Optical hydrogen sensing with high-Q guided-mode resonance of Al2O3/WO3/Pd nanostructure.

Nanostructure based on a dielectric grating (Al2O3), gasochromic oxide (WO3) and catalyst (Pd) is proposed as a hydrogen sensor working at the room temperature. In the fabricated structure, the Pd catalyst film was as thin as 1 nm that allowed a significant decrease in the optical absorption. A high-Q guided-mode resonance was observed in a transmission spectrum at normal incidence and was utilized for hydrogen detection. The spectra were measured at 0-0.12% of hydrogen in a synthetic air (≈ 80% [Formula: see text] and 20% [Formula: see text]). The detection limit below 100 ppm of hydrogen was demonstrated. Hydrogen was detected in the presence of oxygen, which provides the sensor recovery but suppresses the sensor response. Sensor response was treated by the principal component analysis (PCA), which effectively performs noise averaging. Influence of temperature and humidity was measured and processed by PCA, and elimination of the humidity and temperature effects was performed. Square root dependence of the sensor response on the hydrogen concentration (Sievert's law) was observed. Sensor calibration curve was built, and the sensor resolution of 40 ppm was found. Long term stability of the sensor was investigated. Particularly, it was shown that the sensor retains its functionality after 6 months and dozens of acts of response to gas.

Luminescence and energy transfer mechanisms in photo-thermo-refractive glasses co-doped with silver molecular clusters and Eu3.

Silver molecular clusters were synthesized in photo-thermo-refractive glasses using the Na+-Ag+ ion exchange technique followed by heat treatment. Comprehensive study of cluster emission reveals the presence of spectrally separated fluorescence and phosphorescence with nanosecond and microsecond lifetime. Co-doping of glasses with Eu3+ was shown to results in quenching of cluster luminescence caused by energy transfer. The monitoring of silver cluster luminescence quantum yield and lifetime in the presence of Eu3+ indicates the presence of two different mechanisms of energy transfer. The first one affects the decay kinetics of cluster fluorescence and manifests at long distances, while the second one leads to static quenching of cluster emission at shorter distances and becomes prominent at higher doping Eu3+ concentration.

Fluorescence enhancement of monodisperse carbon nanodots treated with aqueous ammonia and hydrogen peroxide.

The treatment of monodisperse carbon nanodots (MCNDs) with a combination of aqueous ammonia and hydrogen peroxide is found to result in a prominent enhancement of their fluorescence efficiency. Depending on the hydrogen peroxide concentration, an increase of the MCNDs quantum yield of up to seven-fold has been achieved. Considering the absence of prominent changes in fluorescence lifetime and fluorescence spectra upon the treatment it is suggested that the observed rise of fluorescence efficiency originates from additional formation of new isolated sp2 domains surrounded by defect sites. The structural modification of MCNDs induced by their treatment with combination of aqueous ammonia and hydrogen peroxide is indicated by both transmission electron microscopy images and infrared spectra. The applied method has insignificant effect on the aggregation properties and size distribution of the studied MCNDs. Taking into account the proposed mechanism, the applied treatment procedure can serve as a basis for a facile approach for modification of emissive properties of various nanocarbon structures.

Controllable spherical aggregation of monodisperse carbon nanodots.

Monodisperse carbon nanodots (MCNDs) having an identical composition, structure, shape and size possess identical chemical and physical properties, making them highly promising for various technical and medical applications. Herein, we report a facile and effective route to obtain monodisperse carbon nanodots 3.5 ± 0.9 nm in size by thermal decomposition of organosilane within the pores of monodisperse mesoporous silica particles with subsequent removal of the silica template. Structural studies demonstrated that the MCNDs we synthesized consist of ∼7-10 defective graphene layers that are misoriented with respect to each other and contain various oxygen-containing functional groups. It was demonstrated that, owing to their identical size and chemical composition, the MCNDs are formed via coagulation primary aggregates ∼10-30 nm in size, which are, in turn, combined into secondary porous spherical aggregates ∼100-200 nm in diameter. The processes of coagulation of MCNDs and peptization of their hierarchical aggregates are fully reversible and can be controlled by varying the MCND concentration or the pH value of the hydrosols. Submicrometer spherical aggregates of MCNDs are not disintegrated as the hydrosol is dried. The thus obtained porous spherical aggregates of MCNDs are promising for drug delivery as a self-disassembling container for medicinal preparations.