Recent advances in synchrotron based x-ray spectroscopy enable materials scientists to emanate fingerprints on important materials properties, e.g., electronic, optical, structural, and magnetic properties, in real-time and under nearly real-world conditions. This characterization in combination with optimized materials synthesis routes and tailored morphological properties could contribute greatly to the advances in solid-state electronics and renewable energy technologies. In connection to this, such perspective reflects the current materials research in the space of emerging energy technologies, namely photocatalysis, with a focus on transition metal oxides, mainly on the Fe2O3- and TiO2-based materials.

Soft x-ray scanning transmission x-ray microscope (STXM) spectromicroscopy has been developed and employed to investigate several aspects of actinide chemistry and materials science at the Advanced Light Source Molecular Environmental Science (ALS-MES) Beamline 11.0.2 STXM end station. The basic approach and fundamentals of STXM experiments for radioactive materials systems is discussed. Representative results from STXM spectromicroscopy investigations of a mixed phase uranium nitride, single crystals of Eu(III)[TREN(Me-3,2-HOPO)]3 2H2O and hydrated Pu2(III)(C2O4)3(6H2O) 3H2O complexes are presented. The STXM images and soft x-ray absorption spectra illustrate the capabilities and utility of soft x-ray STXM for providing information about actinide materials, especially the light element constituents. Lastly, new and future opportunities for actinide science utilizing soft x-ray STXM are discussed in light of the planned upgrades for the STXM end stations at the ALS.

Search for novel multi-functional materials, especially multiferroics, which are ferromagnetic above room temperature and at the same time exhibit a ferroelectric behavior much above room temperature, is an active topic of extensive studies today. Ability to address an entity with an external field, laser beam, and also electric potential is a welcome challenge to develop multifunctional devices enabled by nanoscience. While most of the studies to date have been on various forms of Bi- and Ba based Ferrites, rare earth chromites are a new class of materials which appear to show some promise. However in the powder and bulk form these materials are at best canted antiferromagnetics with the magnetic transition temperatures much below room temperature. In this presentation we show that thin films of YbCrO3 deposited by Pulsed Laser Deposition exhibit robust ferromagnetic properties above room temperature. It is indeed a welcome surprise and a challenge to understand the evolution of above room temperature ferromagnetism in such a thin film. The thin films are amorphous in contrast to the powder and bulk forms which are crystalline. The magnetic properties are those of a soft magnet with low coercivity. We present extensive investigations of the magnetic and ferroelectric properties, and spectroscopic studies using XAS techniques to understand the electronic states of the constituent atoms in this novel Chromite. While the amorphous films are ferromagnetic much above room temperature, we show that any observation of ferroelectric property in these films is an artifact of a leaky highly resistive material.

Advanced nano and micro particulate thin films of 3d transition and post-transition metal oxides consisting of nanorods and microrods with parallel and perpendicular orientation with respect to the substrate normal, have been successfully grown onto various substrates by heteronucleation, without template and/or surfactant, from the aqueous condensation of solution of metal salts or metal complexes (aqueous chemical growth). Three-dimensional arrays of iron oxide nanorods and zinc oxide nanorods with parallel and perpendicular orientation are presented as well as the oxygen K-edge polarization dependent x-ray absorption spectroscopy (XAS) study of anisotropic perpendicularly oriented microrod array of ZnO performed at synchrotron radiation source facility.

Large arrays of perpendicularly oriented anisotropic nanoparticles of ferric oxyhydroxide (Akaganeite, β-FeOOH) and oxide (Hematite, α-Fe2O3) of typically 3-5 nm in diameter, self-assembled as bundles of about 50 nm in diameter and of up to 1 μm in length have been successfully grown onto polycrystalline substrates without template and/or surfactant by heteronucleation from an aqueous solution of ferric salts and their optical and electronic properties investigated.