Enhancing the Spectroelectrochemical Performance of WO₃ Films by Use of Structure-Directing Agents during Film Growth

Thin, porous films of WO3 were fabricated by solution-based synthesis via spin-coating using polyethylene glycol (PEG), a block copolymer (PIB50-b-PEO45), or a combination of PEG and PIB50-b-PEO45 as structure-directing agents. The influence of the polymers on the composition and porosity of WO3 was investigated by microwave plasma atomic emission spectroscopy, energy-dispersive X-ray spectroscopy, scanning electron microscopy, X-ray diffraction, and gas sorption analysis. The electrochromic performance of the WO3 thin films was characterized with LiClO4 in propylene carbonate as electrolyte. To analyze the intercalation of the Li+ ions, time-of-flight secondary ion mass spectrometry, and X-ray photoelectron spectroscopy were performed on films in a pristine or reduced state. The use of PEG led to networks of micropores allowing fast reversible electrochromic switching with a high modulation of the optical transmittance and a high coloration efficiency. The use of PIB50-b-PEO45 provided isolated spherical mesopores leading to an electrochromic performance similar to compact WO3, only. Optimum characteristics were obtained in films which had been prepared in the presence of both, PEG and PIB50-b-PEO45, since WO3 films with mesopores were obtained that were interconnected by a microporous network and showed a clear progress in electrochromic switching beyond compact or microporous WO3

Surface enhanced NMR spectroscopy by dynamic nuclear polarization.

International audienceIt is shown that surface NMR spectra can be greatly enhanced using dynamic nuclear polarization. Polarization is transferred from the protons of the solvent to the rare nuclei (here carbon-13 at natural isotopic abundance) at the surface, yielding at least a 50-fold signal enhancement for surface species covalently incorporated into a silica framework

Synthesis and Physicochemical Characterization of Ce1-xGdxO2-δ: A Case Study on the Impact of the Oxygen Storage Capacity on the HCl Oxidation Reaction

This study reports the synthesis of high-surface-area Ce1−xGdxO2−δ (CGO) fibers that are used as catalysts for the oxidation of HCl. Special emphasis is put on the role of the oxygen storage capacity (OSC) of the CGO fibers on the catalytic performance. An in-depth physicochemical characterization of high-surface-area CGO was achieved by employing a multitude of dedicated spectroscopic techniques. The increasing OSC with Gd content is traced to the development of a space charge region with increased electron concentration as a result of the nano size of the CGO particles. The activity of CGO in the HCl oxidation reaction is shown to decrease with Gd concentration