Controlled Growth of WO3Nanostructures with Three Different Morphologies and Their Structural, Optical, and Photodecomposition Studies

Tungsten trioxide (WO3) nanostructures were synthesized by hydrothermal method using sodium tungstate (Na2WO4·2H2O) alone as starting material, and sodium tungstate in presence of ferrous ammonium sulfate [(NH4)2Fe(SO4)2·6H2O] or cobalt chloride (CoCl2·6H2O) as structure-directing agents. Orthorhombic WO3having a rectangular slab-like morphology was obtained when Na2WO4·2H2O was used alone. When ferrous ammonium sulfate and cobalt chloride were added to sodium tungstate, hexagonal WO3nanowire clusters and hexagonal WO3nanorods were obtained, respectively. The crystal structure and orientation of the synthesized products were studied by X-ray diffraction (XRD), micro-Raman spectroscopy, and high-resolution transmission electron microscopy (HRTEM), and their chemical composition was analyzed by X-ray photoelectron spectroscopy (XPS). The optical properties of the synthesized products were verified by UV–Vis and photoluminescence studies. A photodegradation study on Procion Red MX 5B was also carried out, showing that the hexagonal WO3nanowire clusters had the highest photodegradation efficiency

Colorimetric Properties and Structural Evolution of Cathodic Electrochromic WO3 Thin Films

Cathodic amorphous tungsten trioxide (WO3) thin films have been deposited by reactive direct current magnetron sputtering and have been studied for their colorimetric and electrochromic properties. Those studies were carried out under two different potential cycling process: (i) switching mode (the response between coloration and bleaching in increasing potential steps) and (ii) modulation mode (the stepwise modulation to coloration with increasing potential and back to bleaching). Optical measurements, performed as a function of applied potential, showed excellent transmittance contrasts (∼80%) between colored and bleached states. The color stimuli and the changes that take place upon reversible switching or modulation were recorded based on the Commisson International de l’Éclairage (CIE) system. It was found that, under various potentials, significant changes occurred in the hue and saturation for WO3, as exhibited by the CIE 1931 xy chromaticity coordinates. As WO3 was reduced (W6+ + e– → W5+), a sharp decrease in luminance was observed. Excellent reversibility is demonstrated not only by colorimetric properties, but also by the corresponding intrinsic structures of the films, as investigated by µ-Raman spectroscopy. Furthermore, the WO3 films displayed a fast response time and good long-term cycling durability, which was attributed to their amorphous nature.The accepted manuscript in pdf format is listed with the files at the bottom of this page. The presentation of the authors' names and (or) special characters in the title of the manuscript may differ slightly between what is listed on this page and what is listed in the pdf file of the accepted manuscript; that in the pdf file of the accepted manuscript is what was submitted by the author

Two-Dimensional V2O5 Inverse Opal: Fabrication and Electrochromic Application

The open-layered structure of Vanadium pentoxide (V2O5) has triggered significant interest in exploring its energy-related application as lithium (Li) intercalation cathode material. Various methods are extensively studied to improve the Li diffusion using thin films or nanoarchitecture. In this work, high-quality two-dimensional (2D) inverse opal α-V2O5 films were synthesized via a modified ‘dynamic hard template’ infiltration strategy using sacrificial polystyrene spheres (PS, a diameter of 530 nm) photonic crystal as a template. The new material exhibited an excellent porous array with featured structural colors in a large area. The electrochromic behavior was explored by combining bandgap and electrochemical characterization. On the one hand, the intercalation/deintercalation of Li+ played an important role in the bandgap (Eg), and thereafter on the visible range transmittance through changing the film’s stoichiometry and the valence of vanadium ions. On the other hand, the asymmetry of the lattice due to the disordered distribution of Li+ within the V2O5 interlayer and/or the formation of an irreversible phase explained the change in transmittance with voltage