The relevance of point defects in studying silica-based materials from bulk to nanosystems

The macroscopic properties of silica can be modified by the presence of local microscopic modifications at the scale of the basic molecular units (point defects). Such defects can be generated during the production of glass, devices, or by the environments where the latter have to operate, impacting on the devices’ performance. For these reasons, the identification of defects, their generation processes, and the knowledge of their electrical and optical features are relevant for microelectronics and optoelectronics. The aim of this manuscript is to report some examples of how defects can be generated, how they can impact device performance, and how a defect species or a physical phenomenon that is a disadvantage in some fields can be used as an advantage in others

29Si Hyperfine Structure of the E'_\alpha Center in Amorphous Silicon Dioxide

We report a study by electron paramagnetic resonance (EPR) on the E'_\alpha point defect in amorphous silicon dioxide (a-SiO2). Our experiments were performed on gamma-ray irradiated oxygen-deficient materials and pointed out that the 29Si hyperfine structure of the E'_alpha consists in a pair of lines split by 49 mT. On the basis of the experimental results a microscopic model is proposed for the E'_alpha center, consisting in a hole trapped in an oxygen vacancy with the unpaired electron sp3 orbital pointing away from the vacancy in a back-projected configuration and interacting with an extra oxygen atom of the a-SiO2 matrix.Comment: 4 page

Structure of the FeBTC Metal\u2013Organic Framework: A Model Based on the Local Environment Study

The local environment of iron in FeBTC, a metal organic framework commercially known as Basolite F300, is investigated combining XANES and EXAFS studies of the iron K-edge. The building block of the FeBTC can be described as an iron acetate moiety. Dehydration induces a change in the coordination of the first shell while preserving the network. We propose that the local structure around Fe atoms does not undergo a rearrangement, thus, leading to the formation of an open site. The analysis conveys that the FeBTC is a disordered network of locally ordered blocks

Investigation by raman spectroscopy of the decomposition process of HKUST-1 upon exposure to air

We report an experimental investigation by Raman spectroscopy of the decomposition process of Metal-Organic Framework (MOF) HKUST-1 upon exposure to air moisture (T=300 K, 70% relative humidity). The data collected here are compared with the indications obtained from a model of the process of decomposition of this material proposed in literature. In agreement with that model, the reported Raman measurements indicate that for exposure times longer than 20 days relevant irreversible processes take place, which are related to the occurrence of the hydrolysis of Cu-O bonds. These processes induce small but detectable variations of the peak positions and intensities of the main Raman bands of the material, which can be related to Cu-Cu, Cu-O, and O-C-O stretching modes. The critical analyses of these changes have permitted us to obtain a more detailed description of the process of decomposition taking place in HKUST-1 upon interaction with moisture. Furthermore, the reported Raman data give further strong support to the recently proposed model of decomposition of HKUST-1, contributing significantly to the development of a complete picture of the properties of this considerable deleterious effect

Structural modifications induced in ZIF-8 by interaction with Cu2+ions in water remediation applications

Metal-organic frameworks (MOF) are very promising materials, as they exhibit many exciting properties inspiring many outstanding applications. One very intriguing property of a class of MOF consists in their ability to breath, i.e. to undergo a crystalline to-crystalline structural change, usually induced by modifying the temperature, applying external pressure or by adsorbing of specific gases [1]. Such structural changes in turn affect many properties of the material, further increasing the potential applications of these materials. The advantages of the breathing process in sensing applications, for example, are obvious. One of the most interesting breathing MOF is MIL-53(Al) [2]. It has strong potentialities in many fields, as adsorption, separation and storage of gases, catalysis, drug delivery, sensing [3,4]. Since its first report, MIL-53(Al) has gained the role of prototype system, giving the opportunity to unveil many properties pertaining to such outstanding class of highly reactive (breathing) MOF...

Sensing of transition metals by top-down carbon dots

Carbon quantum dots (CQDs) are a new class of carbon-rich materials with a range of unique optical and structural properties. They can be defined as carbon nanoparticles, with sizes in the range of 1–10 nm, displaying absorption and emission activities in the UV-VIS range. Depending on the structure, CQDs display a wide variability of properties, which provides the possibility of finely tuning them for several applications. The great advantages of CQDs are certainly the ease of synthesis, non-toxicity, and the strong interactions with the surrounding environment. Based on this, CQDs are especially promising as selective chemosensors. The present study reports on carbon quantum dots synthesized with a top-down (TD) approach, and characterized by different optical, spectroscopic, and morphological techniques to identify the selectivity for metal ions belonging to the first transition series. In particular, the study focuses on the interaction between two samples, namely TD and TDA, featuring different surface functionalization, and heavy metal ions. Their sensing towards Co2+, Cu2+, Fe3+, Zn2+, and Ni2+ has been tested by fluorescence (PL), steady state absorption spectroscopy, and time-resolved PL spectroscopy, in order to determine the fluorescence quenching. We found a PL quenching in the presence of concentrations of metal salts starting from 0.5 µM, and a selectivity towards the interacting ions, depending on CQDs’ surface features paving the way for their use for sensing

Stimuli-responsive photoluminescent and structural properties of MIL-53(Al) MOF for sensing applications

Metal-organic frameworks (MOFs) are an intriguing group of porous materials due to their potential influence on the development of indispensable technologies like luminescent sensors and solid-state light devices, luminescent multifunctional nanomaterials. In this research work we explored MIL-53(Al), an exceptional class of MOF that, along with guest adsorption, undergoes structural transitions exhibiting breathing behavior between narrow pore and large pore under temperature and mechanical stress. Therefore, we opted for the time resolved luminescence and FT-Raman spectroscopy to investigate the mechanochromic and thermochromic response of this material under external stimuli. Intriguingly, when subjected to temperature changes, MIL-53(Al) exhibited a ratiometric fluorescence behavior related to the reversible relationship of photoluminescence emission intensity with respect to temperature. Moreover, under higher mechanical stress MIL-53(Al) displayed turn-on behavior in emission intensity, hence offering a thrilling avenue for the application in mechanically deformed-based luminescent sensors and ratiometric fluorescence temperature sensors

Investigation on the luminescence properties of bare and Rhodamine B functionalized Zr-MOF-808

Metal organic frameworks (MOFs) are materials well known for their high surface and catalytic properties as well as because they are relatively easy to synthesize and, in some cases, extremely f lexible.[1] Recently, there has been also a growing interest in the optical properties of these materials, particularly in luminescence, which has potential applications in various fields, such as sensors, LEDs, scintillators, and bioimaging agents....