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2011 Postgraduate Research Competition - UNSW Science - The ...

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Page |23<br />

WO3 Nanostructured Thin Film Prepared by<br />

Cathodic Electrodeposition and its<br />

Photoelectrochemical Properties<br />

Wai Ling Kwong and Charles C Sorrell<br />

School of Materials <strong>Science</strong> & Engineering<br />

Abstract<br />

Nanostructured tungsten trioxide (WO3) has shown great promise as photoelectrode<br />

material for the application in photoelectrochemical water splitting due to its remarkable<br />

stability in acidic aqueous environment, good electrical conductivity, non-toxicity and a<br />

small band gap of 2.6-3.0 eV, leading to the adsorption of a reasonable fraction of the<br />

electromagnetic spectrum. <strong>The</strong> large specific surface area which provides more active<br />

reaction sites and the absence of the conventional space-charge layer which resulted in<br />

different charge separation in a nanocrystalline WO3 play important role in surpassing its<br />

counter part (planar film) in photoelectrochemical performance. In this study,<br />

nanostructured WO3 thin films were synthesized by cathodic electrodeposition technique<br />

because it offers a cost-effective way to deposit adhesive large-area stoichiometric thin films<br />

on electro-conductive substrates at low-temperature without the need of expensive<br />

instrument. <strong>The</strong> films were potentiostatically deposited from peroxotungstic acid aqueous<br />

solutions and its photoelectrochemical properties were studied. Uniform WO3 nanostructured<br />

thin films were obtained and they demonstrated high crystallinity and optical adsorption<br />

upon annealing. <strong>The</strong> optical, structural and photoelectrochemical properties of<br />

nanostructured WO3 were found to be tailored by varying the concentration of tungsten,<br />

electrolyte pH, deposition potential, temperature and post-annealing.<br />

Electric field-induced transformations in the<br />

lead-free piezoceramic 94%(Bi1/2Na1/2)TiO3-6%BaTiO3<br />

Abstract<br />

Hugh Simons and Mark Hoffman<br />

School of Materials <strong>Science</strong> & Engineering<br />

<strong>The</strong> structural origin of the large electric-field-induced strain in bulk 94%(Bi1/2Na1/2)TiO3-<br />

6%BaTiO3 has been investigated using in-situ neutron diffraction. This material is of particular<br />

interest as a substitute for lead zirconate titanate in high strain actuator applications. <strong>The</strong><br />

unpoled structure shows an unusual combination of near-cubic phases with differing tilting<br />

modes of the oxygen octahedra and a periodic modulation of the atomic positions. An<br />

electric field was applied stepwise to a maximum of 4kV/mm with texture patterns collected<br />

at each field value. It was found that low-magnitute electric fields (

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