Recent advances in solid‐state organic lasers

Organic solid‐state lasers are reviewed, with a special emphasis on works published during the last decade. Referring originally to dyes in solid‐state polymeric matrices, organic lasers also include the rich family of organic semiconductors, paced by the rapid development of organic light‐emitting diodes. Organic lasers are broadly tunable coherent sources, potentially compact, convenient and manufactured at low cost. In this review, we describe the basic photophysics of the materials used as gain media in organic lasers with a specific look at the distinctive features of dyes and semiconductors. We also outline the laser architectures used in state‐of‐the‐art organic lasers and the performances of these devices with regard to output power, lifetime and beam quality. A survey of the recent trends in the field is given, highlighting the latest developments in terms of wavelength coverage, wavelength agility, efficiency and compactness, and towards integrated low‐cost sources, with a special focus on the great challenges remaining for achieving direct electrical pumping. Finally, we discuss the very recent demonstration of new kinds of organic lasers based on polaritons or surface plasmons, which open new and very promising routes in the field of organic nanophotonics. Copyright © 2011 Society of Chemical Industry     

Simulation Based Investigation of Triple Heterojunction TFET (THJ-TFET) for Low Power Applications

Silicon - We designed a new model tunnel field-effect transistor (TFET) based on Triple Heterojunction Tunnel Field Effect Transistor (THJ-TFET) is investigated and designed in this paper. This...     

Quasi-Diamond Platelet-Shaped Zinc Oxide Nanostructures Display Enhanced Antibacterial Activity

The current study compares the antibacterial activity of zinc oxide nanostructures (neZnO). For this purpose, two bacterial strains, Escherichia coli (ATCC 4157) and Staphylococcus aureus (ATCC 29213) were challenged in room light conditions with the aforementioned materials. Colloidal and hydrothermal methods were used to obtain the quasi-round and quasi-diamond platelet-shape nanostructures. Thus, the oxygen vacancy (V_O) effects on the surface of neZnO are also considered to assess its effects on antibacterial activity. The neZnO characterization was achieved by X-ray diffraction (XRD), a selected area electron diffraction (SAED) and Raman spectroscopy. The microstructural effects were monitored by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Furthermore, optical absorption ultraviolet visible spectrophotometry (UV-Vis) and X-ray photoelectron spectroscopy (XPS) analyses complement the physical characterization of these nanostructures; neZnO caused 50 % inhibition (IC₅₀) at concentrations from 0.064 to 0.072 mg/mL for S. aureus and from 0.083 to 0.104 mg/mL for E. coli, indicating an increase in activity against S. aureus compared to E. coli. Consequently, quasi-diamond platelet-shaped nanostructures (average particle size of 377.6±10 nm) showed enhanced antibacterial activity compared to quasi-round agglomerated particles (average size of 442.8±12 nm), regardless of Vo presence or absence.     

Synthesis and ex-situ evaluation of quaternized polysulfone as an anion exchange ionomer for AEM technologies

Anion exchange ionomer (AEI) is a critical component used on anion exchange membrane fuel cell (AEMFC) and alkaline water electrolyzer (AWE). In this work, quaternized polysulfone with different functionalization degree were used as an ionomer to evaluate the performance in the oxygen reduction reaction (ORR) and hydrogen oxidation reaction (HOR), both implied in the operation of AEMFC and AWE. The synthesized ionomer exhibited a better performance in both reactions in comparison to the commercial AEI Aemion®. PSf-130 exhibited better performance, since IEC and surface area increases twice regarding the same parameters in the PSf-60. The PSf-130 conductivity increases three times regarding the value exhibited by PSf-60. Finally, the J_lim and J_k increases 67% and 100% for ORR. On the other hand, the same catalytic parameter increased 44% and 35% for HOR comparing both polysulfone-based ionomers. The Tafel slope values do not showed drastically changes for different ionomers indicating the same rate determining step (RDS) and the same mechanism in both reactions for all the ionomers.     

高科技纤维在摩擦制动材料中的应用

本文介绍了一些高科技纤维在聚俣物基摩擦材料中的使用情况，指出在摩擦材料中使用高科技纤维已成为摩擦材料的一个发展趋势，但需要大大提高高科技纤维的性价比和使用纤维混杂技术。     

Physisorption of hydrogen in single-walled carbon nanotubes

The interaction of hydrogen with single-walled carbon nanotubes (SWNTs) was analysed. A SWNT sample was exposed to D₂ or H₂ at a pressure of 2 MPa for 1 h at 298 or 873 K. The desorption spectra were measured by thermal desorption spectroscopy (TDS). A main reversible desorption site was observed throughout the range 77 to 320 K. The activation energy of this peak at about 90 K was calculated assuming first-order desorption. This corresponds to physisorption on the surface of the SWNTs (19.2±1.2 kJ/mol). A desorption peak was also found for multi-walled carbon nanotubes (MWNTs), and also for graphite samples. The hydrogen desorption spectrum showed other small shoulders, but only for the SWNT sample. They are assumed to originate from hydrogen physisorbed at sites on the internal surface of the tubes and on various other forms of carbon in the sample. The nanosized metallic particles (Co:Ni) used for nanotube growth did not play any role in the physisorption of molecular hydrogen on the SWNT sample. Therefore, it is concluded that the desorption of hydrogen from nanotubes is related to the specific surface area of the sample.     

Primary steps of oxidation and electronic interactions in anodic cleavage of α,ω-diisocyanurate substituted dialkyl disulfides

The electrochemical oxidation of 1,1′-bis(3,5-dimethyl-[1,3,5]triazinane-2,4,6-trionyl)-α,α′-diorganyl-ω,ω′-disulfides involves a fast electron transfer followed by two chemical steps according to a ECC scheme. Using MM+, PM3 and ab initio SCF/3-21G^∗ molecular modeling it was shown that the low oxidation potential and the smallest current-determining cleavage rate constant in the reaction series of the disulfide with (CH₂)₆ spacer between SS bridge and the terminal heterocycles is due to an interaction of the π-components of the highest filled orbitals of the two heterocycles (HOMO and HOMO-1) with the LUMO (n-orbital of S) of the cation radical.     

Investigation on La3+ and Dy3+ co-doped ceria ceramics with an optimized average atomic number of dopants for electrolytes in IT-SOFCs

In the present study, we investigate the fundamental properties of CeO₂ by selecting La³⁺ (57), and Dy³⁺ (66) as dopants with optimized average atomic number of 61.5, which lies in between Pm³⁺ (62) and Sm³⁺ (62) in accordance with the criteria for optimum doping. A system of co-doped ceria ceramics Ce_1–x–yLa_xDy_yO_2-δ ((x, y) = (0.00, 0.00), (0.025, 0.025), (0.05, 0.05), (0.075, 0.075), (0.10, 0.10), (0.00, 0.20) and (0.20, 0.00)) as electrolytes for intermediate temperature solid oxide fuel cells were successfully prepared by a well-known sol-gel auto-combustion route. In order to obtain dense samples, the prepared pellets were sintered in air at 1300 °C for 4 h using conventional furnace and relative densities of all the samples were found to be higher than 95%. Single phase cubic structure, microstructural density and elemental composition analysis of all the samples were studied by powder X-ray diffraction, scanning electron microscope and energy dispersive spectroscopy techniques, respectively. Raman spectroscopy analysis confirmed the formation of concentrated O^2-–vacancies in the co-doped ceria system. Impedance spectroscopy measurements revealed the high value of total ionic conductivity and low activation energy for the composition Ce_0.85La_0.075Dy_0.075O_2?δ i.e., 2.08 × 10^–2 S cm^–1 and 0.58 eV, respectively. Linear thermal expansion analyses of all the samples revealed the matched thermal expansion coefficients. Finally, these results recommend that the Ce_0.85La_0.075Dy_0.075O_2?δ sample can be useful as a solid electrolyte in IT-SOFC applications.     

Improving hydrophobicity of polyurethane by PTFE incorporation

A simple and facile method was established of incorporating polytetrafluoroethylene (PTFE) on to polyurethane (PU) to improve hydrophobicity of PU by incorporating low levels of fluorine at a molecular level. Nanocomposites were made by preparing PU in the presence of PTFE using seeded miniemulsion polymerization method. The resulting PTFE/PU nanocomposites were characterized by transmission electron microscopy (TEM), Fourier transform infrared (FTIR) spectrometry, differential scanning calorimetric, and thermo gravimetric analysis (TGA). FTIR and TEM indicated changes observed in their structure, size and morphology. The water contact angle of PTFE/PU nanocomposite films increased with increasing amount of PTFE and more on blending with silica nanoparticles but a slight decrease in thermal stabilities of SiO₂/PTFE/PU nanocomposites were noticed. The hydrophobicity imparted by PTFE to PU surface was found to be at its best for 1 : 2 PTFE/PU latex film. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42779.