Functionalization of an extended-gate field-effect transistor (EGFET) for bacteria detection.

Traditional sensing technologies have drawbacks as they are time-consuming, cost-intensive, and do not attain the required accuracy and reproducibility. Therefore, new methods of measurements are necessary to improve the detection of bacteria. Well-established electrical measurement methods can connect high sensitive sensing systems with biological requirements. One approach is to functionalize an extended-gate field-effect transistor's (EGFET) sensing area with modified porphyrins containing two different linkers. One linker connects the electrode surface with the porphyrin. The other linker bonds bacteria on the functional layer through a specific peptide chain. The negative charge on the surface of the cells regulates the surface potential which has an impact on the electrical behavior of the EGFET. The attendance of attached bacteria on the functionalized sensing area could successfully be detected.

Organic Dye-Doped PMMA Lasing.

Organic thin-film lasers gain interest as potential light sources for application in diverse fields. With the current development, they hold variety of benefits such as: low-cost, high-performance, and color-tunability. Meanwhile, the production is not complicated because both the resonator and the gain medium can be assembled by solution-processable organic materials. To our knowledge, information about using poly(methyl methacrylate) (PMMA) as a matrix for organic dye lasers was insubstantial. Herein, the feasibility of using organic dye-doped PMMA as an organic dye laser was tested. Six different sample designs were introduced to find out the best sample model. The most optimum result was displayed by the sample design, in which the gain medium was sandwiched between the substrate and the photoresist layer with grating structure. The impact of dye concentration and grating period on peak wavelength was also investigated, which resulted in a shift of 6 nm and 25 nm, respectively. Moreover, there were in total six various organic dyes that could function well with PMMA to collectively perform as 'organic dye lasers', and they emitted in the range of 572 nm to 609 nm. Besides, one of the samples was used as a sensor platform. For instance, it was used to detect the concentration of sugar solutions.

A2BC-Type Porphyrin SAM on Gold Surface for Bacteria Detection Applications: Synthesis and Surface Functionalization.

Currently used elaborate technologies for the detection of bacteria can be improved in regard to their time consumption, labor intensity, accuracy and reproducibility. Well-known electrical measurement methods might connect highly sensitive sensing systems with biological requirements. The development of modified sensor surfaces with self-assembled monolayers (SAMs) from functionalized porphyrin for bacteria trapping can lead to a highly sensitive sensor for bacteria detection. Different A2BC-type porphyrin structures were synthesized and examined regarding their optical behavior. We achieved the synthesis of a porphyrin for SAM formation on a gold surface as electrode material. Two possible bio linkers were attached on the opposite meso-position of the porphyrin, which allows the porphyrin to react as a linker on the surface for bacteria trapping. Different porphyrin structures were attached to a gold surface, the SAM formation and the respective coverage was investigated.

Optical and Electrical Measurements Reveal the Orientation Mechanism of Homoleptic Iridium-Carbene Complexes.

Understanding and controlling the driving forces for molecular alignment in optoelectronic thin-film devices is of crucial importance for improving their performance. In this context, the preferential orientation of organometallic iridium complexes is in the focus of research to benefit from their improved light-outcoupling efficiencies in organic light-emitting diodes (OLEDs). Although there has been great progress concerning the orientation behavior for heteroleptic Ir complexes, the mechanism behind the alignment of homoleptic complexes is still unclear yet. In this work, we present a sky-blue phosphorescent dye that shows variable alignment depending on systematic modifications of the ligands bound to the central iridium atom. From an optical study of the transition dipole moment orientation and the electrically accessible alignment of the permanent dipole moment, we conclude that the film morphology is related to both the aspect ratio of the dye and the local electrostatic interaction of the ligands with the film surface during growth. These results indicate a potential strategy to actively control the orientation of iridium-based emitters for the application in OLEDs.

Upconversion Nanocrystal Doped Polymer Fiber Thermometer.

In recent years, lanthanide-doped nanothermometers have been mainly used in thin films or dispersed in organic solvents. However, both approaches have disadvantages such as the short interaction lengths of the active material with the pump beam or complicated handling, which can directly affect the achievable temperature resolution. We investigated the usability of a polymer fiber doped with upconversion nanocrystals as a thermometer. The fiber was excited with a wavelength stabilized diode laser at a wavelength of 976 nm. Emission spectra were recorded in a temperature range from 10 to 35 ∘C and the thermal emission changes were measured. Additionally, the pump power was varied to study the effect of self-induced heating on the thermometer specifications. Our fiber sensor shows a maximal thermal sensitivity of 1.45%/K and the minimal thermal resolution is below 20 mK. These results demonstrate that polymer fibers doped with nanocrystals constitute an attractive alternative to conventional fluorescence thermometers, as they add a long pump interaction length while also being insensitive to strong electrical fields or inert to bio-chemical environments.

Towards Highly Efficient Polymer Fiber Laser Sources for Integrated Photonic Sensors.

Lab-on-a-Chip (LoC) devices combining microfluidic analyte provision with integrated optical analysis are highly desirable for several applications in biological or medical sciences. While the microfluidic approach is already broadly addressed, some work needs to be done regarding the integrated optics, especially provision of highly integrable laser sources. Polymer optical fiber (POF) lasers represent an alignment-free, rugged, and flexible technology platform. Additionally, POFs are intrinsically compatible to polymer microfluidic devices. Home-made Rhodamine B (RB)-doped POFs were characterized with experimental and numerical parameter studies on their lasing potential. High output energies of 1.65 mJ, high slope efficiencies of 56 % , and 50 % -lifetimes of ≥900 k shots were extracted from RB:POFs. Furthermore, RB:POFs show broad spectral tunability over several tens of nanometers. A route to optimize polymer fiber lasers is revealed, providing functionality for a broad range of LoC devices. Spectral tunability, high efficiencies, and output energies enable a broad field of LoC applications.

Homogeneous Distribution of Polymerizable Coumarin Dyes for Active Few Mode POF.

For most kinds of active polymer optical fibers, a homogeneous distribution of dye molecules over the entire fiber length and cross section is required. In this study, chemical bonding of dyes to poly(methyl methacrylate) (PMMA) by copolymerization is achieved within the polymerization process instead of dissolving the dyes in the monomers. In combination with an improved fabrication mechanism, this leads to homogeneous dye distribution within the preforms. A method for proving the integration of the dyes into the polymer chains has been developed using high-performance liquid chromatography (HPLC) and size exclusion chromatography (SEC). Prestructured core-cladding preforms with dye-doped poly(cylohexyl methacrylate-co-methyl methacrylate)-core have been prepared with the Teflon string technique and were heat-drawn to few mode fibers.

Room-Temperature Stimulated Emission and Lasing in Recrystallized Cesium Lead Bromide Perovskite Thin Films.

Cesium lead halide perovskites are of interest for light-emitting diodes and lasers. So far, thin-films of CsPbX3 have typically afforded very low photoluminescence quantum yields (PL-QY < 20%) and amplified spontaneous emission (ASE) only at cryogenic temperatures, as defect related nonradiative recombination dominated at room temperature (RT). There is a current belief that, for efficient light emission from lead halide perovskites at RT, the charge carriers/excitons need to be confined on the nanometer scale, like in CsPbX3 nanoparticles (NPs). Here, thin films of cesium lead bromide, which show a high PL-QY of 68% and low-threshold ASE at RT, are presented. As-deposited layers are recrystallized by thermal imprint, which results in continuous films (100% coverage of the substrate), composed of large crystals with micrometer lateral extension. Using these layers, the first cesium lead bromide thin-film distributed feedback and vertical cavity surface emitting lasers with ultralow threshold at RT that do not rely on the use of NPs are demonstrated. It is foreseen that these results will have a broader impact beyond perovskite lasers and will advise a revision of the paradigm that efficient light emission from CsPbX3 perovskites can only be achieved with NPs.

Characterization of Double-Doped Polymer Optical Fibers as Luminescent Solar Concentrators.

This work reports on a diameter dependence analysis of the performance as luminescent solar concentrators of three self-fabricated polymer optical fibers (POFs) doped with a hybrid combination of dopants. The works carried out include the design and self-fabrication of the different diameter fibers; an experimental analysis of the output power, of the output irradiance and of the fluorescent fiber solar concentrator efficiency; a comparison of the experimental results with a theoretical model; a study of the performance of all the fibers under different simulated lighting conditions; and a calculation of the active fiber length of each of the samples, all of them as a function of the fiber core diameter. To the best of our knowledge, this paper reports the first analysis of the influence of the POF diameter for luminescent solar concentration applications. The results obtained offer a general perspective on the optimal design of solar energy concentrating systems based on doped POFs and pave the way for the implementation of cost-effective solar energy concentrating devices.

Twist it! The acid-dependent isomerization of homoleptic carbenic iridium(iii) complexes.

The first successful meridional to facial isomerization of homoleptic carbenic iridium(iii) complexes is presented. The Brønsted-acid-mediated procedure allows the conversion of large amounts of material and additionally provides an in situ purification because of precipitation of the target material during the reaction. The pronounced acid-dependency of the reaction yield observed for tris(N-phenyl,N-methyl-benzimidazol-2-yl)iridium(iii) and tris(N-phenyl,N-benzyl-benzimidazol-2-yl)iridium(iii) was investigated by labelling experiments and quantum chemical calculations. The results reveal a subtle balance between the strength of the acid, the coordinating power of the corresponding base and steric effects of the ligand sphere. Based on these findings, general rules are given for a systematic and material-specific modification of the reaction conditions for the mer-fac isomerization of homoleptic carbenic Ir(iii) complexes.

Methacrylate-Based Copolymers for Polymer Optical Fibers.

Waveguides made of poly-methyl-methacrylate (PMMA) play a major role in the homogeneous distribution of display backlights as a matrix for solid-state dye lasers and polymer optical fibers (POFs). PMMA is favored because of its transparency in the visible spectrum, low price, and well-controlled processability. Nevertheless, technical drawbacks, such as its limited temperature stability, call for new materials. In this work, the copolymerization technique is used to modify the properties of the corresponding homopolymers. The analytical investigation of fourteen copolymers made of methyl-methacrylate (MMA) or ethyl-methacrylate (EMA) as the basis monomer is summarized. Their polymerization behaviors are examined by NMR spectroscopy with subsequent copolymerization parameter evaluation according to Fineman-Ross and Kelen-Tüdös. Therefore, some r-parameter sets are shown to be capable of copolymerizations with very high conversions. The first applications as high-temperature resistant (HT) materials for HT-POFs are presented. Copolymers containing isobornyl-methacrylate (IBMA) as the comonomer are well-suited for this demanding application.

Moisture barrier properties of thin organic-inorganic multilayers prepared by plasma-enhanced ALD and CVD in one reactor.

A widely used application of the atomic layer deposition (ALD) and chemical vapour deposition (CVD) methods is the preparation of permeation barrier layers against water vapour. Especially in the field of organic electronics, these films are highly demanded as such devices are very sensitive to moisture and oxygen. In this work, multilayers of aluminium oxide (AlO x ) and plasma polymer (PP) were coated on polyethylene naphthalate substrates by plasma-enhanced ALD and plasma-enhanced CVD at 80â"ƒ in the same reactor, respectively. As precursor, trimethylaluminium was used together with oxygen radicals in order to prepare AlO x , and benzene served as precursor to deposit the PP. This hybrid structure allows the decoupling of defects between the single AlO x layers and extends the permeation path for water molecules towards the entire barrier film. Furthermore, the combination of two plasma techniques in a single reactor system enables short process times without vacuum breaks. Single aluminium oxide films by plasma-enhanced ALD were compared to thermally grown layers and showed a significantly better barrier performance. The water vapour transmission rate (WVTR) was determined by means of electrical calcium tests. For a multilayer with 3.5 dyads of 25-nm AlO x and 125-nm PP, a WVTR of 1.2 × 10 (-3) gm (-2) d (-1) at 60â"ƒ and 90% relative humidity could be observed.

Conformal and highly luminescent monolayers of Alq3 prepared by gas-phase molecular layer deposition.

The gas-phase molecular layer deposition (MLD) of conformal and highly luminescent monolayers of tris(8-hydroxyquinolinato)aluminum (Alq3) is reported. The controlled formation of Alq3 monolayers is achieved for the first time by functionalization of the substrate with amino groups, which serve as initial docking sites for trimethyl aluminum (TMA) molecules binding datively to the amine. Thereby, upon exposure to 8-hydroxyquinoline (8-HQ), the self-limiting formation of highly luminescent Alq3 monolayers is afforded. The growth process and monolayer formation were studied and verified by in situ quartz crystal monitoring, optical emission and absorption spectroscopy, and X-ray photoelectron spectroscopy. The nature of the MLD process provides an avenue to coat arbitrarily shaped 3D surfaces and porous structures with high surface areas, as demonstrated in this work for silica aerogels. The concept presented here paves the way to highly sensitive luminescent sensors and dye-sensitized metal oxides for future applications (e.g., in photocatalysis and solar cells).

Synthesis of new pyrrole-pyridine-based ligands using an in situ Suzuki coupling method.

The compounds 6-(pyrrol-2-yl)-2,2'-bipyridine, 2-(pyrrol-2-yl)-1,10-phenanthroline and 2-(2-(N-methylbenz[d,e]imidazole)-6-(pyrrol-2-yl)-pyridine were synthesized by using an in situ generated boronic acid for the Suzuki coupling. Crystals of the products could be grown and exhibited interesting structures by X-ray analysis, one of them showing a chain-like network with the adjacent molecules linked to each other via intermolecular N-H(…)N hydrogen bonds.

Pyrrolo[1,2-a]quinoxalines: novel synthesis via annulation of 2-alkylquinoxalines.

In an attempt to synthesize a novel homoleptic complex 3 from 2-methyl-3-phenylquinoxaline 1 and Ir(acac)(3) for application as a triplet emitter in OLEDs (organic light-emitting diodes) no cyclometalation was observed. Instead, an annulation to 1-methyl-4-phenylpyrrolo[1,2-a]quinoxaline 2 was observed. Since pyrroloquinoxalines are potentially bioactive and few paths for their synthesis are known, selected reactions and conditions were investigated, suggesting Ir(acac)(3) as catalyst and proving glycerol to be a reactant.

mer-Bis[2-(1,3-benzothiazol-2-yl)phenyl-κC,N][3-phenyl-5-(2-pyridyl)-1,2,4-triazol-1-ido-κN,N]iridium(III) deuterochloro-form 3.5-solvate.

In the title compound, [Ir(C(13)H(9)N(4))(C(13)H(8)NS)(2)]·3.5CDCl(3), the coordination at iridium is octa-hedral, but with narrow ligand bite angles. The bond lengths at iridium show the expected trans influence, with the Ir-N bonds trans to C being appreciably longer than those trans to N. The chelate rings are mutually perpendicular, the inter-planar angles between them all lying within 6° of 90°. All ligands are approximately planar; the maximum inter-planar angles within ligands are ca 10°. The three ordered deuterochloro-form mol-ecules are all involved in C⋯D-A contacts that can be inter-preted as hydrogen bonds of various types. The fourth deuterochloroform is disordered over an inversion centre.

mer-[3-Phenyl-5-(2-pyridyl-κN)-1,2,4-triazol-1-ido-κN]bis-(2-quinolylphenyl-κC,N)iridium(III) deuterochloro-form disolvate.

In the title compound, [Ir(C(13)H(9)N(4))(C(15)H(10)N)(2)]·2CDCl(3), the coordination at iridium is octa-hedral, but with narrow ligand bite angles ranging from 74.85 (8) to 83.99 (8)°. The bond lengths at iridium show the expected trans influence, with Ir-N trans to C being appreciably longer than trans to N. The chelate rings are mutually perpendicular to a reasonable approximation [interplanar angles ranging from 77.79 (6) to 83.93 (7)°]. All ligands are approximately planar; the maximum inter-planar angles within ligands are ca 12°. One CDCl(3) solvent molecule is severly disordered and was excluded from the refinement.

Efficient and long-time stable red iridium(III) complexes for organic light-emitting diodes based on quinoxaline ligands.

We report the design and characterization of three heteroleptic orange-red phosphorescent iridium(III) complexes bearing two 2-(4-fluorophenyl)-3-methyl-quinoxaline (fpmqx) cyclometalated ligands combined with three different ancillary ligands, triazolylpyridine (trz), picolinate (pic), and acetylacetonate (acac). All of these complexes emit an orange to red color in the spectral range of 605-628 nm in dichloromethane. Strong spin-orbit coupling of the iridium atom allows the formally forbidden mixing of singlet and triplet states. Because of the structureless phosphorescent line shapes and low Stokes shifts between triplet metal-to-ligand charge-transfer ((3)MLCT) absorption and phosphorescent emission, we propose that emission originates predominantly from the (3)MLCT state with a lesser admixture of totally ligand-based (3)(pi-pi*) states. The influence of 5d-electron densities of the iridium center on highest occupied molecular orbitals leads to high emission quantum yields in toluene (Phi(p) = 0.39-0.42) and to short triplet lifetimes. Cyclovoltammetry measurements show reversible oxidation peaks from 0.74 to 0.92 V and reversible reduction waves with potentials ranging from -1.58 to -2.05 V versus Cp(2)Fe/Cp(2)Fe(+). All complexes have been applied in simple test devices and also in stable, long-living devices to evaluate their electroluminescent device performances, for which we especially report the influence of the chosen ancillary ligands on emission colors, efficiencies, and device lifetimes. We obtained narrowband emission ranging from 613 to 630 nm with a full width at half-maximum of 64-71 nm, and a maximum in power efficiency of eta(p) = 14.6 lm/W at a current density of J = 0.01 mA/cm(2) for [(fpmqx)(2)Ir(pic)]. The operating lifetimes of [(fpmqx)(2)Ir(trz)] in both neat and mixed matrixes were longer than that of the established stable tris(1-phenylisoquinolinato)iridium(III) [Ir(piq)(3)]. From the lifetime measurements, it becomes clear that the stability is strongly correlated to the type of ancillary ligand. An extrapolated lifetime of 58 000 h with an initial brightness of 1000 cd/m(2), together with a very low voltage increase of 0.2 V over a time period of 1000 h (starting voltage of 4.1 V), was achieved. Such a high device lifetime is attributed to the chemical stability of all materials toward both charge carriers and excitons.

A stable enol from a 6-substituted benzanthrone and its unexpected behaviour under acidic conditions.

Treatment of benzanthrone (1) with biphenyl-2-yl lithium leads to the surprisingly stable enol 4, which is converted by dehydrogenation into the benzanthrone derivative 7. Under acidic conditions 4 isomerises to the spiro compound 11 and the bicyclo[4.3.1]decane derivative 12. Furthermore, the formation of 7 and the hydrogenated compound 13 is observed. A mechanism for the formation of the reaction products is proposed and supported by DFT calculations.