Characterization of seed proanthocyanidins of thirty-two red and white hybrid grape varieties

Grape seed extracts are known for their beneficial effects on health and on cardiovascular diseases due to antioxidant activity and the free radical-scavenging properties of proanthocyanidins (PAs). Moreover, grape seed tannins are used in oenology as additives to improve the organoleptic characteristics of wines, and for the clarification of must and wines. PAs in seed extract of 32 hybrid and three V. vinifera grape varieties were characterized by MALDI-TOF mass spectrometry. Signals of 148 compounds were identified as [M+H]+, [M+Na]+ and [M+K]+ adducts of B-type and A-type PAs formed from catechin/epicatechin subunits up to undecamers and with galloylation degree 0-7. The number-average molecular weight (Mn) of the samples, a parameter correlated with the molecular weight of polymers, and the polyphenolic content of extract, were also determined. Profiles of the hybrid grape varieties were compared with those of three V. vinifera samples studied as references. 'Terzi 108-6' showed high content of antioxidant polyphenols and 'Seyve Villard 12-390' higher content of higher oligomers. These two grape varieties are therefore potentially very interesting as sources of antioxidants and tannins for nutraceutical and oenological uses

review of 2h tetraphenylporphyrins metalation in ultra high vacuum on metal surfaces

The formation and conformational adaptation of self-assembled monolayer of 2H- tetraphenylporphyrins (2H-TPPs) on metal surfaces, as well as their metalation processes in ultra-high vacuum (UHV), are reviewed. By means of XPS, NEXAFS and STM measurements we demonstrate that, after the annealing at 550 K, a temperature-induced chemical modification of 2H-TPP monolayer on Ag(111) occurs, resulting in the rotation of the phenyl rings parallel to the substrate plane. Moreover, independently of the conformation, we report three dierent methods to metalate 2H-TPP monolayers in UHV. Experimental evidence indicates that the presence of a metal atom in the TPP macrocycle influences both the conformation of the molecule and its adsorption distance

Electronic structure of MAPbI3 and MAPbCl3: importance of band alignment

Since their first appearance, organic-inorganic perovskite absorbers have been capturing the attention of the scientific community. While high efficiency devices highlight the importance of band level alignment, very little is known on the origin of the strong n-doping character observed in the perovskite. Here, by means of a highly accurate photoemission study, we shed light on the energy alignment in perovskite-based devices. Our results suggest that the interaction with the substrate may be the driver for the observed doping in the perovskite samples

Metadata schema to support FAIR data in scanning electron microscopy

The development and the adoption of metadata schemas and standards are a key aspect in data management. In this paper, we introduce our approach to a metadata model in the field of Materials Science. We present the specific use case of a metadata schema for Scanning Electron Microscopy, a characterization technique which is routinely used in Materials Science. This metadata schema is aiming to be a de-facto standard which will be openly available for reuse and further extension to other electron microscopy techniques

Tuning the Magnetic Anisotropy of Lanthanides on a Metal Substrate by Metal–Organic Coordination

Taming the magnetic anisotropy of lanthanides through coordination environments is crucial to take advantage of the lanthanides properties in thermally robust nanomaterials. In this work, the electronic and magnetic properties of Dy-carboxylate metal–organic networks on Cu(111) based on an eightfold coordination between Dy and ditopic linkers are inspected. This surface science study based on scanning probe microscopy and X-ray magnetic circular dichroism, complemented with density functional theory and multiplet calculations, reveals that the magnetic anisotropy landscape of the system is complex. Surface-supported metal–organic coordination is able to induce a change in the orientation of the easy magnetization axis of the Dy coordinative centers as compared to isolated Dy atoms and Dy clusters, and significantly increases the magnetic anisotropy. Surprisingly, Dy atoms coordinated in the metallosupramolecular networks display a nearly in-plane easy magnetization axis despite the out-of-plane symmetry axis of the coordinative molecular lattice. Multiplet calculations highlight the decisive role of the metal–organic coordination, revealing that the tilted orientation is the result of a very delicate balance between the interaction of Dy with O atoms and the precise geometry of the crystal field. This study opens new avenues to tailor the magnetic anisotropy and magnetic moments of lanthanide elements on surfaces.The ALBA synchrotron is acknowledged for providing beam time at BOREAS beamline (proposal number 2015091454). This project has received funding from the European Research Council (ERC, grant 766555) and Marie Sklodowska-Curie Actions (MSCA, project 894924) under the European Union's Horizon 2020 research and innovation programme. This work has been financed by the Spanish Ministerio de Economía, Industria y Competitividad (projects FIS2016-78591-C3-1-R, RTI2018-097895-B-C42, MAT2016-78293-C6-2-R, MAT2017-85089-C2-1-R, and PID2019-107338RB-C65); the Comunidad de Madrid (Projects S2013/MIT-2850, P2018/NMT4321, and S2018/NMT-4367); the European Regional Development Fund (ERDF) under the program Interreg V-A España-Francia-Andorra (Contract No. EFA 194/16 TNSI); and “Severo Ochoa” Programme for Centres of Excellence in R&D (grants SEV-2016-0686, and SEV-2017-0706)

Tuning the magnetic moment of high density FePc/Ag(110) phases by oxygen dosing

Resumen del trabajo presentado a la 64th Annual Conference on Magnetism and Magnetic Materials (MMM), celebrada en Las Vegas (USA) del 4 al 8 de noviembre de 2019.Peer reviewe

Improved recovery time and sensitivity to H2 and NH3 at room temperature with SnOx vertical nanopillars on ITO

Nanostructured SnO2 is a promising material for the scalable production of portable gas sensors. To fully exploit their potential, these gas sensors need a faster recovery rate and higher sensitivity at room temperature than the current state of the art. Here we demonstrate a chemiresistive gas sensor based on vertical SnOx nanopillars, capable of sensing < 5 ppm of H2 at room temperature and 10 ppt at 230 \ub0C. We test the sample both in vacuum and in air and observe an exceptional improvement in the performance compared to commercially available gas sensors. In particular, the recovery time for sensing NH3 at room temperature is more than one order of magnitude faster than a commercial SnO2 sensor. The sensor shows an unique combination of high sensitivity and fast recovery time, matching the requirements on materials expected to foster widespread use of portable and affordable gas sensors