Copper nanoparticle and point defect formation in Cu+-Na+ ion-exchanged glass using protons of 2 MeV energy.

There are several applications for irradiating materials with protons that could provide alternative methodologies to synthesize and induce the formation of new compounds of different size scales. In this study, we explored the effects of proton irradiation oncommercial glass silicate that was previously subjected to a Cu+-Na+ ion exchange (IE) treatment at 600 °C for a duration of 60 min. The ion-exchanged glass samples were irradiated with protons (p+) of 2 MeV energy at doses in the range of thousands of grays (3.3 × 103, 7.9 × 103 Gy) and hundreds of thousands of grays (3.6 × 105 Gy). Significant changes in the optical and structural properties were observed post the radiation treatment. The UV-Visible absorption spectra of the irradiated samples revealed the appearance of overlapping absorption bands, which could be deconvoluted into three Gaussian-shaped bands peaking at 566, 620 and 680 nm. These three bands could be attributed to the surface plasmon resonance (SPR) of copper nanoparticles, non-bridging oxygen hole centers (NBOHCs) and self-trapped hole (STH) defects, respectively. Prominent photoluminescence (PL) was observed in the Cu-exchanged and irradiated samples, mainly induced by the presence of both Cu+ and Cu2O. Increasing the irradiation dose led to an increase in the PL intensity due to the conversion of Cu2+ ions into Cu+. This result was confirmed by electron paramagnetic resonance (EPR) spectroscopy that shows a decrease in the Cu2+ signal when increasing the dose of proton exposure. Transmission electron microscopy (TEM) and high-resolution TEM (TEM and HRTEM) observations confirmed the presence of copper nanoparticles (CuNPs) in the doped and p+ irradiated Cu-exchanged glass silicate samples. These CuNPs were found to be crystalline with an average size of 12.39 nm.

Time-Resolved Fluorescence Spectroscopy of Molecularly Imprinted Nanoprobes as an Ultralow Detection Nanosensing Tool for Protein Contaminants.

Currently, optical sensors based on molecularly imprinted polymers (MIPs) have been attracting significant interest. MIP sensing relies on the combination of the MIP's selective capability, which is conveyed to the polymeric material by a template-assisted synthesis, with optical techniques that offer exquisite sensitivity. In this work, we devised an MIP nanoparticle optical sensor for the ultralow detection of serum albumin through time-resolved fluorescence spectroscopy. The Fluo-nanoMIPs (∅~120 nm) were synthetized using fluorescein-O-methacrylate (0.1×, 1×, 10× mol:mol versus template) as an organic fluorescent reporter. The ability of 0.1× and 1×Fluo-nanoMIPs to bind albumin (15 fM-150 nM) was confirmed by fluorescence intensity analyses and isothermal titration calorimetry. The apparent dissociation constant (Kapp) was 30 pM. Conversely, the 10× fluorophore content did not enable monitoring binding. Then, the time-resolved fluorescence spectroscopy of the nanosensors was studied. The 1×Fluo-nanoMIPs showed a decrease in fluorescence lifetime upon binding to albumin (100 fM-150 nM), Kapp = 28 pM, linear dynamic range 3.0-83.5 pM, limit of detection (LOD) 1.26 pM. Selectivity was confirmed testing 1×Fluo-nanoMIPs against competitor proteins. Finally, as a proof of concept, the nanosensors demonstrated detection of the albumin (1.5 nM) spiked in wine samples, suggesting a possible scaling up of the method in monitoring allergens in wines.

Novel flexible and conformable composite neutron scintillator based on fully enriched lithium tetraborate.

Thermal neutron detection is a key subject for nuclear physics research and also in a wide variety of applications from homeland security to nuclear medicine. In this work, it is proposed a novel flexible and conformable composite thermal neutron scintillator based on a fully enriched Lithium Tetraborate preparation ([Formula: see text]Li[Formula: see text]B[Formula: see text]O[Formula: see text]) combined with a phosphorescent inorganic scintillator powder (ZnS:Ag), and is then distributed into a polydimethylsiloxane matrix. The proposed scintillator shows a good neutron detection efficiency (max. [Formula: see text] 57% with respect to the commercial EJ-420), an average light output of [Formula: see text] 9000 ph/neutron-capture, a remarkable insensitivity to [Formula: see text]-rays (Gamma Rejection Ratio <10[Formula: see text]), and an extraordinary flexibility, so as to reach extremely small curvature radii, down to 1.5 mm, with no signs of cracking or tearing. Its characteristics make it suitable to be employed in scenarios where non-standard geometries are needed, for example, to optimize the detector performance and/or maximize the detection efficiency. Finally, the response of a hybrid detector made of a plastic scintillator, wrapped with the proposed scintillator, coupled to a silicon photomultiplier array is described, and the excellent discrimination between [Formula: see text]-rays, fast and thermal neutrons resulting from data processing is demonstrated.

MoS2 Based Photodetectors: A Review.

Photodetectors based on transition metal dichalcogenides (TMDs) have been widely reported in the literature and molybdenum disulfide (MoS2) has been the most extensively explored for photodetection applications. The properties of MoS2, such as direct band gap transition in low dimensional structures, strong light-matter interaction and good carrier mobility, combined with the possibility of fabricating thin MoS2 films, have attracted interest for this material in the field of optoelectronics. In this work, MoS2-based photodetectors are reviewed in terms of their main performance metrics, namely responsivity, detectivity, response time and dark current. Although neat MoS2-based detectors already show remarkable characteristics in the visible spectral range, MoS2 can be advantageously coupled with other materials to further improve the detector performance Nanoparticles (NPs) and quantum dots (QDs) have been exploited in combination with MoS2 to boost the response of the devices in the near ultraviolet (NUV) and infrared (IR) spectral range. Moreover, heterostructures with different materials (e.g., other TMDs, Graphene) can speed up the response of the photodetectors through the creation of built-in electric fields and the faster transport of charge carriers. Finally, in order to enhance the stability of the devices, perovskites have been exploited both as passivation layers and as electron reservoirs.

Direct detection of 5-MeV protons by flexible organic thin-film devices.

The direct detection of 5-MeV protons by flexible organic detectors based on thin films is here demonstrated. The organic devices act as a solid-state detector, in which the energy released by the protons within the active layer of the sensor is converted into an electrical current. These sensors can quantitatively and reliably measure the dose of protons impinging on the sensor both in real time and in integration mode. This study shows how to detect and exploit the energy absorbed both by the organic semiconducting layer and by the plastic substrate, allowing to extrapolate information on the present and past irradiation of the detector. The measured sensitivity, S = (5.15 ± 0.13) pC Gy-1, and limit of detection, LOD = (30 ± 6) cGy s-1, of the here proposed detectors assess their efficacy and their potential as proton dosimeters in several fields of application, such as in medical proton therapy.

Preliminary evaluation of the production of non-carrier added 111Ag as core of a therapeutic radiopharmaceutical in the framework of ISOLPHARM_Ag experiment.

Research in the field of radiopharmaceuticals is increasingly promoted by the widespread and growing interest in applying nuclear medicine procedures in both disease diagnosis and treatment. The production of radionuclides of medical interest is however a challenging issue. Along with the conventional techniques other innovative approaches are being investigated and, among those, the ISOLPHARM project is being developed at INFN-LNL (Istituto Nazionale di Fisica Nucleare - Laboratori Nazionali di Legnaro). Such technique foresees the employment of the SPES ISOL facility to produce isobarically pure Radioactive Ion Beams (RIBs), obtained thanks to electromagnetic mass separation and collected on appropriate substrates. The latter are successively recovered and dissolved, allowing thus the chemical separation and harvesting of the nuclides of interest, free from any isotopic contaminant. Although ISOLPHARM can be potentially employed for most of the routinely used medical radioisotopes, its innovation potential is better expressed considering its capability to provide carrier free unconventional nuclides, difficult to produce with state-of-art techniques, such as 111Ag, a ß- emitter potentially interesting for therapeutic applications. Thus, in the framework of ISOLPHARM, INFN supported a two-years experiment, called ISOLPHARM_Ag, aimed at evaluating the feasibility of the production of a111Ag labelled radiopharmaceutical. The ISOL production yields are estimated by computing intensive Monte Carlo codes, that require an appropriate custom Information Technology infrastructure. The presented work is focused on the first part of the production chain including the capability to extract, ionize, and collect stable Ag beams with SPES technologies. MC calculations were used to estimate the expected 111Ag in-target yields, whereas experiments with stable Ag were performed to test the ionization, transport and collection of Ag beams.

Preparation and Statistical Characterization of Tunable Porous Sponge Scaffolds using UV Cross-linking of Methacrylate-Modified Silk Fibroin.

Silk fibroin sponges have been widely studied and reported in literature for tissue engineering applications. Several fabrication methods have been proposed during the years to cover most of the demands in terms of properties, which should be adapted to the considered tissue. Most of these procedures are based on the secondary structure transition of the protein to the stable ß crystalline form. This transition, known as physical cross-linking, makes the sponge resistant to dissolution in water, and, in general, increases the sponge stiffness. In our work, we propose an alternative method to ensure the stability of the sponge based on chemical cross-linking of a methacrylated version of silk fibroin (Sil-MA) obtained via chemical modification. The Sil-MA water solution with the addition of a photoinitiator (LAP) allows the opening, under UV radiation, of a double carbon-carbon bond and radical polymerization. The incorporation of air bubbles (that serves as a template for the pores) was accomplished by a mixer; then, the foam was stabilized under UV light and the excess water was removed by freeze-drying. Because of the cytotoxicity of the photoinitiator (found when used at a high concentration), an additional washing step in water has been introduced to eliminate the residues and improve the cells' viability. Fourier transform infrared (FTIR) analysis confirmed the functionalization of the protein. To evaluate the effect of the composition on the sponge properties, a 23 full factorial design of the experiment has been adopted. FTIR analysis revealed that the sponge composition did not affect the protein's secondary structure. The analysis of images obtained by SEM allowed some statistical measures of the porosity curves to be studied and modeled. The same modeling procedure was applied to the dissolution test in a simulated body fluid, to the water absorption, and to the cell viability (tested by the MTT and LDH assays). An empirical model for each property was built, showing how by changing the composition it is possible to tune the sponge properties.

Versatile and Scalable Strategy To Grow Sol-Gel Derived 2H-MoS2 Thin Films with Superior Electronic Properties: A Memristive Case.

Transition metal dichalcogenides, such as molybdenum disulfide (MoS2), show peculiar chemical/physical properties that enable their use in applications ranging from micro- and nano-optoelectronics to surface catalysis, gas and light detection, and energy harvesting/production. One main limitation to fully harness the potential of MoS2 is given by the lack of scalable and low environmental impact synthesis of MoS2 films with high uniformity, hence setting a significant challenge for industrial applications. In this work, we develop a versatile and scalable sol-gel-derived MoS2 film fabrication by spin coating deposition of an aqueous sol on different technologically relevant, flexible substrates with annealing at low temperatures (300 °C) and without the need of sulfurization and/or supply of hydrogen as compared to cutting-edge techniques. The electronic and physical properties of the MoS2 thin films were extensively investigated by means of surface spectroscopy and structural characterization techniques. Spatially homogenous nanocrystalline 2H-MoS2 thin films were obtained exhibiting high chemical purity and excellent electronic properties such as an energy band gap of 1.35 eV in agreement with the 2H phase of the MoS2, and a density of states that corresponds to the n-type character expected for high-quality 2H-MoS2. The potential use of sol-gel-grown MoS2 as the candidate material for electronic applications was tested via electrical characterization and demonstrated via the reversible switching in resistivity typical for memristors with a measured ON-OFF ratio ≥102. The obtained results highlight that the novel low-cost fabrication method has a great potential to promote the use of high-quality MoS2 in technological and industrial-relevant scalable applications.

AN ONLINE, RADIATION HARD PROTON ENERGY-RESOLVING SCINTILLATOR STACK FOR LASER-DRIVEN PROTON BUNCHES.

We report on a scintillator-based online detection system for the spectral characterization of polychromatic proton bunches. Using up to nine stacked layers of radiation hard polysiloxane scintillators, coupled to and readout edge-on by a large area pixelated CMOS detector, impinging polychromatic proton bunches were characterized. The energy spectra were reconstructed using calibration data and simulated using Monte-Carlo simulations. Despite the scintillator stack showed some problems like thickness inhomogeneities and unequal layer coupling, the prototype allows to obtain a first estimate of the energy spectrum of proton beams.

Carbonate and Silicate Abundance Indexing in Coarse-Grained River Sediments Using Diffuse Reflection Infrared Spectroscopy (DRIFTS) and Ion-Beam-Induced Luminescence (IBIL) Spectroscopies.

Two different types of spectroscopic methods, namely diffuse reflection infrared spectroscopy (DRIFTS) as a vibrational spectroscopy and ion-beam-induced luminescence (IBIL) as an optical spectroscopy, have been exploited for the analysis of three sand samples collected from the Adige, Bacchiglione, and Brenta rivers (Veneto, Northern Italy) with the aim to set up a procedure for the comparison of the relative abundance of silicates, carbonates, and feldspars. By fitting the spectra, the features corresponding to different geological compounds have been identified and descriptive indexes of their relative amount have been obtained by comparing the peak area ratios.

IBIL analysis of road dust samples from San Bernardo tunnel.

Road dust in urban or industrial sites is an important source of atmospheric particulate by re-suspension of finer particles that may contain potentially toxic pollutants. In this work Ion Beam Induced Luminescence (IBIL), Nuclear Magnetic Resonance and fluorescence spectroscopy analyses were used to characterize road dust samples with particle size lower than 250 µm collected on the walls and on the floor of the ventilation air shaft of "Traforo del San Bernardo" highway tunnel. Moreover, for comparison, IBIL analyses were performed both on some possible anthropic sources of particulate matter and on a road dust reference sample (BCR-723). IBIL spectra as a function of the fluence were analyzed with a multivariate approach in order to identify the spectral components evolving with different rate. Nuclear Magnetic Resonance and fluorescence spectroscopy analyses were performed on extracted samples of the road dust in order to study the contribution of organic compounds to the IBIL features. Results point out that IBIL, here performed for the first time for road dust analysis, can be applied for the identification of compounds by characterizing the sample origin.

Deposition and characterization of luminescent Eu(tta)3phen-doped parylene-based thin-film materials.

Herein, novel host-guest films produced by coarse vacuum cosublimation of the parylene C dimer and Eu(tta)3phen are prepared and studied. Eu(tta)3phen sublimation at different temperatures allows films with different concentrations of the Eu complex to be obtained. The films are characterized by Rutherford backscattering spectrometry (RBS), FTIR spectroscopy, X-ray diffraction (XRD), atomic force microscopy (AFM), and UV/Vis absorption and emission spectroscopy. RBS, FTIR, and XRD reveal the incorporation of Eu(tta)3phen into the parylene matrix. AFM evidences the very flat film surface, which is particularly advantageous for optical applications. UV/Vis absorption and emission analyses confirm that the optical properties of Eu(tta)3phen are preserved in the deposited films. Fluorescence measurements evidence the occurrence of an energy-transfer process between parylene and Eu(tta)3phen, and this results in an increase in the light emitted by the Eu complex that is as much as five times higher than that emitted by Eu(tta)3phen alone.

Multivariate analysis of Ion Beam Induced Luminescence spectra of irradiated silver ion-exchanged silicate glasses.

A multivariate analysis is used for the identification of the spectral features in Ion Beam Induced Luminescence (IBIL) spectra of soda-lime silicate glasses doped with silver by Ag(+)-Na(+) ion exchange. Both Principal Component Analysis and multivariate analysis were used to characterize time-evolving IBIL spectra of Ag-doped glasses, by means of the identification of the number and of the wavelength positions of the main luminescent features and the study of their evolution during irradiation. This method helps to identify the spectral features of the samples spectra, even when partially overlapped or less intense. This analysis procedure does not require additional input such as the number of peaks.

Organic semiconducting single crystals as next generation of low-cost, room-temperature electrical X-ray detectors.

Direct, solid-state X-ray detectors based on organic single crystals are shown to operate at room temperature, in air, and at voltages as low as a few volts, delivering a stable and reproducible linear response to increasing X-ray dose rates, with notable radiation hardness and resistance to aging. All-organic and optically transparent devices are reported.

Use of silica microspheres having refractive index similar to bacteria for conversion of flow cytometric forward light scatter into biovolume.

This research describes an alternative approach for the rapid conversion of flow cytometric Forward Angle Light Scattering (FALS) into bacterial biovolume. The Rayleigh-Gans theory was considered for explaining the main parameters affecting FALS intensity: sensitivity analysis of the model was carried out, taking into account the parameters characteristic of bacterial cells and characteristics of the flow cytometer. For particles with size in the typical range of bacteria, the FALS intensity is affected mainly by volume and refractive index of bacterial cells and is approximately independent of the shape of the cells. The proposed conversion from FALS intensity into bacterial biovolume is based on a calibration curve determined by using silica microspheres having relative refractive index as far as possible similar to that of bacteria. The approach was validated for two different flow cytometers (the first equipped with an arc lamp and the second with a laser) by comparing the biovolume distribution obtained from FALS conversion with the biovolume measured conventionally under epifluorescence microscopy. The specific case of bacteria taken from a WWTP was addressed. Compared to the time-consuming conventional microscopic approach, the application of FALS for sizing bacterial biovolume could be a very promising tool being completed in few minutes, simultaneously to the enumeration of bacteria during the flow cytometric analysis.

Effects of proton irradiation on glass filter substrates for the Rosetta mission.

The Optical, Spectroscopic, and Infrared Remote Imaging System (OSIRIS) instrument on board the Rosetta spacecraft, a misson of the European Space Agency to comet P/Wirtanen, includes two cameras for acquiring images of the comet. A set of interference filters deposited upon glass and fused-silica substrates will be added to the cameras for wavelength tuning. For this mission of more than 10/years in an interplanetary environment, the requirement of preserving the optical characteristics of the filters is a critical one. We checked the variation in the transmission of some filter substrates after proton irradiation that simulated the solar wind. To produce a situation that is representative of the interplanetary environment, we irradiated proton fluences at three energies: 1.5 x 10(11) protons/cm2 at 4 MeV, 1.9 x 10(10) protons/cm2 at 8 MeV, and 7.1 x 10(9) protons/cm2 at 18 MeV. Seven substrates were tested: three Suprasil-1; three colored glasses, namely, OG590, KG3, and RG9; and one quartz. In addition, two interference filters were checked. The results obtained show that Suprasil-1 is rather insensitive to this irradiation, whereas very small reductions in transmission, of the order of a few percent, occur for colored glasses. The transmission of these filters was remeasured 2 years after the irradiation, and showed a general decrease in the transmission reduction.