Jiang-Jen Lin

Additive Enhanced Crystallization of Solution‐Processed Perovskite for Highly Efficient Planar‐Heterojunction Solar Cells

P.-W. Liang, C.-Y. Liao, Dr. C.-C. Chueh, Dr. F. Zuo, S. T. Williams, Dr. X.-K. Xin, Prof. A. K.-Y. Jen Department of Materials Science and Engineering University of Washington Seattle , WA 98195 , USA E-mail: ajen@u.washington.edu Prof. A. K.-Y. Jen Department of Chemistry University of Washington Seattle , WA 98195 , USA C.-Y. Liao, Prof. J. J. Lin Institute of Polymer Science and Engineering National Taiwan University Taipei 106 , Taiwan

The disruption of bacterial membrane integrity through ROS generation induced by nanohybrids of silver and clay.

Nanohybrids, synthesized via silver nitrate reduction in the presence of silicate clay, exhibit a high potency against bacterial growth. The plate-like clay, due to its anionic surface charges and a large surface area, serves as the support for the formation of silver nanoparticles (AgNPs) approximately 30 nm in diameter. The nanohybrid consisting of Ag/silicate at a 7/93 weight ratio inhibited the growth of dermal pathogens including Staphylococcus aureus (S. aureus), Pseudomonas aeruginosa and Streptococcus pyrogens, as well as the methicillin- and oxacillin-resistant S. aureus (MRSA and ORSA). Scanning electron microscope revealed that these nanohybrids were adherent on the surface of individual bacteria. The thin silicate plates provide a surface for immobilizing AgNPs in one highly concentrated area but prevent them from entering the cell membrane. Subsequent cytotoxicity studies indicated that surface contact with the reduced AgNPs on clay is sufficient to initiate cell death. This toxicity is related to a loss in membrane integrity due to reactive oxygen species (ROS) generation. The hybridization of AgNPs on clay surface is viable for generating a new class of nanohybrids exhibiting mild cytotoxicity but high efficacy for battling drug-resistant bacteria.

A high performance dye-sensitized solar cell with a novel nanocomposite film of PtNP/MWCNT on the counter electrode

An imide-functionalized material, poly(oxyethylene)-segmented polymer, was synthesized from the reaction of poly(oxyethylene)diamine of 2000 g mol−1Mw and 4,4′-oxydiphthalic anhydride and used to disperse hybrid nanomaterials of platinum nanoparticles and multi-wall carbon nanotubes (PtNP/MWCNT). The composite material was spin-coated into film and further prepared as the counter electrode (PtNP/MWCNT-CE) for a dye-sensitized solar cell (DSSC). The short-circuit current density (JSC) and power-conversion efficiency (η) of the DSSC with PtNP/MWCNT-CE were found to be 18.01 ± 0.91 mA cm−2 and 8.00 ± 0.23%, respectively, while the corresponding values were 14.62 ± 0.19 mA cm−2 and 6.92 ± 0.07% for a DSSC with a bare platinum counter electrode (Pt-CE). The presence and distribution of PtNP/MWCNT on the CE were characterized by using scanning electron microscopy (SEM), atomic force microscopy (AFM), energy dispersive spectroscopy (EDS), and X-ray diffraction (XRD). The attachment of PtNPs on MWCNTs was observed by transmission electron microscopy (TEM). Cyclic voltammetry (CV), incident-photo-to-current efficiency (IPCE) and electrochemical impedance spectra (EIS) were correlated to explain the efficacy of this nanocomposite system.

Flame retardant epoxy polymers based on all phosphorus-containing components

A phosphorus-containing epoxy resin, bis(3-t-butyl-4-glycidyloxyphenyl-2,4-di-t-butylphenyl)resorcinol diphosphate, was synthesized and subsequently cured with non-phosphorus containing amines, and/or novel phosphorus-containing aromatic or polyoxyalkylene amines. Chemical structures of these materials were characterized with FTIR, NMR, elemental analysis, and amine titration. The introduction of soft –P–O– linkage, polyoxyalkyene, or hard aromatic group into the backbones of the synthesized phosphorus-containing amines provides epoxy polymers with high phosphorus contents and tailored flexibility. Thermal analysis of differential scanning calorimeter and thermal gravimetric analysis (TGA) reveals that these resulted epoxy polymers possess moderate Tgs and thermal stability. Furthermore, high char yields in TGA analysis and high limited oxygen index values indicate that these phosphorus-containing epoxy polymers possess excellent flame retardant properties.

Evaluation on Cytotoxicity and Genotoxicity of the Exfoliated Silicate Nanoclay

The concern about toxicity for nanosilicate platelets (NSP) derived from natural montmorillonite clay is addressed. The NSP nanoclay was isolated from polyamine-salt exfoliation of the layered silicate clay into randomized individual plates, possessing multiple ionic charges on the surface of silicate plates with an average geometric dimension of ca. 80 x 80 x 1 nm(3). The material had been previously shown to be effective for antimicrobial and tendency for adhering onto the biomaterial surface based on the direct observation by using scanning electron microscope. The material safety on genotoxic effect was investigated by using three different test systems: the Comet assay test on Chinese Hamster Ovary (CHO) cells in vitro, micronucleus (MN) assay in vivo and the Salmonella gene mutation assay on strain TA98, TA100, TA102, TA1535 and TA1537. The Comet assay showed no DNA damage after 24 h of incubation with NSP of 1000 microg/mL. The MN test indicated no significant micronucleus induction in the CHO cells at the concentrations tested. With all five strains of Salmonella typhimurium, none of mutations was found. Furthermore, cytotoxicity of the same material was assayed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and lactate dehydrogenase (LDH) release, showing a low cytotoxicity on CHO cells below 1000 microg/mL after 12 h incubation period and a dose-dependent effect after 24 h incubation. For feeding to rats, the acute oral toxicity was shown a low lethal dose (LD(50)) or greater than 5700 mg/kg body weight for both male and female Sprague-Dawley rats. Overall, the study has demonstrated the safety of the NSP for potential uses in biomedical areas.

Poly(oxypropylene)-amide grafted polypropylene as novel compatibilizer for PP and PA6 blends

Poly(oxypropylene)-amide grafted polypropylene (PP) was prepared in an extruder by the reaction of poly(oxypropylene) (POP)diamines and maleated PP (PP-g-MA). The resulting POP-grafted PP copolymers are confirmed by the FTIR analysis, and used as compatibilizers for polyamide 6 (PA6) and polypropylene blends. These compatibilizers, POP-functionalized PPs (PP-g-MA-co-POPs), have different amphiphilic properties depending on the content of MA in the starting PP-g-MA and the molar ratio of MA/amine. The compatibilization effect is examined in terms of morphologies, thermal and mechanical properties. The morphologies, affected by the molecular weight of POP diamine in PP-g-MA-co-POP copolymer, show a decreasing size of the dispersed PA6 particles as the molecular weight of POP diamine increasing from 230 to 400 to 2000. Using these PP-g-MA-co-POP copolymers, the compatibilized blends show improvements in mechanical properties, including Izod impact strength and tensile toughness, over a conventional compatibilizer. The POP and amide functionalities in the compatibilizers can facilitate the formation of hydrogen bonding with PA6 and, therefore, the compatibilizing effect. During the compounding process, the compatibilizers further react with PA6 in situ to afford the mixture of PP-g-MA-co-POP-PA6, PP-g-MA-co-POP-co-PA6 and PP-g-MA-co-PA6 copolymers, which further improves the compatibilizing effect.

Evaluation of the antibacterial activity and biocompatibility for silver nanoparticles immobilized on nano silicate platelets.

Silver nanoparticles (AgNPs) are known for their bactericidal abilities. The antibacterial potency is dependent on the particle size and dispersion status. In this study, we synthesized AgNP/NSP nanohybrids in two different weight ratios (1/99 and 8/92) using the fully exfoliated clay, i.e., nanosilicate platelets (NSP), as a dispersing agent and carrier for AgNPs. Due to the size of NSP, the immobilized AgNPs do not enter cells readily, which may lower the risk associated with the cellular uptake of AgNPs. The biocompatibility, immunological response, and antimicrobial activities of AgNP/NSP hybrids were evaluated. The results revealed that AgNP/NSP hybrids elicited merely mild inflammatory response and retained the outstanding antibacterial activity. The hybrids were further embedded in poly(ether)urethane (PEU) to increase the biocompatibility. At the same silver content (20 ppm), the PEU-AgNP/NSP nanocomposites were nontoxic to mouse skin fibroblasts, while simultaneously exhibiting nearly complete bacterial growth reduction (99.9%). PEU containing the same amount of free AgNPs did not display such an effect. Our results verify the better biosafety of the AgNPs/NSP hybrids and their polymer nanocomposites for further clinical use.

Concentration effect of carbon nanotube based saturable absorber on stabilizing and shortening mode-locked pulse

We comprehensively investigated the concentration effect of dispersed single-walled carbon nanotubes (SWCNTs) in polymer films for being a saturable absorber (SA) to stabilize the mode locking performance of the erbium-doped fiber laser (EDFL) pulse through the diagnosis of its nonlinear properties of SA. The measured modulation depth was from 1 to 4.5% as the thickness increased 18 to 265 microm. The full-width half-maximum (FWHM) of the stable mode-locked EDFL (MLEDFL) pulse decreased from 3.43 to 2.02 ps as the concentrations of SWCNTs SA increased 0.125 to 0.5 wt%. At constant concentration of 0.125 wt%, the similar pulse shortening effect of the MLEDFL was also observed when the FWHM decreased from 3.43 to 1.85 ps as the thickness of SWCNTs SA increased 8 to 100 microm. With an erbium-doped fiber length of 80 cm, the shortest pulse width of 1.85 ps were achieved at 1.56 microm with a repetition rate of 11.1 MHz and 0.2 mW of the output power under an output coupling ratio of 5%. An in-depth study on the stable mode-locked pulse formation employing SWCNTs SA, it is possible to fabricate the SWCNT films for use in high performance MLEDFL and utilization of many other low-cost nanodevices.

The cellular responses and antibacterial activities of silver nanoparticles stabilized by different polymers

Silver nanoparticles (AgNPs) are known for their excellent antibacterial activities. The possible toxicity, however, is a major concern for their applications. Three types of AgNPs were prepared in this study by chemical processes. Each was stabilized by a polymer surfactant, which was expected to reduce the exposure of cells to AgNPs and therefore their cytotoxicity. The polymer stabilizers included poly(oxyethylene)-segmented imide (POEM), poly(styrene-co-maleic anhydride)-grafting poly(oxyalkylene) (SMA) and poly(vinyl alcohol) (PVA). The cytotoxicity of these chemically produced AgNPs to mouse skin fibroblasts (L929), human hepatocarcinoma cells (HepG2), and mouse monocyte macrophages (J774A1) was compared to that of physically produced AgNPs and gold nanoparticles (AuNPs) as well as the standard reference material RM8011 AuNPs. Results showed that SMA-AgNPs were the least cytotoxic among all materials, but cytotoxicity was still observed at higher silver concentrations (>30 ppm). Macrophages demonstrated the inflammatory response with cell size increase and viability decrease upon exposure to 10 ppm of the chemically produced AgNPs. SMA-AgNPs did not induce hemolysis at a silver concentration below 1.5 ppm. Regarding the antibacterial activity, POEM-AgNPs and SMA-AgNPs at 1 ppm silver content showed 99.9% and 99.3% growth inhibition against E. coli, while PVA-AgNPs at the same silver concentration displayed 79.1% inhibition. Overall, SMA-AgNPs demonstrated better safety in vitro and greater antibacterial effects than POEM-AgNPs and PVA-AgNPs. This study suggested that polymer stabilizers may play an important role in determining the toxicity of AgNPs.

A novel polymer gel electrolyte for highly efficient dye-sensitized solar cells

A structurally interconnected block copolymer was facilely prepared by the oligomerization of poly(oxyethylene)-segmented diamine and 4,4′-oxydiphthalic anhydride, followed by a late-stage curing to generate amide-imide cross-linked gels. The gel structure, with multiple functionalities including poly(oxyethylene) segments, amido-acid linkers, amine termini, and amide cross-linker was characterized by Fourier transform infrared spectroscopy. The gel-like copolymer was used to absorb a liquid electrolyte; formation of 3D interconnected nanochannels, as could be observed by field emission scanning electronic microscopy has confirmed this absorption of the liquid electrolyte by the copolymer. This elastomeric copolymer was used as the matrix of a polymer gel electrolyte (PGE) for a dye-sensitized solar cell (DSSC), which shows extremely high photovoltaic performance (soaking for 1 h in the electrolyte). In particular, the PGE containing 76.8 wt% of the liquid electrolyte renders a power conversion efficiency of 9.48% for its DSSC, with a short-circuit photocurrent density of 19.50 mA cm−2, an open-circuit voltage of 0.76 V, and a fill factor of 0.64. The outstanding performance of the gel-state DSSC, superior to that (8.84%) of the DSSC with the liquid electrolyte, is mainly ascribed to the suppression of the back electron transfer through the PGE. Electrochemical impedance spectra, and dark current measurements were used to substantiate the explanations of the photovoltaic parameters.