Grazing Incidence Small Angle X-Ray Scattering as a Tool for In- Situ Time-Resolved Studies

With the advent of third-generation synchrotron sources and the development of fast two-dimensional X-ray detectors, X-ray scattering has become an invaluable tool for in-situ time-resolved experiments. In the case of thin films, grazing incidence small angle X-ray scattering (GISAXS) constitutes a powerful technique to extract morphological information not only of the thin film surface but also of buried structures with statistical relevance. Thus, recently in-situ GISAXS experiments with subsecond time resolution have enabled investigating the self-assembly processes during vacuum deposition of metallic and organic thin films as well as the structural changes of polymer and colloidal thin films in the course of wet deposition. Moreover, processing of thin films has also been investigated in-situ employing GISAXS. In this chapter, we review the current trends of time-resolved GISAXS studies. After an introduction to the GISAXS technique, we present exemplary results of metallic and organic thin film preparation, wet deposition of polymer thin films and self-assembly of colloidal thin films, as well as examples of thin film modification in, e.g., microfluidic channels and within working devices. Finally, an overview of the future perspectives in the field is provided

Preparación y caracterización de nanocompuestos poliméricos de PP y PET con nanotubos de carbono: estudio mediante microespectroscopia vibracional

Tesis doctoral inédita. Universidad Autónoma de Madrid, Facultad de Ciencias, Departamento de Física Aplicada. Fecha de lectura: 12-12-201

Infrared synchrotron radiation from bending magnet and edge radiation sources for the study of orientation and conformation in anisotropic materials

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Real time investigations during sputter deposition for tailoring optical properties of metal-polymer interfaces

Poster presented at the 16th International Conference on Small-Angle Scattering, held on 13-18th September, 2015, Berlin (Germany).Tailoring optoelectronic properties of metal-polymer interfaces using self-assembly of nanoparticles is of crucial importance in organic electronics and organic photovoltaics [1]. In particular, metal sputter deposition on block-co-polymers is one widely used method to fabricate nanostructured metal layers on a large scale exploiting the selective wetting and doping of metals on polystyrene domains [2,3]. In order to obtain full control over the nanostructural evolution at the metal-polymer interface and its impact on optoelectronic properties, we employed a combination of in situ time-resolved microfocus Grazing Incidence Small Angle X-ray Scattering (μGISAXS) with in situ UV/Vis Specular Reflectance Spectroscopy (SRS) during sputter deposition of gold (Au) on thin polystyrene films (PS). We monitored the evolution of the metallic layer morphology according to changes in the key scattering features by geometrical modeling [4] and correlate the nanostructural development to optical properties. The changes of optoelectronic properties induced by metal nanoparticle growth during the sputter deposition process were exemplarily monitored using SRS. The morphological characterization is complemented by X-ray reflectivity and electron microscopy. This enables us to identify the different growth regimes including their specific thresholds and permits better understanding of the growth kinetics of gold clusters and their self-organization into complex nanostructures on polymer substrates. Thus, our findings are of great interest for applications in organic photovoltaics [5] and organic electronics, which benefit from tailored metal-polymer interfaces

Is the sub-glass temperature relaxation of furan-based polymers related to their high gas barrier properties?

11th Conference on Broadband Dielectric Spectroscopy and its Applications (BDS2022), Donostia/San Sebastián, 04.Sep - 09.Sep 2022. -- Presentación con 25 diapositivasPoly(alkylene 2,5-furanoate)s, (PAF)s, are fully biobased homopolyesters based on 2,5-furandicarboxylic acid that have recently emerged as promising alternative to petroleum based poly(alkylene terephthalate)s. In addition to a lower production carbon footprint poly(alkylene 2,5-furanoate)s have received significant attention due to their outstanding gas barrier properties in comparison to traditional poly aromatic esters [1]. The influence of chain dynamics on barrier properties has also devoted some attention. Dielectric spectroscopy experiments performed in poly(trimethylene 2,5-furanoate) revealed that the subambient relaxation, below its glass transition temperature, exhibited an inhibition of the mode corresponding to the ester oxygen linked to the aliphatic subunit which efficiently relaxes in the poly(trimethylene terephthalate) counterpart [2]. Fourier Transform Infrared (FT-IR) spectroscopy can provide precise information of intra-molecular motions at the molecular level [3]. By evaluating the vibrational frequencies and the corresponding oscillator, strength from the IR spectra information about the intra-molecular dynamics can be available. In this study, we present a combined IR spectroscopy and BDS study focused on the sub-glass temperature molecular dynamics of poly(trimethylene 2,5-furanoate) in comparison to that of poly(trimethylene terephthalate) in order to shed light on the influence the dynamics on the barrier properties of Poly(alkylene 2,5-furanoate)s.The authors gratefully acknowledge the financial support of the Spanish Ministry of Science and Innovation (MICINN) through PID2019-107514GB-I00 / AEI / 10.13039/501100011033

Inter and intra molecular dynamics in poly(trimethylene 2,5-furanoate) as revealed by infrared and Broadband Dielectric Spectroscopies

9 pags., 9 figs., 2 tabs.Infrared spectroscopy (IR) and Broadband Dielectric Spectroscopy (BDS) experiments have been performed in poly(trimethylene 2,5-furanoate)(PTF) and poly(trimethylene terephthalate)(PTT) below their glass transition temperatures. The BDS experiments reveal a richer inter-molecular dynamic for PTT as characterized by a multimodal β relaxation in contrast with the monomodal one exhibited by PTF. The evolution with temperature of comparable IR absorption bands is very similar for PTF and PTT and shows small shifts in wavenumbers towards lower values, with exception of the band related to the stretching mode of the carbonyl group. In addition, a significant difference appears in the shape of the bands associated with the –C[dbnd]O stretching. While for PTT the absorption feature is comprised of a single component, that for PTF exhibits several components suggesting the presence of hydrogen bonds. This effect may be responsible for the monomodal shape of the β relaxation of PTF since a higher degree of intramolecular coupling between the furan ring and the rest of the monomer is expected. Density Functional Theory (DFT) calculations support the experimental results revealing that as temperature increases an increment of the syn conformations of the 2,5-furandicarboxylic acid (FDCA) moiety is likely to occur in the amorphous state. The energy gain from more stable anti to less stable syn isomers can be compensated by the formation of hydrogen bonds between interchain FDCA moieties in syn conformations. This effect may cause additional hindrance to the intermolecular dynamics of the dielectric β relaxation. It is conceivable that the hindrance exhibited by PTF in both intra and inter-molecular dynamics may play a role in the reduction of gas diffusion and permeability of PTF in comparison with PTT.Grants PID2019-107514 GB-I00/AEI/10.13039/501100011033 and PID2019-106125 GB-I00/AEI/10.13039/501100011033 funded by MCIN/AEI/10.13039/501100011033 and by “ ERDF A way of making Europe”. GS acknowledges grant RYC2020-029810-I funded by MCIN/ AEI/10.13039/501100011033 and by “ ESF Investing in your future”. SP would like to thank for financial support from the National Science Centre within project SONATA no 2018/31/D/ST8/00792.

Experimental Station for Generation, Processing and Diagnostics of Nanoparticles of Astrophysical Interest

Europhysics Sectional Conference on the Atomic and Molecular Physics of Ionized Gases. ESCAMPIG XXIV.Glasgow July 17-21 (2018). .--file:///C:/Users/BIBLIO~1/AppData/Local/Temp/CONGRESOS_Y_CONFERENCIAS752874-1.pd

Astronomical radio-reception techniques for emission spectroscopy of molecular and short lived species in cold plasmas

Santiago de Compostela, Facultade de Química,17-21 julio 2017. -- http://www.bienalrsef2017.com/bienalrsef17/This work has received funding from the European Research Council under the Program (FP/2007- 2013) / ERC-SyG-2013 Grant Agreement n. 610256 NANOCOSMOS and from Spanish MINECO under the Consolider-Ingenio Program CSD2009-00038 (ASTROMOL) and the grants FIS2013- 48087-C2-1-P, FIS2016-77726-C3-1-P.Peer Reviewe

Solution structure of the dimerization domain of ribosomal protein P2 provides insights for the structural organization of eukaryotic stalk

The lateral stalk of ribosome is responsible for kingdom-specific binding of translation factors and activation of GTP hydrolysis that drives protein synthesis. In eukaryotes, the stalk is composed of acidic ribosomal proteins P0, P1 and P2 that constitute a pentameric P-complex in 1: 2: 2 ratio. We have determined the solution structure of the N-terminal dimerization domain of human P2 (NTD-P2), which provides insights into the structural organization of the eukaryotic stalk. Our structure revealed that eukaryotic stalk protein P2 forms a symmetric homodimer in solution, and is structurally distinct from the bacterial counterpart L12 homodimer. The two subunits of NTD-P2 form extensive hydrophobic interactions in the dimeric interface that buries 2400 Å2 of solvent accessible surface area. We have showed that P1 can dissociate P2 homodimer spontaneously to form a more stable P1/P2 1 : 1 heterodimer. By homology modelling, we identified three exposed polar residues on helix-3 of P2 are substituted by conserved hydrophobic residues in P1. Confirmed by mutagenesis, we showed that these residues on helix-3 of P1 are not involved in the dimerization of P1/P2, but instead play a vital role in anchoring P1/P2 heterodimer to P0. Based on our results, models of the eukaryotic stalk complex were proposed

Solution structure of the dimerization domain of ribosomal protein P2 provides insights for the structural organization of eukaryotic stalk

The lateral stalk of ribosome is responsible for kingdom-specific binding of translation factors and activation of GTP hydrolysis that drives protein synthesis. In eukaryotes, the stalk is composed of acidic ribosomal proteins P0, P1 and P2 that constitute a pentameric P-complex in 1: 2: 2 ratio. We have determined the solution structure of the N-terminal dimerization domain of human P2 (NTD-P2), which provides insights into the structural organization of the eukaryotic stalk. Our structure revealed that eukaryotic stalk protein P2 forms a symmetric homodimer in solution, and is structurally distinct from the bacterial counterpart L12 homodimer. The two subunits of NTD-P2 form extensive hydrophobic interactions in the dimeric interface that buries 2400 Å2 of solvent accessible surface area. We have showed that P1 can dissociate P2 homodimer spontaneously to form a more stable P1/P2 1 : 1 heterodimer. By homology modelling, we identified three exposed polar residues on helix-3 of P2 are substituted by conserved hydrophobic residues in P1. Confirmed by mutagenesis, we showed that these residues on helix-3 of P1 are not involved in the dimerization of P1/P2, but instead play a vital role in anchoring P1/P2 heterodimer to P0. Based on our results, models of the eukaryotic stalk complex were proposed