Enhancement of Photoluminescence Properties via Polymer Infiltration in a Colloidal Photonic Glass.

Photonic glasses (PGs) based on the self-assembly of monosized nanoparticles can be an effective tool for realizing disordered structures capable of tailoring light diffusion due to the establishment of Mie resonances. In particular, the wavelength position of these resonances depends mainly on the morphology (dimension) and optical properties (refractive index) of the building blocks. In this study, we report the fabrication and optical characterization of photonic glasses obtained via a self-assembling technique. Furthermore, we have demonstrated that the infiltration of these systems with a green-emitting polymer enhances the properties of the polymer, resulting in a large increase in its photoluminescence quantum yield and a 3 ps growing time of the photoluminescence time decay Finally, the development of the aforementioned system can serve as a suitable low-cost platform for the realization of lasers and fluorescence-based bio-sensors.

Silver Nanoparticle-PEDOT:PSS Composites as Water-Processable Anodes: Correlation between the Synthetic Parameters and the Optical/Morphological Properties.

The morphological, spectroscopic and rheological properties of silver nanoparticles (AgNPs) synthesized in situ within commercial PEDOT:PSS formulations, labeled PP@NPs, were systematically investigated by varying different synthetic parameters (NaBH4/AgNO3 molar ratio, PEDOT:PSS formulation and silver and PEDOT:PSS concentration in the reaction medium), revealing that only the reagent ratio affected the properties of the resulting nanoparticles. Combining the results obtained from the field-emission scanning electron microscopy analysis and UV-Vis characterization, it could be assumed that PP@NPs' stabilization occurs by means of PSS chains, preferably outside of the PEDOT:PSS domains with low silver content. Conversely, with high silver content, the particles also formed in PEDOT-rich domains with the consequent perturbation of the polaron absorption features of the conjugated polymer. Atomic force microscopy was used to characterize the films deposited on glass from the particle-containing PEDOT:PSS suspensions. The film with an optimized morphology, obtained from the suspension sample characterized by the lowest silver and NaBH4 content, was used to fabricate a very initial prototype of a water-processable anode in a solar cell prepared with an active layer constituted by the benchmark blend poly(3-hexylthiophene) and [6,6]-Phenyl C61 butyric acid methyl ester (PC60BM) and a low-temperature, not-evaporated cathode (Field's metal).

Impact of chiral ligands on photophysical and electro-optical properties of ß-diketonate europium complexes in circularly polarized OLEDs.

Luminescent lanthanide complexes exhibiting chiroptical properties are attracting attention for their application in chiral optoelectronics and photonics, thanks to their unique optical properties, allied to intraconfigurational f-f transitions, which are generally electric-dipole-forbidden and can be magnetic dipole-allowed, which in an appropriate environment can lead to high dissymmetry factors and strong luminescence, in the presence of an antenna ligand. However, because luminescence and chiroptical activity are governed by different selection rules, their successful application in commonly used technologies is still an expectation. Recently, we showed that europium complexes bearing ß-diketonates acting as luminescence sensitizers, and chiral bis(oxazolinyl) pyridine derivatives as the chirality inducer, reasonably perform in circularly polarized (CP) organic light-emitting devices (OLEDs). Indeed, europium ß-diketonate complexes are an interesting molecular starting point, given their strong luminescence and their established use in conventional (i.e., nonpolarized) OLEDs. In this context, it is interesting to investigate in detail the impact of the ancillary chiral ligand on complex emission properties and the performances of corresponding CP-OLEDs. Here we show that, by incorporating the chiral compound as emitter in the architecture of solution processed electroluminescent devices, CP emission is retained, and the efficiency of the device is comparable to reference unpolarized OLED. The observed remarkable dissymmetry values strengthen the position of chiral lanthanide-OLEDs as CP-emitting devices.

Bacteria as sensors: Real-time NMR analysis of extracellular metabolites detects sub-lethal amounts of bactericidal molecules released from functionalized materials.

BACKGROUND: Cells exposed to stress factors experience time-dependent variations of metabolite concentration, acting as reliable sensors of the effective concentration of drugs in solution. NMR can detect and quantify changes in metabolite concentration, thus providing an indirect estimate of drug concentration. The quantification of bactericidal molecules released from antimicrobial-treated biomedical materials is crucial to determine their biocompatibility and the potential onset of drug resistance. METHODS: Real-time NMR measurements of extracellular metabolites produced by bacteria grown in the presence of known concentrations of an antibacterial molecule (irgasan) are employed to quantify the bactericidal molecule released from antimicrobial-treated biomedical devices. Viability tests assess their activity against E. coli and S. aureus planktonic and sessile cells. AFM and contact angle measurements assisted in the determination of the mechanism of antibacterial action. RESULTS: NMR-derived concentration kinetics of metabolites produced by bacteria grown in contact with functionalized materials allows for indirectly evaluating the effective concentration of toxic substances released from the device, lowering the detection limit to the nanomolar range. NMR, AFM and contact angle measurements support a surface-killing mechanism of action against bacteria. CONCLUSIONS: The NMR based approach provides a reliable tool to estimate bactericidal molecule release from antimicrobial materials. GENERAL SIGNIFICANCE: The novelty of the proposed NMR-based strategy is that it i) exploits bacteria as sensors of the presence of bactericidal molecules in solution; ii) is independent of the chemo-physical properties of the analyte; iii) establishes the detection limit to nanomolar concentrations.

Amphiphilic PTB7-Based Rod-Coil Block Copolymer for Water-Processable Nanoparticles as an Active Layer for Sustainable Organic Photovoltaic: A Case Study.

We synthetized a new rod-coil block copolymer (BCP) based on the semiconducting polymerpoly({4,8-bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b']dithiophene-2,6-diyl}{3-fluoro-2-[(2-ethylhexyl)carbonyl]thieno[3,4-b]thiophenediyl}) (PTB7) and poly-4-vinylpyridine (P4VP), tailored to produce water-processable nanoparticles (WPNPs) in blend with phenyl-C71-butyric acid methyl ester (PC71BM). The copolymer PTB7-b-P4VP was completely characterized by means of two-dimensional nuclear magnetic resonance (2D-NMR), matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) mass spectrometry (MS), size-exclusion chromatography (SEC), and differential scanning calorimetry (DSC) to confirm the molecular structure. The WPNPs were prepared through an adapted miniemulsion approach without any surfactants. Transmission electron microscopy (TEM) images reveal the nano-segregation of two active materials inside the WPNPs. The nanostructures appear spherical with a Janus-like inner morphology. PTB7 segregated to one side of the nanoparticle, while PC71BM segregated to the other side. This morphology was consistent with the value of the surface energy obtained for the two active materials PTB7-b-P4VP and PC71BM. The WPNPs obtained were deposited as an active layer of organic solar cells (OSCs). The films obtained were characterized by UV-Visible Spectroscopy (UV-vis), atomic force microscopy (AFM), and grazing incidence X-ray diffraction (GIXRD). J-V characteristics of the WPNP-based devices were measured by obtaining a power conversion efficiency of 0.85%. Noticeably, the efficiency of the WPNP-based devices was higher than that achieved for the devices fabricated with the PTB7-based BCP dissolved in chlorinated organic solvent.

Hybrid MoS2/PEDOT:PSS transporting layers for interface engineering of nanoplatelet-based light-emitting diodes.

Colloidal semiconductor nanoplatelets (NPLs) are a subgroup of quantum confined materials that have recently emerged as promising active materials for solution processed light-emitting diodes (LEDs) thanks to their peculiar structural and electronic properties as well as their reduced dimensionality. Nowadays, the conventional structure for NPL-based LEDs makes use of poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) as a hole transporting layer (HTL). This is a well-known conjugated conductive polymer because it leads to high LED efficiency, though it has limited stability in air due to its intrinsic acidity and hygroscopicity. Here, we develop a nanocomposite aqueous ink, obtained by blending commercial PEDOT:PSS with water-based, stable and highly concentrated molybdenum disulfide (MoS2) nanosheets, obtained via liquid phase exfoliation (LPE), which is suitable as a HTL for solution processed NPL-based LEDs. We demonstrate that the MoS2 additive effectively works as a performance booster in unpackaged devices, thereby prolonging the lifetime up to 1000 hours under ambient conditions. Moreover, the addition of MoS2 induces a modification of the anode interface properties, including a change in the work function and a significant enhancement of the permittivity of the HTL.

Sulfonate-Conjugated Polyelectrolytes as Anode Interfacial Layers in Inverted Organic Solar Cells.

Conjugated polymers with ionic pendant groups (CPEs) are receiving increasing attention as solution-processed interfacial materials for organic solar cells (OSCs). Various anionic CPEs have been successfully used, on top of ITO (Indium Tin Oxide) electrodes, as solution-processed anode interlayers (AILs) for conventional devices with direct geometry. However, the development of CPE AILs for OSC devices with inverted geometry is an important topic that still needs to be addressed. Here, we have designed three anionic CPEs bearing alkyl-potassium-sulfonate side chains. Their functional behavior as anode interlayers has been investigated in P3HT:PC61BM (poly(3-hexylthiophene): [6,6]-phenyl C61 butyric acid methyl ester) devices with an inverted geometry, using a hole collecting silver electrode evaporated on top. Our results reveal that to obtain effective anode modification, the CPEs' conjugated backbone has to be tailored to grant self-doping and to have a good energy-level match with the photoactive layer. Furthermore, the sulfonate moieties not only ensure the solubility in polar orthogonal solvents, induce self-doping via a right choice of the conjugated backbone, but also play a role in the gaining of hole selectivity of the top silver electrode.

Rod-Coil Block Copolymer: Fullerene Blend Water-Processable Nanoparticles: How Molecular Structure Addresses Morphology and Efficiency in NP-OPVs.

The use of water-processable nanoparticles (WPNPs) is an emerging strategy for the processing of organic semiconducting materials into aqueous medium, dramatically reducing the use of chlorinated solvents and enabling the control of the nanomorphology in OPV active layers. We studied amphiphilic rod-coil block copolymers (BCPs) with a different chemical structure and length of the hydrophilic coil blocks. Using the BCPs blended with a fullerene acceptor material, we fabricated NP-OPV devices with a sustainable approach. The goal of this work is to clarify how the morphology of the nanodomains of the two active materials is addressed by the hydrophilic coil molecular structures, and in turn how the design of the materials affects the device performances. Exploiting a peculiar application of TEM, EFTEM microscopy on WPNPs, with the contribution of AFM and spectroscopic techniques, we correlate the coil structure with the device performances, demonstrating the pivotal influence of the chemical design over material properties. BCP5, bearing a coil block of five repeating units of 4-vinilpyridine (4VP), leads to working devices with efficiency comparable to the solution-processed ones for the multiple PCBM-rich cores morphology displayed by the blend WPNPs. Otherwise, BCP2 and BCP15, with 2 and 15 repeating units of 4VP, respectively, show a single large PCBM-rich core; the insertion of styrene units into the coil block of BCP100 is detrimental for the device efficiency, even if it produces an intermixed structure.

Biobased Cryogels from Enzymatically Oxidized Starch: Functionalized Materials as Carriers of Active Molecules.

Starch recovered from an agrifood waste, pea pods, was enzymatically modified and used to prepare cryogels applied as drug carriers. The enzymatic modification of starch was performed using the laccase/(2,2,6,6-tetramethylpiperidin-1-yl)oxyl TEMPO system, at a variable molar ratio. The characterization of the ensuing starches by solution NMR spectroscopy showed partial conversion of the primary hydroxyl groups versus aldehyde and carboxyl groups and successive creation of hemiacetal and ester bonds. Enzymatically modified starch after simple freezing and lyophilization process provided stable and compact cryogels with a morphology characterized by irregular pores, as determined by atomic force (AFM) and scanning electron microscopy (SEM). The application of cryogels as carriers of active molecules was successfully evaluated by following two different approaches of loading with drugs: a) as loaded sponge, by adsorption of drug from the liquid phase; and b) as dry-loaded cryogel, from a dehydration step added to loaded cryogel from route (a). The efficiency of the two routes was studied and compared by determining the drug release profile by proton NMR studies over time. Preliminary results demonstrated that cryogels from modified starch are good candidates to act as drug delivery systems due to their stability and prolonged residence times of loaded molecules, opening promising applications in biomedical and food packaging scenarios.

A bifunctional conjugated polyelectrolyte for the interfacial engineering of polymer solar cells.

In this work a novel combination of side chain functionalities, alkyl-phosphonate (EP) and alkyl-ammonium bromide (NBr) groups, on a polyfluorene backbone (PF-NBr-EP) was studied as cathode interfacial material (CIM) in polymer-based solar cells. The devices were made with a conventional geometry, with PTB7:PC71 BM as active layer and aluminum as metal electrode. The CIM showed good solubility in ethanol and film forming ability onto the active layer so that its deposition could be finely tuned. The interface engineering imparted by this CIM was assessed and discussed through kelvin probe force microscopy (KPFM), impedance spectroscopy, charge recombination and electron transport characterizations. To discriminate between the interfacial modifications imparted by the interlayer and its solvent, we included in this study a surface ethanol treated device. In the optimized conditions an average power conversion efficiency of 7.24% was obtained, which is about 60% higher when compared to devices made with bare Al and 26% when compared to devices made with a standard calcium/aluminum cathode. Besides performances, some insights about the devices shelf life stability are also presented. A good persistency through aging was found for the cathode interfacial engineering capabilities of PF-NBr-EP.

Coating ZnO nanoparticle films with DNA nanolayers for enhancing the electron extracting properties and performance of polymer solar cells.

Here we present for the first time polymer solar cells that incorporate biological material that show state of the art efficiencies in excess of 8%. The performance of inverted polymer solar cells was improved significantly after deposition of ZnO nanoparticles (ZnO-NPs) together with a thin deoxyribonucleic acid nanolayer and used as an electron extraction layer (EEL). The ZnO-NPs/DNA double layer improved the rectifying ratio, shunt resistance of the cells as well as lowering the work function of the electron-collecting contact. Importantly, the ZnO-NPs/DNA bilayer enhanced the power conversion efficiency of cells considerably compared to cells with EELs made of only DNA (improvement of 56% in relative terms) or only ZnO-NPs (improvement of 19% in relative terms) reaching a best power conversion efficiency of 8.5%. The ZnO-NPs/DNA double layer cells also outperformed ones made with one of the most efficient previous synthetic composite EELs (i.e. ZnO/PEIE(poly(ethyleneimine)-ethoxylated)). Since all fabrication procedures were carried out at low (<150 °C) or room temperature, we have applied the findings to flexible substrates as well as on glass obtaining a high PCE of 7.2%. The solar cells with the biological/metal-oxide composite EELs also delivered an improvement in the stability (∼20% in relative term) compared to that with ZnO-NPs only. All these findings show that natural materials, in this case DNA, the premium biological material, can be incorporated in organic semiconductor devices in tandem with inorganic devices delivering uncompromising levels of performance as well as significant improvements.

Hierarchical hematite nanoplatelets for photoelectrochemical water splitting.

A new nanostructured α-Fe2O3 photoelectrode synthesized through plasma-enhanced chemical vapor deposition (PE-CVD) is presented. The α-Fe2O3 films consist of nanoplatelets with (001) crystallographic planes strongly oriented perpendicular to the conductive glass surface. This hematite morphology was never obtained before and is strictly linked to the method being used for its production. Structural, electronic, and photocurrent measurements are employed to disclose the nanoscale features of the photoanodes and their relationships with the generated photocurrent. α-Fe2O3 films have a hierarchical morphology consisting of nanobranches (width ∼10 nm, length ∼50 nm) that self-organize in plume-like nanoplatelets (350-700 nm in length). The amount of precursor used in the PE-CVD process mainly affects the nanoplatelets dimension, the platelets density, the roughness, and the photoelectrochemical (PEC) activity. The highest photocurrent (j = 1.39 mA/cm(2) at 1.55 VRHE) is shown by the photoanodes with the best balance between the platelets density and roughness. The so obtained hematite hierarchical morphology assures good photocurrent performance and appears to be an ideal platform for the construction of customized multilayer architecture for PEC water splitting.

Poly(styrene)/oligo(fluorene)-intercalated fluoromica hybrids: synthesis, characterization and self-assembly.

We report on the intercalation of a cationic fluorescent oligo(fluorene) in between the 2D interlayer region of a fluoromica type silicate. The formation of intercalated structures with different fluorophore contents is observed in powders by synchrotron radiation XRD. Successively, the hybrids are dispersed in poly(styrene) through in situ polymerization. Such a procedure allows us to synthesize the materials from solution, to achieve solid films, and to characterize them by optical and morphologic techniques. The polymeric films with homogeneous distribution of the hybrids exhibit ultraviolet-blue photoluminescence with a significantly enhanced photostability compared to the bare oligo(fluorene)s. Finally, under specific conditions, the polymer hybrid with higher oligo(fluorene) content spontaneously assembles into highly ordered microporous films.

Structural iridescent tuned colors from self-assembled polymer opal surfaces.

Structural colors are the object of a wide scientific interest, not only for the potential technical applications of their intriguing optical properties but also for the need of coloring agents to replace toxic and carcinogenic dyes. We present a simple methodology to obtain polymer opal surfaces of self-assembled core-shell nanoparticles with different degree of order for structural color applications. Polymer nanospheres prepared by surfactant-free emulsion radical copolymerization of an hydrophobic and an hydrophilic comonomer (styrene and methacrylic acid) spontaneously assemble into core-shell particles. Nanoparticles with identical composition and different diameters were prepared by modulating the degree of ionization of the weakly acidic comonomer. We report experimental results revealing how the synthesis parameters affect the properties of the core-shell particles and their influence on the optical properties of the final polymer opal surfaces, which depend on size, charge, and packing arrangement of the constituent nanoparticles.

A controlled approach to iron oxide nanoparticles functionalization for magnetic polymer brushes.

In this article, we report a detailed study of surface modification of magnetite nanoparticles by means of three different grafting agents, functional for the preparation of magnetic polymer brushes. 3-Aminopropyltriethoxysilane (APTES), 3-chloropropyltriethoxysilane (CPTES), and 2-(4-chlorosulfonylphenyl)ethyltrichlorosilane (CTCS) were chosen as grafting models through which a wide range of polymer brushes can be obtained. By means of accurate thermogravimetric analysis a good control over the amount of immobilized molecules is achieved, and optimal operating conditions for each grafting agent are consequently determined. Graft densities ranging from approximately 4 to 7 molecules per nm(2) are obtained, depending on the conditions used. In addition, the surface-initiated atom transfer radical polymerization (ATRP) of methyl methacrylate (MMA) carried out with CTCS-coated nanoparticles is presented as an example of polymer brushes, leading to a well-defined and dense polymeric coating of around 0.6 PMMA chains per nm(2).

Evolution of the Pt layer deposited on MgO(001) by pulsed laser deposition as a function of the deposition parameters: a scanning tunneling microscopy and energy dispersive X-ray diffractometry/reflectometry study.

A combined ultrahigh vacuum scanning tunneling microscopy (STM-UHV) and energy dispersive X-ray diffractometry/reflectometry (EDXD/EDXR) study of the evolution of face-centered cubic (fcc) Pt layer growth on MgO(100) by pulsed laser deposition as a function of the process parameters such as deposition temperature and deposition duration has been carried out. The aim of this study is to define the best experimental conditions to obtain a controlled film deposition selective on the Pt growth direction (either [111] or [002]). The evolution of the Pt surface morphology as a function of the deposition temperature (T(dep)) from 300 to 700 degrees C has been studied with STM and ED techniques. Results show that the Pt surface, characterized at T(dep) = 300 degrees C by a 3D island morphology, evolves at higher temperatures to a morphology in which the original islands coexist with a distribution of orthogonal 2D stripes. The two features can be associated with the [111] and [002] Pt growth directions of the fcc phase, respectively. For T(dep) = 700 degrees C, the island morphology of the (111) face completely disappears, while the merging process of the (002) stripes reaches completion. The evolution of the morphology at T(dep) = 600 degrees C as a function of the deposition time and thickness has then been studied with STM-UHV, revealing an initial growth of mosaic-like 3D islands. These independent islands, already interconnected, expand along two orthogonal directions and, for longer deposition times, lead to the texture of orthogonal stripes. The EDXR characterization providing the morphological parameters of the films, i.e., thickness and roughness, confirms the above observation and quantifies the effect of such morphological changes on the surface roughness of the Pt film, an important parameter for applications of Pt films as underlayer in magnetic recording media.