pH-dependent network formation of quantum dots and fluorescent quenching by Au nanoparticle embedding

A simple approach to the creation of colloidal assemblies is in high demand for the development of functional devices. Here, we present the preparation of CdTe-QD (quantum dot) networks in as little as 1 day simply by pH modification without the use of oxidants. The QD network was tractable in water and casting from a droplet produced a porous networked film on both hydrophobic and hydrophilic solid substrates. Further, we found that citrate-protected gold nanoparticles (AuNPs, d = 5 nm) could be incorporated into the QD networks to afford a QD/Au composite network, and that the fluorescence from the QDs was largely decreased by the addition of a small proportion of AuNPs (QD:AuNP = 99.4:0.6), probably due to the efficient charge transfer through the network. These data indicate that our method is suitable for application to the creation of metal/QD hybrid materials that can be integrated into wet-based processes.     

Effects of Microalloying on the Impact Toughness of Ultrahigh-Strength TRIP-Aided Martensitic Steels

The effects of the addition of Cr, Mo, and/or Ni on the Charpy impact toughness of a 0.2 pct C-1.5 pct Si-1.5 pct Mn-0.05 pct Nb transformation-induced plasticity (TRIP)-aided steel with a lath-martensite structure matrix (i.e., a TRIP-aided martensitic steel or TM steel) were investigated with the aim of using the steel in automotive applications. In addition, the relationship between the toughness of the various alloyed steels and their metallurgical characteristics was determined. When Cr, Cr-Mo, or Cr-Mo-Ni was added to the base steel, the TM steel exhibited a high upper-shelf Charpy impact absorbed value that ranged from 100 to 120 J/cm² and a low ductile–brittle fracture appearance transition temperature that ranged from 123 K to 143 K (?150 °C to ?130 °C), while also exhibiting a tensile strength of about 1.5 GPa. This impact toughness of the alloyed steels was far superior to that of conventional martensitic steel and was caused by the presence of (i) a softened wide lath-martensite matrix, which contained only a small amount of carbide and hence had a lower carbon concentration, (ii) a large amount of finely dispersed martensite-retained austenite complex phase, and (iii) a metastable retained austenite phase of 2 to 4 vol pct in the complex phase, which led to plastic relaxation via strain-induced transformation and played an important role in the suppression of the initiation and propagation of voids and/or cleavage cracks.     

Thermal and gas permeation properties of copolymers derived from 3‐methacryloxypropyltris(trimethylsiloxy)silane and adamantyl group‐containing methacrylate derivatives

Novel copolymer membranes derived from three types of adamantyl group‐containing methacrylate derivatives and 3‐methacryloxypropyltris(trimethylsiloxy)silane (SiMA) were synthesized via free radical polymerization. The thermal and permeation properties of these copolymer membranes were investigated. Copolymer membranes with less than 11.9 mol % adamantane content exhibited good membrane forming abilities that are suitable for permeation measurement. The decomposition temperature of all copolymers increased up to approximately 40–80°C with increasing adamantane content compared with poly(SiMA). Moreover, the glass transition temperature (T_g) of all copolymers increased up to approximately 46–60°C with increasing adamantane content compared with the theoretical value, which was estimated from Fox equation. 1‐Adamantyl methacrylate copolymer had the highest fractional free volume among the three types of adamantly group‐containing methacrylate derivatives. The gas permeability coefficient of this copolymer increased by 22–45% with increasing adamantane content compared with that of poly(SiMA). © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43129.     

Preparation of physical gel consisting of syndiotactic polystyrene and poly(ethylene glycol)

Syndiotactic polystyrene (s-PS) was blended with poly(ethylene glycol) (PEG) in 1,2-dichloroethane (DCE) solvent. The mixture became a homogeneous solution at 155 °C depending on the composition ratio of PEG to DCE. When the solution was cooled at the rate of 5 °C/min to room temperature, a thermoreversible gelation was occurred. Wide angle X-ray diffraction (WAXD) measurements revealed that the polymer chain of s-PS in the obtained gel was crystallized with a helical conformation, while that in the non-gelated sample was done with an all-trans planar zigzag conformation.After drying gelated samples at 70 °C for 24 h, a novel polymer blend type of the physical gel consisting of s-PS and PEG was obtained. Dynamic mechanical analysis (DMA) revealed that the physical gel had a high modulus and a long elastic plateau in the temperature range of −80-270 °C.     

Green emitting β$ubeta$-SiAlON:Eu2+ phosphors derived from chemically modified perhydropolysilazanes

We report the first synthesis of β-SiAlON:Eu²⁺ phosphors from single-source precursors, perhydropolysilazane (PHPS), chemically modified with Al(OCH(CH₃)₂)₃, and EuCl₂. The reactions occurring during the precursor synthesis and the subsequent thermal conversion of polymeric precursors into β-SiAlON:Eu²⁺ phosphors have been studied by a complementary set of analytical techniques, including infrared spectroscopy, gas chromatography–mass spectrometry, thermogravimetry–mass spectrometry, X-ray diffraction (XRD), photoluminescence spectroscopy, and scanning electron microscopy. It has been clearly established that Al(OCH(CH₃)₂)₃ immediately reacted with PHPS to afford N–Al bonds at room temperature, whereas N–Eu bond formation was suggested to proceed above 600°C accompanied by the elimination of HCl up to 1000°C in flowing N₂. The subsequent 1800°C-heat treatment for 1 h under an N₂ gas pressure at 980 kPa allowed converting the single-source precursors into fine-grained β-SiAlON:Eu²⁺ phosphors. XRD analysis revealed that the Al/Si of .09 was the critical atomic ratio in the precursor synthesis to afford single-phase β-SiAlON (z = .55). Moreover, Eu²⁺-doping was found to efficiently reduce the carbon impurity in the host β-SiAlON. The polymer-derived β-SiAlON:Eu²⁺ phosphors exhibited green emission under excitation at 460 nm and achieved the highest green emission intensity at the critical dopant Eu²⁺ concentration at 1.48 at%.     

Simulation of dynamic behavior of surfactants on a hydrophobic surface using periodic-shell boundary molecular dynamics

The adsorption and aggregation behaviors of sodium dodecyl sulfate (SDS) and cetyltrimethylammonium bromide (CTAB) on a hydrophobic graphite surface were examined using a novel molecular dynamics (MD) simulation with the periodic-shell boundary condition (PSBC). Differences in the adsorption behavior of SDS and CTAB molecules were clearly shown on the hydrophobic surface. Unexpectedly, the SDS molecules approached the graphite surface with their hydrophilic head groups. This unexpected approach mode was thought to be due to the aqueous layer on the graphite surface. The hydrophobic moiety of SDS molecules repeatedly adsorbed and desorbed on the graphite surface. In addition, SDS molecules kept moving on the graphite surface; thus, they did not form a stable adsorption layer. In contrast to SDS, the hydrophobic moiety of CTAB molecules approached the graphite surface at the primary step of adsorption. The hydrophobic moieties of CTAB molecules came close to each other, whereas the hydrophilic groups separated from one another. This result suggests that the CTAB molecules form molecular assemblies with a curved structure. The simulation results were consistent with the experimental observations. A clear difference between the adsorption behavior of SDS and CTAB molecules was revealed by MD simulations with PSBC.     

Influence of texture feature size on spherical silicon solar cells

The effects of surface texturing on spherical silicon solar cells were investigated. Surface texturing for spherical Si solar cells was prepared by immersing p-type spherical Si crystals in KOH solution with stirring. Two kinds of texture feature sizes (1 and 5μm pyramids) were prepared by changing stirring speed. After fabrication through our baseline processes, these cells were evaluated by solar cell performance and external quantum efficiency. The cell with 1 and 5μm pyramids shows the short circuit current density ( Jsc ) value of 31.9 and 33.2 mA·cm-2 , which is 9% and 13% relative increase compared to the cell without texturing. Furthermore, the cell with 5 μm pyramids has a higher open-circuit voltage (0.589 V) than the cell with 1 μm pyramids (0.577 V). As a result, the conversion efficiency was improved from 11.4% for the cell without texturing to 12.1% for the cell with 5 μm pyramids.