A simple hole-type secondary scintillation structure (2 mm-hole, 5 mm-pitch, 5 mm-thickness) is introduced and its operation demonstrated in pure xenon in the pressure range 2-10 bar. The new device, characteristically translucent, has been manufactured through a collaboration between IGFAE and the CERN workshop, and relies entirely on radiopure materials (acrylic and copper), being extremely rugged in the presence of sparks, mechanically robust, and easily scalable, yet made through a relatively simple process. With an overall figure (at 10 bar) characterized by an energy resolution of 18.9%(FWHM) for 55Fe x-rays, an optical gain of m γ = 500 ph/e, and a stable operation at reduced fields more than twice those of some of the presently running experiments (E EL = 3 kV/cm/bar), this family of structures seems to show great promise for electroluminescence readouts on large scale detectors. As argued below, further improvements have the potential of bringing the energy resolution close to the Fano factor and increasing the optical gain.

Naturally occurring van der Waals crystals have brought unprecedented interest to nanomaterial researchers in recent years. So far, more than 1800 layered materials (LMs) have been identified but only a few insulating and naturally occurring LMs were deeply investigated. Phyllosilicate minerals, which are a class of natural and abundant LMs, have been recently considered as a low-cost source of insulating nanomaterials. Within this family an almost barely explored material emerges: phlogopite [KMg3(AlSi3)O10(OH)2]. Here we carry out a high throughput characterization of this LM by employing several experimental techniques, corroborating the major findings with first-principles calculations. We show that monolayers (1L) and few-layers of this material are air and temperature stable, as well as easily obtained by the standard mechanical exfoliation technique, have an atomically flat surface, and lower bandgap than its bulk counterpart, an unusual trend in LMs. We also systematically study the basic properties of ultrathin phlogopite and demonstrate that natural phlogopite presents iron impurities in its crystal lattice, which decreases its bandgap from about 7 eV to 3.6 eV. Finally, we combine phlogopite crystals with 1L-WS2 in ultrathin van der Waals heterostructures and present a photoluminescence study, revealing a significant enhancement on the 1L-WS2 optical quality (i.e., higher recombination efficiency through neutral excitons) similarly to that obtained on 1L-WS2/hBN heterostructures. Our proof-of-concept study shows that phlogopite should be regarded as a good and promising candidate for LM-based applications as a low-cost layered nanomaterial.

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A new concept for the simultaneous detection of primary and secondary scintillation in time projection chambers is proposed. Its core element is a type of very-thick GEM structure supplied with transparent electrodes and machined from a polyethylene naphthalate plate, a natural wavelength shifter. Such a device has good prospects for scalability and, by virtue of its genuine optical properties, it can improve on the light collection efficiency, energy threshold and resolution of conventional micropattern gas detectors. This, together with the intrinsic radiopurity of its constituting elements, offers advantages for noble gas and liquid based time projection chambers, used for dark matter searches and neutrino experiments. Production, optical and electrical characterization, and first measurements performed with the new device are reported.

TiO2-based visible-light-sensitive nanomaterials are widely studied for photocatalytic applications under UV–Vis radiation. Among the mechanisms of visible-light sensitization, extrinsic oxygen vacancies have been introduced into TiO2 and charge-transfer complexes (CTCs) have been formed between chelating ligands, such as acetylacetone, and nanocrystalline TiO2 (TiO2-ACAC). However, the influence of extrinsic oxygen vacancies on the photocatalytic performance of TiO2-based CTCs is unknown. In this work, surface/bulk extrinsic oxygen vacancies were introduced into TiO2-ACAC through calcination at 270 °C under static air, argon, and hydrogen atmospheres. TiO2-ACAC CTCs were characterized by X-ray powder diffraction, thermogravimetric analysis, diffuse-reflectance spectroscopy, photoluminescence, electron paramagnetic resonance (EPR), and X-ray photoelectron spectroscopy techniques. The correlation between EPR–spin trapping and tetracycline (TC) photodegradation, using scavengers, highlighted the key role of the superoxide radical in TC degradation by TiO2-ACAC CTCs under low-power visible-light radiation. The increased extrinsic oxygen vacancies concentration was not beneficial for the photocatalytic performance of TiO2 CTCs, since bulk extrinsic oxygen vacancies additionally act as recombination centers. In fact, the TiO2-ACAC CTC with the lowest extrinsic oxygen vacancies concentration exhibited the highest photocatalytic performance for TC degradation due to an adequate distribution of extrinsic bulk oxygen vacancies, which led to the trapped electrons undergoing repeated hopping, reducing the recombination rates and improving the efficiency in superoxide radicals production. Our findings indicated that TiO2-ACAC CTCs are able to degrade pollutants via interactions with electronic holes and principally superoxide radicals and also, provided fundamental information about the influence of surface/bulk extrinsic oxygen vacancies on the photocatalytic performance, lattice parameters, and optical and photochemical properties of TiO2-based CTCs.