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CaloCube is an R&D project borne to develop a novel calorimeter design, optimized for high-energy cosmic ray measurements in space. A small prototype made of CsI(Tl) elements has been built and tested on particle beams. A final version, made of 5×5×18 crystals and with dual readout (two photodiodes for each crystal), to cover the full required dynamic range, is under construction and will be tested at CERN SPS in Summer 2016. The dual readout compensation technique were developed and the feasibility to extract Čerenkov signals from CsI crystals verified.

The comparison of the performances of SiO2 and SiOC layers as host matrices for optically active Eu ions is presented. A SiO2 matrix allows to observe light emission from both Eu2+ and Eu3+ ions, owing to a proper tuning of the thermal annealing process used for the optical activation of the rare earth. However, the photoluminescence efficiency of both ions remains relatively low and quite far from the requirements for technological applications, mainly due to the extensive formation of Eu-containing precipitates. A detailed study by transmission electron microscopy allowed us to analyze and elucidate the clustering process and to find suitable strategies for minimizing it. We found that the substitution of SiO2 matrix with a SiOC film allows to obtain a very bright light emission centered at about 440 nm from Eu2+ ions. In fact, SiOC is able to efficiently promote the Eu3+ → Eu2+ reduction; furthermore, Eu ions are characterized by an enhanced mobility and solubility in this matrix, and as a consequence, Eu precipitation is strongly reduced. Since SiOC is a material fully compatible with standard Si technology, Eu-doped SiOC layers can be considered a highly interesting candidate for photonic applications. [ABSTRACT FROM AUTHOR]

We report a systematic study of time-resolved and power-dependent photoresponse in high-efficiency germanium quantum dot photodetectors (Ge-QD PDs), with internal quantum efficiencies greater than 100% over a broad wavelength, reverse bias, and incident power range. Turn-on and turn-off response times (τon and τoff) are shown to depend on series resistance, bias, optical power, and thickness (WQD) of the Ge-QD layer, with measured τoff values down to ∼40 ns. Two different photoconduction regimes are observed at low and high reverse bias, with a transition around -3 V. A transient current overshoot phenomenon is also observed, which depends on bias and illumination power. [ABSTRACT FROM AUTHOR]

Thin films (100-500 nm) of the Si:O alloy have been systematically characterized in the optical absorption and electrical transport behavior, by varying the Si content from 43 up to 100 at. %. Magnetron sputtering or plasma enhanced chemical vapor deposition have been used for the Si:O alloy deposition, followed by annealing up to 1250 °C. Boron implantation (30 keV, 3-30×1014 B/cm2) on selected samples was performed to vary the electrical sheet resistance measured by the four-point collinear probe method. Transmittance and reflectance spectra have been extracted and combined to estimate the absorption spectra and the optical band gap, by means of the Tauc analysis. Raman spectroscopy was also employed to follow the amorphous-crystalline (a-c) transition of the Si domains contained in the Si:O films. The optical absorption and the electrical transport of Si:O films can be continuously and independently modulated by acting on different parameters. The light absorption increases (by one decade) with the Si content in the 43-100 at. % range, determining an optical band gap which can be continuously modulated into the 2.6-1.6 eV range, respectively. The a-c phase transition in Si:O films, causing a significant reduction in the absorption coefficient, occurs at increasing temperatures (from 600 to 1100 °C) as the Si content decreases. The electrical resistivity of Si:O films can be varied among five decades, being essentially dominated by the number of Si grains and by the doping. Si:O alloys with Si content in the 60-90 at. % range (named oxygen rich silicon films), are proved to join an appealing optical gap with a viable conductivity, being a good candidate for increasing the conversion efficiency of thin-film photovoltaic cell. [ABSTRACT FROM AUTHOR]

The photon absorption in Si quantum dots (QDs) embedded in SiO2 has been systematically investigated by varying several parameters of the QD synthesis. Plasma-enhanced chemical vapor deposition (PECVD) or magnetron cosputtering (MS) have been used to deposit, upon quartz substrates, single layer, or multilayer structures of Si-rich-SiO2 (SRO) with different Si content (43–46 at. %). SRO samples have been annealed for 1 h in the 450–1250 °C range and characterized by optical absorption measurements, photoluminescence analysis, Rutherford backscattering spectrometry and x-ray Photoelectron Spectroscopy. After annealing up to 900 °C SRO films grown by MS show a higher absorption coefficient and a lower optical bandgap (∼2.0 eV) in comparison with that of PECVD samples, due to the lower density of Si–Si bonds and to the presence of nitrogen in PECVD materials. By increasing the Si content a reduction in the optical bandgap has been recorded, pointing out the role of Si–Si bonds density in the absorption process in small amorphous Si QDs. Both the photon absorption probability and energy threshold in amorphous Si QDs are higher than in bulk amorphous Si, evidencing a quantum confinement effect. For temperatures higher than 900 °C both the materials show an increase in the optical bandgap due to the amorphous-crystalline transition of the Si QDs. Fixed the SRO stoichiometry, no difference in the optical bandgap trend of multilayer or single layer structures is evidenced. These data can be profitably used to better implement Si QDs for future PV technologies. [ABSTRACT FROM AUTHOR]

Y2-xErxO3 thin films, with x varying between 0 and 0.72, have been successfully grown on crystalline silicon (c-Si) substrates by radio-frequency magnetron cosputtering of Y2O3 and Er2O3 targets. As-deposited films are polycrystalline, showing the body-centered cubic structure of Y2O3, and show only a slight lattice parameter contraction when x is increased, owing to the insertion of Er ions. All the films exhibit intense Er-related optical emission at room temperature both in the visible and infrared regions. By studying the optical properties for different excitation conditions and for different Er contents, all the mechanisms (i.e., cross relaxations, up-conversions, and energy transfers to impurities) responsible for the photoluminescence (PL) emission have been identified, and the existence of two different well-defined Er concentration regimes has been demonstrated. In the low concentration regime (x up to 0.05, Er-doped regime), the visible PL emission reaches its highest intensity, owing to the influence of up-conversions, thus giving the possibility of using Y2-xErxO3 films as an up-converting layer in the rear of silicon solar cells. However, most of the excited Er ions populate the first two excited levels 4I11/2 and 4I13/2, and above a certain excitation flux a population inversion condition between the former and the latter is achieved, opening the route for the realization of amplifiers at 2.75 μm. Instead, in the high concentration regime (Er-compound regime), an increase in the nonradiative decay rates is observed, owing to the occurrence of cross relaxations or energy transfers to impurities. As a consequence, the PL emission at 1.54 μm becomes the most intense, thus determining possible applications for Y2-xErxO3 as an infrared emitting material. [ABSTRACT FROM AUTHOR]

In this paper we demonstrate that the structural and optical properties of Si nanoclusters (Si ncs) formed by thermal annealing of SiOx films prepared by plasma enhanced chemical vapor deposition (PECVD) and magnetron sputtering are very different. In fact, at a fixed Si excess and annealing temperature, photoluminescence (PL) spectra of sputtered samples are redshifted with respect to PECVD samples, denoting a larger Si ncs size. In addition, PL intensity reaches a maximum in sputtered films at annealing temperatures much lower than those needed in PECVD films. These data are correlated with structural properties obtained by energy filtered transmission electron microscopy and electron energy loss spectroscopy. It is shown that in PECVD films only around 30% of the Si excess agglomerates in clusters while an almost complete agglomeration occurs in sputtered films. These data are explained on the basis of the different initial structural properties of the as-deposited films that become crucial for the subsequent evolution. [ABSTRACT FROM AUTHOR]

The structural properties and the room temperature luminescence of Er2O3 thin films deposited by magnetron sputtering have been studied. In spite of the well-known high reactivity of rare earth oxides towards silicon, films characterized by good morphological properties have been obtained by using a SiO2 interlayer between the film and the silicon substrate. The evolution of the properties of the Er2O3 films due to thermal annealing processes in oxygen ambient performed at temperatures in the range of 800–1200 °C has been investigated in detail. The existence of well defined annealing conditions (rapid treatments at a temperature of 1100 °C or higher) allowing to avoid the occurrence of extensive chemical reactions with the oxidized substrate has been demonstrated; under these conditions, the thermal process has a beneficial effect on both structural and optical properties of the film, and an increase of the photoluminescence (PL) intensity by about a factor of 40 with respect to the as-deposited material has been observed. The enhanced efficiency of the photon emission process has been correlated with the longer lifetime of the PL signal. Finally, the conditions leading to a reaction of Er2O3 with the substrate have been also identified, and evidences about the formation of silicate-like phases have been collected. [ABSTRACT FROM AUTHOR]

A combination of the magnetron sputtering and plasma enhanced chemical vapor deposition techniques is employed for the characterization of the different Si:O alloys. The various parameters that are employed for determining the light absorption and the electrical transport properties of these alloys are also discussed.

Several experimental studies are conducted to explain the optical properties, as well as the impact of [Er.sup.3+] concentration on the luminescence in the [Y.2?x][Er.x][O.sub.3] thin films on Si. The high concentration regions are shown to lead to an increase in the nonradiative decay rate of the compounds.

The structural and optical properties of Si-rich silicon oxide (SRSO) layers obtained by plasma enhanced chemical vapor deposition (PECVD) and magnetron sputtering is examined. The studies have shown that in PECVD films only around 30% of the Si excess agglomerates in clusters while an almost complete agglomeration has occurred in sputtered films.

The structural and optical properties and the room temperature luminescence of Er2O3 thin films deposited by magnetron sputtering are analyzed. The enhanced efficiency of the photon emission process is correlated with the longer lifetime of the photoluminescence (PL) signal and the conditions leading to a reaction of Er2O3 with the substrate are identified.

This study reports the structural and stoichiometric modifications of bismuth oxide nanoparticles in the β phase (β-Bi2O3) by UV pulsed laser irradiation in water or ethanol solutions. Scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, UV-vis diffuse reflectance and high-resolution transmission electron microscopy were used to characterize the synthesized nanomaterials. The various analyses demonstrate that the laser irradiation of β-Bi2O3 nanospheres is a green, fast and effective method to produce Bi2O2CO3 nanosheets or metallic Bi nanoparticles depending on the liquid environment used. Bi subcarbonate is obtained by laser irradiation in water, whereas metallic Bi is produced by laser irradiation in ethanol, and in particular the relative amount of metallic Bi is found to depend on the laser fluence. These typologies of materials find application in several fields, such as photocatalytic processes, light filters and environmental sensors. [ABSTRACT FROM AUTHOR]

Er-containing silicon compatible materials have been widely used as infrared emitters for microphotonics application. In this field, the additional introduction of a proper sensitizer permits to increase the Er excitation cross sections, thus increasing its optical efficiency. This work aims to investigate the influence of a post-transition metal, bismuth, on the optical properties of erbiumyttrium disilicate thin films synthesized by magnetron co-sputtering. After thermal treatments at 1000 °C in O2 or N2 environment, the presence of small precipitates, about 6 nm in diameter, was evidenced by transmission electron microscopy analyses. The spatially resolved chemical nature of the nanoparticles was discerned in the Si and O rich environments by means of scanning transmission electron microscopy-energy dispersive X-ray and scanning transmission electron microscopy-electron energy loss spectroscopy analyses performed with nanometric resolution. In particular, metallic Bi nanoparticles were stabilized in the N2 environment, being strongly detrimental for the Er emission. A different scenario was instead observed in O2, where the formation of Bi silicate nanoparticles was demonstrated with the support of photoluminescence excitation spectroscopy. In particular, a broad band peaked at 255 nm, correlated to the excitation band of Bi silicate nanoparticles, was identified in Er excitation spectrum. Thus Bi silicate clusters act as sensitizer for Er ions, permitting to improve Er emission up to 250 times with respect to the resonant condition. Moreover, the Er decay time increases in the presence of the Bi silicate nanoparticles that act as cages for Er ions. These last results permit to further increase Er optical efficiency in the infrared range, suggesting (Bi+Er)-Y disilicate as a good candidate for applications in microphotonics. [ABSTRACT FROM AUTHOR]

We report on the design, fabrication, and electro-optical characterization of a light emitting device operating at 1.54 μm, whose active layer consists of silicon oxide containing Er-doped Si nanoclusters. A photonic crystal (PhC) is fabricated on the top-electrode to enhance the light extraction in the vertical direction, and thus the external efficiency of the device. This occurs if a photonic mode of the PhC slab is resonant with the Er emission energy, as confirmed by theoretical calculations and experimental analyses. We measure an increase of the extraction efficiency by a factor of 3 with a high directionality of light emission in a narrow vertical cone. External quantum efficiency and power efficiency are among the highest reported for this kind of material. These results are important for the realization of CMOS-compatible efficient light emitters at telecom wavelengths. [ABSTRACT FROM AUTHOR]

Multilayers of Ge quantum dots (QDs, 3 nm in diameter) embedded in SiO2, separated by SiO2 barrier layer (3, 9, or 20 nm thick), have been synthesized by sputter deposition and characterized by transmission electron microscopy and light absorption spectroscopy. Quantum confinement affects the optical bandgap energy (1.9 eV for QDs, 0.8 eV for bulk Ge); moreover, the absorption probability greatly depends on the QD-QD distance. A strong electronic coupling among Ge QDs is evidenced, with a significant increase of the light absorption efficiency when the QD-QD distance is reduced. These data unveil promising aspects for light harvesting with nanostructures. [ABSTRACT FROM AUTHOR]

We investigate the optical properties of Er-Yb-Y disilicate thin films in which Er and Yb contents are varied independently. From time-resolved measurements of Yb decay in absence and in presence of Er, we analyzed and modeled the energy transfer mechanism identifying all the de-excitation channels and measuring a coupling constant CYb-Er = 3.0 × 10-39 cm6/s. Finally, we calculated the efficiency of Yb-Er energy transfer process and we correlated it with Er photoluminescence, demonstrating that it is controlled by the energy transfer mechanism. The maximum efficiency is found for 1.5 × 1021 Er/cm3 and 1.5 × 1022 Yb/cm3, by making this material very promising for optical amplifiers. [ABSTRACT FROM AUTHOR]