No abstract

We report the activation energy determination corresponding to the recombination of the radical cation electron moiety created through photoionization of the 1,6-diphenyl-1,3,5-hexatriene molecule incorporated in ZSM-5 zeolite channels. We demonstrate that the charge separated state stabilization in zeolite does not depend only on the Al content but also on the Al repartition.

International audienceThe evolution of plutonium dioxide surface due to water adsorption seems to influence H-2 generation through the radiolysis of adsorbed water. Surface evolution of ceria, a non-radioactive surrogate for plutonium dioxide, was investigated using Inverse Gas Chromatography (IGC), Raman spectroscopy, Environmental Scanning Electronic Microscopy (ESEM) and Atomic Force Microscopy (AFM). IGC highlights the complexity of ceria surface revealing three different adsorption sites on surface and indicate a surface evolution upon hydration. Thermal treatment appears to regenerate at least partially the initial surface state before hydration. IGC points out the influence of calcination temperature of ceria precursor on surface reactivity. The nature of surface modification was investigated by Raman spectroscopy which suggests formation of superficial hydroxide layer. ESEM and AFM were used to study potential surface topology modification upon superficial layer formation. Cerium hydroxide forms as a superficial layer with a nanostructure differing from the one of the oxide. (C) 2013 Elsevier B.V. All rights reserved

The adsorption of DPH in M6.6ZSM‐5 (M=Na+, K+, Rb+, Cs+), RbFER and RbMOR channel zeolites takes place without chemical or structural modification. After photoexcitation of these systems, a radical cation–electron pair is observed and has a sufficiently long lifetime to be studied by diffuse reflectance UV‐visible spectroscopy. The study of the recombination of this radical cation‐electron pair was carried out at different temperatures and allowed the determination of the activation energy as a function of the nature of the charge‐balancing cation but also of the confinement effect. It appears that the activation energy decreases progressively from Na+ to Cs+ but also when the confinement decreases. To go further, the free enthalpies have been calculated from the Marcus theory demonstrating experimentally that these systems are located in the inverted Marcus region.

No abstract