Linear-Shaped Low-Bandgap Asymmetric Conjugated Donor Molecule for Fabrication of Bulk Heterojunction Small-Molecule Organic Solar Cells.

A linear-shaped small organic molecule (E)-4-(5-(3,5-dimethoxy-styryl)thiophen-2-yl)-7-(5″-hexyl-[2,2':5',2″-terthiophen]-5-yl)benzo[c][1,2,5]thiadiazole (MBTR) comprising a benzothiadiazole (BTD) acceptor linked with the terminal donors bithiophene and dimethoxy vinylbenzene through a π-bridge thiophene was synthesized and analyzed. The MBTR efficiently tuned the thermal, absorption, and emission characteristics to enhance the molecular packing and aggregation behaviors in the solid state. The obtained optical bandgap of 1.86 eV and low-lying highest occupied molecular orbital (HOMO) level of -5.42 eV efficiently lowered the energy losses in the fabricated devices, thereby achieving enhanced photovoltaic performances. The optimized MBTR:PC71BM (1:2.5 w/w%) fullerene-based devices showed a maximum power conversion efficiency (PCE) of 7.05%, with an open-circuit voltage (VOC) of 0.943 V, short-circuit current density (JSC) of 12.63 mA/cm2, and fill factor (FF) of 59.2%. With the addition of 3% 1,8-diiodooctane (DIO), the PCE improved to 8.76% with a high VOC of 1.02 V, JSC of 13.78 mA/cm2, and FF of 62.3%, which are associated with improved charge transport at the donor/acceptor interfaces owing to the fibrous active layer morphology and favorable phase separation. These results demonstrate that the introduction of suitable donor/acceptor groups in molecular design and device engineering is an effective approach to enhancing the photovoltaic performances of organic solar cells.

Network formation in graphene oxide composites with surface grafted PNIPAM chains in aqueous solution characterized by rheological experiments.

Poly N-isopropyl acrylamide (PNI) radically polymerized in aqueous solution in the presence of graphene oxide (GO) can significantly change the properties of the resulting solution from a regular polymer solution to a soft solid with a GO content of only 0.176 wt% (3 wt% with respect to PNI). However, these properties require the presence of both grafting and supramolecular interactions between polymer chains and hydrophilic groups on GO (-OH, -COOH), proven by Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), X-ray diffraction and spectroscopy (XRD) and Raman spectra. While very low GO-contents (below 0.05 wt%) only lead to a labile structure, which can be disassembled by shear, higher contents yield composites with solid-like characteristics. This is clearly evident from the rheological behaviour, which changes significantly at a GO content around 0.15 wt%. Intensive shearing destroys the weak network, which cannot reform quickly at lower GO-concentrations, while at intermediate concentrations, restructuring is fast. GO-contents of 0.176 wt% lead to a material behaviour, which almost perfectly recovers from small deformations (creep and creep recovery compliance almost match) but larger deformations lead to permanent damage to the sample.

Screening of novel peptides that specifically interact with vitamin D bound biocomplex proteins.

The majority of the vitamin D that is present in the blood binds to vitamin D binding protein (VDBP) and circulates in the form of a complex (VDBP-Complex). Knowing the level of vitamin D in the body is crucial for vitamin D-related treatments so that the right dosage of vitamin D can be given. In other words, it is essential to distinguish between the protein VDBP and the complex form bound to vitamin D. As a novel way for the detection of VDBP-Complex, a more effective phage display methodology was applied in this study along with the addition of two approaches. In order to screen a sequence specific to the target only, the pre-binding method and after-binding method were performed. VDBP-Complex was directly coated on the petri dishes. In order to select phages that specifically bind to the VDBP-Complex, random phages were attached, and selected by 7 times of biopanning. Individual DNA sequences were analyzed for each biopanning to find specific peptide sequences for VDBP-Complex. The affinity of binding phages was verified by ELISA assay using an anti-M13 antibody. The phage having a sequence of SFTKTSTFTWRD (called as M3) has shown the highest binding affinity to VDBP-Complex. As a result of the removal test of VDBP-Complex using magnetic beads conjugated with M3 peptide, it was confirmed that significant decrease of VDBP-Complex. The unique characteristic of the M3 sequence was confirmed through a sequence-modified peptide (SFT motif). That is, it is expected that the M3 peptide may be used to determine the vitamin D levels in the blood.

Study on Aminated PP-g-GMA Synthesized by Radiation-Induced Graft Polymerization for Silver Adsorption.

In the semiconductor manufacturing process, metallic contaminants remain on the surface of the silicon wafer, which has a serious effect on the physical and electrical characteristics of the semiconductor device. In particular, silver has high electrical conductivity and large reducibility, and it is not easily removed causing a great deal of damage in small amounts. Therefore, it is important to prevent contamination by lowering the silver ion concentration in the etching agent in the wet etching process. In this study, to prepare an effective silver ion adsorbent, glycidyl methacrylate (GMA) was grafted onto polypropylene (PP) through electron beam irradiation. Ethylenediamine (EDA) and diethylenetriamine (DETA) were introduced into the epoxide group of GMA via amination. The prepared adsorbent was packed in a holder and connected to a circulation pump, and 1 L of 200 ppm silver ion solution was circulated at room temperature for 12 hours. The adsorbents aminated with EDA and DETA showed adsorption capacities of 2.0587 mmol/g and 2.3645 mmol/g, respectively.

Improvement of device efficiency by phosphorescent materials in polymers bulk heterojunction solar cells.

To improve the performance of organic solar cells, various methods have been used to increase the light absorbance and electron transfer efficiency or decrease the internal resistance of the device. In this article, red dyes of phosphorescent materials are used to improve the performance of bulk heterojunction organic solar cells based on MDMO-PPV and PCBM. Solar cell devices doped with different red dyes showed higher performances in terms of current, voltage and conversion efficiency than those without red dyes. The efficiency was maximized in the devices with a 10% concentration of red dye 2, which was attributed to the longer exciton lifetimes that were induced by the triplet spin state of the red dyes allowing them to reach the p-n junction and thereby generate more photocurrent.

Effect of Potassium Ions on the Formation of Mixed-Valence Manganese Oxide/Graphene Nanocomposites.

One-pot synthesis of mixed-valence manganese oxide (MnOx)/potassium ion-doped reduced graphene oxide (rGO) composites for efficient electrochemical supercapacitors is introduced. Using manganese nitrate and potassium permanganate as co-precursors for the MnOx and by directly annealing the rGO without tedious purification steps, as described herein, MnOx/rGO composites with a high specific capacitance of 1955.6 F g-1 at a current density of 1 A g-1 are achieved. It is found that the presence of potassium ions helps in the development of mixed-valence MnOx on the surface of the rGO.

NiCo2S4 Nanotrees Directly Grown on the Nickel NP-Doped Reduced Graphene Oxides for Efficient Supercapacitors.

In this work, we report a feasible fabrication of NiCo2S4 nanotree-like structures grown from the Ni nanoparticle (NP)-doped reduced graphene oxides (Ni-rGO) by a simple hydrothermal method. It is found that the presence of Ni NPs on the surface of the rGOs initiates growth of the NiCo2S4 nanotree flocks with enhanced interfacial compatibility, providing excellent cyclic stability and rate performance. The resulting NiCo2S4/Ni-rGO nanocomposites exhibit a superior rate performance, demonstrating 91.6% capacity retention even after 10,000 cycles of charge/discharge tests.

Enhancement of flame retardancy of rubber matrix using nanofillers.

Natural rubber (NR) nanocomposites filled with carbon nanotubes (CNT) and organoclay (O-MMT) were prepared by melt mixing, and their vulcanization, mechanical, thermal and flammability properties were characterized. The obtained results were compared with those of carbon black (CB) and pure NR composites. The incorporation of OC reduced drastically the cure times, when compared with CNT and CB-reinforced compounds. The addition of CNT increased considerably the difference between minimum and maximum torques compared with OC and CB-reinforced composites. The mechanical properties were improved by adding nanofillers of CNT and OC. The nanocomposites filled with OC and CNT showed lower peak heat release rate (PHRR) obtained from a cone calorimeter and corresponding reduced surface cracks of formed chars after burning. A slight synergistic effect was found for NR nanocomposite having equal amount of OC and CNT.

Synthesis of thiourea-immobilized polystyrene nanoparticles and their sorption behavior with respect to silver ions in aqueous phase.

Although a thiourea-immobilized polystyrene sorbent has been reported to exhibit high Ag+ sorption capacity (135mg/g), it is not stable under the acidic conditions commonly employed for desorption. In this research, we synthesized novel thiourea-immobilized polystyrene (TA-PS) nanoparticles to be highly acid resistant via a two-step procedure from polystyrene nanoparticles: acetylation and the subsequent immobilization of thiourea. We investigated the influences of pH, contact time, and initial concentration of AgNO3 solution on the Ag+ sorption of the polymer nanoparticles and estimated the maximum Ag+ sorption capacity to be 190±5mg/g at a pH of 6. The sorption performance did not significantly decrease in tap water containing competing ions. The sorption kinetic data were well fitted to the pseudo-second-order kinetic model. Overall, the TA-PS nanoparticles exhibited a high Ag+ sorption capacity and high selectivity against alkaline and alkaline earth-metal ions. In particular, their high acid resistance allows them to be used for long time periods in sorption-desorption processes.

Enhanced Performance in Bulk Heterojunction Polymer Solar Cell Using Water Soluble Conjugated Polymer.

We have synthesized water-soluble polymer, poly[(9,9-bis((6'-(N,N,N-trimethylammonium)hexyl)-2,7-fluorene))-alt-bisphenylfumaronitrile]dibromide (AHF-alt-PFN), the polymer typically obtained by the Suzuki type of polymerization reaction and shows good solubility in methanol. Bulk heterojunction polymer solar cells (BHJ-PSCs) fabricated by using water soluble conjugated polymer and positive (Cs+) and negative (F-, CO2-(3)) charge ions doping as an interfacial layer for poly(3-hexylthiophene):phenyl-C61 butyric acid methyl ester (P3HT:PCBM). We have achieved an enhancement of the short circuit density and power conversion efficiency in solar cell by introducing poly(AHF-alt-PFN) layer between the active layer and the cathode metal. The device with poly(AHF-alt-PRN) layer containing F-, CO2-(3) showed a short circuit current density more 1.3, 2.3 times higher than those of the device without poly(AHF-alt-PFN) + ion layer. We explain the better performance in solar cell with poly(AHF-alt-PFN) + ion layer was due not only to the increase of electron mobility in poly(AHF-alt-PFN) layer but also to the decrease of the electron barrier near cathode by the addition of the negative ions.

Synthesis of 4-vinylpyridine-divinylbenzene copolymer adsorbents for microwave-assisted desorption of benzene.

Reports on the development of polymer adsorbents for microwave-assisted desorption of nonpolar volatile organic compounds (VOCs) are rare. In this study, we synthesized macroporous polymeric adsorbents with hydrophilic methyl pyridinium units for microwave-assisted desorption of nonpolar VOCs. The benzene adsorption and desorption properties of the adsorbents were investigated under both dry and humid conditions. Under humid conditions, as the content of the hydrophilic methyl pyridinium units in the adsorbents increased from 0 to 20%, the adsorption capacity of benzene decreased from about 21 to 7 mg/g, while the desorption efficiency of benzene increased significantly from 48 to 87%. The maximum concentration of desorbate also increased significantly as the content of the hydrophilic units was increased under humid conditions. We attributed the enhanced desorption efficiency mainly to more adsorbed moisture, which indirectly allowed heating of the polymer adsorbents to higher temperatures upon irradiation with 600 W microwaves.

Transgenic mice with neuron-specific overexpression of HtrA2/Omi suggest a neuroprotective role for HtrA2/Omi.

Mammalian serine protease HtrA2/Omi has been known as an apoptosis inducer involved inactivation of caspase-dependent as well as caspase-independent cell death. Recent studies with the HtrA2/Omi mutant and knockout mouse models, however, suggested that HtrA2/Omi might play a protective role in neurons. It is important to establish a transgenic mouse model with neuron-specific overexpression of HtrA2/Omi to clarify the physiological function of mammalian HtrA2/Omi in neurons. In the present study, a transgene containing HtrA2/Omi cDNA downstream of a rat neuron-specific enolase promoter was constructed and microinjected into the pronuclei of fertilized zygotes to establish transgenic mice. Transgenic mice successfully overexpressed HtrA2/Omi in brain tissue. As expected, HtrA2/Omi-overexpressing transgenic mice showed normal development without any sign of apoptotic cell death. Our results suggest that the primary function of neuronal HtrA2/Omi might be to protect neurons against stress in contrast to its role in the somatic system.

[Usefulness of Anti-HCV ELISA Test and HCV Reverse Transcriptase-PCR for the Diagnosis of Hepatits C Viral Infection.].

BACKGROUND: The diagnosis of hepatitis C virus (HCV) infection is screened by anti-HCV enzymelinked immunosorbant assay (ELISA) and confirmed by recombinant immunoblotting assay (RIBA) or HCV RT-PCR. We attempted to evaluate the results between anti-HCV ELISA and a qualitative HCV RT-PCR. METHODS: Four hundred and twenty patients who were tested with anti-HCV ELISA and HCV RTPCR, simultaneously, from January 2002 to June 2005 were enrolled in this study. Anti-HCV ELISA was performed by AxSYM HCV version 3.0 (Abbott Laboratories, USA). HCV RT-PCR was performed using in-house RT-nested PCR methods from January 2002 to October 2004 and HCV Genotype Amplification Kit (LiPA) (Bayer Healthcare, USA) from November 2004 to June 2005. RESULTS: Of the 420 patients tested, 321 were positive for anti-HCV ELISA, and 204 were positive for RT-PCR. The positive predictability of anti-HCV ELISA was 63.6%. Among anti-HCV positive patients, RT-PCR was positive in 7.3% of the patients with sample/cut-off (S/CO)<6, compared with 82.8% of the patients with S/CO>/=6. Among the 117 patients with positive anti-HCV, but with negative HCV RT-PCR, 64 had liver diseases such as chronic hepatitis C, chronic hepatitis B, or hepatocellular carcinoma. Twelve patients showed positive HCV RT-PCR, but negative anti-HCV results; of these 9 had hepatic dysfunction. CONCLUSIONS: In the patients who were positive for anti-HCV ELISA with a low S/CO, HCV RT-PCR positivity was shown in a low proportion. Therefore, in such cases, the results should be confirmed by RIBA or HCV RT-PCR. The liver function test showed increased levels of hepatic enzymes in patients with positive HCV RT-PCR, but negative anti-HCV. Such findings correlate to an early phase of chronic hepatitis C, suggesting the necessity of continuous follow up.