New materials hold the key to fundamental advances in energy conversion and storage, both of which are vital in order to meet the challenge of global warming and the finite nature of fossil fuels. Nanomaterials in particular offer unique properties or combinations of properties as electrodes and electrolytes in a range of energy devices. This review describes some recent developments in the discovery of nanoelectrolytes and nanoelectrodes for lithium batteries, fuel cells and supercapacitors. The advantages and disadvantages of the nanoscale in materials design for such devices are highlighted.

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Nanostructured materials for advanced energy conversion and storage devices

Metal hydride materials for solid hydrogen storage: a review

In this chapter, we will restrict our attention to the ferrites and a few other closely related materials. The great interest in ferrites stems from their unique combination of a spontaneous magnetization and a high electrical resistivity. The observed magnetization results from the difference in the magnetizations of two non-equivalent sub-lattices of the magnetic ions in the crystal structure. Materials of this type should strictly be designated as “ferrimagnetic” and in some respects are more closely related to anti-ferromagnetic substances than they are to ferromagnetics in which the magnetization results from the parallel alignment of all the magnetic moments present. We shall not adhere to this special nomenclature except to emphasize effects, which are due to the existence of the sub-lattices.

Ferromagnetic materials

This review focuses on key aspects of the thermal decomposition of multinary or mixed hydride materials, with a particular emphasis on the rational control and chemical tuning of the strategically important thermal decomposition temperature of such hydrides, Tdec. An attempt is also made to predict the thermal stability of as-yet unknown, elusive or even unknown hydrides. The future of a particularly promising class of materials for hydrogen storage, namely the catalytically enhanced complex metal hydrides, is discussed. The predictions are supported by thermodynamics considerations, calculations derived from molecular orbital (MO) theory and backed up by simple chemical insights and intuition.

Thermal decomposition of the non-interstitial hydrides for the storage and production of hydrogen.

The purpose of this study was to investigate the influence of Cu-coating on the spreading kinetics and equilibrium contact angles of aluminum on ceramics using a sessile drop technique. Al2O3 and SiC plates were coated by electroless plating. The copper film overcomes the low wetting of the uncoated samples by dissolution in the drop at 800 °C in argon, showing an intrinsically favorable effect on the adhesion energy. Just after 2 min, the contact angle decreased to 12.6° and 26°for Al/Cu–Al2O3 and Al/Cu–SiC, respectively. However, a de-wetting behavior was observed, reaching equilibrium contact angles of 58.3° and 45.5° for the couples. The dissolution reaction rate at the triple junction was so high that the spreading process was controlled by local diffusion rather than chemical reaction kinetics.

Jean-Louis Bobet

Papers

Improvement in hydrogen sorption properties of Mg by reactive mechanical grinding with Cr2O3, Al2O3 and CeO2

Addition of nanosized Cr2O3 to magnesium for improvement of the hydrogen sorption properties

Production of hydrogen from magnesium hydrides hydrolysis

Hydrogen sorption properties of graphite-modified magnesium nanocomposites prepared by ball-milling

Hydrogen sorption of Mg-based mixtures elaborated by reactive mechanical grinding