Challenges and prospects about the graphene role in the design of photoelectrodes for sunlight-driven water splitting.

Graphene and its derivatives have emerged as potential materials for several technological applications including sunlight-driven water splitting reactions. This review critically addresses the latest achievements concerning the use of graphene as a player in the design of hybrid-photoelectrodes for photoelectrochemical cells. Insights about the charge carrier dynamics of graphene-based photocatalysts which include metal oxides and non-metal oxide semiconductors are also discussed.

Defect States Control Effective Band Gap and Photochemistry of Graphene Quantum Dots.

Graphene quantum dots (GQDs) have emerged as a new group of quantum-confined semiconductors in recent years, with possible applications as light absorbers, luminescent labels, electrocatalysts, and photoelectrodes for photoelectrochemical water splitting. However, their semiconductor characteristics, such as the effective band gap, majority carrier type, and photochemistry, are obscured by defects in this material. Herein, we use surface photovoltage spectroscopy (SPS) in combination with photoelectrochemical measurements to determine the parameters that are essential to the use of GQDs as next-generation semiconductor devices and photocatalysts.

Surface Photovoltage Measurements on a Particle Tandem Photocatalyst for Overall Water Splitting.

Surface photovoltage spectroscopy (SPS) is used to measure the photopotential across a Ru-SrTiO:Rh/BiVO particle tandem overall water splitting photocatalyst. The tandem is synthesized from Ru-modified SrTiO:Rh nanocrystals and BiVO microcrystals by electrostatic assembly followed by thermal annealing. It splits water into H and O with an apparent quantum efficiency of 1.

Energetic features of copper and lead sorption by innovative aminoalcohol-functionalized cobalt phyllosilicates.

Inorganic-organic cobalt phyllosilicate hybrids were synthesized by the sol-gel procedure under mild non-hydrothermal conditions with a silicon precursor, formed through individual reactions between the silane 3-glycidoxypropyltriethoxysilane and the aminoalcohols ethanol- or diethanolamine. These procedures generated talc-like phyllosilicates containing pendant organic chains with nitrogen and oxygen basic centres located in the interlamellar region. For organofunctionalized phyllosilicates the lamellar structure obtained through the sol-gel method was confirmed by X-ray powder diffraction, while elemental analysis indicated that the densities of the organic groups attached to the new matrices were 3.