The influence of type-I and type-II triplet multiple quantum well structure on white organic light-emitting diodes

We demonstrate high-efficient white organic light-emitting diodes (WOLEDs) based on triplet multiple quantum well (MQW) structure and focus on the influence on WOLEDs through employing different potential barrier materials to form type-I and type-II MQWs, respectively. It is found that type-I MQW structure WOLEDs based on 1,3,5-tris(N-phenyl-benzimidazol-2-yl)benzene as potential barrier layer (PBL) offers high electroluminescent (EL) performance. That is to say, maximum current efficiency and power efficiency are achieved at about 1,000 cd/m² with 16.4 cd/A and 8.3 lm/W, which increase by 53.3% and 50.9% over traditional three-layer structure WOLEDs, respectively, and a maximum luminance of 17,700 cd/m² is earned simultaneously. The achievement of high EL performance would be attributed to uniform distribution and better confinement of carriers within the emitting layer (EML). However, when 4,7-diphenyl-1,10-phenanthroline or 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline is used as PBL to form type-II MQW structure, poor EL performance is obtained. We attribute that to improper energy level alignment between the interface of EML/PBL, which leads to incomplete confinement and low recombination efficiency of carriers, a more detailed mechanism was argued.     

Uniform SiGe/Si quantum well nanorod and nanodot arrays fabricated using nanosphere lithography

This study fabricates the optically active uniform SiGe/Si multiple quantum well (MQW) nanorod and nanodot arrays from the Si_0.4Ge_0.6/Si MQWs using nanosphere lithography (NSL) combined with the reactive ion etching (RIE) process. Compared to the as-grown sample, we observe an obvious blueshift in photoluminescence (PL) spectra for the SiGe/Si MQW nanorod and nanodot arrays, which can be attributed to the transition of PL emission from the upper multiple quantum dot-like SiGe layers to the lower MQWs. A possible mechanism associated with carrier localization is also proposed for the PL enhancement. In addition, the SiGe/Si MQW nanorod arrays are shown to exhibit excellent antireflective characteristics over a wide wavelength range. These results indicate that SiGe/Si MQW nanorod arrays fabricated using NSL combined with RIE would be potentially useful as an optoelectronic material operating in the telecommunication range.     

分子光化学贮存太阳能 III.双环[2,2,1]-2,5-庚二烯的光诱导电子转移敏化异构化反应

以N,N,N′,N′-四甲基联苯二胺、2,6-二甲氧基萘和2,7-二甲氧基萘为光敏剂,在正己烷溶液中实现了双环[2,2,1]-2,5-庚二烯到四环[2,2,1,0~(2,6),0.(3,5)]庚烷的异构化。测定了反应的量子产率。讨论了反应机理。通过激发态的光敏剂与二烯之间的电子转移反应,形成单重态和三重态处于平衡状态的离子自由基对中间体。处于溶剂笼中的三重态离子自由基对经电子反传,产生激发三重态二烯。最后该激发态二烯经分子内[2+2]环合加成反应异构化为四环烷。     

Dependence of the electrical and optical properties on growth interruption in AlAs/In0.53Ga0.47As/InAs resonant tunneling diodes

ABSTRACT: The dependence of interface roughness of pseudomorphic AlAs/In0.53Ga0.47As/InAs resonant tunneling diodes [RTDs] grown by molecular beam epitaxy on interruption time was studied by current-voltage [I-V] characteristics, photoluminescence [PL] spectroscopy, and transmission electron microscopy [TEM]. We have observed that a splitting in the quantum-well PL due to island formation in the quantum well is sensitive to growth interruption at the AlAs/In0.53Ga0.47As interfaces. TEM images also show flatter interfaces with a few islands which only occur by applying an optimum value of interruption time. The symmetry of I-V characteristics of RTDs with PL and TEM results is consistent because tunneling current is highly dependent on barrier thickness and interface roughness.     

Rice husk as a potentially low-cost biosorbent for heavy metal and dye removal: an overview

Rice husk as a low-value agricultural by-product can be made into sorbent materials which are used in heavy metal and dye removal. It has been investigated as a replacement for currently expensive methods of heavy metal removal from solutions. Currently, the study of rice husk as a low-cost sorbent for removing heavy metals has regained attention. The heavy metals being studied are: As(V) [1], Au [2,3], Cr(IV) [4], Cu and Pb [5,6], Fe, Mn, Zn, Cu [7] and Cd(II) [8-10]. Rice husk is also being used to treat textile dyes such as like malachite green [11,12] and acid yellow 36 [13]. The treatment and preparation of rice husk activated carbon are of importance and became a subject of study [14-16]. In this review an extensive list of previous and current literature on rice husk activated carbons in removing heavy metals and dyes, their preparation or treatment and isotherms studies were complied to provide a summary of available information on rice husk and its potential as a low-cost sorbent.     

Intersubband absorption properties of high Al content AlxGa1?xN/GaN multiple quantum wells grown with different interlayers by metal organic chemical vapor deposition

High Al content Al_xGa_1−xN/GaN multiple quantum well (MQW) films with different interlayers were grown by metal organic chemical vapor deposition. These MQWs were designed to achieve intersubband (ISB) absorption in the mid-infrared spectral range. We have considered two growth conditions, with AlGaN interlayer and GaN/AlN superlattice (SL) interlayer, both deposited on GaN-on-sapphire templates. Atomic force microscopy images show a relatively rough surface with atomic-step terraces and surface depression, mainly dominated by dislocations. High-resolution X-ray diffraction and transmission electron microscopy analyses indicate that good crystalline quality of the AlGaN/GaN MQW layer could be achieved when the AlGaN interlayer is inserted. The ISB absorption with a peak at 3.7 μm was demonstrated in MQW films with AlGaN interlayer. However, we have not observed the infrared absorption in MQW films with GaN/AlN SL interlayer. It is believed that the high dislocation density and weaker polarization that resulted from the rough interface are determinant factors of vanished ISB absorption for MQW films with the GaN/AlN SL interlayer.     

Fabrication of microstructure controlled cathode catalyst layers and their effect on water management in polymer electrolyte fuel cells

Although cathode catalyst layers (CCLs) are at the center of water management in polymer electrolyte fuel cells (PEFCs), the understanding of water movement in CCLs and their roll on fuel cell performance is still limited. In this present study, several CCLs with controlled microstructure, including main pore size, pore volume and porosity ranging from 30 to 70 nm, 0.443 to 0.962 cm³/g_Pt/C, and 45.4 to 64.4%, respectively, were prepared by changing the hot-pressing pressure in a decal process, and their water management ability and cell performance were evaluated. The electrochemical analyses reveal that, as the pore size and pore volume of CCLs increase, the diffusion resistance mainly arising from water accumulation in the pores is evidently reduced by capillary water equilibrium, which leads to better cell performance. Water balancing between accumulation and discharging in the pores also depends on the CCL pore structure, and the CCLs with greater pore sizes and larger pore volumes reveal more stable cell performance by better water management in steady state operation, even under extremely humid conditions. Based on these MEA technologies such as fabrication of CCLs, further study will be performed to understand microscopic phenomena in nano pores of CCLs by combining the experimental approach with CCL numerical modeling.     

Triplet EPR Dynamics of Randomly Oriented Dications and Dianions of Tetraoxaporphyrinoids

This paper deals with the photoexcited triplet state of several tetraoxaporphyrinoids studied by time-resolved electron paramagnetic resonance (EPR). The porphyrinoids studied are tetraoxa[18]porphyrin ( 1a ⁺⁺), octaethyl-tetraoxa[18]porphyrin ( 1b ⁺⁺), tetra-n-butyl tetraoxa[18]porphyrin ( 1c ⁺⁺), octaethyl-tetraoxa[26]porphyrin ( 2 ⁺⁺), and tetraoxa[18]porphycene ( 3 ⁺⁺), all of them as per-chlorate salts. To qualify as stable aromatic 18π- (or 26π-) electron systems, they must exist as dications. Analysis of the triplet EPR spectra is characterized by unique features not found in their parent porphyrins and porphycenes. While in the case of the axially-symmetric tetraphenylporphyrin, the triplet EPR spectra indicate deviation from axial symmetry, the tetraoxaporphyrin 1a ⁺⁺ exhibits, as expected, a vanishing E-term of the zero-field splitting (ZFS) tensor. A conspicuous difference is found between the triplet EPR spectra of the dications and the dianions of all tetraoxa compounds. The results are discussed in terms of the electronic structures of the porphyrinoids.     

Physical and electrochemical properties of 1-butyl-3-methylimidazolium bromide, 1-butyl-3-methylimidazolium iodide,and 1-butyl-3-methylimidazolium tetrafluoroborate

The density, viscosity, refractive index, heat capacity, heat of dilution, ionic conductivity, and electrochemical stability of 1-butyl-3-methylimidazolium bromide ([bmim][Br]), 1-butyl-3-methylimidazolium iodide ([bmim][I]), and 1-butyl-3-methylimidazolium tetrafluoroborate ([bmim][BF₄]) were measured at room temperature or over a temperature range of 293.2 to 323.2 K. The density and refractive index values of [bmim][I] appeared to be the highest among three ionic liquids (ILs). However, the experimental viscosity values of [bmim][Br] were higher than those of [bmim][BF₄], while the heat capacities and heats of dilution of [bmim][BF₄] were higher than those of [bmim][Br]. The cyclic voltammogram of [bmim][br] and [bmim][BF₄] indicated electrochemical windows in the stability range from 2.7 V of [bmim][[Br] to 4.7 V of [bmim][BF₄].     

Electrochemical and spectroscopic measurements for stable nitroxyl radicals

A nitroxyl radical, 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO), is known to be oxidized electrochemically at 3.5 V versus lithium [4] and [5]. Since this reaction is reversible in the aprotic electrolyte, we can use it as a cathode reaction in lithium rechargeable battery. Some nitroxyl radical compounds which have different structures have been prepared and their electrochemical behavior and spectroscopic properties have been studied. The electrochemical measurements in aprotic electrolyte revealed that most nitroxyl radical compounds show reversible redox behavior similar to that of TEMPO independent of their structures in the range of −0.15-0.20 V versus Ag/Ag⁺ (3.69-4.04 V versus Li/Li⁺). The redox potentials for these materials were found to be predictable approximately by quantum calculations. Thus, various molecular designs tailored to desired redox potentials would be possible as active materials for lithium rechargeable batteries, and their specific capacities, mechanical properties and colors can be controlled within limits.     

Hybrid Organic Light-Emitting Diodes with Low Color-Temperature and High Efficiency for Physiologically-Friendly Night Illumination

Low color-temperature (CT) light sources are preferred for physiologically-friendly illumination at night due to their low suppression of melatonin secretion. We fabricated low-CT hybrid organic light-emitting diodes (OLEDs) by constructing a double emissive-layer (EML) structure, with a blue-red fluorescent-phosphorescent hybrid EML and a green phosphorescent EML, separated by a bipolar interlayer. By doping a red phosphor in a blue fluorescent mixed-host with a decent concentration, blue and red emissions from the host and dopant, respectively, were obtained. The CT of the optimized device was tuned to less than 2500 K, with the brightness ranging from 100 to 10,000 cd m⁻². In addition, the low-CT OLED exhibited much higher efficacy than other low-CT light sources, such as incandescent bulbs and candles. The maximum power efficiency and external quantum efficiency of the hybrid OLED reached 54.6 lm W⁻¹ and 24.3 %, respectively, which only rolled off to 44.2 lm W⁻¹ and 23.6 % at 1000 cd m⁻², with a CT of 1910 K. Low-CT OLEDs with high efficacy provide a promising alternative for night lighting that will safeguard human health.     

Some Rheological Properties of Plasticized Polyvinyl Chloride With New Plasticizers

During an earlier research program a series of new plasticizers derived from an intermediate compound (I) [1] were synthesized and characterized [2]. In this paper the effect of benzoate, caproate, and valerate plasticizers on the melt flow rate (MFR) of PVC is studied. These new plasticizers were chosen since we previously found that epoxy plasticizers derived from a similar intermediate were very efficient for PVC [3], polymethyl methacrylate [4], and polystyrene [5].     

Xanthene dyes/amine as photoinitiators of radical polymerization: A comparative and photochemical study in aqueous medium

The efficiency of several xanthene dyes as photoinitiators of the free radical polymerization in aqueous medium was evaluated. These results show that dyes with triplet quantum yield higher than 0.1 present similar efficiencies, independently of their different chemical structure. A detailed study of the photophysics of the dyes under the polymerization conditions was carried out using laser time-resolved spectroscopies. These studies show that the active radicals are those which formed in the interaction of excited triplet state of the dye with the amine through an electron transfer process. In spite of this, the photoinitiation efficiency is not correlated with the triplet quantum yield. Also, the photophysics studies show that the quantum yield of the different pathways of the decomposition of the charge transfer intermediate is an important parameter to predict the efficiency of these photoinitiator systems. The experimentally measured active radical formation is well correlated with that calculated from the polymerization rate. The presence of heavy atoms in the xanthene ring increases the triplet quantum yield, but decreases the active radical yield, and then the polymerization rate.     

Photophysics and photochemical reactions with electron acceptors of an anellated HANTZSCH-ester

3,6-Dimethyl-9-phenyl-1,3,4,5,6,8,9,10-octahydropy-rano-[4,3-b:4′,3′-e]-pyyridine-1,8-dione ( 3 ) was prepared as first derivative of a novel substance class exhibiting a 1,4-dihydropyridine structural element. Diazonium, iodonium, sulfonium and phosphonium salts act as electron acceptors both for ground state charge transfer complex formation and in single electron transfer processes (SET) with excited states of compound 3. Solvents strongly influence the rate constants of fluorescence quenching. Those containing a hydroxyl group decrease these rate constants as well as the quantum yields of SET due to higher solvent reorganization energies. Some expressions have been developed to describe the strong solvent effect. Due to a less effective population of the triplet state, the quantum yields of the SET's are low.     

Design and construction of a hybrid immunoglobulin domain with properties of both heavy and light chain variable regions

The complementarity-determining regions (CDRs) of a human kappa light chain were replaced with CDRs from a murine gamma-1 heavy chain and, by use of molecular modeling, key heavy chain framework residues were identified and thus included to preserve the native conformation of the heavy chain CDRs. Co-expression of this hybrid human kappa chain (V[HB]C[L]) with a human kappa chain counterpart (V[L]C[L], engineered to contain murine light chain CDRs) resulted in the secretion of high levels of a heterodimeric protein (V[HB]C[L]::V[L]C[L]) termed 'kappabody'. This protein also had equivalent affinity for antigen as the Fab' of the parent murine IgG1. High-level secretion was also observed for the hybrid chain as homodimers (V[HB]C[L]::V[HB]C[L]), which is not observed for chimeric chains consisting of a heavy chain variable region and light chain constant region, i.e. V[H]C[L] homodimers or single chains are not secreted. This indicates that regions within the variable domain, required for secretion of light chains, reside outside of the hypervariable regions (CDRs) and that the heavy chain CDRs and supporting residues do not prevent secretion. These results demonstrate the possibility of designing small, single- domain molecules possessing a given binding activity which may be secreted at high levels from mammalian cells.      

Influence of substrate orientation on exciton fine structure splitting of InAs/InP nanowire quantum dots

ABSTRACT: : In this paper, we use an atomistic approach to investigate strain distributions, single particle and many body electronic properties of InAs/InP nanowire quantum dots with substrate orientation varying from [111] to high-index [119], and compared with [001] case. We show that single particle gap for high-index [11k] substrates is increased with respect to [111] and [001] cases, and oscillates with the substrate index due to faceting effects. Surprisingly, the overall shell-like structure of single particle states is preserved even for highly facetted, high-index substrates. On the contrary, we demonstrate that besides two limiting high-symmetry cases, [001] and [111], the bright exciton splitting varies strongly with substrate orientation. For [112]-oriented substrate, the fine structure splitting reaches maximum due to crystal lattice anisotropy despite fully cylindrical isotropic shape of nanowire quantum dot.     

Carrier injection and transport in blue phosphorescent organic light-emitting device with oxadiazole host

In this paper, we investigate the carrier injection and transport characteristics in iridium(III)bis[4,6-(di-fluorophenyl)-pyridinato-N,C2']picolinate (FIrpic) doped phosphorescent organic light-emitting devices (OLEDs) with oxadiazole (OXD) as the bipolar host material of the emitting layer (EML). When doping Firpic inside the OXD, the driving voltage of OLEDs greatly decreases because FIrpic dopants facilitate electron injection and electron transport from the electron-transporting layer (ETL) into the EML. With increasing dopant concentration, the recombination zone shifts toward the anode side, analyzed with electroluminescence (EL) spectra. Besides, EL redshifts were also observed with increasing driving voltage, which means the electron mobility is more sensitive to the electric field than the hole mobility. To further investigate carrier injection and transport characteristics, FIrpic was intentionally undoped at different positions inside the EML. When FIrpic was undoped close to the ETL, driving voltage increased significantly which proves the dopant-assisted-electron-injection characteristic in this OLED. When the undoped layer is near the electron blocking layer, the driving voltage is only slightly increased, but the current efficiency is greatly reduced because the main recombination zone was undoped. However, non-negligible FIrpic emission is still observed which means the recombination zone penetrates inside the EML due to certain hole-transporting characteristics of the OXD.     

Process development for manufacturing of diatomaceous earth filter aids

A pilot plant, capable of treating three tons of diatomaceous earth per day, has been operated to obtain optimum design criteria for scale-up to the commercial plant [1]. High quality filter aids, such as DICALITE [2] have been produced. A commercial plant has been completed in Kyongju city by scale up of this pilot plant test. Selective diatom-earth preparation, homogeneous calcination of diatom-cells-mixture, proper delumping and pneumatic concentration of diatom-cells are main process schemes [3]. The most efficient grinding effect has been obtained using a milling blower, as of two-cage disintegrator [4]. Variable-speed rotary kiln has been operated to convert the diatom-cells into more porous and pure products. Diatom-filter-aids, in the size range of 10-40 microns, are completely separated pneumatically by back wash cyclones.     

Structure of Co-2 × 2 nanoislands grown on Ag/Ge(111)-√3 × √3 surface studied by scanning tunneling microscopy

ABSTRACT: We have found that Co-2 × 2 islands grown on an Ag/Ge(111)-√3 × √3 surface have hcp structure with the (11-20) orientation. The island evolution involves transformation of the unit cell shape from parallelogram into rectangular, which is accompanied by the island shape transformation from hexagonal into stripe-like. Identified are two crystallographic directions for the island growth, the pseudo-[0001] and the pseudo-[1-100]. We have observed the occurrence of a lateral shift between the topmost and the underlying bilayers in the case of the island growth along the pseudo-[0001] direction. In contrast, the topmost and the underlying bilayers are unshifted for the growth along the pseudo-[1-100] direction.