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Broader contextGreat efforts are being focused to search for viable electrocatalysts for the water oxidation reaction (WOR) and the hydrogen evolution reaction (HER) which are preferably composed of only earth-abundant-elements. We report herein two novel ternary suldes, cobalt/nickel-tungsten-suldes, as attractive alternatives to platinum electrocatalysts for the HER. These suldes are easily electrodeposited on conducting electrodes from an aqueous solution of readily available precursors. Implementation of these HER electrocatalysts within a water (photo)electrolysis device is feasible and promising.

Photocorrosion, that causes rapid deactivation of Cu(2)O photocatalysts, was addressed by incorporating this oxide in a composite with reduced graphene oxide which acts as an electron acceptor to extract photogenerated electrons from Cu(2)O. Cu(2)O-rGO composite engineering also allows enhancing significantly photocatalytic activities of Cu(2)O for H(2) generation.

Mild-mannered catalyst: a novel procedure to load a MoS(2) co-catalyst onto the surface of silicon under mild-conditions (room temperature, atmospheric pressure, aqueous solution) by a photo-assisted electrodeposition process employing commercially available precursors is reported. The obtained Si-NW@MoS(2) photocathode showed similar catalytic activity for light-driven H(2) generation compared with a Si-NW@Pt photocathode.

Oxygen conduction at low temperatures in apatites make these materials potentially useful as electrolytes in solid-oxide fuel cells, but our understanding of the defect structures enabling ion migration is incomplete. While conduction along [001] channels is dominant, considerable inter-tunnel mobility has been recognized. Using neutron powder diffraction of stoichiometric 'La(10)(GeO(4))(6)O(3)', it has been shown that this compound is more correctly described as an La(10)(GeO(4))(5-)(GeO(5))O(2) apatite, in which high concentrations of interstitial oxygen reside within the channel walls. It is suggested that these framework interstitial O atoms provide a reservoir of ions that can migrate into the conducting channels of apatite, via a mechanism of inter-tunnel oxygen diffusion that transiently converts GeO(4) tetrahedra to GeO(5) distorted trigonal bipyramids. This structural modification is consistent with known crystal chemistry and may occur generally in oxide apatites.

Ultrathin triangular gold nanoframes are synthesized in high yield through selective gold deposition on the edges of triangular silver nanoprisms and subsequent silver etching with mild wet etchants. These ultrathin gold nanoframes are surfactant-free with tailorable ridge thickness from 1.8 to 6 nm and exhibit adjustable and distinct surface plasmon resonance bands in the visible and near-IR region. In comparison, etching of the nanoprism template by galvanic replacement can only create frame structures with much thicker ridges, which have much lower catalytic activity for 4-nitrophenol reduction than the ultrathin gold nanoframes.