M. parvicella filament, which was beneficial for the fastening of M. parvicella filaments on the plate. The hydrophobic property of the prepared plates was tested by contact angle of water droplets, and the results displayed that the polydimethylsiloxane (PDMS) plate possessed the highest contact angle compared with that of other plates, like polymethylmethacrylate, polystyrene plate, and PDMS plate with no hydrophobic microchannels. Thus, it was concluded that the high separation efficiency of PDMS plates to M. parvicella filaments was due to its best hydrophobic property.

[Photoluminescence investigation of InAs bimodal self-assembled quantum dots state filling].

Self-assembled InAs quantum dots were prepared on GaAs(100) substrate in a solid source molecular beam epitaxy system. The distribution and topographic images of uncapped dots were studied by atomic force microscope. The statistical result shows that the quantum dots are bimodal distribution. The photoluminescence spectrum results shows that the intensity of small size quantum dots dominated, which may be due to: (1) the state density of large quantum dots lower than that of small quantum dots; (2) the carriers capture rate of large size quantum dots is small relative to that of small ones; (3) there is a large strain barrier between large quantum dots and capping layer, and the large strain is likely to produce the defect and dislocation, resulting in a probability of carriers transferring from large quantum dots to small dots that is very small with temperature increasing.