Electron/energy co-transfer behavior and reducibility of Cu-chlorophyllin-bonded carbon-dots.

Cu-chlorophyllin-bonded carbon dots (CCPh-CDs) have been synthesized at room temperature, and the energy/electron co-transfer behavior between Cu-chlorophyllin molecules (CCPh) and carbon dots (CDs) is investigated via various techniques. The mean diameters of CDs and CCPh-CDs are 2.8 nm and 3.1 nm, respectively, measured by HRTEM. The absorption spectra of CCPh-CDs show two parts: the absorptions of CDs and CCPh are in the wavelength range of 300-500 nm. The PL spectra of CCPh-CDs exhibit very weak intensities, and with the decreasing of CCPh content on CDs, the corresponding intensity increases. Luminescent decay spectra show that the PL decay times of CCPh and CCPh-CDs with the highest CCPh content are single-exponentially fitted to be 3.20 ns and 12.64 ns, respectively. Furthermore, based on the electron transfer and reducibility of CCPh-CDs, Ag/Ag2O nanoparticles with a mean diameter of 10 nm can be easily prepared at room temperature under ultraviolet irradiation. The PL measurement result reveals that both electron transfer and FRET behavior take place from CCPh-CDs to Ag.

EDTA-bonded multi-connected carbon-dots and their Eu3+ complex: preparation and optical properties.

EDTA-bonded multi-connected carbon-dots (EDTA-C-dots) were prepared from carbon dot precursors and complexed with Eu3+ to give Eu3+-coordinated EDTA-bonded multi-connected carbon dots (Eu-EDTA-C-dots). Whereas EDTA-C-dots were readily soluble in DMSO, Eu-EDTA-C-dots could not be easily dissolved in DMSO, water, or other common organic solvents. The newly prepared materials were thoroughly characterized. The X-ray diffraction results showed that no crystalline phase of Eu oxides (europium oxide or europium hydroxide) could be observed in Eu-EDTA-C-dots. The infrared and UV-Vis spectra showed that coordination with Eu3+ ions did not damage the structure of the EDTA-C-dots. It was found that EDTA could be easily grafted on the surface of carbon dots and EDTA had minimal influence on the photoluminescence of the carbon dot matrix. In contrast, the existence of Eu3+ ions strongly quenched the photoluminescence of Eu-EDTA-C-dots. The measured and fitted decay lifetime indicated that Eu-EDTA-C-dots possessed two photoluminescence decay processes, i.e., radiative recombination and non-radiative recombination.

Fabrication of Novel Printable Electrically Conductive Adhesives (ECAs) with Excellent Conductivity and Stability Enhanced by the Addition of Polyaniline Nanoparticles.

Electrically conductive adhesives (ECAs) are one of the low temperature bonding materials. It can be used to replace toxic Sn-Pb solder. The key issue for the application of ECAs is how to improve their electrical properties. In the present study, we develop an effective method to promote the electrical properties of ECAs by addition of polyaniline (PANI) nanoparticles. PANIs were synthesized via a facile one-step chemical oxidative polymerization method. After adding 0.5 wt% PANI nanoparticles, the conductivity of ECAs increased dramatically by an order of magnitude. The bulk resistivity of 8.8 × 10-5 Ω·cm is achieved for 65 wt% silver fillers with 0.5 wt% PANIs loaded ECAs. Besides, this improvement has no negative effect on the shear strength and the aging life of ECAs. Moreover, the use of PANIs not only lowers the percolation threshold of ECAs, but also reduces the cost and improves the bonding reliability. Finally, PANIs enhanced ECAs patterns were successfully printed by a stencil printing method, which proved their potential applications in replacing conventional solder pastes and printing functional circuits.

Silver Nanowire-Induced Sensitivity Enhancement of Optical Oxygen Sensors Based on AgNWs-Palladium Octaethylporphine-Poly(methyl methacrylate) Microfiber Mats Prepared by Electrospinning.

Sensitivity enhancement of optical oxygen sensors is crucial for the characterization of nearly anoxic systems and oxygen quantification in trace amounts. In this work, for the first time we presented the introduction of silver nanowires (AgNWs) as a sensitivity booster for optical oxygen sensors based on AgNWs-palladium octaethylporphine-poly(methyl methacrylate) (AgNWs@PdOEP-PMMA) microfiber mats prepared by electrospinning. Herein, a series of sensing microfiber mats with different loading ratios of high aspect ratio AgNWs were fabricated, and the corresponding sensitivity enhancement was systematically investigated. With increasing incorporated ratios, the AgNWs@PdOEP-PMMA-sensing microfiber mats exhibited a swift response (approx. 1.8 s) and a dramatic sensitivity enhancement (by 243% for the range of oxygen concentration 0-10% and 235% for the range of oxygen concentration 0-100%) when compared to the pure PdOEP-PMMA microfiber mat. Additionally, the as-prepared sensing films were experimentally confirmed to be highly photostable and reproducible. The advantages of AgNW-induced sensitivity enhancement could be useful for the rational design and realization of revolutionary highly sensitive sensors and expected to be readily applicable to many other high-performance gas sensor devices.

Preparation and application of ratiometric polystyrene-based microspheres as oxygen sensors.

Mono-dispersed polystyrene-based microspheres with diameters about 1 µm encapsulating rhodamine moieties as oxygen insensitive internal reference probes and platinum octaethylporphyrin units as oxygen sensitive probes were synthesized as new ratiometric oxygen sensors (Rhod-PtOEP-PS). The dual luminophors of rhodamines and platinum porphyrin moieties exhibited emissions maxima at 585 nm and 644 nm, respectively. The microspheres showed good oxygen sensing properties in different oxygen partial pressures (pO2) and dissolved oxygen (DO) concentrations. It was found the oxygen probes and reference probes in microspheres showed higher photo-stability than their corresponding free fluorophores in solution. The microspheres also showed good sensitivity for air-pressure and cellular oxygen in cell culture medium. These microspheres were used to detect DOs in a few kinds of liquids including some daily drinks and it was found the measured errors were within positive/negative 11% as compared with the measured results using traditional oxygen electrodes.

Electrospun nanofibers and spin coated films prepared from side-chain copolymers with chemically bounded platinum (II) porphyrin moieties for oxygen sensing and pressure sensitive paints.

Pressure sensitive paints (PSP) containing oxygen probes were primarily used to measure air pressure. In this perspective, a polymerizable methacrylate-derived tetraphenylporphinato platinum(II) (PtTPP-MA) monomer was copolymerized with acrylic/vinyl monomers to produce four different copolymers. Octafluoropentyl methacrylate (OCFPM) and pentafluorophenyl acrylate (PFPA) were used as fluorinated monomers. Methyl methacrylate (MMA) and styrene (S) were used as non-fluorinated monomers. The structures and physical properties of the polymers were confirmed by 1H NMR, 19F NMR, GPC, and DSC. Experimental conditions were optimized to get fine nanofibers. Pressure sensing electrospun membranes and spin coated films were fabricated. Nanofibers showed fast response and good sensitivity towards gaseous oxygen. The influence of types of substrate and polymer natures on response time, oxygen sensitivity, and pressure responses were deliberated. Among our synthesized copolymers, poly(PS-co-PFPA-co-OCFPM-co-PtTPPMA) (Polymer P3) showed fast response time and good pressure sensitivity both as spin coated films and nanofibers.